{"text_format":"3","workbook":"xlsx","n_sheets":1,"sheets":["Table S1"],"cells_cut":1,"read":"whole","date_system":"1900"}

{"sheet":"Table S1","index":0,"n_rows":90977,"n_cols":38,"rows_kept":2250,"cut":true,"bounds":{"rows_first":1000,"rows_last":250,"rows_between":1000,"halvings":1}}
["Table S1 The open-access mutation data for 983 primary tumor samples of BRCA from TCGA"]
["#version gdc-1.0.0"]
["#filedate 20170515"]
[" #Release Date 20180823"]
["#annotation.spec gdc-1.0.1-public"]
["#n.analyzed.samples 983"]
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["FPGT",8790,"WUGSC","GRCh38","chr1",74205234,74205234,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.1226C>T","ENST00000370898",42829,119,179,"T","ENSG00000254685","ENST00000370898","missense_variant","missense_variant","1254/3254","1226/1824","409/607","S/F","tCt/tTt"]
["CRTC2",200186,"WUGSC","GRCh38","chr1",153954889,153954889,"+","Missense_Mutation","SNP","C","C","T","rs752412661","byFrequency","TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.356G>A","ENST00000368633",42808,105,100,"T","ENSG00000160741","ENST00000368633","missense_variant","missense_variant","484/2644","356/2082","119/693","R/H","cGc/cAc"]
["KIFAP3",22920,"WUGSC","GRCh38","chr1",170035518,170035518,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.553G>A","ENST00000361580",42906,81,139,"T","ENSG00000075945","ENST00000361580","missense_variant","missense_variant","781/2957","553/2379","185/792","E/K","Gaa/Aaa"]
["SLC35F3",148641,"WUGSC","GRCh38","chr1",234316601,234316601,"+","Splice_Site","SNP","G","G","C","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.622-1G>C","ENST00000366617",null,1110,518,"C","ENSG00000183780","ENST00000366617","splice_acceptor_variant","splice_acceptor_variant","-/2762","622/1266","208/421"]
["ZNF35",7584,"WUGSC","GRCh38","chr3",44660194,44660194,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.*247G>A","ENST00000396056",42829,23,17,"A","ENSG00000169981","ENST00000396056","3_prime_UTR_variant","3_prime_UTR_variant","2066/2661","-/1584","-/527"]
["CADPS",8618,"WUGSC","GRCh38","chr3",62592691,62592691,"+","Silent","SNP","C","C","T","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.1383G>A","ENST00000383710",42946,146,244,"T","ENSG00000163618","ENST00000383710","synonymous_variant","synonymous_variant","1733/5471","1383/4062","461/1353","K","aaG/aaA"]
["SLC7A14",57709,"WUGSC","GRCh38","chr3",170483328,170483328,"+","Silent","SNP","G","G","A","rs751620264","byFrequency","TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.1101C>T","ENST00000231706",42894,161,104,"A","ENSG00000013293","ENST00000231706","synonymous_variant","synonymous_variant","1417/10103","1101/2316","367/771","D","gaC/gaT"]
["PCDHGB3",56102,"WUGSC","GRCh38","chr5",141370572,141370572,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.178G>T","ENST00000576222",42739,61,120,"T","ENSG00000262209","ENST00000576222","missense_variant","missense_variant","309/4727","178/2790","60/929","D/Y","Gat/Tat"]
["CMTR1",23070,"WUGSC","GRCh38","chr6",37459672,37459672,"+","Silent","SNP","G","G","A","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.1083G>A","ENST00000373451",43032,553,662,"A","ENSG00000137200","ENST00000373451","synonymous_variant","synonymous_variant","1247/4033","1083/2508","361/835","L","ctG/ctA"]
["MED23",9439,"WUGSC","GRCh38","chr6",131590368,131590368,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.3761C>T","ENST00000368068","27/29",50,139,"A","ENSG00000112282","ENST00000368068","missense_variant","missense_variant","3941/5233","3761/4107","1254/1368","P/L","cCa/cTa"]
["TMEM71",137835,"WUGSC","GRCh38","chr8",132751911,132751911,"+","Missense_Mutation","SNP","C","C","T","rs542588923","by1000G","TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.188G>A","ENST00000356838",42835,430,292,"T","ENSG00000165071","ENST00000356838","missense_variant","missense_variant","331/1993","188/831","63/276","R/Q","cGa/cAa"]
["DOCK8",81704,"WUGSC","GRCh38","chr9",377063,377063,"+","Silent","SNP","C","C","T","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.2292C>T","ENST00000432829","20/48",71,32,"T","ENSG00000107099","ENST00000432829","synonymous_variant","synonymous_variant","2404/7452","2292/6300","764/2099","I","atC/atT"]
["PRUNE2",158471,"WUGSC","GRCh38","chr9",76637483,76637483,"+","Silent","SNP","T","T","C","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.8898A>G","ENST00000376718","14/19",350,248,"C","ENSG00000106772","ENST00000376718","synonymous_variant","synonymous_variant","9022/12584","8898/9267","2966/3088","A","gcA/gcG"]
["VCL",7414,"WUGSC","GRCh38","chr10",74118180,74118180,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.*11G>A","ENST00000211998","22/22",188,205,"A","ENSG00000035403","ENST00000211998","3_prime_UTR_variant","3_prime_UTR_variant","3510/5482","-/3405","-/1134"]
["SSRP1",6749,"WUGSC","GRCh38","chr11",57332396,57332396,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.859C>A","ENST00000278412",42933,297,58,"T","ENSG00000149136","ENST00000278412","missense_variant","missense_variant","1126/2819","859/2130","287/709","L/M","Ctg/Atg"]
["INTS5",80789,"WUGSC","GRCh38","chr11",62647027,62647027,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.3053G>A","ENST00000330574",42768,34,94,"T","ENSG00000185085","ENST00000330574","missense_variant","missense_variant","3106/3285","3053/3060","1018/1019","G/E","gGg/gAg"]
["VWA5A",4013,"WUGSC","GRCh38","chr11",124117459,124117459,"+","Intron","SNP","C","C","G","novel",null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.-15-38C>G","ENST00000392748",null,118,215,"G","ENSG00000110002","ENST00000392748","intron_variant","intron_variant","-/3419","-/2361","-/786"]
["ADAMTS15",170689,"WUGSC","GRCh38","chr11",130473440,130473440,"+","Silent","SNP","C","C","T",null,null,"TCGA-A8-A07J-01A-11W-A019-09","TCGA-A8-A07J-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","c8eac36c-c3a7-4c88-b928-832ab279045b","2dae6992-3060-4e22-9383-698c791cd3b1","c.2472C>T","ENST00000299164",42955,36,38,"T","ENSG00000166106","ENST00000299164","synonymous_variant","synonymous_variant","2472/5673","2472/2853","824/950","S","agC/agT"]
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["ATG2A",23130,"WUGSC","GRCh38","chr11",64892749,64892749,"+","3'Flank","SNP","G","G","C","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613",null,"ENST00000377264",null,46,51,"C","ENSG00000110046","ENST00000377264","downstream_gene_variant","downstream_gene_variant","-/6357","-/5817","-/1938"]
["C11orf71",54494,"WUGSC","GRCh38","chr11",114391560,114391560,"+","3'UTR","SNP","T","T","C","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.*5A>G","ENST00000325636",42768,30,31,"C","ENSG00000180425","ENST00000325636","3_prime_UTR_variant","3_prime_UTR_variant","535/652","-/444","-/147"]
["CKAP4",10970,"WUGSC","GRCh38","chr12",106238093,106238093,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.*931G>C","ENST00000378026",42768,31,28,"G","ENSG00000136026","ENST00000378026","3_prime_UTR_variant","3_prime_UTR_variant","2877/3093","-/1809","-/602"]
["SPTB",6710,"WUGSC","GRCh38","chr14",64753737,64753737,"+","Silent","SNP","C","C","T","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.6402G>A","ENST00000556626","33/36",64,55,"T","ENSG00000070182","ENST00000556626","synonymous_variant","synonymous_variant","6545/10153","6402/6987","2134/2328","Q","caG/caA"]
["CALM1",801,"WUGSC","GRCh38","chr14",90405849,90405849,"+","3'UTR","SNP","G","G","T","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.*1132G>T","ENST00000356978",42892,31,33,"T","ENSG00000198668","ENST00000356978","3_prime_UTR_variant","3_prime_UTR_variant","1830/4242","-/450","-/149"]
["LMF1",64788,"WUGSC","GRCh38","chr16",879647,879647,"+","Missense_Mutation","SNP","C","C","T","rs531415593","by1000G;byCluster","TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.820G>A","ENST00000262301",42897,59,56,"T","ENSG00000103227","ENST00000262301","missense_variant","missense_variant","839/2621","820/1704","274/567","E/K","Gag/Aag"]
["TP53",7157,"WUGSC","GRCh38","chr17",7673802,7673802,"+","Missense_Mutation","SNP","C","C","T","rs28934576","by1000G;byCluster","TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.818G>A","ENST00000269305",42958,45,23,"T","ENSG00000141510","ENST00000269305","missense_variant","missense_variant","1008/2579","818/1182","273/393","R/H","cGt/cAt"]
["SLC13A2",9058,"WUGSC","GRCh38","chr17",28489283,28489283,"+","Missense_Mutation","SNP","G","G","A","rs782617929","byFrequency","TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.172G>A","ENST00000314669",42778,46,41,"A","ENSG00000007216","ENST00000314669","missense_variant","missense_variant","592/2711","172/1779","58/592","V/I","Gtc/Atc"]
["JUP",3728,"WUGSC","GRCh38","chr17",41767460,41767460,"+","Silent","SNP","C","C","T","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.828G>A","ENST00000310706",42870,48,44,"T","ENSG00000173801","ENST00000310706","synonymous_variant","synonymous_variant","947/3200","828/2238","276/745","L","ctG/ctA"]
["INTS2",57508,"WUGSC","GRCh38","chr17",61872339,61872339,"+","Missense_Mutation","SNP","T","T","C","rs558513297","by1000G","TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.2728A>G","ENST00000444766","20/25",109,83,"C","ENSG00000108506","ENST00000444766","missense_variant","missense_variant","2804/5878","2728/3615","910/1204","I/V","Att/Gtt"]
["CHMP6",79643,"WUGSC","GRCh38","chr17",80997341,80997341,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.495G>C","ENST00000325167",42894,47,28,"C","ENSG00000176108","ENST00000325167","missense_variant","missense_variant;splice_region_variant","573/1664","495/606","165/201","Q/H","caG/caC"]
["MUC16",94025,"WUGSC","GRCh38","chr19",8886789,8886789,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.40957C>G","ENST00000397910","59/84",93,94,"C","ENSG00000181143","ENST00000397910","missense_variant","missense_variant","41161/43816","40957/43524","13653/14507","Q/E","Cag/Gag"]
["CYP4F2",8529,"WUGSC","GRCh38","chr19",15878871,15878871,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.1463G>A","ENST00000221700","13/13",167,141,"T","ENSG00000186115","ENST00000221700","missense_variant","missense_variant","1559/2407","1463/1563","488/520","R/H","cGc/cAc"]
["ZNF217",7764,"WUGSC","GRCh38","chr20",53581571,53581571,"+","Missense_Mutation","SNP","G","G","A","rs755258720",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.1256C>T","ENST00000302342",42740,57,27,"A","ENSG00000171940","ENST00000302342","missense_variant","missense_variant","1527/5633","1256/3147","419/1048","T/M","aCg/aTg"]
["ETS2",2114,"WUGSC","GRCh38","chr21",38818580,38818580,"+","Missense_Mutation","SNP","G","G","A","rs116698978","by1000G;byCluster;byFrequency","TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.745G>A","ENST00000360214",42958,44,36,"A","ENSG00000157557","ENST00000360214","missense_variant","missense_variant","1205/3936","745/1410","249/469","V/I","Gtc/Atc"]
["DGCR9",25787,"WUGSC","GRCh38","chr22",19018108,19018108,"+","RNA","SNP","A","A","C","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","n.275A>C","ENST00000609630",42736,81,55,"C","ENSG00000273032","ENST00000609630","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","275/2415"]
["DGCR9",25787,"WUGSC","GRCh38","chr22",19018264,19018264,"+","RNA","SNP","G","G","C","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","n.431G>C","ENST00000609630",42736,77,47,"C","ENSG00000273032","ENST00000609630","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","431/2415"]
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["TRIOBP",11078,"WUGSC","GRCh38","chr22",37725341,37725341,"+","Missense_Mutation","SNP","C","G","G","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.2785C>G","ENST00000406386",42940,17,10,"G","ENSG00000100106","ENST00000406386","missense_variant","missense_variant","3040/10129","2785/7098","929/2365","Q/E","Caa/Gaa"]
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["DCAF8L2",347442,"WUGSC","GRCh38","chrX",27748357,27748357,"+","Missense_Mutation","SNP","G","G","A","rs375048390","by1000G;byCluster","TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.1462G>A","ENST00000451261",42860,128,77,"A","ENSG00000189186","ENST00000451261","missense_variant","missense_variant","1861/2295","1462/1896","488/631","G/S","Ggt/Agt"]
["CLCN5",1184,"WUGSC","GRCh38","chrX",50081728,50081728,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.604G>A","ENST00000307367",42898,135,58,"A","ENSG00000171365","ENST00000307367","missense_variant","missense_variant","895/3177","604/2241","202/746","V/M","Gtg/Atg"]
["CLCN5",1184,"WUGSC","GRCh38","chrX",50092454,50092454,"+","3'UTR","SNP","A","A","T","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.*235A>T","ENST00000307367",43081,216,69,"T","ENSG00000171365","ENST00000307367","3_prime_UTR_variant","3_prime_UTR_variant","2767/3177","-/2241","-/746"]
["CCNB3",85417,"WUGSC","GRCh38","chrX",50311197,50311197,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-LL-A6FR-01A-12D-A31U-09","TCGA-LL-A6FR-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","bfbf8ced-afe1-46bf-80cc-ee16d9cd6f1d","e98bc115-d972-4d48-a210-7b7344030613","c.3028G>A","ENST00000276014",42867,80,21,"A","ENSG00000147082","ENST00000276014","missense_variant","missense_variant","3146/4513","3028/4188","1010/1395","E/K","Gaa/Aaa"]
["ZNF638",27332,"WUGSC","GRCh38","chr2",71427246,71427246,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.5377G>C","ENST00000264447","24/28",110,33,"C","ENSG00000075292","ENST00000264447","missense_variant","missense_variant","5691/6505","5377/5937","1793/1978","E/Q","Gag/Cag"]
["ZNF638",27332,"WUGSC","GRCh38","chr2",71427323,71427323,"+","Silent","SNP","G","G","A","rs777671713",null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.5454G>A","ENST00000264447","24/28",64,21,"A","ENSG00000075292","ENST00000264447","synonymous_variant","synonymous_variant","5768/6505","5454/5937","1818/1978","K","aaG/aaA"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179234297,179234297,"+","Missense_Mutation","SNP","A","A","G","rs121913279","byCluster;byFrequency","TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.3140A>G","ENST00000263967","21/21",83,26,"G","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","3297/9093","3140/3207","1047/1068","H/R","cAt/cGt"]
["ADGRV1",84059,"WUGSC","GRCh38","chr5",90652359,90652359,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.3430C>T","ENST00000405460","19/90",170,61,"T","ENSG00000164199","ENST00000405460","stop_gained","stop_gained","3526/19338","3430/18921","1144/6306","R/*","Cga/Tga"]
["ECT2L",345930,"WUGSC","GRCh38","chr6",138900945,138900945,"+","Splice_Region","SNP","C","C","T","novel",null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.2415-3C>T","ENST00000367682",null,189,55,"T","ENSG00000203734","ENST00000367682","splice_region_variant","splice_region_variant;intron_variant","-/4343","-/2715","-/904"]
["TBC1D4",9882,"WUGSC","GRCh38","chr13",75310065,75310065,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.2470G>A","ENST00000377636","14/21",160,55,"T","ENSG00000136111","ENST00000377636","missense_variant","missense_variant","2817/6364","2470/3897","824/1298","E/K","Gag/Aag"]
["CPNE6",9362,"WUGSC","GRCh38","chr14",24076679,24076679,"+","Intron","SNP","C","C","G","novel",null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.1165+122C>G","ENST00000397016",null,27,9,"G","ENSG00000100884","ENST00000397016","intron_variant","intron_variant","-/2235","-/1674","-/557"]
["ATP10A",57194,"WUGSC","GRCh38","chr15",25721756,25721756,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.1264C>G","ENST00000356865",42937,96,40,"C","ENSG00000206190","ENST00000356865","missense_variant","missense_variant","1376/6680","1264/4500","422/1499","Q/E","Cag/Gag"]
["PRR14",78994,"WUGSC","GRCh38","chr16",30656276,30656276,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.1723G>A","ENST00000300835",43081,31,11,"A","ENSG00000156858","ENST00000300835","missense_variant","missense_variant","2034/2198","1723/1758","575/585","E/K","Gaa/Aaa"]
["CTCF",10664,"WUGSC","GRCh38","chr16",67612031,67612031,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.862C>G","ENST00000264010",42837,76,27,"G","ENSG00000102974","ENST00000264010","missense_variant","missense_variant","1306/3939","862/2184","288/727","H/D","Cac/Gac"]
["DNAH2",146754,"WUGSC","GRCh38","chr17",7805272,7805272,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.9321G>C","ENST00000389173","60/85",102,35,"C","ENSG00000183914","ENST00000389173","missense_variant","missense_variant","9335/13505","9321/13284","3107/4427","K/N","aaG/aaC"]
["MARCH10",162333,"WUGSC","GRCh38","chr17",62788571,62788571,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.119G>A","ENST00000311269",42805,146,56,"T","ENSG00000173838","ENST00000311269","missense_variant","missense_variant","394/3090","119/2427","40/808","R/K","aGa/aAa"]
["SCN4A",6329,"WUGSC","GRCh38","chr17",63941976,63941976,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","c.4306C>G","ENST00000435607","24/24",52,13,"C","ENSG00000007314","ENST00000435607","missense_variant","missense_variant","4383/7805","4306/5511","1436/1836","L/V","Ctg/Gtg"]
["AATK-AS1",388428,"WUGSC","GRCh38","chr17",81179056,81179056,"+","RNA","SNP","G","G","A",null,null,"TCGA-E9-A227-01A-11D-A159-09","TCGA-E9-A227-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","15eb25c4-f4a7-446e-b654-ae39ccd2cf00","1f80b7f1-4b76-4815-9cc7-05318f7fa529","n.548G>A","ENST00000414089",42800,50,25,"A","ENSG00000225180","ENST00000414089","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","548/1577"]
["ABCA4",24,"WUGSC","GRCh38","chr1",94056667,94056667,"+","Silent","SNP","G","G","A",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.2316C>T","ENST00000370225","15/50",58,35,"A","ENSG00000198691","ENST00000370225","synonymous_variant","synonymous_variant","2403/7309","2316/6822","772/2273","L","ctC/ctT"]
["ASH1L",55870,"WUGSC","GRCh38","chr1",155479197,155479197,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.3673C>T","ENST00000368346",42822,105,60,"A","ENSG00000116539","ENST00000368346","missense_variant","missense_variant","4313/11942","3673/8910","1225/2969","H/Y","Cat/Tat"]
["CACYBP",27101,"WUGSC","GRCh38","chr1",175008650,175008650,"+","Silent","SNP","G","G","A","rs771316635",null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.474G>A","ENST00000367679",42861,96,54,"A","ENSG00000116161","ENST00000367679","synonymous_variant","synonymous_variant","922/2766","474/687","158/228","V","gtG/gtA"]
["ATP6V1G3",127124,"WUGSC","GRCh38","chr1",198529110,198529110,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.154G>T","ENST00000281087",42798,113,67,"A","ENSG00000151418","ENST00000281087","missense_variant","missense_variant","260/630","154/357","52/118","D/Y","Gat/Tat"]
["GPAT2",150763,"WUGSC","GRCh38","chr2",96021958,96021958,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.*201C>T","ENST00000359548","22/22",32,13,"A","ENSG00000186281","ENST00000359548","3_prime_UTR_variant","3_prime_UTR_variant","2749/2761","-/2388","-/795"]
["EPB41L5",57669,"WUGSC","GRCh38","chr2",120074162,120074162,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.391C>T","ENST00000263713",42880,128,48,"T","ENSG00000115109","ENST00000263713","missense_variant","missense_variant","605/6628","391/2202","131/733","R/C","Cgt/Tgt"]
["CHN1",1123,"WUGSC","GRCh38","chr2",174878034,174878034,"+","Missense_Mutation","SNP","C","C","T","rs775612525",null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.355G>A","ENST00000409900",42899,129,72,"T","ENSG00000128656","ENST00000409900","missense_variant","missense_variant","669/2447","355/1380","119/459","D/N","Gat/Aat"]
["AQP12A",375318,"WUGSC","GRCh38","chr2",240691975,240691975,"+","Missense_Mutation","SNP","C","C","T","rs145322760","byCluster","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.62C>T","ENST00000337801",42739,54,45,"T","ENSG00000184945","ENST00000337801","missense_variant","missense_variant","131/1084","62/888","21/295","A/V","gCc/gTc"]
["MYLK",4638,"WUGSC","GRCh38","chr3",123739030,123739030,"+","Missense_Mutation","SNP","C","C","T","rs201754358","by1000G;byCluster;byFrequency","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.455G>A","ENST00000360304",12206,38,34,"T","ENSG00000065534","ENST00000360304","missense_variant","missense_variant","641/7738","455/5745","152/1914","R/H","cGt/cAt"]
["SLIT2",9353,"WUGSC","GRCh38","chr4",20617472,20617472,"+","Silent","SNP","G","G","A","rs61746361","by1000G;byCluster;byFrequency","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.4170G>A","ENST00000504154","36/37",76,39,"A","ENSG00000145147","ENST00000504154","synonymous_variant","synonymous_variant","4422/6390","4170/4590","1390/1529","A","gcG/gcA"]
["RFC1",5981,"WUGSC","GRCh38","chr4",39345464,39345464,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.145C>T","ENST00000381897",42819,160,79,"A","ENSG00000035928","ENST00000381897","missense_variant","missense_variant","279/4886","145/3447","49/1148","R/C","Cgt/Tgt"]
["GABRA4",2557,"WUGSC","GRCh38","chr4",46928220,46928220,"+","3'UTR","SNP","C","C","T","rs763689947","byCluster;byFrequency","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.*5G>A","ENST00000264318",42987,35,19,"T","ENSG00000109158","ENST00000264318","3_prime_UTR_variant","3_prime_UTR_variant","2653/11973","-/1665","-/554"]
["CEP120",153241,"WUGSC","GRCh38","chr5",123377388,123377388,"+","Missense_Mutation","SNP","G","G","A","rs774705290",null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.2344C>T","ENST00000306467","16/20",133,69,"A","ENSG00000168944","ENST00000306467","missense_variant","missense_variant","2649/4900","2344/2961","782/986","R/C","Cgc/Tgc"]
["LARS",51520,"WUGSC","GRCh38","chr5",146151866,146151866,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.1421A>T","ENST00000394434","14/32",155,68,"A","ENSG00000133706","ENST00000394434","missense_variant","missense_variant","1588/4766","1421/3531","474/1176","E/V","gAg/gTg"]
["HS3ST5",222537,"WUGSC","GRCh38","chr6",114057712,114057712,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.586G>A","ENST00000312719",42860,139,72,"T","ENSG00000249853","ENST00000312719","missense_variant","missense_variant","1775/3901","586/1041","196/346","V/M","Gtg/Atg"]
["FAM184A",79632,"WUGSC","GRCh38","chr6",118980271,118980271,"+","Missense_Mutation","SNP","G","G","A","rs372303662","by1000G;byCluster","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.2168C>T","ENST00000338891",43026,96,66,"A","ENSG00000111879","ENST00000338891","missense_variant","missense_variant","2612/4141","2168/3423","723/1140","T/M","aCg/aTg"]
["RBAK",57786,"WUGSC","GRCh38","chr7",5063899,5063899,"+","Missense_Mutation","SNP","C","C","T","rs183186992","by1000G;byCluster;byFrequency","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.443C>T","ENST00000353796",42892,85,38,"T","ENSG00000146587","ENST00000353796","missense_variant","missense_variant","767/4125","443/2145","148/714","S/L","tCg/tTg"]
["GPR22",2845,"WUGSC","GRCh38","chr7",107474808,107474808,"+","Missense_Mutation","SNP","C","C","A","rs752096556",null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.748C>A","ENST00000304402",42797,140,43,"A","ENSG00000172209","ENST00000304402","missense_variant","missense_variant","2091/2942","748/1302","250/433","Q/K","Cag/Aag"]
["PIP",5304,"WUGSC","GRCh38","chr7",143132146,143132146,"+","Silent","SNP","C","C","T",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.30C>T","ENST00000291009",42739,46,20,"T","ENSG00000159763","ENST00000291009","synonymous_variant","synonymous_variant","70/585","30/441","10/146","A","gcC/gcT"]
["COL14A1",7373,"WUGSC","GRCh38","chr8",120225087,120225087,"+","Splice_Site","SNP","G","G","A",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.1738-1G>A","ENST00000297848",null,112,50,"A","ENSG00000187955","ENST00000297848","splice_acceptor_variant","splice_acceptor_variant","-/6466","1738/5391","580/1796"]
["PIPSL",266971,"WUGSC","GRCh38","chr10",93960991,93960991,"+","RNA","SNP","C","C","T","rs746789809","byFrequency","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","n.550G>A","ENST00000480546",42736,119,58,"T","ENSG00000180764","ENST00000480546","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","550/3350"]
["ACTN3",89,"WUGSC","GRCh38","chr11",66551584,66551584,"+","Missense_Mutation","SNP","G","G","A","rs765424415","byFrequency","TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.319G>A","ENST00000513398",42815,87,43,"A","ENSG00000248746","ENST00000513398","missense_variant","missense_variant","416/2939","319/2706","107/901","V/I","Gtt/Att"]
["IFNG",3458,"WUGSC","GRCh38","chr12",68157955,68157955,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-A7-A26F-01A-21D-A167-09","TCGA-A7-A26F-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fc73db72-d0ac-48d0-b809-2f7540482ec5","7d94bbca-3e31-4a95-819a-def4981d43e8","c.324C>G","ENST00000229135",42798,138,77,"C","ENSG00000111537","ENST00000229135","missense_variant","missense_variant","456/1218","324/501","108/166","N/K","aaC/aaG"]
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["FAM49A",81553,"WUGSC","GRCh38","chr2",16552743,16552743,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.*193C>G","ENST00000381323",43081,46,110,"C","ENSG00000197872","ENST00000381323","3_prime_UTR_variant","3_prime_UTR_variant","1386/4670","-/972","-/323"]
["HAAO",23498,"WUGSC","GRCh38","chr2",42767327,42767327,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.*110G>T","ENST00000294973",43018,10,37,"A","ENSG00000162882","ENST00000294973","3_prime_UTR_variant","3_prime_UTR_variant","1027/1265","-/861","-/286"]
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["ORC2",4999,"WUGSC","GRCh38","chr2",200911089,200911089,"+","3'UTR","SNP","T","T","C","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.*212A>G","ENST00000234296","18/18",65,101,"C","ENSG00000115942","ENST00000234296","3_prime_UTR_variant","3_prime_UTR_variant","2196/4312","-/1734","-/577"]
["COL4A4",1286,"WUGSC","GRCh38","chr2",227080454,227080454,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.1792C>A","ENST00000396625","24/48",81,141,"T","ENSG00000081052","ENST00000396625","missense_variant","missense_variant","2000/9895","1792/5073","598/1690","P/T","Cca/Aca"]
["BAP1",8314,"WUGSC","GRCh38","chr3",52403147,52403147,"+","Nonsense_Mutation","SNP","G","G","C",null,null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.1881C>G","ENST00000460680","14/17",19,60,"C","ENSG00000163930","ENST00000460680","stop_gained","stop_gained","2353/3937","1881/2190","627/729","Y/*","taC/taG"]
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["PCOLCE2",26577,"WUGSC","GRCh38","chr3",142848334,142848334,"+","Missense_Mutation","SNP","G","G","A","rs751653213","byFrequency","TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.331C>T","ENST00000295992",42803,22,59,"A","ENSG00000163710","ENST00000295992","missense_variant","missense_variant","638/2021","331/1248","111/415","R/W","Cgg/Tgg"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179199690,179199690,"+","Missense_Mutation","SNP","G","G","A","rs587777790",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.353G>A","ENST00000263967",42815,63,128,"A","ENSG00000121879","ENST00000263967","missense_variant","missense_variant;splice_region_variant","510/9093","353/3207","118/1068","G/D","gGt/gAt"]
["LRRC66",339977,"WUGSC","GRCh38","chr4",51995732,51995732,"+","Silent","SNP","T","T","C","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.1290A>G","ENST00000343457",42829,54,130,"C","ENSG00000188993","ENST00000343457","synonymous_variant","synonymous_variant","1297/3327","1290/2643","430/880","E","gaA/gaG"]
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["POLK",51426,"WUGSC","GRCh38","chr5",75581274,75581274,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.760G>A","ENST00000241436",42931,86,159,"A","ENSG00000122008","ENST00000241436","missense_variant","missense_variant","932/5911","760/2613","254/870","E/K","Gaa/Aaa"]
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["GPR6",2830,"WUGSC","GRCh38","chr6",109979133,109979133,"+","Silent","SNP","G","A","A","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.21G>A","ENST00000275169",42736,8,32,"A","ENSG00000146360","ENST00000275169","synonymous_variant","synonymous_variant","21/1089","21/1089","7/362","S","tcG/tcA"]
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["DTX2",113878,"WUGSC","GRCh38","chr7",76482608,76482608,"+","Silent","SNP","C","C","A","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.369C>A","ENST00000324432",42867,78,118,"A","ENSG00000091073","ENST00000324432","synonymous_variant","synonymous_variant","879/2769","369/1869","123/622","A","gcC/gcA"]
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["TRPS1",7227,"WUGSC","GRCh38","chr8",115620046,115620046,"+","Nonsense_Mutation","SNP","T","T","A","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.13A>T","ENST00000220888",42772,55,93,"A","ENSG00000104447","ENST00000220888","stop_gained","stop_gained","173/5480","13/3846","5/1281","K/*","Aag/Tag"]
["PVT1",5820,"WUGSC","GRCh38","chr8",127947523,127947523,"+","Intron","SNP","T","T","A","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","n.540+7847T>A","ENST00000513868",null,31,56,"A","ENSG00000249859","ENST00000513868","intron_variant","intron_variant;non_coding_transcript_variant","-/1699"]
["HSD17B3",3293,"WUGSC","GRCh38","chr9",96249760,96249760,"+","Silent","SNP","G","G","A","novel",null,"TCGA-LL-A9Q3-01A-11D-A41F-09","TCGA-LL-A9Q3-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e1aad5f6-17ae-4170-813d-ec2eee285e75","aae4098d-101f-4990-b52d-b541d34d5200","c.480C>T","ENST00000375263",42897,70,142,"A","ENSG00000130948","ENST00000375263","synonymous_variant","synonymous_variant","528/1135","480/933","160/310","S","tcC/tcT"]
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["RNF213",57674,"WUGSC","GRCh38","chr17",80346921,80346921,"+","Silent","SNP","G","G","A",null,null,"TCGA-A8-A08G-01A-11W-A019-09","TCGA-A8-A08G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8da61928-e935-4a33-8e46-840e637163d7","74a3a4af-c93a-4fcd-af11-1f5eeb847c3c","c.8586G>A","ENST00000582970","29/68",27,23,"A","ENSG00000173821","ENST00000582970","synonymous_variant","synonymous_variant","8729/21055","8586/15624","2862/5207","P","ccG/ccA"]
["SIGLEC10",89790,"WUGSC","GRCh38","chr19",51415250,51415250,"+","Nonsense_Mutation","SNP","C","C","A",null,null,"TCGA-A8-A08G-01A-11W-A019-09","TCGA-A8-A08G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8da61928-e935-4a33-8e46-840e637163d7","74a3a4af-c93a-4fcd-af11-1f5eeb847c3c","c.1261G>T","ENST00000339313",42927,91,85,"A","ENSG00000142512","ENST00000339313","stop_gained","stop_gained","1378/2256","1261/2094","421/697","G/*","Gga/Tga"]
["NLRP5",126206,"WUGSC","GRCh38","chr19",56038140,56038140,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A8-A08G-01A-11W-A019-09","TCGA-A8-A08G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8da61928-e935-4a33-8e46-840e637163d7","74a3a4af-c93a-4fcd-af11-1f5eeb847c3c","c.2731G>T","ENST00000390649",43023,237,176,"T","ENSG00000171487","ENST00000390649","missense_variant","missense_variant","2731/3888","2731/3603","911/1200","V/L","Gta/Tta"]
["ZNF805",390980,"WUGSC","GRCh38","chr19",57253105,57253105,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-A8-A08G-01A-11W-A019-09","TCGA-A8-A08G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8da61928-e935-4a33-8e46-840e637163d7","74a3a4af-c93a-4fcd-af11-1f5eeb847c3c","c.286A>G","ENST00000414468",42829,20,19,"G","ENSG00000204524","ENST00000414468","missense_variant","missense_variant","286/1884","286/1884","96/627","T/A","Acc/Gcc"]
["SNRPB",6628,"WUGSC","GRCh38","chr20",2463874,2463874,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A8-A08G-01A-11W-A019-09","TCGA-A8-A08G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8da61928-e935-4a33-8e46-840e637163d7","74a3a4af-c93a-4fcd-af11-1f5eeb847c3c","c.293C>T","ENST00000438552",42832,361,308,"A","ENSG00000125835","ENST00000438552","missense_variant","missense_variant","456/1008","293/723","98/240","A/V","gCt/gTt"]
["SEMG1",6406,"WUGSC","GRCh38","chr20",45208366,45208366,"+","Nonsense_Mutation","SNP","C","C","T","rs183367221","by1000G;byCluster;byFrequency","TCGA-A8-A08G-01A-11W-A019-09","TCGA-A8-A08G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8da61928-e935-4a33-8e46-840e637163d7","74a3a4af-c93a-4fcd-af11-1f5eeb847c3c","c.1069C>T","ENST00000372781",42769,479,188,"T","ENSG00000124233","ENST00000372781","stop_gained","stop_gained","1126/1662","1069/1389","357/462","R/*","Cga/Tga"]
["BCAS1",8537,"WUGSC","GRCh38","chr20",54028523,54028523,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-A8-A08G-01A-11W-A019-09","TCGA-A8-A08G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8da61928-e935-4a33-8e46-840e637163d7","74a3a4af-c93a-4fcd-af11-1f5eeb847c3c","c.592T>A","ENST00000395961",42837,722,373,"T","ENSG00000064787","ENST00000395961","missense_variant","missense_variant","759/3303","592/1755","198/584","F/I","Ttc/Atc"]
["OR2G3",81469,"WUGSC","GRCh38","chr1",247606019,247606019,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.434C>T","ENST00000320002",42736,623,606,"T","ENSG00000177476","ENST00000320002","missense_variant","missense_variant","434/930","434/930","145/309","A/V","gCa/gTa"]
["OR2T33",391195,"WUGSC","GRCh38","chr1",248273106,248273106,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.709G>T","ENST00000318021",42736,349,345,"A","ENSG00000177212","ENST00000318021","missense_variant","missense_variant","709/963","709/963","237/320","A/S","Gcc/Tcc"]
["PRICKLE2",166336,"WUGSC","GRCh38","chr3",64147388,64147388,"+","Missense_Mutation","SNP","C","C","T","rs544405738",null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.1102G>A","ENST00000295902",42924,85,145,"T","ENSG00000163637","ENST00000295902","missense_variant","missense_variant","1688/8305","1102/2535","368/844","D/N","Gac/Aac"]
["SLC4A4",8671,"WUGSC","GRCh38","chr4",71563793,71563793,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.3100T>C","ENST00000264485","24/26",206,190,"C","ENSG00000080493","ENST00000264485","missense_variant","missense_variant;splice_region_variant","3217/5323","3100/3240","1034/1079","S/P","Tct/Cct"]
["NIM1K",167359,"WUGSC","GRCh38","chr5",43277176,43277176,"+","Missense_Mutation","SNP","G","G","A","rs534141752","by1000G","TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.412G>A","ENST00000326035",42798,282,391,"A","ENSG00000177453","ENST00000326035","missense_variant","missense_variant","1293/2313","412/1311","138/436","E/K","Gaa/Aaa"]
["IL4",3565,"WUGSC","GRCh38","chr5",132682625,132682625,"+","3'UTR","SNP","T","T","A","novel",null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.*38T>A","ENST00000231449",42829,48,38,"A","ENSG00000113520","ENST00000231449","3_prime_UTR_variant","3_prime_UTR_variant","565/616","-/462","-/153"]
["SLC45A4",57210,"WUGSC","GRCh38","chr8",141218632,141218632,"+","Silent","SNP","G","A","A","rs774118130",null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.1008C>T","ENST00000517878",42833,16,34,"A","ENSG00000022567","ENST00000517878","synonymous_variant","synonymous_variant","1008/3470","1008/2427","336/808","H","caC/caT"]
["PTAR1",375743,"WUGSC","GRCh38","chr9",69723368,69723368,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.905T>G","ENST00000340434",42894,350,346,"C","ENSG00000188647","ENST00000340434","missense_variant","missense_variant","909/1417","905/1209","302/402","L/R","cTt/cGt"]
["MCMBP",79892,"WUGSC","GRCh38","chr10",119832072,119832072,"+","Missense_Mutation","SNP","C","C","T","rs745417954",null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.1742G>A","ENST00000360003","15/16",139,125,"T","ENSG00000197771","ENST00000360003","missense_variant","missense_variant","1912/4169","1742/1929","581/642","R/Q","cGg/cAg"]
["RPL13AP20",387841,"WUGSC","GRCh38","chr12",12875910,12875910,"+","RNA","SNP","C","C","T","novel",null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","n.412C>T","ENST00000459725",42736,45,28,"T","ENSG00000234498","ENST00000459725","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","412/609"]
["OVCH1",341350,"WUGSC","GRCh38","chr12",29451475,29451475,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.2625G>A","ENST00000318184","22/28",94,67,"T","ENSG00000187950","ENST00000318184","stop_gained","stop_gained","2625/3405","2625/3405","875/1134","W/*","tgG/tgA"]
["CDH11",1009,"WUGSC","GRCh38","chr16",64998583,64998583,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.502G>A","ENST00000268603",42838,148,306,"T","ENSG00000140937","ENST00000268603","missense_variant","missense_variant","1118/6857","502/2391","168/796","V/M","Gtg/Atg"]
["GSPT2",23708,"WUGSC","GRCh38","chrX",51745257,51745257,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.1631A>C","ENST00000340438",42736,293,291,"C","ENSG00000189369","ENST00000340438","missense_variant","missense_variant","1827/2802","1631/1887","544/628","H/P","cAc/cCc"]
["MAP7D3",79649,"WUGSC","GRCh38","chrX",136219662,136219662,"+","Silent","SNP","G","G","T","novel",null,"TCGA-AO-A0JI-01A-21W-A100-09","TCGA-AO-A0JI-10A-01W-A100-09",null,null,"Somatic","Illumina HiSeq 2000","861297ec-2c88-4717-ae63-eb8e21fe8c52","f1f91ae3-80bd-40ed-b495-d8dd96299105","c.2496C>A","ENST00000316077","17/19",182,217,"T","ENSG00000129680","ENST00000316077","synonymous_variant","synonymous_variant","2717/4567","2496/2631","832/876","S","tcC/tcA"]
["ARHGEF16",27237,"WUGSC","GRCh38","chr1",3467276,3467276,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.743A>G","ENST00000378378",42840,64,46,"G","ENSG00000130762","ENST00000378378","missense_variant","missense_variant","1148/3061","743/2130","248/709","D/G","gAc/gGc"]
["MYOM3",127294,"WUGSC","GRCh38","chr1",24076181,24076181,"+","Silent","SNP","G","G","A","rs528961807","by1000G;byCluster;byFrequency","TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2679C>T","ENST00000374434","21/37",90,99,"A","ENSG00000142661","ENST00000374434","synonymous_variant","synonymous_variant","2842/5804","2679/4314","893/1437","P","ccC/ccT"]
["BCL9",607,"WUGSC","GRCh38","chr1",147624290,147624290,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.3612C>G","ENST00000234739",43018,21,28,"G","ENSG00000116128","ENST00000234739","missense_variant","missense_variant","4352/6278","3612/4281","1204/1426","F/L","ttC/ttG"]
["ANGEL2",90806,"WUGSC","GRCh38","chr1",213000886,213000886,"+","Silent","SNP","C","C","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1161G>T","ENST00000366962",42895,68,300,"A","ENSG00000174606","ENST00000366962","synonymous_variant","synonymous_variant","1316/4649","1161/1635","387/544","R","cgG/cgT"]
["ADCY3",109,"WUGSC","GRCh38","chr2",24824460,24824460,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2654G>A","ENST00000260600","16/21",128,183,"T","ENSG00000138031","ENST00000260600","missense_variant","missense_variant","3506/5050","2654/3435","885/1144","R/Q","cGa/cAa"]
["ARHGEF3",50650,"WUGSC","GRCh38","chr3",56745377,56745377,"+","Missense_Mutation","SNP","C","C","T","rs372602142",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.698G>A","ENST00000296315",42926,108,328,"T","ENSG00000163947","ENST00000296315","missense_variant","missense_variant","867/3602","698/1581","233/526","R/Q","cGa/cAa"]
["CLSTN2",64084,"WUGSC","GRCh38","chr3",140558709,140558709,"+","Silent","SNP","C","C","T","rs187880483","by1000G;byCluster;byFrequency","TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1893C>T","ENST00000458420",43086,52,84,"T","ENSG00000158258","ENST00000458420","synonymous_variant","synonymous_variant","2083/14202","1893/2868","631/955","I","atC/atT"]
["IGSF10",285313,"WUGSC","GRCh38","chr3",151443107,151443107,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.5840C>T","ENST00000282466",42861,165,284,"A","ENSG00000152580","ENST00000282466","missense_variant","missense_variant","5840/11067","5840/7872","1947/2623","S/F","tCc/tTc"]
["TAPT1",202018,"WUGSC","GRCh38","chr4",16176172,16176172,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1054G>A","ENST00000405303",42992,81,385,"T","ENSG00000169762","ENST00000405303","missense_variant","missense_variant","1138/4591","1054/1704","352/567","V/M","Gtg/Atg"]
["ANKRD17",26057,"WUGSC","GRCh38","chr4",73091972,73091972,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.5656C>T","ENST00000358602","29/34",149,301,"A","ENSG00000132466","ENST00000358602","missense_variant","missense_variant","5773/10784","5656/7812","1886/2603","P/S","Cct/Tct"]
["CDS1",1040,"WUGSC","GRCh38","chr4",84604325,84604325,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.200G>C","ENST00000295887",42779,117,371,"C","ENSG00000163624","ENST00000295887","missense_variant","missense_variant","623/4461","200/1386","67/461","R/T","aGa/aCa"]
["MAPK10",5602,"WUGSC","GRCh38","chr4",86107347,86107347,"+","Missense_Mutation","SNP","G","G","A","rs143720396","byCluster","TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.242C>T","ENST00000359221",42869,133,319,"A","ENSG00000109339","ENST00000359221","missense_variant","missense_variant","769/2672","242/1395","81/464","A/V","gCg/gTg"]
["ZNF330",27309,"WUGSC","GRCh38","chr4",141230224,141230224,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.477T>A","ENST00000262990",42926,140,493,"A","ENSG00000109445","ENST00000262990","missense_variant","missense_variant","705/1899","477/963","159/320","F/L","ttT/ttA"]
["LPCAT1",79888,"WUGSC","GRCh38","chr5",1463815,1463815,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1441G>A","ENST00000283415","14/14",207,203,"T","ENSG00000153395","ENST00000283415","missense_variant","missense_variant","1574/3966","1441/1605","481/534","E/K","Gaa/Aaa"]
["CDH18",1016,"WUGSC","GRCh38","chr5",19747146,19747146,"+","Missense_Mutation","SNP","T","T","C","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.319A>G","ENST00000274170",42777,325,431,"C","ENSG00000145526","ENST00000274170","missense_variant","missense_variant","577/2809","319/2373","107/790","T/A","Acg/Gcg"]
["CDH12",1010,"WUGSC","GRCh38","chr5",21755731,21755731,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1745C>T","ENST00000382254","14/15",322,376,"A","ENSG00000154162","ENST00000382254","missense_variant","missense_variant","2832/4164","1745/2385","582/794","T/I","aCa/aTa"]
["BRIX1",55299,"WUGSC","GRCh38","chr5",34925266,34925266,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.833G>C","ENST00000336767",43018,30,92,"C","ENSG00000113460","ENST00000336767","missense_variant","missense_variant","1196/1926","833/1062","278/353","R/T","aGa/aCa"]
["CMYA5",202333,"WUGSC","GRCh38","chr5",79788986,79788986,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.11571C>G","ENST00000446378",43021,81,309,"G","ENSG00000164309","ENST00000446378","missense_variant","missense_variant","11602/12847","11571/12210","3857/4069","I/M","atC/atG"]
["TAF7",6879,"WUGSC","GRCh38","chr5",141319506,141319506,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.539G>C","ENST00000313368",42736,128,324,"G","ENSG00000178913","ENST00000313368","missense_variant","missense_variant","1316/2334","539/1050","180/349","R/P","cGg/cCg"]
["PCDHGA1",56114,"WUGSC","GRCh38","chr5",141332046,141332046,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1362G>T","ENST00000517417",42739,106,358,"T","ENSG00000204956","ENST00000517417","missense_variant","missense_variant","1362/4604","1362/2796","454/931","Q/H","caG/caT"]
["PCDHGA7",56108,"WUGSC","GRCh38","chr5",141384729,141384729,"+","Silent","SNP","G","G","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1830G>A","ENST00000518325",42739,39,60,"A","ENSG00000253537","ENST00000518325","synonymous_variant","synonymous_variant","1830/4605","1830/2799","610/932","K","aaG/aaA"]
["SYNGAP1",8831,"WUGSC","GRCh38","chr6",33442942,33442942,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2390C>T","ENST00000629380","15/19",39,42,"T","ENSG00000197283","ENST00000629380","missense_variant","missense_variant","2585/9862","2390/4032","797/1343","P/L","cCa/cTa"]
["RIMS1",22999,"WUGSC","GRCh38","chr6",72179861,72179861,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.758G>A","ENST00000521978",12540,43,67,"A","ENSG00000079841","ENST00000521978","missense_variant","missense_variant","758/5079","758/5079","253/1692","G/E","gGg/gAg"]
["COL12A1",1303,"WUGSC","GRCh38","chr6",75183374,75183374,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1567A>C","ENST00000322507",24381,77,199,"G","ENSG00000111799","ENST00000322507","missense_variant","missense_variant","1877/11723","1567/9192","523/3063","M/L","Atg/Ctg"]
["SENP6",26054,"WUGSC","GRCh38","chr6",75695863,75695863,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2135C>G","ENST00000447266","17/24",56,132,"G","ENSG00000112701","ENST00000447266","missense_variant","missense_variant","2613/6501","2135/3339","712/1112","S/C","tCt/tGt"]
["CEP162",22832,"WUGSC","GRCh38","chr6",84126387,84126387,"+","Missense_Mutation","SNP","T","T","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.3996A>T","ENST00000403245","26/27",258,880,"A","ENSG00000135315","ENST00000403245","missense_variant","missense_variant","4111/5156","3996/4212","1332/1403","E/D","gaA/gaT"]
["CDK19",23097,"WUGSC","GRCh38","chr6",110627074,110627074,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.718G>A","ENST00000368911",42929,135,422,"T","ENSG00000155111","ENST00000368911","missense_variant","missense_variant","898/6246","718/1509","240/502","D/N","Gat/Aat"]
["RFX6",222546,"WUGSC","GRCh38","chr6",116931372,116931372,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2653T>C","ENST00000332958","19/19",139,375,"C","ENSG00000185002","ENST00000332958","missense_variant","missense_variant","2669/3460","2653/2787","885/928","C/R","Tgt/Cgt"]
["DYNC1I1",1780,"WUGSC","GRCh38","chr7",96039361,96039361,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1500C>A","ENST00000324972","14/17",94,168,"A","ENSG00000158560","ENST00000324972","missense_variant","missense_variant","1693/2950","1500/1938","500/645","D/E","gaC/gaA"]
["TRBV4-2",28616,"WUGSC","GRCh38","chr7",142345874,142345874,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.233G>C","ENST00000390392",42768,226,401,"C","ENSG00000211745","ENST00000390392","missense_variant","missense_variant","344/455","233/344","78/114","S/T","aGt/aCt"]
["ZNF282",8427,"WUGSC","GRCh38","chr7",149198588,149198588,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.421G>A","ENST00000610704",42774,55,64,"A","ENSG00000170265","ENST00000610704","missense_variant","missense_variant","526/3722","421/2016","141/671","V/M","Gtg/Atg"]
["PRDM14",63978,"WUGSC","GRCh38","chr8",70068254,70068254,"+","Silent","SNP","G","G","A","rs191871733","by1000G;byCluster;byFrequency","TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.888C>T","ENST00000276594",42833,214,428,"A","ENSG00000147596","ENST00000276594","synonymous_variant","synonymous_variant","1090/2344","888/1716","296/571","Y","taC/taT"]
["LACTB2",51110,"WUGSC","GRCh38","chr8",70669080,70669080,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.41G>C","ENST00000276590",42742,21,24,"G","ENSG00000147592","ENST00000276590","missense_variant","missense_variant","78/1508","41/867","14/288","R/P","cGa/cCa"]
["OSR2",116039,"WUGSC","GRCh38","chr8",98951523,98951523,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.761C>T","ENST00000297565",42829,46,101,"T","ENSG00000164920","ENST00000297565","missense_variant","missense_variant","1257/1838","761/939","254/312","S/F","tCt/tTt"]
["TRPM6",140803,"WUGSC","GRCh38","chr9",74840162,74840162,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.406C>T","ENST00000360774",14366,103,337,"A","ENSG00000119121","ENST00000360774","missense_variant","missense_variant","644/8425","406/6069","136/2022","P/S","Ccc/Tcc"]
["KIF27",55582,"WUGSC","GRCh38","chr9",83853635,83853635,"+","Silent","SNP","G","G","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.3351C>T","ENST00000297814","15/18",23,143,"A","ENSG00000165115","ENST00000297814","synonymous_variant","synonymous_variant","3495/4653","3351/4206","1117/1401","F","ttC/ttT"]
["ARID5B",84159,"WUGSC","GRCh38","chr10",61902302,61902302,"+","Silent","SNP","G","G","C",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.165G>C","ENST00000279873",42776,88,214,"C","ENSG00000150347","ENST00000279873","synonymous_variant","synonymous_variant","575/7891","165/3567","55/1188","A","gcG/gcC"]
["C10orf99",387695,"WUGSC","GRCh38","chr10",84173831,84173831,"+","5'UTR","SNP","G","G","A","rs761101365","byFrequency","TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.-21G>A","ENST00000372126",42738,239,437,"A","ENSG00000188373","ENST00000372126","5_prime_UTR_variant","5_prime_UTR_variant","94/888","-/246","-/81"]
["C10orf2",56652,"WUGSC","GRCh38","chr10",100993593,100993593,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.*83G>A","ENST00000311916",42860,13,24,"A","ENSG00000107815","ENST00000311916","3_prime_UTR_variant","3_prime_UTR_variant","2323/3131","-/2055","-/684"]
["RAG1",5896,"WUGSC","GRCh38","chr11",36575903,36575903,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2599G>A","ENST00000299440",42768,139,181,"A","ENSG00000166349","ENST00000299440","missense_variant","missense_variant","2711/6564","2599/3132","867/1043","D/N","Gat/Aat"]
["ANAPC5",51433,"WUGSC","GRCh38","chr12",121309773,121309773,"+","Missense_Mutation","SNP","G","G","A","rs778284423","byFrequency","TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1984C>T","ENST00000261819","16/17",33,56,"A","ENSG00000089053","ENST00000261819","missense_variant","missense_variant","2106/2513","1984/2268","662/755","R/C","Cgt/Tgt"]
["BRCA2",675,"WUGSC","GRCh38","chr13",32346895,32346895,"+","Missense_Mutation","SNP","C","C","T","rs431825347","byCluster","TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.7006C>T","ENST00000380152","13/27",129,468,"T","ENSG00000139618","ENST00000380152","missense_variant","missense_variant;splice_region_variant","7239/11986","7006/10257","2336/3418","R/C","Cgc/Tgc"]
["MYH7",4625,"WUGSC","GRCh38","chr14",23424961,23424961,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2487G>T","ENST00000355349","22/40",92,263,"A","ENSG00000092054","ENST00000355349","missense_variant","missense_variant","2650/6087","2487/5808","829/1935","W/C","tgG/tgT"]
["PRKD1",5587,"WUGSC","GRCh38","chr14",29626526,29626526,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1756G>C","ENST00000331968",43087,39,193,"G","ENSG00000184304","ENST00000331968","missense_variant","missense_variant","1986/3726","1756/2739","586/912","D/H","Gat/Cat"]
["IGHG1",3500,"WUGSC","GRCh38","chr14",106062274,106062274,"+","Intron","SNP","C","C","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.268-43G>T","ENST00000618756",null,239,519,"A","ENSG00000211896","ENST00000618756","intron_variant","intron_variant","-/1639","-/1428","-/475"]
["DUOX2",50506,"WUGSC","GRCh38","chr15",45100775,45100775,"+","Silent","SNP","C","C","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.2985G>C","ENST00000603300","23/34",108,367,"G","ENSG00000140279","ENST00000603300","synonymous_variant","synonymous_variant","3188/6345","2985/4647","995/1548","L","ctG/ctC"]
["DMXL2",23312,"WUGSC","GRCh38","chr15",51474588,51474588,"+","Silent","SNP","C","C","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.6966G>C","ENST00000251076","28/43",66,225,"G","ENSG00000104093","ENST00000251076","synonymous_variant","synonymous_variant","7254/10672","6966/9111","2322/3036","V","gtG/gtC"]
["TSR3",115939,"WUGSC","GRCh38","chr16",1350124,1350124,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.637G>A","ENST00000007390",42831,61,60,"T","ENSG00000007520","ENST00000007390","missense_variant","missense_variant","744/1243","637/939","213/312","E/K","Gag/Aag"]
["PDXDC1",23042,"WUGSC","GRCh38","chr16",15018882,15018882,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1006C>T","ENST00000396410",43092,504,1225,"T","ENSG00000179889","ENST00000396410","missense_variant","missense_variant","1103/4521","1006/2367","336/788","L/F","Ctc/Ttc"]
["PSMD7",5713,"WUGSC","GRCh38","chr16",74300188,74300188,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.148G>A","ENST00000219313",42773,169,331,"A","ENSG00000103035","ENST00000219313","missense_variant","missense_variant","288/1670","148/975","50/324","V/I","Gta/Ata"]
["TP53",7157,"WUGSC","GRCh38","chr17",7673812,7673812,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.808T>A","ENST00000269305",42958,77,160,"T","ENSG00000141510","ENST00000269305","missense_variant","missense_variant","998/2579","808/1182","270/393","F/I","Ttt/Att"]
["MPP2",4355,"WUGSC","GRCh38","chr17",43883202,43883202,"+","Splice_Site","SNP","C","C","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.375+1G>T","ENST00000461854",null,34,25,"A","ENSG00000108852","ENST00000461854","splice_donor_variant","splice_donor_variant","-/3462","375/1731","125/576"]
["USP32",84669,"WUGSC","GRCh38","chr17",60198421,60198421,"+","Silent","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.3273G>A","ENST00000300896","27/34",162,449,"T","ENSG00000170832","ENST00000300896","synonymous_variant","synonymous_variant","3468/5171","3273/4815","1091/1604","L","ctG/ctA"]
["SCN4A",6329,"WUGSC","GRCh38","chr17",63966535,63966535,"+","Missense_Mutation","SNP","T","T","C","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1046A>G","ENST00000435607",42940,80,124,"C","ENSG00000007314","ENST00000435607","missense_variant","missense_variant","1123/7805","1046/5511","349/1836","Y/C","tAc/tGc"]
["MC5R",4161,"WUGSC","GRCh38","chr18",13826449,13826449,"+","Silent","SNP","G","G","A",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.684G>A","ENST00000324750",42736,147,186,"A","ENSG00000176136","ENST00000324750","synonymous_variant","synonymous_variant","906/1200","684/978","228/325","A","gcG/gcA"]
["OR7C1",26664,"WUGSC","GRCh38","chr19",14799396,14799396,"+","Silent","SNP","C","C","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.741G>T","ENST00000248073",42736,76,215,"A","ENSG00000127530","ENST00000248073","synonymous_variant","synonymous_variant","816/1066","741/963","247/320","V","gtG/gtT"]
["ZNF675",171392,"WUGSC","GRCh38","chr19",23653978,23653978,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.955A>C","ENST00000359788",42829,46,207,"G","ENSG00000197372","ENST00000359788","missense_variant","missense_variant","1124/2301","955/1707","319/568","K/Q","Aag/Cag"]
["ZNF420",147923,"WUGSC","GRCh38","chr19",37128278,37128278,"+","Missense_Mutation","SNP","T","T","A","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1287T>A","ENST00000337995",42860,129,273,"A","ENSG00000197050","ENST00000337995","missense_variant","missense_variant","1502/3535","1287/2067","429/688","N/K","aaT/aaA"]
["ACTN4",81,"WUGSC","GRCh38","chr19",38717993,38717993,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.1210G>C","ENST00000252699",43060,63,75,"C","ENSG00000130402","ENST00000252699","missense_variant","missense_variant","1286/4963","1210/2736","404/911","E/Q","Gag/Cag"]
["CYP2A13",1553,"WUGSC","GRCh38","chr19",41088972,41088972,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.224C>T","ENST00000330436",42775,139,144,"T","ENSG00000197838","ENST00000330436","missense_variant","missense_variant","224/1739","224/1485","75/494","P/L","cCc/cTc"]
["ZNF582",147948,"WUGSC","GRCh38","chr19",56384722,56384722,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.695G>A","ENST00000301310",42860,81,232,"T","ENSG00000018869","ENST00000301310","missense_variant","missense_variant","854/2824","695/1554","232/517","C/Y","tGt/tAt"]
["PDRG1",81572,"WUGSC","GRCh38","chr20",31946505,31946505,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.310G>C","ENST00000202017",42830,217,291,"G","ENSG00000088356","ENST00000202017","missense_variant","missense_variant","441/1998","310/402","104/133","E/Q","Gag/Cag"]
["PKDREJ",10343,"WUGSC","GRCh38","chr22",46258823,46258823,"+","Silent","SNP","A","A","C",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.4500T>G","ENST00000253255",42736,221,427,"C","ENSG00000130943","ENST00000253255","synonymous_variant","synonymous_variant","4533/7693","4500/6762","1500/2253","P","ccT/ccG"]
["TAF1",6872,"WUGSC","GRCh38","chrX",71398615,71398615,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.3661C>T","ENST00000373790","24/38",225,539,"T","ENSG00000147133","ENST00000373790","stop_gained","stop_gained","3712/7629","3661/5619","1221/1872","R/*","Cga/Tga"]
["DOCK11",139818,"WUGSC","GRCh38","chrX",118545370,118545370,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.440A>T","ENST00000276202",19480,89,325,"T","ENSG00000147251","ENST00000276202","missense_variant","missense_variant","503/6625","440/6222","147/2073","D/V","gAt/gTt"]
["CMC4",100272147,"WUGSC","GRCh38","chrX",155061898,155061898,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-AR-A1AI-01A-11D-A12Q-09","TCGA-AR-A1AI-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","842846ea-881c-4d79-88d2-fc1703c58350","e1aef6e6-ad91-48f0-8d2e-52c680cd81f8","c.152C>A","ENST00000369479",42797,113,415,"T","ENSG00000182712","ENST00000369479","stop_gained","stop_gained","594/864","152/207","51/68","S/*","tCa/tAa"]
["TNFRSF8",943,"WUGSC","GRCh38","chr1",12115690,12115690,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.907T>A","ENST00000263932",42962,46,45,"A","ENSG00000120949","ENST00000263932","missense_variant","missense_variant","1129/3686","907/1788","303/595","Y/N","Tac/Aac"]
["AADACL4",343066,"WUGSC","GRCh38","chr1",12644556,12644556,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.10C>T","ENST00000376221",42739,88,103,"T","ENSG00000204518","ENST00000376221","missense_variant","missense_variant","10/1575","10/1224","4/407","P/S","Ccc/Tcc"]
["ZYG11B",79699,"WUGSC","GRCh38","chr1",52801896,52801896,"+","Silent","SNP","T","T","A",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1563T>A","ENST00000294353",42992,61,86,"A","ENSG00000162378","ENST00000294353","synonymous_variant","synonymous_variant","1708/8093","1563/2235","521/744","L","ctT/ctA"]
["KIAA1107",23285,"WUGSC","GRCh38","chr1",92182043,92182043,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.3046G>C","ENST00000370378",42956,37,71,"C","ENSG00000069712","ENST00000370378","missense_variant","missense_variant","3144/4556","3046/4065","1016/1354","E/Q","Gaa/Caa"]
["RPTN",126638,"WUGSC","GRCh38","chr1",152155566,152155566,"+","Silent","SNP","A","A","G",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1533T>C","ENST00000316073",42797,462,313,"G","ENSG00000215853","ENST00000316073","synonymous_variant","synonymous_variant","1598/3569","1533/2355","511/784","Y","taT/taC"]
["INSRR",3645,"WUGSC","GRCh38","chr1",156843011,156843011,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.3119A>T","ENST00000368195","17/22",38,32,"A","ENSG00000027644","ENST00000368195","missense_variant","missense_variant","3516/5101","3119/3894","1040/1297","H/L","cAc/cTc"]
["KIFAP3",22920,"WUGSC","GRCh38","chr1",170038428,170038428,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.379G>A","ENST00000361580",42875,52,54,"T","ENSG00000075945","ENST00000361580","missense_variant","missense_variant","607/2957","379/2379","127/792","D/N","Gat/Aat"]
["SLC5A6",8884,"WUGSC","GRCh38","chr2",27202857,27202857,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1231C>G","ENST00000310574",43086,41,50,"C","ENSG00000138074","ENST00000310574","missense_variant","missense_variant","1705/3231","1231/1908","411/635","L/V","Cta/Gta"]
["SPAST",6683,"WUGSC","GRCh38","chr2",32136885,32136885,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1330G>T","ENST00000315285",43056,94,96,"T","ENSG00000021574","ENST00000315285","missense_variant","missense_variant","1455/5117","1330/1851","444/616","D/Y","Gat/Tat"]
["NEB",4703,"WUGSC","GRCh38","chr2",151724344,151724344,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.528G>A","ENST00000172853","8/149",93,90,"T","ENSG00000183091","ENST00000172853","stop_gained","stop_gained","731/20634","528/20010","176/6669","W/*","tgG/tgA"]
["EPHA3",2042,"WUGSC","GRCh38","chr3",89472485,89472485,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.2712C>G","ENST00000336596","16/17",58,52,"G","ENSG00000044524","ENST00000336596","missense_variant","missense_variant","2937/5809","2712/2952","904/983","D/E","gaC/gaG"]
["TFG",10342,"WUGSC","GRCh38","chr3",100748493,100748493,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1165G>T","ENST00000240851",42955,21,31,"T","ENSG00000114354","ENST00000240851","missense_variant","missense_variant","1505/1978","1165/1203","389/400","G/C","Ggt/Tgt"]
["PSMD2",5708,"WUGSC","GRCh38","chr3",184300388,184300388,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.301C>G","ENST00000310118",42815,46,36,"G","ENSG00000175166","ENST00000310118","missense_variant","missense_variant","859/3449","301/2727","101/908","P/A","Cca/Gca"]
["CHRNA9",55584,"WUGSC","GRCh38","chr4",40335840,40335840,"+","Silent","SNP","A","A","C","novel",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.78A>C","ENST00000310169",42771,65,77,"C","ENSG00000174343","ENST00000310169","synonymous_variant","synonymous_variant","217/2276","78/1440","26/479","A","gcA/gcC"]
["PDGFRA",5156,"WUGSC","GRCh38","chr4",54264083,54264083,"+","Intron","SNP","A","A","G","novel",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.628+156A>G","ENST00000257290",null,11,9,"G","ENSG00000134853","ENST00000257290","intron_variant","intron_variant","-/6576","-/3270","-/1089"]
["OSTC",58505,"WUGSC","GRCh38","chr4",108650654,108650654,"+","5'UTR","SNP","A","A","G","novel",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.-2A>G","ENST00000361564",42739,46,29,"G","ENSG00000198856","ENST00000361564","5_prime_UTR_variant","5_prime_UTR_variant","71/1077","-/450","-/149"]
["EXOSC9",5393,"WUGSC","GRCh38","chr4",121816435,121816435,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1223C>G","ENST00000243498",43051,55,58,"G","ENSG00000123737","ENST00000243498","missense_variant","missense_variant","1331/1481","1223/1320","408/439","P/R","cCa/cGa"]
["C4orf47",441054,"WUGSC","GRCh38","chr4",185449610,185449610,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.896A>G","ENST00000378850",42923,102,76,"G","ENSG00000205129","ENST00000378850","missense_variant","missense_variant","918/1134","896/930","299/309","K/R","aAg/aGg"]
["ITGA1",3672,"WUGSC","GRCh38","chr5",52944956,52944956,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.3299G>C","ENST00000282588","27/29",50,79,"C","ENSG00000213949","ENST00000282588","missense_variant","missense_variant","3757/10757","3299/3540","1100/1179","S/T","aGc/aCc"]
["FBXL17",64839,"WUGSC","GRCh38","chr5",107881123,107881123,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1879T>C","ENST00000542267",42956,58,77,"G","ENSG00000145743","ENST00000542267","missense_variant","missense_variant","2286/5188","1879/2106","627/701","C/R","Tgt/Cgt"]
["PCDHGA7",56108,"WUGSC","GRCh38","chr5",141385052,141385052,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.2153G>A","ENST00000518325",42739,60,36,"A","ENSG00000253537","ENST00000518325","missense_variant","missense_variant","2153/4605","2153/2799","718/932","R/H","cGc/cAc"]
["GFPT2",9945,"WUGSC","GRCh38","chr5",180318913,180318913,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.838G>A","ENST00000253778",43027,27,27,"T","ENSG00000131459","ENST00000253778","missense_variant","missense_variant","1008/3093","838/2049","280/682","D/N","Gat/Aat"]
["HLA-J",3137,"WUGSC","GRCh38","chr6",30007014,30007014,"+","RNA","SNP","G","G","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","n.298G>C","ENST00000462773",42772,52,58,"C","ENSG00000204622","ENST00000462773","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","298/1306"]
["ADGRB3",577,"WUGSC","GRCh38","chr6",69048262,69048262,"+","Missense_Mutation","SNP","G","G","T","rs757620134","byFrequency","TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.2185G>T","ENST00000370598","14/32",47,44,"T","ENSG00000135298","ENST00000370598","missense_variant","missense_variant","3006/6010","2185/4569","729/1522","V/F","Gtt/Ttt"]
["ADGRB3",577,"WUGSC","GRCh38","chr6",69048267,69048267,"+","Silent","SNP","C","C","T","novel",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.2190C>T","ENST00000370598","14/32",45,45,"T","ENSG00000135298","ENST00000370598","synonymous_variant","synonymous_variant","3011/6010","2190/4569","730/1522","D","gaC/gaT"]
["VWDE",221806,"WUGSC","GRCh38","chr7",12351651,12351651,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.3808A>G","ENST00000275358","19/29",111,118,"C","ENSG00000146530","ENST00000275358","missense_variant","missense_variant","3997/5260","3808/4773","1270/1590","S/G","Agt/Ggt"]
["SBSPON",157869,"WUGSC","GRCh38","chr8",73069925,73069925,"+","Nonsense_Mutation","SNP","C","C","T","rs767631429",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.557G>A","ENST00000297354",42830,99,62,"T","ENSG00000164764","ENST00000297354","stop_gained","stop_gained","762/3801","557/795","186/264","W/*","tGg/tAg"]
["ASAP1",50807,"WUGSC","GRCh38","chr8",130214558,130214558,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.403C>G","ENST00000518721",42885,110,79,"C","ENSG00000153317","ENST00000518721","missense_variant","missense_variant;splice_region_variant","631/5507","403/3390","135/1129","L/V","Ctg/Gtg"]
["GLDC",2731,"WUGSC","GRCh38","chr9",6605176,6605176,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.816G>C","ENST00000321612",42911,37,67,"G","ENSG00000178445","ENST00000321612","missense_variant","missense_variant","967/3767","816/3063","272/1020","K/N","aaG/aaC"]
["TLR4",7099,"WUGSC","GRCh38","chr9",117712772,117712772,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.644T>C","ENST00000355622",42797,41,43,"C","ENSG00000136869","ENST00000355622","missense_variant","missense_variant","745/4844","644/2520","215/839","M/T","aTg/aCg"]
["TLR4",7099,"WUGSC","GRCh38","chr9",117713566,117713566,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1438G>T","ENST00000355622",42797,38,33,"T","ENSG00000136869","ENST00000355622","missense_variant","missense_variant","1539/4844","1438/2520","480/839","G/C","Ggc/Tgc"]
["SH3GLB2",56904,"WUGSC","GRCh38","chr9",129009851,129009851,"+","Silent","SNP","G","G","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.759C>A","ENST00000372559",42990,41,31,"T","ENSG00000148341","ENST00000372559","synonymous_variant","synonymous_variant","819/1365","759/1188","253/395","L","ctC/ctA"]
["ITIH5",80760,"WUGSC","GRCh38","chr10",7563229,7563229,"+","Missense_Mutation","SNP","T","T","A","novel",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.2683A>T","ENST00000397146","14/14",78,71,"A","ENSG00000123243","ENST00000397146","missense_variant","missense_variant","2762/6721","2683/2829","895/942","I/F","Att/Ttt"]
["VPS11",55823,"WUGSC","GRCh38","chr11",119078264,119078264,"+","Missense_Mutation","SNP","C","C","T","rs781917185",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.221C>T","ENST00000620429",42993,39,31,"T","ENSG00000160695","ENST00000620429","missense_variant","missense_variant","1426/2739","221/1455","74/484","S/L","tCa/tTa"]
["KCNA6",3742,"WUGSC","GRCh38","chr12",4810837,4810837,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.796G>T","ENST00000280684",42736,38,20,"T","ENSG00000151079","ENST00000280684","missense_variant","missense_variant","1662/4237","796/1590","266/529","V/L","Gtg/Ttg"]
["IRAK4",51135,"WUGSC","GRCh38","chr12",43786813,43786813,"+","3'UTR","SNP","A","A","T","novel",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.*98A>T","ENST00000551736","13/13",21,27,"T","ENSG00000198001","ENST00000551736","3_prime_UTR_variant","3_prime_UTR_variant","1594/1684","-/1383","-/460"]
["AGAP2",116986,"WUGSC","GRCh38","chr12",57734670,57734670,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1237G>A","ENST00000547588",42813,36,38,"T","ENSG00000135439","ENST00000547588","missense_variant","missense_variant","1237/3579","1237/3579","413/1192","G/S","Ggc/Agc"]
["TXNRD1",7296,"WUGSC","GRCh38","chr12",104319557,104319557,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.961C>T","ENST00000525566",42995,33,38,"T","ENSG00000198431","ENST00000525566","missense_variant","missense_variant","985/3836","961/1950","321/649","P/S","Cct/Tct"]
["ADAL",161823,"WUGSC","GRCh38","chr15",43351929,43351929,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1052G>C","ENST00000562188",43018,49,48,"C","ENSG00000168803","ENST00000562188","missense_variant","missense_variant","1068/1228","1052/1068","351/355","R/T","aGa/aCa"]
["FBN1",2200,"WUGSC","GRCh38","chr15",48474591,48474591,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.4024A>G","ENST00000316623","33/66",92,91,"C","ENSG00000166147","ENST00000316623","missense_variant","missense_variant","4480/11756","4024/8616","1342/2871","T/A","Aca/Gca"]
["ADCY7",113,"WUGSC","GRCh38","chr16",50294746,50294746,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.943G>A","ENST00000254235",42911,31,33,"A","ENSG00000121281","ENST00000254235","missense_variant","missense_variant","1211/6138","943/3243","315/1080","A/T","Gcc/Acc"]
["RHOT1",55288,"WUGSC","GRCh38","chr17",32209514,32209514,"+","Intron","SNP","C","C","G","novel",null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1739+1205C>G","ENST00000333942",null,26,17,"G","ENSG00000126858","ENST00000333942","intron_variant","intron_variant","-/3133","-/1857","-/618"]
["PTRF",284119,"WUGSC","GRCh38","chr17",42405196,42405196,"+","Nonsense_Mutation","SNP","T","T","A",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.664A>T","ENST00000357037",42768,68,35,"A","ENSG00000177469","ENST00000357037","stop_gained","stop_gained","1084/3828","664/1173","222/390","K/*","Aag/Tag"]
["LAMA1",284217,"WUGSC","GRCh38","chr18",7011428,7011428,"+","Silent","SNP","A","A","G","rs141269552","by1000G;byCluster;byFrequency","TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.3559T>C","ENST00000389658","25/63",16,22,"G","ENSG00000101680","ENST00000389658","synonymous_variant","synonymous_variant","3653/9657","3559/9228","1187/3075","L","Ttg/Ctg"]
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["WIZ",58525,"WUGSC","GRCh38","chr19",15425641,15425641,"+","Silent","SNP","G","G","C",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1209C>G","ENST00000263381",42863,23,23,"C","ENSG00000011451","ENST00000263381","synonymous_variant","synonymous_variant","1423/5695","1209/2385","403/794","V","gtC/gtG"]
["SLC5A5",6528,"WUGSC","GRCh38","chr19",17877840,17877840,"+","Silent","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.816C>T","ENST00000222248",42901,79,69,"T","ENSG00000105641","ENST00000222248","synonymous_variant","synonymous_variant","1163/3576","816/1932","272/643","C","tgC/tgT"]
["AKT2",208,"WUGSC","GRCh38","chr19",40236066,40236066,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.999G>A","ENST00000392038",43053,62,58,"T","ENSG00000105221","ENST00000392038","stop_gained","stop_gained","1298/5300","999/1446","333/481","W/*","tgG/tgA"]
["PRX",57716,"WUGSC","GRCh38","chr19",40396375,40396375,"+","Silent","SNP","G","G","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.1977C>A","ENST00000324001",42923,45,63,"T","ENSG00000105227","ENST00000324001","synonymous_variant","synonymous_variant","2248/4855","1977/4386","659/1461","L","ctC/ctA"]
["FAM47B",170062,"WUGSC","GRCh38","chrX",34943297,34943297,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.466G>T","ENST00000329357",42736,52,55,"T","ENSG00000189132","ENST00000329357","stop_gained","stop_gained","502/2120","466/1938","156/645","E/*","Gag/Tag"]
["RBM3",5935,"WUGSC","GRCh38","chrX",48575642,48575642,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-E9-A1R2-01A-11D-A14G-09","TCGA-E9-A1R2-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","b321a2d9-5345-4891-b450-bfd696c6cfb0","bedecc9f-4e3f-4853-b683-2c901c6d3743","c.185T>A","ENST00000376755",42772,65,55,"A","ENSG00000102317","ENST00000376755","missense_variant","missense_variant","414/1130","185/474","62/157","V/D","gTt/gAt"]
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["FLG",2312,"WUGSC","GRCh38","chr1",152305933,152305933,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-E2-A14Y-01A-21D-A12B-09","TCGA-E2-A14Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f63f0927-5186-4558-853d-4eed95ba0ac8","1297e0da-fbf8-4566-8f22-17095e4031f4","c.8953T>A","ENST00000368799",42797,692,449,"T","ENSG00000143631","ENST00000368799","missense_variant","missense_variant","8989/12747","8953/12186","2985/4061","S/T","Tca/Aca"]
["OR10K1",391109,"WUGSC","GRCh38","chr1",158466483,158466483,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-E2-A14Y-01A-21D-A12B-09","TCGA-E2-A14Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f63f0927-5186-4558-853d-4eed95ba0ac8","1297e0da-fbf8-4566-8f22-17095e4031f4","c.922A>T","ENST00000289451",42736,291,232,"T","ENSG00000173285","ENST00000289451","missense_variant","missense_variant","922/942","922/942","308/313","T/S","Act/Tct"]
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["LAMB2",3913,"WUGSC","GRCh38","chr3",49121999,49121999,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E2-A14Y-01A-21D-A12B-09","TCGA-E2-A14Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f63f0927-5186-4558-853d-4eed95ba0ac8","1297e0da-fbf8-4566-8f22-17095e4031f4","c.4868G>A","ENST00000305544","29/32",128,113,"T","ENSG00000172037","ENST00000305544","missense_variant","missense_variant","5021/5643","4868/5397","1623/1798","G/D","gGt/gAt"]
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["MTRR",4552,"WUGSC","GRCh38","chr5",7889149,7889149,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E2-A14Y-01A-21D-A12B-09","TCGA-E2-A14Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f63f0927-5186-4558-853d-4eed95ba0ac8","1297e0da-fbf8-4566-8f22-17095e4031f4","c.1282C>G","ENST00000264668",42993,497,258,"G","ENSG00000124275","ENST00000264668","missense_variant","missense_variant","1312/3274","1282/2178","428/725","L/V","Cta/Gta"]
["B3GALT4",8705,"WUGSC","GRCh38","chr6",33278670,33278670,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-E2-A14Y-01A-21D-A12B-09","TCGA-E2-A14Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f63f0927-5186-4558-853d-4eed95ba0ac8","1297e0da-fbf8-4566-8f22-17095e4031f4","c.*114C>T","ENST00000451237",42736,71,79,"T","ENSG00000235863","ENST00000451237","3_prime_UTR_variant","3_prime_UTR_variant","1539/1694","-/1137","-/378"]
["ACTB",60,"WUGSC","GRCh38","chr7",5529576,5529576,"+","Silent","SNP","G","G","T",null,null,"TCGA-E2-A14Y-01A-21D-A12B-09","TCGA-E2-A14Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f63f0927-5186-4558-853d-4eed95ba0ac8","1297e0da-fbf8-4566-8f22-17095e4031f4","c.82C>A","ENST00000331789",42772,28,26,"T","ENSG00000075624","ENST00000331789","synonymous_variant","synonymous_variant","274/1917","82/1128","28/375","R","Cgg/Agg"]
["POM121",9883,"WUGSC","GRCh38","chr7",72948190,72948190,"+","3'Flank","SNP","A","A","T","novel",null,"TCGA-E2-A14Y-01A-21D-A12B-09","TCGA-E2-A14Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f63f0927-5186-4558-853d-4eed95ba0ac8","1297e0da-fbf8-4566-8f22-17095e4031f4",null,"ENST00000434423",null,14,13,"T","ENSG00000196313","ENST00000434423","downstream_gene_variant","downstream_gene_variant","-/3750","-/3750","-/1249"]
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["ENPP4",22875,"WUGSC","GRCh38","chr6",46141093,46141093,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.868C>T","ENST00000321037",42798,49,33,"T","ENSG00000001561","ENST00000321037","missense_variant","missense_variant","1098/4651","868/1362","290/453","H/Y","Cat/Tat"]
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["LRRC17",10234,"WUGSC","GRCh38","chr7",102933967,102933967,"+","Silent","SNP","G","G","A","rs778069913","byFrequency","TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.54G>A","ENST00000339431",42770,75,74,"A","ENSG00000128606","ENST00000339431","synonymous_variant","synonymous_variant","349/1963","54/1326","18/441","L","ctG/ctA"]
["TNKS",8658,"WUGSC","GRCh38","chr8",9770219,9770219,"+","Missense_Mutation","SNP","A","A","G","rs767692118","byFrequency","TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.3854A>G","ENST00000310430","26/27",40,41,"G","ENSG00000173273","ENST00000310430","missense_variant","missense_variant","3880/9620","3854/3984","1285/1327","N/S","aAt/aGt"]
["CA13",377677,"WUGSC","GRCh38","chr8",85245747,85245747,"+","5'UTR","SNP","G","G","A","novel",null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.-82G>A","ENST00000321764",42742,47,35,"A","ENSG00000185015","ENST00000321764","5_prime_UTR_variant","5_prime_UTR_variant","221/3815","-/789","-/262"]
["AHNAK",79026,"WUGSC","GRCh38","chr11",62527128,62527128,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.7289A>C","ENST00000378024",42860,121,108,"G","ENSG00000124942","ENST00000378024","missense_variant","missense_variant","7564/18787","7289/17673","2430/5890","E/A","gAg/gCg"]
["SPTBN2",6712,"WUGSC","GRCh38","chr11",66699062,66699062,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.3797C>A","ENST00000309996","18/37",45,48,"T","ENSG00000173898","ENST00000309996","missense_variant","missense_variant","3869/7866","3797/7173","1266/2390","A/E","gCa/gAa"]
["CHD4",1108,"WUGSC","GRCh38","chr12",6601053,6601053,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.800G>T","ENST00000357008",14793,60,62,"A","ENSG00000111642","ENST00000357008","missense_variant","missense_variant;splice_region_variant","964/6496","800/5739","267/1912","G/V","gGt/gTt"]
["NYNRIN",57523,"WUGSC","GRCh38","chr14",24414867,24414867,"+","Missense_Mutation","SNP","C","C","T","rs201775736","byCluster;byFrequency","TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.3118C>T","ENST00000382554",42987,62,59,"T","ENSG00000205978","ENST00000382554","missense_variant","missense_variant","3436/7857","3118/5697","1040/1898","R/W","Cgg/Tgg"]
["EIF3J",8669,"WUGSC","GRCh38","chr15",44561818,44561818,"+","3'UTR","SNP","A","A","G","rs377707157","byCluster","TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.*669A>G","ENST00000261868",42955,35,28,"G","ENSG00000104131","ENST00000261868","3_prime_UTR_variant","3_prime_UTR_variant","1584/2569","-/777","-/258"]
["PALB2",79728,"WUGSC","GRCh38","chr16",23636202,23636202,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.344G>A","ENST00000261584",42838,110,106,"T","ENSG00000083093","ENST00000261584","missense_variant","missense_variant","497/4003","344/3561","115/1186","G/E","gGa/gAa"]
["CDH1",999,"WUGSC","GRCh38","chr16",68833355,68833355,"+","Nonsense_Mutation","SNP","T","T","A",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.2505T>A","ENST00000261769","16/16",55,85,"A","ENSG00000039068","ENST00000261769","stop_gained","stop_gained","2696/4889","2505/2649","835/882","Y/*","taT/taA"]
["GSDMB",55876,"WUGSC","GRCh38","chr17",39906963,39906963,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.725T>C","ENST00000418519",42927,31,23,"G","ENSG00000073605","ENST00000418519","missense_variant","missense_variant;splice_region_variant","856/1597","725/1251","242/416","L/S","tTa/tCa"]
["CPAMD8",27151,"WUGSC","GRCh38","chr19",16952075,16952075,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.2543C>A","ENST00000443236","20/42",51,57,"T","ENSG00000160111","ENST00000443236","missense_variant","missense_variant","2575/5992","2543/5799","848/1932","T/N","aCc/aAc"]
["SYMPK",8189,"WUGSC","GRCh38","chr19",45830159,45830159,"+","Silent","SNP","G","G","A","rs773340509","byFrequency","TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.1644C>T","ENST00000245934","13/27",191,186,"A","ENSG00000125755","ENST00000245934","synonymous_variant","synonymous_variant","1889/4195","1644/3825","548/1274","D","gaC/gaT"]
["USP29",57663,"WUGSC","GRCh38","chr19",57129535,57129535,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.860T>C","ENST00000254181",42829,52,57,"C","ENSG00000131864","ENST00000254181","missense_variant","missense_variant","1314/3705","860/2769","287/922","F/S","tTc/tCc"]
["HNF4A",3172,"WUGSC","GRCh38","chr20",44401301,44401301,"+","5'UTR","SNP","G","G","A","novel",null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.-72G>A","ENST00000316099",42745,45,26,"A","ENSG00000101076","ENST00000316099","5_prime_UTR_variant","5_prime_UTR_variant","18/6445","-/1425","-/474"]
["WISP2",8839,"WUGSC","GRCh38","chr20",44724829,44724829,"+","Silent","SNP","C","C","T",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.369C>T","ENST00000190983",42798,188,177,"T","ENSG00000064205","ENST00000190983","synonymous_variant","synonymous_variant","515/1403","369/753","123/250","C","tgC/tgT"]
["KRTAP12-3",386683,"WUGSC","GRCh38","chr21",44657973,44657973,"+","5'UTR","SNP","C","C","T","rs201126322","by1000G;byCluster","TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.-7C>T","ENST00000397907",42736,79,80,"T","ENSG00000205439","ENST00000397907","5_prime_UTR_variant","5_prime_UTR_variant","42/410","-/291","-/96"]
["PRKX",5613,"WUGSC","GRCh38","chrX",3674603,3674603,"+","Silent","SNP","G","G","A",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.330C>T","ENST00000262848",42775,118,105,"A","ENSG00000183943","ENST00000262848","synonymous_variant","synonymous_variant","685/6031","330/1077","110/358","I","atC/atT"]
["FAM47A",158724,"WUGSC","GRCh38","chrX",34131062,34131062,"+","Missense_Mutation","SNP","G","G","T","rs772251379","byFrequency","TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.1217C>A","ENST00000346193",42736,167,111,"T","ENSG00000185448","ENST00000346193","missense_variant","missense_variant","1250/2556","1217/2376","406/791","T/N","aCt/aAt"]
["RPL36A",6173,"WUGSC","GRCh38","chrX",101391815,101391815,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.170G>A","ENST00000553110",42799,63,75,"A","ENSG00000241343","ENST00000553110","missense_variant","missense_variant","231/429","170/321","57/106","R/Q","cGg/cAg"]
["MAGEA4",4103,"WUGSC","GRCh38","chrX",151924758,151924758,"+","3'UTR","SNP","A","A","C","novel",null,"TCGA-A2-A4S2-01A-12D-A25Q-09","TCGA-A2-A4S2-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","1452df07-b990-46ec-8b2c-b6a17bd464c3","1196567b-472e-44b1-adfa-ca04fce2438f","c.*140A>C","ENST00000276344",42797,110,127,"C","ENSG00000147381","ENST00000276344","3_prime_UTR_variant","3_prime_UTR_variant","1312/1724","-/954","-/317"]
["PTCHD2",57540,"WUGSC","GRCh38","chr1",11531012,11531012,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.3208G>A","ENST00000294484","16/21",32,30,"A","ENSG00000204624","ENST00000294484","missense_variant","missense_variant","3346/5215","3208/4179","1070/1392","G/R","Ggg/Agg"]
["SCP2",6342,"WUGSC","GRCh38","chr1",52995729,52995729,"+","Intron","SNP","A","A","C","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1081+7593A>C","ENST00000371514",null,43,36,"C","ENSG00000116171","ENST00000371514","intron_variant","intron_variant","-/2811","-/1644","-/547"]
["CD53",963,"WUGSC","GRCh38","chr1",110892433,110892433,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.152C>G","ENST00000271324",42802,147,132,"G","ENSG00000143119","ENST00000271324","missense_variant","missense_variant","264/1505","152/660","51/219","T/R","aCg/aGg"]
["TTF2",8458,"WUGSC","GRCh38","chr1",117075412,117075412,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.828G>C","ENST00000369466",42878,30,19,"C","ENSG00000116830","ENST00000369466","missense_variant","missense_variant","872/9462","828/3489","276/1162","Q/H","caG/caC"]
["DCAF6",55827,"WUGSC","GRCh38","chr1",168075433,168075433,"+","Nonstop_Mutation","SNP","T","T","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.2581T>A","ENST00000312263","19/19",177,75,"A","ENSG00000143164","ENST00000312263","stop_lost","stop_lost","2785/3186","2581/2583","861/860","*/K","Taa/Aaa"]
["APOB",338,"WUGSC","GRCh38","chr2",21022869,21022869,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.2778T>G","ENST00000233242","18/29",47,44,"C","ENSG00000084674","ENST00000233242","missense_variant","missense_variant","2906/14121","2778/13692","926/4563","I/M","atT/atG"]
["PLEK",5341,"WUGSC","GRCh38","chr2",68386521,68386521,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.492G>T","ENST00000234313",42864,89,66,"T","ENSG00000115956","ENST00000234313","missense_variant","missense_variant","671/2869","492/1053","164/350","W/C","tgG/tgT"]
["NMS",129521,"WUGSC","GRCh38","chr2",100470549,100470549,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.61C>T","ENST00000376865",42745,159,172,"T","ENSG00000204640","ENST00000376865","stop_gained","stop_gained","68/485","61/462","21/153","Q/*","Cag/Tag"]
["ULK4",54986,"WUGSC","GRCh38","chr3",41900773,41900773,"+","Silent","SNP","G","G","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1239C>T","ENST00000301831","13/37",130,73,"A","ENSG00000168038","ENST00000301831","synonymous_variant","synonymous_variant","1702/4613","1239/3828","413/1275","I","atC/atT"]
["CCDC80",151887,"WUGSC","GRCh38","chr3",112638640,112638640,"+","Silent","SNP","C","C","T",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1266G>A","ENST00000206423",42774,75,81,"T","ENSG00000091986","ENST00000206423","synonymous_variant","synonymous_variant","2220/12430","1266/2853","422/950","Q","caG/caA"]
["ETV5",2119,"WUGSC","GRCh38","chr3",186065957,186065957,"+","Missense_Mutation","SNP","G","G","A","rs763950262",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.766C>T","ENST00000306376",42960,94,49,"A","ENSG00000244405","ENST00000306376","missense_variant","missense_variant","1013/4111","766/1533","256/510","P/S","Ccc/Tcc"]
["NFKB1",4790,"WUGSC","GRCh38","chr4",102580537,102580537,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.730G>A","ENST00000394820",43002,118,83,"A","ENSG00000109320","ENST00000394820","missense_variant","missense_variant;splice_region_variant","1195/3693","730/2907","244/968","A/T","Gcc/Acc"]
["TRIM60",166655,"WUGSC","GRCh38","chr4",165040539,165040539,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.467A>G","ENST00000341062",42768,48,55,"G","ENSG00000176979","ENST00000341062","missense_variant","missense_variant","662/1867","467/1416","156/471","E/G","gAa/gGa"]
["ZNF76",7629,"WUGSC","GRCh38","chr6",35294483,35294483,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1522G>T","ENST00000373953","13/14",138,129,"T","ENSG00000065029","ENST00000373953","missense_variant","missense_variant","1788/2716","1522/1713","508/570","V/L","Gtg/Ttg"]
["SPAG1",6674,"WUGSC","GRCh38","chr8",100194365,100194365,"+","Intron","SNP","C","C","T","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1096+97C>T","ENST00000251809",null,12,10,"T","ENSG00000104450","ENST00000251809","intron_variant","intron_variant","-/3748","-/2781","-/926"]
["PKHD1L1",93035,"WUGSC","GRCh38","chr8",109452163,109452163,"+","Silent","SNP","C","C","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.6390C>A","ENST00000378402","42/78",69,64,"A","ENSG00000205038","ENST00000378402","synonymous_variant","synonymous_variant","6494/13076","6390/12732","2130/4243","A","gcC/gcA"]
["TNFRSF11B",4982,"WUGSC","GRCh38","chr8",118924627,118924627,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.953C>G","ENST00000297350",42860,156,164,"C","ENSG00000164761","ENST00000297350","missense_variant","missense_variant","1332/2402","953/1206","318/401","A/G","gCa/gGa"]
["CD72",971,"WUGSC","GRCh38","chr9",35612975,35612975,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.707G>C","ENST00000259633",42895,107,101,"G","ENSG00000137101","ENST00000259633","missense_variant","missense_variant","831/1548","707/1080","236/359","G/A","gGa/gCa"]
["EGFL7",51162,"WUGSC","GRCh38","chr9",136672070,136672070,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.781G>C","ENST00000308874",43019,17,24,"C","ENSG00000172889","ENST00000308874","missense_variant","missense_variant","1315/1747","781/822","261/273","E/Q","Gag/Cag"]
["KNDC1",85442,"WUGSC","GRCh38","chr10",133206976,133206976,"+","Intron","SNP","T","T","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.3579+23T>A","ENST00000304613",null,47,41,"A","ENSG00000171798","ENST00000304613","intron_variant","intron_variant","-/6793","-/5250","-/1749"]
["TRIM66",9866,"WUGSC","GRCh38","chr11",8648474,8648474,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.232G>C","ENST00000299550",42845,69,73,"G","ENSG00000166436","ENST00000299550","missense_variant","missense_variant","427/9753","232/3651","78/1216","E/Q","Gag/Cag"]
["OR5D18",219438,"WUGSC","GRCh38","chr11",55819717,55819717,"+","Silent","SNP","C","C","T","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.88C>T","ENST00000333976",42736,122,109,"T","ENSG00000186119","ENST00000333976","synonymous_variant","synonymous_variant","88/942","88/942","30/313","L","Ctg/Ttg"]
["MYO7A",4647,"WUGSC","GRCh38","chr11",77192279,77192279,"+","Splice_Site","SNP","G","G","T",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.4152+1G>T","ENST00000409709",null,67,67,"T","ENSG00000137474","ENST00000409709","splice_donor_variant","splice_donor_variant","-/7462","4152/6648","1384/2215"]
["PIWIL4",143689,"WUGSC","GRCh38","chr11",94597837,94597837,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1302G>C","ENST00000299001",43059,113,120,"C","ENSG00000134627","ENST00000299001","missense_variant","missense_variant","1513/3199","1302/2559","434/852","W/C","tgG/tgC"]
["OR10S1",219873,"WUGSC","GRCh38","chr11",123977488,123977488,"+","Silent","SNP","G","G","T",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.204C>A","ENST00000531945",42736,36,46,"T","ENSG00000196248","ENST00000531945","synonymous_variant","synonymous_variant","294/1121","204/996","68/331","L","ctC/ctA"]
["ALX1",8092,"WUGSC","GRCh38","chr12",85286969,85286969,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.648C>A","ENST00000316824",42798,61,45,"A","ENSG00000180318","ENST00000316824","missense_variant","missense_variant","803/1445","648/981","216/326","D/E","gaC/gaA"]
["SERPINA12",145264,"WUGSC","GRCh38","chr14",94487342,94487342,"+","Silent","SNP","C","C","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1206G>C","ENST00000341228",42892,28,24,"G","ENSG00000165953","ENST00000341228","synonymous_variant","synonymous_variant","2002/2061","1206/1245","402/414","V","gtG/gtC"]
["PPP2R5C",5527,"WUGSC","GRCh38","chr14",101819087,101819087,"+","Intron","SNP","T","T","C","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.94+9051T>C","ENST00000334743",null,70,72,"C","ENSG00000078304","ENST00000334743","intron_variant","intron_variant","-/4328","-/1575","-/524"]
["HERC2P3",283755,"WUGSC","GRCh38","chr15",20453954,20453954,"+","5'Flank","SNP","C","C","T","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b",null,"ENST00000426501",null,455,452,"T","ENSG00000180229","ENST00000426501","upstream_gene_variant","upstream_gene_variant","-/5995"]
["CHRNB4",1143,"WUGSC","GRCh38","chr15",78635575,78635575,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.68T>C","ENST00000261751",42772,154,192,"G","ENSG00000117971","ENST00000261751","missense_variant","missense_variant","180/2623","68/1497","23/498","V/A","gTg/gCg"]
["CCDC78",124093,"WUGSC","GRCh38","chr16",725286,725286,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.443C>T","ENST00000293889",42869,45,32,"A","ENSG00000162004","ENST00000293889","missense_variant","missense_variant","549/1611","443/1317","148/438","P/L","cCc/cTc"]
["MED24",9862,"WUGSC","GRCh38","chr17",40019851,40019851,"+","Silent","SNP","C","C","T",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.2787G>A","ENST00000394128","25/26",55,36,"T","ENSG00000008838","ENST00000394128","synonymous_variant","synonymous_variant","2869/3479","2787/2970","929/989","E","gaG/gaA"]
["TCF4",6925,"WUGSC","GRCh38","chr18",55232591,55232591,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1567C>G","ENST00000356073","17/20",90,80,"C","ENSG00000196628","ENST00000356073","missense_variant","missense_variant","2179/8317","1567/2004","523/667","L/V","Ctg/Gtg"]
["UNC13A",23025,"WUGSC","GRCh38","chr19",17617734,17617734,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.4526T>C","ENST00000519716","41/44",72,52,"G","ENSG00000130477","ENST00000519716","missense_variant","missense_variant","4526/9838","4526/5112","1509/1703","I/T","aTc/aCc"]
["ACTN4",81,"WUGSC","GRCh38","chr19",38723677,38723677,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.1506G>C","ENST00000252699","13/21",28,20,"C","ENSG00000130402","ENST00000252699","missense_variant","missense_variant","1582/4963","1506/2736","502/911","W/C","tgG/tgC"]
["PDYN",5173,"WUGSC","GRCh38","chr20",1980572,1980572,"+","Silent","SNP","G","G","C",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.516C>G","ENST00000217305",42829,72,63,"C","ENSG00000101327","ENST00000217305","synonymous_variant","synonymous_variant","742/2555","516/765","172/254","V","gtC/gtG"]
["LAMP5",24141,"WUGSC","GRCh38","chr20",9518088,9518088,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.524C>G","ENST00000246070",42861,43,54,"G","ENSG00000125869","ENST00000246070","missense_variant","missense_variant","1016/2039","524/843","175/280","P/R","cCc/cGc"]
["RALGAPB",57148,"WUGSC","GRCh38","chr20",38548770,38548770,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.2984C>G","ENST00000262879","20/30",196,117,"G","ENSG00000170471","ENST00000262879","missense_variant","missense_variant","3268/8663","2984/4485","995/1494","P/R","cCc/cGc"]
["MN1",4330,"WUGSC","GRCh38","chr22",27799795,27799795,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.749C>G","ENST00000302326",42737,22,17,"C","ENSG00000169184","ENST00000302326","missense_variant","missense_variant","1704/7556","749/3963","250/1320","S/C","tCt/tGt"]
["KIAA2022",340533,"WUGSC","GRCh38","chrX",74739369,74739369,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-AR-A24L-01A-11D-A167-09","TCGA-AR-A24L-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2a93298a-d272-487c-ae4a-ec385844536e","7bb4ec17-22de-45cf-8ec8-637526f4752b","c.*36G>A","ENST00000055682",42829,62,51,"T","ENSG00000050030","ENST00000055682","3_prime_UTR_variant","3_prime_UTR_variant","5199/11719","-/4551","-/1516"]
["EPS15",2060,"WUGSC","GRCh38","chr1",51440420,51440420,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.967T>C","ENST00000371733",43094,41,51,"G","ENSG00000085832","ENST00000371733","missense_variant","missense_variant","1064/5225","967/2691","323/896","S/P","Tca/Cca"]
["APCS",325,"WUGSC","GRCh38","chr1",159587959,159587959,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.38G>A","ENST00000255040",42737,46,46,"A","ENSG00000132703","ENST00000255040","missense_variant","missense_variant","135/926","38/672","13/223","S/N","aGc/aAc"]
["FMN2",56776,"WUGSC","GRCh38","chr1",240206894,240206894,"+","Silent","SNP","G","G","A",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.2082G>A","ENST00000319653",42873,40,33,"A","ENSG00000155816","ENST00000319653","synonymous_variant","synonymous_variant","2312/6434","2082/5169","694/1722","E","gaG/gaA"]
["PPARG",5468,"WUGSC","GRCh38","chr3",12405986,12405986,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.724C>G","ENST00000287820",42862,29,34,"G","ENSG00000132170","ENST00000287820","missense_variant","missense_variant","845/1850","724/1518","242/505","L/V","Ctg/Gtg"]
["NAA50",80218,"WUGSC","GRCh38","chr3",113719158,113719158,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.*2602G>T","ENST00000240922",42860,60,61,"A","ENSG00000121579","ENST00000240922","3_prime_UTR_variant","3_prime_UTR_variant","3437/6135","-/510","-/169"]
["SPARCL1",8404,"WUGSC","GRCh38","chr4",87490386,87490386,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.1418G>C","ENST00000282470",42927,37,43,"G","ENSG00000152583","ENST00000282470","missense_variant","missense_variant","1889/2906","1418/1995","473/664","G/A","gGc/gCc"]
["LMBRD2",92255,"WUGSC","GRCh38","chr5",36114519,36114519,"+","Splice_Region","SNP","A","A","T",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.1545T>A","ENST00000296603","13/18",21,31,"T","ENSG00000164187","ENST00000296603","splice_region_variant","splice_region_variant;synonymous_variant","2008/8185","1545/2088","515/695","I","atT/atA"]
["IRAK1BP1",134728,"WUGSC","GRCh38","chr6",78867615,78867615,"+","Silent","SNP","G","G","A",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.39G>A","ENST00000369940",42739,45,29,"A","ENSG00000146243","ENST00000369940","synonymous_variant","synonymous_variant","144/5656","39/783","13/260","V","gtG/gtA"]
["KMT2C",58508,"WUGSC","GRCh38","chr7",152252614,152252614,"+","Nonsense_Mutation","SNP","A","A","T",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.1401T>A","ENST00000262189",21824,47,35,"T","ENSG00000055609","ENST00000262189","stop_gained","stop_gained","1620/16862","1401/14736","467/4911","C/*","tgT/tgA"]
["RP1L1",94137,"WUGSC","GRCh38","chr8",10607133,10607133,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.6965A>T","ENST00000382483",42829,41,52,"A","ENSG00000183638","ENST00000382483","missense_variant","missense_variant","7189/7973","6965/7203","2322/2400","D/V","gAc/gTc"]
["TMEM26",219623,"WUGSC","GRCh38","chr10",61410618,61410618,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.811G>C","ENST00000399298",42892,46,31,"G","ENSG00000196932","ENST00000399298","missense_variant","missense_variant","1180/5151","811/1107","271/368","V/L","Gtg/Ctg"]
["GPALPP1",55425,"WUGSC","GRCh38","chr13",45006287,45006287,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.307G>A","ENST00000379151",42802,61,59,"A","ENSG00000133114","ENST00000379151","missense_variant","missense_variant","410/1393","307/1023","103/340","D/N","Gat/Aat"]
["BMF",90427,"WUGSC","GRCh38","chr15",40090367,40090367,"+","3'UTR","SNP","G","G","A","rs781644111",null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.*1420C>T","ENST00000354670",42860,121,136,"A","ENSG00000104081","ENST00000354670","3_prime_UTR_variant","3_prime_UTR_variant","2210/4687","-/555","-/184"]
["C15orf65",145788,"WUGSC","GRCh38","chr15",55408613,55408613,"+","5'UTR","SNP","G","G","C","rs58847654","by1000G;byCluster;byFrequency","TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.-156G>C","ENST00000569691",42737,17,11,"C","ENSG00000261652","ENST00000569691","5_prime_UTR_variant","5_prime_UTR_variant","66/729","-/366","-/121"]
["HES7",84667,"WUGSC","GRCh38","chr17",8121298,8121298,"+","3'Flank","SNP","G","G","T","novel",null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9",null,"ENST00000317814",null,18,33,"T","ENSG00000179111","ENST00000317814","downstream_gene_variant","downstream_gene_variant","-/678","-/678","-/225"]
["SLC47A2",146802,"WUGSC","GRCh38","chr17",19681567,19681567,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.1376T>C","ENST00000325411","14/17",60,56,"G","ENSG00000180638","ENST00000325411","missense_variant","missense_variant","1427/2258","1376/1809","459/602","L/P","cTg/cCg"]
["CCDC144NL-AS1",440416,"WUGSC","GRCh38","chr17",20902646,20902646,"+","RNA","SNP","C","C","A","novel",null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","n.1143C>A","ENST00000577537",42829,40,33,"A","ENSG00000233098","ENST00000577537","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","1143/3727"]
["OR1M1",125963,"WUGSC","GRCh38","chr19",9093695,9093695,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.451T>A","ENST00000429566",42736,34,40,"A","ENSG00000170929","ENST00000429566","missense_variant","missense_variant","517/1035","451/942","151/313","F/I","Ttt/Att"]
["DLGAP4",22839,"WUGSC","GRCh38","chr20",36527164,36527164,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.*133C>T","ENST00000339266","13/13",28,25,"T","ENSG00000080845","ENST00000339266","3_prime_UTR_variant","3_prime_UTR_variant","3547/5016","-/2979","-/992"]
["NUP50",10762,"WUGSC","GRCh38","chr22",45178353,45178353,"+","Silent","SNP","C","C","A",null,null,"TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.456C>A","ENST00000347635",42863,120,132,"A","ENSG00000093000","ENST00000347635","synonymous_variant","synonymous_variant","922/5233","456/1407","152/468","V","gtC/gtA"]
["PHKA2",5256,"WUGSC","GRCh38","chrX",18901600,18901600,"+","Missense_Mutation","SNP","C","C","T","rs376405603","byCluster;byFrequency","TCGA-OL-A66H-01A-11D-A29N-09","TCGA-OL-A66H-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","069ecb6d-ce1e-4091-a953-a968d851c0d7","6301b1ed-a989-4fea-994c-96fcd75a42d9","c.2912G>A","ENST00000379942","27/33",85,82,"T","ENSG00000044446","ENST00000379942","missense_variant","missense_variant","3578/5559","2912/3708","971/1235","R/H","cGc/cAc"]
["MACF1",23499,"WUGSC","GRCh38","chr1",39331417,39331417,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.4844A>G","ENST00000372915","36/97",14,40,"G","ENSG00000127603","ENST00000372915","missense_variant","missense_variant","4931/23440","4844/22167","1615/7388","Q/R","cAg/cGg"]
["FOXJ3",22887,"WUGSC","GRCh38","chr1",42191329,42191329,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1325C>G","ENST00000361346",42991,176,279,"C","ENSG00000198815","ENST00000361346","missense_variant","missense_variant","1516/5225","1325/1869","442/622","P/R","cCc/cGc"]
["FLG",2312,"WUGSC","GRCh38","chr1",152307611,152307611,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.7275G>C","ENST00000368799",42797,342,247,"G","ENSG00000143631","ENST00000368799","missense_variant","missense_variant","7311/12747","7275/12186","2425/4061","E/D","gaG/gaC"]
["FMO3",2328,"WUGSC","GRCh38","chr1",171117418,171117418,"+","Silent","SNP","C","C","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1575C>T","ENST00000367755",42987,228,179,"T","ENSG00000007933","ENST00000367755","synonymous_variant","synonymous_variant","1686/2087","1575/1599","525/532","I","atC/atT"]
["TOR1AIP2",163590,"WUGSC","GRCh38","chr1",179864614,179864614,"+","Intron","SNP","T","T","G","novel",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.-146-11803A>C","ENST00000367612",null,14,10,"G","ENSG00000169905","ENST00000367612","intron_variant","intron_variant","-/7905","-/1413","-/470"]
["TLR5",7100,"WUGSC","GRCh38","chr1",223112008,223112008,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1024A>C","ENST00000366881",42892,100,46,"G","ENSG00000187554","ENST00000366881","missense_variant","missense_variant","1665/3368","1024/2577","342/858","N/H","Aat/Cat"]
["FH",2271,"WUGSC","GRCh38","chr1",241506129,241506129,"+","Missense_Mutation","SNP","T","T","C","novel",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.778A>G","ENST00000366560",42896,174,104,"C","ENSG00000091483","ENST00000366560","missense_variant","missense_variant","817/1797","778/1533","260/510","T/A","Aca/Gca"]
["ZAP70",7535,"WUGSC","GRCh38","chr2",97738040,97738040,"+","Missense_Mutation","SNP","C","C","T","rs200513049","byCluster","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1669C>T","ENST00000264972","13/14",37,74,"T","ENSG00000115085","ENST00000264972","missense_variant","missense_variant","1884/2437","1669/1860","557/619","R/W","Cgg/Tgg"]
["LCT",3938,"WUGSC","GRCh38","chr2",135808876,135808876,"+","Silent","SNP","G","G","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.3471C>A","ENST00000264162",42964,38,54,"T","ENSG00000115850","ENST00000264162","synonymous_variant","synonymous_variant","3482/6279","3471/5784","1157/1927","P","ccC/ccA"]
["TTN",7273,"WUGSC","GRCh38","chr2",178593643,178593643,"+","Missense_Mutation","SNP","G","G","A","rs372959465","byCluster;byFrequency","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.53734C>T","ENST00000591111","248/313",50,74,"A","ENSG00000155657","ENST00000591111","missense_variant","missense_variant","53959/104301","53734/103053","17912/34350","R/W","Cgg/Tgg"]
["TTN",7273,"WUGSC","GRCh38","chr2",178672207,178672207,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.33869A>G","ENST00000591111","151/313",38,51,"C","ENSG00000155657","ENST00000591111","missense_variant","missense_variant","34094/104301","33869/103053","11290/34350","E/G","gAa/gGa"]
["SLC40A1",30061,"WUGSC","GRCh38","chr2",189572889,189572889,"+","Nonsense_Mutation","SNP","A","A","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.344T>G","ENST00000261024",42833,19,32,"C","ENSG00000138449","ENST00000261024","stop_gained","stop_gained","771/3442","344/1716","115/571","L/*","tTa/tGa"]
["PRKCD",5580,"WUGSC","GRCh38","chr3",53189057,53189057,"+","Splice_Site","SNP","G","C","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1555-1G>C","ENST00000330452",null,79,89,"C","ENSG00000163932","ENST00000330452","splice_acceptor_variant","splice_acceptor_variant","-/2680","1555/2031","519/676"]
["PHC3",80012,"WUGSC","GRCh38","chr3",170171332,170171332,"+","Intron","SNP","T","T","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.378+41A>G","ENST00000494943",null,19,16,"C","ENSG00000173889","ENST00000494943","intron_variant","intron_variant","-/5030","-/2952","-/983"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179234297,179234297,"+","Missense_Mutation","SNP","A","A","G","rs121913279","byCluster;byFrequency","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.3140A>G","ENST00000263967","21/21",53,57,"G","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","3297/9093","3140/3207","1047/1068","H/R","cAt/cGt"]
["MUC20",200958,"WUGSC","GRCh38","chr3",195733168,195733168,"+","Missense_Mutation","SNP","G","G","A","rs368678088","byCluster;byFrequency","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.2080G>A","ENST00000447234",42829,42,25,"A","ENSG00000176945","ENST00000447234","missense_variant","missense_variant","2206/2589","2080/2130","694/709","A/T","Gcc/Acc"]
["BMPR1B",658,"WUGSC","GRCh38","chr4",95131313,95131313,"+","Missense_Mutation","SNP","T","T","C","novel",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.877T>C","ENST00000264568",42958,55,56,"C","ENSG00000138696","ENST00000264568","missense_variant","missense_variant","1031/1807","877/1509","293/502","S/P","Tcc/Ccc"]
["TLR3",7098,"WUGSC","GRCh38","chr4",186083514,186083514,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1828G>C","ENST00000296795",42830,45,42,"C","ENSG00000164342","ENST00000296795","missense_variant","missense_variant","1932/6015","1828/2715","610/904","V/L","Gtg/Ctg"]
["SV2C",22987,"WUGSC","GRCh38","chr5",76132056,76132056,"+","Silent","SNP","G","G","A","rs553883859","by1000G","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.306G>A","ENST00000502798",42779,96,86,"A","ENSG00000122012","ENST00000502798","synonymous_variant","synonymous_variant","748/11035","306/2184","102/727","A","gcG/gcA"]
["TRPC7",57113,"WUGSC","GRCh38","chr5",136315620,136315620,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.940G>A","ENST00000513104",42806,112,91,"T","ENSG00000069018","ENST00000513104","missense_variant","missense_variant","1223/2987","940/2589","314/862","A/T","Gcc/Acc"]
["MDC1",9656,"WUGSC","GRCh38","chr6",30704205,30704205,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.4978C>T","ENST00000376406",43023,82,102,"A","ENSG00000137337","ENST00000376406","missense_variant","missense_variant","5626/7576","4978/6270","1660/2089","L/F","Ctt/Ttt"]
["XPO7",23039,"WUGSC","GRCh38","chr8",21980119,21980119,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.873A>T","ENST00000252512",43006,127,105,"T","ENSG00000130227","ENST00000252512","missense_variant","missense_variant","973/4861","873/3264","291/1087","R/S","agA/agT"]
["FAM135B",51059,"WUGSC","GRCh38","chr8",138151834,138151834,"+","Nonsense_Mutation","SNP","T","T","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.2641A>T","ENST00000395297","13/20",87,77,"A","ENSG00000147724","ENST00000395297","stop_gained","stop_gained","2812/6962","2641/4221","881/1406","K/*","Aaa/Taa"]
["OPLAH",26873,"WUGSC","GRCh38","chr8",144053329,144053329,"+","Silent","SNP","G","G","A","novel",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.2751C>T","ENST00000618853","20/27",39,29,"A","ENSG00000178814","ENST00000618853","synonymous_variant","synonymous_variant","2855/4031","2751/3867","917/1288","H","caC/caT"]
["ZNF658B",401509,"WUGSC","GRCh38","chr9",39445663,39445663,"+","RNA","SNP","G","G","T","novel",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","n.2049C>A","ENST00000602828",42829,110,107,"T","ENSG00000198416","ENST00000602828","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","2049/3408"]
["CEL",1056,"WUGSC","GRCh38","chr9",133068761,133068761,"+","Missense_Mutation","SNP","G","G","A","rs746397927","byFrequency","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.994G>A","ENST00000372080",42958,106,115,"A","ENSG00000170835","ENST00000372080","missense_variant","missense_variant","1010/2384","994/2271","332/756","D/N","Gac/Aac"]
["MED22",6837,"WUGSC","GRCh38","chr9",133344236,133344236,"+","Missense_Mutation","SNP","C","C","T","rs782125745",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.302G>A","ENST00000343730",42830,39,50,"T","ENSG00000148297","ENST00000343730","missense_variant","missense_variant","536/1437","302/603","101/200","R/H","cGc/cAc"]
["EGFL7",51162,"WUGSC","GRCh38","chr9",136672378,136672378,"+","3'UTR","SNP","C","C","T","rs750500312",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.*92C>T","ENST00000308874",43050,33,22,"T","ENSG00000172889","ENST00000308874","3_prime_UTR_variant","3_prime_UTR_variant","1448/1747","-/822","-/273"]
["OR51E1",143503,"WUGSC","GRCh38","chr11",4653331,4653331,"+","Missense_Mutation","SNP","C","C","T","rs201979094","byCluster;byFrequency","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.805C>T","ENST00000396952",42768,84,113,"T","ENSG00000180785","ENST00000396952","missense_variant","missense_variant","1455/3612","805/957","269/318","R/W","Cgg/Tgg"]
["OR5L2",26338,"WUGSC","GRCh38","chr11",55827892,55827892,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.674T>A","ENST00000378397",42736,102,100,"A","ENSG00000205030","ENST00000378397","missense_variant","missense_variant","674/936","674/936","225/311","I/N","aTc/aAc"]
["SLCO1B3",28234,"WUGSC","GRCh38","chr12",20875309,20875309,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.802T>C","ENST00000261196",42930,235,234,"C","ENSG00000111700","ENST00000261196","missense_variant","missense_variant","869/2840","802/2109","268/702","F/L","Ttt/Ctt"]
["CALCOCO1",57658,"WUGSC","GRCh38","chr12",53716395,53716395,"+","Silent","SNP","T","T","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.870A>G","ENST00000550804",42962,46,76,"C","ENSG00000012822","ENST00000550804","synonymous_variant","synonymous_variant","931/2291","870/2076","290/691","Q","caA/caG"]
["CIT",11113,"WUGSC","GRCh38","chr12",119690434,119690434,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.5777C>T","ENST00000261833","46/47",19,20,"A","ENSG00000122966","ENST00000261833","missense_variant","missense_variant","5830/8578","5777/6084","1926/2027","P/L","cCa/cTa"]
["RB1",5925,"WUGSC","GRCh38","chr13",48379624,48379624,"+","Nonsense_Mutation","SNP","C","T","T","rs121913302",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1363C>T","ENST00000267163","14/27",10,25,"T","ENSG00000139687","ENST00000267163","stop_gained","stop_gained","1501/4840","1363/2787","455/928","R/*","Cga/Tga"]
["SLC22A17",51310,"WUGSC","GRCh38","chr14",23349325,23349325,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.473G>T","ENST00000206544",42803,40,26,"A","ENSG00000092096","ENST00000206544","missense_variant","missense_variant","810/2284","473/1617","158/538","R/L","cGa/cTa"]
["LRFN5",145581,"WUGSC","GRCh38","chr14",41891545,41891545,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1681C>T","ENST00000298119",42831,73,64,"T","ENSG00000165379","ENST00000298119","missense_variant","missense_variant","2870/3723","1681/2160","561/719","H/Y","Cac/Tac"]
["PTGR2",145482,"WUGSC","GRCh38","chr14",73874082,73874082,"+","Silent","SNP","A","A","G",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.216A>G","ENST00000267568",42835,91,114,"G","ENSG00000140043","ENST00000267568","synonymous_variant","synonymous_variant","437/2559","216/1056","72/351","Q","caA/caG"]
["ZNF710",374655,"WUGSC","GRCh38","chr15",90068051,90068051,"+","Missense_Mutation","SNP","C","C","T","rs764750149",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.914C>T","ENST00000268154",42771,46,41,"T","ENSG00000140548","ENST00000268154","missense_variant","missense_variant","1165/4617","914/1995","305/664","T/M","aCg/aTg"]
["CACNG3",10368,"WUGSC","GRCh38","chr16",24361887,24361887,"+","3'UTR","SNP","C","C","T","rs368106492","by1000G;byCluster","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.*24C>T","ENST00000005284",42829,33,20,"T","ENSG00000006116","ENST00000005284","3_prime_UTR_variant","3_prime_UTR_variant","2174/3088","-/948","-/315"]
["NUTF2",10204,"WUGSC","GRCh38","chr16",67868348,67868348,"+","Silent","SNP","G","G","A","rs750611785","byFrequency","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.108G>A","ENST00000219169",42799,64,90,"A","ENSG00000102898","ENST00000219169","synonymous_variant","synonymous_variant","391/2321","108/384","36/127","A","gcG/gcA"]
["GIP",2695,"WUGSC","GRCh38","chr17",48960985,48960985,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.353C>T","ENST00000357424",42861,41,56,"A","ENSG00000159224","ENST00000357424","missense_variant","missense_variant;splice_region_variant","454/716","353/462","118/153","S/F","tCc/tTc"]
["NOL11",25926,"WUGSC","GRCh38","chr17",67717948,67717948,"+","Translation_Start_Site","SNP","A","A","C",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1A>C","ENST00000253247",42753,27,25,"C","ENSG00000130935","ENST00000253247","start_lost","start_lost","116/2947",94965,"1/719","M/L","Atg/Ctg"]
["TBCD",6904,"WUGSC","GRCh38","chr17",82772488,82772488,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.619G>T","ENST00000355528",14397,91,163,"T","ENSG00000141556","ENST00000355528","missense_variant","missense_variant","749/7168","619/3579","207/1192","A/S","Gct/Tct"]
["ZNF555",148254,"WUGSC","GRCh38","chr19",2852516,2852516,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.451G>T","ENST00000334241",42829,51,74,"T","ENSG00000186300","ENST00000334241","missense_variant","missense_variant","589/8557","451/1887","151/628","V/F","Gtc/Ttc"]
["OR10H5",284433,"WUGSC","GRCh38","chr19",15794108,15794108,"+","Silent","SNP","C","C","T",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.60C>T","ENST00000308940",42736,86,193,"T","ENSG00000172519","ENST00000308940","synonymous_variant","synonymous_variant","158/1132","60/948","20/315","F","ttC/ttT"]
["COMMD7",149951,"WUGSC","GRCh38","chr20",32727925,32727925,"+","Missense_Mutation","SNP","C","C","T","rs755648030",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.209G>A","ENST00000278980",42803,118,116,"T","ENSG00000149600","ENST00000278980","missense_variant","missense_variant","815/1900","209/603","70/200","S/N","aGc/aAc"]
["DOK5",55816,"WUGSC","GRCh38","chr20",54591762,54591762,"+","Missense_Mutation","SNP","C","C","T","rs147632330","byCluster","TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.556C>T","ENST00000262593",42863,102,101,"T","ENSG00000101134","ENST00000262593","missense_variant","missense_variant","906/1963","556/921","186/306","R/W","Cgg/Tgg"]
["EGFL6",25975,"WUGSC","GRCh38","chrX",13569845,13569845,"+","5'UTR","SNP","G","G","A","novel",null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.-17G>A","ENST00000361306",42747,32,42,"A","ENSG00000198759","ENST00000361306","5_prime_UTR_variant","5_prime_UTR_variant","241/2398","-/1662","-/553"]
["CNKSR2",22866,"WUGSC","GRCh38","chrX",21432784,21432784,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.401C>A","ENST00000379510",42816,74,97,"A","ENSG00000149970","ENST00000379510","missense_variant","missense_variant","437/5315","401/3105","134/1034","A/E","gCa/gAa"]
["ELF4",2000,"WUGSC","GRCh38","chrX",130069374,130069374,"+","Silent","SNP","G","G","A",null,null,"TCGA-E9-A1RC-01A-11D-A159-09","TCGA-E9-A1RC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","5b5e7eb2-8efc-4681-ab8c-49a9cc4ac6d6","2c3fdd88-5419-495a-b52b-45fd9de1bd51","c.1113C>T","ENST00000308167",42956,33,64,"A","ENSG00000102034","ENST00000308167","synonymous_variant","synonymous_variant","1493/4165","1113/1992","371/663","D","gaC/gaT"]
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["TIAL1",7073,"WUGSC","GRCh38","chr10",119578723,119578723,"+","Splice_Region","SNP","T","T","A","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.556+3A>T","ENST00000436547",null,222,191,"A","ENSG00000151923","ENST00000436547","splice_region_variant","splice_region_variant;intron_variant","-/1401","-/1128","-/375"]
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["RSF1",51773,"WUGSC","GRCh38","chr11",77701584,77701584,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.1645G>T","ENST00000308488",42902,1170,345,"A","ENSG00000048649","ENST00000308488","missense_variant","missense_variant","1948/11550","1645/4326","549/1441","D/Y","Gat/Tat"]
["ME3",10873,"WUGSC","GRCh38","chr11",86671824,86671824,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.121G>A","ENST00000393324",42749,57,20,"T","ENSG00000151376","ENST00000393324","missense_variant","missense_variant","375/2240","121/1815","41/604","A/T","Gcg/Acg"]
["GAPDH",2597,"WUGSC","GRCh38","chr12",6538176,6538176,"+","3'UTR","SNP","C","C","T","rs3211592",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.*6C>T","ENST00000229239",42987,87,64,"T","ENSG00000111640","ENST00000229239","3_prime_UTR_variant","3_prime_UTR_variant","1680/1875","-/1008","-/335"]
["NR1H4",9971,"WUGSC","GRCh38","chr12",100563571,100563571,"+","3'Flank","SNP","C","C","T","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228",null,"ENST00000551379",null,38,33,"T","ENSG00000012504","ENST00000551379","downstream_gene_variant","downstream_gene_variant","-/1489","-/1461","-/486"]
["KIAA1033",23325,"WUGSC","GRCh38","chr12",105127276,105127276,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.1186C>G","ENST00000332180","13/33",213,220,"G","ENSG00000136051","ENST00000332180","missense_variant","missense_variant","1273/5812","1186/3522","396/1173","Q/E","Caa/Gaa"]
["POLE",5426,"WUGSC","GRCh38","chr12",132672728,132672728,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.1585G>T","ENST00000320574","15/49",323,249,"A","ENSG00000177084","ENST00000320574","missense_variant","missense_variant","1629/7840","1585/6861","529/2286","D/Y","Gac/Tac"]
["PRPF39",55015,"WUGSC","GRCh38","chr14",45114912,45114912,"+","Silent","SNP","G","G","A","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.2009G>A","ENST00000355765","14/14",334,366,"A","ENSG00000185246","ENST00000355765","stop_retained_variant","stop_retained_variant","2179/2868","2009/2010","670/669","*","tGa/tAa"]
["PRPF39",55015,"WUGSC","GRCh38","chr14",45114917,45114917,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.*4G>A","ENST00000355765","14/14",314,352,"A","ENSG00000185246","ENST00000355765","3_prime_UTR_variant","3_prime_UTR_variant","2184/2868","-/2010","-/669"]
["ATP2A3",489,"WUGSC","GRCh38","chr17",3928016,3928016,"+","Intron","SNP","G","G","A","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.3068+224C>T","ENST00000352011",null,78,63,"A","ENSG00000074370","ENST00000352011","intron_variant","intron_variant","-/3274","-/3132","-/1043"]
["TUBD1",51174,"WUGSC","GRCh38","chr17",59886117,59886117,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.286C>A","ENST00000325752",42803,2341,314,"T","ENSG00000108423","ENST00000325752","missense_variant","missense_variant","574/2490","286/1362","96/453","Q/K","Caa/Aaa"]
["UNC13D",201294,"WUGSC","GRCh38","chr17",75842875,75842875,"+","Silent","SNP","G","G","A","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.370C>T","ENST00000207549",11810,224,51,"A","ENSG00000092929","ENST00000207549","synonymous_variant","synonymous_variant","750/4393","370/3273","124/1090","L","Ctg/Ttg"]
["UNC13D",201294,"WUGSC","GRCh38","chr17",75843496,75843496,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.141C>G","ENST00000207549",11720,446,130,"C","ENSG00000092929","ENST00000207549","missense_variant","missense_variant","521/4393","141/3273","47/1090","F/L","ttC/ttG"]
["YES1",7525,"WUGSC","GRCh38","chr18",743380,743380,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.760G>C","ENST00000314574",42928,131,131,"G","ENSG00000176105","ENST00000314574","missense_variant","missense_variant","893/4441","760/1632","254/543","V/L","Gtg/Ctg"]
["C3",718,"WUGSC","GRCh38","chr19",6697358,6697358,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.2782T>G","ENST00000245907","21/41",68,78,"C","ENSG00000125730","ENST00000245907","missense_variant","missense_variant","2875/5263","2782/4992","928/1663","S/A","Tcc/Gcc"]
["STXBP2",6813,"WUGSC","GRCh38","chr19",7639806,7639806,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.245A>C","ENST00000221283",42844,231,153,"C","ENSG00000076944","ENST00000221283","missense_variant","missense_variant;splice_region_variant","276/1876","245/1782","82/593","K/T","aAg/aCg"]
["SHANK1",50944,"WUGSC","GRCh38","chr19",50704129,50704129,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.1213C>A","ENST00000293441",43001,268,155,"T","ENSG00000161681","ENST00000293441","missense_variant","missense_variant","1232/6643","1213/6486","405/2161","Q/K","Cag/Aag"]
["LRRN4",164312,"WUGSC","GRCh38","chr20",6041018,6041018,"+","3'UTR","SNP","T","T","G","novel",null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.*4A>C","ENST00000378858",42860,25,20,"G","ENSG00000125872","ENST00000378858","3_prime_UTR_variant","3_prime_UTR_variant","2452/2692","-/2223","-/740"]
["GPR143",4935,"WUGSC","GRCh38","chrX",9739593,9739593,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.1012G>A","ENST00000467482",42956,113,111,"T","ENSG00000101850","ENST00000467482","missense_variant","missense_variant","1159/1762","1012/1215","338/404","E/K","Gag/Aag"]
["MAGEH1",28986,"WUGSC","GRCh38","chrX",55452475,55452475,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0DG-01A-21D-A12Q-09","TCGA-BH-A0DG-11A-43D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","ec4d4cbc-d5d1-418d-a292-cad9576624fd","d0d81468-73f6-4a8a-8f00-b99bd127c228","c.101C>A","ENST00000342972",42736,26,22,"A","ENSG00000187601","ENST00000342972","missense_variant","missense_variant","371/1462","101/660","34/219","P/H","cCt/cAt"]
["KCNK2",3776,"WUGSC","GRCh38","chr1",215235026,215235026,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.1162C>T","ENST00000444842",42923,254,168,"T","ENSG00000082482","ENST00000444842","missense_variant","missense_variant","1312/3379","1162/1281","388/426","H/Y","Cac/Tac"]
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["TRIM11",81559,"WUGSC","GRCh38","chr1",228395130,228395130,"+","Missense_Mutation","SNP","C","C","T","rs759457960",null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.982G>A","ENST00000284551",42892,55,46,"T","ENSG00000154370","ENST00000284551","missense_variant","missense_variant","1261/2715","982/1407","328/468","G/S","Ggc/Agc"]
["EIF2AK3",9451,"WUGSC","GRCh38","chr2",88585880,88585880,"+","Silent","SNP","C","C","A",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.1611G>T","ENST00000303236",42995,221,261,"A","ENSG00000172071","ENST00000303236","synonymous_variant","synonymous_variant","1913/4646","1611/3351","537/1116","T","acG/acT"]
["RNF182",221687,"WUGSC","GRCh38","chr6",13977964,13977964,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.*101C>T","ENST00000488300",42797,8,15,"T","ENSG00000180537","ENST00000488300","3_prime_UTR_variant","3_prime_UTR_variant","1368/3706","-/744","-/247"]
["HIST1H2AE",3012,"WUGSC","GRCh38","chr6",26217139,26217139,"+","Silent","SNP","G","G","A",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.165G>A","ENST00000303910",42736,159,85,"A","ENSG00000277075","ENST00000303910","synonymous_variant","synonymous_variant","165/393","165/393","55/130","V","gtG/gtA"]
["THNSL1",79896,"WUGSC","GRCh38","chr10",25024077,25024077,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.854G>T","ENST00000376356",42797,242,232,"T","ENSG00000185875","ENST00000376356","missense_variant","missense_variant","1104/3691","854/2232","285/743","G/V","gGa/gTa"]
["TRHDE",29953,"WUGSC","GRCh38","chr12",72562982,72562982,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.1849C>G","ENST00000261180",42997,94,62,"G","ENSG00000072657","ENST00000261180","missense_variant","missense_variant","1945/10733","1849/3075","617/1024","Q/E","Cag/Gag"]
["AKT1",207,"WUGSC","GRCh38","chr14",104780214,104780214,"+","Missense_Mutation","SNP","C","C","T","rs121434592","byCluster","TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.49G>A","ENST00000349310",42840,236,95,"T","ENSG00000142208","ENST00000349310","missense_variant","missense_variant;splice_region_variant","480/2866","49/1443","17/480","E/K","Gag/Aag"]
["GP1BA",2811,"WUGSC","GRCh38","chr17",4934406,4934406,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.1802C>G","ENST00000329125",42768,183,98,"G","ENSG00000185245","ENST00000329125","missense_variant","missense_variant","1877/2501","1802/1959","601/652","S/W","tCg/tGg"]
["SLC46A1",113235,"WUGSC","GRCh38","chr17",28405087,28405087,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.610C>T","ENST00000612814",42771,41,46,"A","ENSG00000076351","ENST00000612814","missense_variant","missense_variant","706/6376","610/1380","204/459","R/W","Cgg/Tgg"]
["RUNX1",861,"WUGSC","GRCh38","chr21",34880556,34880556,"+","Splice_Site","SNP","C","C","G",null,null,"TCGA-D8-A141-01A-11D-A10Y-09","TCGA-D8-A141-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","807791d8-b6c0-4722-bf5c-d5fa30baffc6","8bd52c2f-131d-40cc-8c24-f8021128cb93","c.427+1G>C","ENST00000344691",null,227,183,"G","ENSG00000159216","ENST00000344691","splice_donor_variant","splice_donor_variant","-/7274","427/1362","143/453"]
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["C6orf136",221545,"WUGSC","GRCh38","chr6",30647525,30647525,"+","Intron","SNP","G","G","A",null,null,"TCGA-JL-A3YX-01A-11D-A22X-09","TCGA-JL-A3YX-10A-01D-A22X-09",null,null,"Somatic","Illumina HiSeq 2000","72f91ad5-8d24-4a74-960c-646a15dd8d50","349f79fa-f1fa-4669-a522-7d33a00f78d6","c.72+222G>A","ENST00000376473",null,68,77,"A","ENSG00000204564","ENST00000376473","intron_variant","intron_variant","-/1402","-/948","-/315"]
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["SPSB4",92369,"WUGSC","GRCh38","chr3",141147229,141147229,"+","Missense_Mutation","SNP","C","C","T","rs143524410","by1000G;byCluster","TCGA-LL-A5YP-01A-21D-A28B-09","TCGA-LL-A5YP-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","a6206343-6d41-485a-8992-3a466df43286","fe144218-875d-423c-80d7-05de5b2e1496","c.782C>T","ENST00000310546",42797,43,51,"T","ENSG00000175093","ENST00000310546","missense_variant","missense_variant","1526/2908","782/822","261/273","P/L","cCc/cTc"]
["SPSB4",92369,"WUGSC","GRCh38","chr3",141147230,141147230,"+","Silent","SNP","C","C","T","novel",null,"TCGA-LL-A5YP-01A-21D-A28B-09","TCGA-LL-A5YP-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","a6206343-6d41-485a-8992-3a466df43286","fe144218-875d-423c-80d7-05de5b2e1496","c.783C>T","ENST00000310546",42797,42,50,"T","ENSG00000175093","ENST00000310546","synonymous_variant","synonymous_variant","1527/2908","783/822","261/273","P","ccC/ccT"]
["EGFEM1P",93556,"WUGSC","GRCh38","chr3",168821192,168821192,"+","Splice_Site","SNP","G","G","T",null,null,"TCGA-LL-A5YP-01A-21D-A28B-09","TCGA-LL-A5YP-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","a6206343-6d41-485a-8992-3a466df43286","fe144218-875d-423c-80d7-05de5b2e1496","n.548-1G>T","ENST00000483846",null,58,55,"T","ENSG00000206120","ENST00000483846","splice_acceptor_variant","splice_acceptor_variant;non_coding_transcript_variant","-/2327"]
["IRX4",50805,"WUGSC","GRCh38","chr5",1877673,1877673,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-LL-A5YP-01A-21D-A28B-09","TCGA-LL-A5YP-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","a6206343-6d41-485a-8992-3a466df43286","fe144218-875d-423c-80d7-05de5b2e1496","c.*296G>C","ENST00000231357",42860,57,80,"G","ENSG00000113430","ENST00000231357","3_prime_UTR_variant","3_prime_UTR_variant","1975/2221","-/1560","-/519"]
["C5orf38",153571,"WUGSC","GRCh38","chr5",2755162,2755162,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-LL-A5YP-01A-21D-A28B-09","TCGA-LL-A5YP-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","a6206343-6d41-485a-8992-3a466df43286","fe144218-875d-423c-80d7-05de5b2e1496","c.*121G>C","ENST00000334000",42829,13,8,"C","ENSG00000186493","ENST00000334000","3_prime_UTR_variant","3_prime_UTR_variant","655/890","-/417","-/138"]
["POLK",51426,"WUGSC","GRCh38","chr5",75581473,75581473,"+","Intron","SNP","A","A","T","novel",null,"TCGA-LL-A5YP-01A-21D-A28B-09","TCGA-LL-A5YP-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","a6206343-6d41-485a-8992-3a466df43286","fe144218-875d-423c-80d7-05de5b2e1496","c.934+25A>T","ENST00000241436",null,14,9,"T","ENSG00000122008","ENST00000241436","intron_variant","intron_variant","-/5911","-/2613","-/870"]
["PCDHB6",56130,"WUGSC","GRCh38","chr5",141157937,141157937,"+","3'Flank","SNP","A","A","G","novel",null,"TCGA-LL-A5YP-01A-21D-A28B-09","TCGA-LL-A5YP-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","a6206343-6d41-485a-8992-3a466df43286","fe144218-875d-423c-80d7-05de5b2e1496",null,"ENST00000231136",null,148,245,"G","ENSG00000113211","ENST00000231136","downstream_gene_variant","downstream_gene_variant","-/3266","-/2385","-/794"]
["PRKD3",23683,"WUGSC","GRCh38","chr2",37269654,37269654,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-AO-A0JC-01A-11W-A071-09","TCGA-AO-A0JC-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","120f55df-5d1d-4073-a21a-632c892d3da9","a9132e75-b777-4399-969c-d1e8fab91117","c.1738G>C","ENST00000234179",43087,240,146,"G","ENSG00000115825","ENST00000234179","missense_variant","missense_variant","2293/5900","1738/2673","580/890","E/Q","Gag/Cag"]
["NELFCD",51497,"WUGSC","GRCh38","chr20",58988980,58988980,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-B6-A0RV-01A-11D-A099-09","TCGA-B6-A0RV-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","39b0b605-29ae-4e2c-81dc-319446c807dd","00bd0921-b765-4fbd-ab79-4d85aba0d1f6","c.517G>A","ENST00000602795",42870,126,201,"A","ENSG00000101158","ENST00000602795","missense_variant","missense_variant","565/2305","517/1800","173/599","E/K","Gaa/Aaa"]
["ZMAT1",84460,"WUGSC","GRCh38","chrX",101897897,101897897,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A8-A06Z-01A-11W-A019-09","TCGA-A8-A06Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","f540c4f8-75b3-47d7-a7cf-53cbf7a2c814","d8d09274-b620-4783-96d1-7b1ba32f89e6","c.476C>A","ENST00000372782",42862,733,435,"T","ENSG00000166432","ENST00000372782","missense_variant","missense_variant","524/3185","476/1917","159/638","A/E","gCa/gAa"]
["CWH43",80157,"WUGSC","GRCh38","chr4",49030935,49030935,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A209-01A-11D-A17G-09","TCGA-BH-A209-11A-42D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4eaf8116-4733-4865-8e22-5d03887bbc9b","68d5b797-ff7c-41ab-aedf-8a816ed290e2","c.1483C>T","ENST00000226432",43055,42,40,"T","ENSG00000109182","ENST00000226432","missense_variant","missense_variant","1666/2472","1483/2100","495/699","P/S","Cca/Tca"]
["GDF2",2658,"WUGSC","GRCh38","chr10",47325503,47325503,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-BH-A209-01A-11D-A17G-09","TCGA-BH-A209-11A-42D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4eaf8116-4733-4865-8e22-5d03887bbc9b","68d5b797-ff7c-41ab-aedf-8a816ed290e2","c.1009G>A","ENST00000581492",42768,34,42,"A","ENSG00000263761","ENST00000581492","missense_variant","missense_variant","1188/1955","1009/1290","337/429","E/K","Gag/Aag"]
["RNF144B",255488,"WUGSC","GRCh38","chr6",18387390,18387390,"+","5'UTR","SNP","C","C","T","rs530615611","by1000G;byCluster","TCGA-BH-A5J0-01A-11D-A27P-09","TCGA-BH-A5J0-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","b2273518-7fe0-4c1e-85f6-5c5ef7bbdcab","213426e8-ddbf-4920-813e-74f7f68823fe","c.-277C>T","ENST00000259939",42743,23,31,"T","ENSG00000137393","ENST00000259939","5_prime_UTR_variant","5_prime_UTR_variant","41/5036","-/912","-/303"]
["RNASE9",390443,"WUGSC","GRCh38","chr14",20556604,20556604,"+","Missense_Mutation","SNP","C","C","T","rs779466707","byFrequency","TCGA-GI-A2C8-01A-11D-A16D-09","TCGA-GI-A2C8-11A-22D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","535a899d-67ca-4500-8dda-63a331a3611c","2ec9bc9e-0d87-48ed-bccf-679c08d9c5a4","c.466G>A","ENST00000338904",42768,44,63,"T","ENSG00000188655","ENST00000338904","missense_variant","missense_variant","538/1049","466/618","156/205","E/K","Gaa/Aaa"]
["GRIA3",2892,"WUGSC","GRCh38","chrX",123185842,123185842,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-GI-A2C8-01A-11D-A16D-09","TCGA-GI-A2C8-11A-22D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","535a899d-67ca-4500-8dda-63a331a3611c","2ec9bc9e-0d87-48ed-bccf-679c08d9c5a4","c.120C>A","ENST00000541091",42781,31,53,"A","ENSG00000125675","ENST00000541091","missense_variant","missense_variant","173/2740","120/2685","40/894","F/L","ttC/ttA"]
["CRYBG3",131544,"WUGSC","GRCh38","chr3",97888411,97888411,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E2-A15M-01A-11D-A12B-09","TCGA-E2-A15M-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","06b28922-49b5-4633-a07b-c0bd51b2aee5","e71af20f-596d-4bad-8af3-4ded35614825","c.7360G>C","ENST00000389622",43000,72,206,"C","ENSG00000080200","ENST00000389622","missense_variant","missense_variant","7527/10729","7360/8913","2454/2970","E/Q","Gag/Cag"]
["DCST1",149095,"WUGSC","GRCh38","chr1",155041755,155041755,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A0DK-01A-21W-A071-09","TCGA-BH-A0DK-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","24973c7f-21be-48c6-9a24-636cbf7e39dd","0d68bf71-2788-4cda-a04d-ddf7de2fa8c9","c.790G>T","ENST00000295542",42964,82,55,"T","ENSG00000163357","ENST00000295542","missense_variant","missense_variant","886/2279","790/2121","264/706","D/Y","Gac/Tac"]
["NACAD",23148,"WUGSC","GRCh38","chr7",45084098,45084098,"+","Silent","SNP","C","C","T",null,null,"TCGA-D8-A1XS-01A-11D-A14K-09","TCGA-D8-A1XS-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","5d302c04-302e-4040-9429-37cd672e8d53","9b6db1ae-c8eb-4b02-9913-76070077fedf","c.2082G>A","ENST00000490531",42774,82,68,"T","ENSG00000136274","ENST00000490531","synonymous_variant","synonymous_variant","2102/4780","2082/4689","694/1562","S","tcG/tcA"]
["FAM174A",345757,"WUGSC","GRCh38","chr5",100586185,100586185,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-AR-A250-01A-31D-A167-09","TCGA-AR-A250-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","f7d9a372-fcd1-4462-9e0b-7eb46ddb68fd","0035e0c2-0376-4050-a03e-df556d408b94","c.*1G>C","ENST00000312637",42797,45,26,"C","ENSG00000174132","ENST00000312637","3_prime_UTR_variant","3_prime_UTR_variant","800/1356","-/573","-/190"]
["C2orf71",388939,"WUGSC","GRCh38","chr2",29072822,29072822,"+","Silent","SNP","A","A","G",null,null,"TCGA-A2-A3XT-01A-11D-A22X-09","TCGA-A2-A3XT-10A-01D-A22X-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina HiSeq 2500","f5afb86a-e57a-422a-abdb-6bab20273cc0","47db5812-3372-46bd-a59f-5fac0d3d1a97","c.1440T>C","ENST00000331664",42737,192,124,"G","ENSG00000179270","ENST00000331664","synonymous_variant","synonymous_variant","1440/7044","1440/3867","480/1288","S","tcT/tcC"]
["POM121L9P",29774,"WUGSC","GRCh38","chr22",24261015,24261015,"+","RNA","SNP","C","C","G","novel",null,"TCGA-A2-A3XT-01A-11D-A22X-09","TCGA-A2-A3XT-10A-01D-A22X-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina HiSeq 2500","f5afb86a-e57a-422a-abdb-6bab20273cc0","47db5812-3372-46bd-a59f-5fac0d3d1a97","n.2056C>G","ENST00000414583",42862,151,154,"G","ENSG00000128262","ENST00000414583","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","2056/5018"]
["DUSP4",1846,"WUGSC","GRCh38","chr8",29337412,29337412,"+","Splice_Site","SNP","C","C","T","novel",null,"TCGA-B6-A0IK-01A-12W-A071-09","TCGA-B6-A0IK-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","c5b1f426-562e-44e4-bcce-ce2ff6d969c8","79f55c96-edea-4b81-a4de-5df5e55df162","c.800-1G>A","ENST00000240100",null,14,22,"T","ENSG00000120875","ENST00000240100","splice_acceptor_variant","splice_acceptor_variant","-/5537","800/1185","267/394"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179234297,179234297,"+","Missense_Mutation","SNP","A","A","G","rs121913279","byCluster;byFrequency","TCGA-BH-A1F8-01A-11D-A13L-09","TCGA-BH-A1F8-11B-21D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","030cfc8a-7b43-4d73-8bfa-b68a47749e49","05c094da-381f-4c2d-bec1-aa0259f7793f","c.3140A>G","ENST00000263967","21/21",128,45,"G","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","3297/9093","3140/3207","1047/1068","H/R","cAt/cGt"]
["SLC6A12",6539,"WUGSC","GRCh38","chr12",204568,204568,"+","Silent","SNP","G","G","A",null,null,"TCGA-BH-A1F8-01A-11D-A13L-09","TCGA-BH-A1F8-11B-21D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","030cfc8a-7b43-4d73-8bfa-b68a47749e49","05c094da-381f-4c2d-bec1-aa0259f7793f","c.345C>T","ENST00000359674",42841,34,21,"A","ENSG00000111181","ENST00000359674","synonymous_variant","synonymous_variant","674/3165","345/1845","115/614","F","ttC/ttT"]
["TARS2",80222,"WUGSC","GRCh38","chr1",150499231,150499231,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-BH-A0C0-01A-21W-A071-09","TCGA-BH-A0C0-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","cb9d68dd-d159-4a7e-b914-18d2498b19d6","58a1d50c-1674-4db6-8ed7-d2aa04826142","c.1555C>A","ENST00000369064","13/18",300,419,"A","ENSG00000143374","ENST00000369064","missense_variant","missense_variant","1589/2729","1555/2157","519/718","L/M","Ctg/Atg"]
["XPO6",23214,"WUGSC","GRCh38","chr16",28146148,28146148,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-B6-A0IH-01A-11D-A10Y-09","TCGA-B6-A0IH-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","4a4488b9-74d9-4eb1-a7ef-c894c32db942","348ca096-ee86-4a96-9a09-a90b24e84060","c.1280A>G","ENST00000304658",43002,327,346,"C","ENSG00000169180","ENST00000304658","missense_variant","missense_variant","1781/4422","1280/3378","427/1125","Y/C","tAt/tGt"]
["BICC1",80114,"WUGSC","GRCh38","chr10",58800967,58800967,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-D8-A143-01A-11D-A10Y-09","TCGA-D8-A143-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","db1763d1-fcae-4a01-a0cb-3019e292aa10","a8bb9607-a942-4e01-a4e3-faeeff223d0d","c.1936A>T","ENST00000373886","14/21",164,106,"T","ENSG00000122870","ENST00000373886","missense_variant","missense_variant","1940/5475","1936/2925","646/974","M/L","Atg/Ttg"]
["PPP1R3B",79660,"WUGSC","GRCh38","chr8",9141273,9141273,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-EW-A1IW-01A-11D-A13L-09","TCGA-EW-A1IW-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","8b8732c3-78b1-409b-bc8c-c482575361bb","853ff819-807d-4569-b4e9-16f7f4cb59b3","c.379C>T","ENST00000310455",42768,65,28,"A","ENSG00000173281","ENST00000310455","stop_gained","stop_gained","530/5548","379/858","127/285","R/*","Cga/Tga"]
["NES",10763,"WUGSC","GRCh38","chr1",156670482,156670482,"+","Nonsense_Mutation","SNP","G","G","A","novel",null,"TCGA-BH-A0E9-01B-11D-A10Y-09","TCGA-BH-A0E9-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","48ccd30d-0c71-4117-8ccb-013986f14e95","244a360a-b8b8-4a85-b86d-8138b3d6e397","c.3706C>T","ENST00000368223",42829,62,39,"A","ENSG00000132688","ENST00000368223","stop_gained","stop_gained","3839/5558","3706/4866","1236/1621","Q/*","Cag/Tag"]
["HIST1H2AH",85235,"WUGSC","GRCh38","chr6",27147470,27147470,"+","Silent","SNP","C","C","G","rs574744122","by1000G;byFrequency","TCGA-A8-A0A9-01A-11W-A019-09","TCGA-A8-A0A9-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","228e66eb-1dc6-4c01-8252-c557a8f53916","80968de5-1de3-4be8-8697-1764f28db89f","c.342C>G","ENST00000377459",42736,78,97,"G","ENSG00000274997","ENST00000377459","synonymous_variant","synonymous_variant","342/387","342/387","114/128","A","gcC/gcG"]
["SI",6476,"WUGSC","GRCh38","chr3",164998606,164998606,"+","Nonsense_Mutation","SNP","G","G","A","rs747584061",null,"TCGA-B6-A0RH-01A-21D-A10Y-09","TCGA-B6-A0RH-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","6e59b987-b4f0-4078-af2d-482c299103b6","6041e087-636b-4f3c-96d9-202e0d102899","c.4474C>T","ENST00000264382","38/48",246,372,"A","ENSG00000090402","ENST00000264382","stop_gained","stop_gained","4537/6011","4474/5484","1492/1827","R/*","Cga/Tga"]
["RAD51",5888,"WUGSC","GRCh38","chr15",40729513,40729513,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-BH-A0HW-01A-11W-A050-09","TCGA-BH-A0HW-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","706ec3be-bd65-4f42-b5cc-603f7f62c91a","76e4b953-efcc-401c-916a-e3c7ecbe8de6","c.653T>G","ENST00000267868",42957,51,75,"G","ENSG00000051180","ENST00000267868","missense_variant","missense_variant","921/2449","653/1020","218/339","L/R","cTg/cGg"]
["SLITRK1",114798,"WUGSC","GRCh38","chr13",83879530,83879530,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A7-A26H-01A-11D-A167-09","TCGA-A7-A26H-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fbeade79-28ef-4e85-8282-67e691630ca3","73459869-08fc-408a-bdf0-6ca346113171","c.1978G>A","ENST00000377084",42736,27,33,"T","ENSG00000178235","ENST00000377084","missense_variant","missense_variant","2864/5189","1978/2091","660/696","E/K","Gag/Aag"]
["TNRC6B",23112,"WUGSC","GRCh38","chr22",40308521,40308521,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A7-A26H-01A-11D-A167-09","TCGA-A7-A26H-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fbeade79-28ef-4e85-8282-67e691630ca3","73459869-08fc-408a-bdf0-6ca346113171","c.4130C>T","ENST00000454349","16/23",63,83,"T","ENSG00000100354","ENST00000454349","missense_variant","missense_variant","4341/18279","4130/5502","1377/1833","S/F","tCt/tTt"]
["TMEM132C",92293,"WUGSC","GRCh38","chr12",128415129,128415129,"+","Silent","SNP","C","C","T","rs138627815","by1000G;byFrequency","TCGA-C8-A9FZ-01A-11D-A41F-09","TCGA-C8-A9FZ-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","97aabeff-bd2d-4c9e-914d-90e0c766daf7","8cfc64e3-5b44-4cc6-b8af-3d73bd6b3cde","c.483C>T","ENST00000435159",42775,77,138,"T","ENSG00000181234","ENST00000435159","synonymous_variant","synonymous_variant","483/4947","483/3327","161/1108","H","caC/caT"]
["ZNF366",167465,"WUGSC","GRCh38","chr5",72456409,72456409,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AO-A03O-01A-11W-A019-09","TCGA-AO-A03O-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","1578b356-7f42-4722-bc54-cd5f37954f6a","4b2392a1-ce32-47dd-83d2-be2342be7a58","c.1519T>A","ENST00000318442",42799,173,193,"T","ENSG00000178175","ENST00000318442","missense_variant","missense_variant","2010/3830","1519/2235","507/744","C/S","Tgc/Agc"]
["THADA",63892,"WUGSC","GRCh38","chr2",43590859,43590859,"+","Silent","SNP","C","C","T","novel",null,"TCGA-A8-A07U-01A-11W-A050-09","TCGA-A8-A07U-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","e6409415-8453-489d-a731-49257cade2a3","bd1d1390-403b-4e65-9ecc-430b52d2f8af","c.267G>A","ENST00000405006",13971,380,223,"T","ENSG00000115970","ENST00000405006","synonymous_variant","synonymous_variant","619/6310","267/5862","89/1953","L","ttG/ttA"]
["ZNF208",7757,"WUGSC","GRCh38","chr19",21974389,21974389,"+","Silent","SNP","G","G","T","rs764030563",null,"TCGA-A7-A0CD-01A-11W-A019-09","TCGA-A7-A0CD-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d29ba065-28ca-4dfb-9588-06be857f67b2","1f53f23c-bb31-4247-ba6a-fa2b4d7d9fbf","c.645C>A","ENST00000397126",42829,511,513,"T","ENSG00000160321","ENST00000397126","synonymous_variant","synonymous_variant","794/3992","645/3843","215/1280","T","acC/acA"]
["ZNF37BP",100129482,"WUGSC","GRCh38","chr10",42520104,42520104,"+","RNA","SNP","G","G","A",null,null,"TCGA-A7-A26I-01A-11D-A167-09","TCGA-A7-A26I-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","81fff2d1-d6ed-4963-a5f6-5899cde6b359","d4ad0739-04d5-4d68-a794-7fe9aa13ff38","n.2043C>T","ENST00000452075",42955,17,27,"A","ENSG00000234420","ENST00000452075","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","2043/8637"]
["BMP15",9210,"WUGSC","GRCh38","chrX",50910804,50910804,"+","Silent","SNP","T","T","C","novel",null,"TCGA-XX-A899-01A-11D-A36J-09","TCGA-XX-A899-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","49fb101d-f242-4abf-bf85-6a8c3ced711d","0ffd9ad1-6643-42ff-af29-13389bfb1364","c.21T>C","ENST00000252677",42737,88,99,"C","ENSG00000130385","ENST00000252677","synonymous_variant","synonymous_variant","21/1179","21/1179","7/392","L","ctT/ctC"]
["CCDC124",115098,"WUGSC","GRCh38","chr19",17942674,17942674,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-UL-AAZ6-01A-11D-A41F-09","TCGA-UL-AAZ6-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","878a8452-abfa-48b4-8a6a-75d01dbad458","37d7fd9b-94b5-4bd9-a0cb-02ae7eab5712","c.178C>T","ENST00000445755",42799,148,193,"T","ENSG00000007080","ENST00000445755","missense_variant","missense_variant","222/938","178/672","60/223","R/C","Cgc/Tgc"]
["SLC6A17",388662,"WUGSC","GRCh38","chr1",110167078,110167078,"+","Missense_Mutation","SNP","C","C","T","rs770557467","byFrequency","TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.149C>T","ENST00000331565",42778,226,232,"T","ENSG00000197106","ENST00000331565","missense_variant","missense_variant","634/6427","149/2184","50/727","A/V","gCg/gTg"]
["IGSF9",57549,"WUGSC","GRCh38","chr1",159934809,159934809,"+","Silent","SNP","G","G","A",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.687C>T","ENST00000368094",42937,393,164,"A","ENSG00000085552","ENST00000368094","synonymous_variant","synonymous_variant","885/4044","687/3540","229/1179","I","atC/atT"]
["GALM",130589,"WUGSC","GRCh38","chr2",38731770,38731770,"+","Missense_Mutation","SNP","T","T","C","rs570948999","by1000G","TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.812T>C","ENST00000272252",42893,271,231,"C","ENSG00000143891","ENST00000272252","missense_variant","missense_variant","1064/2484","812/1029","271/342","V/A","gTa/gCa"]
["EPHB1",2047,"WUGSC","GRCh38","chr3",134925861,134925861,"+","Missense_Mutation","SNP","C","C","T","rs536029159","by1000G","TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.104C>T","ENST00000398015",42782,247,285,"T","ENSG00000154928","ENST00000398015","missense_variant","missense_variant","474/4672","104/2955","35/984","T/M","aCg/aTg"]
["FBXL7",23194,"WUGSC","GRCh38","chr5",15936571,15936571,"+","Silent","SNP","C","C","T",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.861C>T","ENST00000504595",42829,107,114,"T","ENSG00000183580","ENST00000504595","synonymous_variant","synonymous_variant","1342/4562","861/1476","287/491","D","gaC/gaT"]
["ADGRF5",221395,"WUGSC","GRCh38","chr6",46867066,46867066,"+","Silent","SNP","G","G","A",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.1693C>T","ENST00000265417","13/21",343,316,"A","ENSG00000069122","ENST00000265417","synonymous_variant","synonymous_variant","1927/5668","1693/4041","565/1346","L","Ctg/Ttg"]
["ZNF34",80778,"WUGSC","GRCh38","chr8",144773975,144773975,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.974A>G","ENST00000343459",42892,130,122,"C","ENSG00000196378","ENST00000343459","missense_variant","missense_variant","1040/1901","974/1683","325/560","H/R","cAc/cGc"]
["NUDT13",25961,"WUGSC","GRCh38","chr10",73126697,73126697,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.728G>A","ENST00000357321",42956,321,285,"A","ENSG00000166321","ENST00000357321","missense_variant","missense_variant","846/2102","728/1059","243/352","R/H","cGc/cAc"]
["ZDHHC13",54503,"WUGSC","GRCh38","chr11",19175970,19175970,"+","3'UTR","SNP","A","A","G","novel",null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.*10A>G","ENST00000446113","17/17",278,234,"G","ENSG00000177054","ENST00000446113","3_prime_UTR_variant","3_prime_UTR_variant","2000/2445","-/1869","-/622"]
["AQP6",363,"WUGSC","GRCh38","chr12",49975369,49975369,"+","Intron","SNP","G","G","T","novel",null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.643-96G>T","ENST00000315520",null,22,19,"T","ENSG00000086159","ENST00000315520","intron_variant","intron_variant","-/1398","-/849","-/282"]
["XPO4",64328,"WUGSC","GRCh38","chr13",20842933,20842933,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.689C>T","ENST00000255305",42909,158,113,"A","ENSG00000132953","ENST00000255305","missense_variant","missense_variant","761/9921","689/3456","230/1151","A/V","gCc/gTc"]
["ADCY7",113,"WUGSC","GRCh38","chr16",50290588,50290588,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.303G>T","ENST00000254235",42791,242,237,"T","ENSG00000121281","ENST00000254235","missense_variant","missense_variant","571/6138","303/3243","101/1080","W/C","tgG/tgT"]
["DHX58",79132,"WUGSC","GRCh38","chr17",42110732,42110732,"+","Silent","SNP","G","G","A",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.552C>T","ENST00000251642",42869,78,152,"A","ENSG00000108771","ENST00000251642","synonymous_variant","synonymous_variant","775/2617","552/2037","184/678","H","caC/caT"]
["KRI1",65095,"WUGSC","GRCh38","chr19",10557594,10557594,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.1593C>A","ENST00000312962","16/19",221,197,"T","ENSG00000129347","ENST00000312962","stop_gained","stop_gained","1613/3023","1593/2130","531/709","Y/*","taC/taA"]
["ZNF780B",163131,"WUGSC","GRCh38","chr19",40034996,40034996,"+","Silent","SNP","G","G","T",null,null,"TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.1863C>A","ENST00000434248",42860,401,358,"T","ENSG00000128000","ENST00000434248","synonymous_variant","synonymous_variant","1929/8665","1863/2502","621/833","A","gcC/gcA"]
["SLC2A10",81031,"WUGSC","GRCh38","chr20",46725217,46725217,"+","Missense_Mutation","SNP","G","G","A","rs768203290","byFrequency","TCGA-BH-A18G-01A-11D-A12B-09","TCGA-BH-A18G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5f080655-65bd-42af-8cde-15dc2d255f3c","fdeda5fc-8cdb-45d8-bd01-1caa1c068af0","c.181G>A","ENST00000359271",42771,265,255,"A","ENSG00000197496","ENST00000359271","missense_variant","missense_variant","431/4389","181/1626","61/541","A/T","Gcc/Acc"]
["MROH2B",133558,"WUGSC","GRCh38","chr5",41052500,41052500,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A0XV-01A-11D-A10G-09","TCGA-AN-A0XV-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","6f0e5a39-e2c7-4a93-bd63-f1bab1e7c16e","ad602351-e61a-4469-97b0-fedfa3320fdf","c.1195G>A","ENST00000399564",15676,113,106,"T","ENSG00000171495","ENST00000399564","missense_variant","missense_variant","1646/5239","1195/4758","399/1585","V/I","Gtc/Atc"]
["FMN2",56776,"WUGSC","GRCh38","chr1",240092387,240092387,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0HK-01A-11W-A071-09","TCGA-BH-A0HK-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","fe131f38-d0a6-446b-831f-6f1f9e382594","2765bf65-94df-4c9a-91c2-0bb653729c02","c.278C>T","ENST00000319653",42753,15,11,"T","ENSG00000155816","ENST00000319653","missense_variant","missense_variant","508/6434","278/5169","93/1722","S/F","tCc/tTc"]
["C17orf53",78995,"WUGSC","GRCh38","chr17",44152636,44152636,"+","Splice_Site","SNP","G","G","C",null,null,"TCGA-BH-A0HK-01A-11W-A071-09","TCGA-BH-A0HK-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","fe131f38-d0a6-446b-831f-6f1f9e382594","2765bf65-94df-4c9a-91c2-0bb653729c02","c.1309-1G>C","ENST00000319977",null,72,83,"C","ENSG00000125319","ENST00000319977","splice_acceptor_variant","splice_acceptor_variant","-/2725","1309/1944","437/647"]
["AKAP12",9590,"WUGSC","GRCh38","chr6",151349221,151349221,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-A7-A6VW-01A-21D-A33E-09","TCGA-A7-A6VW-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","20340d40-2959-4c8e-a364-0749088b0649","b4911a5d-e94b-479f-8756-9d8eb685044f","c.830C>A","ENST00000253332",42798,52,30,"A","ENSG00000131016","ENST00000253332","missense_variant","missense_variant","1019/6597","830/5349","277/1782","P/H","cCt/cAt"]
["ZNF814",730051,"WUGSC","GRCh38","chr19",57874753,57874753,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-3C-AALK-01A-11D-A41F-09","TCGA-3C-AALK-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","e15261e6-6ab7-4a24-a04e-4f992a1da251","bcf4018a-98f3-4f38-a23a-7bb3e84d596c","c.637C>T","ENST00000435989",42797,43,124,"A","ENSG00000204514","ENST00000435989","missense_variant","missense_variant","872/3146","637/2568","213/855","H/Y","Cac/Tac"]
["OR6P1",128366,"WUGSC","GRCh38","chr1",158563088,158563088,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-D8-A1JD-01A-11D-A13L-09","TCGA-D8-A1JD-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","7df92725-fa63-494d-af9d-65c6ed76e023","c27dea12-3973-44a8-b150-da7a22ff80e3","c.517A>T","ENST00000334632",42736,48,70,"A","ENSG00000186440","ENST00000334632","missense_variant","missense_variant","517/954","517/954","173/317","I/F","Att/Ttt"]
["OPHN1",4983,"WUGSC","GRCh38","chrX",68192937,68192937,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-D8-A1JD-01A-11D-A13L-09","TCGA-D8-A1JD-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","7df92725-fa63-494d-af9d-65c6ed76e023","c27dea12-3973-44a8-b150-da7a22ff80e3","c.1258C>A","ENST00000355520","15/25",155,61,"T","ENSG00000079482","ENST00000355520","missense_variant","missense_variant","1900/7879","1258/2409","420/802","L/M","Ctg/Atg"]
["TYRP1",7306,"WUGSC","GRCh38","chr9",12695736,12695736,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-A8-A07W-01A-11W-A019-09","TCGA-A8-A07W-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","9bc8dbab-c700-498c-8ff7-ccc62c911349","efeb884c-b13d-46ba-90b0-5b23593b53f3","c.607G>C","ENST00000388918",42802,394,403,"C","ENSG00000107165","ENST00000388918","missense_variant","missense_variant","736/2851","607/1614","203/537","V/L","Gta/Cta"]
["ZXDB",158586,"WUGSC","GRCh38","chrX",57594951,57594951,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-E2-A9RU-01A-11D-A41F-09","TCGA-E2-A9RU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","4b0e06a6-27c9-4c9a-b230-c1054f2380f7","71f73bdb-7b6b-45bb-a696-1a461b5cb707","c.*491C>A","ENST00000374888",42736,46,99,"A","ENSG00000198455","ENST00000374888","3_prime_UTR_variant","3_prime_UTR_variant","3300/5894","-/2412","-/803"]
["MIR8078",102466878,"WUGSC","GRCh38","chr18",117294,117294,"+","5'Flank","SNP","T","T","C",null,null,"TCGA-AC-A3YJ-01A-11D-A22X-09","TCGA-AC-A3YJ-10A-01D-A22X-09",null,null,"Somatic","Illumina HiSeq 2000","6fecea7a-e8f4-4d95-bcd6-52cf363104e7","aee3b032-58c1-4ba5-ae5f-9008ca914a5b",null,"ENST00000619811",null,58,58,"C","ENSG00000277521","ENST00000619811","upstream_gene_variant","upstream_gene_variant","-/84"]
["AKT1",207,"WUGSC","GRCh38","chr14",104780214,104780214,"+","Missense_Mutation","SNP","C","C","T","rs121434592","byCluster","TCGA-GM-A2DL-01A-11D-A18P-09","TCGA-GM-A2DL-10C-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","05618052-7f63-45dc-9a47-df92fce1bad9","9f1ebbdb-32b6-4e83-80e9-d87433f83958","c.49G>A","ENST00000349310",42840,31,49,"T","ENSG00000142208","ENST00000349310","missense_variant","missense_variant;splice_region_variant","480/2866","49/1443","17/480","E/K","Gag/Aag"]
["CARD11",84433,"WUGSC","GRCh38","chr7",2919412,2919412,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A2-A0D2-01A-21W-A050-09","TCGA-A2-A0D2-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","05656575-69e7-4745-a89d-ca0568eb5559","c830c663-95f6-40e0-9fd6-16586fa7d344","c.2470G>C","ENST00000396946","18/25",49,91,"G","ENSG00000198286","ENST00000396946","missense_variant","missense_variant","2874/4366","2470/3465","824/1154","D/H","Gac/Cac"]
["CPT2",1376,"WUGSC","GRCh38","chr1",53210955,53210955,"+","Silent","SNP","C","C","T","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.1281C>T","ENST00000371486",42830,75,51,"T","ENSG00000157184","ENST00000371486","synonymous_variant","synonymous_variant","1796/3094","1281/1977","427/658","I","atC/atT"]
["VANGL2",57216,"WUGSC","GRCh38","chr1",160419542,160419542,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.733C>T","ENST00000368061",42833,63,27,"T","ENSG00000162738","ENST00000368061","stop_gained","stop_gained","1207/5340","733/1566","245/521","Q/*","Cag/Tag"]
["TFB2M",64216,"WUGSC","GRCh38","chr1",246541054,246541054,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.1168G>C","ENST00000366514",42955,150,68,"G","ENSG00000162851","ENST00000366514","missense_variant","missense_variant","1354/1848","1168/1191","390/396","D/H","Gat/Cat"]
["LRP1B",53353,"WUGSC","GRCh38","chr2",140950265,140950265,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.3106G>C","ENST00000389484","20/91",243,139,"G","ENSG00000168702","ENST00000389484","missense_variant","missense_variant","4078/16535","3106/13800","1036/4599","D/H","Gat/Cat"]
["IDH1",3417,"WUGSC","GRCh38","chr2",208242067,208242067,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.777G>A","ENST00000345146",42926,102,55,"T","ENSG00000138413","ENST00000345146","missense_variant","missense_variant","1062/2382","777/1245","259/414","M/I","atG/atA"]
["ARHGAP24",83478,"WUGSC","GRCh38","chr4",86000774,86000774,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.*52C>G","ENST00000395184",43018,69,31,"G","ENSG00000138639","ENST00000395184","3_prime_UTR_variant","3_prime_UTR_variant","2765/4661","-/2247","-/748"]
["MCC",4163,"WUGSC","GRCh38","chr5",113027452,113027452,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.2340G>C","ENST00000302475","17/17",128,62,"G","ENSG00000171444","ENST00000302475","missense_variant","missense_variant","2904/8257","2340/2490","780/829","K/N","aaG/aaC"]
["N4BP3",23138,"WUGSC","GRCh38","chr5",178120343,178120343,"+","Missense_Mutation","SNP","C","C","G","rs772816113","byFrequency","TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.496C>G","ENST00000274605",42799,109,70,"G","ENSG00000145911","ENST00000274605","missense_variant","missense_variant","855/6080","496/1635","166/544","Q/E","Cag/Gag"]
["ADGB",79747,"WUGSC","GRCh38","chr6",146717050,146717050,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.1909G>C","ENST00000397944","15/36",91,40,"C","ENSG00000118492","ENST00000397944","missense_variant","missense_variant","1985/5325","1909/5004","637/1667","D/H","Gat/Cat"]
["ZFPM2",23414,"WUGSC","GRCh38","chr8",105798837,105798837,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.853G>A","ENST00000407775",42924,105,60,"A","ENSG00000169946","ENST00000407775","missense_variant","missense_variant","1103/4700","853/3456","285/1151","E/K","Gag/Aag"]
["FAM73B",84895,"WUGSC","GRCh38","chr9",129049439,129049439,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.479G>T","ENST00000358369",42871,76,56,"T","ENSG00000148343","ENST00000358369","missense_variant","missense_variant","705/3637","479/1782","160/593","R/I","aGa/aTa"]
["PLCE1",51196,"WUGSC","GRCh38","chr10",94298568,94298568,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.5357G>A","ENST00000260766","24/33",81,51,"A","ENSG00000138193","ENST00000260766","missense_variant","missense_variant","5991/7992","5357/6909","1786/2302","R/K","aGa/aAa"]
["NXF1",10482,"WUGSC","GRCh38","chr11",62794272,62794272,"+","Silent","SNP","G","G","A","rs181325349","by1000G;byCluster;byFrequency","TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.1746C>T","ENST00000294172","19/21",49,29,"A","ENSG00000162231","ENST00000294172","synonymous_variant","synonymous_variant","1882/2346","1746/1860","582/619","L","ctC/ctT"]
["FAM186A",121006,"WUGSC","GRCh38","chr12",50351679,50351679,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.5153C>T","ENST00000327337",42833,183,100,"A","ENSG00000185958","ENST00000327337","missense_variant","missense_variant","5153/7127","5153/7056","1718/2351","S/L","tCg/tTg"]
["DIO3",1735,"WUGSC","GRCh38","chr14",101562880,101562880,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.*469G>C","ENST00000510508",42736,84,63,"C","ENSG00000197406","ENST00000510508","3_prime_UTR_variant","3_prime_UTR_variant","1530/2102","-/915","-/304"]
["ERCC4",2072,"WUGSC","GRCh38","chr16",13920187,13920187,"+","Nonsense_Mutation","SNP","C","C","T","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.22C>T","ENST00000311895",42746,208,144,"T","ENSG00000175595","ENST00000311895","stop_gained","stop_gained","31/6758","22/2751","8/916","R/*","Cga/Tga"]
["KRT33A",3883,"WUGSC","GRCh38","chr17",41346935,41346935,"+","Missense_Mutation","SNP","G","G","A","rs779297022",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.785C>T","ENST00000007735",42862,167,93,"A","ENSG00000006059","ENST00000007735","missense_variant","missense_variant","830/1287","785/1215","262/404","S/L","tCg/tTg"]
["SMIM21",284274,"WUGSC","GRCh38","chr18",75410282,75410282,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.*582G>A","ENST00000579022",42797,101,54,"T","ENSG00000206026","ENST00000579022","3_prime_UTR_variant","3_prime_UTR_variant","1028/1834","-/306","-/101"]
["FAM217B",63939,"WUGSC","GRCh38","chr20",59946499,59946499,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.*1404G>A","ENST00000358293",42860,197,81,"A","ENSG00000196227","ENST00000358293","3_prime_UTR_variant","3_prime_UTR_variant","2971/5152","-/1152","-/383"]
["FOXO4",4303,"WUGSC","GRCh38","chrX",71101278,71101278,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-5L-AAT1-01A-12D-A41F-09","TCGA-5L-AAT1-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","af6872d5-0475-437f-b4d6-5115e71c442e","9db372b8-f687-49c1-844a-53d3e1246ef4","c.1048G>A","ENST00000374259",42769,68,38,"A","ENSG00000184481","ENST00000374259","missense_variant","missense_variant","1380/3301","1048/1518","350/505","E/K","Gag/Aag"]
["USP42",84132,"WUGSC","GRCh38","chr7",6115383,6115383,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-E2-A14Q-01A-11D-A12B-09","TCGA-E2-A14Q-10A-01D-A12B-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","ee51cf6d-351f-48f8-ab93-639c27c50e9f","323a490c-8dd7-4715-b083-f238c565b60d","c.302T>G","ENST00000306177",42812,231,57,"G","ENSG00000106346","ENST00000306177","missense_variant","missense_variant","460/5155","302/3951","101/1316","L/R","cTt/cGt"]
["CACNA2D2",9254,"WUGSC","GRCh38","chr3",50367416,50367416,"+","Silent","SNP","G","G","A",null,null,"TCGA-E9-A228-01A-31D-A159-09","TCGA-E9-A228-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","4a804a8d-7dc8-4b5b-9537-b7f8f7133bda","c618a148-78cb-425d-b026-e2f1c10773bd","c.2400C>T","ENST00000479441","28/39",74,50,"A","ENSG00000007402","ENST00000479441","synonymous_variant","synonymous_variant","2400/3453","2400/3453","800/1150","V","gtC/gtT"]
["ZBTB37",84614,"WUGSC","GRCh38","chr1",173865371,173865371,"+","5'Flank","SNP","C","C","G",null,null,"TCGA-AN-A0AL-01A-11W-A019-09","TCGA-AN-A0AL-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","47849ee3-b59e-4ccf-a261-65f7e252b885","2f79e4ef-5112-4d70-8320-ca2148b47621",null,"ENST00000367701",null,29,43,"G","ENSG00000185278","ENST00000367701","upstream_gene_variant","upstream_gene_variant","-/19128","-/1512","-/503"]
["FAM122B",159090,"WUGSC","GRCh38","chrX",134789100,134789100,"+","Silent","SNP","A","A","G",null,null,"TCGA-D8-A1JI-01A-11D-A13L-09","TCGA-D8-A1JI-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","2c6a885b-0452-492c-8829-13ba4b2ac455","011f9e39-3f8f-48df-b392-ab2963cfde84","c.261T>C","ENST00000370790",42834,172,86,"G","ENSG00000156504","ENST00000370790","synonymous_variant","synonymous_variant","1190/4246","261/744","87/247","D","gaT/gaC"]
["CA9",768,"WUGSC","GRCh38","chr9",35674293,35674293,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A04X-01A-21W-A050-09","TCGA-A2-A04X-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","66a73891-2fea-450c-8224-0865d98b4346","20662b69-e7e6-4f78-a7fb-2c1562ca4223","c.334G>T","ENST00000378357",42746,132,179,"T","ENSG00000107159","ENST00000378357","missense_variant","missense_variant","438/1618","334/1380","112/459","D/Y","Gat/Tat"]
["KIF21B",23046,"WUGSC","GRCh38","chr1",200990609,200990609,"+","Silent","SNP","G","G","C",null,null,"TCGA-AO-A0J3-01A-11W-A050-09","TCGA-AO-A0J3-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","ff706355-867e-4968-99ad-0af4e24ece51","ac697d39-8c85-4acf-8ca9-fe8cb8cc77f8","c.2802C>G","ENST00000422435","19/35",109,148,"C","ENSG00000116852","ENST00000422435","synonymous_variant","synonymous_variant","3119/5519","2802/4914","934/1637","V","gtC/gtG"]
["UNC93A",54346,"WUGSC","GRCh38","chr6",167296069,167296069,"+","Missense_Mutation","SNP","G","G","A","rs775793583",null,"TCGA-B6-A0I9-01A-11W-A050-09","TCGA-B6-A0I9-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","d2291482-9bbb-4f8f-a65b-c0737cf3acea","eba08b28-762e-4d9d-a5ee-c180ce7621ec","c.307G>A","ENST00000230256",42802,135,143,"A","ENSG00000112494","ENST00000230256","missense_variant","missense_variant","482/2116","307/1374","103/457","G/R","Ggg/Agg"]
["CASQ2",845,"WUGSC","GRCh38","chr1",115738269,115738269,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A2-A0D0-01A-11W-A019-09","TCGA-A2-A0D0-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","3f20d0fe-aaa1-40f1-b2c1-7f070f93aef5","bbf1c43d-d7b3-4574-a074-d22ad537829c","c.487G>C","ENST00000261448",42836,628,304,"G","ENSG00000118729","ENST00000261448","missense_variant","missense_variant","727/2674","487/1200","163/399","D/H","Gac/Cac"]
["FAM219B",57184,"WUGSC","GRCh38","chr15",74905188,74905188,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AO-A0J4-01A-11W-A050-09","TCGA-AO-A0J4-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","7667f49c-449d-44ce-bab8-02a491bb6775","211ddcb7-5fea-46cf-86f5-dc6d5f4cae36","c.346C>T","ENST00000357635",42799,45,38,"A","ENSG00000178761","ENST00000357635","missense_variant","missense_variant","667/3550","346/597","116/198","P/S","Cca/Tca"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179234297,179234297,"+","Missense_Mutation","SNP","A","A","G","rs121913279","byCluster;byFrequency","TCGA-BH-A18F-01A-11D-A12B-09","TCGA-BH-A18F-11A-22D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","d414b3fe-b768-4a98-b285-5284bffa66f9","8404ab78-054d-4cd1-b92e-951f3047ff45","c.3140A>G","ENST00000263967","21/21",189,224,"G","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","3297/9093","3140/3207","1047/1068","H/R","cAt/cGt"]
["NPTX2",4885,"WUGSC","GRCh38","chr7",98628497,98628497,"+","Silent","SNP","T","T","C",null,null,"TCGA-BH-A1F6-01A-11D-A13L-09","TCGA-BH-A1F6-11B-94D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","34eb095d-3d44-4c59-9ef5-94592ba97900","9a86338f-4176-4931-ba32-457e92d4b0dc","c.1164T>C","ENST00000265634",42860,67,72,"C","ENSG00000106236","ENST00000265634","synonymous_variant","synonymous_variant","1329/2700","1164/1296","388/431","I","atT/atC"]
["CACNA1G",8913,"WUGSC","GRCh38","chr17",50617569,50617569,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0HX-01A-21W-A071-09","TCGA-BH-A0HX-10A-02W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","27df78cd-1f39-42f3-92e6-56664d4c472c","ec32084a-c085-4ef6-b50e-212ae61944ec","c.5153G>A","ENST00000359106","29/38",58,32,"A","ENSG00000006283","ENST00000359106","missense_variant","missense_variant;splice_region_variant","5153/7648","5153/7134","1718/2377","R/Q","cGa/cAa"]
["INADL",10207,"WUGSC","GRCh38","chr1",61990240,61990240,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-GM-A2DD-01A-11D-A17W-09","TCGA-GM-A2DD-10C-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","42a8b6bb-6b28-4663-8b48-2928fa8c71c2","f86d9ca8-d705-4041-bdde-f7e3014f8ae3","c.3743G>A","ENST00000371158","28/43",63,53,"A","ENSG00000132849","ENST00000371158","missense_variant","missense_variant","3857/8505","3743/5406","1248/1801","G/E","gGa/gAa"]
["CUBN",8029,"WUGSC","GRCh38","chr10",17084408,17084408,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A13Y-01A-11D-A10Y-09","TCGA-D8-A13Y-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","8bb90325-028e-491a-bbaf-2cf4b3b87cd6","527b325c-63e5-4f66-9caf-6081829fbc2a","c.2164C>T","ENST00000377833","17/67",122,116,"A","ENSG00000107611","ENST00000377833","missense_variant","missense_variant","2230/11949","2164/10872","722/3623","P/S","Cct/Tct"]
["LRBA",987,"WUGSC","GRCh38","chr4",150302717,150302717,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A7-A13G-01A-11D-A13L-09","TCGA-A7-A13G-11A-51D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ef847b83-eb88-435b-bcfd-4b51d4dfa5fe","7eaacabd-76fe-4080-9e1c-7277bffe8b89","c.7958G>C","ENST00000357115","54/58",110,122,"G","ENSG00000198589","ENST00000357115","missense_variant","missense_variant","8202/9899","7958/8592","2653/2863","G/A","gGa/gCa"]
["PRKCG",5582,"WUGSC","GRCh38","chr19",53900428,53900428,"+","Silent","SNP","G","G","A","rs373576217","byCluster;byFrequency","TCGA-C8-A12O-01A-11D-A10Y-09","TCGA-C8-A12O-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","51dbda2a-106b-4597-aa49-609b677866c8","5d34bbb4-54c8-4a35-baee-80c72548ca34","c.1383G>A","ENST00000263431","13/18",124,76,"A","ENSG00000126583","ENST00000263431","synonymous_variant","synonymous_variant","1665/3133","1383/2094","461/697","A","gcG/gcA"]
["MPLKIP",136647,"WUGSC","GRCh38","chr7",40133117,40133117,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E2-A14R-01A-11D-A10Y-09","TCGA-E2-A14R-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","c7212115-1007-40cf-b9b5-7b25e2f5f2a4","7b38de28-3b9d-4a67-bf94-5fd17317d1a9","c.482G>C","ENST00000306984",42768,728,335,"G","ENSG00000168303","ENST00000306984","missense_variant","missense_variant","574/7668","482/540","161/179","S/T","aGc/aCc"]
["RECQL4",9401,"WUGSC","GRCh38","chr8",144516641,144516641,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A7-A425-01A-11D-A243-09","TCGA-A7-A425-10A-01D-A243-09",null,null,"Somatic","Illumina HiSeq 2000","c67181dd-3934-4e63-b0b0-ddb61a5d1306","1a65e4d5-1db5-44b8-8c9c-c014a6e22760","c.478C>T","ENST00000617875",42876,57,59,"A","ENSG00000160957","ENST00000617875","missense_variant","missense_variant","520/3809","478/3627","160/1208","P/S","Cca/Tca"]
["KLHL24",54800,"WUGSC","GRCh38","chr3",183672455,183672455,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-A7-A0DA-01A-31D-A10Y-09","TCGA-A7-A0DA-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","878337fe-9f41-44f5-9760-3977e7d75308","47723567-39d1-40e9-a8ea-1bf9548db03e","c.1573A>G","ENST00000242810",42924,185,83,"G","ENSG00000114796","ENST00000242810","missense_variant","missense_variant","1923/2345","1573/1803","525/600","M/V","Atg/Gtg"]
["FANCM",57697,"WUGSC","GRCh38","chr14",45175529,45175529,"+","Silent","SNP","A","A","G",null,null,"TCGA-A7-A0DA-01A-31D-A10Y-09","TCGA-A7-A0DA-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","878337fe-9f41-44f5-9760-3977e7d75308","47723567-39d1-40e9-a8ea-1bf9548db03e","c.2775A>G","ENST00000267430","14/23",179,35,"G","ENSG00000187790","ENST00000267430","synonymous_variant","synonymous_variant","2860/7111","2775/6147","925/2048","T","acA/acG"]
["KLRF1",51348,"WUGSC","GRCh38","chr12",9833329,9833329,"+","Nonsense_Mutation","SNP","C","C","T","novel",null,"TCGA-AR-A1AR-01A-31D-A135-09","TCGA-AR-A1AR-10A-01D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","008ba655-a0a3-42c4-8c72-f1341365ef02","0395a62f-3f37-4068-bab6-4c1d29cef2d5","c.211C>T","ENST00000617889",42800,248,282,"T","ENSG00000150045","ENST00000617889","stop_gained","stop_gained","275/1241","211/696","71/231","Q/*","Caa/Taa"]
["AKNA",80709,"WUGSC","GRCh38","chr9",114362528,114362528,"+","Missense_Mutation","SNP","G","G","C","rs755632366","byFrequency","TCGA-B6-A0RS-01A-11D-A099-09","TCGA-B6-A0RS-10A-01W-A097-09",null,null,"Somatic","Illumina Genome Analyzer II","6b3ff733-402d-4390-8f57-57a9ad9b9969","791db435-e2b8-42b6-a490-2e0783c0c237","c.1794C>G","ENST00000307564",42969,108,40,"C","ENSG00000106948","ENST00000307564","missense_variant","missense_variant","1956/7380","1794/4320","598/1439","F/L","ttC/ttG"]
["USH2A",7399,"WUGSC","GRCh38","chr1",216198503,216198503,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-AR-A1AH-01A-11D-A12B-09","TCGA-AR-A1AH-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","ff4a0f5a-9f30-4a2b-9915-62f2df5ad155","430fb469-2c87-469e-8d23-0473caeefab3","c.3893A>C","ENST00000307340","18/72",334,272,"G","ENSG00000042781","ENST00000307340","missense_variant","missense_variant","4280/18883","3893/15609","1298/5202","Q/P","cAg/cCg"]
["CNTN1",1272,"WUGSC","GRCh38","chr12",40943651,40943651,"+","Silent","SNP","T","T","C","novel",null,"TCGA-AR-A1AH-01A-11D-A12B-09","TCGA-AR-A1AH-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","ff4a0f5a-9f30-4a2b-9915-62f2df5ad155","430fb469-2c87-469e-8d23-0473caeefab3","c.1434T>C","ENST00000347616",43092,1319,299,"C","ENSG00000018236","ENST00000347616","synonymous_variant","synonymous_variant","1513/5507","1434/3057","478/1018","D","gaT/gaC"]
["VLDLR",7436,"WUGSC","GRCh38","chr9",2643403,2643403,"+","Missense_Mutation","SNP","G","G","A","rs767529669","byFrequency","TCGA-A2-A04U-01A-11D-A10Y-09","TCGA-A2-A04U-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","f819433a-44db-4022-abdb-d6123cfa30b2","85bbbb48-4570-41e6-9e53-b38b2d463cbf","c.692G>A","ENST00000382100",42874,210,49,"A","ENSG00000147852","ENST00000382100","missense_variant","missense_variant","1048/9163","692/2622","231/873","R/H","cGt/cAt"]
["FZD6",8323,"WUGSC","GRCh38","chr8",103300101,103300101,"+","5'UTR","SNP","G","G","C","novel",null,"TCGA-LL-A73Y-01A-11D-A33E-09","TCGA-LL-A73Y-10B-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","ac077103-6e1b-423f-bf85-4ba798e08ce2","5f044f10-3304-4071-8d16-906af45517dd","c.-7G>C","ENST00000358755",42773,251,85,"C","ENSG00000164930","ENST00000358755","5_prime_UTR_variant","5_prime_UTR_variant","311/3788","-/2121","-/706"]
["RBFOX3",146713,"WUGSC","GRCh38","chr17",79090681,79090681,"+","3'Flank","SNP","C","C","G","novel",null,"TCGA-LL-A73Y-01A-11D-A33E-09","TCGA-LL-A73Y-10B-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","ac077103-6e1b-423f-bf85-4ba798e08ce2","5f044f10-3304-4071-8d16-906af45517dd",null,"ENST00000580155",null,153,50,"G","ENSG00000167281","ENST00000580155","downstream_gene_variant","downstream_gene_variant","-/1519","-/939","-/312"]
["ITPR1",3708,"WUGSC","GRCh38","chr3",4811454,4811454,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A8-A09B-01A-11W-A019-09","TCGA-A8-A09B-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","a8be37d2-2743-4fde-9aae-2623b5a03b60","6acddb6d-f866-498b-9b57-f46cbca2cdf9","c.7462G>A","ENST00000354582","56/62",147,195,"A","ENSG00000150995","ENST00000354582","missense_variant","missense_variant","7812/10242","7462/8277","2488/2758","V/I","Gtt/Att"]
["PSMA5",5686,"WUGSC","GRCh38","chr1",109415307,109415307,"+","Silent","SNP","C","C","T",null,null,"TCGA-AR-A256-01A-11D-A167-09","TCGA-AR-A256-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","ea43434b-197e-48ac-ae2e-46bc7f3776de","09f34836-fc9a-4ff4-a0c9-fd93259e32f3","c.153G>A","ENST00000271308",42803,66,50,"T","ENSG00000143106","ENST00000271308","synonymous_variant","synonymous_variant","174/3729","153/726","51/241","E","gaG/gaA"]
["ABCA6",23460,"WUGSC","GRCh38","chr17",69084357,69084357,"+","Splice_Site","SNP","T","T","C",null,null,"TCGA-AR-A256-01A-11D-A167-09","TCGA-AR-A256-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","ea43434b-197e-48ac-ae2e-46bc7f3776de","09f34836-fc9a-4ff4-a0c9-fd93259e32f3","c.4261-2A>G","ENST00000284425",null,96,78,"C","ENSG00000154262","ENST00000284425","splice_acceptor_variant","splice_acceptor_variant","-/5300","4261/4854","1421/1617"]
["KLHL38",340359,"WUGSC","GRCh38","chr8",123652398,123652398,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E2-A154-01A-11D-A10Y-09","TCGA-E2-A154-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","336e39fb-d407-4ced-b7bb-e8ff5329abdb","2a64a2d9-2683-40fb-9e22-43cb3185321c","c.529G>A","ENST00000325995",42738,33,19,"T","ENSG00000175946","ENST00000325995","missense_variant","missense_variant","553/1982","529/1746","177/581","A/T","Gcc/Acc"]
["HZGJ",0,"WUGSC","GRCh38","chr2",68186571,68186571,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A1FL-01A-11D-A13L-09","TCGA-BH-A1FL-11A-13D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","bb84cbb1-7244-4d92-8977-a37dbafc47b4","d669a784-1fb6-417f-b4e6-34486d51f2e0","c.551G>A","ENST00000614162",42902,123,126,"T","ENSG00000273398","ENST00000614162","missense_variant","missense_variant","551/3387","551/2298","184/765","G/E","gGg/gAg"]
["KRT7",3855,"WUGSC","GRCh38","chr12",52243114,52243114,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-EW-A1PH-01A-11D-A14K-09","TCGA-EW-A1PH-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","ce860c6f-c87a-4a45-92df-ca34bfb2e8b2","28823da8-d29d-48c6-ae45-0ea4cdc23f52","c.961G>C","ENST00000331817",42895,56,34,"C","ENSG00000135480","ENST00000331817","missense_variant","missense_variant","1144/1754","961/1410","321/469","E/Q","Gag/Cag"]
["CDC14A",8556,"WUGSC","GRCh38","chr1",100496031,100496031,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-D8-A1XL-01A-11D-A14K-09","TCGA-D8-A1XL-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","28d44e6e-c73f-4788-8ad4-2bd6572f643d","a64ed39f-0699-4997-b8f4-011090174b75","c.1280C>A","ENST00000336454","13/16",115,139,"A","ENSG00000079335","ENST00000336454","missense_variant","missense_variant","1635/4137","1280/1785","427/594","A/E","gCa/gAa"]
["CPA1",1357,"WUGSC","GRCh38","chr7",130383430,130383430,"+","Missense_Mutation","SNP","G","G","A","rs782556361","byFrequency","TCGA-BH-A0AW-01A-11W-A071-09","TCGA-BH-A0AW-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","82057159-dd32-49fd-9ee7-82b4668f39c3","959f61e0-33ba-4464-a04a-efd0372eedb5","c.523G>A","ENST00000011292",42865,41,39,"A","ENSG00000091704","ENST00000011292","missense_variant","missense_variant","673/1487","523/1260","175/419","D/N","Gac/Aac"]
["PRMT2",3275,"WUGSC","GRCh38","chr21",46651969,46651969,"+","Intron","SNP","C","C","T","novel",null,"TCGA-BH-A0AW-01A-11W-A071-09","TCGA-BH-A0AW-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","82057159-dd32-49fd-9ee7-82b4668f39c3","959f61e0-33ba-4464-a04a-efd0372eedb5","c.654+2230C>T","ENST00000355680",null,144,77,"T","ENSG00000160310","ENST00000355680","intron_variant","intron_variant","-/2688","-/1302","-/433"]
["NUP54",53371,"WUGSC","GRCh38","chr4",76117667,76117667,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-AC-A5EH-01A-11D-A28B-09","TCGA-AC-A5EH-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","571dac9a-a2d6-4d29-ae22-111cd9822c1a","8eea835b-f1ff-4efc-805e-149e5e2bd9c5","c.1392G>T","ENST00000264883",43051,36,25,"A","ENSG00000138750","ENST00000264883","missense_variant","missense_variant","1533/2367","1392/1524","464/507","K/N","aaG/aaT"]
["PEAK1",79834,"WUGSC","GRCh38","chr15",77180012,77180012,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-AC-A5EH-01A-11D-A28B-09","TCGA-AC-A5EH-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","571dac9a-a2d6-4d29-ae22-111cd9822c1a","8eea835b-f1ff-4efc-805e-149e5e2bd9c5","c.1915G>C","ENST00000312493",42771,84,72,"G","ENSG00000173517","ENST00000312493","missense_variant","missense_variant","2194/11512","1915/5241","639/1746","A/P","Gct/Cct"]
["DST",667,"WUGSC","GRCh38","chr6",56608182,56608182,"+","Intron","SNP","T","T","C","novel",null,"TCGA-E2-A1B6-01A-31D-A12Q-09","TCGA-E2-A1B6-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","1aaf88fc-f7cb-4239-a420-224352194160","409d90e2-1252-4a42-95d6-9625033b2c8f","c.4770+2245A>G","ENST00000312431",null,247,234,"C","ENSG00000151914","ENST00000312431","intron_variant","intron_variant","-/17756","-/16614","-/5537"]
["DENND5B",160518,"WUGSC","GRCh38","chr12",31460303,31460303,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-D8-A27K-01A-11D-A16D-09","TCGA-D8-A27K-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","09fa0bc7-acb3-45b0-b687-977869c31d12","a25f38d9-48a6-4b15-a83b-d1a963324e96","c.983C>G","ENST00000389082",42846,64,106,"C","ENSG00000170456","ENST00000389082","missense_variant","missense_variant","1248/9470","983/3825","328/1274","P/R","cCc/cGc"]
["IGKV1D-16",28901,"WUGSC","GRCh38","chr2",90100680,90100680,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-PE-A5DD-01A-12D-A27P-09","TCGA-PE-A5DD-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","240ff9b5-d5c6-4d0f-b2a3-dbbdf7e3aff0","5069f07e-fae4-47fc-8512-0ca8b9f19494","c.293G>T","ENST00000492446",42768,206,165,"T","ENSG00000241244","ENST00000492446","missense_variant","missense_variant","320/378","293/351","98/117","S/I","aGc/aTc"]
["HCRTR2",3062,"WUGSC","GRCh38","chr6",55277504,55277504,"+","Missense_Mutation","SNP","T","T","C","novel",null,"TCGA-EW-A6SB-01A-12D-A32I-09","TCGA-EW-A6SB-10A-01D-A32I-09",null,null,"Somatic","Illumina HiSeq 2000","9eee3c8a-d354-4d59-8a02-d35e7476a06f","29e10811-487d-433e-95bd-a5b96066a804","c.887T>C","ENST00000370862",42862,73,51,"C","ENSG00000137252","ENST00000370862","missense_variant","missense_variant","1223/1837","887/1335","296/444","I/T","aTc/aCc"]
["TNS4",84951,"WUGSC","GRCh38","chr17",40488751,40488751,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-A8-A06O-01A-11W-A019-09","TCGA-A8-A06O-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","29cd408e-a04b-418a-85e2-6ef95840ddbc","62c57a4a-eaa6-42ee-b8b2-80d44d3edcf8","c.658G>T","ENST00000254051",42807,40,37,"A","ENSG00000131746","ENST00000254051","missense_variant","missense_variant","817/4067","658/2148","220/715","G/C","Ggt/Tgt"]
["DPPA2",151871,"WUGSC","GRCh38","chr3",109312624,109312624,"+","Silent","SNP","G","G","A","rs572153453","by1000G;byFrequency","TCGA-EW-A1P6-01A-11D-A142-09","TCGA-EW-A1P6-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","eef5cea9-82f6-4001-8e2c-701e43a9787a","9363f17c-f3ba-4219-8de9-15f0cf99dcd2","c.102C>T","ENST00000478945",42803,87,68,"A","ENSG00000163530","ENST00000478945","synonymous_variant","synonymous_variant","349/1383","102/897","34/298","D","gaC/gaT"]
["DNAJB5",25822,"WUGSC","GRCh38","chr9",34993356,34993356,"+","Silent","SNP","T","T","C","novel",null,"TCGA-EW-A6SA-01A-21D-A32I-09","TCGA-EW-A6SA-10A-01D-A32I-09",null,null,"Somatic","Illumina HiSeq 2000","4c9de093-e72d-4cad-a4e9-c76aaa5856b5","728de241-d4c8-4c5f-8e33-75a5f6336a4b","c.123T>C","ENST00000312316",42770,96,65,"C","ENSG00000137094","ENST00000312316","synonymous_variant","synonymous_variant","295/2391","123/1047","41/348","A","gcT/gcC"]
["ADAM19",8728,"WUGSC","GRCh38","chr5",157530866,157530866,"+","Silent","SNP","G","G","A","rs150188867","byCluster","TCGA-C8-A26V-01A-11D-A16D-09","TCGA-C8-A26V-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","6c5a83f5-983f-434c-ac29-ddb84a7f1019","c546d2fb-09e7-4b5d-a39e-24d6a26e6341","c.348C>T","ENST00000517905",42877,40,34,"A","ENSG00000135074","ENST00000517905","synonymous_variant","synonymous_variant","393/3312","348/2868","116/955","H","caC/caT"]
["ADGB",79747,"WUGSC","GRCh38","chr6",146726168,146726168,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A04Y-01A-21W-A050-09","TCGA-A2-A04Y-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","3669bbbd-2e75-4b57-a5a8-8eebc25a97c2","f2467587-34f3-406d-8b3a-143c1bb52667","c.2323G>A","ENST00000397944","19/36",276,150,"A","ENSG00000118492","ENST00000397944","missense_variant","missense_variant","2399/5325","2323/5004","775/1667","E/K","Gaa/Aaa"]
["CNOT3",4849,"WUGSC","GRCh38","chr19",54153585,54153585,"+","Intron","SNP","G","G","A","novel",null,"TCGA-AQ-A04J-01A-02W-A050-09","TCGA-AQ-A04J-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","cce21f2b-784b-4fa0-9809-ae532c528f8e","a53132c6-21f2-4083-9b0b-5e927d63e199","c.2038-130G>A","ENST00000221232",null,17,13,"A","ENSG00000088038","ENST00000221232","intron_variant","intron_variant","-/2852","-/2262","-/753"]
["ZXDB",158586,"WUGSC","GRCh38","chrX",57594267,57594267,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A2LO-01A-31D-A18P-09","TCGA-AR-A2LO-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","c65887cd-2df3-46ac-9787-f1ad62279055","67693f81-bf05-4221-ba0b-3a4ce2217bf3","c.2219C>T","ENST00000374888",42736,93,93,"T","ENSG00000198455","ENST00000374888","missense_variant","missense_variant","2616/5894","2219/2412","740/803","S/L","tCg/tTg"]
["NDUFS2",4720,"WUGSC","GRCh38","chr1",161214164,161214164,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A0YJ-01A-11D-A10G-09","TCGA-A2-A0YJ-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","3fe8e99f-dce5-4df9-983e-efe63d56bdd5","0fb6d352-b236-4ecf-9d79-39d49a387277","c.1363G>A","ENST00000367993","15/15",214,46,"A","ENSG00000158864","ENST00000367993","missense_variant","missense_variant","1811/2042","1363/1392","455/463","D/N","Gat/Aat"]
["FCRL1",115350,"WUGSC","GRCh38","chr1",157803868,157803868,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A08X-01A-21W-A019-09","TCGA-A8-A08X-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","67c7d350-5c82-49b0-a7eb-6ca829ffcbc9","263fb74b-c2f8-4ad7-8b3e-0e02749d167e","c.296G>A","ENST00000368176",42805,232,173,"T","ENSG00000163534","ENST00000368176","missense_variant","missense_variant","364/2596","296/1290","99/429","R/K","aGg/aAg"]
["PROM2",150696,"WUGSC","GRCh38","chr2",95287171,95287171,"+","Silent","SNP","G","G","A",null,null,"TCGA-A2-A0EY-01A-11W-A050-09","TCGA-A2-A0EY-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","a8cde596-e3f5-4b20-9e7f-45d079893176","b1d7c034-0cf5-40ce-8620-35248ca45e08","c.2133G>A","ENST00000317620","19/24",91,109,"A","ENSG00000155066","ENST00000317620","synonymous_variant","synonymous_variant","2266/4728","2133/2505","711/834","L","ctG/ctA"]
["LMAN1L",79748,"WUGSC","GRCh38","chr15",74819249,74819249,"+","Nonsense_Mutation","SNP","C","C","G",null,null,"TCGA-A2-A0EY-01A-11W-A050-09","TCGA-A2-A0EY-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","a8cde596-e3f5-4b20-9e7f-45d079893176","b1d7c034-0cf5-40ce-8620-35248ca45e08","c.695C>G","ENST00000309664",42900,38,114,"G","ENSG00000140506","ENST00000309664","stop_gained","stop_gained","834/1873","695/1581","232/526","S/*","tCa/tGa"]
["RCAN3",11123,"WUGSC","GRCh38","chr1",24535383,24535383,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-A8-A095-01A-11W-A019-09","TCGA-A8-A095-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","d16f025a-4187-4632-b833-02a3ffa54210","9dafa22c-39df-467b-920b-a1e42c820671","c.*106G>A","ENST00000374395",42860,37,23,"A","ENSG00000117602","ENST00000374395","3_prime_UTR_variant","3_prime_UTR_variant","1145/6802","-/726","-/241"]
["KIAA1549",57670,"WUGSC","GRCh38","chr7",138837847,138837847,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-A8-A095-01A-11W-A019-09","TCGA-A8-A095-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","d16f025a-4187-4632-b833-02a3ffa54210","9dafa22c-39df-467b-920b-a1e42c820671","c.*59G>A","ENST00000422774","20/20",56,22,"T","ENSG00000122778","ENST00000422774","3_prime_UTR_variant","3_prime_UTR_variant","5961/6283","-/5853","-/1950"]
["FBXL19",54620,"WUGSC","GRCh38","chr16",30930268,30930268,"+","Missense_Mutation","SNP","G","G","A","rs761311601",null,"TCGA-A8-A095-01A-11W-A019-09","TCGA-A8-A095-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","d16f025a-4187-4632-b833-02a3ffa54210","9dafa22c-39df-467b-920b-a1e42c820671","c.1045G>A","ENST00000380310",42927,54,32,"A","ENSG00000099364","ENST00000380310","missense_variant","missense_variant","1203/3796","1045/2085","349/694","E/K","Gag/Aag"]
["KIR2DL4",3805,"WUGSC","GRCh38","chr19",54813280,54813280,"+","Intron","SNP","G","G","A",null,null,"TCGA-D8-A1JJ-01A-31D-A14K-09","TCGA-D8-A1JJ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","412f96a6-6599-40a6-9dd2-afba8c643910","a022c9a2-3e8a-4377-abed-33cdfbc85b18","c.707-410G>A","ENST00000345540",null,382,498,"A","ENSG00000189013","ENST00000345540","intron_variant","intron_variant","-/1447","-/1029","-/342"]
["MT1HL1",645745,"WUGSC","GRCh38","chr1",237004406,237004406,"+","5'UTR","SNP","A","A","T","novel",null,"TCGA-AO-A124-01A-11D-A10M-09","TCGA-AO-A124-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","987528ac-437a-4eb8-a335-4f2076d5c006","0c4d979c-75f8-49bd-8e65-f980cbeae267","c.-34T>A","ENST00000464121",42736,121,33,"T","ENSG00000244020","ENST00000464121","5_prime_UTR_variant","5_prime_UTR_variant","13/316","-/186","-/61"]
["GSPT1",2935,"WUGSC","GRCh38","chr16",11896693,11896693,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-AO-A124-01A-11D-A10M-09","TCGA-AO-A124-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","987528ac-437a-4eb8-a335-4f2076d5c006","0c4d979c-75f8-49bd-8e65-f980cbeae267","c.115G>T","ENST00000420576",42840,655,292,"A","ENSG00000103342","ENST00000420576","missense_variant","missense_variant","218/1603","115/1500","39/499","D/Y","Gat/Tat"]
["FBXL13",222235,"WUGSC","GRCh38","chr7",102963541,102963541,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A092-01A-11W-A019-09","TCGA-A8-A092-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","732dd0ab-c869-4d35-973f-9db064680fb1","40550f2e-0413-4ddf-85e3-edce4f47f62e","c.716G>A","ENST00000313221",42967,145,179,"T","ENSG00000161040","ENST00000313221","missense_variant","missense_variant","1143/2744","716/2208","239/735","R/K","aGa/aAa"]
["ABCG1",9619,"WUGSC","GRCh38","chr21",42225712,42225712,"+","Silent","SNP","G","G","A","rs751989691","byFrequency","TCGA-D8-A1Y0-01A-11D-A14K-09","TCGA-D8-A1Y0-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","33ff7870-fa76-4e48-a223-a8e2441d8f53","95048722-2664-4839-9814-dfa4aeb66198","c.84G>A","ENST00000361802",42781,60,102,"A","ENSG00000160179","ENST00000361802","synonymous_variant","synonymous_variant","229/3034","84/2037","28/678","S","tcG/tcA"]
["NAMPT",10135,"WUGSC","GRCh38","chr7",106253145,106253145,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A1JC-01A-11D-A13L-09","TCGA-D8-A1JC-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","63a9d14f-d91a-47af-8ef6-8124193aa110","d6936adf-adbc-4cb1-b7cb-c7ef255864d1","c.1237G>C","ENST00000222553",43019,85,92,"G","ENSG00000105835","ENST00000222553","missense_variant","missense_variant","1545/4582","1237/1476","413/491","V/L","Gtc/Ctc"]
["HPDL",84842,"WUGSC","GRCh38","chr1",45328036,45328036,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-B6-A0RE-01A-11W-A071-09","TCGA-B6-A0RE-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","db2bd5cf-f0a7-4874-89eb-15029447dae1","21d6d4ec-23c7-470d-8654-59d20f56c9a6","c.888G>C","ENST00000334815",42736,67,101,"C","ENSG00000186603","ENST00000334815","missense_variant","missense_variant","1132/1629","888/1116","296/371","Q/H","caG/caC"]
["HEMGN",55363,"WUGSC","GRCh38","chr9",97927426,97927426,"+","Missense_Mutation","SNP","C","C","G","rs751804933","byFrequency","TCGA-B6-A0RE-01A-11W-A071-09","TCGA-B6-A0RE-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","db2bd5cf-f0a7-4874-89eb-15029447dae1","21d6d4ec-23c7-470d-8654-59d20f56c9a6","c.1413G>C","ENST00000259456",42860,77,47,"G","ENSG00000136929","ENST00000259456","missense_variant","missense_variant","1557/2192","1413/1455","471/484","E/D","gaG/gaC"]
["ARID1A",8289,"WUGSC","GRCh38","chr1",26761067,26761067,"+","Nonsense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A2LE-01A-11D-A17W-09","TCGA-AR-A2LE-10A-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","2684cf0d-9cc7-45f3-86bd-96f9bb17d749","f7ffd8c1-3b0b-477c-97c5-467710171bbf","c.2132C>G","ENST00000324856",42875,72,56,"G","ENSG00000117713","ENST00000324856","stop_gained","stop_gained","2503/8577","2132/6858","711/2285","S/*","tCa/tGa"]
["OPN1SW",611,"WUGSC","GRCh38","chr7",128775718,128775718,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A2LE-01A-11D-A17W-09","TCGA-AR-A2LE-10A-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","2684cf0d-9cc7-45f3-86bd-96f9bb17d749","f7ffd8c1-3b0b-477c-97c5-467710171bbf","c.73C>T","ENST00000249389",42740,28,33,"A","ENSG00000128617","ENST00000249389","stop_gained","stop_gained","73/1096","73/1047","25/348","Q/*","Cag/Tag"]
["C12orf40",283461,"WUGSC","GRCh38","chr12",39716809,39716809,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A2LE-01A-11D-A17W-09","TCGA-AR-A2LE-10A-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","2684cf0d-9cc7-45f3-86bd-96f9bb17d749","f7ffd8c1-3b0b-477c-97c5-467710171bbf","c.1465G>C","ENST00000324616",43082,197,148,"C","ENSG00000180116","ENST00000324616","missense_variant","missense_variant","1619/2776","1465/1959","489/652","D/H","Gac/Cac"]
["ASXL3",80816,"WUGSC","GRCh38","chr18",33739250,33739250,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AR-A2LE-01A-11D-A17W-09","TCGA-AR-A2LE-10A-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","2684cf0d-9cc7-45f3-86bd-96f9bb17d749","f7ffd8c1-3b0b-477c-97c5-467710171bbf","c.1846G>C","ENST00000269197",43051,60,46,"C","ENSG00000141431","ENST00000269197","missense_variant","missense_variant","1846/11344","1846/6747","616/2248","E/Q","Gag/Cag"]
["TRPM6",140803,"WUGSC","GRCh38","chr9",74820427,74820427,"+","Splice_Region","SNP","C","C","G","novel",null,"TCGA-HN-A2NL-01A-11D-A18P-09","TCGA-HN-A2NL-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","73d09eab-d3f5-442d-aea8-690b282fd68a","e21e6d93-3bb6-4ba1-8c65-e20c13cfdf16","c.1011G>C","ENST00000360774",14489,70,60,"G","ENSG00000119121","ENST00000360774","splice_region_variant","splice_region_variant;synonymous_variant","1249/8425","1011/6069","337/2022","G","ggG/ggC"]
["CYP4F12",66002,"WUGSC","GRCh38","chr19",15696498,15696498,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AN-A0AM-01A-11W-A050-09","TCGA-AN-A0AM-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","a238f21f-ca46-4759-b5b7-f8c3810dfbdb","d2910522-0610-4cef-a499-7bb1d7cb7c84","c.1383C>G","ENST00000550308",43082,228,211,"G","ENSG00000186204","ENST00000550308","missense_variant","missense_variant","1763/2044","1383/1575","461/524","F/L","ttC/ttG"]
["MEIS2",4212,"WUGSC","GRCh38","chr15",36894796,36894796,"+","Intron","SNP","C","C","T",null,null,"TCGA-A2-A0CP-01A-11W-A050-09","TCGA-A2-A0CP-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","a776e274-fe9f-49a9-83ab-95ca6819c96b","a1bb0524-fef9-405d-8e55-4c8ab74efb16","c.1147+355G>A","ENST00000561208",null,248,140,"T","ENSG00000134138","ENST00000561208","intron_variant","intron_variant","-/4822","-/1434","-/477"]
["MCOLN3",55283,"WUGSC","GRCh38","chr1",85034207,85034207,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-D8-A1XQ-01A-11D-A14K-09","TCGA-D8-A1XQ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","6907fb6b-34d8-4376-961b-f073f0b5f700","241a754b-92a3-4a10-a8ad-ee7e2e29ad19","c.441G>T","ENST00000370589",42838,120,141,"A","ENSG00000055732","ENST00000370589","missense_variant","missense_variant","494/2756","441/1662","147/553","E/D","gaG/gaT"]
["FAM161A",84140,"WUGSC","GRCh38","chr2",61836069,61836069,"+","Silent","SNP","G","G","A","novel",null,"TCGA-D8-A1XQ-01A-11D-A14K-09","TCGA-D8-A1XQ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","6907fb6b-34d8-4376-961b-f073f0b5f700","241a754b-92a3-4a10-a8ad-ee7e2e29ad19","c.1624C>T","ENST00000405894",42831,327,290,"A","ENSG00000170264","ENST00000405894","synonymous_variant","synonymous_variant","1726/3684","1624/1983","542/660","L","Cta/Tta"]
["CELSR3",1951,"WUGSC","GRCh38","chr3",48658950,48658950,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A1XQ-01A-11D-A14K-09","TCGA-D8-A1XQ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","6907fb6b-34d8-4376-961b-f073f0b5f700","241a754b-92a3-4a10-a8ad-ee7e2e29ad19","c.3685C>T","ENST00000164024",12785,88,86,"A","ENSG00000008300","ENST00000164024","stop_gained","stop_gained","3966/11956","3685/9939","1229/3312","R/*","Cga/Tga"]
["EPHB6",2051,"WUGSC","GRCh38","chr7",142869820,142869820,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-D8-A1XQ-01A-11D-A14K-09","TCGA-D8-A1XQ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","6907fb6b-34d8-4376-961b-f073f0b5f700","241a754b-92a3-4a10-a8ad-ee7e2e29ad19","c.2464C>G","ENST00000619012","17/20",77,75,"G","ENSG00000106123","ENST00000619012","missense_variant","missense_variant","3216/4011","2464/3069","822/1022","P/A","Cca/Gca"]
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["PCF11",51585,"WUGSC","GRCh38","chr11",83184765,83184765,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-D8-A1XQ-01A-11D-A14K-09","TCGA-D8-A1XQ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","6907fb6b-34d8-4376-961b-f073f0b5f700","241a754b-92a3-4a10-a8ad-ee7e2e29ad19","c.4539A>T","ENST00000298281","16/16",189,168,"T","ENSG00000165494","ENST00000298281","missense_variant","missense_variant","4991/7677","4539/4668","1513/1555","E/D","gaA/gaT"]
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["MAP2K2",5605,"WUGSC","GRCh38","chr19",4101076,4101076,"+","Silent","SNP","G","G","A","rs147276536","byCluster","TCGA-D8-A1XQ-01A-11D-A14K-09","TCGA-D8-A1XQ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","6907fb6b-34d8-4376-961b-f073f0b5f700","241a754b-92a3-4a10-a8ad-ee7e2e29ad19","c.648C>T","ENST00000262948",42897,87,88,"A","ENSG00000126934","ENST00000262948","synonymous_variant","synonymous_variant","902/1734","648/1203","216/400","S","agC/agT"]
["CEACAM1",634,"WUGSC","GRCh38","chr19",42518973,42518973,"+","Silent","SNP","G","G","A",null,null,"TCGA-D8-A1XQ-01A-11D-A14K-09","TCGA-D8-A1XQ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","6907fb6b-34d8-4376-961b-f073f0b5f700","241a754b-92a3-4a10-a8ad-ee7e2e29ad19","c.1221C>T","ENST00000161559",42864,230,213,"A","ENSG00000079385","ENST00000161559","synonymous_variant","synonymous_variant","1356/3519","1221/1581","407/526","S","agC/agT"]
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["HRNR",388697,"WUGSC","GRCh38","chr1",152219110,152219110,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-D8-A142-01A-11D-A10Y-09","TCGA-D8-A142-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","86c9c056-e9c7-4653-a0b5-29f2b140534b","45e9f8c4-5eac-44fe-b1bd-4e9285524e60","c.2519G>C","ENST00000368801",42797,302,219,"G","ENSG00000197915","ENST00000368801","missense_variant","missense_variant","2595/9623","2519/8553","840/2850","S/T","aGc/aCc"]
["GDPD1",284161,"WUGSC","GRCh38","chr17",59257137,59257137,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A04N-01A-11D-A10Y-09","TCGA-A2-A04N-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","389dd52b-a7b7-46f0-83ae-308e485466a8","6bc7c00e-9bf1-4d08-b69e-a73942d9afd5","c.383G>A","ENST00000284116",42865,134,177,"A","ENSG00000153982","ENST00000284116","missense_variant","missense_variant","520/1821","383/945","128/314","G/E","gGa/gAa"]
["SAP25",100316904,"WUGSC","GRCh38","chr7",100572404,100572404,"+","Silent","SNP","G","G","C",null,null,"TCGA-BH-A0BG-01A-11D-A10Y-09","TCGA-BH-A0BG-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","923ee16a-2c42-46ee-b2cb-82075f2dd603","483a4feb-931f-40f8-964d-29104030ebe7","c.483C>G","ENST00000538735",42892,23,23,"C","ENSG00000205307","ENST00000538735","synonymous_variant","synonymous_variant","661/837","483/600","161/199","S","tcC/tcG"]
["CTNNAL1",8727,"WUGSC","GRCh38","chr9",108979399,108979399,"+","Missense_Mutation","SNP","C","C","T","rs142466437","by1000G;byCluster;byFrequency","TCGA-AO-A1KS-01A-11D-A13L-09","TCGA-AO-A1KS-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","21074661-4b0f-4adc-b406-5801688a3ae9","460a9133-a189-42d2-acf0-ae61ca265d76","c.983G>A","ENST00000325551",42935,70,153,"T","ENSG00000119326","ENST00000325551","missense_variant","missense_variant","1070/2490","983/2205","328/734","R/H","cGt/cAt"]
["SH3KBP1",30011,"WUGSC","GRCh38","chrX",19836257,19836257,"+","Silent","SNP","G","G","A",null,null,"TCGA-C8-A12U-01A-11D-A10Y-09","TCGA-C8-A12U-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000","444a1ef9-819a-41dc-baef-22057225efcd","e7b0ba1b-04c8-48f1-ba7d-844ae3f70916","c.30C>T","ENST00000397821",42784,248,149,"A","ENSG00000147010","ENST00000397821","synonymous_variant","synonymous_variant","321/4731","30/1998","10/665","Y","taC/taT"]
["CYP26B1",56603,"WUGSC","GRCh38","chr2",72134910,72134910,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.712C>G","ENST00000001146",42831,62,32,"C","ENSG00000003137","ENST00000001146","missense_variant","missense_variant","916/4732","712/1539","238/512","Q/E","Cag/Gag"]
["TERT",7015,"WUGSC","GRCh38","chr5",1293728,1293728,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.1158C>A","ENST00000310581",42782,20,9,"T","ENSG00000164362","ENST00000310581","stop_gained","stop_gained","1216/4018","1158/3399","386/1132","Y/*","taC/taA"]
["SMPDL3A",10924,"WUGSC","GRCh38","chr6",122809340,122809340,"+","Missense_Mutation","SNP","A","A","G","rs377120956","by1000G;byCluster","TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.1294A>G","ENST00000368440",42955,34,25,"G","ENSG00000172594","ENST00000368440","missense_variant","missense_variant","1471/1851","1294/1362","432/453","I/V","Att/Gtt"]
["KMT2C",58508,"WUGSC","GRCh38","chr7",152183104,152183104,"+","Nonsense_Mutation","SNP","G","G","C",null,null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.5135C>G","ENST00000262189","35/59",151,71,"C","ENSG00000055609","ENST00000262189","stop_gained","stop_gained","5354/16862","5135/14736","1712/4911","S/*","tCa/tGa"]
["DSCAML1",57453,"WUGSC","GRCh38","chr11",117437134,117437134,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.4888G>A","ENST00000321322","26/33",20,26,"T","ENSG00000177103","ENST00000321322","missense_variant","missense_variant","4890/6899","4888/6342","1630/2113","D/N","Gac/Aac"]
["NOX5",79400,"WUGSC","GRCh38","chr15",69023178,69023178,"+","Intron","SNP","G","G","C","novel",null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.51-3350G>C","ENST00000388866",null,11,18,"C","ENSG00000255346","ENST00000388866","intron_variant","intron_variant","-/2804","-/2298","-/765"]
["NAGS",162417,"WUGSC","GRCh38","chr17",44008557,44008557,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.1561C>G","ENST00000293404",42923,59,47,"G","ENSG00000161653","ENST00000293404","missense_variant","missense_variant","1679/2182","1561/1605","521/534","L/V","Ctg/Gtg"]
["LIPE",3991,"WUGSC","GRCh38","chr19",42427261,42427261,"+","5'UTR","SNP","C","C","G","novel",null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.-112G>C","ENST00000244289",42745,21,13,"G","ENSG00000079435","ENST00000244289","5_prime_UTR_variant","5_prime_UTR_variant","166/3813","-/3231","-/1076"]
["SREBF2",6721,"WUGSC","GRCh38","chr22",41894839,41894839,"+","Silent","SNP","C","C","T",null,null,"TCGA-C8-A26Y-01A-11D-A16D-09","TCGA-C8-A26Y-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","b1c77e8b-cc4a-40aa-b858-5928aa761aa3","4a97d15d-98ec-4107-bfa4-21be8b5fba25","c.2397C>T","ENST00000361204","13/19",30,17,"T","ENSG00000198911","ENST00000361204","synonymous_variant","synonymous_variant","2563/5240","2397/3426","799/1141","V","gtC/gtT"]
["PCDHA8",56140,"WUGSC","GRCh38","chr5",140842782,140842782,"+","Silent","SNP","C","C","T",null,null,"TCGA-AR-A1AY-01A-21D-A12Q-09","TCGA-AR-A1AY-10A-01D-A12Q-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","15f90ef0-831b-40a3-98bd-ec226a9e8b26","1c6d0926-e635-4f26-97a6-642c012e930d","c.1461C>T","ENST00000531613",42739,93,29,"T","ENSG00000204962","ENST00000531613","synonymous_variant","synonymous_variant","1461/5260","1461/2853","487/950","N","aaC/aaT"]
["C9orf62",157927,"WUGSC","GRCh38","chr9",135344124,135344124,"+","RNA","SNP","A","A","G","novel",null,"TCGA-LL-A7SZ-01A-32D-A351-09","TCGA-LL-A7SZ-10A-01D-A351-09",null,null,"Somatic","Illumina HiSeq 2000","cfa25da5-b3f0-4f8d-8a7e-eb6a6e83cd64","84859c58-edcc-4caf-babe-2f07fbc29040","n.326A>G","ENST00000623103",42769,15,55,"G","ENSG00000178243","ENST00000623103","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","326/1924"]
["TEX14",56155,"WUGSC","GRCh38","chr17",58599366,58599366,"+","Missense_Mutation","SNP","A","A","G","rs143467737","by1000G;byCluster","TCGA-LL-A7SZ-01A-32D-A351-09","TCGA-LL-A7SZ-10A-01D-A351-09",null,null,"Somatic","Illumina HiSeq 2000","cfa25da5-b3f0-4f8d-8a7e-eb6a6e83cd64","84859c58-edcc-4caf-babe-2f07fbc29040","c.1997T>C","ENST00000240361","14/33",16,41,"G","ENSG00000121101","ENST00000240361","missense_variant","missense_variant","2083/4911","1997/4494","666/1497","M/T","aTg/aCg"]
["KLHL18",23276,"WUGSC","GRCh38","chr3",47340603,47340603,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-BH-A0B4-01A-11W-A019-09","TCGA-BH-A0B4-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","83bee702-eb97-4216-a47e-d4e4eece279a","cf1209cc-b0f9-40d1-9f55-f04a74981a96","c.1153A>T","ENST00000232766",42957,80,176,"T","ENSG00000114648","ENST00000232766","missense_variant","missense_variant","1173/4620","1153/1725","385/574","I/F","Atc/Ttc"]
["ANKRD28",23243,"WUGSC","GRCh38","chr3",15712167,15712167,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A09D-01A-11W-A019-09","TCGA-A8-A09D-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d0ef396f-4e9f-40ba-a09c-0a96832cabf9","4cc17aa7-57b9-4618-bd04-42378c11d27b","c.1156G>A","ENST00000399451",43067,34,23,"T","ENSG00000206560","ENST00000399451","missense_variant","missense_variant","1524/6564","1156/3162","386/1053","D/N","Gat/Aat"]
["THNSL2",55258,"WUGSC","GRCh38","chr2",88174658,88174658,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-AR-A0TX-01A-11D-A099-09","TCGA-AR-A0TX-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","63d635fa-d136-4e8a-a534-966ee678bb66","3c3cfe65-4e86-4c42-85d0-9daaeff2fc26","c.243C>G","ENST00000324166",42774,120,251,"G","ENSG00000144115","ENST00000324166","missense_variant","missense_variant","1934/3649","243/1455","81/484","F/L","ttC/ttG"]
["TTN",7273,"WUGSC","GRCh38","chr2",178591343,178591343,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A0TX-01A-11D-A099-09","TCGA-AR-A0TX-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","63d635fa-d136-4e8a-a534-966ee678bb66","3c3cfe65-4e86-4c42-85d0-9daaeff2fc26","c.55459G>A","ENST00000591111","254/313",111,166,"T","ENSG00000155657","ENST00000591111","missense_variant","missense_variant","55684/104301","55459/103053","18487/34350","E/K","Gaa/Aaa"]
["FAM35A",54537,"WUGSC","GRCh38","chr10",87187152,87187152,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A0TX-01A-11D-A099-09","TCGA-AR-A0TX-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","63d635fa-d136-4e8a-a534-966ee678bb66","3c3cfe65-4e86-4c42-85d0-9daaeff2fc26","c.2260G>A","ENST00000298784",42956,114,372,"A","ENSG00000122376","ENST00000298784","missense_variant","missense_variant","2374/3402","2260/2508","754/835","E/K","Gag/Aag"]
["FOPNL",123811,"WUGSC","GRCh38","chr16",15884092,15884092,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-AR-A0TX-01A-11D-A099-09","TCGA-AR-A0TX-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","63d635fa-d136-4e8a-a534-966ee678bb66","3c3cfe65-4e86-4c42-85d0-9daaeff2fc26","c.142C>A","ENST00000255759",42771,177,167,"T","ENSG00000133393","ENST00000255759","missense_variant","missense_variant","172/2275","142/525","48/174","H/N","Cat/Aat"]
["MIR513A1",574509,"WUGSC","GRCh38","chrX",147213566,147213566,"+","RNA","SNP","C","C","T","rs782486524","byFrequency","TCGA-AR-A0TX-01A-11D-A099-09","TCGA-AR-A0TX-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","63d635fa-d136-4e8a-a534-966ee678bb66","3c3cfe65-4e86-4c42-85d0-9daaeff2fc26","n.26G>A","ENST00000385138",42736,258,394,"T","ENSG00000207873","ENST00000385138","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","26/129"]
["ABCD1",215,"WUGSC","GRCh38","chrX",153744531,153744531,"+","3'UTR","SNP","G","G","T","novel",null,"TCGA-GM-A3NW-01A-21D-A228-09","TCGA-GM-A3NW-10A-01D-A22A-09",null,null,"Somatic","Illumina HiSeq 2000","b7ba9ef1-b3c6-45a1-a059-5aea15561d95","70a26034-3902-4c3c-b9bb-40720ae1bb73","c.*796G>T","ENST00000218104",43018,8,10,"T","ENSG00000101986","ENST00000218104","3_prime_UTR_variant","3_prime_UTR_variant","3433/3664","-/2238","-/745"]
["LHX9",56956,"WUGSC","GRCh38","chr1",197921599,197921599,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A0AS-01A-11W-A019-09","TCGA-AN-A0AS-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","2257c942-1274-47e7-86ad-b92ecfafc205","0ec33f45-45dc-4fd6-b1c9-0312bff04da4","c.673G>A","ENST00000367387",42799,38,24,"A","ENSG00000143355","ENST00000367387","missense_variant","missense_variant","1098/7836","673/1194","225/397","G/R","Ggg/Agg"]
["PARP9",83666,"WUGSC","GRCh38","chr3",122540664,122540664,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-GM-A2DO-01A-11D-A19Y-09","TCGA-GM-A2DO-10D-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","fc563803-d0e6-4b04-86b1-ff00ae342a12","c247eeab-2b71-4019-a24b-d4648fa38deb","c.1678G>T","ENST00000360356",42958,138,98,"A","ENSG00000138496","ENST00000360356","missense_variant","missense_variant","1906/3198","1678/2565","560/854","D/Y","Gac/Tac"]
["CEP350",9857,"WUGSC","GRCh38","chr1",180093318,180093318,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A09E-01A-11W-A019-09","TCGA-A8-A09E-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d6465963-5ea6-44a5-96b0-dff0b0fae4c4","950408ef-e597-4d7c-852d-865fbc66f75d","c.7213C>T","ENST00000367607","34/38",57,33,"T","ENSG00000135837","ENST00000367607","missense_variant","missense_variant","7631/13491","7213/9354","2405/3117","L/F","Ctc/Ttc"]
["MED23",9439,"WUGSC","GRCh38","chr6",131615947,131615947,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-AR-A0TZ-01A-12D-A099-09","TCGA-AR-A0TZ-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","90a26d5e-356b-424c-80bc-4723d24c594f","1d7bc726-8fc1-4a06-8c5f-4e08291b8952","c.836C>G","ENST00000368068",43037,73,220,"C","ENSG00000112282","ENST00000368068","missense_variant","missense_variant","1016/5233","836/4107","279/1368","S/C","tCc/tGc"]
["BMP6",654,"WUGSC","GRCh38","chr6",7845307,7845307,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E2-A15S-01A-11D-A10Y-09","TCGA-E2-A15S-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","01f78efa-ba0b-4263-81fd-d3d8ea1bc5fd","9c963e55-136d-498c-b440-09d4fc3f74de","c.832C>G","ENST00000283147",42773,164,176,"G","ENSG00000153162","ENST00000283147","missense_variant","missense_variant","991/2780","832/1542","278/513","Q/E","Caa/Gaa"]
["ADGRF5",221395,"WUGSC","GRCh38","chr6",46863050,46863050,"+","Silent","SNP","C","C","T","rs144652122","by1000G;byCluster;byFrequency","TCGA-BH-A0H7-01A-13W-A071-09","TCGA-BH-A0H7-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","8623830e-3fdd-4707-83e9-5f528105aa55","bd560d56-fd13-4213-8e29-2a99fee0a055","c.2037G>A","ENST00000265417","15/21",195,185,"T","ENSG00000069122","ENST00000265417","synonymous_variant","synonymous_variant","2271/5668","2037/4041","679/1346","P","ccG/ccA"]
["OR2L13",284521,"WUGSC","GRCh38","chr1",248099867,248099867,"+","Silent","SNP","T","T","C","rs376300250","byCluster","TCGA-BH-A0BW-01A-11D-A10Y-09","TCGA-BH-A0BW-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","07b5141f-ac79-439b-883b-b0183bbe7ff5","4fe9e340-5314-4633-befe-c09aad28d7bf","c.492T>C","ENST00000358120",42768,529,343,"C","ENSG00000196071","ENST00000358120","synonymous_variant","synonymous_variant","637/1692","492/939","164/312","H","caT/caC"]
["CAPN6",827,"WUGSC","GRCh38","chrX",111253150,111253150,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0BW-01A-11D-A10Y-09","TCGA-BH-A0BW-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","07b5141f-ac79-439b-883b-b0183bbe7ff5","4fe9e340-5314-4633-befe-c09aad28d7bf","c.364C>T","ENST00000324068",42838,192,305,"A","ENSG00000077274","ENST00000324068","missense_variant","missense_variant","532/3568","364/1926","122/641","H/Y","Cac/Tac"]
["ATP6V1G1",9550,"WUGSC","GRCh38","chr9",114592585,114592585,"+","Missense_Mutation","SNP","A","A","C","rs72752535","by1000G;byCluster;byFrequency","TCGA-C8-A274-01A-11D-A16D-09","TCGA-C8-A274-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","5e6e7c20-47b3-4f0e-a3c7-8293993e39cf","88dcd89c-7af1-48c2-9973-4ffee5c6ee50","c.116A>C","ENST00000374050",42769,106,66,"C","ENSG00000136888","ENST00000374050","missense_variant","missense_variant","209/1080","116/357","39/118","E/A","gAa/gCa"]
["RFXANK",8625,"WUGSC","GRCh38","chr19",19194043,19194043,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-C8-A274-01A-11D-A16D-09","TCGA-C8-A274-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","5e6e7c20-47b3-4f0e-a3c7-8293993e39cf","88dcd89c-7af1-48c2-9973-4ffee5c6ee50","c.97G>C","ENST00000303088",42804,79,57,"C","ENSG00000064490","ENST00000303088","missense_variant","missense_variant","571/1407","97/783","33/260","D/H","Gat/Cat"]
["FREM2",341640,"WUGSC","GRCh38","chr13",38689448,38689448,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-LL-A5YO-01A-21D-A28B-09","TCGA-LL-A5YO-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","5af23455-a0dc-4c6e-8577-e90599523caa","463b9a58-79b7-4b1c-abcb-25fe9c4de4e0","c.2104G>C","ENST00000280481",42759,54,86,"C","ENSG00000150893","ENST00000280481","missense_variant","missense_variant","2320/16070","2104/9510","702/3169","E/Q","Gag/Cag"]
["FZD9",8326,"WUGSC","GRCh38","chr7",73434841,73434841,"+","Silent","SNP","G","G","A","rs782349557","byFrequency","TCGA-A8-A093-01A-11W-A019-09","TCGA-A8-A093-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8f64ba22-0958-4fdb-8161-f83cfe57c95d","4f97de65-e2ea-444d-b824-70905e5059c2","c.834G>A","ENST00000344575",42736,14,31,"A","ENSG00000188763","ENST00000344575","synonymous_variant","synonymous_variant","1059/2338","834/1776","278/591","S","tcG/tcA"]
["GON4L",54856,"WUGSC","GRCh38","chr1",155765275,155765275,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-PL-A8LV-01A-21D-A41F-09","TCGA-PL-A8LV-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","d1020f41-997b-4f08-957e-2e798c51e20f","ee83a007-0ea7-4df1-ba6d-01fd724e5843","c.4198G>C","ENST00000368331","21/32",17,34,"G","ENSG00000116580","ENST00000368331","missense_variant","missense_variant","4373/7823","4198/6726","1400/2241","G/R","Gga/Cga"]
["SS18L1",26039,"WUGSC","GRCh38","chr20",62181557,62181557,"+","3'UTR","SNP","T","T","C","novel",null,"TCGA-PL-A8LV-01A-21D-A41F-09","TCGA-PL-A8LV-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","d1020f41-997b-4f08-957e-2e798c51e20f","ee83a007-0ea7-4df1-ba6d-01fd724e5843","c.*2349T>C","ENST00000331758",43050,180,242,"C","ENSG00000184402","ENST00000331758","3_prime_UTR_variant","3_prime_UTR_variant","3566/4493","-/1191","-/396"]
["MUC4",4585,"WUGSC","GRCh38","chr3",195780614,195780614,"+","Missense_Mutation","SNP","A","A","T","novel",null,"TCGA-A2-A1FW-01A-11D-A13L-09","TCGA-A2-A1FW-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","6ccdb42e-1ad1-4175-b83a-a24b019dc640","c2563fdc-a603-4974-a849-a938ca683f7c","c.10966T>A","ENST00000463781",42791,545,279,"T","ENSG00000145113","ENST00000463781","missense_variant","missense_variant","11426/17110","10966/16239","3656/5412","S/T","Tca/Aca"]
["TUBBP5",643224,"WUGSC","GRCh38","chr9",138176680,138176680,"+","3'Flank","SNP","C","C","T","novel",null,"TCGA-AC-A6NO-01A-12D-A33E-09","TCGA-AC-A6NO-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","b1e44cd8-c488-4bd7-a622-c09aef256569","c0a823d7-0501-4a82-b08d-3d1f05c96c23",null,"ENST00000503395",null,224,116,"T","ENSG00000159247","ENST00000503395","downstream_gene_variant","downstream_gene_variant","-/1735"]
["HUWE1",10075,"WUGSC","GRCh38","chrX",53630965,53630965,"+","Nonsense_Mutation","SNP","G","G","A","novel",null,"TCGA-AR-A1AO-01A-11D-A12Q-09","TCGA-AR-A1AO-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","b841db95-2eff-4181-8d44-3cde2f2f9e70","1569c114-c779-4135-9978-99aa3ac67035","c.832C>T","ENST00000262854",31017,125,193,"A","ENSG00000086758","ENST00000262854","stop_gained","stop_gained","1235/14739","832/13125","278/4374","Q/*","Cag/Tag"]
["ERICH3",127254,"WUGSC","GRCh38","chr1",74572164,74572164,"+","Silent","SNP","C","C","T","novel",null,"TCGA-A2-A0YL-01A-21D-A10G-09","TCGA-A2-A0YL-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","3cc80b41-603d-4735-85c7-71f540dc6e5c","f570e581-5f15-4113-93d7-a4bbeb7ec394","c.3546G>A","ENST00000326665","14/15",133,95,"T","ENSG00000178965","ENST00000326665","synonymous_variant","synonymous_variant","3765/7159","3546/4593","1182/1530","L","ctG/ctA"]
["SSPO",23145,"WUGSC","GRCh38","chr7",149817899,149817899,"+","Splice_Site","SNP","A","A","G","novel",null,"TCGA-PE-A5DC-01A-12D-A27P-09","TCGA-PE-A5DC-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","7b62179b-7b95-441a-8fe2-6e1f604ee077","d9f3df49-ebb8-4208-985d-aa9fee51715f","c.11382-2A>G","ENST00000378016",null,63,68,"G","ENSG00000197558","ENST00000378016","splice_acceptor_variant","splice_acceptor_variant","-/15589","11382/15453","3794/5150"]
["TSHZ1",10194,"WUGSC","GRCh38","chr18",75287798,75287798,"+","Silent","SNP","C","C","T","novel",null,"TCGA-PE-A5DC-01A-12D-A27P-09","TCGA-PE-A5DC-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","7b62179b-7b95-441a-8fe2-6e1f604ee077","d9f3df49-ebb8-4208-985d-aa9fee51715f","c.2391C>T","ENST00000580243",42768,19,20,"T","ENSG00000179981","ENST00000580243","synonymous_variant","synonymous_variant","2739/3582","2391/3234","797/1077","A","gcC/gcT"]
["CPA6",57094,"WUGSC","GRCh38","chr8",67483747,67483747,"+","Intron","SNP","C","C","T","novel",null,"TCGA-A2-A0SY-01A-31D-A099-09","TCGA-A2-A0SY-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","efaa9c0b-c14b-4141-b48c-cc2c6b89ab73","95699bf2-296b-4b90-8328-3e423c69e282","c.838+21G>A","ENST00000297770",null,156,137,"T","ENSG00000165078","ENST00000297770","intron_variant","intron_variant","-/1861","-/1314","-/437"]
["C7orf25",79020,"WUGSC","GRCh38","chr7",42910716,42910716,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A8-A06R-01A-11D-A015-09","TCGA-A8-A06R-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","c6b00eff-6c4e-4d79-a9b1-8fb1f3090816","bf64ab88-5956-4a6a-a303-6a2cbb82f649","c.185C>T","ENST00000350427",42768,1024,159,"A","ENSG00000136197","ENST00000350427","missense_variant","missense_variant","461/2451","185/1266","62/421","S/F","tCt/tTt"]
["JMJD6",23210,"WUGSC","GRCh38","chr17",76720496,76720496,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-E9-A1N8-01A-11D-A142-09","TCGA-E9-A1N8-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","cac57844-0e46-489b-8d94-ceea5788c050","91eb46af-a239-4482-ac32-b4a930aa91c3","c.944T>G","ENST00000397625",42861,25,22,"C","ENSG00000070495","ENST00000397625","missense_variant","missense_variant;splice_region_variant","1059/1603","944/1212","315/403","I/S","aTt/aGt"]
["METTL5",29081,"WUGSC","GRCh38","chr2",169815507,169815507,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-D8-A146-01A-31D-A10Y-09","TCGA-D8-A146-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","9a7548dc-fc79-4ad4-a324-0e9f63c91a20","6d63e128-669b-4ac6-b2d3-10f6d7cf82d1","c.511G>A","ENST00000260953",42862,599,535,"T","ENSG00000138382","ENST00000260953","missense_variant","missense_variant","828/1010","511/630","171/209","E/K","Gaa/Aaa"]
["DEFB113",245927,"WUGSC","GRCh38","chr6",49969620,49969620,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A0TU-01A-31D-A10G-09","TCGA-AR-A0TU-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","31922dbe-3b4a-4ac1-98fc-db88ae851462","406d5b1c-1023-40c4-bd89-aaa03b36ac39","c.6G>C","ENST00000398718",42737,41,195,"G","ENSG00000214642","ENST00000398718","missense_variant","missense_variant","6/249","6/249",29983,"K/N","aaG/aaC"]
["CFH",3075,"WUGSC","GRCh38","chr1",196701342,196701342,"+","Intron","SNP","G","G","A","rs781371850","byFrequency","TCGA-A1-A0SF-01A-11D-A142-09","TCGA-A1-A0SF-10B-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","b291200e-3c22-411a-85d0-fbe1570acda2","cc8ae8d4-315d-492a-84e9-7ed8630e9c70","c.1336+11103G>A","ENST00000367429",null,78,43,"A","ENSG00000000971","ENST00000367429","intron_variant","intron_variant","-/4127","-/3696","-/1231"]
["NAT10",55226,"WUGSC","GRCh38","chr11",34131527,34131527,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-OL-A66L-01A-12D-A31U-09","TCGA-OL-A66L-10A-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","a2158183-5c33-4f1b-bcae-66c8b1d7de30","9f8120cf-4fd1-4404-9e87-a91a7c19e7a6","c.1516G>A","ENST00000257829","14/29",97,101,"A","ENSG00000135372","ENST00000257829","missense_variant","missense_variant","1722/4002","1516/3078","506/1025","E/K","Gaa/Aaa"]
["SMG1P5",595101,"WUGSC","GRCh38","chr16",30281394,30281394,"+","RNA","SNP","A","A","G","novel",null,"TCGA-AQ-A1H2-01A-11D-A13L-09","TCGA-AQ-A1H2-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1ab2dc63-51ce-4a96-b7ad-f0d9eb198d10","164f69db-8ade-412a-935c-2f2b05203616","n.2042T>C","ENST00000529428","15/29",69,40,"G","ENSG00000183604","ENST00000529428","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","2042/4219"]
["TGFBR2",7048,"WUGSC","GRCh38","chr3",30688440,30688440,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AP-01A-11D-A12Q-09","TCGA-AR-A1AP-10A-01D-A12Q-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","597e37c9-f0c9-4839-800e-6e9519ec3add","db345a86-cbeb-4514-b490-b730372b90dc","c.1453G>A","ENST00000295754",42893,202,110,"A","ENSG00000163513","ENST00000295754","missense_variant","missense_variant","1835/4621","1453/1704","485/567","E/K","Gaa/Aaa"]
["ALDH16A1",126133,"WUGSC","GRCh38","chr19",49459787,49459787,"+","Silent","SNP","C","C","G","novel",null,"TCGA-AO-A03V-01A-11D-A10Y-09","TCGA-AO-A03V-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","d88c365f-366a-49d5-9860-b930aab3eb1b","95a2e03d-1cc6-4565-b63f-99c7f2165c4d","c.438C>G","ENST00000293350",42842,44,43,"G","ENSG00000161618","ENST00000293350","synonymous_variant","synonymous_variant","601/3153","438/2409","146/802","L","ctC/ctG"]
["TSPYL2",64061,"WUGSC","GRCh38","chrX",53085361,53085361,"+","Intron","SNP","A","A","T","novel",null,"TCGA-AR-A24W-01A-11D-A17G-09","TCGA-AR-A24W-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","454e7cd4-8424-4cad-8fbb-f69affa5d1bf","781a3f88-4ca5-4f67-bcef-dcfe30dced42","c.1238+40A>T","ENST00000375442",null,119,80,"T","ENSG00000184205","ENST00000375442","intron_variant","intron_variant","-/2815","-/2082","-/693"]
["GALNT3",2591,"WUGSC","GRCh38","chr2",165755015,165755015,"+","Nonsense_Mutation","SNP","G","G","A","rs137853089",null,"TCGA-EW-A1PB-01A-11D-A142-09","TCGA-EW-A1PB-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","9ddf2119-a222-4fa5-a9f3-0bec7eeea36b","26aa0f07-c813-4659-88fa-fdbae73a937e","c.1441C>T","ENST00000392701",42958,82,41,"A","ENSG00000115339","ENST00000392701","stop_gained","stop_gained","2217/3868","1441/1902","481/633","Q/*","Cag/Tag"]
["POLR3D",661,"WUGSC","GRCh38","chr8",22250455,22250455,"+","Silent","SNP","C","C","T",null,null,"TCGA-EW-A1PB-01A-11D-A142-09","TCGA-EW-A1PB-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","9ddf2119-a222-4fa5-a9f3-0bec7eeea36b","26aa0f07-c813-4659-88fa-fdbae73a937e","c.1134C>T","ENST00000306433",42987,102,66,"T","ENSG00000168495","ENST00000306433","synonymous_variant","synonymous_variant","1219/1931","1134/1197","378/398","H","caC/caT"]
["SLC35A2",7355,"WUGSC","GRCh38","chrX",48904841,48904841,"+","Silent","SNP","G","G","A","rs201330204","by1000G;byCluster","TCGA-EW-A1PB-01A-11D-A142-09","TCGA-EW-A1PB-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","9ddf2119-a222-4fa5-a9f3-0bec7eeea36b","26aa0f07-c813-4659-88fa-fdbae73a937e","c.1068C>T","ENST00000247138",42830,31,35,"A","ENSG00000102100","ENST00000247138","synonymous_variant","synonymous_variant","1072/1451","1068/1191","356/396","S","tcC/tcT"]
["DEFB119",245932,"WUGSC","GRCh38","chr20",31390497,31390497,"+","5'UTR","SNP","G","G","A","novel",null,"TCGA-BH-A0DP-01A-21W-A071-09","TCGA-BH-A0DP-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","5a83cbfe-1803-42ca-820b-a4045e413f90","63666721-38a8-46c4-b519-89dba2c58eb1","c.-14C>T","ENST00000376321",42737,184,208,"A","ENSG00000180483","ENST00000376321","5_prime_UTR_variant","5_prime_UTR_variant","107/457","-/255","-/84"]
["AKR1C1",1645,"WUGSC","GRCh38","chr10",4968321,4968321,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AK-01A-21D-A12Q-09","TCGA-AR-A1AK-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","52f7c22f-84cb-4263-93bf-1ae8cf8abbd2","eccf2a84-ba31-455f-942a-2c1dc7b08cc8","c.382G>A","ENST00000380872",42834,1175,910,"A","ENSG00000187134","ENST00000380872","missense_variant","missense_variant","574/6705","382/972","128/323","V/M","Gtg/Atg"]
["MUC16",94025,"WUGSC","GRCh38","chr19",8961634,8961634,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-AO-A1KT-01A-11D-A13L-09","TCGA-AO-A1KT-10A-01D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","97b33dc3-6a62-419a-aa6c-cb84c9f92102","f5386f22-b79a-48ba-b98d-8110ae94009b","c.15136T>C","ENST00000397910",30742,79,92,"G","ENSG00000181143","ENST00000397910","missense_variant","missense_variant","15340/43816","15136/43524","5046/14507","S/P","Tca/Cca"]
["LOXHD1",125336,"WUGSC","GRCh38","chr18",46560401,46560401,"+","5'Flank","SNP","G","G","A","rs766698872","byFrequency","TCGA-E2-A1LA-01A-11D-A142-09","TCGA-E2-A1LA-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","bdcd4800-3258-446f-b6e5-3c8e2f46c656","d3d4282c-2865-42e6-b9b3-0d69ffd11ccb",null,"ENST00000300591",null,70,35,"A","ENSG00000167210","ENST00000300591","upstream_gene_variant","upstream_gene_variant","-/3970","-/3345","-/1114"]
["MX1",4599,"WUGSC","GRCh38","chr21",41458752,41458752,"+","Silent","SNP","C","C","T","novel",null,"TCGA-BH-A1EO-01A-11D-A135-09","TCGA-BH-A1EO-11A-31D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","20131381-8a11-425d-8954-980e6ec7c427","cb2284f3-6d08-40ec-bf36-dfa349354c59","c.1983C>T","ENST00000398598","17/17",21,22,"T","ENSG00000157601","ENST00000398598","synonymous_variant","synonymous_variant","2388/2850","1983/1989","661/662","P","ccC/ccT"]
["CTNND2",1501,"WUGSC","GRCh38","chr5",11082755,11082755,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-E9-A1RH-01A-21D-A167-09","TCGA-E9-A1RH-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","2ecb84c0-c307-4fa9-85e3-2f722dd365a3","eb6b01e0-150f-4c06-81a8-bd7df58aa879","c.2729G>T","ENST00000304623","16/22",105,59,"A","ENSG00000169862","ENST00000304623","missense_variant","missense_variant","2919/5481","2729/3678","910/1225","C/F","tGc/tTc"]
["SDHAF4",135154,"WUGSC","GRCh38","chr6",70566935,70566935,"+","5'UTR","SNP","G","G","A","novel",null,"TCGA-PL-A8LZ-01A-31D-A36J-09","TCGA-PL-A8LZ-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","3910f2f6-6d7d-4657-bd6b-56e1ecd8dfc5","25b79b90-d886-4437-978e-be42a9bf8324","c.-6G>A","ENST00000370474",42738,59,54,"A","ENSG00000154079","ENST00000370474","5_prime_UTR_variant","5_prime_UTR_variant","19/1196","-/327","-/108"]
["SCP2",6342,"WUGSC","GRCh38","chr1",52995985,52995985,"+","Intron","SNP","G","G","A","novel",null,"TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.1081+7849G>A","ENST00000371514",null,22,33,"A","ENSG00000116171","ENST00000371514","intron_variant","intron_variant","-/2811","-/1644","-/547"]
["PLEKHH2",130271,"WUGSC","GRCh38","chr2",43644790,43644790,"+","Silent","SNP","A","A","G",null,null,"TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.117A>G","ENST00000282406",10990,85,89,"G","ENSG00000152527","ENST00000282406","synonymous_variant","synonymous_variant","227/6981","117/4482","39/1493","A","gcA/gcG"]
["GATB",5188,"WUGSC","GRCh38","chr4",151671161,151671161,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.*13C>T","ENST00000263985","13/13",90,139,"A","ENSG00000059691","ENST00000263985","3_prime_UTR_variant","3_prime_UTR_variant","1728/2385","-/1674","-/557"]
["SLC26A8",116369,"WUGSC","GRCh38","chr6",35955412,35955412,"+","Missense_Mutation","SNP","C","C","T","rs767361951","byFrequency","TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.1972G>A","ENST00000355574","17/20",281,240,"T","ENSG00000112053","ENST00000355574","missense_variant","missense_variant","2143/3463","1972/2913","658/970","E/K","Gaa/Aaa"]
["TRIM24",8805,"WUGSC","GRCh38","chr7",138584925,138584925,"+","Missense_Mutation","SNP","A","A","G","rs780616900",null,"TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.3127A>G","ENST00000343526","19/19",42,21,"G","ENSG00000122779","ENST00000343526","missense_variant","missense_variant","3342/8410","3127/3153","1043/1050","I/V","Att/Gtt"]
["BUD13",84811,"WUGSC","GRCh38","chr11",116763047,116763047,"+","Missense_Mutation","SNP","C","C","T","rs117864209","by1000G;byCluster;byFrequency","TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.542G>A","ENST00000260210",42835,15,42,"T","ENSG00000137656","ENST00000260210","missense_variant","missense_variant","566/2196","542/1860","181/619","R/H","cGt/cAt"]
["NOP2",4839,"WUGSC","GRCh38","chr12",6563164,6563164,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.895G>A","ENST00000322166",42994,50,64,"T","ENSG00000111641","ENST00000322166","missense_variant","missense_variant","1017/2683","895/2439","299/812","E/K","Gag/Aag"]
["ARMC5",79798,"WUGSC","GRCh38","chr16",31466607,31466607,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.2526C>A","ENST00000268314",42892,23,44,"A","ENSG00000140691","ENST00000268314","missense_variant","missense_variant","3055/3612","2526/2808","842/935","F/L","ttC/ttA"]
["CALR3",125972,"WUGSC","GRCh38","chr19",16490428,16490428,"+","Silent","SNP","G","G","C","rs185241971","by1000G;byCluster","TCGA-D8-A1J8-01A-11D-A13L-09","TCGA-D8-A1J8-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1857f611-3082-45d3-801c-800e685ade07","58ca54bc-8f1a-4ffc-916c-f96b993e3c45","c.336C>G","ENST00000269881",42803,142,144,"C","ENSG00000269058","ENST00000269881","synonymous_variant","synonymous_variant","399/1292","336/1155","112/384","V","gtC/gtG"]
["LAMB3",3914,"WUGSC","GRCh38","chr1",209633086,209633086,"+","Silent","SNP","T","T","C","rs772335033",null,"TCGA-S3-AA0Z-01A-11D-A41F-09","TCGA-S3-AA0Z-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1eea16c3-4637-4690-bd74-ba6238addeb8","a89971b0-b2d3-4bea-beca-97805891d409","c.612A>G","ENST00000356082",42939,128,123,"C","ENSG00000196878","ENST00000356082","synonymous_variant","synonymous_variant","747/4055","612/3519","204/1172","Q","caA/caG"]
["TTN",7273,"WUGSC","GRCh38","chr2",178526793,178526793,"+","3'UTR","SNP","C","C","T","rs566063792","by1000G","TCGA-S3-AA0Z-01A-11D-A41F-09","TCGA-S3-AA0Z-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1eea16c3-4637-4690-bd74-ba6238addeb8","a89971b0-b2d3-4bea-beca-97805891d409","c.*219G>A","ENST00000591111","313/313",118,223,"T","ENSG00000155657","ENST00000591111","3_prime_UTR_variant","3_prime_UTR_variant","103497/104301","-/103053","-/34350"]
["PRCC",5546,"WUGSC","GRCh38","chr1",156767937,156767937,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-PE-A5DE-01A-11D-A27P-09","TCGA-PE-A5DE-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","b59ec69e-e93a-4415-9c18-9d139b852919","7ff240ac-2b8f-4e5c-8184-980b3f9322a5","c.166C>G","ENST00000271526",42742,59,30,"G","ENSG00000143294","ENST00000271526","missense_variant","missense_variant","438/2105","166/1476","56/491","Q/E","Cag/Gag"]
["AC073869.20",0,"WUGSC","GRCh38","chr2",131442676,131442676,"+","RNA","SNP","C","C","T","novel",null,"TCGA-PE-A5DE-01A-11D-A27P-09","TCGA-PE-A5DE-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","b59ec69e-e93a-4415-9c18-9d139b852919","7ff240ac-2b8f-4e5c-8184-980b3f9322a5","n.1912G>A","ENST00000407594",42736,161,143,"T","ENSG00000217950","ENST00000407594","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","1912/1944"]
["PMS2CL",441194,"WUGSC","GRCh38","chr7",6737234,6737234,"+","RNA","SNP","C","C","G","novel",null,"TCGA-PE-A5DE-01A-11D-A27P-09","TCGA-PE-A5DE-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","b59ec69e-e93a-4415-9c18-9d139b852919","7ff240ac-2b8f-4e5c-8184-980b3f9322a5","n.244C>G","ENST00000403974",42772,162,121,"G","ENSG00000187953","ENST00000403974","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","244/1529"]
["XPNPEP1",7511,"WUGSC","GRCh38","chr10",109907809,109907809,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-PE-A5DE-01A-11D-A27P-09","TCGA-PE-A5DE-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","b59ec69e-e93a-4415-9c18-9d139b852919","7ff240ac-2b8f-4e5c-8184-980b3f9322a5","c.128G>A","ENST00000502935",42815,39,60,"T","ENSG00000108039","ENST00000502935","missense_variant","missense_variant","248/2539","128/2001","43/666","R/K","aGa/aAa"]
["DCC",1630,"WUGSC","GRCh38","chr18",53531147,53531147,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-PE-A5DE-01A-11D-A27P-09","TCGA-PE-A5DE-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","b59ec69e-e93a-4415-9c18-9d139b852919","7ff240ac-2b8f-4e5c-8184-980b3f9322a5","c.*494G>A","ENST00000442544","29/29",31,41,"A","ENSG00000187323","ENST00000442544","3_prime_UTR_variant","3_prime_UTR_variant","5454/10206","-/4344","-/1447"]
["POLR3F",10621,"WUGSC","GRCh38","chr20",18467403,18467403,"+","5'UTR","SNP","C","C","T","novel",null,"TCGA-PE-A5DE-01A-11D-A27P-09","TCGA-PE-A5DE-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","b59ec69e-e93a-4415-9c18-9d139b852919","7ff240ac-2b8f-4e5c-8184-980b3f9322a5","c.-104C>T","ENST00000377603",42744,91,55,"T","ENSG00000132664","ENST00000377603","5_prime_UTR_variant","5_prime_UTR_variant","277/2416","-/951","-/316"]
["RRM2",6241,"WUGSC","GRCh38","chr2",10129082,10129082,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A25A-01A-12D-A16D-09","TCGA-A2-A25A-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","5739a7e1-7fa3-434c-b1c3-c0a9e570c858","ad66f1d8-3521-4acf-a50f-76c6842df466","c.945G>A","ENST00000304567",42988,272,105,"A","ENSG00000171848","ENST00000304567","missense_variant","missense_variant","1014/3271","945/1170","315/389","M/I","atG/atA"]
["TMEM67",91147,"WUGSC","GRCh38","chr8",93758537,93758537,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A25A-01A-12D-A16D-09","TCGA-A2-A25A-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","5739a7e1-7fa3-434c-b1c3-c0a9e570c858","ad66f1d8-3521-4acf-a50f-76c6842df466","c.367G>T","ENST00000453321",42822,107,59,"T","ENSG00000164953","ENST00000453321","missense_variant","missense_variant","425/4651","367/2988","123/995","A/S","Gcc/Tcc"]
["ZNFX1",57169,"WUGSC","GRCh38","chr20",49271394,49271394,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-A2-A25A-01A-12D-A16D-09","TCGA-A2-A25A-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","5739a7e1-7fa3-434c-b1c3-c0a9e570c858","ad66f1d8-3521-4acf-a50f-76c6842df466","c.418C>A","ENST00000371752",42808,103,50,"T","ENSG00000124201","ENST00000371752","missense_variant","missense_variant","503/7212","418/5757","140/1918","Q/K","Cag/Aag"]
["SPHKAP",80309,"WUGSC","GRCh38","chr2",228018157,228018157,"+","Silent","SNP","G","G","T",null,null,"TCGA-BH-A1EY-01A-11D-A13L-09","TCGA-BH-A1EY-11B-21D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","7c035023-8ea9-4504-8f03-9573745cb6ef","278795b3-a369-43fb-9d82-4d6d3b92ade3","c.2697C>A","ENST00000392056",42928,210,129,"T","ENSG00000153820","ENST00000392056","synonymous_variant","synonymous_variant","2744/6917","2697/5103","899/1700","V","gtC/gtA"]
["MSLN",10232,"WUGSC","GRCh38","chr16",764721,764721,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-A1-A0SJ-01A-11D-A099-09","TCGA-A1-A0SJ-10A-02D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","a55c6a44-c0f5-4300-8df4-4a70befe2d3b","aaf63cff-b2e2-4f9b-868e-e7a1637cc14b","c.375C>A","ENST00000382862",42903,52,27,"A","ENSG00000102854","ENST00000382862","missense_variant","missense_variant","470/2116","375/1893","125/630","F/L","ttC/ttA"]
["PDYN",5173,"WUGSC","GRCh38","chr20",1980666,1980666,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A0DX-01A-11D-A10Y-09","TCGA-BH-A0DX-10A-02D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","bca403d9-48ff-4534-ba33-94b8fb9fee0f","edc2ac11-3828-41d0-abf8-976ea7c5b348","c.422C>A","ENST00000217305",42829,149,222,"T","ENSG00000101327","ENST00000217305","missense_variant","missense_variant","648/2555","422/765","141/254","A/E","gCa/gAa"]
["SEC16A",9919,"WUGSC","GRCh38","chr9",136447305,136447305,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-EW-A1P4-01A-21D-A142-09","TCGA-EW-A1P4-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","204e4ef3-e6b8-469f-9024-56c6f6f07afd","99c296d2-1d17-47c0-b036-239170e2ff1a","c.6619C>T","ENST00000313050","25/30",16,30,"A","ENSG00000148396","ENST00000313050","missense_variant","missense_variant","6693/8806","6619/7074","2207/2357","P/S","Ccg/Tcg"]
["MROH1",727957,"WUGSC","GRCh38","chr8",144258845,144258845,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-B6-A0I1-01A-11D-A21Q-09","TCGA-B6-A0I1-10A-01D-A21Q-09",null,null,"Somatic","Illumina HiSeq 2000","2290b078-6a5b-4c83-9dfb-b525bbf14e4e","82b4b870-3cc6-429f-bb9a-d53757437517","c.3860A>G","ENST00000326134","34/42",186,54,"G","ENSG00000179832","ENST00000326134","missense_variant","missense_variant","3917/5183","3860/4926","1287/1641","D/G","gAc/gGc"]
["SASH1",23328,"WUGSC","GRCh38","chr6",148548489,148548489,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-OL-A6VQ-01A-12D-A41F-09","TCGA-OL-A6VQ-10B-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","08d5d362-c2d8-4d2b-8323-6bf07963c798","ac23b58d-de5f-4d93-896f-83804822aa89","c.3675G>C","ENST00000367467","20/20",11,23,"C","ENSG00000111961","ENST00000367467","missense_variant","missense_variant","4150/7711","3675/3744","1225/1247","E/D","gaG/gaC"]
["TTN",7273,"WUGSC","GRCh38","chr2",178577412,178577412,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-LL-A8F5-01A-11D-A36J-09","TCGA-LL-A8F5-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","b8dc8ba9-9bd3-422f-b86f-34a2b6bdfd10","0a7e0566-9399-435b-bf5b-37bb75fd017c","c.64000C>A","ENST00000591111","274/313",57,69,"T","ENSG00000155657","ENST00000591111","missense_variant","missense_variant","64225/104301","64000/103053","21334/34350","P/T","Ccc/Acc"]
["ZSCAN30",100101467,"WUGSC","GRCh38","chr18",35284613,35284613,"+","Intron","SNP","A","A","T","novel",null,"TCGA-LL-A8F5-01A-11D-A36J-09","TCGA-LL-A8F5-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","b8dc8ba9-9bd3-422f-b86f-34a2b6bdfd10","0a7e0566-9399-435b-bf5b-37bb75fd017c","c.-104+5471T>A","ENST00000333206",null,53,37,"T","ENSG00000186814","ENST00000333206","intron_variant","intron_variant","-/4097","-/1485","-/494"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179234297,179234297,"+","Missense_Mutation","SNP","A","A","G","rs121913279","byCluster;byFrequency","TCGA-BH-A0EA-01A-11D-A10Y-09","TCGA-BH-A0EA-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","561b8777-801a-49ed-a306-e7dafeb044b6","cfbd5476-e83a-401d-9f9a-639c73a0e35b","c.3140A>G","ENST00000263967","21/21",123,225,"G","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","3297/9093","3140/3207","1047/1068","H/R","cAt/cGt"]
["NID1",4811,"WUGSC","GRCh38","chr1",236042093,236042093,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AO-A0J6-01A-11W-A050-09","TCGA-AO-A0J6-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","7d21a0c4-03c7-4641-8b4d-7a5877960360","2014e5c3-3ac5-4d79-8942-3ee4e0cbf60d","c.952C>G","ENST00000264187",42845,66,82,"C","ENSG00000116962","ENST00000264187","missense_variant","missense_variant","1035/5864","952/3744","318/1247","L/V","Ctg/Gtg"]
["ACP5",54,"WUGSC","GRCh38","chr19",11575246,11575246,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AO-A0J6-01A-11W-A050-09","TCGA-AO-A0J6-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","7d21a0c4-03c7-4641-8b4d-7a5877960360","2014e5c3-3ac5-4d79-8942-3ee4e0cbf60d","c.742C>G","ENST00000218758",42923,15,33,"C","ENSG00000102575","ENST00000218758","missense_variant","missense_variant","1044/1630","742/978","248/325","Q/E","Caa/Gaa"]
["LY9",4063,"WUGSC","GRCh38","chr1",160799888,160799888,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-A8-A08F-01A-11W-A019-09","TCGA-A8-A08F-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","4975eeda-984e-4a7a-8193-43d8b6e0271c","f3828bb5-e811-4992-ba01-0fe463d82cab","c.260T>C","ENST00000263285",42776,134,104,"C","ENSG00000122224","ENST00000263285","missense_variant","missense_variant","290/2443","260/1968","87/655","L/P","cTt/cCt"]
["THAP1",55145,"WUGSC","GRCh38","chr8",42838316,42838316,"+","Silent","SNP","T","T","C",null,null,"TCGA-A8-A08F-01A-11W-A019-09","TCGA-A8-A08F-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","4975eeda-984e-4a7a-8193-43d8b6e0271c","f3828bb5-e811-4992-ba01-0fe463d82cab","c.288A>G","ENST00000254250",42797,119,78,"C","ENSG00000131931","ENST00000254250","synonymous_variant","synonymous_variant","519/2161","288/642","96/213","P","ccA/ccG"]
["EMC1",23065,"WUGSC","GRCh38","chr1",19237168,19237168,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.1283A>G","ENST00000477853",43092,159,170,"C","ENSG00000127463","ENST00000477853","missense_variant","missense_variant","1326/6664","1283/2982","428/993","H/R","cAt/cGt"]
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["ZNF841",284371,"WUGSC","GRCh38","chr19",52065932,52065932,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.1602G>T","ENST00000426391",42860,266,269,"A","ENSG00000197608","ENST00000426391","missense_variant","missense_variant","2154/3620","1602/2427","534/808","E/D","gaG/gaT"]
["MROH8",140699,"WUGSC","GRCh38","chr20",37141220,37141220,"+","Missense_Mutation","SNP","C","C","T","rs759428520","byFrequency","TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.1510G>A","ENST00000343811",43063,175,139,"T","ENSG00000101353","ENST00000343811","missense_variant","missense_variant","1510/3425","1511/3210","504/1069","R/Q","cGa/cAa"]
["SUMO1P1",391257,"WUGSC","GRCh38","chr20",53875273,53875273,"+","RNA","SNP","G","G","A","novel",null,"TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","n.285C>T","ENST00000497904",42736,204,156,"A","ENSG00000241721","ENST00000497904","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","285/306"]
["TUBA8",51807,"WUGSC","GRCh38","chr22",18126597,18126597,"+","Missense_Mutation","SNP","G","G","A","rs770431044",null,"TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.619G>A","ENST00000330423",42830,322,293,"A","ENSG00000183785","ENST00000330423","missense_variant","missense_variant","692/2018","619/1350","207/449","E/K","Gaa/Aaa"]
["SHROOM2",357,"WUGSC","GRCh38","chrX",9932194,9932194,"+","Missense_Mutation","SNP","C","C","T","rs763499301","byFrequency","TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.2911C>T","ENST00000380913",42896,104,155,"T","ENSG00000146950","ENST00000380913","missense_variant","missense_variant","3001/7447","2911/4851","971/1616","R/W","Cgg/Tgg"]
["CFAP47",286464,"WUGSC","GRCh38","chrX",35948431,35948431,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.635G>A","ENST00000297866",42841,358,386,"A","ENSG00000165164","ENST00000297866","missense_variant","missense_variant","701/3608","635/2931","212/976","R/K","aGa/aAa"]
["PJA1",64219,"WUGSC","GRCh38","chrX",69162213,69162213,"+","Silent","SNP","T","T","C",null,null,"TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.1026A>G","ENST00000361478",42768,75,82,"C","ENSG00000181191","ENST00000361478","synonymous_variant","synonymous_variant","1404/2755","1026/1932","342/643","R","cgA/cgG"]
["KIAA1210",57481,"WUGSC","GRCh38","chrX",119088943,119088943,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.2287C>A","ENST00000402510",43053,37,69,"T","ENSG00000250423","ENST00000402510","missense_variant","missense_variant","2287/7824","2287/5130","763/1709","P/T","Cct/Act"]
["AFF2",2334,"WUGSC","GRCh38","chrX",148662459,148662459,"+","Silent","SNP","C","C","T","rs370542676","by1000G;byCluster","TCGA-AN-A046-01A-21W-A050-09","TCGA-AN-A046-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","696dfa31-8ff8-4b4f-a6e5-b59c34fae1f7","7fd1a063-e742-4ebc-acbd-c81ba11f1cc3","c.732C>T","ENST00000370460",42815,317,454,"T","ENSG00000155966","ENST00000370460","synonymous_variant","synonymous_variant","1211/13746","732/3936","244/1311","F","ttC/ttT"]
["AHCTF1",25909,"WUGSC","GRCh38","chr1",246853276,246853276,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E2-A1IF-01A-11D-A142-09","TCGA-E2-A1IF-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","7751c2d5-e548-4439-aac1-e7b9dce97583","34cbed4d-6aff-4293-8f12-931ad2f174ca","c.4405G>A","ENST00000326225","32/36",67,35,"T","ENSG00000153207","ENST00000326225","missense_variant","missense_variant","4502/8633","4405/6828","1469/2275","G/S","Ggt/Agt"]
["TBCE",6905,"WUGSC","GRCh38","chr1",235430730,235430730,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AN-A0FZ-01A-11W-A050-09","TCGA-AN-A0FZ-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","d77f59f7-8cff-41f3-a1bb-0de14524d4f4","5605aad9-7f20-4db3-9ed8-cae136f5773b","c.586G>A","ENST00000366601",42933,358,231,"A","ENSG00000116957","ENST00000366601","missense_variant","missense_variant","762/1966","586/1584","196/527","G/S","Ggt/Agt"]
["MYBPC2",4606,"WUGSC","GRCh38","chr19",50454136,50454136,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AN-A0FZ-01A-11W-A050-09","TCGA-AN-A0FZ-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","d77f59f7-8cff-41f3-a1bb-0de14524d4f4","5605aad9-7f20-4db3-9ed8-cae136f5773b","c.1866C>A","ENST00000357701","17/28",161,142,"A","ENSG00000086967","ENST00000357701","missense_variant","missense_variant","1917/3593","1866/3426","622/1141","N/K","aaC/aaA"]
["ADORA3",140,"WUGSC","GRCh38","chr1",111499967,111499967,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-LD-A74U-01A-13D-A33E-09","TCGA-LD-A74U-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","405f804a-1c3f-423a-ba2c-b555f6c80c28","3c243237-0372-440a-ab44-711f482ccc17","c.940G>A","ENST00000241356",42768,60,52,"T","ENSG00000121933","ENST00000241356","missense_variant","missense_variant","1346/1884","940/957","314/318","E/K","Gag/Aag"]
["ARMC3",219681,"WUGSC","GRCh38","chr10",23002029,23002029,"+","Silent","SNP","G","G","A","novel",null,"TCGA-LD-A74U-01A-13D-A33E-09","TCGA-LD-A74U-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","405f804a-1c3f-423a-ba2c-b555f6c80c28","3c243237-0372-440a-ab44-711f482ccc17","c.1536G>A","ENST00000298032",43088,30,33,"A","ENSG00000165309","ENST00000298032","synonymous_variant","synonymous_variant","1620/2811","1536/2619","512/872","L","ctG/ctA"]
["SNRPD2",6633,"WUGSC","GRCh38","chr19",45687489,45687489,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-LD-A74U-01A-13D-A33E-09","TCGA-LD-A74U-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","405f804a-1c3f-423a-ba2c-b555f6c80c28","3c243237-0372-440a-ab44-711f482ccc17","c.*64G>A","ENST00000342669",42797,41,31,"T","ENSG00000125743","ENST00000342669","3_prime_UTR_variant","3_prime_UTR_variant","866/901","-/357","-/118"]
["ATP10B",23120,"WUGSC","GRCh38","chr5",160670488,160670488,"+","Missense_Mutation","SNP","C","C","T","rs751974766",null,"TCGA-AR-A1AS-01A-11D-A12Q-09","TCGA-AR-A1AS-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","3f26f93c-e11a-4ec9-b73b-98fcadc209f4","97a055bf-af49-4c79-bc12-0b3644f21638","c.650G>A","ENST00000327245",42942,130,268,"T","ENSG00000118322","ENST00000327245","missense_variant","missense_variant","1497/7566","650/4386","217/1461","C/Y","tGt/tAt"]
["AKIRIN2",55122,"WUGSC","GRCh38","chr6",87675476,87675476,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-BH-A18T-01A-11D-A12B-09","TCGA-BH-A18T-11A-42D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","4e0ddfcb-e847-4132-bdce-aaee2e027b28","9cfbb971-1628-4eda-9d96-efa55b7d4138","c.*121G>C","ENST00000257787",42860,32,40,"G","ENSG00000135334","ENST00000257787","3_prime_UTR_variant","3_prime_UTR_variant","1258/1662","-/612","-/203"]
["GRIPAP1",56850,"WUGSC","GRCh38","chrX",48981257,48981257,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A0XO-01A-11D-A10G-09","TCGA-AN-A0XO-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","f63863f5-cb60-4961-a5b4-ed5ea1fb3dc8","ea2d9f54-744b-4e56-bc97-d9492168db87","c.1888G>A","ENST00000376423","21/26",115,191,"T","ENSG00000068400","ENST00000376423","missense_variant","missense_variant","1923/3031","1888/2526","630/841","E/K","Gag/Aag"]
["C2orf73",129852,"WUGSC","GRCh38","chr2",54334966,54334966,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0BZ-01A-31D-A12Q-09","TCGA-BH-A0BZ-11A-61D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","1f07765a-3f2b-4b6f-88ef-0d7aab17a758","be00304b-7a7a-464c-b5f7-d784d0c2c0ab","c.176C>A","ENST00000398634",42771,349,219,"A","ENSG00000177994","ENST00000398634","missense_variant","missense_variant","218/1921","176/864","59/287","A/E","gCa/gAa"]
["CDH8",1006,"WUGSC","GRCh38","chr16",61821089,61821089,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-BH-A0BZ-01A-31D-A12Q-09","TCGA-BH-A0BZ-11A-61D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","1f07765a-3f2b-4b6f-88ef-0d7aab17a758","be00304b-7a7a-464c-b5f7-d784d0c2c0ab","c.860A>C","ENST00000577390",42898,179,226,"G","ENSG00000150394","ENST00000577390","missense_variant","missense_variant","1815/9721","860/2400","287/799","E/A","gAa/gCa"]
["ZNF552",79818,"WUGSC","GRCh38","chr19",57808234,57808234,"+","Nonsense_Mutation","SNP","T","T","A",null,null,"TCGA-BH-A0BZ-01A-31D-A12Q-09","TCGA-BH-A0BZ-11A-61D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","1f07765a-3f2b-4b6f-88ef-0d7aab17a758","be00304b-7a7a-464c-b5f7-d784d0c2c0ab","c.1030A>T","ENST00000391701",42797,273,476,"A","ENSG00000178935","ENST00000391701","stop_gained","stop_gained","1200/2352","1030/1224","344/407","R/*","Aga/Tga"]
["LAMTOR1",55004,"WUGSC","GRCh38","chr11",72097712,72097712,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-C8-A12Y-01A-11D-A12B-09","TCGA-C8-A12Y-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","d5c0a1a0-3d38-497b-9f47-107f06659cb1","9fdfe86f-477c-410d-8258-c253254ffe13","c.*110C>G","ENST00000278671",42860,166,42,"C","ENSG00000149357","ENST00000278671","3_prime_UTR_variant","3_prime_UTR_variant","759/1179","-/486","-/161"]
["BSN",8927,"WUGSC","GRCh38","chr3",49658086,49658086,"+","Nonsense_Mutation","SNP","A","A","T",null,null,"TCGA-A8-A094-01A-11W-A019-09","TCGA-A8-A094-10A-01W-A021-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","ab9bf7a6-688e-4388-9682-6b1616723fde","81550760-c58d-4ae7-90eb-9a436d664442","c.8530A>T","ENST00000296452",42867,17,81,"T","ENSG00000164061","ENST00000296452","stop_gained","stop_gained","8644/15955","8530/11781","2844/3926","K/*","Aag/Tag"]
["SUPT20HL2",170067,"WUGSC","GRCh38","chrX",24311469,24311469,"+","RNA","SNP","G","G","A","novel",null,"TCGA-A8-A094-01A-11W-A019-09","TCGA-A8-A094-10A-01W-A021-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","ab9bf7a6-688e-4388-9682-6b1616723fde","81550760-c58d-4ae7-90eb-9a436d664442","n.1847C>T","ENST00000486479",42736,135,107,"A","ENSG00000223611","ENST00000486479","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","1847/2409"]
["CATSPER4",378807,"WUGSC","GRCh38","chr1",26201403,26201403,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1249G>C","ENST00000456354",42988,39,49,"C","ENSG00000188782","ENST00000456354","missense_variant","missense_variant","1316/1912","1249/1419","417/472","E/Q","Gag/Cag"]
["RLF",6018,"WUGSC","GRCh38","chr1",40239824,40239824,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.5122G>C","ENST00000372771",42955,16,18,"C","ENSG00000117000","ENST00000372771","missense_variant","missense_variant","5149/6246","5122/5745","1708/1914","E/Q","Gaa/Caa"]
["FPGT-TNNI3K",100526835,"WUGSC","GRCh38","chr1",74369233,74369233,"+","Nonsense_Mutation","SNP","C","C","T","rs757261707","byFrequency","TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1783C>T","ENST00000557284","17/27",56,84,"T","ENSG00000259030","ENST00000557284","stop_gained","stop_gained","1788/2855","1783/2850","595/949","R/*","Cga/Tga"]
["WDR77",79084,"WUGSC","GRCh38","chr1",111447476,111447476,"+","Silent","SNP","C","C","T","rs74387335","byCluster;suspect","TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.402G>A","ENST00000235090",42804,78,91,"T","ENSG00000116455","ENST00000235090","synonymous_variant","synonymous_variant","609/2576","402/1029","134/342","L","ttG/ttA"]
["SHC1",6464,"WUGSC","GRCh38","chr1",154970222,154970222,"+","Nonsense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.305C>G","ENST00000368445",42747,34,23,"C","ENSG00000160691","ENST00000368445","stop_gained","stop_gained","520/3472","305/1752","102/583","S/*","tCa/tGa"]
["ZBTB41",360023,"WUGSC","GRCh38","chr1",197159496,197159496,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.2593C>T","ENST00000367405",43018,280,199,"A","ENSG00000177888","ENST00000367405","stop_gained","stop_gained","2662/8478","2593/2730","865/909","Q/*","Caa/Taa"]
["EPRS",2058,"WUGSC","GRCh38","chr1",219982790,219982790,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.3355C>T","ENST00000366923","23/32",121,114,"A","ENSG00000136628","ENST00000366923","missense_variant","missense_variant","3625/5014","3355/4539","1119/1512","R/C","Cgt/Tgt"]
["IFT172",26160,"WUGSC","GRCh38","chr2",27483309,27483309,"+","Nonsense_Mutation","SNP","C","C","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.550G>T","ENST00000260570",17715,110,92,"A","ENSG00000138002","ENST00000260570","stop_gained","stop_gained","654/5415","550/5250","184/1749","E/*","Gaa/Taa"]
["ALMS1",7840,"WUGSC","GRCh38","chr2",73452481,73452481,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.5954C>T","ENST00000613296",42970,43,44,"T","ENSG00000116127","ENST00000613296","missense_variant","missense_variant","6065/12925","5954/12507","1985/4168","S/F","tCt/tTt"]
["FOXD4L1",200350,"WUGSC","GRCh38","chr2",113499655,113499655,"+","Silent","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.399C>T","ENST00000306507",42736,70,93,"T","ENSG00000184492","ENST00000306507","synonymous_variant","synonymous_variant","991/2491","399/1227","133/408","I","atC/atT"]
["SCN1A",6323,"WUGSC","GRCh38","chr2",165991406,165991406,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.5869G>C","ENST00000303395","28/28",192,164,"G","ENSG00000144285","ENST00000303395","missense_variant","missense_variant","6287/8533","5869/6030","1957/2009","E/Q","Gaa/Caa"]
["STAT4",6775,"WUGSC","GRCh38","chr2",191029608,191029608,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.*232G>C","ENST00000358470","24/24",36,44,"G","ENSG00000138378","ENST00000358470","3_prime_UTR_variant","3_prime_UTR_variant","2737/2769","-/2247","-/748"]
["KANSL1L",151050,"WUGSC","GRCh38","chr2",210031364,210031364,"+","Intron","SNP","C","C","T","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.2155+57G>A","ENST00000281772",null,128,143,"T","ENSG00000144445","ENST00000281772","intron_variant","intron_variant","-/4754","-/2964","-/987"]
["SCN10A",6336,"WUGSC","GRCh38","chr3",38763545,38763545,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.651C>G","ENST00000449082",42882,165,129,"C","ENSG00000185313","ENST00000449082","missense_variant","missense_variant","651/6418","651/5871","217/1956","F/L","ttC/ttG"]
["CACNA2D3",55799,"WUGSC","GRCh38","chr3",54320529,54320529,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.292A>T","ENST00000288197",13940,112,77,"T","ENSG00000157445","ENST00000288197","missense_variant","missense_variant","340/3671","292/3276","98/1091","M/L","Atg/Ttg"]
["STXBP5L",9515,"WUGSC","GRCh38","chr3",121239044,121239044,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1258G>C","ENST00000273666","13/28",77,77,"C","ENSG00000145087","ENST00000273666","missense_variant","missense_variant","1529/9496","1258/3561","420/1186","D/H","Gat/Cat"]
["ATP2C1",27032,"WUGSC","GRCh38","chr3",130999635,130999635,"+","Nonsense_Mutation","SNP","C","C","T","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.2605C>T","ENST00000428331","26/27",152,106,"T","ENSG00000017260","ENST00000428331","stop_gained","stop_gained","2840/4795","2605/2760","869/919","Q/*","Cag/Tag"]
["TAPT1",202018,"WUGSC","GRCh38","chr4",16176181,16176181,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1045G>C","ENST00000405303",42992,90,106,"G","ENSG00000169762","ENST00000405303","missense_variant","missense_variant","1129/4591","1045/1704","349/567","E/Q","Gaa/Caa"]
["FRYL",285527,"WUGSC","GRCh38","chr4",48515119,48515119,"+","Missense_Mutation","SNP","C","C","T","rs545267489","by1000G","TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.7846G>A","ENST00000358350","56/64",102,131,"T","ENSG00000075539","ENST00000358350","missense_variant","missense_variant","8451/11706","7846/9042","2616/3013","E/K","Gag/Aag"]
["KIAA1109",84162,"WUGSC","GRCh38","chr4",122264359,122264359,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.7249C>A","ENST00000264501","45/86",111,106,"A","ENSG00000138688","ENST00000264501","missense_variant","missense_variant","7622/15896","7249/15018","2417/5005","Q/K","Cag/Aag"]
["ICE1",23379,"WUGSC","GRCh38","chr5",5460894,5460894,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1560G>C","ENST00000296564","13/19",78,76,"C","ENSG00000164151","ENST00000296564","missense_variant","missense_variant","1782/7927","1560/6801","520/2266","E/D","gaG/gaC"]
["PCDHA6",56142,"WUGSC","GRCh38","chr5",140830468,140830468,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.2377G>A","ENST00000529310",42739,33,39,"A","ENSG00000081842","ENST00000529310","missense_variant","missense_variant","2491/5374","2377/2853","793/950","E/K","Gaa/Aaa"]
["HMMR",3161,"WUGSC","GRCh38","chr5",163483038,163483038,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1548G>C","ENST00000358715","14/18",29,17,"C","ENSG00000072571","ENST00000358715","missense_variant","missense_variant","1584/2988","1548/2175","516/724","Q/H","caG/caC"]
["HIST1H4B",8366,"WUGSC","GRCh38","chr6",26027030,26027030,"+","Nonsense_Mutation","SNP","C","C","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.223G>T","ENST00000377745",42736,71,73,"A","ENSG00000278705","ENST00000377745","stop_gained","stop_gained","223/438","223/312","75/103","E/*","Gag/Tag"]
["DNAH8",1769,"WUGSC","GRCh38","chr6",39012498,39012498,"+","Silent","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.12924C>G","ENST00000359357","89/91",124,128,"G","ENSG00000124721","ENST00000359357","synonymous_variant","synonymous_variant","13178/13864","12924/13473","4308/4490","L","ctC/ctG"]
["SYNCRIP",10492,"WUGSC","GRCh38","chr6",85615304,85615304,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1324C>T","ENST00000369622",43050,19,12,"A","ENSG00000135316","ENST00000369622","missense_variant","missense_variant","1825/3023","1324/1872","442/623","P/S","Cca/Tca"]
["THBS2",7058,"WUGSC","GRCh38","chr6",169248813,169248813,"+","Silent","SNP","G","G","A","rs770340323","byFrequency","TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.213C>T","ENST00000366787",42848,89,94,"A","ENSG00000186340","ENST00000366787","synonymous_variant","synonymous_variant","463/5811","213/3519","71/1172","L","ctC/ctT"]
["SBDS",51119,"WUGSC","GRCh38","chr7",66995367,66995367,"+","Silent","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.51G>C","ENST00000246868",42740,48,49,"G","ENSG00000126524","ENST00000246868","synonymous_variant","synonymous_variant","235/1631","51/753","17/250","V","gtG/gtC"]
["DNAJC2",27000,"WUGSC","GRCh38","chr7",103316920,103316920,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1337G>T","ENST00000379263","13/17",265,283,"A","ENSG00000105821","ENST00000379263","missense_variant","missense_variant","1588/2167","1337/1866","446/621","G/V","gGa/gTa"]
["PIP",5304,"WUGSC","GRCh38","chr7",143139715,143139715,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.*73C>T","ENST00000291009",42829,26,20,"T","ENSG00000159763","ENST00000291009","3_prime_UTR_variant","3_prime_UTR_variant","554/585","-/441","-/146"]
["ABRA",137735,"WUGSC","GRCh38","chr8",106761182,106761182,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1001G>C","ENST00000311955",42768,142,87,"G","ENSG00000174429","ENST00000311955","missense_variant","missense_variant","1056/2755","1001/1146","334/381","G/A","gGa/gCa"]
["FREM1",158326,"WUGSC","GRCh38","chr9",14824947,14824947,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1927G>C","ENST00000380880",13820,87,107,"G","ENSG00000164946","ENST00000380880","missense_variant","missense_variant","2711/7324","1927/6540","643/2179","E/Q","Gag/Cag"]
["PCSK5",5125,"WUGSC","GRCh38","chr9",75986167,75986167,"+","Silent","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.333G>A","ENST00000545128",13575,123,111,"A","ENSG00000099139","ENST00000545128","synonymous_variant","synonymous_variant","871/9538","333/5583","111/1860","R","cgG/cgA"]
["UGCG",7357,"WUGSC","GRCh38","chr9",111929647,111929647,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.706G>C","ENST00000374279",42895,102,101,"C","ENSG00000148154","ENST00000374279","missense_variant","missense_variant","1156/4007","706/1185","236/394","D/H","Gat/Cat"]
["SGMS1-AS1",104355295,"WUGSC","GRCh38","chr10",50631064,50631064,"+","RNA","SNP","G","G","A","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","n.2013G>A","ENST00000443374",42829,65,91,"A","ENSG00000226200","ENST00000443374","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","2013/12400"]
["AS3MT",57412,"WUGSC","GRCh38","chr10",102877008,102877008,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.583G>T","ENST00000369880",42927,110,184,"T","ENSG00000214435","ENST00000369880","stop_gained","stop_gained","660/2404","583/1128","195/375","E/*","Gaa/Taa"]
["OR6A2",8590,"WUGSC","GRCh38","chr11",6795265,6795265,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.444G>C","ENST00000332601",42736,97,60,"G","ENSG00000184933","ENST00000332601","missense_variant","missense_variant","519/1157","444/984","148/327","Q/H","caG/caC"]
["WDR74",54663,"WUGSC","GRCh38","chr11",62834482,62834482,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.664G>C","ENST00000278856",42927,32,24,"G","ENSG00000133316","ENST00000278856","missense_variant","missense_variant","755/1289","664/1158","222/385","E/Q","Gag/Cag"]
["MEN1",4221,"WUGSC","GRCh38","chr11",64809786,64809786,"+","Silent","SNP","T","T","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.324A>T","ENST00000337652",42776,95,46,"A","ENSG00000133895","ENST00000337652","synonymous_variant","synonymous_variant","828/3162","324/1848","108/615","R","cgA/cgT"]
["SCNN1A",6337,"WUGSC","GRCh38","chr12",6348798,6348798,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1558G>A","ENST00000228916",43082,47,61,"T","ENSG00000111319","ENST00000228916","missense_variant","missense_variant","1657/3135","1558/2010","520/669","G/R","Gga/Aga"]
["KANSL2",54934,"WUGSC","GRCh38","chr12",48679809,48679809,"+","Silent","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.276C>T","ENST00000420613",42804,91,71,"A","ENSG00000139620","ENST00000420613","synonymous_variant","synonymous_variant","324/2155","276/1479","92/492","V","gtC/gtT"]
["USP15",9958,"WUGSC","GRCh38","chr12",62401213,62401213,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.2701G>A","ENST00000280377","21/22",90,70,"A","ENSG00000135655","ENST00000280377","missense_variant","missense_variant","2759/4748","2701/2946","901/981","D/N","Gat/Aat"]
["VEZT",55591,"WUGSC","GRCh38","chr12",95300243,95300243,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1910G>T","ENST00000436874",43081,46,60,"T","ENSG00000028203","ENST00000436874","missense_variant","missense_variant","2015/4562","1910/2340","637/779","G/V","gGa/gTa"]
["VPS33A",65082,"WUGSC","GRCh38","chr12",122263617,122263617,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.251G>A","ENST00000267199",42807,166,115,"T","ENSG00000139719","ENST00000267199","missense_variant","missense_variant","364/4586","251/1791","84/596","R/K","aGa/aAa"]
["FANCM",57697,"WUGSC","GRCh38","chr14",45196471,45196471,"+","Silent","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.5640C>T","ENST00000267430","21/23",54,66,"T","ENSG00000187790","ENST00000267430","synonymous_variant","synonymous_variant","5725/7111","5640/6147","1880/2048","F","ttC/ttT"]
["DIO2",1734,"WUGSC","GRCh38","chr14",80211371,80211371,"+","Silent","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.102C>T","ENST00000438257",42737,33,39,"A","ENSG00000211448","ENST00000438257","synonymous_variant","synonymous_variant","257/6136","102/822","34/273","L","ctC/ctT"]
["LTK",4058,"WUGSC","GRCh38","chr15",41504113,41504113,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.2478G>C","ENST00000263800","20/20",54,34,"G","ENSG00000062524","ENST00000263800","missense_variant","missense_variant","2575/3046","2478/2595","826/864","E/D","gaG/gaC"]
["UNC13C",440279,"WUGSC","GRCh38","chr15",54013095,54013095,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.192G>C","ENST00000260323",11689,98,94,"C","ENSG00000137766","ENST00000260323","missense_variant","missense_variant","192/12946","192/6645","64/2214","K/N","aaG/aaC"]
["TELO2",9894,"WUGSC","GRCh38","chr16",1497068,1497068,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.646C>T","ENST00000262319",42846,128,70,"T","ENSG00000100726","ENST00000262319","stop_gained","stop_gained","925/3314","646/2514","216/837","Q/*","Cag/Tag"]
["STX1B",112755,"WUGSC","GRCh38","chr16",30992849,30992849,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.839C>T","ENST00000215095",43018,27,32,"A","ENSG00000099365","ENST00000215095","missense_variant","missense_variant","1071/4664","839/867","280/288","S/L","tCa/tTa"]
["IL34",146433,"WUGSC","GRCh38","chr16",70660101,70660101,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.643C>T","ENST00000288098",42892,43,18,"T","ENSG00000157368","ENST00000288098","missense_variant","missense_variant","1026/1607","643/729","215/242","P/S","Ccg/Tcg"]
["TSR1",55720,"WUGSC","GRCh38","chr17",2333014,2333014,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1252G>C","ENST00000301364",42931,145,145,"G","ENSG00000167721","ENST00000301364","missense_variant","missense_variant","2332/5188","1252/2415","418/804","E/Q","Gaa/Caa"]
["RASD1",51655,"WUGSC","GRCh38","chr17",17495496,17495496,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.475G>A","ENST00000225688",42768,34,15,"T","ENSG00000108551","ENST00000225688","missense_variant","missense_variant","687/1746","475/846","159/281","E/K","Gag/Aag"]
["COX11",1353,"WUGSC","GRCh38","chr17",54963262,54963262,"+","Intron","SNP","C","C","G","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.648+44G>C","ENST00000299335",null,115,56,"G","ENSG00000166260","ENST00000299335","intron_variant","intron_variant","-/2497","-/831","-/276"]
["ICAM2",3384,"WUGSC","GRCh38","chr17",64005052,64005052,"+","Intron","SNP","G","G","C","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.328+55C>G","ENST00000412356",null,51,14,"C","ENSG00000108622","ENST00000412356","intron_variant","intron_variant","-/1334","-/828","-/275"]
["MIB1",57534,"WUGSC","GRCh38","chr18",21844161,21844161,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.2119C>G","ENST00000261537","15/21",93,99,"G","ENSG00000101752","ENST00000261537","missense_variant","missense_variant","2383/9576","2119/3021","707/1006","L/V","Cta/Gta"]
["PIK3C3",5289,"WUGSC","GRCh38","chr18",41987889,41987889,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.609G>T","ENST00000262039",42880,52,94,"T","ENSG00000078142","ENST00000262039","missense_variant","missense_variant","695/9443","609/2664","203/887","M/I","atG/atT"]
["TMEM161A",54929,"WUGSC","GRCh38","chr19",19120058,19120058,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1312C>G","ENST00000162044",43081,18,16,"C","ENSG00000064545","ENST00000162044","missense_variant","missense_variant","1377/1820","1312/1440","438/479","L/V","Ctg/Gtg"]
["ZNF570",148268,"WUGSC","GRCh38","chr19",37484303,37484303,"+","Silent","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.681C>T","ENST00000330173",42860,23,58,"T","ENSG00000171827","ENST00000330173","synonymous_variant","synonymous_variant","1210/5559","681/1611","227/536","F","ttC/ttT"]
["ZNF701",55762,"WUGSC","GRCh38","chr19",52575892,52575892,"+","Splice_Region","SNP","C","C","T","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.214-3C>T","ENST00000301093",null,143,144,"T","ENSG00000167562","ENST00000301093","splice_region_variant","splice_region_variant;intron_variant","-/2610","-/1596","-/531"]
["TNNT1",7138,"WUGSC","GRCh38","chr19",55133925,55133925,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.753C>G","ENST00000588981","13/14",67,58,"C","ENSG00000105048","ENST00000588981","missense_variant","missense_variant;splice_region_variant","958/1163","753/837","251/278","I/M","atC/atG"]
["TGM2",7052,"WUGSC","GRCh38","chr20",38142138,38142138,"+","Silent","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.921G>A","ENST00000361475",42929,251,160,"T","ENSG00000198959","ENST00000361475","synonymous_variant","synonymous_variant","1095/5070","921/2064","307/687","Q","caG/caA"]
["GNAS",2778,"WUGSC","GRCh38","chr20",58855113,58855113,"+","Silent","SNP","C","C","T","novel",null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.1848C>T","ENST00000371100",42748,56,33,"T","ENSG00000087460","ENST00000371100","synonymous_variant","synonymous_variant","2400/4029","1848/3114","616/1037","F","ttC/ttT"]
["GNB1L",54584,"WUGSC","GRCh38","chr22",19806707,19806707,"+","Silent","SNP","C","C","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.468G>T","ENST00000329517",42894,61,33,"A","ENSG00000185838","ENST00000329517","synonymous_variant","synonymous_variant","705/6706","468/984","156/327","P","ccG/ccT"]
["PICK1",9463,"WUGSC","GRCh38","chr22",38065053,38065053,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.205G>A","ENST00000356976",42838,162,83,"A","ENSG00000100151","ENST00000356976","missense_variant","missense_variant","443/2055","205/1248","69/415","E/K","Gag/Aag"]
["BMX",660,"WUGSC","GRCh38","chrX",15526067,15526067,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.856G>T","ENST00000342014",42997,169,177,"T","ENSG00000102010","ENST00000342014","stop_gained","stop_gained","957/2499","856/2028","286/675","E/*","Gaa/Taa"]
["ZC3H12B",340554,"WUGSC","GRCh38","chrX",65488928,65488928,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.127G>C","ENST00000338957",42740,63,50,"C","ENSG00000102053","ENST00000338957","missense_variant","missense_variant","194/7256","127/2511","43/836","E/Q","Gag/Cag"]
["MTCP1",4515,"WUGSC","GRCh38","chrX",155065959,155065959,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AC-A23H-01A-11D-A159-09","TCGA-AC-A23H-11A-12D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","cee435b5-c424-4f9d-a834-ec90c1807913","15408151-7d19-4d24-a9a1-bc9f913d5e36","c.52G>A","ENST00000362018",42771,40,33,"T","ENSG00000214827","ENST00000362018","missense_variant","missense_variant","215/570","52/324","18/107","E/K","Gag/Aag"]
["THRB",7068,"WUGSC","GRCh38","chr3",24127544,24127544,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A06X-01A-21W-A019-09","TCGA-A8-A06X-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","dc306402-3a55-4996-b786-f3f738f13dd3","09c30f57-516c-4a4f-bf63-943f09904d21","c.1099G>A","ENST00000356447",42988,212,90,"T","ENSG00000151090","ENST00000356447","missense_variant","missense_variant","1384/6345","1099/1386","367/461","D/N","Gac/Aac"]
["CFAP58",159686,"WUGSC","GRCh38","chr10",104454487,104454487,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A8-A06X-01A-21W-A019-09","TCGA-A8-A06X-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","dc306402-3a55-4996-b786-f3f738f13dd3","09c30f57-516c-4a4f-bf63-943f09904d21","c.2576C>G","ENST00000369704","18/18",281,175,"G","ENSG00000120051","ENST00000369704","missense_variant","missense_variant","2710/3313","2576/2619","859/872","T/S","aCt/aGt"]
["GUCY1A3",2982,"WUGSC","GRCh38","chr4",155708251,155708251,"+","Silent","SNP","A","A","G",null,null,"TCGA-GM-A2DN-01A-11D-A17W-09","TCGA-GM-A2DN-10C-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","e6101e95-5296-4040-af52-0159a21e63b5","70bb3d92-770c-426e-98c5-35362229d54a","c.333A>G","ENST00000296518",42865,34,39,"G","ENSG00000164116","ENST00000296518","synonymous_variant","synonymous_variant","542/4400","333/2073","111/690","R","agA/agG"]
["LRRD1",401387,"WUGSC","GRCh38","chr7",92164660,92164660,"+","Silent","SNP","C","C","A","novel",null,"TCGA-S3-AA17-01A-11D-A41F-09","TCGA-S3-AA17-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","15f0aaf4-2a28-44ed-a2d5-2224eaf8d3e4","111aeeed-3c67-4325-8e1b-29070534fc99","c.543G>T","ENST00000430130",42740,72,93,"A","ENSG00000240720","ENST00000430130","synonymous_variant","synonymous_variant","617/2661","543/2583","181/860","G","ggG/ggT"]
["MFHAS1",9258,"WUGSC","GRCh38","chr8",8786011,8786011,"+","3'UTR","SNP","A","A","C","novel",null,"TCGA-B6-A0WY-01A-11D-A10G-09","TCGA-B6-A0WY-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","c973a902-abdf-41a3-8250-57011dfef1f4","d6007264-3412-46b3-8775-f2c42146de20","c.*11T>G","ENST00000276282",42797,172,94,"C","ENSG00000147324","ENST00000276282","3_prime_UTR_variant","3_prime_UTR_variant","3757/6414","-/3159","-/1052"]
["NOTCH4",4855,"WUGSC","GRCh38","chr6",32215372,32215372,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A5FL-01A-11D-A27P-09","TCGA-E9-A5FL-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","20b0e3b8-7fc9-414a-848a-602614fa2727","8a6dbb92-338b-4fa8-bb83-803f333ea743","c.1875G>C","ENST00000375023",43099,89,112,"G","ENSG00000204301","ENST00000375023","missense_variant","missense_variant","2014/6745","1875/6012","625/2003","E/D","gaG/gaC"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179234297,179234297,"+","Missense_Mutation","SNP","A","A","G","rs121913279","byCluster;byFrequency","TCGA-A7-A6VX-01A-12D-A33E-09","TCGA-A7-A6VX-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","ae3350b5-794c-4f87-b79a-6a43bf20dca8","9fd4a260-7077-471f-a505-9185d9a50fe2","c.3140A>G","ENST00000263967","21/21",23,36,"G","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","3297/9093","3140/3207","1047/1068","H/R","cAt/cGt"]
["BCL11B",64919,"WUGSC","GRCh38","chr14",99171369,99171369,"+","3'UTR","SNP","T","T","A","novel",null,"TCGA-A7-A6VX-01A-12D-A33E-09","TCGA-A7-A6VX-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","ae3350b5-794c-4f87-b79a-6a43bf20dca8","9fd4a260-7077-471f-a505-9185d9a50fe2","c.*2782A>T","ENST00000357195",42829,129,96,"A","ENSG00000127152","ENST00000357195","3_prime_UTR_variant","3_prime_UTR_variant","5477/7559","-/2685","-/894"]
["FHL2",2274,"WUGSC","GRCh38","chr2",105363389,105363389,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-D8-A1JP-01A-11D-A13L-09","TCGA-D8-A1JP-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","1e21a355-0cb6-4a43-b134-50ff88dacf92","6eeba22a-d922-4fc8-abc1-ae8bc9eee928","c.584T>A","ENST00000322142",42893,25,43,"T","ENSG00000115641","ENST00000322142","missense_variant","missense_variant","751/1462","584/840","195/279","L/Q","cTg/cAg"]
["CHRNB2",1141,"WUGSC","GRCh38","chr1",154571343,154571343,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A2-A0T2-01A-11W-A097-09","TCGA-A2-A0T2-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","c7918143-dbce-45b3-8d24-2993a9e2b7f4","5b5581e0-8d87-47db-a789-bc943c4cd6e9","c.520C>T","ENST00000368476",42861,96,56,"T","ENSG00000160716","ENST00000368476","missense_variant","missense_variant","784/5867","520/1509","174/502","R/C","Cgt/Tgt"]
["LCT",3938,"WUGSC","GRCh38","chr2",135822022,135822022,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-D8-A1X9-01A-12D-A159-09","TCGA-D8-A1X9-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","b5f65c3a-b922-4a81-863d-59b72b08d1bf","451900d1-a2da-4536-8db3-b56433500ab8","c.984A>T","ENST00000264162",42872,61,83,"A","ENSG00000115850","ENST00000264162","missense_variant","missense_variant;splice_region_variant","995/6279","984/5784","328/1927","K/N","aaA/aaT"]
["GJB5",2709,"WUGSC","GRCh38","chr1",34758049,34758049,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-E2-A1IH-01A-11D-A188-09","TCGA-E2-A1IH-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","cd886e35-4201-4732-90c6-142d8fe309b1","cb1773b7-2caf-4e7f-8dd8-ef6b62fbca62","c.719A>C","ENST00000338513",42768,107,98,"C","ENSG00000189280","ENST00000338513","missense_variant","missense_variant","892/1355","719/822","240/273","Q/P","cAa/cCa"]
["PLXNA1",5361,"WUGSC","GRCh38","chr3",127017661,127017661,"+","Silent","SNP","C","C","T",null,null,"TCGA-E9-A1R5-01A-11D-A14K-09","TCGA-E9-A1R5-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","a04ba6e9-2bc4-4cab-96d8-0820e0390d84","bda47415-2577-4d09-874a-2a85e999c9cd","c.3513C>T","ENST00000393409","17/31",37,87,"T","ENSG00000114554","ENST00000393409","synonymous_variant","synonymous_variant","3513/9066","3513/5691","1171/1896","L","ctC/ctT"]
["ZNF35",7584,"WUGSC","GRCh38","chr3",44659305,44659305,"+","Silent","SNP","C","C","T","novel",null,"TCGA-C8-A12M-01A-11D-A135-09","TCGA-C8-A12M-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","9a0a7b93-da6e-45b7-9a6f-190d79552b49","5f9aae0c-1d2f-4bb2-b801-32478f7058a2","c.942C>T","ENST00000396056",42829,76,68,"T","ENSG00000169981","ENST00000396056","synonymous_variant","synonymous_variant","1177/2661","942/1584","314/527","A","gcC/gcT"]
["GULP1",51454,"WUGSC","GRCh38","chr2",188587934,188587934,"+","Silent","SNP","A","A","G",null,null,"TCGA-EW-A1PD-01A-11D-A142-09","TCGA-EW-A1PD-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","5a288561-bf14-4cb9-b2f5-9ece0e038319","8e2913c9-4903-4d07-a706-a42e19b2ed7a","c.828A>G","ENST00000359135",43051,53,68,"G","ENSG00000144366","ENST00000359135","synonymous_variant","synonymous_variant","1340/3347","828/915","276/304","K","aaA/aaG"]
["CDS1",1040,"WUGSC","GRCh38","chr4",84609445,84609445,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-BH-A1ES-01A-11D-A135-09","TCGA-BH-A1ES-11A-33D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","7ecda44b-e942-4077-9d18-2a844ec53c9d","b281f983-29fc-4389-bea2-cabf4c90b3df","c.262A>G","ENST00000295887",42807,602,635,"G","ENSG00000163624","ENST00000295887","missense_variant","missense_variant","685/4461","262/1386","88/461","I/V","Ata/Gta"]
["POMGNT1",55624,"WUGSC","GRCh38","chr1",46192408,46192408,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.1313C>T","ENST00000371984","16/22",34,24,"A","ENSG00000085998","ENST00000371984","missense_variant","missense_variant","1471/2728","1313/1983","438/660","A/V","gCa/gTa"]
["ARHGAP31",57514,"WUGSC","GRCh38","chr3",119402378,119402378,"+","Silent","SNP","G","G","A","novel",null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.1626G>A","ENST00000264245",43020,95,51,"A","ENSG00000031081","ENST00000264245","synonymous_variant","synonymous_variant","2158/9317","1626/4335","542/1444","L","ctG/ctA"]
["PCDHB1",29930,"WUGSC","GRCh38","chr5",141051657,141051657,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.187G>C","ENST00000306549",42736,51,34,"C","ENSG00000171815","ENST00000306549","missense_variant","missense_variant","523/8210","187/2457","63/818","G/R","Ggg/Cgg"]
["SPDYE5",442590,"WUGSC","GRCh38","chr7",75501384,75501384,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.778G>A","ENST00000625065",42894,273,136,"A","ENSG00000170092","ENST00000625065","missense_variant","missense_variant","1201/1700","778/1209","260/402","E/K","Gag/Aag"]
["P2RX3",5024,"WUGSC","GRCh38","chr11",57348702,57348702,"+","Splice_Region","SNP","G","G","A",null,null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.561G>A","ENST00000263314",42898,53,34,"A","ENSG00000109991","ENST00000263314","splice_region_variant","splice_region_variant;synonymous_variant","595/1831","561/1194","187/397","E","gaG/gaA"]
["PRTG",283659,"WUGSC","GRCh38","chr15",55672630,55672630,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.1856C>G","ENST00000389286",43059,124,49,"C","ENSG00000166450","ENST00000389286","missense_variant","missense_variant","1904/11967","1856/3453","619/1150","P/R","cCt/cGt"]
["TBC1D3B",414059,"WUGSC","GRCh38","chr17",36165757,36165757,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.*238G>C","ENST00000611257","14/14",259,56,"G","ENSG00000274808","ENST00000611257","3_prime_UTR_variant","3_prime_UTR_variant","2005/2081","-/1650","-/549"]
["ZNF568",374900,"WUGSC","GRCh38","chr19",36936815,36936815,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-3C-AALI-01A-11D-A41F-09","TCGA-3C-AALI-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d5c2f3c-7ddc-48d6-96b4-06d60cf964e8","4cc302f2-78dc-4f9c-b7ad-f78635184899","c.205C>G","ENST00000333987",42862,89,91,"G","ENSG00000198453","ENST00000333987","missense_variant","missense_variant","711/2441","205/1935","69/644","Q/E","Caa/Gaa"]
["DGKQ",1609,"WUGSC","GRCh38","chr4",962035,962035,"+","Silent","SNP","C","C","G",null,null,"TCGA-E2-A14V-01A-11D-A12B-09","TCGA-E2-A14V-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","703314fe-bfd5-45d5-9ed5-fcdce8a19fd6","e49f6bc1-0933-4500-9068-aa7d8c276b22","c.2262G>C","ENST00000273814","19/23",105,97,"G","ENSG00000145214","ENST00000273814","synonymous_variant","synonymous_variant","2336/4636","2262/2829","754/942","L","ctG/ctC"]
["TXLNA",200081,"WUGSC","GRCh38","chr1",32188007,32188007,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-BH-A2L8-01A-11D-A18P-09","TCGA-BH-A2L8-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","ce4179d3-b31d-4242-8ec1-f6785f9af2e1","b0e8676c-6f2d-4691-96c5-b323dded9687","c.651G>C","ENST00000373609",42835,25,32,"C","ENSG00000084652","ENST00000373609","missense_variant","missense_variant","932/5012","651/1641","217/546","Q/H","caG/caC"]
["ANKAR",150709,"WUGSC","GRCh38","chr2",189741382,189741382,"+","Silent","SNP","C","C","T",null,null,"TCGA-BH-A2L8-01A-11D-A18P-09","TCGA-BH-A2L8-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","ce4179d3-b31d-4242-8ec1-f6785f9af2e1","b0e8676c-6f2d-4691-96c5-b323dded9687","c.3741C>T","ENST00000313581","19/22",48,32,"T","ENSG00000151687","ENST00000313581","synonymous_variant","synonymous_variant","3805/4391","3741/4305","1247/1434","I","atC/atT"]
["COL12A1",1303,"WUGSC","GRCh38","chr6",75142145,75142145,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A2L8-01A-11D-A18P-09","TCGA-BH-A2L8-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","ce4179d3-b31d-4242-8ec1-f6785f9af2e1","b0e8676c-6f2d-4691-96c5-b323dded9687","c.4844C>T","ENST00000322507","27/66",79,92,"A","ENSG00000111799","ENST00000322507","missense_variant","missense_variant","5154/11723","4844/9192","1615/3063","S/L","tCa/tTa"]
["CDH17",1015,"WUGSC","GRCh38","chr8",94177603,94177603,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-BH-A2L8-01A-11D-A18P-09","TCGA-BH-A2L8-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","ce4179d3-b31d-4242-8ec1-f6785f9af2e1","b0e8676c-6f2d-4691-96c5-b323dded9687","c.269C>G","ENST00000027335",42843,87,106,"C","ENSG00000079112","ENST00000027335","missense_variant","missense_variant","394/3693","269/2499","90/832","S/C","tCt/tGt"]
["GPATCH8",23131,"WUGSC","GRCh38","chr17",44399831,44399831,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-BH-A2L8-01A-11D-A18P-09","TCGA-BH-A2L8-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","ce4179d3-b31d-4242-8ec1-f6785f9af2e1","b0e8676c-6f2d-4691-96c5-b323dded9687","c.2246G>A","ENST00000591680",42955,97,66,"T","ENSG00000186566","ENST00000591680","missense_variant","missense_variant","2277/4692","2246/4509","749/1502","R/K","aGa/aAa"]
["GBP1",2633,"WUGSC","GRCh38","chr1",89060305,89060305,"+","Silent","SNP","C","C","T","rs149168400","by1000G;byCluster","TCGA-A2-A1G4-01A-11D-A13L-09","TCGA-A2-A1G4-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","420a4771-6376-4b52-a2e3-e62aaf4d4ed6","e8a9a187-4df7-41af-b0aa-389e4319b9ab","c.210G>A","ENST00000370473",42805,114,75,"T","ENSG00000117228","ENST00000370473","synonymous_variant","synonymous_variant","430/3035","210/1779","70/592","T","acG/acA"]
["SSR3",6747,"WUGSC","GRCh38","chr3",156543206,156543206,"+","Silent","SNP","T","T","C","rs773174876",null,"TCGA-A8-A08L-01A-11W-A019-09","TCGA-A8-A08L-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8b819a59-f0c1-456a-9e81-64b5bed025c1","3f7a64f1-bed9-4e3f-9109-09c320e2fc96","c.555A>G","ENST00000265044",42860,101,118,"C","ENSG00000114850","ENST00000265044","synonymous_variant","synonymous_variant","650/3716","555/558","185/185","K","aaA/aaG"]
["FAM184A",79632,"WUGSC","GRCh38","chr6",118975991,118975991,"+","Silent","SNP","G","G","T","rs772310108","byFrequency","TCGA-A8-A08L-01A-11W-A019-09","TCGA-A8-A08L-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8b819a59-f0c1-456a-9e81-64b5bed025c1","3f7a64f1-bed9-4e3f-9109-09c320e2fc96","c.2509C>A","ENST00000338891",43087,128,53,"T","ENSG00000111879","ENST00000338891","synonymous_variant","synonymous_variant","2953/4141","2509/3423","837/1140","R","Cgg/Agg"]
["ASAP3",55616,"WUGSC","GRCh38","chr1",23442263,23442263,"+","Silent","SNP","G","G","C",null,null,"TCGA-A2-A0YK-01A-22D-A117-09","TCGA-A2-A0YK-10A-01D-A117-09",null,null,"Somatic","Illumina Genome Analyzer II","7c27f81e-62fb-478c-9cee-8e20db9300f2","134d71cc-c1c7-40b7-9cc1-927b8f6f393d","c.594C>G","ENST00000336689",42941,185,230,"C","ENSG00000088280","ENST00000336689","synonymous_variant","synonymous_variant","639/4050","594/2712","198/903","L","ctC/ctG"]
["KIAA1143",57456,"WUGSC","GRCh38","chr3",44754356,44754356,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A0YK-01A-22D-A117-09","TCGA-A2-A0YK-10A-01D-A117-09",null,null,"Somatic","Illumina Genome Analyzer II","7c27f81e-62fb-478c-9cee-8e20db9300f2","134d71cc-c1c7-40b7-9cc1-927b8f6f393d","c.121C>A","ENST00000296121",42769,228,232,"T","ENSG00000163807","ENST00000296121","missense_variant","missense_variant","181/5122","121/465","41/154","Q/K","Cag/Aag"]
["ASH2L",9070,"WUGSC","GRCh38","chr8",38110801,38110801,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A2-A0YK-01A-22D-A117-09","TCGA-A2-A0YK-10A-01D-A117-09",null,null,"Somatic","Illumina Genome Analyzer II","7c27f81e-62fb-478c-9cee-8e20db9300f2","134d71cc-c1c7-40b7-9cc1-927b8f6f393d","c.553G>A","ENST00000343823",42871,278,180,"A","ENSG00000129691","ENST00000343823","missense_variant","missense_variant","862/3090","553/1887","185/628","E/K","Gaa/Aaa"]
["HNRNPA1L2",144983,"WUGSC","GRCh38","chr13",52642421,52642421,"+","5'UTR","SNP","C","C","T","novel",null,"TCGA-A2-A0YK-01A-22D-A117-09","TCGA-A2-A0YK-10A-01D-A117-09",null,null,"Somatic","Illumina Genome Analyzer II","7c27f81e-62fb-478c-9cee-8e20db9300f2","134d71cc-c1c7-40b7-9cc1-927b8f6f393d","c.-72C>T","ENST00000357495",42736,51,49,"T","ENSG00000139675","ENST00000357495","5_prime_UTR_variant","5_prime_UTR_variant","1636/3011","-/963","-/320"]
["GIN1",54826,"WUGSC","GRCh38","chr5",103097370,103097370,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-E2-A1LG-01A-21D-A14K-09","TCGA-E2-A1LG-11A-42D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","7cdbe0e8-f614-4f54-b864-fd6b39e8ef1c","583d989c-fa07-46f5-b463-6ce5a2744927","c.952G>C","ENST00000399004",42894,184,92,"G","ENSG00000145723","ENST00000399004","missense_variant","missense_variant","1047/3229","952/1569","318/522","D/H","Gat/Cat"]
["THEMIS",387357,"WUGSC","GRCh38","chr6",127900852,127900852,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E2-A1LG-01A-21D-A14K-09","TCGA-E2-A1LG-11A-42D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","7cdbe0e8-f614-4f54-b864-fd6b39e8ef1c","583d989c-fa07-46f5-b463-6ce5a2744927","c.81C>G","ENST00000368248",42741,158,164,"C","ENSG00000172673","ENST00000368248","missense_variant","missense_variant","230/3866","81/1926","27/641","I/M","atC/atG"]
["C1orf112",55732,"WUGSC","GRCh38","chr1",169829444,169829444,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A24Q-01A-12D-A167-09","TCGA-AR-A24Q-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","a9d691f2-ad2a-4a3b-ae30-ed4af96d75f2","cc88b2b8-d0af-45be-9b32-7849fa97deae","c.1309G>A","ENST00000286031","13/24",119,136,"A","ENSG00000000460","ENST00000286031","missense_variant","missense_variant","2009/4355","1309/2562","437/853","E/K","Gaa/Aaa"]
["NOL6",65083,"WUGSC","GRCh38","chr9",33466364,33466364,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A24Q-01A-12D-A167-09","TCGA-AR-A24Q-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","a9d691f2-ad2a-4a3b-ae30-ed4af96d75f2","cc88b2b8-d0af-45be-9b32-7849fa97deae","c.2153C>T","ENST00000297990","17/26",44,50,"A","ENSG00000165271","ENST00000297990","missense_variant","missense_variant","2241/4741","2153/3441","718/1146","S/F","tCc/tTc"]
["NUCB1",4924,"WUGSC","GRCh38","chr19",48919007,48919007,"+","Intron","SNP","C","C","A","novel",null,"TCGA-AR-A24Q-01A-12D-A167-09","TCGA-AR-A24Q-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","a9d691f2-ad2a-4a3b-ae30-ed4af96d75f2","cc88b2b8-d0af-45be-9b32-7849fa97deae","c.817-23C>A","ENST00000405315",null,35,26,"A","ENSG00000104805","ENST00000405315","intron_variant","intron_variant","-/2668","-/1386","-/461"]
["PGPEP1",54858,"WUGSC","GRCh38","chr19",18363448,18363448,"+","Silent","SNP","C","C","T",null,null,"TCGA-E2-A1IL-01A-11D-A14G-09","TCGA-E2-A1IL-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","1540ae03-7bb4-418b-afbc-44bf3ad60a31","6a5f0824-3724-42a3-af37-ca7215491e63","c.495C>T","ENST00000269919",42860,57,61,"T","ENSG00000130517","ENST00000269919","synonymous_variant","synonymous_variant","590/7092","495/630","165/209","A","gcC/gcT"]
["ESRP1",54845,"WUGSC","GRCh38","chr8",94674351,94674351,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-E2-A1LH-01A-11D-A14G-09","TCGA-E2-A1LH-11A-22D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","605f1d27-db45-449a-a68f-4888b8c786a1","4feb8572-68f1-403c-8d3c-198fbe6e9fa4","c.1496A>G","ENST00000433389",43085,105,56,"G","ENSG00000104413","ENST00000433389","missense_variant","missense_variant","1686/3770","1496/2046","499/681","D/G","gAc/gGc"]
["LTN1",26046,"WUGSC","GRCh38","chr21",28984892,28984892,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-E2-A1LH-01A-11D-A14G-09","TCGA-E2-A1LH-11A-22D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","605f1d27-db45-449a-a68f-4888b8c786a1","4feb8572-68f1-403c-8d3c-198fbe6e9fa4","c.376C>G","ENST00000361371",42855,128,77,"C","ENSG00000198862","ENST00000361371","missense_variant","missense_variant","456/7685","376/5301","126/1766","Q/E","Caa/Gaa"]
["OR8B2",26595,"WUGSC","GRCh38","chr11",124382850,124382850,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-B6-A0X1-01A-11D-A10G-09","TCGA-B6-A0X1-10A-01D-A117-09",null,null,"Somatic","Illumina Genome Analyzer II","a492abf9-0cd3-402c-89e2-c49d650ef540","8c39f4bf-c997-41a9-8b36-37e9e9e6124b","c.494G>C","ENST00000375013",42736,74,76,"G","ENSG00000204293","ENST00000375013","missense_variant","missense_variant","513/968","494/942","165/313","R/T","aGa/aCa"]
["YEATS2",55689,"WUGSC","GRCh38","chr3",183790905,183790905,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-GM-A2D9-01A-11D-A18P-09","TCGA-GM-A2D9-11A-42D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","1e314f3c-88c6-4453-96a7-5d616f1c4e9b","1d25f976-3635-49f6-8d0b-f1501be6b0f4","c.3022G>A","ENST00000305135","21/31",56,58,"A","ENSG00000163872","ENST00000305135","missense_variant","missense_variant","3217/6506","3022/4269","1008/1422","A/T","Gcc/Acc"]
["TPD52L3",89882,"WUGSC","GRCh38","chr9",6330015,6330015,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-GM-A2D9-01A-11D-A18P-09","TCGA-GM-A2D9-11A-42D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","1e314f3c-88c6-4453-96a7-5d616f1c4e9b","1d25f976-3635-49f6-8d0b-f1501be6b0f4","c.*997G>A","ENST00000344545",42736,17,16,"A","ENSG00000170777","ENST00000344545","3_prime_UTR_variant","3_prime_UTR_variant","1641/2296","-/423","-/140"]
["TEAD4",7004,"WUGSC","GRCh38","chr12",3038048,3038048,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-GM-A2D9-01A-11D-A18P-09","TCGA-GM-A2D9-11A-42D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","1e314f3c-88c6-4453-96a7-5d616f1c4e9b","1d25f976-3635-49f6-8d0b-f1501be6b0f4","c.978G>C","ENST00000359864",43052,34,32,"C","ENSG00000197905","ENST00000359864","missense_variant","missense_variant","1168/1690","978/1305","326/434","M/I","atG/atC"]
["IGHV3OR16-9",28307,"WUGSC","GRCh38","chr16",32066252,32066252,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-GM-A2D9-01A-11D-A18P-09","TCGA-GM-A2D9-11A-42D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","1e314f3c-88c6-4453-96a7-5d616f1c4e9b","1d25f976-3635-49f6-8d0b-f1501be6b0f4","c.188C>G","ENST00000354689",42736,63,77,"G","ENSG00000270472","ENST00000354689","missense_variant","missense_variant","188/294","188/294","63/98","S/C","tCt/tGt"]
["SBNO2",22904,"WUGSC","GRCh38","chr19",1119544,1119544,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-GM-A2D9-01A-11D-A18P-09","TCGA-GM-A2D9-11A-42D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","1e314f3c-88c6-4453-96a7-5d616f1c4e9b","1d25f976-3635-49f6-8d0b-f1501be6b0f4","c.1345G>C","ENST00000361757","13/32",19,27,"G","ENSG00000064932","ENST00000361757","missense_variant","missense_variant","1583/4923","1345/4101","449/1366","E/Q","Gag/Cag"]
["AASDH",132949,"WUGSC","GRCh38","chr4",56384226,56384226,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-AC-A5XU-01A-11D-A28B-09","TCGA-AC-A5XU-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","9bb1dbae-1f3c-4986-8493-e49981155689","f3058a74-3da8-4367-b662-dc1cf4e4392b","c.74G>C","ENST00000205214",42781,47,62,"G","ENSG00000157426","ENST00000205214","missense_variant","missense_variant","255/3590","74/3297","25/1098","C/S","tGc/tCc"]
["NOL6",65083,"WUGSC","GRCh38","chr9",33467830,33467830,"+","Missense_Mutation","SNP","C","C","T","rs771212659","byFrequency","TCGA-A8-A0A1-01A-11W-A019-09","TCGA-A8-A0A1-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","73aa20fe-b74b-41ae-88d3-2d5a66908c25","c356aae0-c3f1-4c70-962d-e0d592174bbc","c.1463G>A","ENST00000297990",43095,39,70,"T","ENSG00000165271","ENST00000297990","missense_variant","missense_variant","1551/4741","1463/3441","488/1146","R/Q","cGg/cAg"]
["SH3D19",152503,"WUGSC","GRCh38","chr4",151122171,151122171,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-E9-A1NA-01A-11D-A142-09","TCGA-E9-A1NA-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","a3d223eb-20e6-40b9-9f07-e5f865bd2439","6c9a17cd-a638-47f4-ba5d-3ec57d96b56e","c.2293G>T","ENST00000304527","21/21",59,65,"A","ENSG00000109686","ENST00000304527","missense_variant","missense_variant","3383/5273","2293/2373","765/790","D/Y","Gat/Tat"]
["TNRC6B",23112,"WUGSC","GRCh38","chr22",40265711,40265711,"+","Missense_Mutation","SNP","A","A","G","rs751692063",null,"TCGA-EW-A1PE-01A-11D-A142-09","TCGA-EW-A1PE-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","54377bac-8f52-4116-b7e5-b71a8a721ac4","e18ccc97-6ed5-48fb-85ce-6a9484ce18bd","c.1481A>G","ENST00000454349",42878,23,32,"G","ENSG00000100354","ENST00000454349","missense_variant","missense_variant","1692/18279","1481/5502","494/1833","N/S","aAc/aGc"]
["MYH11",4629,"WUGSC","GRCh38","chr16",15756459,15756459,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A0T0-01A-22D-A099-09","TCGA-A2-A0T0-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","3c107ce4-a6ac-469b-b1c0-cd86674b5766","94629e5b-195d-495b-bfa5-e10c46930a47","c.1631C>A","ENST00000300036","14/41",137,40,"T","ENSG00000133392","ENST00000300036","missense_variant","missense_variant","1741/6029","1631/5919","544/1972","A/D","gCc/gAc"]
["ERF",2077,"WUGSC","GRCh38","chr19",42249996,42249996,"+","Intron","SNP","G","G","T","novel",null,"TCGA-AN-A03X-01A-21W-A019-09","TCGA-AN-A03X-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","f177234e-e0a7-4f85-b73d-48e0080c805d","222e0fba-5b47-4ee3-b4ff-81e1a15372c1","c.258-54C>A","ENST00000222329",null,22,45,"T","ENSG00000105722","ENST00000222329","intron_variant","intron_variant","-/2698","-/1647","-/548"]
["ATG2B",55102,"WUGSC","GRCh38","chr14",96311605,96311605,"+","Silent","SNP","C","C","A",null,null,"TCGA-BH-A1F2-01A-31D-A13L-09","TCGA-BH-A1F2-11A-32D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","a5c67494-d843-4b14-ba9c-d077396ed2dc","3b15c929-09bb-49b8-914c-b0a5e32ddd3e","c.3927G>T","ENST00000359933","27/42",81,52,"A","ENSG00000066739","ENST00000359933","synonymous_variant","synonymous_variant","4821/13684","3927/6237","1309/2078","V","gtG/gtT"]
["GLB1L2",89944,"WUGSC","GRCh38","chr11",134368717,134368717,"+","Silent","SNP","C","C","T","novel",null,"TCGA-BH-A0EE-01A-11W-A050-09","TCGA-BH-A0EE-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","68d16e6a-20a5-428f-89d0-a8a0deda80cc","f4528a3f-aa6b-4964-80fd-afa642427616","c.963C>T","ENST00000339772",43028,134,54,"T","ENSG00000149328","ENST00000339772","synonymous_variant","synonymous_variant","1151/3152","963/1911","321/636","T","acC/acT"]
["MIR1204",100302185,"WUGSC","GRCh38","chr8",127796011,127796011,"+","RNA","SNP","G","G","C",null,null,"TCGA-BH-A0EB-01A-11W-A050-09","TCGA-BH-A0EB-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","3861ca01-bcc3-42a9-835d-1ef9f1a053bd","991496de-9acd-43e0-b853-2c19c155254e","n.50G>C","ENST00000408388",42736,149,103,"C","ENSG00000275264","ENST00000408388","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","50/67"]
["DNAH8",1769,"WUGSC","GRCh38","chr6",38924007,38924007,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-BH-A0DZ-01A-11W-A019-09","TCGA-BH-A0DZ-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d6418b7f-96b4-424a-8737-d382ece37afe","dfd32478-8fa8-42a1-b5f7-329c02aa8f87","c.10156C>G","ENST00000359357","71/91",388,195,"G","ENSG00000124721","ENST00000359357","missense_variant","missense_variant","10410/13864","10156/13473","3386/4490","L/V","Ctg/Gtg"]
["ADCY8",114,"WUGSC","GRCh38","chr8",130814079,130814079,"+","Missense_Mutation","SNP","C","C","T","rs374456387","byCluster;byFrequency","TCGA-BH-A0DZ-01A-11W-A019-09","TCGA-BH-A0DZ-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d6418b7f-96b4-424a-8737-d382ece37afe","dfd32478-8fa8-42a1-b5f7-329c02aa8f87","c.2903G>A","ENST00000286355","14/18",140,106,"T","ENSG00000155897","ENST00000286355","missense_variant","missense_variant","4996/5938","2903/3756","968/1251","R/Q","cGa/cAa"]
["SNW1",22938,"WUGSC","GRCh38","chr14",77732493,77732493,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0DZ-01A-11W-A019-09","TCGA-BH-A0DZ-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d6418b7f-96b4-424a-8737-d382ece37afe","dfd32478-8fa8-42a1-b5f7-329c02aa8f87","c.883G>T","ENST00000261531",42992,183,101,"A","ENSG00000100603","ENST00000261531","missense_variant","missense_variant","946/2163","883/1611","295/536","D/Y","Gat/Tat"]
["ABCA5",23461,"WUGSC","GRCh38","chr17",69264776,69264776,"+","Missense_Mutation","SNP","G","G","A","rs139096664","byCluster;byFrequency","TCGA-BH-A0DZ-01A-11W-A019-09","TCGA-BH-A0DZ-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d6418b7f-96b4-424a-8737-d382ece37afe","dfd32478-8fa8-42a1-b5f7-329c02aa8f87","c.3274C>T","ENST00000392676","24/39",142,73,"A","ENSG00000154265","ENST00000392676","missense_variant","missense_variant","3339/8220","3274/4929","1092/1642","H/Y","Cat/Tat"]
["SMG7",9887,"WUGSC","GRCh38","chr1",183553117,183553117,"+","3'UTR","SNP","C","C","G",null,null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.*1186C>G","ENST00000347615","22/22",19,23,"G","ENSG00000116698","ENST00000347615","3_prime_UTR_variant","3_prime_UTR_variant","4719/5788","-/3414","-/1137"]
["ZNF197",10168,"WUGSC","GRCh38","chr3",44629503,44629503,"+","Missense_Mutation","SNP","G","G","A","rs375070406","by1000G;byCluster","TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.349G>A","ENST00000344387",42772,34,27,"A","ENSG00000186448","ENST00000344387","missense_variant","missense_variant","534/3275","349/3090","117/1029","V/I","Gta/Ata"]
["LETM1",3954,"WUGSC","GRCh38","chr4",1836480,1836480,"+","Silent","SNP","C","C","A",null,null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.687G>T","ENST00000302787",42839,122,86,"A","ENSG00000168924","ENST00000302787","synonymous_variant","synonymous_variant","984/5462","687/2220","229/739","V","gtG/gtT"]
["ZSCAN23",222696,"WUGSC","GRCh38","chr6",28434813,28434813,"+","Silent","SNP","C","C","T",null,null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.822G>A","ENST00000289788",42829,92,51,"T","ENSG00000187987","ENST00000289788","synonymous_variant","synonymous_variant","968/3126","822/1170","274/389","E","gaG/gaA"]
["PEX1",5189,"WUGSC","GRCh38","chr7",92494298,92494298,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.3025G>C","ENST00000248633","19/24",24,26,"G","ENSG00000127980","ENST00000248633","missense_variant","missense_variant","3121/4385","3025/3852","1009/1283","D/H","Gat/Cat"]
["RASSF10",644943,"WUGSC","GRCh38","chr11",13010199,13010199,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.623C>T","ENST00000529419",42736,79,44,"T","ENSG00000189431","ENST00000529419","missense_variant","missense_variant","623/2530","623/1524","208/507","S/L","tCg/tTg"]
["NAB2",4665,"WUGSC","GRCh38","chr12",57093084,57093084,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.1165G>A","ENST00000300131",42862,64,38,"A","ENSG00000166886","ENST00000300131","missense_variant","missense_variant","1543/2711","1165/1578","389/525","E/K","Gaa/Aaa"]
["C16orf52",730094,"WUGSC","GRCh38","chr16",22083926,22083926,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.*3046C>G","ENST00000542527",42797,16,10,"G","ENSG00000185716","ENST00000542527","3_prime_UTR_variant","3_prime_UTR_variant","3643/4360","-/504","-/167"]
["PKD1L3",342372,"WUGSC","GRCh38","chr16",71933951,71933951,"+","Silent","SNP","C","C","T","novel",null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.4788G>A","ENST00000620267","27/30",38,38,"T","ENSG00000277481","ENST00000620267","synonymous_variant","synonymous_variant","4788/5199","4788/5199","1596/1732","L","ctG/ctA"]
["DOPEY2",9980,"WUGSC","GRCh38","chr21",36199193,36199193,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.262G>C","ENST00000399151",13575,77,73,"C","ENSG00000142197","ENST00000399151","missense_variant","missense_variant","347/7685","262/6897","88/2298","E/Q","Gag/Cag"]
["TBC1D8B",54885,"WUGSC","GRCh38","chrX",106839366,106839366,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0B6-01A-11D-A19Y-09","TCGA-BH-A0B6-10A-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","9e575ee5-731c-49fd-80fc-944b861e0ea7","7b99568d-3c2e-41a9-b8b8-0ba296a21aaf","c.1262C>T","ENST00000357242",42968,57,43,"T","ENSG00000133138","ENST00000357242","missense_variant","missense_variant","1436/5717","1262/3363","421/1120","T/I","aCa/aTa"]
["KDM4D",55693,"WUGSC","GRCh38","chr11",94997742,94997742,"+","Nonsense_Mutation","SNP","A","A","T",null,null,"TCGA-AO-A12H-01A-11D-A10Y-09","TCGA-AO-A12H-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","5a535c49-d42e-43c6-9d32-dc76f28d4f0f","ef348ec7-f3d5-41d6-af09-65f81ebd2b46","c.370A>T","ENST00000335080",42797,106,81,"T","ENSG00000186280","ENST00000335080","stop_gained","stop_gained","1202/2978","370/1572","124/523","K/*","Aaa/Taa"]
["GFPT2",9945,"WUGSC","GRCh38","chr5",180304877,180304877,"+","Silent","SNP","C","C","A","novel",null,"TCGA-A2-A0CW-01A-21D-A10Y-09","TCGA-A2-A0CW-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","da4f0f85-b16f-40fa-95c6-524d70d7ac4d","b6b51168-dc64-4bb1-aca5-346a1f1c8b67","c.1737G>T","ENST00000253778","17/19",117,168,"A","ENSG00000131459","ENST00000253778","synonymous_variant","synonymous_variant","1907/3093","1737/2049","579/682","G","ggG/ggT"]
["LRRC31",79782,"WUGSC","GRCh38","chr3",169869817,169869817,"+","5'UTR","SNP","G","G","T","novel",null,"TCGA-E2-A10C-01A-21D-A10M-09","TCGA-E2-A10C-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","2750ed41-0bd4-4cf4-98f5-762957cf80b7","92567dce-0f9e-4885-8260-0196fef7a91b","c.-10C>A","ENST00000316428",42744,130,199,"T","ENSG00000114248","ENST00000316428","5_prime_UTR_variant","5_prime_UTR_variant","49/2520","-/1659","-/552"]
["TAS2R16",50833,"WUGSC","GRCh38","chr7",122995599,122995599,"+","Silent","SNP","G","G","A","rs747794465","byFrequency","TCGA-E2-A10C-01A-21D-A10M-09","TCGA-E2-A10C-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","2750ed41-0bd4-4cf4-98f5-762957cf80b7","92567dce-0f9e-4885-8260-0196fef7a91b","c.36C>T","ENST00000249284",42736,32,31,"A","ENSG00000128519","ENST00000249284","synonymous_variant","synonymous_variant","102/997","36/876","12/291","I","atC/atT"]
["HYOU1",10525,"WUGSC","GRCh38","chr11",119056137,119056137,"+","Silent","SNP","C","C","T",null,null,"TCGA-E2-A10C-01A-21D-A10M-09","TCGA-E2-A10C-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","2750ed41-0bd4-4cf4-98f5-762957cf80b7","92567dce-0f9e-4885-8260-0196fef7a91b","c.24G>A","ENST00000617285",42792,107,44,"T","ENSG00000149428","ENST00000617285","synonymous_variant","synonymous_variant","149/4529","24/3000","8/999","Q","caG/caA"]
["GPATCH2L",55668,"WUGSC","GRCh38","chr14",76154741,76154741,"+","Silent","SNP","C","C","G",null,null,"TCGA-E2-A10C-01A-21D-A10M-09","TCGA-E2-A10C-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","2750ed41-0bd4-4cf4-98f5-762957cf80b7","92567dce-0f9e-4885-8260-0196fef7a91b","c.378C>G","ENST00000261530",42776,79,33,"G","ENSG00000089916","ENST00000261530","synonymous_variant","synonymous_variant","444/14007","378/1449","126/482","L","ctC/ctG"]
["CYP4F3",4051,"WUGSC","GRCh38","chr19",15647089,15647089,"+","Silent","SNP","C","C","T",null,null,"TCGA-E2-A10C-01A-21D-A10M-09","TCGA-E2-A10C-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","2750ed41-0bd4-4cf4-98f5-762957cf80b7","92567dce-0f9e-4885-8260-0196fef7a91b","c.381C>T","ENST00000221307",42838,185,125,"T","ENSG00000186529","ENST00000221307","synonymous_variant","synonymous_variant","428/5050","381/1563","127/520","F","ttC/ttT"]
["MLLT3",4300,"WUGSC","GRCh38","chr9",20622430,20622430,"+","5'UTR","SNP","G","G","T","novel",null,"TCGA-AC-A8OQ-01A-11D-A41F-09","TCGA-AC-A8OQ-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","9ea8e9fa-c9cf-48cd-8949-6976c1ad46b2","ea85a93c-cf16-4e88-824f-d697caf2693b","c.-174C>A","ENST00000380338",42746,129,74,"T","ENSG00000171843","ENST00000380338","5_prime_UTR_variant","5_prime_UTR_variant","114/6772","-/1707","-/568"]
["DPP10",57628,"WUGSC","GRCh38","chr2",115762605,115762605,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E9-A1R4-01A-21D-A14G-09","TCGA-E9-A1R4-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","15d9c916-a12e-48a0-8a0f-8c240c54bd37","769c4e3f-5ee1-4a17-840e-84cfdba07434","c.1108C>G","ENST00000410059",43095,149,162,"G","ENSG00000175497","ENST00000410059","missense_variant","missense_variant","1588/6278","1108/2391","370/796","Q/E","Cag/Gag"]
["GLB1L3",112937,"WUGSC","GRCh38","chr11",134318683,134318683,"+","Nonsense_Mutation","SNP","G","G","A","novel",null,"TCGA-E9-A1R4-01A-21D-A14G-09","TCGA-E9-A1R4-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","15d9c916-a12e-48a0-8a0f-8c240c54bd37","769c4e3f-5ee1-4a17-840e-84cfdba07434","c.1832G>A","ENST00000431683","19/20",142,149,"A","ENSG00000166105","ENST00000431683","stop_gained","stop_gained","1832/2583","1832/1962","611/653","W/*","tGg/tAg"]
["PLEKHG4",25894,"WUGSC","GRCh38","chr16",67286809,67286809,"+","Missense_Mutation","SNP","C","C","T","rs762486532","byFrequency","TCGA-BH-A18S-01A-11D-A12B-09","TCGA-BH-A18S-11A-43D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","a01c12fc-a33e-4a06-8b69-ebe6d4f59c2b","cee84481-1eca-4469-b2be-77830f5a9510","c.2815C>T","ENST00000360461","16/21",39,60,"T","ENSG00000196155","ENST00000360461","missense_variant","missense_variant","5350/6782","2815/3576","939/1191","R/C","Cgc/Tgc"]
["GUK1",2987,"WUGSC","GRCh38","chr1",228147668,228147668,"+","Silent","SNP","G","G","A",null,null,"TCGA-D8-A1Y1-01A-21D-A14K-09","TCGA-D8-A1Y1-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","2ea6e540-6e2f-48a5-99e3-27a0107d07b7","0400d779-78d9-4645-add6-2a9f94d55e1c","c.444G>A","ENST00000312726",42925,25,32,"A","ENSG00000143774","ENST00000312726","synonymous_variant","synonymous_variant","685/1084","444/594","148/197","R","cgG/cgA"]
["ZDHHC20",253832,"WUGSC","GRCh38","chr13",21376614,21376614,"+","3'UTR","SNP","A","A","G","novel",null,"TCGA-D8-A1Y1-01A-21D-A14K-09","TCGA-D8-A1Y1-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","2ea6e540-6e2f-48a5-99e3-27a0107d07b7","0400d779-78d9-4645-add6-2a9f94d55e1c","c.*82T>C","ENST00000400590","13/13",58,39,"G","ENSG00000180776","ENST00000400590","3_prime_UTR_variant","3_prime_UTR_variant","1379/1869","-/1098","-/365"]
["CCL26",10344,"WUGSC","GRCh38","chr7",75769624,75769624,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-AN-A0XR-01A-11D-A10G-09","TCGA-AN-A0XR-10A-01D-A117-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","e7dc7492-3a84-49c7-8dea-8f508b53dc40","974aff12-3ec4-41e2-852a-837a513edd6c","c.*69C>T","ENST00000005180",42797,237,157,"A","ENSG00000006606","ENST00000005180","3_prime_UTR_variant","3_prime_UTR_variant","435/526","-/285","-/94"]
["SPARCL1",8404,"WUGSC","GRCh38","chr4",87494133,87494133,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A2-A0CR-01A-11D-A228-09","TCGA-A2-A0CR-10A-01D-A22A-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina HiSeq 2500","f573c3c3-7b61-4955-8772-215b7cb9a763","3bdb54b4-1e26-4274-a1bd-800416ffbd34","c.667G>C","ENST00000282470",42836,55,65,"G","ENSG00000152583","ENST00000282470","missense_variant","missense_variant","1138/2906","667/1995","223/664","E/Q","Gaa/Caa"]
["CACNA1S",779,"WUGSC","GRCh38","chr1",201061293,201061293,"+","Nonsense_Mutation","SNP","T","T","A","novel",null,"TCGA-E9-A22E-01A-11D-A159-09","TCGA-E9-A22E-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","a1d7dafc-a755-44a6-b45b-dc6aae309d3e","126314e2-cbf4-40e6-9277-05857e870852","c.3229A>T","ENST00000362061","25/44",193,70,"A","ENSG00000081248","ENST00000362061","stop_gained","stop_gained","3456/6166","3229/5622","1077/1873","K/*","Aag/Tag"]
["AHCTF1",25909,"WUGSC","GRCh38","chr1",246863957,246863957,"+","Silent","SNP","T","T","C",null,null,"TCGA-E9-A5UO-01A-11D-A28B-09","TCGA-E9-A5UO-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","dc23e9b3-7347-405e-8a21-72955541757e","ff54d8e4-64f8-48eb-8b2e-314142645eb6","c.3534A>G","ENST00000326225","27/36",33,54,"C","ENSG00000153207","ENST00000326225","synonymous_variant","synonymous_variant","3631/8633","3534/6828","1178/2275","E","gaA/gaG"]
["CFL1P1",142913,"WUGSC","GRCh38","chr10",87844118,87844118,"+","RNA","SNP","C","C","G","novel",null,"TCGA-AR-A1AV-01A-21D-A12Q-09","TCGA-AR-A1AV-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","0a0dd89c-5ec8-4015-9616-733e41361a64","77cb1c29-4009-4669-bdb6-3ec5e74b65d1","n.626C>G","ENST00000438248",42829,28,29,"G","ENSG00000223820","ENST00000438248","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","626/2120"]
["RYR2",6262,"WUGSC","GRCh38","chr1",237809000,237809000,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.14398G>A","ENST00000366574","100/105",124,95,"A","ENSG00000198626","ENST00000366574","missense_variant","missense_variant","14715/16562","14398/14904","4800/4967","D/N","Gat/Aat"]
["ATP6V1E2",90423,"WUGSC","GRCh38","chr2",46512591,46512591,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.121G>C","ENST00000306448",42768,109,116,"G","ENSG00000250565","ENST00000306448","missense_variant","missense_variant","1235/1979","121/681","41/226","E/Q","Gag/Cag"]
["CCDC109B",55013,"WUGSC","GRCh38","chr4",109682639,109682639,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.509G>A","ENST00000394650",42863,48,45,"A","ENSG00000005059","ENST00000394650","missense_variant","missense_variant","642/2278","509/1011","170/336","R/K","aGa/aAa"]
["PTCHD4",442213,"WUGSC","GRCh38","chr6",47878304,47878304,"+","Nonstop_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.2540G>C","ENST00000339488",42797,61,48,"G","ENSG00000244694","ENST00000339488","stop_lost","stop_lost","2574/2850","2540/2541","847/846","*/S","tGa/tCa"]
["INTS10",55174,"WUGSC","GRCh38","chr8",19845781,19845781,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.1960C>G","ENST00000397977","16/17",79,82,"G","ENSG00000104613","ENST00000397977","missense_variant","missense_variant","2358/2804","1960/2133","654/710","Q/E","Caa/Gaa"]
["OR13F1",138805,"WUGSC","GRCh38","chr9",104504546,104504546,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.284C>T","ENST00000334726",42736,51,65,"T","ENSG00000186881","ENST00000334726","missense_variant","missense_variant","284/960","284/960","95/319","S/L","tCa/tTa"]
["MRPL21",219927,"WUGSC","GRCh38","chr11",68891325,68891325,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.*6G>C","ENST00000362034",42923,44,71,"G","ENSG00000197345","ENST00000362034","3_prime_UTR_variant","3_prime_UTR_variant","634/683","-/618","-/205"]
["HERC1",8925,"WUGSC","GRCh38","chr15",63725505,63725505,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.3355G>A","ENST00000443617","18/78",41,36,"T","ENSG00000103657","ENST00000443617","missense_variant","missense_variant","3443/15137","3355/14586","1119/4861","E/K","Gaa/Aaa"]
["AMZ2",51321,"WUGSC","GRCh38","chr17",68250232,68250232,"+","Silent","SNP","C","C","T",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.45C>T","ENST00000359904",42773,84,65,"T","ENSG00000196704","ENST00000359904","synonymous_variant","synonymous_variant","1177/2402","45/1083","15/360","L","ctC/ctT"]
["ZNF85",7639,"WUGSC","GRCh38","chr19",20949765,20949765,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.1251G>C","ENST00000328178",42829,48,33,"C","ENSG00000105750","ENST00000328178","missense_variant","missense_variant","1364/2296","1251/1788","417/595","K/N","aaG/aaC"]
["APOL6",80830,"WUGSC","GRCh38","chr22",35658744,35658744,"+","Silent","SNP","C","C","T",null,null,"TCGA-D8-A27G-01A-11D-A16D-09","TCGA-D8-A27G-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","c8bc172c-0986-481e-a4ce-54fa55db4871","4e47a193-cf64-45ab-afb0-0167661972a2","c.180C>T","ENST00000409652",42797,74,74,"T","ENSG00000221963","ENST00000409652","synonymous_variant","synonymous_variant","456/10121","180/1032","60/343","L","ctC/ctT"]
["SP110",3431,"WUGSC","GRCh38","chr2",230212938,230212938,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A0YG-01A-21D-A10G-09","TCGA-A2-A0YG-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","bf82035c-9cd1-4355-acdd-8a007708e976","d2825bbf-6083-40da-bd62-f6e7c0cb0204","c.406C>A","ENST00000358662",42843,192,52,"T","ENSG00000135899","ENST00000358662","missense_variant","missense_variant","485/2337","406/2070","136/689","P/T","Cca/Aca"]
["MYO10",4651,"WUGSC","GRCh38","chr5",16680082,16680082,"+","Nonsense_Mutation","SNP","G","G","C",null,null,"TCGA-B6-A0IJ-01A-11W-A050-09","TCGA-B6-A0IJ-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","c63f9ddb-6301-400e-a0e8-197eea2efe75","aa5b770f-1e5f-459b-8ef5-cfbbb5ecd737","c.4407C>G","ENST00000513610","33/41",73,70,"C","ENSG00000145555","ENST00000513610","stop_gained","stop_gained","4862/8038","4407/6177","1469/2058","Y/*","taC/taG"]
["ZNF646",9726,"WUGSC","GRCh38","chr16",31081251,31081251,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-B6-A0IJ-01A-11W-A050-09","TCGA-B6-A0IJ-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","c63f9ddb-6301-400e-a0e8-197eea2efe75","aa5b770f-1e5f-459b-8ef5-cfbbb5ecd737","c.4927G>C","ENST00000394979",42736,38,73,"C","ENSG00000167395","ENST00000394979","missense_variant","missense_variant","5350/8118","4927/5490","1643/1829","E/Q","Gag/Cag"]
["SF3A3",10946,"WUGSC","GRCh38","chr1",37980632,37980632,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.644C>T","ENST00000373019",42964,135,133,"A","ENSG00000183431","ENST00000373019","missense_variant","missense_variant","1600/3673","644/1506","215/501","A/V","gCt/gTt"]
["LAMB3",3914,"WUGSC","GRCh38","chr1",209615362,209615362,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.3428G>A","ENST00000356082","23/23",83,68,"T","ENSG00000196878","ENST00000356082","missense_variant","missense_variant","3563/4055","3428/3519","1143/1172","R/H","cGc/cAc"]
["C3orf58",205428,"WUGSC","GRCh38","chr3",143989731,143989731,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.1183C>T","ENST00000315691",42797,162,136,"T","ENSG00000181744","ENST00000315691","missense_variant","missense_variant","1718/4346","1183/1293","395/430","L/F","Ctc/Ttc"]
["MRPS27",23107,"WUGSC","GRCh38","chr5",72228360,72228360,"+","Silent","SNP","C","C","T",null,null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.600G>A","ENST00000261413",42958,184,300,"T","ENSG00000113048","ENST00000261413","synonymous_variant","synonymous_variant","640/2785","600/1245","200/414","E","gaG/gaA"]
["RTN4IP1",84816,"WUGSC","GRCh38","chr6",106572024,106572024,"+","Missense_Mutation","SNP","C","C","T","rs760835047",null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.1163G>A","ENST00000369063",42987,165,129,"T","ENSG00000130347","ENST00000369063","missense_variant","missense_variant","1629/1682","1163/1191","388/396","R/Q","cGa/cAa"]
["TACC1",6867,"WUGSC","GRCh38","chr8",38820328,38820328,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.1084G>A","ENST00000317827",42807,353,240,"A","ENSG00000147526","ENST00000317827","missense_variant","missense_variant","1463/7802","1084/2418","362/805","A/T","Gca/Aca"]
["FAT3",120114,"WUGSC","GRCh38","chr11",92353701,92353701,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.1139C>T","ENST00000525166",42762,178,226,"T","ENSG00000165323","ENST00000525166","missense_variant","missense_variant","1161/18699","1139/13320","380/4439","T/I","aCa/aTa"]
["OAS3",4940,"WUGSC","GRCh38","chr12",112968070,112968070,"+","Silent","SNP","G","G","A",null,null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.3000G>A","ENST00000228928","14/16",39,69,"A","ENSG00000111331","ENST00000228928","synonymous_variant","synonymous_variant","3179/6719","3000/3264","1000/1087","E","gaG/gaA"]
["HS3ST4",9951,"WUGSC","GRCh38","chr16",26136224,26136224,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.1347G>A","ENST00000331351",42768,89,84,"A","ENSG00000182601","ENST00000331351","stop_gained","stop_gained","1739/3203","1347/1371","449/456","W/*","tgG/tgA"]
["ZC3H18",124245,"WUGSC","GRCh38","chr16",88630503,88630503,"+","Missense_Mutation","SNP","C","C","T","rs749335369",null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.2585C>T","ENST00000301011","17/18",13,11,"T","ENSG00000158545","ENST00000301011","missense_variant","missense_variant","2785/3729","2585/2862","862/953","S/L","tCa/tTa"]
["EP300",2033,"WUGSC","GRCh38","chr22",41131454,41131454,"+","Missense_Mutation","SNP","C","C","T","rs769721803",null,"TCGA-BH-A0HF-01A-11W-A071-09","TCGA-BH-A0HF-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","464a1d47-a56a-4667-b4c5-911e5d4a7363","6116e3af-4c46-4be9-98b3-ef1d6c3cdf65","c.1349C>T","ENST00000263253",11475,245,226,"T","ENSG00000100393","ENST00000263253","missense_variant","missense_variant","2568/9585","1349/7245","450/2414","A/V","gCc/gTc"]
["TIAM2",26230,"WUGSC","GRCh38","chr6",155254274,155254274,"+","Intron","SNP","C","C","A","novel",null,"TCGA-BH-A204-01A-11D-A159-09","TCGA-BH-A204-11A-53D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","2454d30f-1ca5-4f01-bfce-6ae10e84e75a","38726a6a-7c67-43c9-b795-71512b2a6f7f","c.4314-145C>A","ENST00000318981",null,28,23,"A","ENSG00000146426","ENST00000318981","intron_variant","intron_variant","-/5916","-/5106","-/1701"]
["PHLDA3",23612,"WUGSC","GRCh38","chr1",201465853,201465853,"+","3'Flank","SNP","C","C","G","novel",null,"TCGA-AC-A6IW-01A-12D-A33E-09","TCGA-AC-A6IW-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","c3d40a81-01f9-4f16-bfc5-84a038f72482","abfc0a6a-6c65-4b20-bba2-b958cd564acc",null,"ENST00000367309",null,71,40,"G","ENSG00000174307","ENST00000367309","downstream_gene_variant","downstream_gene_variant","-/896","-/384","-/127"]
["DYNLL1",8655,"WUGSC","GRCh38","chr12",120496100,120496100,"+","5'UTR","SNP","C","C","G","novel",null,"TCGA-AC-A6IW-01A-12D-A33E-09","TCGA-AC-A6IW-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","c3d40a81-01f9-4f16-bfc5-84a038f72482","abfc0a6a-6c65-4b20-bba2-b958cd564acc","c.-123C>G","ENST00000242577",42738,32,25,"G","ENSG00000088986","ENST00000242577","5_prime_UTR_variant","5_prime_UTR_variant","45/720","-/270","-/89"]
["GRID1",2894,"WUGSC","GRCh38","chr10",85856078,85856078,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E2-A14W-01A-11D-A12B-09","TCGA-E2-A14W-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","fbdc8659-e9cc-483f-bd0a-1a24b5ada1cf","7dfbdd33-5e89-45ef-a636-fe72cc25f3b9","c.1064C>G","ENST00000327946",42932,266,309,"C","ENSG00000182771","ENST00000327946","missense_variant","missense_variant","1150/5834","1064/3030","355/1009","S/C","tCc/tGc"]
["TP53",7157,"WUGSC","GRCh38","chr17",7673802,7673802,"+","Missense_Mutation","SNP","C","C","T","rs28934576","by1000G;byCluster","TCGA-AR-A1AJ-01A-21D-A12Q-09","TCGA-AR-A1AJ-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","4e1f9084-4729-4b3f-b036-6226d64fd25b","63ee3781-4578-4d19-88e4-c8785fc7987e","c.818G>A","ENST00000269305",42958,165,180,"T","ENSG00000141510","ENST00000269305","missense_variant","missense_variant","1008/2579","818/1182","273/393","R/H","cGt/cAt"]
["FMN2",56776,"WUGSC","GRCh38","chr1",240333902,240333902,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AN-A0AT-01A-11D-A045-09","TCGA-AN-A0AT-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","f848b66f-bd9e-4fba-afd4-eb58848d1ef4","1dab1c73-daeb-4900-9fa1-61656237024a","c.4600C>A","ENST00000319653",43087,256,145,"A","ENSG00000155816","ENST00000319653","missense_variant","missense_variant","4830/6434","4600/5169","1534/1722","L/I","Ctt/Att"]
["UPF3B",65109,"WUGSC","GRCh38","chrX",119837977,119837977,"+","Missense_Mutation","SNP","C","C","T","rs773491980","byFrequency","TCGA-AN-A0AT-01A-11D-A045-09","TCGA-AN-A0AT-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","f848b66f-bd9e-4fba-afd4-eb58848d1ef4","1dab1c73-daeb-4900-9fa1-61656237024a","c.1082G>A","ENST00000276201",43019,413,247,"T","ENSG00000125351","ENST00000276201","missense_variant","missense_variant","1152/2378","1082/1452","361/483","R/Q","cGa/cAa"]
["ZNF598",90850,"WUGSC","GRCh38","chr16",1998315,1998315,"+","Missense_Mutation","SNP","C","C","T","rs761148339",null,"TCGA-BH-A1FM-01A-11D-A13L-09","TCGA-BH-A1FM-11B-23D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","7cb17736-03da-4f77-8397-145585a25b1e","e50ac0fd-6812-4747-b18d-243a19c00af5","c.2467G>A","ENST00000563630",43081,31,51,"T","ENSG00000167962","ENST00000563630","missense_variant","missense_variant","2710/3371","2467/2550","823/849","D/N","Gat/Aat"]
["DNM1",1759,"WUGSC","GRCh38","chr9",128248678,128248678,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-E2-A1LS-01A-12D-A159-09","TCGA-E2-A1LS-11A-32W-A16L-09",null,null,"Somatic","Illumina HiSeq 2000","40087f80-85f6-4cc4-95c9-0639153dd3f4","a8f9516d-822f-4888-b66b-f42bb8e6a814","c.2001C>A","ENST00000372923","19/22",52,185,"A","ENSG00000106976","ENST00000372923","missense_variant","missense_variant","2120/3244","2001/2595","667/864","D/E","gaC/gaA"]
["GPATCH4",54865,"WUGSC","GRCh38","chr1",156595090,156595090,"+","3'Flank","SNP","G","G","A","novel",null,"TCGA-C8-A3M7-01A-12D-A21Q-09","TCGA-C8-A3M7-10A-01D-A21Q-09",null,null,"Somatic","Illumina HiSeq 2000","1cbe3a4c-23ef-45a3-a01c-59ba13f053e4","d04ce8a0-807d-478f-adae-56fdef6c1ecc",null,"ENST00000438976",null,137,84,"A","ENSG00000160818","ENST00000438976","downstream_gene_variant","downstream_gene_variant","-/1159","-/1128","-/375"]
["TIGD3",220359,"WUGSC","GRCh38","chr11",65357192,65357192,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-C8-A3M7-01A-12D-A21Q-09","TCGA-C8-A3M7-10A-01D-A21Q-09",null,null,"Somatic","Illumina HiSeq 2000","1cbe3a4c-23ef-45a3-a01c-59ba13f053e4","d04ce8a0-807d-478f-adae-56fdef6c1ecc","c.1384G>C","ENST00000309880",42768,38,19,"C","ENSG00000173825","ENST00000309880","missense_variant","missense_variant","1591/2012","1384/1416","462/471","E/Q","Gag/Cag"]
["PHLDB3",653583,"WUGSC","GRCh38","chr19",43495611,43495611,"+","Silent","SNP","G","G","A",null,null,"TCGA-C8-A3M7-01A-12D-A21Q-09","TCGA-C8-A3M7-10A-01D-A21Q-09",null,null,"Somatic","Illumina HiSeq 2000","1cbe3a4c-23ef-45a3-a01c-59ba13f053e4","d04ce8a0-807d-478f-adae-56fdef6c1ecc","c.835C>T","ENST00000292140",42932,51,32,"A","ENSG00000176531","ENST00000292140","synonymous_variant","synonymous_variant","1196/2591","835/1923","279/640","L","Ctg/Ttg"]
["HSD11B1",3290,"WUGSC","GRCh38","chr1",209705829,209705829,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-BH-A5IZ-01A-11D-A27P-09","TCGA-BH-A5IZ-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","a6db0ecd-0328-4bc3-b2d6-9f1a9c8e320f","24076c1c-df28-40d1-9696-221716c279cf","c.107A>G","ENST00000367027",42772,60,37,"G","ENSG00000117594","ENST00000367027","missense_variant","missense_variant","204/1405","107/879","36/292","K/R","aAa/aGa"]
["TMEM161A",54929,"WUGSC","GRCh38","chr19",19121643,19121643,"+","Missense_Mutation","SNP","G","G","A","rs72993472","by1000G;byCluster;byFrequency","TCGA-BH-A5IZ-01A-11D-A27P-09","TCGA-BH-A5IZ-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","a6db0ecd-0328-4bc3-b2d6-9f1a9c8e320f","24076c1c-df28-40d1-9696-221716c279cf","c.682C>T","ENST00000162044",42959,82,60,"A","ENSG00000064545","ENST00000162044","missense_variant","missense_variant","747/1820","682/1440","228/479","R/C","Cgc/Tgc"]
["IL37",27178,"WUGSC","GRCh38","chr2",112918564,112918564,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E2-A152-01A-11D-A12B-09","TCGA-E2-A152-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","b266b370-425c-4146-8b72-59248436618e","61e9e215-f15b-4968-9afc-4931ad991c80","c.412G>C","ENST00000263326",42860,118,146,"C","ENSG00000125571","ENST00000263326","missense_variant","missense_variant","454/772","412/657","138/218","E/Q","Gag/Cag"]
["FAM45A",404636,"WUGSC","GRCh38","chr10",119104170,119104170,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E2-A152-01A-11D-A12B-09","TCGA-E2-A152-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","b266b370-425c-4146-8b72-59248436618e","61e9e215-f15b-4968-9afc-4931ad991c80","c.28C>G","ENST00000361432",42744,39,25,"G","ENSG00000119979","ENST00000361432","missense_variant","missense_variant","54/1648","28/1074","10/357","Q/E","Cag/Gag"]
["ANKRD19P",138649,"WUGSC","GRCh38","chr9",92884610,92884610,"+","RNA","SNP","C","C","A","novel",null,"TCGA-AO-A0J2-01A-11W-A050-09","TCGA-AO-A0J2-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","84b66e02-1b37-4424-b752-363f7861fe74","e3d65145-2dc6-4be3-a3b9-b53940c920fe","n.2243C>A","ENST00000473204",43019,675,406,"A","ENSG00000187984","ENST00000473204","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","2243/2370"]
["SLC9A2",6549,"WUGSC","GRCh38","chr2",102657995,102657995,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-BH-A18V-01A-11D-A12B-09","TCGA-BH-A18V-11A-52D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","6150dd25-a8f4-4d9f-9da0-f956855ab67d","e968461c-7bb9-4db0-87c6-5e7c77c5042c","c.721G>C","ENST00000233969",42778,254,220,"C","ENSG00000115616","ENST00000233969","missense_variant","missense_variant","863/5410","721/2439","241/812","G/R","Gga/Cga"]
["DLX5",1749,"WUGSC","GRCh38","chr7",97021016,97021016,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-BH-A18V-01A-11D-A12B-09","TCGA-BH-A18V-11A-52D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","6150dd25-a8f4-4d9f-9da0-f956855ab67d","e968461c-7bb9-4db0-87c6-5e7c77c5042c","c.590A>C","ENST00000222598",42797,219,263,"G","ENSG00000105880","ENST00000222598","missense_variant","missense_variant","1064/1688","590/870","197/289","K/T","aAa/aCa"]
["MYO1A",4640,"WUGSC","GRCh38","chr12",57030214,57030214,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-BH-A18V-01A-11D-A12B-09","TCGA-BH-A18V-11A-52D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","6150dd25-a8f4-4d9f-9da0-f956855ab67d","e968461c-7bb9-4db0-87c6-5e7c77c5042c","c.2587C>G","ENST00000300119","24/28",130,224,"C","ENSG00000166866","ENST00000300119","missense_variant","missense_variant","2838/3621","2587/3132","863/1043","Q/E","Cag/Gag"]
["RNF207",388591,"WUGSC","GRCh38","chr1",6212824,6212824,"+","Intron","SNP","G","G","A","novel",null,"TCGA-A8-A06Q-01A-11W-A050-09","TCGA-A8-A06Q-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","473d5422-978a-48be-be32-2b7516d6d2d5","c66176ec-6088-430c-a3f3-3c03ba2b5b1a","c.1534+91G>A","ENST00000377939",null,41,107,"A","ENSG00000158286","ENST00000377939","intron_variant","intron_variant","-/3924","-/1905","-/634"]
["RAB30",27314,"WUGSC","GRCh38","chr11",82982355,82982355,"+","Nonsense_Mutation","SNP","G","G","C","novel",null,"TCGA-A8-A06Q-01A-11W-A050-09","TCGA-A8-A06Q-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","473d5422-978a-48be-be32-2b7516d6d2d5","c66176ec-6088-430c-a3f3-3c03ba2b5b1a","c.422C>G","ENST00000260056",42860,95,113,"C","ENSG00000137502","ENST00000260056","stop_gained","stop_gained","828/1393","422/612","141/203","S/*","tCa/tGa"]
["SMARCA4",6597,"WUGSC","GRCh38","chr19",11060114,11060114,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A8-A06Q-01A-11W-A050-09","TCGA-A8-A06Q-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","473d5422-978a-48be-be32-2b7516d6d2d5","c66176ec-6088-430c-a3f3-3c03ba2b5b1a","c.4838G>A","ENST00000344626","34/35",51,87,"A","ENSG00000127616","ENST00000344626","missense_variant","missense_variant","5043/5392","4838/4944","1613/1647","R/Q","cGg/cAg"]
["APPL2",55198,"WUGSC","GRCh38","chr12",105176969,105176969,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AN-A0XP-01A-11D-A117-09","TCGA-AN-A0XP-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","6179b498-2cea-4f7a-82a8-b7ec71431ea8","6c4eee86-8839-4a74-a786-b37e7dd35b21","c.1719G>C","ENST00000258530","19/21",163,196,"G","ENSG00000136044","ENST00000258530","missense_variant","missense_variant","1945/3239","1719/1995","573/664","K/N","aaG/aaC"]
["TTN",7273,"WUGSC","GRCh38","chr2",178728122,178728122,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-E2-A158-01A-11D-A12B-09","TCGA-E2-A158-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","5517dcca-46e7-4d0c-ba4f-193343f590d6","671469b6-2cc7-4236-95d3-3e3f73e08ea3","c.18751T>G","ENST00000591111","65/313",156,150,"C","ENSG00000155657","ENST00000591111","missense_variant","missense_variant","18976/104301","18751/103053","6251/34350","L/V","Tta/Gta"]
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["DRGX",644168,"WUGSC","GRCh38","chr10",49391239,49391239,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-A1-A0SH-01A-11D-A099-09","TCGA-A1-A0SH-10A-03D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","473d6ae4-162a-4136-b44f-fad42529a31a","7df4bbf4-7ac5-4fd3-b0b9-ca6e49674cfd","c.57C>G","ENST00000374139",42772,76,62,"C","ENSG00000165606","ENST00000374139","missense_variant","missense_variant","68/2738","57/792","19/263","H/Q","caC/caG"]
["DHRS13",147015,"WUGSC","GRCh38","chr17",28898584,28898584,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A1-A0SH-01A-11D-A099-09","TCGA-A1-A0SH-10A-03D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","473d6ae4-162a-4136-b44f-fad42529a31a","7df4bbf4-7ac5-4fd3-b0b9-ca6e49674cfd","c.991G>C","ENST00000378895",42860,65,58,"G","ENSG00000167536","ENST00000378895","missense_variant","missense_variant","1118/1921","991/1134","331/377","E/Q","Gag/Cag"]
["SH3TC1",54436,"WUGSC","GRCh38","chr4",8219519,8219519,"+","Silent","SNP","C","C","A","novel",null,"TCGA-WT-AB44-01A-11D-A41F-09","TCGA-WT-AB44-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","74482437-8aa2-4731-88f2-499e2addb5d3","925ac60b-fdc8-4990-a4ee-57738b4cbb76","c.1101C>A","ENST00000245105",42996,244,177,"A","ENSG00000125089","ENST00000245105","synonymous_variant","synonymous_variant","1168/4226","1101/4011","367/1336","G","ggC/ggA"]
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["IKBKE",9641,"WUGSC","GRCh38","chr1",206480448,206480448,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-S3-AA15-01A-11D-A41F-09","TCGA-S3-AA15-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","227a0e1c-9c7b-4262-b726-fef4a5518ffe","a50130ee-07df-4bb2-9d20-162ed9fe2f49","c.1342G>A","ENST00000581977","13/22",30,59,"A","ENSG00000263528","ENST00000581977","missense_variant","missense_variant;splice_region_variant","1668/3221","1342/2151","448/716","E/K","Gag/Aag"]
["BRE",9577,"WUGSC","GRCh38","chr2",27894617,27894617,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A1JG-01B-11D-A13L-09","TCGA-D8-A1JG-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","0b15c6f7-8e3e-48ad-a4a2-97d2ada56c44","56cc7ef4-ecf0-41d0-a692-88b352939918","c.61G>A","ENST00000342045",42807,173,105,"A","ENSG00000158019","ENST00000342045","missense_variant","missense_variant","202/1681","61/1152","21/383","V/M","Gtg/Atg"]
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["XKR4",114786,"WUGSC","GRCh38","chr8",55454933,55454933,"+","Intron","SNP","G","G","T","novel",null,"TCGA-BH-A18L-01A-32D-A12B-09","TCGA-BH-A18L-11A-42D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","883cd3c9-2681-4822-8b22-29149a027514","dc231f7a-c0b8-4639-9885-06ec9a0405a0","c.1007-68348G>T","ENST00000327381",null,232,133,"T","ENSG00000206579","ENST00000327381","intron_variant","intron_variant","-/19880","-/1953","-/650"]
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["CEP44",80817,"WUGSC","GRCh38","chr4",174303813,174303813,"+","Silent","SNP","G","G","C",null,null,"TCGA-E9-A22B-01A-11D-A159-09","TCGA-E9-A22B-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","e46a5d19-2dd7-4c34-8fff-6276278c58b3","f948182a-f814-4e3c-83ee-82b78aa423c1","c.348G>C","ENST00000296519",42804,91,102,"C","ENSG00000164118","ENST00000296519","synonymous_variant","synonymous_variant","400/4173","348/1173","116/390","V","gtG/gtC"]
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["BNC2",54796,"WUGSC","GRCh38","chr9",16419371,16419371,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-AR-A0TT-01A-31D-A099-09","TCGA-AR-A0TT-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","29cfdc11-2f20-436e-8913-340909684c06","cbcfa0ba-0d96-4484-913a-c9079d24690d","c.2918G>A","ENST00000380672",42923,165,129,"T","ENSG00000173068","ENST00000380672","missense_variant","missense_variant","2976/12844","2918/3300","973/1099","S/N","aGt/aAt"]
["TP53",7157,"WUGSC","GRCh38","chr17",7674945,7674945,"+","Nonsense_Mutation","SNP","G","G","A","rs397516435","byCluster","TCGA-B6-A0RU-01A-11D-A099-09","TCGA-B6-A0RU-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","251371ac-ef46-4e11-b45e-a2aaa986a2d2","5a22cccd-1c8a-425c-bc7c-3043bf4d8d15","c.586C>T","ENST00000269305",42897,109,146,"A","ENSG00000141510","ENST00000269305","stop_gained","stop_gained","776/2579","586/1182","196/393","R/*","Cga/Tga"]
["FAM200A",221786,"WUGSC","GRCh38","chr7",99547649,99547649,"+","Missense_Mutation","SNP","A","A","C","novel",null,"TCGA-AC-A8OP-01A-11D-A36J-09","TCGA-AC-A8OP-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","115a26e2-23e0-435c-9fa1-9b8df49e7ffe","6a367098-6007-413f-b4ad-d1aa2acbdf0e","c.759T>G","ENST00000449309",42768,68,92,"C","ENSG00000221909","ENST00000449309","missense_variant","missense_variant","1139/2480","759/1722","253/573","I/M","atT/atG"]
["FNIP1",96459,"WUGSC","GRCh38","chr5",131710616,131710616,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AR-A1AQ-01A-11D-A12Q-09","TCGA-AR-A1AQ-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","88ff7728-ecc9-4ec5-817e-4793619ab5a4","3f1960e3-339f-42e6-a925-fa21d1d6e2a5","c.668G>T","ENST00000510461",42934,74,95,"A","ENSG00000217128","ENST00000510461","missense_variant","missense_variant","764/3845","668/3501","223/1166","G/V","gGt/gTt"]
["CCDC120",90060,"WUGSC","GRCh38","chrX",49065579,49065579,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-OL-A97C-01A-32D-A41F-09","TCGA-OL-A97C-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1bef6c28-e4ab-4abe-8060-434dd9a850b4","30f5cf58-3a70-4f3e-9806-6022ad9653d7","c.808C>A","ENST00000496529",42957,194,176,"A","ENSG00000147144","ENST00000496529","missense_variant","missense_variant","1103/2415","808/1893","270/630","L/I","Ctt/Att"]
["SEMA4F",10505,"WUGSC","GRCh38","chr2",74675371,74675371,"+","Silent","SNP","C","C","G","rs752008980",null,"TCGA-A8-A075-01A-11D-A099-09","TCGA-A8-A075-10B-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","085dd125-1f95-46aa-a480-2965090e8591","d67faef9-d467-4476-bbe9-181225c15e7b","c.1359C>G","ENST00000357877",43022,111,84,"G","ENSG00000135622","ENST00000357877","synonymous_variant","synonymous_variant","1508/4312","1359/2313","453/770","L","ctC/ctG"]
["KLF15",28999,"WUGSC","GRCh38","chr3",126352867,126352867,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-E2-A56Z-01A-12D-A29N-09","TCGA-E2-A56Z-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","da5821cd-8653-41e5-b2ee-d60e2e541f2f","fd447987-24d9-46ec-8f43-5525d8f42fde","c.56T>C","ENST00000296233",42769,14,44,"G","ENSG00000163884","ENST00000296233","missense_variant","missense_variant","287/2574","56/1251","19/416","V/A","gTt/gCt"]
["FER1L4",80307,"WUGSC","GRCh38","chr20",35583218,35583218,"+","RNA","SNP","T","T","C",null,null,"TCGA-A2-A3KD-01A-12D-A20S-09","TCGA-A2-A3KD-10A-01D-A20S-09",null,null,"Somatic","Illumina HiSeq 2000","37ddccc5-9ff1-4733-a5a9-595bba074e54","4d1c9503-ba24-449f-8f5c-8eb3a54067a1","n.2992A>G","ENST00000430275","24/26",33,33,"C","ENSG00000088340","ENST00000430275","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","2992/3281"]
["MEGF8",1954,"WUGSC","GRCh38","chr19",42371462,42371462,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-AR-A24X-01A-11D-A167-09","TCGA-AR-A24X-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","53d55f5a-df86-44d7-a3a2-2dccc2557b7b","68357e67-adff-4cd3-a458-c6ed719032d2","c.7249C>T","ENST00000251268","41/42",23,25,"T","ENSG00000105429","ENST00000251268","stop_gained","stop_gained","7249/9549","7249/8538","2417/2845","R/*","Cga/Tga"]
["ZNF468",90333,"WUGSC","GRCh38","chr19",52841314,52841314,"+","Missense_Mutation","SNP","T","T","C","novel",null,"TCGA-UU-A93S-01A-21D-A41F-09","TCGA-UU-A93S-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6a917da8-aaa0-4c7a-9433-30f00a3d5311","2d4e6b65-036a-42bc-950b-d6ddb1218271","c.980A>G","ENST00000595646",42829,49,95,"C","ENSG00000204604","ENST00000595646","missense_variant","missense_variant","1101/4407","980/1569","327/522","Y/C","tAc/tGc"]
["URB1",9875,"WUGSC","GRCh38","chr21",32393307,32393307,"+","5'Flank","SNP","G","G","C",null,null,"TCGA-E2-A15E-01A-11D-A12B-09","TCGA-E2-A15E-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","c6f107df-1186-4d6d-b5b5-2393e9369dd1","1cdbe17e-c0ed-45a4-b4bb-6464cfb60817",null,"ENST00000382751",null,67,105,"C","ENSG00000142207","ENST00000382751","upstream_gene_variant","upstream_gene_variant","-/10832","-/6816","-/2271"]
["SCN2A",6326,"WUGSC","GRCh38","chr2",165367226,165367226,"+","Missense_Mutation","SNP","G","G","A","rs773202451",null,"TCGA-D8-A27T-01A-11D-A16D-09","TCGA-D8-A27T-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","ecabcc6a-2767-4ad8-ac4f-54cc3d081b6e","bb595689-dcda-48af-b114-e0fe28c3d794","c.3530G>A","ENST00000283256","19/27",76,97,"A","ENSG00000136531","ENST00000283256","missense_variant","missense_variant","3686/8660","3530/6018","1177/2005","R/Q","cGg/cAg"]
["NES",10763,"WUGSC","GRCh38","chr1",156670507,156670507,"+","Silent","SNP","C","C","A",null,null,"TCGA-BH-A18P-01A-11D-A12B-09","TCGA-BH-A18P-11A-43D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","add624a3-57e9-46be-9bcc-3e53d7c2dfb7","5cae8dca-b28a-4483-9c03-6f0645161c04","c.3681G>T","ENST00000368223",42829,68,46,"A","ENSG00000132688","ENST00000368223","synonymous_variant","synonymous_variant","3814/5558","3681/4866","1227/1621","P","ccG/ccT"]
["SH2D3C",10044,"WUGSC","GRCh38","chr9",127778727,127778727,"+","5'UTR","SNP","C","C","G","novel",null,"TCGA-BH-A18P-01A-11D-A12B-09","TCGA-BH-A18P-11A-43D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","add624a3-57e9-46be-9bcc-3e53d7c2dfb7","5cae8dca-b28a-4483-9c03-6f0645161c04","c.-100G>C","ENST00000314830",42747,272,169,"G","ENSG00000095370","ENST00000314830","5_prime_UTR_variant","5_prime_UTR_variant","15/3124","-/2583","-/860"]
["SLC39A5",283375,"WUGSC","GRCh38","chr12",56232780,56232780,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A18P-01A-11D-A12B-09","TCGA-BH-A18P-11A-43D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","add624a3-57e9-46be-9bcc-3e53d7c2dfb7","5cae8dca-b28a-4483-9c03-6f0645161c04","c.379C>T","ENST00000266980",42805,119,86,"T","ENSG00000139540","ENST00000266980","missense_variant","missense_variant","672/2031","379/1623","127/540","H/Y","Cac/Tac"]
["ST6GALNAC1",55808,"WUGSC","GRCh38","chr17",76627479,76627479,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-BH-A18P-01A-11D-A12B-09","TCGA-BH-A18P-11A-43D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","add624a3-57e9-46be-9bcc-3e53d7c2dfb7","5cae8dca-b28a-4483-9c03-6f0645161c04","c.936G>C","ENST00000156626",42803,145,157,"G","ENSG00000070526","ENST00000156626","missense_variant","missense_variant","1136/2570","936/1803","312/600","Q/H","caG/caC"]
["YIPF6",286451,"WUGSC","GRCh38","chrX",68522770,68522770,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-BH-A18P-01A-11D-A12B-09","TCGA-BH-A18P-11A-43D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","add624a3-57e9-46be-9bcc-3e53d7c2dfb7","5cae8dca-b28a-4483-9c03-6f0645161c04","c.445C>G","ENST00000462683",42893,598,565,"G","ENSG00000181704","ENST00000462683","missense_variant","missense_variant","1189/6741","445/711","149/236","Q/E","Cag/Gag"]
["ME3",10873,"WUGSC","GRCh38","chr11",86449939,86449939,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-C8-A12Q-01A-11D-A10Y-09","TCGA-C8-A12Q-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","b6b4af38-7ebb-4fa8-9876-6d88d2b1e7e4","c393110b-afe2-4838-bc8f-998ca23058d9","c.1081G>A","ENST00000393324",42992,296,185,"T","ENSG00000151376","ENST00000393324","missense_variant","missense_variant","1335/2240","1081/1815","361/604","E/K","Gag/Aag"]
["ABCA13",154664,"WUGSC","GRCh38","chr7",48528337,48528337,"+","Silent","SNP","T","T","A",null,null,"TCGA-B6-A0IB-01A-11W-A050-09","TCGA-B6-A0IB-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","ff80d5cd-7aed-499f-a472-153cc40f65de","0caeac20-293e-4c97-8074-3f9d78e5ef3e","c.14346T>A","ENST00000435803","55/62",356,218,"A","ENSG00000179869","ENST00000435803","synonymous_variant","synonymous_variant","14370/17184","14346/15177","4782/5058","T","acT/acA"]
["RASAL2",9462,"WUGSC","GRCh38","chr1",178466094,178466094,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A0BP-01A-11D-A10Y-09","TCGA-BH-A0BP-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","51405cf1-e844-4316-be17-85e8ad1de4a3","f1b6fe69-8f67-4fc8-8650-664ab02d7cfb","c.3139G>T","ENST00000462775","14/16",107,99,"T","ENSG00000075391","ENST00000462775","missense_variant","missense_variant","3264/14453","3139/3420","1047/1139","D/Y","Gat/Tat"]
["OR8H2",390151,"WUGSC","GRCh38","chr11",56105365,56105365,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A0BP-01A-11D-A10Y-09","TCGA-BH-A0BP-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","51405cf1-e844-4316-be17-85e8ad1de4a3","f1b6fe69-8f67-4fc8-8650-664ab02d7cfb","c.323G>T","ENST00000313503",42736,325,388,"T","ENSG00000181767","ENST00000313503","missense_variant","missense_variant","323/939","323/939","108/312","G/V","gGt/gTt"]
["CPZ",8532,"WUGSC","GRCh38","chr4",8618468,8618468,"+","Missense_Mutation","SNP","G","G","A","rs138232433","byCluster","TCGA-AR-A0U1-01A-11D-A10Y-09","TCGA-AR-A0U1-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","265ceec6-e9a8-499e-adf6-0c18c598532e","30329e31-a2b2-4c2e-8291-f775e3c9fa14","c.1543G>A","ENST00000360986",43019,80,46,"A","ENSG00000109625","ENST00000360986","missense_variant","missense_variant","1717/2267","1543/1959","515/652","G/S","Ggc/Agc"]
["RP11-1220K2.2",93432,"WUGSC","GRCh38","chr7",142196281,142196281,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-A2-A0T6-01A-11D-A099-09","TCGA-A2-A0T6-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","e4dcb280-c309-4ebb-a58d-e6389a0306ee","f0f5e37a-90f7-4800-b7d2-a514e8be3a13","c.4474A>G","ENST00000477922","38/48",9,18,"G","ENSG00000257743","ENST00000477922","missense_variant","missense_variant","4528/7867","4474/7548","1492/2515","I/V","Atc/Gtc"]
["EIF2AK4",440275,"WUGSC","GRCh38","chr15",39939596,39939596,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A7-A6VV-01A-22D-A33E-09","TCGA-A7-A6VV-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","c4a8a1c2-c84f-42c8-a107-9af40023dca0","d356f157-7990-43c8-8348-56038d3590a9","c.236G>A","ENST00000263791",14277,49,80,"A","ENSG00000128829","ENST00000263791","missense_variant","missense_variant","279/5499","236/4950","79/1649","C/Y","tGc/tAc"]
["FAT1",2195,"WUGSC","GRCh38","chr4",186620360,186620360,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A7-A0CE-01A-11W-A019-09","TCGA-A7-A0CE-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","e8c1bd4a-69aa-4496-96d0-d580d1ccc04c","40f1c52b-2063-4541-8600-865735b708b0","c.6226G>A","ENST00000441802",43035,356,675,"T","ENSG00000083857","ENST00000441802","missense_variant","missense_variant","6436/14786","6226/13767","2076/4588","D/N","Gat/Aat"]
["MTR",4548,"WUGSC","GRCh38","chr1",236838425,236838425,"+","Silent","SNP","C","C","T","novel",null,"TCGA-A8-A09I-01A-22W-A050-09","TCGA-A8-A09I-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","96d5070d-1fa9-4fa5-b2c9-472240dfd3b9","ac8bb292-dad8-4f5b-b9d1-8c7aeb24bbac","c.1341C>T","ENST00000366577","15/33",189,180,"T","ENSG00000116984","ENST00000366577","synonymous_variant","synonymous_variant","1735/10529","1341/3798","447/1265","C","tgC/tgT"]
["NCOR1",9611,"WUGSC","GRCh38","chr17",16072217,16072217,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-A8-A09I-01A-22W-A050-09","TCGA-A8-A09I-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","96d5070d-1fa9-4fa5-b2c9-472240dfd3b9","ac8bb292-dad8-4f5b-b9d1-8c7aeb24bbac","c.3823C>T","ENST00000268712","29/46",47,76,"A","ENSG00000141027","ENST00000268712","stop_gained","stop_gained","4081/10720","3823/7323","1275/2440","R/*","Cga/Tga"]
["CHTF18",63922,"WUGSC","GRCh38","chr16",795995,795995,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-BH-AB28-01A-31D-A41F-09","TCGA-BH-AB28-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","79234fb0-ea9d-45ac-9b43-a75462cabd94","53ce37b0-ad1e-4f47-9832-f7a6f5ad664b","c.2374C>A","ENST00000262315","18/22",36,17,"A","ENSG00000127586","ENST00000262315","missense_variant","missense_variant","2437/3090","2374/2928","792/975","L/M","Ctg/Atg"]
["PSMD14",10213,"WUGSC","GRCh38","chr2",161318840,161318840,"+","Silent","SNP","T","T","G",null,null,"TCGA-AN-A04A-01A-21W-A050-09","TCGA-AN-A04A-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","7e8f250c-6162-4049-8559-5bfdf054b021","2761c6e7-affc-4ffe-a72a-1d1203d574c4","c.15T>G","ENST00000409682",42806,321,508,"G","ENSG00000115233","ENST00000409682","synonymous_variant","synonymous_variant","719/1954","15/933","5/310","L","ctT/ctG"]
["DNAH6",1768,"WUGSC","GRCh38","chr2",84557786,84557786,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0DT-01A-21D-A12B-09","TCGA-BH-A0DT-11A-12D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","30dbe353-86d5-40ed-84c2-dbddf7beb17b","03c623e2-04d7-43ea-ade1-5f5a619cd5c8","c.1654C>T","ENST00000237449",28034,208,300,"T","ENSG00000115423","ENST00000237449","missense_variant","missense_variant","1662/12666","1654/12477","552/4158","P/S","Cct/Tct"]
["SLC2A4RG",56731,"WUGSC","GRCh38","chr20",63741891,63741891,"+","Silent","SNP","G","G","A",null,null,"TCGA-E9-A1N3-01A-12D-A159-09","TCGA-E9-A1N3-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","6c3891a9-baa9-4309-9974-d82fd5f97417","dbbc85cd-811a-4d6a-b515-3ea1f6f01ea5","c.414G>A","ENST00000266077",42833,13,11,"A","ENSG00000125520","ENST00000266077","synonymous_variant","synonymous_variant","466/1731","414/1164","138/387","K","aaG/aaA"]
["MYO1E",4643,"WUGSC","GRCh38","chr15",59231742,59231742,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-E2-A1LB-01A-11D-A142-09","TCGA-E2-A1LB-11A-22D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","377b1816-61e1-431a-9952-71e4d58bbd48","f159d3d3-831d-47ee-8fb0-7665405a5581","c.470G>T","ENST00000288235",42914,62,47,"A","ENSG00000157483","ENST00000288235","missense_variant","missense_variant","870/8673","470/3327","157/1108","G/V","gGg/gTg"]
["CWF19L2",143884,"WUGSC","GRCh38","chr11",107428935,107428935,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-A2-A3XZ-01A-42D-A23C-09","TCGA-A2-A3XZ-10A-01D-A23C-09",null,null,"Somatic","Illumina HiSeq 2000","e8c2a05d-7caa-4362-9be1-17ac4bbeb721","7bcc1bd0-f9a3-4d1c-ba0d-1cc038653aae","c.1297C>G","ENST00000282251",42965,142,216,"C","ENSG00000152404","ENST00000282251","missense_variant","missense_variant","1325/3278","1297/2685","433/894","Q/E","Caa/Gaa"]
["BRS3",680,"WUGSC","GRCh38","chrX",136492276,136492276,"+","Silent","SNP","G","G","A",null,null,"TCGA-E2-A15G-01A-11D-A12B-09","TCGA-E2-A15G-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","d45bb60a-e73b-4b95-8637-e8d17fcca745","9b5d1a2f-ccca-45de-b995-85754015b39c","c.1101G>A","ENST00000370648",42797,162,168,"A","ENSG00000102239","ENST00000370648","synonymous_variant","synonymous_variant","1329/2833","1101/1200","367/399","V","gtG/gtA"]
["BNC1",646,"WUGSC","GRCh38","chr15",83264504,83264504,"+","Silent","SNP","G","G","A",null,null,"TCGA-C8-A275-01A-21D-A16D-09","TCGA-C8-A275-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","7751a837-2656-4e3b-9182-556314c4f6a3","8775eb88-4ca6-43b1-b4c1-00767ac1b3de","c.747C>T","ENST00000345382",42830,47,61,"A","ENSG00000169594","ENST00000345382","synonymous_variant","synonymous_variant","833/4610","747/2985","249/994","F","ttC/ttT"]
["SEPT1",1731,"WUGSC","GRCh38","chr16",30381464,30381464,"+","Silent","SNP","C","C","A",null,null,"TCGA-E2-A1AZ-01A-11D-A12Q-09","TCGA-E2-A1AZ-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","f961c932-cf37-47c8-8520-8d0d444dc94f","d486a6d4-f7b9-4df1-b14f-df434c457363","c.456G>T","ENST00000321367",42898,155,122,"A","ENSG00000180096","ENST00000321367","synonymous_variant","synonymous_variant","502/1592","456/1245","152/414","P","ccG/ccT"]
["RICTOR",253260,"WUGSC","GRCh38","chr5",38952257,38952257,"+","Silent","SNP","T","T","C",null,null,"TCGA-BH-A0HL-01A-11W-A050-09","TCGA-BH-A0HL-10A-11W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","1fd1db26-79e0-4018-8548-8fd20a96c479","f3a79920-cdfb-4dc7-b10b-9c143fd3d274","c.3066A>G","ENST00000357387","30/38",116,118,"C","ENSG00000164327","ENST00000357387","synonymous_variant","synonymous_variant","3097/9543","3066/5127","1022/1708","L","ctA/ctG"]
["POLQ",10721,"WUGSC","GRCh38","chr3",121488168,121488168,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0AY-01A-21W-A019-09","TCGA-BH-A0AY-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","16ae1ccf-0a1e-4a67-9cbe-d0746ee68dac","635d1b45-ef87-457e-9ea9-bd97f6ee70c0","c.4763C>T","ENST00000264233","16/30",328,420,"A","ENSG00000051341","ENST00000264233","missense_variant","missense_variant","4892/8775","4763/7773","1588/2590","P/L","cCt/cTt"]
["NSD1",64324,"WUGSC","GRCh38","chr5",177210363,177210363,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A7-A26G-01A-21D-A167-09","TCGA-A7-A26G-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","36d1a85e-a09b-4537-86e0-eaf1eb03aed8","5f0452c9-2310-4118-b895-cf8aa79f1ccf","c.1964G>A","ENST00000439151",42878,47,42,"A","ENSG00000165671","ENST00000439151","missense_variant","missense_variant","2009/12892","1964/8091","655/2696","S/N","aGc/aAc"]
["SDK2",54549,"WUGSC","GRCh38","chr17",73379209,73379209,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-A7-A26E-01A-11D-A272-09","TCGA-A7-A26E-10A-01D-A272-09",null,null,"Somatic","Illumina HiSeq 2000","a2bbb02b-3046-4633-9b5c-6ff4222a10d8","d2ed0f51-2c5c-44b5-97a2-b3e83b1467ed","c.4948G>T","ENST00000392650","36/45",93,84,"A","ENSG00000069188","ENST00000392650","missense_variant","missense_variant","4949/10723","4948/6519","1650/2172","D/Y","Gac/Tac"]
["NRF1",4899,"WUGSC","GRCh38","chr7",129657413,129657413,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A0XN-01A-21D-A10G-09","TCGA-AN-A0XN-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","94a6c172-25e2-4438-945c-9b310f89ae22","b840005e-ca83-4444-ad1d-e3e263ae4fed","c.62C>T","ENST00000223190",42777,76,95,"T","ENSG00000106459","ENST00000223190","missense_variant","missense_variant","140/2424","62/1512","21/503","A/V","gCc/gTc"]
["MYH9",4627,"WUGSC","GRCh38","chr22",36293822,36293822,"+","Silent","SNP","G","G","A",null,null,"TCGA-AN-A0XN-01A-21D-A10G-09","TCGA-AN-A0XN-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","94a6c172-25e2-4438-945c-9b310f89ae22","b840005e-ca83-4444-ad1d-e3e263ae4fed","c.3879C>T","ENST00000216181","29/41",50,83,"A","ENSG00000100345","ENST00000216181","synonymous_variant","synonymous_variant","4110/7501","3879/5883","1293/1960","D","gaC/gaT"]
["PEG3",5178,"WUGSC","GRCh38","chr19",56817537,56817537,"+","Missense_Mutation","SNP","C","C","T","rs549894601","by1000G","TCGA-D8-A1XR-01A-11D-A14K-09","TCGA-D8-A1XR-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","5913c8ff-26ce-4f26-909e-3ed292d3c538","596c1603-ee4c-4f54-9641-27a67edf30a4","c.905G>A","ENST00000326441",43018,28,44,"T","ENSG00000198300","ENST00000326441","missense_variant","missense_variant","1269/8723","905/4767","302/1588","R/Q","cGg/cAg"]
["FMO5",2330,"WUGSC","GRCh38","chr1",147212445,147212445,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-A8-A07F-01A-11W-A019-09","TCGA-A8-A07F-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","73d907e6-4ba0-431f-a009-8366644ffaf0","5281a45b-e0b8-404f-ae25-91cd7ae5bf30","c.578T>A","ENST00000254090",42864,389,137,"T","ENSG00000131781","ENST00000254090","missense_variant","missense_variant","967/2632","578/1602","193/533","I/N","aTt/aAt"]
["TDRD1",56165,"WUGSC","GRCh38","chr10",114204738,114204738,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-A2-A04P-01A-31D-A128-09","TCGA-A2-A04P-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","a85cf239-ff51-46e7-9b88-4c2cb49c66b9","aaef2ada-b81d-4e89-8add-a571603d67bb","c.1142T>C","ENST00000251864",43034,131,123,"C","ENSG00000095627","ENST00000251864","missense_variant","missense_variant","1295/4510","1142/3570","381/1189","V/A","gTa/gCa"]
["IL1RAPL1",11141,"WUGSC","GRCh38","chrX",29955817,29955817,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A04P-01A-31D-A128-09","TCGA-A2-A04P-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","a85cf239-ff51-46e7-9b88-4c2cb49c66b9","aaef2ada-b81d-4e89-8add-a571603d67bb","c.2088G>T","ENST00000378993",43050,52,49,"T","ENSG00000169306","ENST00000378993","missense_variant","missense_variant","2761/3667","2088/2091","696/696","W/C","tgG/tgT"]
["MYOM2",9172,"WUGSC","GRCh38","chr8",2106503,2106503,"+","Nonsense_Mutation","SNP","C","C","G",null,null,"TCGA-AR-A251-01A-12D-A167-09","TCGA-AR-A251-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","68b4de6d-352d-44e8-911a-f4541f28fc78","59a8266d-0a43-4abf-bfe8-2c90002cf0bd","c.2904C>G","ENST00000262113","23/37",53,81,"G","ENSG00000036448","ENST00000262113","stop_gained","stop_gained","3045/5014","2904/4398","968/1465","Y/*","taC/taG"]
["DSE",29940,"WUGSC","GRCh38","chr6",116436266,116436266,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AO-A0JE-01A-11W-A071-09","TCGA-AO-A0JE-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","4f311714-ebb4-47fb-b471-62c6951d9066","f08265fa-cf7d-4d5b-a516-a319b0595cc1","c.1798G>C","ENST00000331677",42923,81,89,"C","ENSG00000111817","ENST00000331677","missense_variant","missense_variant","2242/7237","1798/2877","600/958","D/H","Gat/Cat"]
["NHS",4810,"WUGSC","GRCh38","chrX",17725941,17725941,"+","Missense_Mutation","SNP","C","C","T","rs745597127",null,"TCGA-AN-A0FS-01A-11W-A050-09","TCGA-AN-A0FS-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","9bb76d20-cefb-4f7a-80c2-aa2178e302a9","608d90c1-f205-43fa-a9cd-dcdf54bb927d","c.1772C>T","ENST00000380060",42894,79,135,"T","ENSG00000188158","ENST00000380060","missense_variant","missense_variant","2110/8761","1772/4893","591/1630","T/M","aCg/aTg"]
["PTPRQ",374462,"WUGSC","GRCh38","chr12",80534900,80534900,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-A2-A259-01A-11D-A16D-09","TCGA-A2-A259-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","93febb0a-587c-47f2-9a59-117f7aa475c5","492d903f-0464-44a3-8984-39b13c6fbcf7","c.2848G>C","ENST00000614701","19/45",71,65,"C","ENSG00000139304","ENST00000614701","missense_variant","missense_variant","3026/8289","2848/6900","950/2299","D/H","Gat/Cat"]
["TROVE2",6738,"WUGSC","GRCh38","chr1",193075900,193075900,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-C8-A8HP-01A-11D-A36J-09","TCGA-C8-A8HP-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","48431b7a-8d34-4d4d-ab64-ddbab7e8c866","359094ae-674f-4ef7-96f9-feab1a40573f","c.661G>C","ENST00000367441",42774,76,63,"C","ENSG00000116747","ENST00000367441","missense_variant","missense_variant","700/1791","661/1617","221/538","E/Q","Gag/Cag"]
["KCNQ3",3786,"WUGSC","GRCh38","chr8",132184277,132184277,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-C8-A8HP-01A-11D-A36J-09","TCGA-C8-A8HP-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","48431b7a-8d34-4d4d-ab64-ddbab7e8c866","359094ae-674f-4ef7-96f9-feab1a40573f","c.568C>T","ENST00000388996",42809,89,61,"A","ENSG00000184156","ENST00000388996","stop_gained","stop_gained","989/11441","568/2619","190/872","R/*","Cga/Tga"]
["HUWE1",10075,"WUGSC","GRCh38","chrX",53545072,53545072,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-C8-A8HP-01A-11D-A36J-09","TCGA-C8-A8HP-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","48431b7a-8d34-4d4d-ab64-ddbab7e8c866","359094ae-674f-4ef7-96f9-feab1a40573f","c.11005G>A","ENST00000262854","71/84",112,84,"T","ENSG00000086758","ENST00000262854","missense_variant","missense_variant","11408/14739","11005/13125","3669/4374","E/K","Gag/Aag"]
["FCAR",2204,"WUGSC","GRCh38","chr19",54885414,54885414,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A3W5-01A-11D-A228-09","TCGA-AC-A3W5-10A-01D-A22A-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina HiSeq 2500","21da489e-0eea-4cb5-9b50-98ce50c9a617","b7bae67a-42a2-4fe7-b469-ef0725971eed","c.250G>A","ENST00000355524",42799,52,47,"A","ENSG00000186431","ENST00000355524","missense_variant","missense_variant","260/1483","250/864","84/287","E/K","Gag/Aag"]
["TANC2",26115,"WUGSC","GRCh38","chr17",63314462,63314462,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-EW-A2FR-01A-11D-A21Q-09","TCGA-EW-A2FR-10A-01D-A21Q-09",null,null,"Somatic","Illumina HiSeq 2000","91439f81-e2ff-4d75-9fcc-aee49fc9c5aa","d5b0ec6a-964e-45ca-bfdd-31757e3dfeaf","c.1012G>C","ENST00000424789",42972,42,43,"C","ENSG00000170921","ENST00000424789","missense_variant","missense_variant","1016/11721","1012/5973","338/1990","E/Q","Gag/Cag"]
["GABRB2",2561,"WUGSC","GRCh38","chr5",161290060,161290060,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-A7-A4SE-01A-11D-A25Q-09","TCGA-A7-A4SE-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","0e477299-592b-4018-bd17-0c2a646c7672","15e93d8f-1db4-4cf1-99dd-81d3fd90a898","c.*4021G>T","ENST00000274547",43050,28,67,"A","ENSG00000145864","ENST00000274547","3_prime_UTR_variant","3_prime_UTR_variant","5778/7409","-/1539","-/512"]
["MBD2",8932,"WUGSC","GRCh38","chr18",54154825,54154825,"+","3'UTR","SNP","G","G","T","novel",null,"TCGA-A7-A4SE-01A-11D-A25Q-09","TCGA-A7-A4SE-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","0e477299-592b-4018-bd17-0c2a646c7672","15e93d8f-1db4-4cf1-99dd-81d3fd90a898","c.*499C>A","ENST00000256429",42923,30,56,"T","ENSG00000134046","ENST00000256429","3_prime_UTR_variant","3_prime_UTR_variant","1964/5188","-/1236","-/411"]
["LRFN4",78999,"WUGSC","GRCh38","chr11",66860147,66860147,"+","Nonsense_Mutation","SNP","C","C","A","novel",null,"TCGA-AC-A7VB-01A-11D-A351-09","TCGA-AC-A7VB-10A-01D-A351-09",null,null,"Somatic","Illumina HiSeq 2000","1390a2a2-b3c1-4289-91d2-2be43e2f1cab","02cc24bb-ae71-484e-b317-8ad89f4f6b36","c.1860C>A","ENST00000309602",42768,37,64,"A","ENSG00000173621","ENST00000309602","stop_gained","stop_gained","2103/2431","1860/1908","620/635","C/*","tgC/tgA"]
["RNF128",79589,"WUGSC","GRCh38","chrX",106694018,106694018,"+","Missense_Mutation","SNP","A","A","G","rs764287121",null,"TCGA-A8-A099-01A-11W-A019-09","TCGA-A8-A099-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","1066cb38-e051-42fa-a8bc-20b659c17a13","f683d650-e338-4347-a0a3-b7e28cb096f8","c.16A>G","ENST00000324342",42742,156,314,"G","ENSG00000133135","ENST00000324342","missense_variant","missense_variant","181/2654","16/1209","6/402","R/G","Agg/Ggg"]
["IL17RB",55540,"WUGSC","GRCh38","chr3",53865261,53865261,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-C8-A12L-01A-11D-A10Y-09","TCGA-C8-A12L-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","998a465a-d084-4d7f-8c02-8c5be1e1ee27","8fedd128-c3e3-451c-8a22-fc76a2e8103e","c.1462G>A","ENST00000288167",43050,59,63,"A","ENSG00000056736","ENST00000288167","missense_variant","missense_variant","1471/2010","1462/1509","488/502","A/T","Gca/Aca"]
["RP11-571M6.15",0,"WUGSC","GRCh38","chr12",57783202,57783202,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A7-A5ZW-01A-12D-A29N-09","TCGA-A7-A5ZW-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","625e623d-6b89-4f8d-8b99-21e8d3178b73","3e7894de-ba96-4306-844b-f675ef3f4566","c.169C>T","ENST00000546504",42770,25,27,"T","ENSG00000257921","ENST00000546504","missense_variant","missense_variant","169/373","169/373","57/124","H/Y","Cat/Tat"]
["CREBRF",153222,"WUGSC","GRCh38","chr5",173090550,173090550,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E2-A155-01A-11D-A12B-09","TCGA-E2-A155-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","a966904f-e8dd-473c-8626-84c25d7e0d6c","ff422b83-8a29-41b3-8e73-2909fe3521da","c.371C>G","ENST00000296953",42834,247,196,"G","ENSG00000164463","ENST00000296953","missense_variant","missense_variant","690/7778","371/1920","124/639","S/C","tCt/tGt"]
["MTOR",2475,"WUGSC","GRCh38","chr1",11114874,11114874,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E9-A54Y-01A-11D-A25Q-09","TCGA-E9-A54Y-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","fafdb0f0-8793-4fa5-aad9-7edb0fe378a3","dd45289a-3543-448a-ad91-b35d282448f5","c.7103G>A","ENST00000361445","52/58",32,45,"T","ENSG00000198793","ENST00000361445","missense_variant","missense_variant","7180/8677","7103/7650","2368/2549","R/Q","cGa/cAa"]
["CHRNB3",1142,"WUGSC","GRCh38","chr8",42708780,42708780,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A2JS-01A-11D-A17W-09","TCGA-E9-A2JS-10A-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","ca32f508-7c87-4747-b6d5-e27e3f28b211","d8eec44c-d3a2-4ba6-9fa7-a36a9fc338bd","c.116G>T","ENST00000289957",42772,256,112,"T","ENSG00000147432","ENST00000289957","missense_variant","missense_variant","244/2294","116/1377","39/458","G/V","gGt/gTt"]
["IMP4",92856,"WUGSC","GRCh38","chr2",130346270,130346270,"+","Silent","SNP","G","G","A",null,null,"TCGA-Z7-A8R6-01A-11D-A41F-09","TCGA-Z7-A8R6-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","1d60d16a-5dc4-4cc9-9d63-ef6e40dcc5a9","2277fdd6-120a-4272-a5cb-7b61ae0f568f","c.759G>A","ENST00000259239",42956,51,17,"A","ENSG00000136718","ENST00000259239","synonymous_variant","synonymous_variant","1467/1740","759/876","253/291","L","ctG/ctA"]
["FAM135A",57579,"WUGSC","GRCh38","chr6",70477231,70477231,"+","Silent","SNP","C","C","A",null,null,"TCGA-AO-A0JB-01A-11W-A071-09","TCGA-AO-A0JB-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","8f4f06be-2a16-4ae2-9dd4-5d87f480810b","f51b5a75-a541-4589-b883-7f651a2612c9","c.441C>A","ENST00000370479",42906,117,65,"A","ENSG00000082269","ENST00000370479","synonymous_variant","synonymous_variant","574/5930","441/4548","147/1515","G","ggC/ggA"]
["PDZRN4",29951,"WUGSC","GRCh38","chr12",41572744,41572744,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-E9-A295-01A-11D-A16D-09","TCGA-E9-A295-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","f3d5e986-046f-4f75-8abc-67a3b99f742d","cd761feb-9a20-4495-8943-c6243532a5cf","c.1965T>A","ENST00000402685",43018,54,49,"A","ENSG00000165966","ENST00000402685","missense_variant","missense_variant","1973/3347","1965/3111","655/1036","N/K","aaT/aaA"]
["NAT16",375607,"WUGSC","GRCh38","chr7",101174428,101174428,"+","Intron","SNP","C","C","T","novel",null,"TCGA-AO-A0J9-01A-11W-A050-09","TCGA-AO-A0J9-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","9932232f-a7b0-4962-9b14-adb8316a4661","635a03b8-f873-4ec7-bb1d-82dbcc6cb02a","c.312+68G>A","ENST00000300303",null,66,16,"T","ENSG00000167011","ENST00000300303","intron_variant","intron_variant","-/2935","-/1110","-/369"]
["PRR14L",253143,"WUGSC","GRCh38","chr22",31715834,31715834,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AO-A0J9-01A-11W-A050-09","TCGA-AO-A0J9-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","9932232f-a7b0-4962-9b14-adb8316a4661","635a03b8-f873-4ec7-bb1d-82dbcc6cb02a","c.2005G>A","ENST00000327423",42834,155,187,"T","ENSG00000183530","ENST00000327423","missense_variant","missense_variant","2195/10826","2005/6456","669/2151","D/N","Gac/Aac"]
["CALCRL",10203,"WUGSC","GRCh38","chr2",187345401,187345401,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-LL-A740-01A-21D-A32I-09","TCGA-LL-A740-10B-01D-A32I-09",null,null,"Somatic","Illumina HiSeq 2000","b3e4fee3-8e7e-47fd-8278-abac0f13b82b","2724d919-0335-4e3f-aa30-439c28d4f214","c.*783G>T","ENST00000392370","15/15",93,130,"A","ENSG00000064989","ENST00000392370","3_prime_UTR_variant","3_prime_UTR_variant","2883/5155","-/1386","-/461"]
["TSPAN2",10100,"WUGSC","GRCh38","chr1",115057583,115057583,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A7-A6VY-01A-12D-A33E-09","TCGA-A7-A6VY-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","890d77cd-eefd-4711-ae9c-9716079bf3e9","5c6da671-b9a7-46a5-98fc-397ddfb2a1b2","c.470C>T","ENST00000369516",42894,75,50,"A","ENSG00000134198","ENST00000369516","missense_variant","missense_variant","502/3177","470/666","157/221","S/F","tCc/tTc"]
["MCMBP",79892,"WUGSC","GRCh38","chr10",119831523,119831523,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A7-A6VY-01A-12D-A33E-09","TCGA-A7-A6VY-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","890d77cd-eefd-4711-ae9c-9716079bf3e9","5c6da671-b9a7-46a5-98fc-397ddfb2a1b2","c.1880G>A","ENST00000360003","16/16",22,21,"T","ENSG00000197771","ENST00000360003","missense_variant","missense_variant","2050/4169","1880/1929","627/642","R/K","aGa/aAa"]
["ITGB3",3690,"WUGSC","GRCh38","chr17",47283418,47283418,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-A7-A6VY-01A-12D-A33E-09","TCGA-A7-A6VY-10A-01D-A33H-09",null,null,"Somatic","Illumina HiSeq 2000","890d77cd-eefd-4711-ae9c-9716079bf3e9","5c6da671-b9a7-46a5-98fc-397ddfb2a1b2","c.230C>A","ENST00000559488",42809,44,57,"A","ENSG00000259207","ENST00000559488","missense_variant","missense_variant","246/3995","230/2367","77/788","P/Q","cCa/cAa"]
["XKR4",114786,"WUGSC","GRCh38","chr8",55454873,55454873,"+","Intron","SNP","C","C","T","novel",null,"TCGA-BH-A18J-01A-11D-A12B-09","TCGA-BH-A18J-11A-31D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","fd9923db-2a27-432e-a0c6-4c44e6ee1f53","c5149cdb-2765-4c64-8f19-308562782032","c.1007-68408C>T","ENST00000327381",null,138,148,"T","ENSG00000206579","ENST00000327381","intron_variant","intron_variant","-/19880","-/1953","-/650"]
["BCO1",53630,"WUGSC","GRCh38","chr16",81270164,81270164,"+","Nonsense_Mutation","SNP","T","T","A",null,null,"TCGA-AR-A1AW-01A-21D-A12Q-09","TCGA-AR-A1AW-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","33c6b6b5-1484-4002-8f84-ba67525a8777","e93c2d61-5212-4796-8a2c-950db804fddf","c.849T>A","ENST00000258168",42927,101,113,"A","ENSG00000135697","ENST00000258168","stop_gained","stop_gained","1310/2670","849/1644","283/547","Y/*","taT/taA"]
["DAGLA",747,"WUGSC","GRCh38","chr11",61740544,61740544,"+","Silent","SNP","C","C","G",null,null,"TCGA-C8-A12Z-01A-11D-A10Y-09","TCGA-C8-A12Z-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","ae68cac5-e561-4094-98fa-2303cdaa6dbb","812e038c-91bd-4e32-bf6b-99922a18b5c0","c.1935C>G","ENST00000257215","18/20",40,89,"G","ENSG00000134780","ENST00000257215","synonymous_variant","synonymous_variant","2051/5757","1935/3129","645/1042","A","gcC/gcG"]
["CBLB",868,"WUGSC","GRCh38","chr3",105720244,105720244,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0B5-01A-11D-A12Q-09","TCGA-BH-A0B5-11A-23W-A14O-09",null,null,"Somatic","Illumina HiSeq 2000","dfa0f8ea-ae94-4673-9751-f6cdad26022a","74428f88-9ecb-427b-83a6-faee8ee09c24","c.1210G>A","ENST00000264122",43027,109,116,"T","ENSG00000114423","ENST00000264122","missense_variant","missense_variant","1532/6780","1210/2949","404/982","D/N","Gat/Aat"]
["ZFP36L1",677,"WUGSC","GRCh38","chr14",68790090,68790090,"+","Nonsense_Mutation","SNP","T","T","A",null,null,"TCGA-C8-A1HN-01A-11D-A135-09","TCGA-C8-A1HN-10A-01D-A135-09",null,null,"Somatic","Illumina Genome Analyzer II","a2576147-28eb-460f-9b97-916892d801e2","66a18ff8-0467-4423-aca0-0cbcec0e4513","c.460A>T","ENST00000336440",42769,58,137,"A","ENSG00000185650","ENST00000336440","stop_gained","stop_gained","2258/3026","460/1017","154/338","K/*","Aag/Tag"]
["TTR",7276,"WUGSC","GRCh38","chr18",31591848,31591848,"+","5'UTR","SNP","A","A","T","novel",null,"TCGA-B6-A40B-01A-11D-A23C-09","TCGA-B6-A40B-10A-01D-A23C-09",null,null,"Somatic","Illumina HiSeq 2500;Illumina HiSeq 2000","4879bc18-31b9-4cd6-967c-2891a1fd416e","dc05c74e-86e4-4b00-9824-a7c8c69acf7c","c.-55A>T","ENST00000237014",42739,72,74,"T","ENSG00000118271","ENST00000237014","5_prime_UTR_variant","5_prime_UTR_variant","123/957","-/444","-/147"]
["LOXL3",84695,"WUGSC","GRCh38","chr2",74550258,74550258,"+","Missense_Mutation","SNP","G","G","A","rs762811068",null,"TCGA-D8-A147-01A-11D-A10Y-09","TCGA-D8-A147-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","1f292323-cafc-4e45-bb4e-f5428e1a3276","4e55052d-a439-4da0-b799-29bd2d174444","c.404C>T","ENST00000264094",42808,53,63,"A","ENSG00000115318","ENST00000264094","missense_variant","missense_variant","476/3502","404/2262","135/753","T/M","aCg/aTg"]
["LPPR2",64748,"WUGSC","GRCh38","chr19",11357682,11357682,"+","Silent","SNP","A","A","G",null,null,"TCGA-D8-A147-01A-11D-A10Y-09","TCGA-D8-A147-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","1f292323-cafc-4e45-bb4e-f5428e1a3276","4e55052d-a439-4da0-b799-29bd2d174444","c.9A>G","ENST00000251473",42804,188,117,"G","ENSG00000105520","ENST00000251473","synonymous_variant","synonymous_variant","385/2727","9/1032","3/343","G","ggA/ggG"]
["ZNF655",79027,"WUGSC","GRCh38","chr7",99564175,99564175,"+","Intron","SNP","C","C","G","novel",null,"TCGA-AC-A8OS-01A-12D-A41F-09","TCGA-AC-A8OS-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","05613d4c-71c6-43da-80bf-81be30e6c3f3","d6d8c373-416e-480e-a446-2a195e105843","c.136+3480C>G","ENST00000252713",null,27,11,"G","ENSG00000197343","ENST00000252713","intron_variant","intron_variant","-/2535","-/1476","-/491"]
["CACNA1G",8913,"WUGSC","GRCh38","chr17",50607122,50607122,"+","Intron","SNP","G","G","A","novel",null,"TCGA-C8-A1HO-01A-11D-A13L-09","TCGA-C8-A1HO-10A-01D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","c6fb921c-78fe-4852-b2a5-edd5a02ae923","dd0c6efe-1e1d-4031-aaaa-6823475036af","c.4512+133G>A","ENST00000359106",null,115,38,"A","ENSG00000006283","ENST00000359106","intron_variant","intron_variant","-/7648","-/7134","-/2377"]
["ZNF536",9745,"WUGSC","GRCh38","chr19",30445603,30445603,"+","Nonsense_Mutation","SNP","C","C","T","novel",null,"TCGA-GM-A3XL-01A-11D-A22X-09","TCGA-GM-A3XL-10A-01D-A22X-09",null,null,"Somatic","Illumina HiSeq 2000","b27d75ba-5989-4200-bfe9-f1b7d7cf8008","90469bfb-140c-4856-be28-a9b04c183157","c.2041C>T","ENST00000355537",42771,76,51,"T","ENSG00000198597","ENST00000355537","stop_gained","stop_gained","2188/4945","2041/3903","681/1300","Q/*","Cag/Tag"]
["NUTM1",256646,"WUGSC","GRCh38","chr15",34348122,34348122,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A2-A04W-01A-31D-A10Y-09","TCGA-A2-A04W-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","7822a6b1-68c8-4675-993c-c4b54a510c09","62188c38-1f49-4f09-bd46-f60922cd3e4a","c.170C>T","ENST00000333756",42773,77,180,"T","ENSG00000184507","ENST00000333756","missense_variant","missense_variant","325/3795","170/3399","57/1132","P/L","cCa/cTa"]
["WISP3",8838,"WUGSC","GRCh38","chr6",112061144,112061144,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-B6-A0WX-01A-11D-A10G-09","TCGA-B6-A0WX-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","47b5d831-5287-4f62-b17a-6e5eff2e4184","57c92229-f196-429c-8c85-874e2906a3d4","c.202G>A","ENST00000230529",42800,157,176,"A","ENSG00000112761","ENST00000230529","missense_variant","missense_variant","312/1235","202/1065","68/354","V/M","Gtg/Atg"]
["WDR46",9277,"WUGSC","GRCh38","chr6",33280808,33280808,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A0YM-01A-11D-A10G-09","TCGA-A2-A0YM-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","1125ec93-6d24-4537-9c89-526f2d6b2299","1b5a4092-b33a-442c-808c-abbaf60d033c","c.1295C>T","ENST00000374617",43054,72,55,"A","ENSG00000227057","ENST00000374617","missense_variant","missense_variant","1652/2358","1295/1833","432/610","A/V","gCc/gTc"]
["EML6",400954,"WUGSC","GRCh38","chr2",54853758,54853758,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A7-A13D-01A-13D-A272-09","TCGA-A7-A13D-10A-02D-A272-09",null,null,"Somatic","Illumina HiSeq 2000","3e0f9b90-88f4-41f1-91b2-2f4bcdfaaebb","2fc0129f-0a1c-4f01-85a1-d447fc9d348b","c.1560C>G","ENST00000356458",15250,37,37,"G","ENSG00000214595","ENST00000356458","missense_variant","missense_variant","2080/8320","1560/5877","520/1958","D/E","gaC/gaG"]
["RFPL1",5988,"WUGSC","GRCh38","chr22",29441635,29441635,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A1AT-01A-11D-A12Q-09","TCGA-AR-A1AT-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","7e00d4fa-b951-44d8-8fbf-fc7b9f19772e","f4c41f30-2984-49b6-87a7-e27893a7fc71","c.467G>A","ENST00000354373",42768,225,371,"A","ENSG00000128250","ENST00000354373","missense_variant","missense_variant","676/1496","467/954","156/317","R/Q","cGg/cAg"]
["PTGIS",5740,"WUGSC","GRCh38","chr20",49507999,49507999,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-A7-A26J-01A-11D-A272-09","TCGA-A7-A26J-10A-01D-A272-09",null,null,"Somatic","Illumina HiSeq 2000","6f2b1732-2f2d-46a9-8665-9f5373768a5e","14e32cc8-ff98-4842-9ab9-022358584e94","c.1424A>C","ENST00000244043",43018,170,90,"G","ENSG00000124212","ENST00000244043","missense_variant","missense_variant","1454/5579","1424/1503","475/500","E/A","gAg/gCg"]
["SMG1",23049,"WUGSC","GRCh38","chr16",18811758,18811758,"+","Splice_Region","SNP","C","C","T","novel",null,"TCGA-B6-A0RG-01A-11W-A071-09","TCGA-B6-A0RG-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","9431c642-610e-4325-97b8-8b4c5c81cacd","83830a90-9963-4aa2-8bc1-ae3a292de36a","c.10908+3G>A","ENST00000446231",null,623,476,"T","ENSG00000157106","ENST00000446231","splice_region_variant","splice_region_variant;intron_variant","-/16115","-/10986","-/3661"]
["GSKIP",51527,"WUGSC","GRCh38","chr14",96385559,96385559,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-D8-A1XB-01A-11D-A14G-09","TCGA-D8-A1XB-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","e5ca0f82-6fa9-4d54-adc7-385721f351f3","665d057d-7d5f-41ef-98f1-5d71dded62b5","c.295T>A","ENST00000438650",42797,80,79,"A","ENSG00000100744","ENST00000438650","missense_variant","missense_variant","413/2140","295/420","99/139","L/I","Tta/Ata"]
["SGIP1",84251,"WUGSC","GRCh38","chr1",66682295,66682295,"+","Missense_Mutation","SNP","C","C","T","rs369259312",null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.1241C>T","ENST00000371037","15/25",20,26,"T","ENSG00000118473","ENST00000371037","missense_variant","missense_variant","1318/7768","1241/2487","414/828","P/L","cCa/cTa"]
["AMMECR1L",83607,"WUGSC","GRCh38","chr2",127864009,127864009,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.*1085G>T","ENST00000272647",42955,15,8,"A","ENSG00000144233","ENST00000272647","3_prime_UTR_variant","3_prime_UTR_variant","2279/4658","-/933","-/310"]
["GNB2L1",10399,"WUGSC","GRCh38","chr5",181237279,181237279,"+","Intron","SNP","C","C","G",null,null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.889-237G>C","ENST00000512805",null,46,61,"G","ENSG00000204628","ENST00000512805","intron_variant","intron_variant","-/1403","-/954","-/317"]
["DST",667,"WUGSC","GRCh38","chr6",56619800,56619800,"+","Intron","SNP","C","C","T",null,null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.4416+4730G>A","ENST00000312431",null,39,69,"T","ENSG00000151914","ENST00000312431","intron_variant","intron_variant","-/17756","-/16614","-/5537"]
["ACTL7A",10881,"WUGSC","GRCh38","chr9",108863093,108863093,"+","Silent","SNP","G","G","T",null,null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.771G>T","ENST00000333999",42736,45,70,"T","ENSG00000187003","ENST00000333999","synonymous_variant","synonymous_variant","828/1494","771/1308","257/435","L","ctG/ctT"]
["SPNS1",83985,"WUGSC","GRCh38","chr16",28984469,28984469,"+","3'UTR","SNP","G","G","A",null,null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.*170G>A","ENST00000311008",43081,46,48,"A","ENSG00000169682","ENST00000311008","3_prime_UTR_variant","3_prime_UTR_variant","2134/2208","-/1587","-/528"]
["PET100",100131801,"WUGSC","GRCh38","chr19",7629824,7629824,"+","5'UTR","SNP","G","G","C","novel",null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.-10G>C","ENST00000594797",42739,89,92,"C","ENSG00000229833","ENST00000594797","5_prime_UTR_variant","5_prime_UTR_variant","88/719","-/222","-/73"]
["WNK3",65267,"WUGSC","GRCh38","chrX",54294686,54294686,"+","Silent","SNP","C","C","T",null,null,"TCGA-AC-A5XS-01A-11D-A29N-09","TCGA-AC-A5XS-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","bc7a5f17-00b0-4724-965b-4e2c7d571676","5feed130-1b8e-483b-9187-3e9c6de3d51d","c.1560G>A","ENST00000354646",42971,49,57,"T","ENSG00000196632","ENST00000354646","synonymous_variant","synonymous_variant","1999/11341","1560/5403","520/1800","Q","caG/caA"]
["SACM1L",22908,"WUGSC","GRCh38","chr3",45735208,45735208,"+","Intron","SNP","G","G","C","novel",null,"TCGA-E2-A1IN-01A-11D-A13L-09","TCGA-E2-A1IN-10A-01D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","9e85559f-098e-4b0f-8034-4798789e710b","8dd6fca4-007f-45de-a569-bfb899254977","c.1101-27G>C","ENST00000389061",null,101,103,"C","ENSG00000211456","ENST00000389061","intron_variant","intron_variant","-/3723","-/1764","-/587"]
["DEGS2",123099,"WUGSC","GRCh38","chr14",100159557,100159557,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-E2-A1IN-01A-11D-A13L-09","TCGA-E2-A1IN-10A-01D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","9e85559f-098e-4b0f-8034-4798789e710b","8dd6fca4-007f-45de-a569-bfb899254977","c.31G>C","ENST00000305631",42738,17,22,"G","ENSG00000168350","ENST00000305631","missense_variant","missense_variant","607/4352","31/972","11/323","E/Q","Gag/Cag"]
["TTLL11",158135,"WUGSC","GRCh38","chr9",121989537,121989537,"+","Silent","SNP","G","G","C",null,null,"TCGA-AN-A0FV-01A-11W-A019-09","TCGA-AN-A0FV-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","c70259c1-f561-43d7-9829-6852815baa87","6cbd9cc2-e405-49d5-b512-cae7c4460f19","c.1197C>G","ENST00000321582",42834,460,232,"C","ENSG00000175764","ENST00000321582","synonymous_variant","synonymous_variant","1385/3250","1197/2403","399/800","P","ccC/ccG"]
["GOT1",2805,"WUGSC","GRCh38","chr10",99430600,99430600,"+","5'Flank","SNP","C","C","T","novel",null,"TCGA-B6-A0I5-01A-11W-A100-09","TCGA-B6-A0I5-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","f1139266-fade-4d27-ac67-60870e666295","2a5bbcf0-d39c-4f1b-a200-f778e586d42e",null,"ENST00000370508",null,51,39,"T","ENSG00000120053","ENST00000370508","upstream_gene_variant","upstream_gene_variant","-/1947","-/1242","-/413"]
["ABCC8",6833,"WUGSC","GRCh38","chr11",17442813,17442813,"+","Missense_Mutation","SNP","C","C","T","rs761748692","byFrequency","TCGA-AN-A0AJ-01A-11W-A019-09","TCGA-AN-A0AJ-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","97fbce82-0eed-4d70-9af2-57918a4ea8da","4450b82b-beee-4327-a851-3b7488a3273c","c.1537G>A","ENST00000389817",14519,140,138,"T","ENSG00000006071","ENST00000389817","missense_variant","missense_variant","1606/4921","1537/4746","513/1581","A/T","Gcc/Acc"]
["ZNF7",7553,"WUGSC","GRCh38","chr8",144841350,144841350,"+","Splice_Region","SNP","T","T","C","novel",null,"TCGA-AC-A2BK-01A-11D-A21Q-09","TCGA-AC-A2BK-11A-13D-A21Q-09",null,null,"Somatic","Illumina HiSeq 2000","bfa13c0e-cc3d-4a4d-9307-75571f89c37f","8f640fe4-aa25-444a-95b1-ca7a17baeb52","c.248-5T>C","ENST00000528372",null,28,19,"C","ENSG00000147789","ENST00000528372","splice_region_variant","splice_region_variant;intron_variant","-/2905","-/2061","-/686"]
["TBC1D8",11138,"WUGSC","GRCh38","chr2",101050625,101050625,"+","Silent","SNP","C","C","T","rs769096172","byFrequency","TCGA-EW-A423-01A-11D-A243-09","TCGA-EW-A423-10A-01D-A243-09",null,null,"Somatic","Illumina HiSeq 2500;Illumina HiSeq 2000","0077cf20-d598-4e04-863c-534e3386580e","5c24d17e-b10e-4b8e-9250-f0ed71fd4e3b","c.603G>A","ENST00000376840",42875,52,20,"T","ENSG00000204634","ENST00000376840","synonymous_variant","synonymous_variant","603/3627","603/3423","201/1140","P","ccG/ccA"]
["CPT2",1376,"WUGSC","GRCh38","chr1",53202401,53202401,"+","Missense_Mutation","SNP","A","A","T","novel",null,"TCGA-D8-A1JK-01A-11D-A13L-09","TCGA-D8-A1JK-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","fadaa39d-ebd2-4887-ae54-1fca12287fcf","e61906d0-87d8-4d8a-9ccb-a075759744ff","c.312A>T","ENST00000371486",42799,101,55,"T","ENSG00000157184","ENST00000371486","missense_variant","missense_variant","827/3094","312/1977","104/658","K/N","aaA/aaT"]
["AMBN",258,"WUGSC","GRCh38","chr4",70597010,70597010,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-D8-A1JK-01A-11D-A13L-09","TCGA-D8-A1JK-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","fadaa39d-ebd2-4887-ae54-1fca12287fcf","e61906d0-87d8-4d8a-9ccb-a075759744ff","c.96G>T","ENST00000322937",42807,217,92,"T","ENSG00000178522","ENST00000322937","missense_variant","missense_variant","199/2005","96/1344","32/447","Q/H","caG/caT"]
["TAS2R8",50836,"WUGSC","GRCh38","chr12",10806567,10806567,"+","Silent","SNP","A","A","G",null,null,"TCGA-D8-A1JK-01A-11D-A13L-09","TCGA-D8-A1JK-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","fadaa39d-ebd2-4887-ae54-1fca12287fcf","e61906d0-87d8-4d8a-9ccb-a075759744ff","c.414T>C","ENST00000240615",42736,126,53,"G","ENSG00000121314","ENST00000240615","synonymous_variant","synonymous_variant","727/1243","414/930","138/309","F","ttT/ttC"]
["TNK2",10188,"WUGSC","GRCh38","chr3",195867492,195867492,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-LL-A5YL-01A-12D-A29N-09","TCGA-LL-A5YL-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","85de3ba8-3c04-4590-a620-c7a602f0b266","e606da36-cc93-4759-886c-1fe07d617705","c.2761G>A","ENST00000333602",43084,16,9,"T","ENSG00000061938","ENST00000333602","missense_variant","missense_variant","3379/4552","2761/3117","921/1038","A/T","Gcc/Acc"]
["DMD",1756,"WUGSC","GRCh38","chrX",32573590,32573590,"+","Silent","SNP","C","C","T",null,null,"TCGA-LL-A5YL-01A-12D-A29N-09","TCGA-LL-A5YL-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","85de3ba8-3c04-4590-a620-c7a602f0b266","e606da36-cc93-4759-886c-1fe07d617705","c.1752G>A","ENST00000357033","15/79",49,63,"T","ENSG00000198947","ENST00000357033","synonymous_variant","synonymous_variant","1959/13956","1752/11058","584/3685","K","aaG/aaA"]
["DCD",117159,"WUGSC","GRCh38","chr12",54645654,54645654,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-D8-A1XM-01A-21D-A14K-09","TCGA-D8-A1XM-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","07418962-0a82-43a2-a66f-614903ea8380","647a05dc-3959-4997-a775-7b6a2c4cba59","c.151T>A","ENST00000293371",42799,142,141,"T","ENSG00000161634","ENST00000293371","missense_variant","missense_variant","341/645","151/333","51/110","L/I","Tta/Ata"]
["F5",2153,"WUGSC","GRCh38","chr1",169515576,169515576,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-A8-A07L-01A-11W-A019-09","TCGA-A8-A07L-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","4cc86f29-061e-4058-8e8f-4c48191f52aa","44a4c963-3b68-4537-a0da-e47fe5f1d7ac","c.6396G>T","ENST00000367797","24/25",544,260,"A","ENSG00000198734","ENST00000367797","missense_variant","missense_variant","6598/7024","6396/6675","2132/2224","K/N","aaG/aaT"]
["HYDIN",54768,"WUGSC","GRCh38","chr16",70908326,70908326,"+","Silent","SNP","G","G","A",null,null,"TCGA-A8-A07L-01A-11W-A019-09","TCGA-A8-A07L-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","4cc86f29-061e-4058-8e8f-4c48191f52aa","44a4c963-3b68-4537-a0da-e47fe5f1d7ac","c.8322C>T","ENST00000393567","49/86",186,73,"A","ENSG00000157423","ENST00000393567","synonymous_variant","synonymous_variant","8473/15719","8322/15366","2774/5121","I","atC/atT"]
["SERPINB9",5272,"WUGSC","GRCh38","chr6",2896169,2896169,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A1-A0SO-01A-22D-A099-09","TCGA-A1-A0SO-10A-03D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","b3568259-c63c-4eb1-bbc7-af711ddd33db","17ba8cdb-e35b-4496-a787-d1a7ee7d4a1e","c.190G>A","ENST00000380698",42801,411,153,"T","ENSG00000170542","ENST00000380698","missense_variant","missense_variant","280/4118","190/1131","64/376","E/K","Gaa/Aaa"]
["SPAG6",9576,"WUGSC","GRCh38","chr10",22386930,22386930,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-A1-A0SO-01A-22D-A099-09","TCGA-A1-A0SO-10A-03D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","b3568259-c63c-4eb1-bbc7-af711ddd33db","17ba8cdb-e35b-4496-a787-d1a7ee7d4a1e","c.649A>G","ENST00000376624",42866,165,117,"G","ENSG00000077327","ENST00000376624","missense_variant","missense_variant","791/2605","649/1530","217/509","M/V","Atg/Gtg"]
["GH2",2689,"WUGSC","GRCh38","chr17",63880755,63880755,"+","Intron","SNP","C","C","A","novel",null,"TCGA-A1-A0SO-01A-22D-A099-09","TCGA-A1-A0SO-10A-03D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","b3568259-c63c-4eb1-bbc7-af711ddd33db","17ba8cdb-e35b-4496-a787-d1a7ee7d4a1e","c.456+17G>T","ENST00000423893",null,182,103,"A","ENSG00000136487","ENST00000423893","intron_variant","intron_variant","-/819","-/654","-/217"]
["NFIB",4781,"WUGSC","GRCh38","chr9",14307140,14307140,"+","Silent","SNP","C","C","G",null,null,"TCGA-A2-A1G1-01A-21D-A13L-09","TCGA-A2-A1G1-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","afe70076-1044-4fdd-bebc-14a97b1a8363","24968a8a-5969-4b98-9d06-f286f771fb53","c.411G>C","ENST00000380959",42775,53,85,"G","ENSG00000147862","ENST00000380959","synonymous_variant","synonymous_variant","885/8198","411/1263","137/420","L","ctG/ctC"]
["SELP",6403,"WUGSC","GRCh38","chr1",169612276,169612276,"+","Missense_Mutation","SNP","G","G","A","rs6124","by1000G;byCluster;byHapMap","TCGA-A8-A09N-01A-11W-A019-09","TCGA-A8-A09N-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","304a2945-f134-45c7-9eaa-c6c9c2435552","03c46c7b-9609-47ca-8ae5-714ce4a77860","c.902C>T","ENST00000263686",42903,119,149,"A","ENSG00000174175","ENST00000263686","missense_variant","missense_variant","940/3142","902/2493","301/830","P/L","cCg/cTg"]
["HPD",3242,"WUGSC","GRCh38","chr12",121846910,121846910,"+","Silent","SNP","G","G","A","rs369152577","byCluster;byFrequency","TCGA-A8-A09N-01A-11W-A019-09","TCGA-A8-A09N-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","304a2945-f134-45c7-9eaa-c6c9c2435552","03c46c7b-9609-47ca-8ae5-714ce4a77860","c.783C>T","ENST00000289004",43053,34,38,"A","ENSG00000158104","ENST00000289004","synonymous_variant","synonymous_variant","819/1419","783/1182","261/393","G","ggC/ggT"]
["ALOX5AP",241,"WUGSC","GRCh38","chr13",30735593,30735593,"+","5'UTR","SNP","G","G","T","novel",null,"TCGA-E2-A1LL-01A-11D-A142-09","TCGA-E2-A1LL-11A-21D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","47312f61-5ef4-4f25-9320-8fbb4758790e","ed257922-f940-4fb3-9a92-fde82d130aef","c.-13G>T","ENST00000380490",42740,33,58,"T","ENSG00000132965","ENST00000380490","5_prime_UTR_variant","5_prime_UTR_variant","86/904","-/486","-/161"]
["CXCL11",6373,"WUGSC","GRCh38","chr4",76035094,76035094,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-BH-A1FN-01A-11D-A13L-09","TCGA-BH-A1FN-11A-34D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","bf92d76e-31ff-4273-82ea-982c4c26394b","a5d31e3a-08d6-40c1-a1e5-ee2b2eb6c544","c.214C>A","ENST00000306621",42798,258,243,"T","ENSG00000169248","ENST00000306621","missense_variant","missense_variant","424/1606","214/285","72/94","Q/K","Caa/Aaa"]
["ZNF831",128611,"WUGSC","GRCh38","chr20",59193134,59193134,"+","Silent","SNP","T","T","G","rs762733401",null,"TCGA-BH-A1FN-01A-11D-A13L-09","TCGA-BH-A1FN-11A-34D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","bf92d76e-31ff-4273-82ea-982c4c26394b","a5d31e3a-08d6-40c1-a1e5-ee2b2eb6c544","c.2115T>G","ENST00000371030",42740,28,36,"G","ENSG00000124203","ENST00000371030","synonymous_variant","synonymous_variant","2115/9404","2115/5034","705/1677","T","acT/acG"]
["FSHR",2492,"WUGSC","GRCh38","chr2",49068268,49068268,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A0YH-01A-11D-A10G-09","TCGA-A2-A0YH-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","e5558a39-eab2-4216-ba88-b63c2de48b01","b5036146-9005-41b6-ad70-1906a7c6c8c7","c.175C>T","ENST00000406846",42776,55,92,"A","ENSG00000170820","ENST00000406846","stop_gained","stop_gained","295/2784","175/2088","59/695","R/*","Cga/Tga"]
["DNAH14",127602,"WUGSC","GRCh38","chr1",225144579,225144579,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-E2-A573-01A-11D-A29N-09","TCGA-E2-A573-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","5cf9c046-c6bb-4872-827b-9d1dfe6d28f9","45873e30-7f35-4727-ba6e-3301004bef48","c.3488C>A","ENST00000445597","18/61",54,48,"A","ENSG00000185842","ENST00000445597","missense_variant","missense_variant","3488/10524","3488/10524","1163/3507","A/D","gCc/gAc"]
["ZNF644",84146,"WUGSC","GRCh38","chr1",90938961,90938961,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-GM-A2DB-01A-31D-A19Y-09","TCGA-GM-A2DB-10C-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","c13e05b6-0b3e-4c1f-800e-4a49c5d417aa","7bba57a5-c11e-43a2-ab14-5b33f5afa6d9","c.2393A>G","ENST00000337393",42800,39,37,"C","ENSG00000122482","ENST00000337393","missense_variant","missense_variant","2676/5763","2393/3984","798/1327","E/G","gAa/gGa"]
["RPRM",56475,"WUGSC","GRCh38","chr2",153478163,153478163,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-C8-A8HQ-01A-11D-A36J-09","TCGA-C8-A8HQ-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","8a0981fc-75c7-493b-b91d-a58c4755a37a","492cb306-4521-4767-b634-338fc782663e","c.*73C>G","ENST00000325926",42736,23,14,"C","ENSG00000177519","ENST00000325926","3_prime_UTR_variant","3_prime_UTR_variant","646/1471","-/330","-/109"]
["ZC2HC1B",153918,"WUGSC","GRCh38","chr6",143903071,143903071,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-C8-A8HQ-01A-11D-A36J-09","TCGA-C8-A8HQ-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","8a0981fc-75c7-493b-b91d-a58c4755a37a","492cb306-4521-4767-b634-338fc782663e","c.517G>C","ENST00000237275",42894,85,46,"C","ENSG00000118491","ENST00000237275","missense_variant","missense_variant","621/1002","517/669","173/222","E/Q","Gaa/Caa"]
["MEN1",4221,"WUGSC","GRCh38","chr11",64808010,64808010,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-C8-A8HQ-01A-11D-A36J-09","TCGA-C8-A8HQ-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","8a0981fc-75c7-493b-b91d-a58c4755a37a","492cb306-4521-4767-b634-338fc782663e","c.550G>A","ENST00000337652",42804,57,56,"T","ENSG00000133895","ENST00000337652","missense_variant","missense_variant","1054/3162","550/1848","184/615","E/K","Gag/Aag"]
["FXR2",9513,"WUGSC","GRCh38","chr17",7591914,7591914,"+","Silent","SNP","G","G","A","novel",null,"TCGA-C8-A8HQ-01A-11D-A36J-09","TCGA-C8-A8HQ-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","8a0981fc-75c7-493b-b91d-a58c4755a37a","492cb306-4521-4767-b634-338fc782663e","c.1938C>T","ENST00000250113","17/17",50,57,"A","ENSG00000129245","ENST00000250113","synonymous_variant","synonymous_variant","2273/2957","1938/2022","646/673","V","gtC/gtT"]
["TOP1",7150,"WUGSC","GRCh38","chr20",41123609,41123609,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-C8-A8HQ-01A-11D-A36J-09","TCGA-C8-A8HQ-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","8a0981fc-75c7-493b-b91d-a58c4755a37a","492cb306-4521-4767-b634-338fc782663e","c.*312C>T","ENST00000361337","21/21",52,58,"T","ENSG00000198900","ENST00000361337","3_prime_UTR_variant","3_prime_UTR_variant","2860/3738","-/2298","-/765"]
["SYTL5",94122,"WUGSC","GRCh38","chrX",38126615,38126615,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-A8-A08H-01A-21W-A019-09","TCGA-A8-A08H-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","26161c06-f816-489a-8800-e0a68a4ce78a","c384d5d9-b1d6-4553-8f3f-7602dbaca681","c.2078G>A","ENST00000297875","17/17",109,70,"A","ENSG00000147041","ENST00000297875","stop_gained","stop_gained","2521/4722","2078/2193","693/730","W/*","tGg/tAg"]
["CFAP44",55779,"WUGSC","GRCh38","chr3",113379358,113379358,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A0CX-01A-21W-A019-09","TCGA-A2-A0CX-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","975adb76-3561-41a0-959a-68da470816c7","dd43a88d-fd04-4ce4-8bac-1478975304aa","c.2246C>A","ENST00000295868","17/21",645,313,"T","ENSG00000206530","ENST00000295868","missense_variant","missense_variant","2409/3377","2246/2949","749/982","S/Y","tCt/tAt"]
["ZNRF2",223082,"WUGSC","GRCh38","chr7",30323683,30323683,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A2-A0CX-01A-21W-A019-09","TCGA-A2-A0CX-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","975adb76-3561-41a0-959a-68da470816c7","dd43a88d-fd04-4ce4-8bac-1478975304aa","c.511G>A","ENST00000323037",42771,299,166,"A","ENSG00000180233","ENST00000323037","missense_variant","missense_variant","1562/3460","511/729","171/242","E/K","Gaa/Aaa"]
["CCDC88C",440193,"WUGSC","GRCh38","chr14",91313632,91313632,"+","Silent","SNP","C","C","T",null,null,"TCGA-A2-A0CX-01A-21W-A019-09","TCGA-A2-A0CX-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","975adb76-3561-41a0-959a-68da470816c7","dd43a88d-fd04-4ce4-8bac-1478975304aa","c.2184G>A","ENST00000389857","15/30",97,126,"T","ENSG00000015133","ENST00000389857","synonymous_variant","synonymous_variant","2271/7474","2184/6087","728/2028","R","agG/agA"]
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["TTC29",83894,"WUGSC","GRCh38","chr4",146909066,146909066,"+","Silent","SNP","C","C","T",null,null,"TCGA-GM-A2DH-01A-11D-A17W-09","TCGA-GM-A2DH-10C-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","3925c12c-b388-40ab-addf-2c3bf2c8398b","7f09df95-48bb-490a-9937-9a3d604760f2","c.360G>A","ENST00000325106",42868,103,99,"T","ENSG00000137473","ENST00000325106","synonymous_variant","synonymous_variant","587/1785","360/1428","120/475","L","ctG/ctA"]
["CCDC24",149473,"WUGSC","GRCh38","chr1",43995828,43995828,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-EW-A1IZ-01A-11D-A188-09","TCGA-EW-A1IZ-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","18db4143-48cc-424c-8d23-46cf23056528","e528b9ef-53e6-49d4-a86c-648a752d1835","c.673G>A","ENST00000372318",42956,25,43,"A","ENSG00000159214","ENST00000372318","missense_variant","missense_variant","844/1463","673/924","225/307","G/R","Ggg/Agg"]
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["FEZF2",55079,"WUGSC","GRCh38","chr3",62372807,62372807,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-D8-A1JN-01A-11D-A13L-09","TCGA-D8-A1JN-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","c83c7d48-8671-4f27-b3dd-05411fa2f784","c14cac2a-e308-44fa-b1af-ee51511ee0ee","c.62C>T","ENST00000283268",42771,12,12,"A","ENSG00000153266","ENST00000283268","missense_variant","missense_variant","357/2074","62/1380","21/459","S/L","tCg/tTg"]
["SEMA5B",54437,"WUGSC","GRCh38","chr3",122948520,122948520,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-D8-A1JN-01A-11D-A13L-09","TCGA-D8-A1JN-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","c83c7d48-8671-4f27-b3dd-05411fa2f784","c14cac2a-e308-44fa-b1af-ee51511ee0ee","c.314C>A","ENST00000357599",42817,35,20,"T","ENSG00000082684","ENST00000357599","missense_variant","missense_variant","701/4792","314/3456","105/1151","T/N","aCc/aAc"]
["ZNF780B",163131,"WUGSC","GRCh38","chr19",40034536,40034536,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A1JN-01A-11D-A13L-09","TCGA-D8-A1JN-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","c83c7d48-8671-4f27-b3dd-05411fa2f784","c14cac2a-e308-44fa-b1af-ee51511ee0ee","c.2323C>T","ENST00000434248",42860,105,65,"A","ENSG00000128000","ENST00000434248","missense_variant","missense_variant","2389/8665","2323/2502","775/833","H/Y","Cat/Tat"]
["EPS8",2059,"WUGSC","GRCh38","chr12",15647187,15647187,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AQ-A04H-01B-11D-A10M-09","TCGA-AQ-A04H-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","73c13e04-1400-4ebb-aa80-f54becbe036c","751944ed-705b-43b8-99fc-a49a6514941d","c.1508A>G","ENST00000281172","15/21",94,131,"C","ENSG00000151491","ENST00000281172","missense_variant","missense_variant","1945/4061","1508/2469","503/822","H/R","cAc/cGc"]
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["HFE",3077,"WUGSC","GRCh38","chr6",26096707,26096707,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-XX-A89A-01A-11D-A36J-09","TCGA-XX-A89A-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","2fcf6df4-8e93-4dd2-907b-68fec9c1ecf6","274fd888-94ca-4099-8527-8d57f6c157f6","c.*2481G>A","ENST00000357618",42892,31,9,"A","ENSG00000010704","ENST00000357618","3_prime_UTR_variant","3_prime_UTR_variant","3650/5286","-/1047","-/348"]
["KIAA1598",57698,"WUGSC","GRCh38","chr10",116929886,116929886,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-XX-A89A-01A-11D-A36J-09","TCGA-XX-A89A-10A-01D-A36M-09",null,null,"Somatic","Illumina HiSeq 2000","2fcf6df4-8e93-4dd2-907b-68fec9c1ecf6","274fd888-94ca-4099-8527-8d57f6c157f6","c.975G>C","ENST00000355371",43025,71,43,"G","ENSG00000187164","ENST00000355371","missense_variant","missense_variant","1473/5361","975/1896","325/631","Q/H","caG/caC"]
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["MKI67",4288,"WUGSC","GRCh38","chr10",128114981,128114981,"+","Missense_Mutation","SNP","G","G","C","rs761799390","byFrequency","TCGA-BH-A18U-01A-21D-A12B-09","TCGA-BH-A18U-11A-23D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","a8400863-c145-4c6c-bcf3-e4cc4d816d22","f0d1235d-8fc6-4849-8506-9d8dce2eabaa","c.1427C>G","ENST00000368654",42931,169,197,"C","ENSG00000148773","ENST00000368654","missense_variant","missense_variant","1803/12678","1427/9771","476/3256","S/C","tCt/tGt"]
["TP53BP2",7159,"WUGSC","GRCh38","chr1",223802188,223802188,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-A8-A08R-01A-11W-A050-09","TCGA-A8-A08R-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","05362091-8e04-46e2-81e7-1efddc0d8c63","f1681b14-25e1-4bc6-a97d-18928662d45b","c.1153C>G","ENST00000343537",42996,139,84,"C","ENSG00000143514","ENST00000343537","missense_variant","missense_variant","1445/4651","1153/3405","385/1134","Q/E","Cag/Gag"]
["NUP205",23165,"WUGSC","GRCh38","chr7",135616042,135616042,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-A8-A08R-01A-11W-A050-09","TCGA-A8-A08R-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","05362091-8e04-46e2-81e7-1efddc0d8c63","f1681b14-25e1-4bc6-a97d-18928662d45b","c.3437A>G","ENST00000285968","24/43",152,199,"G","ENSG00000155561","ENST00000285968","missense_variant","missense_variant","3463/6266","3437/6039","1146/2012","D/G","gAc/gGc"]
["TRIM47",91107,"WUGSC","GRCh38","chr17",75876085,75876085,"+","Silent","SNP","T","T","G",null,null,"TCGA-A8-A08R-01A-11W-A050-09","TCGA-A8-A08R-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","05362091-8e04-46e2-81e7-1efddc0d8c63","f1681b14-25e1-4bc6-a97d-18928662d45b","c.1017A>C","ENST00000254816",42831,23,30,"G","ENSG00000132481","ENST00000254816","synonymous_variant","synonymous_variant","1044/2266","1017/1917","339/638","L","ctA/ctC"]
["GBP7",388646,"WUGSC","GRCh38","chr1",89147584,89147584,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A0AK-01A-21W-A019-09","TCGA-AN-A0AK-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","30870af5-e46e-47c6-b7fb-af6f4c91861e","9243b0f3-5c29-4922-902c-8348cd53537c","c.1348C>T","ENST00000294671",42958,324,363,"A","ENSG00000213512","ENST00000294671","missense_variant","missense_variant","1487/2454","1348/1917","450/638","P/S","Ccc/Tcc"]
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["C3orf17",25871,"WUGSC","GRCh38","chr3",113005999,113005999,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AN-A0AK-01A-21W-A019-09","TCGA-AN-A0AK-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","30870af5-e46e-47c6-b7fb-af6f4c91861e","9243b0f3-5c29-4922-902c-8348cd53537c","c.1241C>T","ENST00000314400",42987,93,76,"A","ENSG00000163608","ENST00000314400","missense_variant","missense_variant","1433/4992","1241/1704","414/567","P/L","cCa/cTa"]
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["ZNF79",7633,"WUGSC","GRCh38","chr9",127444109,127444109,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AN-A0AK-01A-21W-A019-09","TCGA-AN-A0AK-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","30870af5-e46e-47c6-b7fb-af6f4c91861e","9243b0f3-5c29-4922-902c-8348cd53537c","c.409C>A","ENST00000342483",42860,263,306,"A","ENSG00000196152","ENST00000342483","missense_variant","missense_variant","815/2078","409/1497","137/498","P/T","Cct/Act"]
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["PIAS2",9063,"WUGSC","GRCh38","chr18",46828010,46828010,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A0AK-01A-21W-A019-09","TCGA-AN-A0AK-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","30870af5-e46e-47c6-b7fb-af6f4c91861e","9243b0f3-5c29-4922-902c-8348cd53537c","c.1457C>T","ENST00000585916",43053,166,180,"A","ENSG00000078043","ENST00000585916","missense_variant","missense_variant","1457/11075","1457/1866","486/621","A/V","gCc/gTc"]
["EDEM2",55741,"WUGSC","GRCh38","chr20",35137894,35137894,"+","Missense_Mutation","SNP","C","C","T","rs754555510",null,"TCGA-AN-A0AK-01A-21W-A019-09","TCGA-AN-A0AK-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","30870af5-e46e-47c6-b7fb-af6f4c91861e","9243b0f3-5c29-4922-902c-8348cd53537c","c.476G>A","ENST00000374492",42866,137,117,"T","ENSG00000088298","ENST00000374492","missense_variant","missense_variant","582/1919","476/1737","159/578","R/Q","cGa/cAa"]
["SUPT20HL1",100130302,"WUGSC","GRCh38","chrX",24364719,24364719,"+","RNA","SNP","T","T","C","novel",null,"TCGA-AN-A0AK-01A-21W-A019-09","TCGA-AN-A0AK-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","30870af5-e46e-47c6-b7fb-af6f4c91861e","9243b0f3-5c29-4922-902c-8348cd53537c","n.1959T>C","ENST00000436466",42736,75,75,"C","ENSG00000223731","ENST00000436466","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","1959/2618"]
["FAM160A2",84067,"WUGSC","GRCh38","chr11",6223812,6223812,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A62Y-01A-11D-A29N-09","TCGA-AC-A62Y-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","305901ca-3086-4ca5-81d1-825a0ca5bdf3","5cb6799d-58c1-4424-a38d-a1e6d50ff772","c.575C>T","ENST00000449352",42806,18,25,"A","ENSG00000051009","ENST00000449352","missense_variant","missense_variant","839/3354","575/2919","192/972","S/L","tCa/tTa"]
["SLC16A14",151473,"WUGSC","GRCh38","chr2",230046059,230046059,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E2-A1IG-01A-11D-A142-09","TCGA-E2-A1IG-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","84da47a3-49e1-4f94-bea9-dd20b6627adb","9859da9f-72c1-4f68-a054-4d103170d785","c.1067C>T","ENST00000295190",42830,35,32,"A","ENSG00000163053","ENST00000295190","missense_variant","missense_variant","1526/4398","1067/1533","356/510","T/M","aCg/aTg"]
["ZFPM2",23414,"WUGSC","GRCh38","chr8",105801495,105801495,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-A2-A04R-01A-41D-A117-09","TCGA-A2-A04R-10B-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","1f8e4326-dfc7-4635-a9b7-a9207a392748","6234c5ee-14f2-427c-9ebc-4911da27a849","c.1413G>T","ENST00000407775",42955,135,79,"T","ENSG00000169946","ENST00000407775","missense_variant","missense_variant","1663/4700","1413/3456","471/1151","K/N","aaG/aaT"]
["MRPL46",26589,"WUGSC","GRCh38","chr15",88465643,88465643,"+","Missense_Mutation","SNP","A","A","G","novel",null,"TCGA-E9-A6HE-01A-11D-A31U-09","TCGA-E9-A6HE-10A-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","6a114c34-c16d-43f0-9fb9-a96228bb9a0e","4f4db15d-8c72-4910-b98d-0b0dd72e13ad","c.359T>C","ENST00000312475",42770,42,56,"G","ENSG00000259494","ENST00000312475","missense_variant","missense_variant","401/1019","359/840","120/279","L/S","tTg/tCg"]
["ADCY5",111,"WUGSC","GRCh38","chr3",123319747,123319747,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-D8-A1XZ-01A-11D-A14K-09","TCGA-D8-A1XZ-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","381a9211-1f2b-4c14-895b-ee7fb6eb8c7f","1f6f5abe-614f-4f57-930c-e0ea2384cde6","c.2183G>A","ENST00000462833",43029,57,81,"T","ENSG00000173175","ENST00000462833","missense_variant","missense_variant","3396/7311","2183/3786","728/1261","S/N","aGc/aAc"]
["ABCG5",64240,"WUGSC","GRCh38","chr2",43813130,43813130,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-A8-A0A7-01A-11W-A019-09","TCGA-A8-A0A7-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","28be7b14-730d-44f7-bf93-a7590b4a08f8","42c2f167-31c5-4e16-8957-a01fd498e05d","c.1942C>G","ENST00000260645","13/13",66,73,"C","ENSG00000138075","ENST00000260645","missense_variant","missense_variant","2082/2740","1942/1956","648/651","L/V","Ctc/Gtc"]
["CCDC102B",79839,"WUGSC","GRCh38","chr18",68838850,68838850,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A8-A0A7-01A-11W-A019-09","TCGA-A8-A0A7-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","28be7b14-730d-44f7-bf93-a7590b4a08f8","42c2f167-31c5-4e16-8957-a01fd498e05d","c.751G>A","ENST00000319445",42802,203,249,"A","ENSG00000150636","ENST00000319445","missense_variant","missense_variant","801/2644","751/1542","251/513","E/K","Gaa/Aaa"]
["SESN2",83667,"WUGSC","GRCh38","chr1",28274860,28274860,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-A8-A09G-01A-21W-A019-09","TCGA-A8-A09G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","3bd68e94-d902-4079-8fdb-16edcc90de1c","f53ea676-2475-408e-9b54-29324a255a2e","c.1056C>G","ENST00000253063",42957,215,155,"G","ENSG00000130766","ENST00000253063","missense_variant","missense_variant","1377/3453","1056/1443","352/480","I/M","atC/atG"]
["ZEB2",9839,"WUGSC","GRCh38","chr2",144389816,144389816,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A09G-01A-21W-A019-09","TCGA-A8-A09G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","3bd68e94-d902-4079-8fdb-16edcc90de1c","f53ea676-2475-408e-9b54-29324a255a2e","c.3280G>A","ENST00000409487",43018,220,149,"T","ENSG00000169554","ENST00000409487","missense_variant","missense_variant","3563/5361","3280/3645","1094/1214","E/K","Gag/Aag"]
["INTS8",55656,"WUGSC","GRCh38","chr8",94842480,94842480,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-A8-A09G-01A-21W-A019-09","TCGA-A8-A09G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","3bd68e94-d902-4079-8fdb-16edcc90de1c","f53ea676-2475-408e-9b54-29324a255a2e","c.1252C>G","ENST00000523731",43035,356,164,"G","ENSG00000164941","ENST00000523731","missense_variant","missense_variant","1385/4633","1252/2988","418/995","L/V","Ctt/Gtt"]
["BCKDHA",593,"WUGSC","GRCh38","chr19",41422267,41422267,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-A8-A09G-01A-21W-A019-09","TCGA-A8-A09G-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","3bd68e94-d902-4079-8fdb-16edcc90de1c","f53ea676-2475-408e-9b54-29324a255a2e","c.750C>A","ENST00000269980",42895,35,38,"A","ENSG00000248098","ENST00000269980","missense_variant","missense_variant","1118/2103","750/1338","250/445","F/L","ttC/ttA"]
["CCDC110",256309,"WUGSC","GRCh38","chr4",185462709,185462709,"+","Splice_Site","SNP","C","C","G",null,null,"TCGA-AN-A0FJ-01A-11W-A019-09","TCGA-AN-A0FJ-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","6b988737-0504-42bb-8c75-d70d7a312e68","02ed13b6-5cc2-423d-9b5a-b1c802c33569","c.172-1G>C","ENST00000307588",null,33,69,"G","ENSG00000168491","ENST00000307588","splice_acceptor_variant","splice_acceptor_variant","-/2898","172/2502","58/833"]
["AMIGO2",347902,"WUGSC","GRCh38","chr12",47077574,47077574,"+","Missense_Mutation","SNP","C","C","T","rs140364757",null,"TCGA-AN-A0FJ-01A-11W-A019-09","TCGA-AN-A0FJ-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","6b988737-0504-42bb-8c75-d70d7a312e68","02ed13b6-5cc2-423d-9b5a-b1c802c33569","c.1429G>A","ENST00000266581",42768,44,75,"T","ENSG00000139211","ENST00000266581","missense_variant","missense_variant","1896/3763","1429/1569","477/522","A/T","Gca/Aca"]
["PRSS53",339105,"WUGSC","GRCh38","chr16",31086462,31086462,"+","Missense_Mutation","SNP","G","G","A","rs760392898",null,"TCGA-B6-A1KN-01A-11D-A13L-09","TCGA-B6-A1KN-10A-01D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","c1ad09c8-4237-48f0-b04c-7ee8ccaf8cf1","2a8d9494-2d88-4577-bb21-05a62a07d8f9","c.538C>T","ENST00000280606",42866,92,41,"A","ENSG00000151006","ENST00000280606","missense_variant","missense_variant","692/2181","538/1662","180/553","R/C","Cgt/Tgt"]
["ZNRD1-AS1",80862,"WUGSC","GRCh38","chr6",30035887,30035887,"+","5'Flank","SNP","G","G","C",null,null,"TCGA-A7-A56D-01A-11D-A27P-09","TCGA-A7-A56D-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","dc8ca430-e89c-4f9b-8745-bccf6373accc","74901ecc-d370-42c5-812e-8e842cd8532f",null,"ENST00000444051",null,123,65,"C","ENSG00000204623","ENST00000444051","upstream_gene_variant","upstream_gene_variant","-/9771"]
["HFM1",164045,"WUGSC","GRCh38","chr1",91262250,91262250,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-B6-A0RN-01A-12D-A099-09","TCGA-B6-A0RN-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","bbbcb493-2937-4a7b-8454-0abbbb379927","5465e36a-97f7-4408-81c1-9f8e836c1279","c.4229T>C","ENST00000370425","38/39",101,107,"G","ENSG00000162669","ENST00000370425","missense_variant","missense_variant","4328/4931","4229/4308","1410/1435","V/A","gTt/gCt"]
["MRPS35",60488,"WUGSC","GRCh38","chr12",27737563,27737563,"+","Silent","SNP","C","C","T",null,null,"TCGA-A8-A07P-01A-11W-A019-09","TCGA-A8-A07P-10A-01W-A021-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","2b88ff64-bf43-43e8-9ea9-0de571520d72","43c44bf2-cb01-4747-8481-ce0c65be4863","c.657C>T","ENST00000081029",42924,93,144,"T","ENSG00000061794","ENST00000081029","synonymous_variant","synonymous_variant","728/1888","657/972","219/323","Y","taC/taT"]
["PI16",221476,"WUGSC","GRCh38","chr6",36954808,36954808,"+","Silent","SNP","A","A","G",null,null,"TCGA-D8-A1X5-01A-11D-A14G-09","TCGA-D8-A1X5-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","db4526d4-e344-4b5a-bb66-fd43b41764ca","6d77bba9-4db6-4277-b5ce-b7e3d2f1d7cc","c.48A>G","ENST00000373674",42742,25,36,"G","ENSG00000164530","ENST00000373674","synonymous_variant","synonymous_variant","376/2190","48/1392","16/463","L","ctA/ctG"]
["CFL1",1072,"WUGSC","GRCh38","chr11",65855609,65855609,"+","Intron","SNP","C","C","G","novel",null,"TCGA-D8-A27M-01A-11D-A16D-09","TCGA-D8-A27M-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","cb9257f9-ca3f-4c14-a680-6632175dd526","d57d98db-8901-497c-b97e-1fc813a6d1ab","c.388+45G>C","ENST00000308162",null,29,16,"G","ENSG00000172757","ENST00000308162","intron_variant","intron_variant","-/1234","-/501","-/166"]
["MAEL",84944,"WUGSC","GRCh38","chr1",166992794,166992794,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-AR-A0TV-01A-21D-A099-09","TCGA-AR-A0TV-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","0ec80200-12fe-479c-8ea0-982a9995f55a","7df70a01-366a-48ed-992a-3959d56bddde","c.434C>T","ENST00000367872",42837,159,121,"T","ENSG00000143194","ENST00000367872","missense_variant","missense_variant","678/1908","434/1305","145/434","S/F","tCt/tTt"]
["NUDT6",11162,"WUGSC","GRCh38","chr4",122893178,122893178,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A07O-01A-11W-A019-09","TCGA-A8-A07O-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","4574b64d-8848-46e4-913e-5d318c1f6162","edde47bb-2b18-4fcf-8c3a-10ea98983e62","c.601G>A","ENST00000304430",42860,131,170,"T","ENSG00000170917","ENST00000304430","missense_variant","missense_variant","635/1169","601/951","201/316","E/K","Gaa/Aaa"]
["NFKB1",4790,"WUGSC","GRCh38","chr4",102578817,102578817,"+","Intron","SNP","A","A","C","novel",null,"TCGA-E9-A1NC-01A-12W-A16L-09","TCGA-E9-A1NC-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","2ba4c398-b94b-49f8-bb88-9d0cb3347d2c","ebb77710-bd6f-435d-83c5-2600f9e422db","c.569-64A>C","ENST00000394820",null,17,22,"C","ENSG00000109320","ENST00000394820","intron_variant","intron_variant","-/3693","-/2907","-/968"]
["MUC4",4585,"WUGSC","GRCh38","chr3",195783009,195783009,"+","Silent","SNP","C","C","T",null,null,"TCGA-AO-A0J8-01A-21D-A045-09","TCGA-AO-A0J8-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","24ba5501-8097-4af6-b12c-bb6dcbe10cac","a6efdded-0dee-4407-a1b2-bdfdb1649a07","c.8571G>A","ENST00000463781",42791,1071,57,"T","ENSG00000145113","ENST00000463781","synonymous_variant","synonymous_variant","9031/17110","8571/16239","2857/5412","V","gtG/gtA"]
["APOA1BP",128240,"WUGSC","GRCh38","chr1",156592448,156592448,"+","Silent","SNP","G","G","C",null,null,"TCGA-C8-A1HJ-01A-11D-A13L-09","TCGA-C8-A1HJ-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","a62c3601-b90f-402f-8212-ffdfde3c6df8","913051a1-919a-436c-8fc2-9110968c19c3","c.375G>C","ENST00000368235",42800,231,64,"C","ENSG00000163382","ENST00000368235","synonymous_variant","synonymous_variant","418/1125","375/867","125/288","L","ctG/ctC"]
["OR2V1",26693,"WUGSC","GRCh38","chr5",181124841,181124841,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-BH-A0BL-01A-11D-A10Y-09","TCGA-BH-A0BL-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000","1eb22fbe-6108-46c9-b51b-814861c3e104","10add567-cef4-464f-98a7-23a153bc1c40","c.464T>A","ENST00000329365",42736,81,176,"T","ENSG00000185372","ENST00000329365","missense_variant","missense_variant","464/948","464/948","155/315","I/K","aTa/aAa"]
["NHLH1",4807,"WUGSC","GRCh38","chr1",160370945,160370945,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AC-A62V-01A-11D-A31U-09","TCGA-AC-A62V-10A-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","8f3a1eea-b417-4a3e-a7e9-f64d70b6b34f","200832d5-bc97-458f-b3c4-8ac15410b312","c.214G>A","ENST00000302101",42768,47,45,"A","ENSG00000171786","ENST00000302101","missense_variant","missense_variant","660/2563","214/402","72/133","A/T","Gcc/Acc"]
["UBE3A",7337,"WUGSC","GRCh38","chr15",25375582,25375582,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AC-A62V-01A-11D-A31U-09","TCGA-AC-A62V-10A-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","8f3a1eea-b417-4a3e-a7e9-f64d70b6b34f","200832d5-bc97-458f-b3c4-8ac15410b312","c.253C>T","ENST00000397954",42900,65,68,"A","ENSG00000114062","ENST00000397954","missense_variant","missense_variant","498/2873","253/2628","85/875","P/S","Cct/Tct"]
["CSNK1A1L",122011,"WUGSC","GRCh38","chr13",37104841,37104841,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-E2-A15R-01A-11D-A10Y-09","TCGA-E2-A15R-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","11799240-0275-48fe-84ef-85e188839bbe","463d72c3-0e93-4d3e-b1c8-39827372fa08","c.416C>A","ENST00000379800",42736,288,604,"T","ENSG00000180138","ENST00000379800","missense_variant","missense_variant","824/2406","416/1014","139/337","P/Q","cCa/cAa"]
["GAA",2548,"WUGSC","GRCh38","chr17",80107617,80107617,"+","Silent","SNP","G","G","A","rs761363283",null,"TCGA-BH-A8FZ-01A-11D-A351-09","TCGA-BH-A8FZ-10A-01D-A351-09",null,null,"Somatic","Illumina HiSeq 2000","34e3c8bb-e881-451c-a3ff-60db39101b43","0a8ebc6c-83fd-4881-af82-5f2c10aa3d66","c.753G>A","ENST00000302262",42845,62,71,"A","ENSG00000171298","ENST00000302262","synonymous_variant","synonymous_variant","972/3626","753/2859","251/952","S","tcG/tcA"]
["STK35",140901,"WUGSC","GRCh38","chr20",2116817,2116817,"+","Silent","SNP","T","T","C",null,null,"TCGA-E9-A1NF-01A-11D-A14G-09","TCGA-E9-A1NF-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","cd428bec-fc31-4d2d-9e6c-c8f30608d797","edffc09c-201a-44d1-b758-5d9d64f5f6a6","c.1044T>C","ENST00000381482",42798,76,101,"C","ENSG00000125834","ENST00000381482","synonymous_variant","synonymous_variant","1315/6685","1044/1605","348/534","I","atT/atC"]
["C1orf177",163747,"WUGSC","GRCh38","chr1",54813859,54813859,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.808G>C","ENST00000371273",42926,97,83,"C","ENSG00000162398","ENST00000371273","missense_variant","missense_variant","823/1651","808/1257","270/418","E/Q","Gaa/Caa"]
["RMDN2",151393,"WUGSC","GRCh38","chr2",37975290,37975290,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.706G>C","ENST00000354545",42836,153,94,"C","ENSG00000115841","ENST00000354545","missense_variant","missense_variant","829/1381","706/1233","236/410","E/Q","Gaa/Caa"]
["EGR4",1961,"WUGSC","GRCh38","chr2",73291496,73291496,"+","Silent","SNP","G","G","A","novel",null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.1731C>T","ENST00000545030",42768,12,12,"A","ENSG00000135625","ENST00000545030","synonymous_variant","synonymous_variant","1806/2372","1731/1770","577/589","L","ctC/ctT"]
["ARHGAP24",83478,"WUGSC","GRCh38","chr4",86000545,86000545,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.2070G>C","ENST00000395184",43018,117,56,"C","ENSG00000138639","ENST00000395184","missense_variant","missense_variant","2536/4661","2070/2247","690/748","E/D","gaG/gaC"]
["BTN3A3",10384,"WUGSC","GRCh38","chr6",26444250,26444250,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.379T>C","ENST00000244519",42836,154,136,"C","ENSG00000111801","ENST00000244519","missense_variant","missense_variant","622/3002","379/1755","127/584","Y/H","Tat/Cat"]
["SKAP2",8935,"WUGSC","GRCh38","chr7",26738858,26738858,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.406G>C","ENST00000345317",42899,107,85,"G","ENSG00000005020","ENST00000345317","missense_variant","missense_variant","720/3998","406/1080","136/359","E/Q","Gaa/Caa"]
["KAT6A",7994,"WUGSC","GRCh38","chr8",42048644,42048644,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.334G>C","ENST00000265713",42783,145,69,"G","ENSG00000083168","ENST00000265713","missense_variant","missense_variant","746/9153","334/6015","112/2004","E/Q","Gag/Cag"]
["ABTB2",25841,"WUGSC","GRCh38","chr11",34164704,34164704,"+","Nonsense_Mutation","SNP","G","G","C",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.1970C>G","ENST00000435224",42995,35,99,"C","ENSG00000166016","ENST00000435224","stop_gained","stop_gained","2395/4902","1970/3078","657/1025","S/*","tCa/tGa"]
["CNPY2",10330,"WUGSC","GRCh38","chr12",56315142,56315142,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.76C>G","ENST00000273308",42772,54,30,"C","ENSG00000257727","ENST00000273308","missense_variant","missense_variant","617/1214","76/549","26/182","L/V","Ctc/Gtc"]
["PLEKHH1",57475,"WUGSC","GRCh38","chr14",67581886,67581886,"+","Intron","SNP","G","G","C","novel",null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.3285-183G>C","ENST00000329153",null,15,11,"C","ENSG00000054690","ENST00000329153","intron_variant","intron_variant","-/6604","-/4095","-/1364"]
["TICRR",90381,"WUGSC","GRCh38","chr15",89625491,89625491,"+","Silent","SNP","C","C","G",null,null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.5181C>G","ENST00000268138","20/22",39,28,"G","ENSG00000140534","ENST00000268138","synonymous_variant","synonymous_variant","5286/6775","5181/5733","1727/1910","L","ctC/ctG"]
["SLC35B1",10237,"WUGSC","GRCh38","chr17",49705956,49705956,"+","Intron","SNP","G","G","C","novel",null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.451-60C>G","ENST00000240333",null,216,57,"C","ENSG00000121073","ENST00000240333","intron_variant","intron_variant","-/1850","-/1080","-/359"]
["ABHD12",26090,"WUGSC","GRCh38","chr20",25294773,25294773,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-D8-A1JA-01A-11D-A13L-09","TCGA-D8-A1JA-10A-01W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","6ffcb6e0-9850-47c8-a75a-5ff47a6f1a2f","a20d8bfb-53ad-4a4e-bbc5-4f204a08b812","c.*200G>C","ENST00000376542","13/13",21,14,"G","ENSG00000100997","ENST00000376542","3_prime_UTR_variant","3_prime_UTR_variant","1695/1725","-/1215","-/404"]
["YBX1",4904,"WUGSC","GRCh38","chr1",42696203,42696203,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.269C>T","ENST00000321358",42833,229,263,"T","ENSG00000065978","ENST00000321358","missense_variant","missense_variant","408/1514","269/975","90/324","A/V","gCc/gTc"]
["FAM189B",10712,"WUGSC","GRCh38","chr1",155254664,155254664,"+","Missense_Mutation","SNP","C","C","T","rs764162205",null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.214G>A","ENST00000361361",42747,77,51,"T","ENSG00000160767","ENST00000361361","missense_variant","missense_variant","724/3082","214/2007","72/668","A/T","Gct/Act"]
["LYST",1130,"WUGSC","GRCh38","chr1",235782033,235782033,"+","Silent","SNP","A","A","G",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.4917T>C","ENST00000389793","15/53",101,95,"G","ENSG00000143669","ENST00000389793","synonymous_variant","synonymous_variant","5092/13480","4917/11406","1639/3801","S","tcT/tcC"]
["ACPP",55,"WUGSC","GRCh38","chr3",132357078,132357078,"+","3'UTR","SNP","A","A","G","novel",null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.*200A>G","ENST00000336375",43018,21,32,"G","ENSG00000014257","ENST00000336375","3_prime_UTR_variant","3_prime_UTR_variant","1451/3125","-/1161","-/386"]
["H2AFZ",3015,"WUGSC","GRCh38","chr4",99948895,99948895,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.241C>T","ENST00000296417",42830,123,172,"A","ENSG00000164032","ENST00000296417","missense_variant","missense_variant","459/979","241/387","81/128","R/C","Cgt/Tgt"]
["PDE6A",5145,"WUGSC","GRCh38","chr5",149899469,149899469,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.1169T>C","ENST00000255266",43000,358,491,"G","ENSG00000132915","ENST00000255266","missense_variant","missense_variant","1289/5642","1169/2583","390/860","I/T","aTt/aCt"]
["CALN1",83698,"WUGSC","GRCh38","chr7",71787834,71787834,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.601T>C","ENST00000329008",42892,41,45,"G","ENSG00000183166","ENST00000329008","missense_variant","missense_variant","900/9243","601/660","201/219","F/L","Ttc/Ctc"]
["GBA2",57704,"WUGSC","GRCh38","chr9",35740055,35740055,"+","Missense_Mutation","SNP","C","C","T","rs200048828","byCluster","TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.1352G>A","ENST00000378103",42964,169,162,"T","ENSG00000070610","ENST00000378103","missense_variant","missense_variant","1876/3611","1352/2784","451/927","R/Q","cGa/cAa"]
["PLA2G12B",84647,"WUGSC","GRCh38","chr10",72954565,72954565,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.121G>A","ENST00000373032",42739,190,202,"T","ENSG00000138308","ENST00000373032","missense_variant","missense_variant","214/1128","121/588","41/195","G/R","Gga/Aga"]
["MS4A12",54860,"WUGSC","GRCh38","chr11",60502032,60502032,"+","Missense_Mutation","SNP","G","G","A","rs111546873","byCluster","TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.464G>A","ENST00000016913",42832,403,391,"A","ENSG00000071203","ENST00000016913","missense_variant","missense_variant","521/1167","464/804","155/267","R/H","cGt/cAt"]
["LPAR6",10161,"WUGSC","GRCh38","chr13",48411550,48411550,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.874T>A","ENST00000345941",42860,123,186,"T","ENSG00000139679","ENST00000345941","missense_variant","missense_variant","2017/2428","874/1035","292/344","Y/N","Tac/Aac"]
["DAAM1",23002,"WUGSC","GRCh38","chr14",59352550,59352550,"+","Missense_Mutation","SNP","A","A","G","rs150686067","byCluster","TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.2215A>G","ENST00000395125","18/25",77,67,"G","ENSG00000100592","ENST00000395125","missense_variant","missense_variant","2238/5806","2215/3237","739/1078","S/G","Agt/Ggt"]
["FAM83G",644815,"WUGSC","GRCh38","chr17",18978845,18978845,"+","Missense_Mutation","SNP","G","G","A","rs753302947",null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.821C>T","ENST00000345041",42861,11,14,"A","ENSG00000188522","ENST00000345041","missense_variant","missense_variant","987/2929","821/2472","274/823","T/M","aCg/aTg"]
["MYO5B",4645,"WUGSC","GRCh38","chr18",49835406,49835406,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.5332C>T","ENST00000285039","39/40",113,157,"A","ENSG00000167306","ENST00000285039","missense_variant","missense_variant","5632/9505","5332/5547","1778/1848","L/F","Ctt/Ttt"]
["FGF21",26291,"WUGSC","GRCh38","chr19",48756331,48756331,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.95C>T","ENST00000222157",42738,20,27,"T","ENSG00000105550","ENST00000222157","missense_variant","missense_variant","245/885","95/630","32/209","P/L","cCt/cTt"]
["PPM1F",9647,"WUGSC","GRCh38","chr22",21923402,21923402,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-A8-A09Z-01A-11W-A019-09","TCGA-A8-A09Z-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","8a59b247-da3f-4334-ad5c-f43f86164d5b","9e2abf15-6ef5-43a4-a4cb-60813371b770","c.1055A>G","ENST00000263212",42955,17,29,"C","ENSG00000100034","ENST00000263212","missense_variant","missense_variant","1161/5143","1055/1365","352/454","E/G","gAg/gGg"]
["ZNF213",7760,"WUGSC","GRCh38","chr16",3137253,3137253,"+","5'UTR","SNP","G","G","T","novel",null,"TCGA-LL-A6FP-01A-11D-A31U-09","TCGA-LL-A6FP-10A-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","a9d40165-b2c4-4bef-9406-7dbcabdab9fe","3ba91f1f-a638-4282-867f-5c2c6df6d248","c.-28G>T","ENST00000396878",42772,101,50,"T","ENSG00000085644","ENST00000396878","5_prime_UTR_variant","5_prime_UTR_variant","448/3313","-/1380","-/459"]
["BHLHB9",80823,"WUGSC","GRCh38","chrX",102751934,102751934,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-LL-A6FP-01A-11D-A31U-09","TCGA-LL-A6FP-10A-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","a9d40165-b2c4-4bef-9406-7dbcabdab9fe","3ba91f1f-a638-4282-867f-5c2c6df6d248","c.*1295C>T","ENST00000361229",42797,63,77,"T","ENSG00000198908","ENST00000361229","3_prime_UTR_variant","3_prime_UTR_variant","3467/3974","-/1644","-/547"]
["TFAP2D",83741,"WUGSC","GRCh38","chr6",50715493,50715493,"+","Silent","SNP","C","C","A",null,null,"TCGA-AR-A5QM-01A-11D-A27P-09","TCGA-AR-A5QM-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","be9c46db-f3c8-46d6-bb9e-b885a4c33e7e","bf63d4f2-a6df-4146-9ef6-5892fc21db95","c.417C>A","ENST00000008391",42774,63,71,"A","ENSG00000008197","ENST00000008391","synonymous_variant","synonymous_variant","645/1711","417/1359","139/452","A","gcC/gcA"]
["ANKRD52",283373,"WUGSC","GRCh38","chr12",56244434,56244434,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-AR-A254-01A-21D-A167-09","TCGA-AR-A254-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","fe2bdac0-832e-4268-bd8f-5dcfffda1979","d139e454-63f2-42da-8ab5-997fca0482b8","c.2724A>T","ENST00000267116","25/28",24,34,"A","ENSG00000139645","ENST00000267116","missense_variant","missense_variant;splice_region_variant","2846/8688","2724/3231","908/1076","E/D","gaA/gaT"]
["LGALS9B",284194,"WUGSC","GRCh38","chr17",20460393,20460393,"+","Silent","SNP","C","C","T","novel",null,"TCGA-A7-A0D9-01A-31W-A071-09","TCGA-A7-A0D9-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","c730a631-f3d0-4d7d-945a-b65c7a5a4d58","f671adda-19b8-4329-85a0-e25c344a92db","c.90G>A","ENST00000423676",42777,173,168,"T","ENSG00000170298","ENST00000423676","synonymous_variant","synonymous_variant","154/1713","90/1071","30/356","Q","caG/caA"]
["MEF2C",4208,"WUGSC","GRCh38","chr5",88721414,88721414,"+","3'UTR","SNP","A","A","C","novel",null,"TCGA-D8-A3Z6-01A-11D-A23C-09","TCGA-D8-A3Z6-10A-01D-A23C-09",null,null,"Somatic","Illumina HiSeq 2000","67a233d6-6e32-4224-a9af-c5579672d155","0ca11874-f9f6-4631-9a0a-1814a35f238c","c.*1190T>G","ENST00000437473",43050,58,42,"C","ENSG00000081189","ENST00000437473","3_prime_UTR_variant","3_prime_UTR_variant","3263/4340","-/1422","-/473"]
["GPC6",10082,"WUGSC","GRCh38","chr13",93227602,93227602,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-A2-A0YT-01A-11D-A10G-09","TCGA-A2-A0YT-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","827c6a2f-fb1b-4845-9cb1-11013a16da3f","75eb756e-e38e-4f94-867e-b4eabdf71c79","c.146A>T","ENST00000377047",42744,37,66,"T","ENSG00000183098","ENST00000377047","missense_variant","missense_variant","761/6467","146/1668","49/555","Y/F","tAc/tTc"]
["RFX1",5989,"WUGSC","GRCh38","chr19",13962862,13962862,"+","Nonsense_Mutation","SNP","C","A","A",null,null,"TCGA-AN-A0FY-01A-11W-A050-09","TCGA-AN-A0FY-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","a6a8bd08-0e60-442d-adce-de020177f82c","aa5cbdd2-e1f7-4d59-962a-3362278d401a","c.2773G>T","ENST00000254325","21/21",8,12,"A","ENSG00000132005","ENST00000254325","stop_gained","stop_gained;splice_region_variant","3008/4332","2773/2940","925/979","E/*","Gag/Tag"]
["TRPV6",55503,"WUGSC","GRCh38","chr7",142875550,142875550,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AC-A2B8-01A-11D-A17D-09","TCGA-AC-A2B8-10A-01D-A17D-09",null,null,"Somatic","Illumina HiSeq 2000","006faa97-572b-4015-a803-e1c9fa4a1be2","ca7ebf6b-a461-462e-9dbd-323b5aeba931","c.1040G>A","ENST00000359396",42962,43,55,"T","ENSG00000165125","ENST00000359396","missense_variant","missense_variant","1286/2928","1040/2178","347/725","C/Y","tGc/tAc"]
["GDPD4",220032,"WUGSC","GRCh38","chr11",77217252,77217252,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-E2-A2P6-01A-11D-A19Y-09","TCGA-E2-A2P6-10B-01D-A19Y-09",null,null,"Somatic","Illumina HiSeq 2000","b5d4557a-10ec-430e-a01a-c8b79c6fe3ea","bf78c46f-db59-42d8-85a1-56bb2498126e","c.1557G>A","ENST00000376217","17/17",83,51,"T","ENSG00000178795","ENST00000376217","missense_variant","missense_variant","1808/2502","1557/1872","519/623","M/I","atG/atA"]
["ARSK",153642,"WUGSC","GRCh38","chr5",95591520,95591520,"+","Missense_Mutation","SNP","G","G","A","rs375563497","byCluster;byFrequency","TCGA-E2-A1L6-01A-11D-A13L-09","TCGA-E2-A1L6-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","f610239f-5610-4d7b-bc31-ae3ccb9c425d","3388c646-ffac-43bf-b8a6-c5f216b17af0","c.991G>A","ENST00000380009",42894,193,63,"A","ENSG00000164291","ENST00000380009","missense_variant","missense_variant","1196/3354","991/1611","331/536","E/K","Gag/Aag"]
["OR52J3",119679,"WUGSC","GRCh38","chr11",5046982,5046982,"+","Missense_Mutation","SNP","C","C","T","rs774802089",null,"TCGA-AC-A4ZE-01A-11D-A41F-09","TCGA-AC-A4ZE-10B-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","bd2c5c5d-e623-4ff2-b890-d887a16d8e9f","78bcd852-ddd4-4b2b-b16f-a03ca9dc7a85","c.457C>T","ENST00000380370",42736,44,36,"T","ENSG00000205495","ENST00000380370","missense_variant","missense_variant","457/936","457/936","153/311","R/C","Cgt/Tgt"]
["OR5D16",390144,"WUGSC","GRCh38","chr11",55839529,55839529,"+","Missense_Mutation","SNP","C","C","G","rs375832312","byCluster;byFrequency","TCGA-A8-A081-01A-11W-A019-09","TCGA-A8-A081-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d29c3a5b-aab5-4d1b-bdaf-eb6fa405bc80","a28d918c-2d16-49c9-a5f8-0cf66224f940","c.778C>G","ENST00000378396",42736,466,236,"G","ENSG00000205029","ENST00000378396","missense_variant","missense_variant","778/987","778/987","260/328","L/V","Ctc/Gtc"]
["PRICKLE3",4007,"WUGSC","GRCh38","chrX",49175895,49175895,"+","Silent","SNP","C","C","T","rs782053613",null,"TCGA-A8-A081-01A-11W-A019-09","TCGA-A8-A081-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","d29c3a5b-aab5-4d1b-bdaf-eb6fa405bc80","a28d918c-2d16-49c9-a5f8-0cf66224f940","c.1626G>A","ENST00000599218",42987,130,86,"T","ENSG00000012211","ENST00000599218","synonymous_variant","synonymous_variant","1721/2062","1626/1848","542/615","S","tcG/tcA"]
["TDRD7",23424,"WUGSC","GRCh38","chr9",97473553,97473553,"+","Missense_Mutation","SNP","G","G","T","rs530102296",null,"TCGA-A2-A3Y0-01A-11D-A23C-09","TCGA-A2-A3Y0-10A-01D-A23C-09",null,null,"Somatic","Illumina HiSeq 2000","d8fbb398-d1da-4444-984a-22c8523625da","46e1fd58-c2ea-46ef-bfc9-26d61e7be608","c.2006G>T","ENST00000355295",43056,117,78,"T","ENSG00000196116","ENST00000355295","missense_variant","missense_variant","2301/3834","2006/3297","669/1098","C/F","tGc/tTc"]
["FXYD5",53827,"WUGSC","GRCh38","chr19",35155350,35155350,"+","5'UTR","SNP","G","G","A","novel",null,"TCGA-A2-A3Y0-01A-11D-A23C-09","TCGA-A2-A3Y0-10A-01D-A23C-09",null,null,"Somatic","Illumina HiSeq 2000","d8fbb398-d1da-4444-984a-22c8523625da","46e1fd58-c2ea-46ef-bfc9-26d61e7be608","c.-201G>A","ENST00000342879",42743,20,14,"A","ENSG00000089327","ENST00000342879","5_prime_UTR_variant","5_prime_UTR_variant","578/1580","-/537","-/178"]
["DDX55",57696,"WUGSC","GRCh38","chr12",123609964,123609964,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-D8-A1JE-01A-11D-A13L-09","TCGA-D8-A1JE-10A-01D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","bb34512b-2432-4256-968c-d7fdf38f126a","35afe2e2-1bdd-49ce-ba61-8a6f98749a17","c.577C>G","ENST00000238146",42930,78,50,"G","ENSG00000111364","ENST00000238146","missense_variant","missense_variant","627/2654","577/1803","193/600","P/A","Cca/Gca"]
["HPS3",84343,"WUGSC","GRCh38","chr3",149162326,149162326,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-D8-A27F-01A-11D-A16D-09","TCGA-D8-A27F-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","fc6d77a9-121b-48ab-a899-713c3d1319a2","a070d518-b1fe-4505-86b5-fc08201a4b61","c.2285T>A","ENST00000296051",43086,108,47,"A","ENSG00000163755","ENST00000296051","missense_variant","missense_variant","2425/4665","2285/3015","762/1004","F/Y","tTt/tAt"]
["ZNF524",147807,"WUGSC","GRCh38","chr19",55602499,55602499,"+","Silent","SNP","G","G","A","novel",null,"TCGA-A2-A25B-01A-11D-A167-09","TCGA-A2-A25B-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","6e839eaf-1dbb-43f5-8846-c980e05540c7","c16cf182-b4b2-42c0-a2b1-ce071638de2f","c.387G>A","ENST00000301073",42768,14,11,"A","ENSG00000171443","ENST00000301073","synonymous_variant","synonymous_variant","465/1102","387/795","129/264","L","ctG/ctA"]
["CLIP4",79745,"WUGSC","GRCh38","chr2",29143801,29143801,"+","Silent","SNP","C","C","A",null,null,"TCGA-A2-A0T3-01A-21D-A10Y-09","TCGA-A2-A0T3-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","0ca029bb-3b3a-48ec-8ade-5591e8e8629f","2c1a2795-e195-4f8d-a062-373aab5c50fc","c.741C>A","ENST00000320081",42932,127,68,"A","ENSG00000115295","ENST00000320081","synonymous_variant","synonymous_variant","996/4293","741/2118","247/705","I","atC/atA"]
["HSD3BP2",440606,"WUGSC","GRCh38","chr1",119445583,119445583,"+","RNA","SNP","C","C","T","novel",null,"TCGA-AR-A2LR-01A-12D-A18P-09","TCGA-AR-A2LR-10A-01D-A18P-09",null,null,"Somatic","Illumina HiSeq 2000","ed8d901f-d8ed-4c26-a7a0-a0baa383b0d2","8f2265a8-ea26-41f4-acf5-89c798d85e8f","n.615C>T","ENST00000457615",42797,25,19,"T","ENSG00000203858","ENST00000457615","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","615/1118"]
["PHTF2",57157,"WUGSC","GRCh38","chr7",77940597,77940597,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0DI-01A-21D-A12Q-09","TCGA-BH-A0DI-11A-32D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","3777748c-5614-4826-8cde-eb7ecefb8101","505bcff2-103a-4183-80cd-203ae6a5a31c","c.1810C>T","ENST00000248550","14/19",304,377,"T","ENSG00000006576","ENST00000248550","missense_variant","missense_variant","1886/4778","1810/2358","604/785","H/Y","Cat/Tat"]
["WAS",7454,"WUGSC","GRCh38","chrX",48689433,48689433,"+","Splice_Region","SNP","C","C","T",null,null,"TCGA-A7-A2KD-01A-31D-A21Q-09","TCGA-A7-A2KD-10A-01D-A21Q-09",null,null,"Somatic","Illumina HiSeq 2000","f8d373ee-1874-4d50-93ce-baea3d91bcf3","534d0ac4-dc2f-427f-911f-1b7b2a003306","c.1452C>T","ENST00000376701",43051,84,54,"T","ENSG00000015285","ENST00000376701","splice_region_variant","splice_region_variant;synonymous_variant","1527/1849","1452/1509","484/502","S","tcC/tcT"]
["EXOC3",11336,"WUGSC","GRCh38","chr5",447583,447583,"+","Silent","SNP","C","C","T",null,null,"TCGA-E2-A1BC-01A-11D-A14G-09","TCGA-E2-A1BC-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","5947a9db-7d13-44ff-86ad-eb5e6c8dcec5","6a4cd52f-2247-4caf-9b37-e90b02fd4d8b","c.195C>T","ENST00000512944",42807,35,50,"T","ENSG00000180104","ENST00000512944","synonymous_variant","synonymous_variant","384/2825","195/2238","65/745","L","ctC/ctT"]
["RINT1",60561,"WUGSC","GRCh38","chr7",105532153,105532153,"+","5'UTR","SNP","C","C","T","novel",null,"TCGA-5L-AAT0-01A-12D-A41F-09","TCGA-5L-AAT0-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","9a0adcc0-11a4-49c9-8aea-2b4274e3ee7b","a5f14a36-4024-4067-b4cd-b52fc8ef77db","c.-163C>T","ENST00000257700",42750,21,11,"T","ENSG00000135249","ENST00000257700","5_prime_UTR_variant","5_prime_UTR_variant","69/2976","-/2379","-/792"]
["OXA1L",5018,"WUGSC","GRCh38","chr14",22771323,22771323,"+","Silent","SNP","G","G","A","novel",null,"TCGA-5L-AAT0-01A-12D-A41F-09","TCGA-5L-AAT0-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","9a0adcc0-11a4-49c9-8aea-2b4274e3ee7b","a5f14a36-4024-4067-b4cd-b52fc8ef77db","c.1338G>A","ENST00000612549",42988,108,35,"A","ENSG00000155463","ENST00000612549","synonymous_variant","synonymous_variant","1338/2971","1338/1488","446/495","R","cgG/cgA"]
["TGM4",7047,"WUGSC","GRCh38","chr3",44901907,44901907,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A2-A04T-01A-21W-A050-09","TCGA-A2-A04T-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","d9ddc397-9cb7-4095-a7d2-1c1396891587","9482fe83-a4b1-424a-baf1-8b0f8e40c9b7","c.947C>T","ENST00000296125",42961,89,114,"T","ENSG00000163810","ENST00000296125","missense_variant","missense_variant","1015/3388","947/2055","316/684","T/I","aCc/aTc"]
["ZFAND5",7763,"WUGSC","GRCh38","chr9",72356050,72356050,"+","Missense_Mutation","SNP","T","T","A","novel",null,"TCGA-S3-AA10-01A-21D-A41F-09","TCGA-S3-AA10-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","c9d01f5d-66ef-45bc-b868-2b0151a8f9ee","0c0a48d4-aaac-4626-abbe-9370e5058f83","c.545A>T","ENST00000237937",42892,133,173,"A","ENSG00000107372","ENST00000237937","missense_variant","missense_variant","685/5310","545/642","182/213","D/V","gAc/gTc"]
["PALB2",79728,"WUGSC","GRCh38","chr16",23626389,23626389,"+","Silent","SNP","T","T","A","novel",null,"TCGA-B6-A0RT-01A-21D-A099-09","TCGA-B6-A0RT-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","e1a297ed-1951-4d97-978c-56b452111ba5","61f83071-b7fd-4037-aaf2-1db0349d8238","c.2595A>T","ENST00000261584",42929,137,116,"A","ENSG00000083093","ENST00000261584","synonymous_variant","synonymous_variant","2748/4003","2595/3561","865/1186","S","tcA/tcT"]
["KATNB1",10300,"WUGSC","GRCh38","chr16",57755212,57755212,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E9-A1N9-01A-11D-A14G-09","TCGA-E9-A1N9-10A-01D-A14G-09",null,null,"Somatic","Illumina HiSeq 2000","2aa7a1db-40a5-421b-97ab-1031e6fa7f04","8ad40192-c404-4cfa-b30c-1e76452dadbc","c.1390G>C","ENST00000379661","15/20",19,24,"C","ENSG00000140854","ENST00000379661","missense_variant","missense_variant","1782/2664","1390/1968","464/655","G/R","Ggg/Cgg"]
["PQLC2",54896,"WUGSC","GRCh38","chr1",19317730,19317730,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.53C>A","ENST00000375153",42774,308,240,"A","ENSG00000040487","ENST00000375153","missense_variant","missense_variant","693/2153","53/876","18/291","S/Y","tCc/tAc"]
["ARMC9",80210,"WUGSC","GRCh38","chr2",231256585,231256585,"+","Splice_Site","SNP","G","G","A",null,null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.880-1G>A","ENST00000611582",null,650,463,"A","ENSG00000135931","ENST00000611582","splice_acceptor_variant","splice_acceptor_variant","-/5759","880/2457","294/818"]
["VWA5B2",90113,"WUGSC","GRCh38","chr3",184234863,184234863,"+","Intron","SNP","G","G","A","novel",null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.945+108G>A","ENST00000426955",null,21,10,"A","ENSG00000145198","ENST00000426955","intron_variant","intron_variant","-/4120","-/3729","-/1242"]
["LAMA4",3910,"WUGSC","GRCh38","chr6",112109469,112109469,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.5440G>A","ENST00000230538","39/39",30,136,"T","ENSG00000112769","ENST00000230538","missense_variant","missense_variant","5838/6547","5440/5472","1814/1823","A/T","Gcc/Acc"]
["TLN1",7094,"WUGSC","GRCh38","chr9",35707174,35707174,"+","Missense_Mutation","SNP","C","C","T","rs780560798","byFrequency","TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.4853G>A","ENST00000314888","37/57",75,41,"T","ENSG00000137076","ENST00000314888","missense_variant","missense_variant","5207/8823","4853/7626","1618/2541","R/Q","cGg/cAg"]
["LETMD1",25875,"WUGSC","GRCh38","chr12",51049087,51049087,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.176A>G","ENST00000262055",42775,163,176,"G","ENSG00000050426","ENST00000262055","missense_variant","missense_variant","215/2112","176/1083","59/360","Y/C","tAt/tGt"]
["DENND4A",10260,"WUGSC","GRCh38","chr15",65752415,65752415,"+","Silent","SNP","C","C","T","rs201670474","by1000G;byCluster","TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.525G>A","ENST00000431932",11780,105,320,"T","ENSG00000174485","ENST00000431932","synonymous_variant","synonymous_variant","734/5875","525/5592","175/1863","T","acG/acA"]
["FAM134C",162427,"WUGSC","GRCh38","chr17",42586061,42586061,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.581A>G","ENST00000309428",42864,130,211,"C","ENSG00000141699","ENST00000309428","missense_variant","missense_variant","641/3759","581/1401","194/466","Y/C","tAc/tGc"]
["ILF3",3609,"WUGSC","GRCh38","chr19",10684057,10684057,"+","Intron","SNP","C","C","T","novel",null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.2059+87C>T","ENST00000590261",null,348,172,"T","ENSG00000129351","ENST00000590261","intron_variant","intron_variant","-/3219","-/2685","-/894"]
["RALGAPA2",57186,"WUGSC","GRCh38","chr20",20512826,20512826,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AO-A128-01A-11D-A10M-09","TCGA-AO-A128-10A-01D-A10M-09",null,null,"Somatic","Illumina Genome Analyzer II","46ae2a1c-e694-4a86-b127-e6fbaa676b69","cf7bd3e2-fe1d-43bc-a1dd-14197984162e","c.4543G>A","ENST00000202677","32/40",66,189,"T","ENSG00000188559","ENST00000202677","missense_variant","missense_variant","4551/6152","4543/5622","1515/1873","E/K","Gag/Aag"]
["NUAK2",81788,"WUGSC","GRCh38","chr1",205308333,205308333,"+","Intron","SNP","C","C","T","novel",null,"TCGA-A8-A07I-01A-11W-A019-09","TCGA-A8-A07I-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","7718c3f0-1c90-4940-bc30-ea4f417851bb","cca486f4-dbe7-4629-b5bc-bce1d97f9bfc","c.505-103G>A","ENST00000367157",null,113,30,"T","ENSG00000163545","ENST00000367157","intron_variant","intron_variant","-/3405","-/1887","-/628"]
["DDX20",11218,"WUGSC","GRCh38","chr1",111762714,111762714,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-BH-A0HA-01A-11D-A12Q-09","TCGA-BH-A0HA-11A-31D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","95f2ee35-a485-4995-8205-01623d97da2d","eb1421a0-3424-4a55-be66-9bea2d867c12","c.1142T>C","ENST00000369702",42989,565,392,"C","ENSG00000064703","ENST00000369702","missense_variant","missense_variant","1762/4212","1142/2475","381/824","V/A","gTt/gCt"]
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["CPSF1",29894,"WUGSC","GRCh38","chr8",144399613,144399613,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-A8-A08S-01A-11W-A050-09","TCGA-A8-A08S-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","9c981525-80af-4f79-b94a-be00131ab872","91135c15-292f-49d0-9eb0-ca16ac6a6a32","c.1217G>T","ENST00000616140",14215,43,35,"A","ENSG00000071894","ENST00000616140","missense_variant","missense_variant","1292/4494","1217/4332","406/1443","S/I","aGt/aTt"]
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["SRF",6722,"WUGSC","GRCh38","chr6",43173960,43173960,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-BH-A0BF-01A-21D-A12Q-09","TCGA-BH-A0BF-11A-31D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000;Illumina Genome Analyzer II","39221056-704b-4a23-9b8d-3178dd9e790d","df0f49fe-e68c-42d3-8dbf-fc08672ac4fb","c.627G>C","ENST00000265354",42773,133,187,"C","ENSG00000112658","ENST00000265354","missense_variant","missense_variant","985/4202","627/1527","209/508","E/D","gaG/gaC"]
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["GK2",2712,"WUGSC","GRCh38","chr4",79407874,79407874,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-C8-A12T-01A-11D-A10Y-09","TCGA-C8-A12T-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","961fae8a-d944-4866-b198-ea6f1e59a979","7ccbb62c-9382-43ef-ba5f-3f81d0074e07","c.327C>A","ENST00000358842",42736,141,218,"T","ENSG00000196475","ENST00000358842","stop_gained","stop_gained","420/1942","327/1662","109/553","Y/*","taC/taA"]
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["KCNH5",27133,"WUGSC","GRCh38","chr14",63006463,63006463,"+","Silent","SNP","A","A","G",null,null,"TCGA-B6-A0I8-01A-11W-A050-09","TCGA-B6-A0I8-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","ba80b13a-e20a-441b-b845-b617cc861ce7","4ff30155-adbf-49dd-a3f2-d040142f0b6f","c.207T>C","ENST00000322893",42805,218,154,"G","ENSG00000140015","ENST00000322893","synonymous_variant","synonymous_variant","476/11290","207/2967","69/988","Y","taT/taC"]
["SLC1A4",6509,"WUGSC","GRCh38","chr2",65010676,65010676,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-OL-A5DA-01A-11D-A27P-09","TCGA-OL-A5DA-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","df98fc00-d39c-4d26-a90a-76543158ddca","036cd1a3-6f1d-4099-93c3-125e1b280698","c.713A>C","ENST00000234256",42833,86,94,"C","ENSG00000115902","ENST00000234256","missense_variant","missense_variant","956/4561","713/1599","238/532","K/T","aAg/aCg"]
["NPHS1",4868,"WUGSC","GRCh38","chr19",35830859,35830859,"+","Silent","SNP","G","G","A","rs747950877",null,"TCGA-D8-A1XO-01A-11D-A14K-09","TCGA-D8-A1XO-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","b5ff68a2-da74-4608-941e-dbac40153077","19f00cd8-b25b-4b38-a55d-b6360c693945","c.3579C>T","ENST00000378910","28/29",62,46,"A","ENSG00000161270","ENST00000378910","synonymous_variant","synonymous_variant","3579/4276","3579/3726","1193/1241","Y","taC/taT"]
["ZNF829",374899,"WUGSC","GRCh38","chr19",36892182,36892182,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-C8-A12P-01A-11D-A10Y-09","TCGA-C8-A12P-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","540fe594-0186-40d3-b519-c1ccebe82247","323e0bfd-8f8f-41a8-a94a-8d2d862a15b1","c.609G>C","ENST00000391711",42892,86,130,"G","ENSG00000185869","ENST00000391711","missense_variant","missense_variant","974/1805","609/1299","203/432","Q/H","caG/caC"]
["ATP11C",286410,"WUGSC","GRCh38","chrX",139743570,139743570,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-EW-A1OZ-01A-11D-A142-09","TCGA-EW-A1OZ-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","a73152be-2293-403d-940b-74ac05810808","86f8904b-36e9-4dbf-9cd4-dafefc783b32","c.3028G>A","ENST00000327569","26/30",39,65,"T","ENSG00000101974","ENST00000327569","missense_variant","missense_variant","3127/6115","3028/3399","1010/1132","V/I","Gta/Ata"]
["PNPLA8",50640,"WUGSC","GRCh38","chr7",108515073,108515073,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-E2-A15A-01A-11D-A12B-09","TCGA-E2-A15A-10A-01D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","b7e3eff1-65d5-491f-a726-35dc6752b370","e33c2754-8dec-4bab-b626-1886a5756536","c.419C>G","ENST00000257694",42805,234,274,"C","ENSG00000135241","ENST00000257694","missense_variant","missense_variant","714/3490","419/2349","140/782","S/W","tCg/tGg"]
["IFNA10",3446,"WUGSC","GRCh38","chr9",21206511,21206511,"+","3'UTR","SNP","C","C","T","rs765972463","byFrequency","TCGA-C8-A134-01A-11D-A10Y-09","TCGA-C8-A134-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","a3e8738b-2456-4f08-bb3d-5debb4265f85","b25af510-abd7-402a-96bf-6532cb18ec71","c.*17G>A","ENST00000357374",42736,544,365,"T","ENSG00000186803","ENST00000357374","3_prime_UTR_variant","3_prime_UTR_variant","633/963","-/570","-/189"]
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["ZNF622",90441,"WUGSC","GRCh38","chr5",16463684,16463684,"+","Silent","SNP","G","G","A",null,null,"TCGA-AR-A24M-01A-11D-A167-09","TCGA-AR-A24M-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","722a8960-3a69-4f66-b972-74e6de94a1e8","89946989-b650-4ddd-86dc-b6e459588d38","c.684C>T","ENST00000308683",42772,57,58,"A","ENSG00000173545","ENST00000308683","synonymous_variant","synonymous_variant","811/1699","684/1434","228/477","D","gaC/gaT"]
["LRRC4B",94030,"WUGSC","GRCh38","chr19",50518697,50518697,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0AV-01A-31D-A10Y-09","TCGA-BH-A0AV-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","9032b7fe-e38a-4641-a45e-67041668adc4","3ab50b2e-8b0c-4ccd-b6bf-d577f5e9fc94","c.1016G>T","ENST00000389201",42797,72,75,"A","ENSG00000131409","ENST00000389201","missense_variant","missense_variant","1153/2958","1016/2142","339/713","R/L","cGc/cTc"]
["GARS",2617,"WUGSC","GRCh38","chr7",30603537,30603537,"+","Missense_Mutation","SNP","G","G","A","rs373326652","byCluster;byFrequency","TCGA-C8-A135-01A-11D-A10Y-09","TCGA-C8-A135-10A-02D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","6b47c22f-8b4e-40fd-9a12-18b539521224","4fef2aff-1a1d-434a-910b-ce94fff48677","c.700G>A","ENST00000389266",42903,177,226,"A","ENSG00000106105","ENST00000389266","missense_variant","missense_variant","941/2634","700/2220","234/739","E/K","Gaa/Aaa"]
["PKNOX2",63876,"WUGSC","GRCh38","chr11",125431343,125431343,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A2-A0D3-01A-11D-A10Y-09","TCGA-A2-A0D3-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","8183420e-7f44-4024-b3db-6b53ad293988","e23f0ac2-c466-4431-a23a-94bf6a1f5db6","c.1370C>T","ENST00000298282","13/13",95,31,"T","ENSG00000165495","ENST00000298282","missense_variant","missense_variant","1641/3687","1370/1419","457/472","T/M","aCg/aTg"]
["BCAR3",8412,"WUGSC","GRCh38","chr1",93582559,93582559,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-BH-A1F0-01A-11D-A135-09","TCGA-BH-A1F0-11B-23D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","3903b485-366d-4318-b17d-a0194f032bd8","64613d52-ad24-4f06-8668-3e058043911b","c.1428G>C","ENST00000260502",42928,231,235,"G","ENSG00000137936","ENST00000260502","missense_variant","missense_variant","1671/3171","1428/2478","476/825","L/F","ttG/ttC"]
["FSHB",2488,"WUGSC","GRCh38","chr11",30233994,30233994,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-A8-A09W-01A-11W-A019-09","TCGA-A8-A09W-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","9a2690ce-485f-4d4f-9673-d86f91be27a4","e6862e84-130f-487b-8d60-43c783d2a8bf","c.*194G>C","ENST00000254122",42797,21,19,"C","ENSG00000131808","ENST00000254122","3_prime_UTR_variant","3_prime_UTR_variant","653/1698","-/390","-/129"]
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["DDX21",9188,"WUGSC","GRCh38","chr10",68977659,68977659,"+","Missense_Mutation","SNP","G","G","A","rs766890848",null,"TCGA-C8-A12K-01A-21D-A10Y-09","TCGA-C8-A12K-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","bcf92c27-3aa7-4449-9c7a-fc715789788f","5516f85d-911f-451a-b9b2-3bf9b4e5d74b","c.1873G>A","ENST00000354185",43084,121,65,"A","ENSG00000165732","ENST00000354185","missense_variant","missense_variant","1971/4711","1873/2352","625/783","D/N","Gac/Aac"]
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["ATR",545,"WUGSC","GRCh38","chr3",142450232,142450232,"+","Intron","SNP","C","C","T","novel",null,"TCGA-AO-A03T-01A-21W-A050-09","TCGA-AO-A03T-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","cbea866d-da66-4f7c-994b-c1ec35aa2d4b","467c3965-5537-4c89-a3f0-ba3eca9854b4","c.7762-630G>A","ENST00000350721",null,25,34,"T","ENSG00000175054","ENST00000350721","intron_variant","intron_variant","-/8249","-/7935","-/2644"]
["MTPAP",55149,"WUGSC","GRCh38","chr10",30313851,30313851,"+","Nonsense_Mutation","SNP","G","G","A","rs754233439","byFrequency","TCGA-BH-A1ET-01A-11D-A135-09","TCGA-BH-A1ET-11B-23D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","9bd66613-68ad-42c1-ab43-dac1386027f9","55ca01bf-18c0-48b3-b83f-4e13b5161bde","c.1507C>T","ENST00000263063",42987,179,208,"A","ENSG00000107951","ENST00000263063","stop_gained","stop_gained","1551/5601","1507/1749","503/582","R/*","Cga/Tga"]
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["DKC1",1736,"WUGSC","GRCh38","chrX",154764921,154764921,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-AR-A24H-01A-11D-A167-09","TCGA-AR-A24H-10A-01D-A167-09",null,null,"Somatic","Illumina HiSeq 2000","6bb61dce-289d-4e39-8298-df5abe8049a2","c1697a30-99bb-4999-b91a-36d587c1faab","c.39T>G","ENST00000369550",42781,78,203,"G","ENSG00000130826","ENST00000369550","missense_variant","missense_variant","249/2577","39/1545","13/514","H/Q","caT/caG"]
["ANP32A",8125,"WUGSC","GRCh38","chr15",68780076,68780076,"+","3'UTR","SNP","T","T","C","novel",null,"TCGA-D8-A140-01A-11D-A10Y-09","TCGA-D8-A140-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","795f051e-01c4-4b49-b179-bd18ba24433c","3294b1ce-7e97-4973-86d3-71866f5a16c7","c.*5A>G","ENST00000465139",42923,99,123,"C","ENSG00000140350","ENST00000465139","3_prime_UTR_variant","3_prime_UTR_variant","899/2440","-/750","-/249"]
["PRR27",401137,"WUGSC","GRCh38","chr4",70156077,70156077,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-AR-A2LK-01A-11D-A17W-09","TCGA-AR-A2LK-10A-01D-A17W-09",null,null,"Somatic","Illumina HiSeq 2000","7b0b60c7-5fa0-440e-937f-8d82119330d6","adfefa9c-2e3e-444d-8018-f364999f5f42","c.75G>T","ENST00000344526",42771,78,82,"T","ENSG00000187533","ENST00000344526","missense_variant","missense_variant;splice_region_variant","264/3127","75/660","25/219","E/D","gaG/gaT"]
["TNXB",7148,"WUGSC","GRCh38","chr6",32053554,32053554,"+","Silent","SNP","C","C","T",null,null,"TCGA-BH-A1EN-01A-11D-A17G-09","TCGA-BH-A1EN-11A-23W-A14R-09",null,null,"Somatic","Illumina HiSeq 2000","ca100ef0-be45-415f-909d-7172261d0084","ac317f91-d40e-4c6c-bca4-9220150a5af9","c.8625G>A","ENST00000375244","25/44",20,19,"T","ENSG00000168477","ENST00000375244","synonymous_variant","synonymous_variant","8827/13132","8625/12735","2875/4244","L","ctG/ctA"]
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["RBMS1",5937,"WUGSC","GRCh38","chr2",160284833,160284833,"+","Missense_Mutation","SNP","C","C","G","novel",null,"TCGA-E2-A576-01A-11D-A31U-09","TCGA-E2-A576-10B-01D-A31U-09",null,null,"Somatic","Illumina HiSeq 2000","ecfc6434-115c-46e4-a5cf-ce441cb67a86","44b61726-1130-4060-9c99-6b6a7918ae53","c.842G>C","ENST00000348849",42992,64,96,"G","ENSG00000153250","ENST00000348849","missense_variant","missense_variant","1273/4273","842/1221","281/406","R/P","cGa/cCa"]
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["FERMT2",10979,"WUGSC","GRCh38","chr14",52858541,52858541,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-C8-A1HF-01A-11D-A135-09","TCGA-C8-A1HF-10A-01D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","508a26f2-d117-44aa-b579-00a119b8bcc4","7ab5304c-1c60-4d91-8009-808ae01ee432","c.1879G>C","ENST00000341590","15/15",263,249,"G","ENSG00000073712","ENST00000341590","missense_variant","missense_variant","2065/3338","1879/2043","627/680","E/Q","Gag/Cag"]
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["ZNF22",7570,"WUGSC","GRCh38","chr10",45003781,45003781,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-A2-A0CM-01A-31W-A050-09","TCGA-A2-A0CM-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","fe8023d4-5476-4c58-bf70-cbf65cdd4327","be44d49f-6519-4d7c-a1ba-577c7b365a37","c.413C>T","ENST00000298299",42768,81,124,"T","ENSG00000165512","ENST00000298299","missense_variant","missense_variant","1006/2551","413/675","138/224","P/L","cCc/cTc"]
["MYLK",4638,"WUGSC","GRCh38","chr3",123726055,123726055,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AO-A0JA-01A-11W-A071-09","TCGA-AO-A0JA-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","0215d4f1-6697-4e8f-afc4-ff7c6439e56d","55ed9925-691d-43df-8472-2d6a52bc9068","c.1540C>T","ENST00000360304",12359,18,24,"A","ENSG00000065534","ENST00000360304","missense_variant","missense_variant","1726/7738","1540/5745","514/1914","P/S","Ccc/Tcc"]
["N4BP3",23138,"WUGSC","GRCh38","chr5",178119576,178119576,"+","5'UTR","SNP","G","G","T","novel",null,"TCGA-E2-A1L7-01A-11D-A142-09","TCGA-E2-A1L7-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","33a09072-6554-4d46-b738-0852624940af","f5286adc-5c10-4b09-a433-daeca4c1f377","c.-8G>T","ENST00000274605",42771,24,26,"T","ENSG00000145911","ENST00000274605","5_prime_UTR_variant","5_prime_UTR_variant","352/6080","-/1635","-/544"]
["TEX14",56155,"WUGSC","GRCh38","chr17",58587976,58587976,"+","Silent","SNP","C","C","T",null,null,"TCGA-D8-A4Z1-01A-21D-A25Q-09","TCGA-D8-A4Z1-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","c74f345b-5217-42db-88d0-ab14aab1b1f3","032b2649-73ad-4838-bd51-afd845fee9b1","c.2640G>A","ENST00000240361","16/33",70,55,"T","ENSG00000121101","ENST00000240361","synonymous_variant","synonymous_variant","2726/4911","2640/4494","880/1497","Q","caG/caA"]
["CISD1",55847,"WUGSC","GRCh38","chr10",58277302,58277302,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A8-A0A4-01A-11W-A019-09","TCGA-A8-A0A4-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","1fc4d542-86ac-42bc-9fbb-272c23e6aa72","db493df5-6038-4dc3-8bc7-eab44d4d9dcb","c.217C>T","ENST00000333926",42769,161,144,"T","ENSG00000122873","ENST00000333926","missense_variant","missense_variant","433/2479","217/327","73/108","R/C","Cgt/Tgt"]
["GNPTAB",79158,"WUGSC","GRCh38","chr12",101766156,101766156,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-A8-A076-01A-21W-A019-09","TCGA-A8-A076-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","dfa06058-320b-4cc6-ac18-a42e59019b1c","20b982d3-ac52-4a42-8b01-05bc860a6b2b","c.1547A>G","ENST00000299314",43090,617,408,"C","ENSG00000111670","ENST00000299314","missense_variant","missense_variant","1810/5701","1547/3771","516/1256","D/G","gAt/gGt"]
["ADRBK1",156,"WUGSC","GRCh38","chr11",67282437,67282437,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-A8-A0A2-01A-11W-A050-09","TCGA-A8-A0A2-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","b681dba3-a608-47c2-9ae8-5d761d1e800e","74e986b0-8284-4f30-8bbd-6132f40ed403","c.1055G>A","ENST00000308595","13/21",16,44,"A","ENSG00000173020","ENST00000308595","missense_variant","missense_variant;splice_region_variant","1345/3466","1055/2070","352/689","G/D","gGc/gAc"]
["MSH4",4438,"WUGSC","GRCh38","chr1",75880089,75880089,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A1FC-01A-11D-A13L-09","TCGA-BH-A1FC-11A-32D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","84c77098-03d0-4b22-afb1-797703e85c6c","ba3a5382-893d-4365-88cd-b4922f5c070e","c.1717G>A","ENST00000263187","13/20",220,84,"A","ENSG00000057468","ENST00000263187","missense_variant","missense_variant","1821/3266","1717/2811","573/936","D/N","Gat/Aat"]
["C16orf62",57020,"WUGSC","GRCh38","chr16",19616699,19616699,"+","Missense_Mutation","SNP","C","C","T","rs749175686","byFrequency","TCGA-BH-A1FC-01A-11D-A13L-09","TCGA-BH-A1FC-11A-32D-A188-09",null,null,"Somatic","Illumina HiSeq 2000","84c77098-03d0-4b22-afb1-797703e85c6c","ba3a5382-893d-4365-88cd-b4922f5c070e","c.1115C>T","ENST00000417362","14/31",146,99,"T","ENSG00000103544","ENST00000417362","missense_variant","missense_variant","1125/3115","1115/2892","372/963","T/M","aCg/aTg"]
["RAB23",51715,"WUGSC","GRCh38","chr6",57190454,57190454,"+","3'UTR","SNP","A","A","T","novel",null,"TCGA-B6-A0WZ-01A-11D-A10G-09","TCGA-B6-A0WZ-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","f6b8b1a9-370c-4023-b8bd-934e2a3d913a","a477963b-b0e1-4394-bfa3-cfc26c651ac8","c.*7T>A","ENST00000317483",42923,199,233,"T","ENSG00000112210","ENST00000317483","3_prime_UTR_variant","3_prime_UTR_variant","875/2546","-/714","-/237"]
["ARCN1",372,"WUGSC","GRCh38","chr11",118597872,118597872,"+","Silent","SNP","A","A","G","rs782702821","byFrequency","TCGA-BH-A0AU-01A-11D-A12Q-09","TCGA-BH-A0AU-11A-11D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","d06209b8-8aba-44d8-b94a-990861c2324a","9b7a36f8-d6c8-49f5-bfaf-26661bac3be3","c.1407A>G","ENST00000264028",42988,217,319,"G","ENSG00000095139","ENST00000264028","synonymous_variant","synonymous_variant","1502/3845","1407/1536","469/511","Q","caA/caG"]
["HEPH",9843,"WUGSC","GRCh38","chrX",66189773,66189773,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-E9-A22G-01A-11D-A159-09","TCGA-E9-A22G-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","2be1b92a-6041-4d2b-9cf8-b9723921987f","b88f0c85-3a9c-44fa-a09a-563e6cf8521f","c.898G>A","ENST00000343002",42875,77,105,"A","ENSG00000089472","ENST00000343002","missense_variant","missense_variant","1562/4854","898/3477","300/1158","E/K","Gaa/Aaa"]
["RYR1",6261,"WUGSC","GRCh38","chr19",38528322,38528322,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-BH-A0B9-01A-11W-A071-09","TCGA-BH-A0B9-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","c57595bb-7953-4611-b0d1-3c2c40feb3b9","02613b8d-b01c-401a-a0be-71f258dea92a","c.10841A>G","ENST00000359596","74/106",68,50,"G","ENSG00000196218","ENST00000359596","missense_variant","missense_variant","10841/15117","10841/15117","3614/5038","K/R","aAg/aGg"]
["DCDC1",341019,"WUGSC","GRCh38","chr11",31306386,31306386,"+","Missense_Mutation","SNP","A","A","G","rs143406648",null,"TCGA-AN-A0FT-01A-11W-A050-09","TCGA-AN-A0FT-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","0598fc5f-9651-4ace-bf4e-56759d544e52","520abbc0-ff40-4a8e-b002-c36bac79cb72","c.437T>C","ENST00000452803",42864,39,77,"G","ENSG00000170959","ENST00000452803","missense_variant","missense_variant;splice_region_variant","639/1706","437/1065","146/354","V/A","gTt/gCt"]
["FREM2",341640,"WUGSC","GRCh38","chr13",38861490,38861490,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-B6-A0RP-01A-21D-A099-09","TCGA-B6-A0RP-10A-01D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","efbdb449-b885-44bb-9054-9e97d6603cad","d989e1d9-e13d-4767-b907-b450b745a00e","c.7579C>T","ENST00000280481","15/24",53,103,"T","ENSG00000150893","ENST00000280481","missense_variant","missense_variant","7795/16070","7579/9510","2527/3169","R/C","Cgc/Tgc"]
["NPHP1",4867,"WUGSC","GRCh38","chr2",110125679,110125679,"+","Missense_Mutation","SNP","A","A","T","novel",null,"TCGA-A8-A09A-01A-11W-A019-09","TCGA-A8-A09A-10A-01W-A062-09",null,null,"Somatic","Illumina Genome Analyzer II","ecfedc29-5c31-4d3d-b599-fc0a1c0beafa","c3017ca7-a84a-4cc3-9eb0-0336f130be31","c.1884T>A","ENST00000393272","19/20",310,289,"T","ENSG00000144061","ENST00000393272","missense_variant","missense_variant;splice_region_variant","1982/2752","1884/2199","628/732","S/R","agT/agA"]
["OR1S1",219959,"WUGSC","GRCh38","chr11",58215330,58215330,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A8-A09A-01A-11W-A019-09","TCGA-A8-A09A-10A-01W-A062-09",null,null,"Somatic","Illumina Genome Analyzer II","ecfedc29-5c31-4d3d-b599-fc0a1c0beafa","c3017ca7-a84a-4cc3-9eb0-0336f130be31","c.586C>T","ENST00000309433",42736,212,137,"T","ENSG00000172774","ENST00000309433","missense_variant","missense_variant","586/978","586/978","196/325","P/S","Cct/Tct"]
["NCOR1",9611,"WUGSC","GRCh38","chr17",16158827,16158827,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-D8-A1XJ-01A-11D-A14K-09","TCGA-D8-A1XJ-10A-01W-A16I-09",null,null,"Somatic","Illumina HiSeq 2000","a37b27a2-c3b0-4f62-82a2-94e9205b1d6e","bb7de09d-aefe-45f2-8e12-7af57c30cbf4","c.665C>A","ENST00000268712",16954,62,99,"T","ENSG00000141027","ENST00000268712","missense_variant","missense_variant","923/10720","665/7323","222/2440","P/H","cCc/cAc"]
["CHRNA1",1134,"WUGSC","GRCh38","chr2",174759333,174759333,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A0HU-01A-11W-A050-09","TCGA-BH-A0HU-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","b46f2619-5937-4847-bb38-fe6022225ab9","630a5659-c666-4da0-bb90-969cf071fde3","c.232C>A","ENST00000261007",42804,94,146,"T","ENSG00000138435","ENST00000261007","missense_variant","missense_variant;splice_region_variant","299/1980","232/1449","78/482","Q/K","Cag/Aag"]
["UQCRC2",7385,"WUGSC","GRCh38","chr16",21983096,21983096,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-C8-A137-01A-11D-A10Y-09","TCGA-C8-A137-10A-02D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","08778f40-d895-46f1-8e7b-122fc598418b","16cfd410-cb75-4177-884e-c3abf7e4aebb","c.1287G>C","ENST00000268379","14/14",150,70,"C","ENSG00000140740","ENST00000268379","missense_variant","missense_variant","2051/2615","1287/1362","429/453","K/N","aaG/aaC"]
["MFSD11",79157,"WUGSC","GRCh38","chr17",76778247,76778247,"+","Silent","SNP","C","C","G","novel",null,"TCGA-C8-A1HI-01A-11D-A135-09","TCGA-C8-A1HI-10A-01D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","75dc3bff-75da-4734-b930-a18fd3d1ebfe","6944644c-a43b-4a5b-b506-7427227f3eb0","c.1245C>G","ENST00000336509","14/14",907,813,"G","ENSG00000092931","ENST00000336509","synonymous_variant","synonymous_variant","1499/2538","1245/1350","415/449","L","ctC/ctG"]
["CAMSAP3",57662,"WUGSC","GRCh38","chr19",7617578,7617578,"+","Missense_Mutation","SNP","A","A","C","novel",null,"TCGA-A2-A0D4-01A-11W-A019-09","TCGA-A2-A0D4-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","f3accede-1716-4d44-bad4-5427a9ebd675","9223d8eb-db2b-469a-94fc-857f5b62996c","c.3361A>C","ENST00000160298","16/17",22,34,"C","ENSG00000076826","ENST00000160298","missense_variant","missense_variant","3462/3889","3361/3750","1121/1249","N/H","Aac/Cac"]
["SLITRK6",84189,"WUGSC","GRCh38","chr13",85795773,85795773,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0DL-01A-11D-A10Y-09","TCGA-BH-A0DL-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","6d1b5971-5b99-41a9-9a7d-79adc0d6dd5f","261ed647-077d-4071-978f-ca030947436b","c.736G>T","ENST00000400286",42768,53,58,"A","ENSG00000184564","ENST00000400286","missense_variant","missense_variant","1335/4318","736/2526","246/841","V/F","Gtc/Ttc"]
["TFAP2A",7020,"WUGSC","GRCh38","chr6",10419520,10419520,"+","5'Flank","SNP","C","C","T","novel",null,"TCGA-D8-A27L-01A-11D-A16D-09","TCGA-D8-A27L-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","10666107-dffb-4c51-b3ee-71e70cde7c88","39acbfee-141d-4c6a-bf04-abb40344659f",null,"ENST00000482890",null,20,30,"T","ENSG00000137203","ENST00000482890","upstream_gene_variant","upstream_gene_variant","-/2071","-/1314","-/437"]
["CIT",11113,"WUGSC","GRCh38","chr12",119712314,119712314,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AR-A0TY-01A-12W-A12T-09","TCGA-AR-A0TY-10A-01D-A110-09",null,null,"Somatic","Illumina HiSeq 2000","f915733b-aaf4-406d-af52-00de113e8e0c","f5cfd725-897e-4728-91bc-ba3957d43764","c.4592C>T","ENST00000261833","36/47",581,623,"A","ENSG00000122966","ENST00000261833","missense_variant","missense_variant","4645/8578","4592/6084","1531/2027","P/L","cCg/cTg"]
["PRDM11",56981,"WUGSC","GRCh38","chr11",45224299,45224299,"+","Silent","SNP","G","G","A",null,null,"TCGA-AO-A03P-01A-11W-A019-09","TCGA-AO-A03P-10A-01W-A021-09",null,null,"Somatic","Illumina HiSeq 2000","185c5e15-c068-4a72-8d5e-468624bf958a","bac92eb4-e818-4d79-b4b0-b10c31ba6d4e","c.927G>A","ENST00000530656",42923,356,601,"A","ENSG00000019485","ENST00000530656","synonymous_variant","synonymous_variant","927/1536","927/1536","309/511","V","gtG/gtA"]
["ADGRE1",2015,"WUGSC","GRCh38","chr19",6919723,6919723,"+","Silent","SNP","C","C","T",null,null,"TCGA-E2-A1B0-01A-11D-A12Q-09","TCGA-E2-A1B0-10A-01D-A12Q-09",null,null,"Somatic","Illumina HiSeq 2000","14e3b00c-cbec-4733-8fa4-829b8e7d9808","ce4b0897-884b-4483-b105-7677ddcb341d","c.1596C>T","ENST00000312053","13/21",102,161,"T","ENSG00000174837","ENST00000312053","synonymous_variant","synonymous_variant","1633/3128","1596/2661","532/886","I","atC/atT"]
["ENPP6",133121,"WUGSC","GRCh38","chr4",184124167,184124167,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A1EV-01A-11D-A135-09","TCGA-BH-A1EV-11A-24D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","43fbe2a9-078a-4be2-b67c-b855329091f0","5a28c2e5-4aec-49d5-beaa-3546005f5ba5","c.527C>T","ENST00000296741",42802,218,353,"A","ENSG00000164303","ENST00000296741","missense_variant","missense_variant","669/3936","527/1323","176/440","S/F","tCc/tTc"]
["PPEF1",5475,"WUGSC","GRCh38","chrX",18749829,18749829,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A1EV-01A-11D-A135-09","TCGA-BH-A1EV-11A-24D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","43fbe2a9-078a-4be2-b67c-b855329091f0","5a28c2e5-4aec-49d5-beaa-3546005f5ba5","c.273G>A","ENST00000361511",42935,202,195,"A","ENSG00000086717","ENST00000361511","missense_variant","missense_variant","767/2890","273/1962","91/653","M/I","atG/atA"]
["GYPA",2993,"WUGSC","GRCh38","chr4",144111146,144111146,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-A2-A0EQ-01A-11W-A050-09","TCGA-A2-A0EQ-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","2c449ea9-c3ff-4726-8566-5933e2b7056d","282ea476-ac8e-4aa3-ac9e-49fced7a4eb2","c.*248C>T","ENST00000360771",42923,32,26,"A","ENSG00000170180","ENST00000360771","3_prime_UTR_variant","3_prime_UTR_variant","817/2659","-/453","-/150"]
["PLD3",23646,"WUGSC","GRCh38","chr19",40374597,40374597,"+","Silent","SNP","T","T","G",null,null,"TCGA-A2-A0EQ-01A-11W-A050-09","TCGA-A2-A0EQ-10A-01W-A055-09",null,null,"Somatic","Illumina HiSeq 2000","2c449ea9-c3ff-4726-8566-5933e2b7056d","282ea476-ac8e-4aa3-ac9e-49fced7a4eb2","c.996T>G","ENST00000356508",43021,58,65,"G","ENSG00000105223","ENST00000356508","synonymous_variant","synonymous_variant","1119/1906","996/1473","332/490","T","acT/acG"]
["GATA3",2625,"WUGSC","GRCh38","chr10",8073783,8073783,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AR-A0U2-01A-11D-A10G-09","TCGA-AR-A0U2-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","f0194733-2347-43c4-a4a3-131642c27798","15bcbeef-a0ab-4b73-878e-34328e6270f4","c.1092A>T","ENST00000346208",42892,86,76,"T","ENSG00000107485","ENST00000346208","missense_variant","missense_variant","1547/2654","1092/1332","364/443","R/S","agA/agT"]
["ERMAP",114625,"WUGSC","GRCh38","chr1",42830730,42830730,"+","Intron","SNP","C","C","T","rs565545614","by1000G","TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.86-38C>T","ENST00000372514",null,41,21,"T","ENSG00000164010","ENST00000372514","intron_variant","intron_variant","-/3369","-/1428","-/475"]
["ANKRD45",339416,"WUGSC","GRCh38","chr1",173624808,173624808,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.709T>C","ENST00000333279",42861,270,174,"G","ENSG00000183831","ENST00000333279","missense_variant","missense_variant","770/1446","709/801","237/266","F/L","Ttc/Ctc"]
["RNF149",284996,"WUGSC","GRCh38","chr2",101294932,101294932,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.710A>G","ENST00000295317",42773,34,31,"C","ENSG00000163162","ENST00000295317","missense_variant","missense_variant;splice_region_variant","818/2458","710/1203","237/400","Q/R","cAg/cGg"]
["C5orf42",65250,"WUGSC","GRCh38","chr5",37195860,37195860,"+","Missense_Mutation","SNP","A","A","C","novel",null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.3809T>G","ENST00000425232","21/52",151,92,"C","ENSG00000197603","ENST00000425232","missense_variant","missense_variant;splice_region_variant","4040/11199","3809/9594","1270/3197","I/R","aTa/aGa"]
["PKHD1",5314,"WUGSC","GRCh38","chr6",51746719,51746719,"+","Splice_Site","SNP","A","A","G","novel",null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.9998+2T>C","ENST00000371117",null,267,147,"G","ENSG00000170927","ENST00000371117","splice_donor_variant","splice_donor_variant","-/16282","9998/12225","3333/4074"]
["SLC26A4",5172,"WUGSC","GRCh38","chr7",107694632,107694632,"+","Silent","SNP","A","A","G",null,null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.1353A>G","ENST00000265715",43090,250,174,"G","ENSG00000091137","ENST00000265715","synonymous_variant","synonymous_variant","1577/4930","1353/2343","451/780","A","gcA/gcG"]
["JAK2",3717,"WUGSC","GRCh38","chr9",5089672,5089672,"+","Splice_Site","SNP","A","A","G","novel",null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.2572-2A>G","ENST00000381652",null,321,125,"G","ENSG00000096968","ENST00000381652","splice_acceptor_variant","splice_acceptor_variant","-/5285","2572/3399","858/1132"]
["PLET1",349633,"WUGSC","GRCh38","chr11",112248929,112248929,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.494T>G","ENST00000338832",42829,92,61,"C","ENSG00000188771","ENST00000338832","missense_variant","missense_variant","765/1215","494/624","165/207","F/C","tTc/tGc"]
["CARKD",55739,"WUGSC","GRCh38","chr13",110622292,110622292,"+","Silent","SNP","T","T","C","novel",null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.177T>C","ENST00000309957",42776,204,176,"C","ENSG00000213995","ENST00000309957","synonymous_variant","synonymous_variant","191/2659","177/1173","59/390","N","aaT/aaC"]
["MYLK3",91807,"WUGSC","GRCh38","chr16",46727178,46727178,"+","Intron","SNP","A","A","T","novel",null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.1914+58T>A","ENST00000394809",null,40,42,"T","ENSG00000140795","ENST00000394809","intron_variant","intron_variant","-/6911","-/2460","-/819"]
["ZFP3",124961,"WUGSC","GRCh38","chr17",5093047,5093047,"+","3'UTR","SNP","T","T","G","novel",null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.*34T>G","ENST00000318833",42768,24,21,"G","ENSG00000180787","ENST00000318833","3_prime_UTR_variant","3_prime_UTR_variant","1879/5206","-/1509","-/502"]
["PDYN",5173,"WUGSC","GRCh38","chr20",1980564,1980564,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.524A>G","ENST00000217305",42829,104,84,"C","ENSG00000101327","ENST00000217305","missense_variant","missense_variant","750/2555","524/765","175/254","Y/C","tAt/tGt"]
["CELSR1",9620,"WUGSC","GRCh38","chr22",46367007,46367007,"+","Missense_Mutation","SNP","C","C","T","rs775423517","byFrequency","TCGA-D8-A1XK-01A-21D-A14K-09","TCGA-D8-A1XK-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","8b704b7c-56d2-4816-8c47-055a794afb69","9f5b3aca-b473-43e0-9dc5-6339152822a5","c.8191G>A","ENST00000262738","29/35",20,20,"T","ENSG00000075275","ENST00000262738","missense_variant","missense_variant","8191/11389","8191/9045","2731/3014","A/T","Gcc/Acc"]
["DENND1B",163486,"WUGSC","GRCh38","chr1",197642733,197642733,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-A8-A06U-01A-11W-A019-09","TCGA-A8-A06U-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","277c2e8a-dd28-4b8f-96d3-ea790a1986b6","115bb522-26a3-418d-90bb-e786e9c87b88","c.650T>G","ENST00000367396",43024,64,67,"C","ENSG00000213047","ENST00000367396","missense_variant","missense_variant","820/2177","650/1281","217/426","I/S","aTt/aGt"]
["ATXN2L",11273,"WUGSC","GRCh38","chr16",28836271,28836271,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-A8-A06U-01A-11W-A019-09","TCGA-A8-A06U-10A-01W-A021-09",null,null,"Somatic","Illumina Genome Analyzer II","277c2e8a-dd28-4b8f-96d3-ea790a1986b6","115bb522-26a3-418d-90bb-e786e9c87b88","c.*6C>G","ENST00000336783","22/22",65,36,"G","ENSG00000168488","ENST00000336783","3_prime_UTR_variant","3_prime_UTR_variant","3401/4367","-/3228","-/1075"]
["FCGBP",8857,"WUGSC","GRCh38","chr19",39883304,39883304,"+","Splice_Site","SNP","C","C","T","novel",null,"TCGA-E2-A14N-01A-31D-A135-09","TCGA-E2-A14N-10A-01D-A135-09",null,null,"Somatic","Illumina HiSeq 2000","00c8d151-2223-4e36-8c66-6c09e42d8777","d2ad26e4-a4a8-45de-9f85-c681a2a49f43","c.8530+1G>A","ENST00000616721",null,211,240,"T","ENSG00000275395","ENST00000616721","splice_donor_variant","splice_donor_variant","-/12787","8530/12615","2844/4204"]
["GP6",51206,"WUGSC","GRCh38","chr19",55014890,55014890,"+","3'UTR","SNP","C","C","G",null,null,"TCGA-D8-A1XW-01A-11D-A14K-09","TCGA-D8-A1XW-10A-01D-A14K-09",null,null,"Somatic","Illumina HiSeq 2000","f29405cc-d712-4562-ac02-ca3c89fb82af","df416cf7-8ddc-4ee0-b925-78a7e849ad84","c.*31G>C","ENST00000417454",42955,52,80,"G","ENSG00000088053","ENST00000417454","3_prime_UTR_variant","3_prime_UTR_variant","1079/2264","-/1020","-/339"]
["FAM208A",23272,"WUGSC","GRCh38","chr3",56647128,56647128,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A1J9-01A-11D-A13L-09","TCGA-D8-A1J9-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","6627e4b1-b34c-4aa2-836e-093061442a6d","6014c1c1-0619-4ea0-9f83-1e7a2523a083","c.1609C>T","ENST00000493960","14/24",30,36,"A","ENSG00000163946","ENST00000493960","stop_gained","stop_gained","1620/5600","1609/4539","537/1512","Q/*","Cag/Tag"]
["CATSPERB",79820,"WUGSC","GRCh38","chr14",91617650,91617650,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-D8-A1J9-01A-11D-A13L-09","TCGA-D8-A1J9-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","6627e4b1-b34c-4aa2-836e-093061442a6d","6014c1c1-0619-4ea0-9f83-1e7a2523a083","c.2347G>A","ENST00000256343","20/27",119,85,"T","ENSG00000133962","ENST00000256343","missense_variant","missense_variant","2504/3623","2347/3351","783/1116","D/N","Gat/Aat"]
["ZNF460",10794,"WUGSC","GRCh38","chr19",57290716,57290716,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-D8-A1J9-01A-11D-A13L-09","TCGA-D8-A1J9-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","6627e4b1-b34c-4aa2-836e-093061442a6d","6014c1c1-0619-4ea0-9f83-1e7a2523a083","c.175G>A","ENST00000360338",42797,35,15,"A","ENSG00000197714","ENST00000360338","missense_variant","missense_variant","497/3350","175/1689","59/562","E/K","Gag/Aag"]
["RAET1G",353091,"WUGSC","GRCh38","chr6",149919620,149919620,"+","Silent","SNP","C","C","T",null,null,"TCGA-E2-A159-01A-11D-A10Y-09","TCGA-E2-A159-10A-01D-A110-09",null,null,"Somatic","Illumina Genome Analyzer II","757c8a2d-90cf-4dab-a4dd-45f3cbdeaeeb","deb6d361-2e35-4b88-8f3b-db1382e05f18","c.282G>A","ENST00000367360",42771,1203,1581,"T","ENSG00000203722","ENST00000367360","synonymous_variant","synonymous_variant","350/1107","282/1005","94/334","L","ctG/ctA"]
["OR51E2",81285,"WUGSC","GRCh38","chr11",4681906,4681906,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-D8-A27N-01A-11D-A16D-09","TCGA-D8-A27N-10A-01D-A16D-09",null,null,"Somatic","Illumina HiSeq 2000","6a411174-582a-4c68-bb04-5ea2e504bf7c","de420622-f742-4781-873a-e9faffc94dd3","c.806C>A","ENST00000396950",42768,37,42,"T","ENSG00000167332","ENST00000396950","missense_variant","missense_variant","1046/2781","806/963","269/320","P/H","cCc/cAc"]
["CYP2C19",1557,"WUGSC","GRCh38","chr10",94762850,94762850,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-OL-A5D7-01A-11D-A27P-09","TCGA-OL-A5D7-10A-01D-A27P-09",null,null,"Somatic","Illumina HiSeq 2000","eec1b52b-f280-4731-8860-a57a790cdaac","1928b73f-4080-4d99-980f-7b7cd456a955","c.145G>T","ENST00000371321",42744,48,31,"T","ENSG00000165841","ENST00000371321","missense_variant","missense_variant","227/1901","145/1473","49/490","D/Y","Gat/Tat"]
["ARHGEF17",9828,"WUGSC","GRCh38","chr11",73311230,73311230,"+","Silent","SNP","C","C","T",null,null,"TCGA-A8-A07G-01A-11W-A050-09","TCGA-A8-A07G-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II","49f77aa5-446b-49f6-bd1b-02d3ff7b9dfc","a50c80c4-329f-456f-b86c-c97d2443ab75","c.2592C>T","ENST00000263674",42756,16,22,"T","ENSG00000110237","ENST00000263674","synonymous_variant","synonymous_variant","2942/7853","2592/6192","864/2063","P","ccC/ccT"]
["BRPF3",27154,"WUGSC","GRCh38","chr6",36214354,36214354,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-OL-A66J-01A-11D-A29N-09","TCGA-OL-A66J-10A-01D-A29N-09",null,null,"Somatic","Illumina HiSeq 2000","b2b9b36e-1584-453c-a2cb-6455ef27e088","65db66df-0e02-40dd-9c2a-cc353d980700","c.2957G>A","ENST00000357641",42960,28,87,"A","ENSG00000096070","ENST00000357641","missense_variant","missense_variant","3210/6052","2957/3618","986/1205","G/E","gGg/gAg"]
["UNC5D",137970,"WUGSC","GRCh38","chr8",35683726,35683726,"+","Splice_Region","SNP","C","C","T","rs141886860","by1000G;byCluster;byFrequency","TCGA-E9-A1RE-01A-11D-A159-09","TCGA-E9-A1RE-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","4a9c0873-f496-48a4-853c-2b41b2dbaa9e","56e80c27-e4b1-4c17-a104-61ae05c5ce82","c.750C>T","ENST00000404895",42872,32,36,"T","ENSG00000156687","ENST00000404895","splice_region_variant","splice_region_variant;synonymous_variant","1078/3252","750/2862","250/953","Y","taC/taT"]
["CA1",759,"WUGSC","GRCh38","chr8",85341646,85341646,"+","5'UTR","SNP","T","T","A","novel",null,"TCGA-BH-A18Q-01A-12D-A12B-09","TCGA-BH-A18Q-11A-34D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","a4de6680-33c3-4f6f-8696-453470a00bcb","7a579f39-1175-4207-a069-b49b9cd87782","c.-11A>T","ENST00000431316",42774,434,540,"A","ENSG00000133742","ENST00000431316","5_prime_UTR_variant","5_prime_UTR_variant","105/1232","-/786","-/261"]
["VPS13A",23230,"WUGSC","GRCh38","chr9",77177737,77177737,"+","Silent","SNP","G","G","A",null,null,"TCGA-EW-A1OV-01A-11D-A142-09","TCGA-EW-A1OV-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","e27ca8f5-3f76-4531-87ea-ba3a44f6830d","39d05c29-a4bb-4b5f-a818-c94045721134","c.33G>A","ENST00000360280",26299,51,33,"A","ENSG00000197969","ENST00000360280","synonymous_variant","synonymous_variant","293/15320","33/9525",465625,"L","ttG/ttA"]
["KRI1",65095,"WUGSC","GRCh38","chr19",10561664,10561664,"+","Splice_Region","SNP","C","C","T","novel",null,"TCGA-EW-A1OV-01A-11D-A142-09","TCGA-EW-A1OV-10A-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","e27ca8f5-3f76-4531-87ea-ba3a44f6830d","39d05c29-a4bb-4b5f-a818-c94045721134","c.506+3G>A","ENST00000312962",null,72,61,"T","ENSG00000129347","ENST00000312962","splice_region_variant","splice_region_variant;intron_variant","-/3023","-/2130","-/709"]
["CALM1",801,"WUGSC","GRCh38","chr14",90406167,90406167,"+","3'UTR","SNP","G","G","T","novel",null,"TCGA-S3-AA11-01A-31D-A41F-09","TCGA-S3-AA11-10B-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","d75dce39-dd23-42b0-a8b8-f75f33ebfa30","258a07ab-aafc-4d28-ac91-86eeeb6b7d16","c.*1450G>T","ENST00000356978",42892,133,118,"T","ENSG00000198668","ENST00000356978","3_prime_UTR_variant","3_prime_UTR_variant","2148/4242","-/450","-/149"]
["USP9X",8239,"WUGSC","GRCh38","chrX",41162861,41162861,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-A1-A0SP-01A-11D-A099-09","TCGA-A1-A0SP-10A-02D-A099-09",null,null,"Somatic","Illumina Genome Analyzer II","d3ae9617-b6cd-4d98-b631-39bd4afd3c4e","a409caa8-efd1-4fc8-9753-fa253e65c58d","c.1969C>T","ENST00000324545","15/45",216,404,"T","ENSG00000124486","ENST00000324545","missense_variant","missense_variant","2602/12401","1969/7713","657/2570","R/W","Cgg/Tgg"]
["CRTAC1",55118,"WUGSC","GRCh38","chr10",97895980,97895980,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-BH-A0B8-01A-21W-A071-09","TCGA-BH-A0B8-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","29798513-2bb1-49f8-8cf3-c903d72072c3","362512ab-407f-47d5-9d9a-dd29647fd176","c.1222G>A","ENST00000370597",43023,134,57,"T","ENSG00000095713","ENST00000370597","missense_variant","missense_variant","1578/2890","1222/1986","408/661","V/M","Gtg/Atg"]
["KLF17",128209,"WUGSC","GRCh38","chr1",44129716,44129716,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AR-A0U3-01A-11D-A10G-09","TCGA-AR-A0U3-10A-01D-A10G-09",null,null,"Somatic","Illumina Genome Analyzer II","c8251555-77d3-4a20-9cc0-f7df0fda5955","264507ec-fd44-4bf0-94aa-abbe52c03810","c.445G>A","ENST00000372299",42770,28,65,"A","ENSG00000171872","ENST00000372299","missense_variant","missense_variant","503/3131","445/1170","149/389","G/R","Ggg/Agg"]
["ADCK4",79934,"WUGSC","GRCh38","chr19",40705395,40705395,"+","Silent","SNP","C","C","T","novel",null,"TCGA-BH-A18K-01A-11D-A12B-09","TCGA-BH-A18K-11A-13D-A12B-09",null,null,"Somatic","Illumina HiSeq 2000","f75de986-bc8a-4ffe-9b35-011eee3a1446","1a1312ef-4a37-445c-80e5-529fdf7827ee","c.420G>A","ENST00000324464",42901,30,42,"T","ENSG00000123815","ENST00000324464","synonymous_variant","synonymous_variant","722/2443","420/1635","140/544","E","gaG/gaA"]
["VWC2L",402117,"WUGSC","GRCh38","chr2",214414266,214414266,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-OL-A5RW-01A-11D-A28B-09","TCGA-OL-A5RW-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","8e4c566c-99f9-4ca5-a8df-c2535130630a","5b3549a7-5b4e-4942-a53d-471d76c3341a","c.73A>G","ENST00000312504",42770,139,63,"G","ENSG00000174453","ENST00000312504","missense_variant","missense_variant","875/4610","73/669","25/222","S/G","Agt/Ggt"]
["EIF3A",8661,"WUGSC","GRCh38","chr10",119042614,119042614,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-OL-A5RW-01A-11D-A28B-09","TCGA-OL-A5RW-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","8e4c566c-99f9-4ca5-a8df-c2535130630a","5b3549a7-5b4e-4942-a53d-471d76c3341a","c.2906G>C","ENST00000369144","19/22",69,53,"G","ENSG00000107581","ENST00000369144","missense_variant","missense_variant","3034/6646","2906/4149","969/1382","R/T","aGa/aCa"]
["MIR527",574497,"WUGSC","GRCh38","chr19",53754102,53754102,"+","RNA","SNP","A","A","G",null,null,"TCGA-OL-A5RW-01A-11D-A28B-09","TCGA-OL-A5RW-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","8e4c566c-99f9-4ca5-a8df-c2535130630a","5b3549a7-5b4e-4942-a53d-471d76c3341a","n.85A>G","ENST00000385244",42736,107,55,"G","ENSG00000207979","ENST00000385244","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","85/85"]
["FAHD2B",151313,"WUGSC","GRCh38","chr2",97091658,97091658,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-A1-A0SI-01A-11D-A142-09","TCGA-A1-A0SI-10B-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","e218c272-a7e1-4bc9-b8c5-d2d1c903550f","fbcab9dc-4a6b-4928-9459-699c9932e3e1","c.49C>T","ENST00000272610",42774,54,38,"A","ENSG00000144199","ENST00000272610","stop_gained","stop_gained","237/1305","49/945","17/314","Q/*","Cag/Tag"]
["HSP90B1",7184,"WUGSC","GRCh38","chr12",103943737,103943737,"+","Splice_Site","SNP","G","G","C",null,null,"TCGA-A1-A0SI-01A-11D-A142-09","TCGA-A1-A0SI-10B-01D-A142-09",null,null,"Somatic","Illumina HiSeq 2000","e218c272-a7e1-4bc9-b8c5-d2d1c903550f","fbcab9dc-4a6b-4928-9459-699c9932e3e1","c.1891-1G>C","ENST00000299767",null,52,32,"C","ENSG00000166598","ENST00000299767","splice_acceptor_variant","splice_acceptor_variant","-/2858","1891/2412","631/803"]
["LETM1",3954,"WUGSC","GRCh38","chr4",1832900,1832900,"+","Silent","SNP","A","A","G",null,null,"TCGA-E9-A1RF-01A-11D-A159-09","TCGA-E9-A1RF-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","43983619-d863-4816-a334-445f6ca36541","0c36d388-c63d-4ab1-8303-6d5005708525","c.924T>C","ENST00000302787",42900,43,64,"G","ENSG00000168924","ENST00000302787","synonymous_variant","synonymous_variant","1221/5462","924/2220","308/739","F","ttT/ttC"]
["SRCAP",10847,"WUGSC","GRCh38","chr16",30733916,30733916,"+","Nonsense_Mutation","SNP","G","G","T",null,null,"TCGA-E9-A1RF-01A-11D-A159-09","TCGA-E9-A1RF-10A-01D-A159-09",null,null,"Somatic","Illumina HiSeq 2000","43983619-d863-4816-a334-445f6ca36541","0c36d388-c63d-4ab1-8303-6d5005708525","c.6517G>T","ENST00000262518","30/34",53,125,"T","ENSG00000080603","ENST00000262518","stop_gained","stop_gained","6902/11754","6517/9693","2173/3230","E/*","Gag/Tag"]
["ATR",545,"WUGSC","GRCh38","chr3",142451516,142451516,"+","Intron","SNP","G","G","C","novel",null,"TCGA-A8-A0AD-01A-11W-A071-09","TCGA-A8-A0AD-10A-01W-A071-09",null,null,"Somatic","Illumina Genome Analyzer II","6e6511fa-4f6e-4184-84b8-9e9e7a863632","6efc67f6-3999-44ca-859b-c1fb69c7c699","c.7761+1612C>G","ENST00000350721",null,29,42,"C","ENSG00000175054","ENST00000350721","intron_variant","intron_variant","-/8249","-/7935","-/2644"]
["NLRP11",204801,"WUGSC","GRCh38","chr19",55809402,55809402,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.1208G>A","ENST00000589093",42804,42,34,"T","ENSG00000179873","ENST00000589093","missense_variant","missense_variant","1302/3417","1208/3102","403/1033","G/E","gGa/gAa"]
["SCRT2",85508,"WUGSC","GRCh38","chr20",662817,662817,"+","3'UTR","SNP","G","G","T","novel",null,"TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.*854C>A","ENST00000246104",42768,40,31,"T","ENSG00000215397","ENST00000246104","3_prime_UTR_variant","3_prime_UTR_variant","2356/3577","-/924","-/307"]
["DIP2A",23181,"WUGSC","GRCh38","chr21",46547055,46547055,"+","Intron","SNP","G","G","A","rs375260481","by1000G;byCluster","TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.2522+13G>A","ENST00000417564",null,59,72,"A","ENSG00000160305","ENST00000417564","intron_variant","intron_variant","-/6967","-/4716","-/1571"]
["SLC25A1",6576,"WUGSC","GRCh38","chr22",19175958,19175958,"+","3'UTR","SNP","A","A","C","novel",null,"TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.*172T>G","ENST00000215882",42987,32,18,"C","ENSG00000100075","ENST00000215882","3_prime_UTR_variant","3_prime_UTR_variant","1265/1648","-/936","-/311"]
["ERCC6L",54821,"WUGSC","GRCh38","chrX",72207213,72207213,"+","Silent","SNP","T","T","C",null,null,"TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.1554A>G","ENST00000334463",42768,53,60,"C","ENSG00000186871","ENST00000334463","synonymous_variant","synonymous_variant","1690/4243","1554/3753","518/1250","K","aaA/aaG"]
["TMEM164",84187,"WUGSC","GRCh38","chrX",110003552,110003552,"+","5'UTR","SNP","C","C","A","novel",null,"TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.-223C>A","ENST00000372068",42773,74,76,"A","ENSG00000157600","ENST00000372068","5_prime_UTR_variant","5_prime_UTR_variant","117/5566","-/894","-/297"]
["HCFC1",3054,"WUGSC","GRCh38","chrX",153949114,153949114,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.*233C>T","ENST00000310441","26/26",57,39,"A","ENSG00000172534","ENST00000310441","3_prime_UTR_variant","3_prime_UTR_variant","7308/8869","-/6108","-/2035"]
["HCFC1",3054,"WUGSC","GRCh38","chrX",153955374,153955374,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-LL-A5YM-01A-11D-A28B-09","TCGA-LL-A5YM-10A-01D-A28E-09",null,null,"Somatic","Illumina HiSeq 2000","ad4322ee-f3f7-42de-8510-6b7e64a91662","2453a8b7-bf16-47c9-9452-cecd1c18f2d3","c.3025G>A","ENST00000310441","17/26",90,94,"T","ENSG00000172534","ENST00000310441","missense_variant","missense_variant","3992/8869","3025/6108","1009/2035","V/I","Gtc/Atc"]
["SRSF10",10772,"WUGSC","GRCh38","chr1",23980312,23980312,"+","5'UTR","SNP","C","C","T","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.-57G>A","ENST00000492112",42741,28,21,"T","ENSG00000188529","ENST00000492112","5_prime_UTR_variant","5_prime_UTR_variant","8/1631","-/789","-/262"]
["ZFP69",339559,"WUGSC","GRCh38","chr1",40495494,40495494,"+","Missense_Mutation","SNP","G","G","A","rs752437339",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1016G>A","ENST00000372705",42892,33,27,"A","ENSG00000187815","ENST00000372705","missense_variant","missense_variant","1310/2104","1016/1581","339/526","R/H","cGc/cAc"]
["ZCCHC11",23318,"WUGSC","GRCh38","chr1",52425495,52425495,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.4721G>A","ENST00000371544","29/30",35,24,"T","ENSG00000134744","ENST00000371544","missense_variant","missense_variant","4984/5858","4721/4935","1574/1644","R/Q","cGa/cAa"]
["LRP8",7804,"WUGSC","GRCh38","chr1",53264229,53264229,"+","Missense_Mutation","SNP","C","C","T","rs758211330","byFrequency","TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1595G>A","ENST00000306052",43027,51,26,"T","ENSG00000157193","ENST00000306052","missense_variant","missense_variant","1697/7648","1595/2892","532/963","R/H","cGc/cAc"]
["AGL",178,"WUGSC","GRCh38","chr1",99884453,99884453,"+","Splice_Site","SNP","T","T","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.2546+2T>C","ENST00000294724",null,25,32,"C","ENSG00000162688","ENST00000294724","splice_donor_variant","splice_donor_variant","-/7446","2546/4599","849/1532"]
["SWT1",54823,"WUGSC","GRCh38","chr1",185290894,185290894,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.*91G>C","ENST00000367500","19/19",16,11,"C","ENSG00000116668","ENST00000367500","3_prime_UTR_variant","3_prime_UTR_variant","2959/3830","-/2703","-/900"]
["ZNF281",23528,"WUGSC","GRCh38","chr1",200408596,200408596,"+","Silent","SNP","G","G","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1110C>G","ENST00000294740",42768,59,52,"C","ENSG00000162702","ENST00000294740","synonymous_variant","synonymous_variant","1235/4891","1110/2688","370/895","V","gtC/gtG"]
["CACNA1S",779,"WUGSC","GRCh38","chr1",201069577,201069577,"+","Silent","SNP","G","G","T","rs200730765","by1000G;byCluster","TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.2385C>A","ENST00000362061","18/44",56,23,"T","ENSG00000081248","ENST00000362061","synonymous_variant","synonymous_variant","2612/6166","2385/5622","795/1873","I","atC/atA"]
["CNST",163882,"WUGSC","GRCh38","chr1",246642009,246642009,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.909G>C","ENST00000366513",42958,47,40,"C","ENSG00000162852","ENST00000366513","missense_variant","missense_variant","1178/5126","909/2178","303/725","K/N","aaG/aaC"]
["OR2L13",284521,"WUGSC","GRCh38","chr1",248099600,248099600,"+","Silent","SNP","C","C","A",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.225C>A","ENST00000358120",42768,101,77,"A","ENSG00000196071","ENST00000358120","synonymous_variant","synonymous_variant","370/1692","225/939","75/312","T","acC/acA"]
["WDR82",80335,"WUGSC","GRCh38","chr3",52268316,52268316,"+","Intron","SNP","G","G","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.260-1298C>G","ENST00000296490",null,38,35,"C","ENSG00000164091","ENST00000296490","intron_variant","intron_variant","-/4293","-/942","-/313"]
["DNAH1",25981,"WUGSC","GRCh38","chr3",52331296,52331296,"+","Silent","SNP","G","G","T",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1020G>T","ENST00000420323",28672,23,23,"T","ENSG00000114841","ENST00000420323","synonymous_variant","synonymous_variant","1281/13104","1020/12798","340/4265","G","ggG/ggT"]
["CACNA1D",776,"WUGSC","GRCh38","chr3",53776951,53776951,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.4582T>A","ENST00000350061","37/48",60,35,"A","ENSG00000157388","ENST00000350061","missense_variant","missense_variant","5093/7636","4582/6486","1528/2161","C/S","Tgc/Agc"]
["ADAMTS9",56999,"WUGSC","GRCh38","chr3",64681254,64681254,"+","Missense_Mutation","SNP","C","C","T","rs146464879","by1000G;byCluster;byFrequency","TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.626G>A","ENST00000498707",14671,156,155,"T","ENSG00000163638","ENST00000498707","missense_variant","missense_variant","969/7624","626/5808","209/1935","R/H","cGc/cAc"]
["SLC9A9",285195,"WUGSC","GRCh38","chr3",143652293,143652293,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.717G>C","ENST00000316549",42902,51,28,"G","ENSG00000181804","ENST00000316549","missense_variant","missense_variant","926/3627","717/1938","239/645","E/D","gaG/gaC"]
["ZBBX",79740,"WUGSC","GRCh38","chr3",167350456,167350456,"+","Silent","SNP","T","T","C","rs376791064","byCluster","TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.492A>G","ENST00000392766",42999,101,71,"C","ENSG00000169064","ENST00000392766","synonymous_variant","synonymous_variant","833/3250","492/2403","164/800","K","aaA/aaG"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179210291,179210291,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1357G>A","ENST00000263967",42968,68,49,"A","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","1514/9093","1357/3207","453/1068","E/K","Gaa/Aaa"]
["AC226119.5",0,"WUGSC","GRCh38","chr4",3940271,3940271,"+","Intron","SNP","C","C","G","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","n.159+12840G>C","ENST00000514073",null,43,50,"G","ENSG00000253917","ENST00000514073","intron_variant","intron_variant;non_coding_transcript_variant","-/682"]
["CCSER1",401145,"WUGSC","GRCh38","chr4",90628217,90628217,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1917G>C","ENST00000509176",42897,36,17,"C","ENSG00000184305","ENST00000509176","missense_variant","missense_variant","2205/5847","1917/2703","639/900","K/N","aaG/aaC"]
["EGFLAM",133584,"WUGSC","GRCh38","chr5",38451443,38451443,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.2696G>C","ENST00000354891","20/23",48,38,"C","ENSG00000164318","ENST00000354891","missense_variant","missense_variant","3042/3963","2696/3054","899/1017","G/A","gGa/gCa"]
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["DUSP22",56940,"WUGSC","GRCh38","chr6",350668,350668,"+","Intron","SNP","T","T","C","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.509-154T>C","ENST00000344450",null,32,27,"C","ENSG00000112679","ENST00000344450","intron_variant","intron_variant","-/1485","-/555","-/184"]
["TINAG",27283,"WUGSC","GRCh38","chr6",54349810,54349810,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.994C>T","ENST00000259782",42927,38,30,"T","ENSG00000137251","ENST00000259782","missense_variant","missense_variant","1090/1754","994/1431","332/476","R/W","Cgg/Tgg"]
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["TNS3",64759,"WUGSC","GRCh38","chr7",47368449,47368449,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.2197C>G","ENST00000311160","17/31",30,25,"C","ENSG00000136205","ENST00000311160","missense_variant","missense_variant","2555/7618","2197/4338","733/1445","P/A","Cca/Gca"]
["MUC12",10071,"WUGSC","GRCh38","chr7",101005073,101005073,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.14939C>T","ENST00000379442",42870,52,99,"T","ENSG00000205277","ENST00000379442","missense_variant","missense_variant","14939/16737","14939/16437","4980/5478","S/L","tCa/tTa"]
["CUL1",8454,"WUGSC","GRCh38","chr7",148760428,148760428,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.721G>C","ENST00000325222",42938,65,43,"C","ENSG00000055130","ENST00000325222","missense_variant","missense_variant","1000/3064","721/2331","241/776","E/Q","Gag/Cag"]
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["TMEM71",137835,"WUGSC","GRCh38","chr8",132751911,132751911,"+","Missense_Mutation","SNP","C","C","T","rs542588923","by1000G","TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.188G>A","ENST00000356838",42835,76,39,"T","ENSG00000165071","ENST00000356838","missense_variant","missense_variant","331/1993","188/831","63/276","R/Q","cGa/cAa"]
["PPRC1",23082,"WUGSC","GRCh38","chr10",102139338,102139338,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.830A>C","ENST00000278070",42869,57,37,"C","ENSG00000148840","ENST00000278070","missense_variant","missense_variant","869/5330","830/4995","277/1664","H/P","cAt/cCt"]
["PTDSS2",81490,"WUGSC","GRCh38","chr11",489687,489687,"+","Missense_Mutation","SNP","G","G","A","rs777043477",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1069G>A","ENST00000308020",43020,56,25,"A","ENSG00000174915","ENST00000308020","missense_variant","missense_variant","1245/2445","1069/1464","357/487","V/M","Gtg/Atg"]
["UBQLN3",50613,"WUGSC","GRCh38","chr11",5508352,5508352,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1207A>C","ENST00000311659",42768,90,59,"G","ENSG00000175520","ENST00000311659","missense_variant","missense_variant","1355/2407","1207/1968","403/655","I/L","Atc/Ctc"]
["SLC22A6",9356,"WUGSC","GRCh38","chr11",62983591,62983591,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.574C>T","ENST00000377871",42804,64,37,"A","ENSG00000197901","ENST00000377871","missense_variant","missense_variant","841/2151","574/1692","192/563","R/W","Cgg/Tgg"]
["DSCAML1",57453,"WUGSC","GRCh38","chr11",117435789,117435789,"+","Silent","SNP","T","T","C",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.4911A>G","ENST00000321322","27/33",62,33,"C","ENSG00000177103","ENST00000321322","synonymous_variant","synonymous_variant","4913/6899","4911/6342","1637/2113","P","ccA/ccG"]
["CACNA1C",775,"WUGSC","GRCh38","chr12",2493344,2493344,"+","Silent","SNP","C","C","T",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1071C>T","ENST00000347598",18080,55,42,"T","ENSG00000151067","ENST00000347598","synonymous_variant","synonymous_variant","1071/6655","1071/6561","357/2186","F","ttC/ttT"]
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["C17orf85",55421,"WUGSC","GRCh38","chr17",3822019,3822019,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.830G>C","ENST00000389005",42960,90,58,"G","ENSG00000074356","ENST00000389005","missense_variant","missense_variant","858/12770","830/1863","277/620","S/T","aGt/aCt"]
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["RHPN2",85415,"WUGSC","GRCh38","chr19",33002846,33002846,"+","Silent","SNP","G","G","A",null,null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.915C>T","ENST00000254260",42962,58,26,"A","ENSG00000131941","ENST00000254260","synonymous_variant","synonymous_variant","951/3500","915/2061","305/686","F","ttC/ttT"]
["AP2A1",160,"WUGSC","GRCh38","chr19",49799686,49799686,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1192G>A","ENST00000359032",43032,29,10,"A","ENSG00000196961","ENST00000359032","missense_variant","missense_variant","1192/3286","1192/2934","398/977","D/N","Gac/Aac"]
["TPX2",22974,"WUGSC","GRCh38","chr20",31801104,31801104,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.*24C>A","ENST00000300403","18/18",43,19,"A","ENSG00000088325","ENST00000300403","3_prime_UTR_variant","3_prime_UTR_variant","2796/3497","-/2244","-/747"]
["RALY",22913,"WUGSC","GRCh38","chr20",34073853,34073853,"+","Missense_Mutation","SNP","G","G","A","rs768865097",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.364G>A","ENST00000246194",42865,34,27,"A","ENSG00000125970","ENST00000246194","missense_variant","missense_variant","866/1789","364/921","122/306","D/N","Gac/Aac"]
["ADORA2A",135,"WUGSC","GRCh38","chr22",24441357,24441357,"+","Silent","SNP","G","G","A","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.1107G>A","ENST00000337539",42797,11,10,"A","ENSG00000128271","ENST00000337539","synonymous_variant","synonymous_variant","1566/2569","1107/1239","369/412","G","ggG/ggA"]
["ZNF711",7552,"WUGSC","GRCh38","chrX",85271736,85271736,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-AQ-A0Y5-01A-11D-A14K-09","TCGA-AQ-A0Y5-10A-01D-A17G-09",null,null,"Somatic","Illumina HiSeq 2000","4aa80fbd-a337-49b6-9371-223cbcfbc85d","d116ee66-1d8f-4319-b8d6-be4213550093","c.2194C>A","ENST00000276123",43018,29,19,"A","ENSG00000147180","ENST00000276123","missense_variant","missense_variant","2702/2887","2194/2286","732/761","P/T","Cca/Aca"]
["LRRC7",57554,"WUGSC","GRCh38","chr1",69919619,69919619,"+","Intron","SNP","G","G","A",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.534-11888G>A","ENST00000035383",null,21,16,"A","ENSG00000033122","ENST00000035383","intron_variant","intron_variant","-/5000","-/4614","-/1537"]
["NES",10763,"WUGSC","GRCh38","chr1",156669566,156669566,"+","Missense_Mutation","SNP","T","T","C","rs748107921","byFrequency","TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.4622A>G","ENST00000368223",42829,64,34,"C","ENSG00000132688","ENST00000368223","missense_variant","missense_variant","4755/5558","4622/4866","1541/1621","N/S","aAc/aGc"]
["OTOF",9381,"WUGSC","GRCh38","chr2",26474656,26474656,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.3145G>A","ENST00000272371","26/47",64,41,"T","ENSG00000115155","ENST00000272371","missense_variant","missense_variant","3272/7156","3145/5994","1049/1997","G/S","Ggc/Agc"]
["MARCO",8685,"WUGSC","GRCh38","chr2",118993258,118993258,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1387C>A","ENST00000327097","16/17",126,67,"A","ENSG00000019169","ENST00000327097","missense_variant","missense_variant","1522/1838","1387/1563","463/520","L/M","Ctg/Atg"]
["SPHKAP",80309,"WUGSC","GRCh38","chr2",228019533,228019533,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1321T>G","ENST00000392056",42928,70,56,"C","ENSG00000153820","ENST00000392056","missense_variant","missense_variant","1368/6917","1321/5103","441/1700","S/A","Tct/Gct"]
["RAP1GDS1",5910,"WUGSC","GRCh38","chr4",98434010,98434010,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1515A>G","ENST00000408927","13/15",133,60,"G","ENSG00000138698","ENST00000408927","missense_variant","missense_variant","1628/3681","1515/1824","505/607","I/M","atA/atG"]
["ABCE1",6059,"WUGSC","GRCh38","chr4",145117361,145117361,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.869A>G","ENST00000296577",43026,224,131,"G","ENSG00000164163","ENST00000296577","missense_variant","missense_variant","1384/3921","869/1800","290/599","Y/C","tAt/tGt"]
["SLC6A19",340024,"WUGSC","GRCh38","chr5",1216567,1216567,"+","Silent","SNP","C","C","T","rs201851669","by1000G;byCluster","TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.897C>T","ENST00000304460",42928,150,73,"T","ENSG00000174358","ENST00000304460","synonymous_variant","synonymous_variant","953/5174","897/1905","299/634","C","tgC/tgT"]
["ZFR",51663,"WUGSC","GRCh38","chr5",32364225,32364225,"+","Silent","SNP","C","C","T",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.2886G>A","ENST00000265069","18/20",98,32,"T","ENSG00000056097","ENST00000265069","synonymous_variant","synonymous_variant","2989/4738","2886/3225","962/1074","Q","caG/caA"]
["FLT4",2324,"WUGSC","GRCh38","chr5",180629385,180629385,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.859A>G","ENST00000261937",42946,147,62,"C","ENSG00000037280","ENST00000261937","missense_variant","missense_variant","938/5857","859/4092","287/1363","T/A","Acc/Gcc"]
["NQO2",4835,"WUGSC","GRCh38","chr6",3019528,3019528,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.569G>C","ENST00000338130",43018,159,119,"C","ENSG00000124588","ENST00000338130","missense_variant","missense_variant","1281/1515","569/696","190/231","S/T","aGc/aCc"]
["PRDM1",639,"WUGSC","GRCh38","chr6",106088249,106088249,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.91G>A","ENST00000369096",42773,114,80,"A","ENSG00000057657","ENST00000369096","missense_variant","missense_variant","325/5164","91/2478","31/825","E/K","Gag/Aag"]
["VPS13B",157680,"WUGSC","GRCh38","chr8",99776827,99776827,"+","Missense_Mutation","SNP","A","A","G","rs781276701",null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.7375A>G","ENST00000358544","41/62",162,113,"G","ENSG00000132549","ENST00000358544","missense_variant","missense_variant","7486/14094","7375/12069","2459/4022","T/A","Aca/Gca"]
["ASS1",445,"WUGSC","GRCh38","chr9",130501169,130501169,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.*148C>T","ENST00000352480","15/15",17,40,"T","ENSG00000130707","ENST00000352480","3_prime_UTR_variant","3_prime_UTR_variant","1459/1564","-/1239","-/412"]
["CCDC6",8030,"WUGSC","GRCh38","chr10",59793069,59793069,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1273C>T","ENST00000263102",42987,332,212,"A","ENSG00000108091","ENST00000263102","missense_variant","missense_variant","1505/5811","1273/1425","425/474","R/W","Cgg/Tgg"]
["NRXN2",9379,"WUGSC","GRCh38","chr11",64685726,64685726,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1072G>A","ENST00000265459",42909,143,191,"T","ENSG00000110076","ENST00000265459","missense_variant","missense_variant","1534/6621","1072/5139","358/1712","E/K","Gag/Aag"]
["BIVM-ERCC5",100533467,"WUGSC","GRCh38","chr13",102838643,102838643,"+","Splice_Region","SNP","A","A","G",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1036A>G","ENST00000602836",42968,101,63,"G","ENSG00000270181","ENST00000602836","splice_region_variant","splice_region_variant;synonymous_variant","1036/4155","1038/4157","346/1385","K","aaA/aaG"]
["SHISA9",729993,"WUGSC","GRCh38","chr16",12916741,12916741,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.617A>G","ENST00000558583",42771,95,42,"G","ENSG00000237515","ENST00000558583","missense_variant","missense_variant","1062/6724","617/1275","206/424","E/G","gAg/gGg"]
["EFCAB5",374786,"WUGSC","GRCh38","chr17",30051148,30051148,"+","Missense_Mutation","SNP","G","G","C",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1231G>C","ENST00000394835",43001,177,63,"C","ENSG00000176927","ENST00000394835","missense_variant","missense_variant","1423/5132","1231/4512","411/1503","A/P","Gcc/Ccc"]
["ZPBP2",124626,"WUGSC","GRCh38","chr17",39875253,39875253,"+","Splice_Site","SNP","G","G","A",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.709-1G>A","ENST00000348931",null,956,52,"A","ENSG00000186075","ENST00000348931","splice_acceptor_variant","splice_acceptor_variant","-/1543","709/1017","237/338"]
["MED24",9862,"WUGSC","GRCh38","chr17",40033106,40033106,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.772G>A","ENST00000394128",42973,453,32,"T","ENSG00000008838","ENST00000394128","missense_variant","missense_variant","854/3479","772/2970","258/989","G/S","Ggc/Agc"]
["MED24",9862,"WUGSC","GRCh38","chr17",40033178,40033178,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.700G>C","ENST00000394128",42973,459,28,"G","ENSG00000008838","ENST00000394128","missense_variant","missense_variant","782/3479","700/2970","234/989","E/Q","Gag/Cag"]
["MED24",9862,"WUGSC","GRCh38","chr17",40033437,40033437,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.579G>C","ENST00000394128",42942,362,23,"G","ENSG00000008838","ENST00000394128","missense_variant","missense_variant","661/3479","579/2970","193/989","E/D","gaG/gaC"]
["KRT25",147183,"WUGSC","GRCh38","chr17",40749326,40749326,"+","Splice_Site","SNP","C","C","T","novel",null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.1176-1G>A","ENST00000312150",null,621,68,"T","ENSG00000204897","ENST00000312150","splice_acceptor_variant","splice_acceptor_variant","-/1670","1176/1353","392/450"]
["OXLD1",339229,"WUGSC","GRCh38","chr17",81665127,81665127,"+","3'UTR","SNP","A","A","C","novel",null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.*74T>G","ENST00000374741",42768,16,11,"C","ENSG00000204237","ENST00000374741","3_prime_UTR_variant","3_prime_UTR_variant","529/620","-/444","-/147"]
["VAV1",7409,"WUGSC","GRCh38","chr19",6850683,6850683,"+","Missense_Mutation","SNP","G","G","A","rs775206603","byFrequency","TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.2143G>A","ENST00000602142","24/27",63,53,"A","ENSG00000141968","ENST00000602142","missense_variant","missense_variant","2225/2620","2143/2538","715/845","V/I","Gtc/Atc"]
["MUC16",94025,"WUGSC","GRCh38","chr19",8927444,8927444,"+","Silent","SNP","T","T","A",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.36156A>T","ENST00000397910",30895,111,54,"A","ENSG00000181143","ENST00000397910","synonymous_variant","synonymous_variant","36360/43816","36156/43524","12052/14507","T","acA/acT"]
["MAVS",57506,"WUGSC","GRCh38","chr20",3854654,3854654,"+","Silent","SNP","G","G","A","rs765934516",null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.30G>A","ENST00000428216",42773,171,107,"A","ENSG00000088888","ENST00000428216","synonymous_variant","synonymous_variant","158/11714","30/1623","10/540","K","aaG/aaA"]
["PIWIL3",440822,"WUGSC","GRCh38","chr22",24762449,24762449,"+","Silent","SNP","C","C","T",null,null,"TCGA-EW-A1J3-01A-11D-A13L-09","TCGA-EW-A1J3-10A-01D-A13O-09",null,null,"Somatic","Illumina HiSeq 2000","ac13b81a-ca05-432c-918a-0c9c8170bf46","3e0f2e32-d64a-416a-be72-eb34ff190ed6","c.51G>A","ENST00000332271",42787,51,27,"T","ENSG00000184571","ENST00000332271","synonymous_variant","synonymous_variant","468/3504","51/2649","17/882","E","gaG/gaA"]
["FOXD3",27022,"WUGSC","GRCh38","chr1",63323535,63323535,"+","Silent","SNP","G","G","A",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.477G>A","ENST00000371116",42736,36,30,"A","ENSG00000187140","ENST00000371116","synonymous_variant","synonymous_variant","495/2086","477/1437","159/478","Q","caG/caA"]
["KPRP",448834,"WUGSC","GRCh38","chr1",152760163,152760163,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.575G>A","ENST00000606109",42736,415,171,"A","ENSG00000203786","ENST00000606109","missense_variant","missense_variant","603/2492","575/1740","192/579","G/D","gGc/gAc"]
["SFT2D2",375035,"WUGSC","GRCh38","chr1",168246650,168246650,"+","3'UTR","SNP","T","T","G","novel",null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.*4110T>G","ENST00000271375",42955,70,38,"G","ENSG00000213064","ENST00000271375","3_prime_UTR_variant","3_prime_UTR_variant","4665/11040","-/483","-/160"]
["KIAA1407",57577,"WUGSC","GRCh38","chr3",113965097,113965097,"+","3'UTR","SNP","A","A","C","novel",null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.*58T>G","ENST00000295878","17/17",196,92,"C","ENSG00000163617","ENST00000295878","3_prime_UTR_variant","3_prime_UTR_variant","3016/3976","-/2811","-/936"]
["FNDC3B",64778,"WUGSC","GRCh38","chr3",172133474,172133474,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.115A>G","ENST00000336824",42820,340,350,"G","ENSG00000075420","ENST00000336824","missense_variant","missense_variant","214/7904","115/3615","39/1204","I/V","Att/Gtt"]
["RAI14",26064,"WUGSC","GRCh38","chr5",34812204,34812204,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.761A>C","ENST00000265109",43026,403,401,"C","ENSG00000039560","ENST00000265109","missense_variant","missense_variant","1048/5092","761/2943","254/980","K/T","aAg/aCg"]
["ITGA2",3673,"WUGSC","GRCh38","chr5",53060960,53060960,"+","Missense_Mutation","SNP","C","C","T","rs377150294","byCluster;byFrequency","TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.1372C>T","ENST00000296585",43099,195,156,"T","ENSG00000164171","ENST00000296585","missense_variant","missense_variant","1515/7869","1372/3546","458/1181","R/W","Cgg/Tgg"]
["GABRA1",2554,"WUGSC","GRCh38","chr5",161897518,161897518,"+","3'UTR","SNP","T","T","C","novel",null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.*96T>C","ENST00000023897",43050,103,24,"C","ENSG00000022355","ENST00000023897","3_prime_UTR_variant","3_prime_UTR_variant","1935/2083","-/1371","-/456"]
["DOCK2",1794,"WUGSC","GRCh38","chr5",169700100,169700100,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.1219G>A","ENST00000256935","13/52",135,121,"A","ENSG00000134516","ENST00000256935","missense_variant","missense_variant","1299/6097","1219/5493","407/1830","V/M","Gtg/Atg"]
["POLR2J4",84820,"WUGSC","GRCh38","chr7",44016487,44016487,"+","RNA","SNP","G","G","A",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","n.126C>T","ENST00000427076",42782,872,834,"A","ENSG00000214783","ENST00000427076","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","126/6466"]
["POLD2",5425,"WUGSC","GRCh38","chr7",44116913,44116913,"+","Silent","SNP","G","G","A","rs144701499","byCluster;byFrequency","TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.684C>T","ENST00000406581",42928,59,32,"A","ENSG00000106628","ENST00000406581","synonymous_variant","synonymous_variant","1334/2158","684/1410","228/469","D","gaC/gaT"]
["ZAN",7455,"WUGSC","GRCh38","chr7",100792533,100792533,"+","Intron","SNP","G","G","C",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.7787+54G>C","ENST00000613979",null,29,12,"C","ENSG00000146839","ENST00000613979","intron_variant","intron_variant","-/8669","-/8439","-/2812"]
["PLEC",5339,"WUGSC","GRCh38","chr8",143927022,143927022,"+","Silent","SNP","G","G","A",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.4311C>T","ENST00000322810","29/32",25,21,"A","ENSG00000178209","ENST00000322810","synonymous_variant","synonymous_variant","4481/15249","4311/14055","1437/4684","A","gcC/gcT"]
["ZBTB43",23099,"WUGSC","GRCh38","chr9",126832815,126832815,"+","Silent","SNP","T","T","C",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.306T>C","ENST00000373457",42736,119,41,"C","ENSG00000169155","ENST00000373457","synonymous_variant","synonymous_variant","1407/5695","306/1404","102/467","S","agT/agC"]
["EDRF1",26098,"WUGSC","GRCh38","chr10",125741263,125741263,"+","Intron","SNP","T","T","C","novel",null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.2371+62T>C","ENST00000356792",null,162,76,"C","ENSG00000107938","ENST00000356792","intron_variant","intron_variant","-/4128","-/3717","-/1238"]
["CCDC89",220388,"WUGSC","GRCh38","chr11",85686135,85686135,"+","5'UTR","SNP","T","T","C","novel",null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.-5A>G","ENST00000316398",42736,90,27,"C","ENSG00000179071","ENST00000316398","5_prime_UTR_variant","5_prime_UTR_variant","143/1412","-/1125","-/374"]
["CHST11",50515,"WUGSC","GRCh38","chr12",104757161,104757161,"+","Silent","SNP","C","C","T","rs768446172","byFrequency","TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.417C>T","ENST00000303694",42797,103,81,"T","ENSG00000171310","ENST00000303694","synonymous_variant","synonymous_variant","856/5709","417/1059","139/352","T","acC/acT"]
["NDN",4692,"WUGSC","GRCh38","chr15",23686793,23686793,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.425G>A","ENST00000331837",42736,27,23,"T","ENSG00000182636","ENST00000331837","missense_variant","missense_variant","538/1931","425/966","142/321","R/H","cGc/cAc"]
["LINGO1",84894,"WUGSC","GRCh38","chr15",77615479,77615479,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.428G>A","ENST00000355300",42768,131,59,"T","ENSG00000169783","ENST00000355300","missense_variant","missense_variant","603/3055","428/1863","143/620","S/N","aGc/aAc"]
["GOLGA6L9",440295,"WUGSC","GRCh38","chr15",82436020,82436020,"+","Missense_Mutation","SNP","G","G","C","novel",null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.1117G>C","ENST00000618348",42956,163,97,"C","ENSG00000197978","ENST00000618348","missense_variant","missense_variant","1177/1710","1117/1299","373/432","A/P","Gct/Cct"]
["SMCHD1",23347,"WUGSC","GRCh38","chr18",2747544,2747544,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.3824G>T","ENST00000320876","30/48",110,151,"T","ENSG00000101596","ENST00000320876","missense_variant","missense_variant","4162/8821","3824/6018","1275/2005","R/I","aGa/aTa"]
["FCGBP",8857,"WUGSC","GRCh38","chr19",39886484,39886484,"+","Silent","SNP","C","C","T","novel",null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.7695G>A","ENST00000616721","16/28",209,105,"T","ENSG00000275395","ENST00000616721","synonymous_variant","synonymous_variant","7703/12787","7695/12615","2565/4204","L","ctG/ctA"]
["TMC4",147798,"WUGSC","GRCh38","chr19",54173077,54173077,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.41C>T","ENST00000617472",42750,88,47,"A","ENSG00000167608","ENST00000617472","missense_variant","missense_variant","174/2413","41/2139","14/712","S/F","tCc/tTc"]
["BACH1",571,"WUGSC","GRCh38","chr21",29326995,29326995,"+","Nonsense_Mutation","SNP","C","C","T",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.1171C>T","ENST00000286800",42799,234,94,"T","ENSG00000156273","ENST00000286800","stop_gained","stop_gained","1314/5669","1171/2211","391/736","R/*","Cga/Tga"]
["ENTHD1",150350,"WUGSC","GRCh38","chr22",39765421,39765421,"+","Nonsense_Mutation","SNP","C","C","A",null,null,"TCGA-BH-A0HO-01A-11W-A050-09","TCGA-BH-A0HO-10A-01W-A055-09",null,null,"Somatic","Illumina Genome Analyzer II;Illumina HiSeq 2000","354172e7-3e54-4ec4-88fa-fd7781cc86ae","32f59f61-3335-4cfe-93f3-5931705e312e","c.1021G>T","ENST00000325157",42893,191,153,"A","ENSG00000176177","ENST00000325157","stop_gained","stop_gained","1272/2710","1021/1824","341/607","E/*","Gag/Tag"]
["HIST2H3PS2",440686,"WUGSC","GRCh38","chr1",143904312,143904312,"+","3'Flank","SNP","C","C","A","novel",null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6",null,"ENST00000392948",null,142,174,"A","ENSG00000203818","ENST00000392948","downstream_gene_variant","downstream_gene_variant","-/412","-/411","-/136"]
["FCRLA",84824,"WUGSC","GRCh38","chr1",161711946,161711946,"+","Missense_Mutation","SNP","C","C","T","rs140395904","by1000G;byCluster;byFrequency","TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.581C>T","ENST00000367959",42861,40,62,"T","ENSG00000132185","ENST00000367959","missense_variant","missense_variant","823/2362","581/1149","194/382","A/V","gCg/gTg"]
["ARPC5",10092,"WUGSC","GRCh38","chr1",183627081,183627081,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.*451C>T","ENST00000359856",42829,34,44,"A","ENSG00000162704","ENST00000359856","3_prime_UTR_variant","3_prime_UTR_variant","974/7209","-/456","-/151"]
["LRRTM1",347730,"WUGSC","GRCh38","chr2",80303649,80303649,"+","Silent","SNP","G","G","A",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.171C>T","ENST00000295057",42768,23,32,"A","ENSG00000162951","ENST00000295057","synonymous_variant","synonymous_variant","828/2599","171/1569","57/522","L","ctC/ctT"]
["ERBB4",2066,"WUGSC","GRCh38","chr2",211722443,211722443,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.833A>G","ENST00000342788",42944,64,100,"C","ENSG00000178568","ENST00000342788","missense_variant","missense_variant","1144/12136","833/3927","278/1308","N/S","aAt/aGt"]
["GBE1",2632,"WUGSC","GRCh38","chr3",81581169,81581169,"+","Missense_Mutation","SNP","T","T","A",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.1442A>T","ENST00000429644",43055,40,52,"A","ENSG00000114480","ENST00000429644","missense_variant","missense_variant","2086/3461","1442/2109","481/702","D/V","gAt/gTt"]
["ZBTB38",253461,"WUGSC","GRCh38","chr3",141448242,141448242,"+","3'Flank","SNP","C","C","T","novel",null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6",null,"ENST00000321464",null,61,83,"T","ENSG00000177311","ENST00000321464","downstream_gene_variant","downstream_gene_variant","-/3588","-/3588","-/1195"]
["PIK3CA",5290,"WUGSC","GRCh38","chr3",179218303,179218303,"+","Missense_Mutation","SNP","G","G","A","rs104886003","byCluster","TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.1633G>A","ENST00000263967",43029,34,71,"A","ENSG00000121879","ENST00000263967","missense_variant","missense_variant","1790/9093","1633/3207","545/1068","E/K","Gag/Aag"]
["LRBA",987,"WUGSC","GRCh38","chr4",150277867,150277867,"+","Silent","SNP","C","C","A",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.8487G>T","ENST00000357115","57/58",53,92,"A","ENSG00000198589","ENST00000357115","synonymous_variant","synonymous_variant","8731/9899","8487/8592","2829/2863","L","ctG/ctT"]
["PCLO",27445,"WUGSC","GRCh38","chr7",82952402,82952402,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.8551G>A","ENST00000333891",42880,110,109,"T","ENSG00000186472","ENST00000333891","missense_variant","missense_variant","8889/20329","8551/15429","2851/5142","A/T","Gca/Aca"]
["CA2",760,"WUGSC","GRCh38","chr8",85480750,85480750,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.744G>T","ENST00000285379",42923,58,59,"T","ENSG00000104267","ENST00000285379","missense_variant","missense_variant","974/1717","744/783","248/260","Q/H","caG/caT"]
["MAML2",84441,"WUGSC","GRCh38","chr11",95979551,95979551,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.2868G>A","ENST00000524717",42860,93,230,"T","ENSG00000184384","ENST00000524717","missense_variant","missense_variant","4153/7106","2868/3471","956/1156","M/I","atG/atA"]
["OS9",10956,"WUGSC","GRCh38","chr12",57694235,57694235,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.74C>G","ENST00000315970",42750,37,54,"G","ENSG00000135506","ENST00000315970","missense_variant","missense_variant","115/2691","74/2004","25/667","T/S","aCc/aGc"]
["BAZ1A",11177,"WUGSC","GRCh38","chr14",34800338,34800338,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.1014G>T","ENST00000360310",43005,18,25,"A","ENSG00000198604","ENST00000360310","missense_variant","missense_variant","1582/6010","1014/4671","338/1556","K/N","aaG/aaT"]
["FLRT2",23768,"WUGSC","GRCh38","chr14",85622479,85622479,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.965C>T","ENST00000330753",42768,82,155,"T","ENSG00000185070","ENST00000330753","missense_variant","missense_variant","1732/33679","965/1983","322/660","T/I","aCa/aTa"]
["EML5",161436,"WUGSC","GRCh38","chr14",88688350,88688350,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.2663G>A","ENST00000380664","18/42",52,130,"T","ENSG00000165521","ENST00000380664","missense_variant","missense_variant","2663/5910","2663/5910","888/1969","C/Y","tGt/tAt"]
["OTUD7A",161725,"WUGSC","GRCh38","chr15",31655133,31655133,"+","Silent","SNP","C","C","T","rs772949592",null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.114G>A","ENST00000307050",42746,94,151,"T","ENSG00000169918","ENST00000307050","synonymous_variant","synonymous_variant","207/10770","114/2781","38/926","T","acG/acA"]
["ANP32A",8125,"WUGSC","GRCh38","chr15",68787534,68787534,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.206T>G","ENST00000465139",42801,39,59,"C","ENSG00000140350","ENST00000465139","missense_variant","missense_variant;splice_region_variant","350/2440","206/750","69/249","L/R","cTt/cGt"]
["IGF1R",3480,"WUGSC","GRCh38","chr15",98962642,98962642,"+","3'UTR","SNP","A","A","G","novel",null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.*5200A>G","ENST00000268035","21/21",13,34,"G","ENSG00000140443","ENST00000268035","3_prime_UTR_variant","3_prime_UTR_variant","9915/11803","-/4104","-/1367"]
["TOM1L2",146691,"WUGSC","GRCh38","chr17",17882783,17882783,"+","Silent","SNP","C","C","T",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.582G>A","ENST00000379504",42901,21,53,"T","ENSG00000175662","ENST00000379504","synonymous_variant","synonymous_variant","666/2418","582/1524","194/507","S","tcG/tcA"]
["GALNT1",2589,"WUGSC","GRCh38","chr18",35677596,35677596,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.320A>G","ENST00000269195",42805,21,38,"G","ENSG00000141429","ENST00000269195","missense_variant","missense_variant","423/3847","320/1680","107/559","K/R","aAa/aGa"]
["ODF3L2",284451,"WUGSC","GRCh38","chr19",474621,474621,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.127G>A","ENST00000315489",42739,42,82,"T","ENSG00000181781","ENST00000315489","missense_variant","missense_variant;splice_region_variant","363/1604","127/870","43/289","G/S","Ggc/Agc"]
["FBL",2091,"WUGSC","GRCh38","chr19",39834649,39834649,"+","Intron","SNP","T","T","C","novel",null,"TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.941+19A>G","ENST00000221801",null,77,132,"C","ENSG00000105202","ENST00000221801","intron_variant","intron_variant","-/1160","-/966","-/321"]
["CCDC61",729440,"WUGSC","GRCh38","chr19",46003457,46003457,"+","Nonsense_Mutation","SNP","C","C","T","rs768308257","byFrequency","TCGA-AQ-A54O-01A-11D-A25Q-09","TCGA-AQ-A54O-10A-01D-A25Q-09",null,null,"Somatic","Illumina HiSeq 2000","f4481d7e-4544-4c76-be94-4cdc1ccce963","f1b073ac-cdeb-482f-bc59-1e8376aa7cc6","c.187C>T","ENST00000595358",42808,35,53,"T","ENSG00000104983","ENST00000595358","stop_gained","stop_gained","236/1817","187/1539","63/512","Q/*","Cag/Tag"]
["DDAH1",23576,"WUGSC","GRCh38","chr1",85324885,85324885,"+","Splice_Site","SNP","T","T","A","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.598-2A>T","ENST00000284031",null,52,57,"A","ENSG00000153904","ENST00000284031","splice_acceptor_variant","splice_acceptor_variant","-/3920","598/858","200/285"]
["CELSR2",1952,"WUGSC","GRCh38","chr1",109274629,109274629,"+","3'UTR","SNP","C","C","G","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.*580C>G","ENST00000271332","34/34",114,110,"G","ENSG00000143126","ENST00000271332","3_prime_UTR_variant","3_prime_UTR_variant","9413/10534","-/8772","-/2923"]
["PLEKHO1",51177,"WUGSC","GRCh38","chr1",150155828,150155828,"+","Intron","SNP","G","G","C","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.178-238G>C","ENST00000369124",null,62,22,"C","ENSG00000023902","ENST00000369124","intron_variant","intron_variant","-/2050","-/1230","-/409"]
["PLEKHO1",51177,"WUGSC","GRCh38","chr1",150155993,150155993,"+","Intron","SNP","G","G","T","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.178-73G>T","ENST00000369124",null,899,160,"T","ENSG00000023902","ENST00000369124","intron_variant","intron_variant","-/2050","-/1230","-/409"]
["SRBD1",55133,"WUGSC","GRCh38","chr2",45553668,45553668,"+","Missense_Mutation","SNP","T","T","C","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.1472A>G","ENST00000263736",43060,109,163,"C","ENSG00000068784","ENST00000263736","missense_variant","missense_variant","1535/3681","1472/2988","491/995","D/G","gAt/gGt"]
["FHL2",2274,"WUGSC","GRCh38","chr2",105399357,105399357,"+","5'Flank","SNP","C","C","T","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438",null,"ENST00000322142",null,39,57,"T","ENSG00000115641","ENST00000322142","upstream_gene_variant","upstream_gene_variant","-/1462","-/840","-/279"]
["ZEB2",9839,"WUGSC","GRCh38","chr2",144398518,144398518,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.2669G>A","ENST00000409487",42957,34,76,"T","ENSG00000169554","ENST00000409487","missense_variant","missense_variant","2952/5361","2669/3645","890/1214","S/N","aGt/aAt"]
["XIRP2",129446,"WUGSC","GRCh38","chr2",167210760,167210760,"+","Silent","SNP","G","G","A",null,null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.63G>A","ENST00000628543",42775,56,109,"A","ENSG00000163092","ENST00000628543","synonymous_variant","synonymous_variant","188/12182","63/10125","21/3374","E","gaG/gaA"]
["PAX3",5077,"WUGSC","GRCh38","chr2",222201216,222201216,"+","3'UTR","SNP","C","C","T","rs764232120",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.*708G>A","ENST00000350526",42955,61,76,"T","ENSG00000135903","ENST00000350526","3_prime_UTR_variant","3_prime_UTR_variant","2285/3610","-/1440","-/479"]
["PF4",5196,"WUGSC","GRCh38","chr4",73981141,73981141,"+","3'UTR","SNP","A","A","T","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.*63T>A","ENST00000296029",42797,830,103,"T","ENSG00000163737","ENST00000296029","3_prime_UTR_variant","3_prime_UTR_variant","540/604","-/306","-/101"]
["FAM71B",153745,"WUGSC","GRCh38","chr5",157166081,157166081,"+","Nonsense_Mutation","SNP","G","G","A","rs370119273","byCluster","TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.88C>T","ENST00000302938",42737,107,111,"A","ENSG00000170613","ENST00000302938","stop_gained","stop_gained","184/2515","88/1818","30/605","R/*","Cga/Tga"]
["PLG",5340,"WUGSC","GRCh38","chr6",160718377,160718377,"+","Missense_Mutation","SNP","G","G","T","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.871G>T","ENST00000308192",42966,34,105,"T","ENSG00000122194","ENST00000308192","missense_variant","missense_variant","934/2741","871/2433","291/810","V/L","Gtg/Ttg"]
["CCT6A",908,"WUGSC","GRCh38","chr7",56062757,56062757,"+","Splice_Site","SNP","T","T","C","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.1523+2T>C","ENST00000275603",null,127,134,"C","ENSG00000146731","ENST00000275603","splice_donor_variant","splice_donor_variant","-/2719","1523/1596","508/531"]
["CLIP2",7461,"WUGSC","GRCh38","chr7",74376128,74376128,"+","Missense_Mutation","SNP","C","C","T","rs150588666","by1000G;byCluster;byFrequency","TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.1727C>T","ENST00000223398",43025,72,91,"T","ENSG00000106665","ENST00000223398","missense_variant","missense_variant","2054/5563","1727/3141","576/1046","A/V","gCg/gTg"]
["CSMD1",64478,"WUGSC","GRCh38","chr8",3367246,3367246,"+","Splice_Region","SNP","T","T","C","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.2904A>G","ENST00000520002","21/71",51,50,"C","ENSG00000183117","ENST00000520002","splice_region_variant","splice_region_variant;synonymous_variant","3460/11740","2904/10698","968/3565","G","ggA/ggG"]
["CDC37L1",55664,"WUGSC","GRCh38","chr9",4679763,4679763,"+","5'UTR","SNP","C","C","T","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.-5C>T","ENST00000381854",42742,238,333,"T","ENSG00000106993","ENST00000381854","5_prime_UTR_variant","5_prime_UTR_variant","198/3502","-/1014","-/337"]
["DNAI1",27019,"WUGSC","GRCh38","chr9",34493292,34493292,"+","Silent","SNP","G","G","A","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.780G>A","ENST00000242317",42998,46,49,"A","ENSG00000122735","ENST00000242317","synonymous_variant","synonymous_variant","951/2504","780/2100","260/699","K","aaG/aaA"]
["PGM5P2",595135,"WUGSC","GRCh38","chr9",41039663,41039663,"+","RNA","SNP","T","T","C","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","n.1160A>G","ENST00000613141",42895,128,245,"C","ENSG00000277778","ENST00000613141","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","1160/1980"]
["MAN1B1",11253,"WUGSC","GRCh38","chr9",137107290,137107290,"+","Missense_Mutation","SNP","G","G","A","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.1607G>A","ENST00000371589",43052,23,63,"A","ENSG00000177239","ENST00000371589","missense_variant","missense_variant","1680/2769","1607/2100","536/699","G/D","gGc/gAc"]
["WDR11",55717,"WUGSC","GRCh38","chr10",120909443,120909443,"+","3'UTR","SNP","G","G","A","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.*730G>A","ENST00000263461","29/29",94,143,"A","ENSG00000120008","ENST00000263461","3_prime_UTR_variant","3_prime_UTR_variant","4651/4732","-/3675","-/1224"]
["NPAS4",266743,"WUGSC","GRCh38","chr11",66426181,66426181,"+","3'UTR","SNP","G","G","C","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.*192G>C","ENST00000311034",42955,146,104,"C","ENSG00000174576","ENST00000311034","3_prime_UTR_variant","3_prime_UTR_variant","2777/3303","-/2409","-/802"]
["NAALAD2",10003,"WUGSC","GRCh38","chr11",90159199,90159199,"+","Intron","SNP","G","G","A","novel",null,"TCGA-3C-AAAU-01A-11D-A41F-09","TCGA-3C-AAAU-10A-01D-A41F-09",null,null,"Somatic","Illumina HiSeq 2000","6c3b8e04-6582-42e9-b3cf-9220b8c1f136","180b06bb-30e0-432a-b824-06e45b102438","c.891-40G>A","ENST00000534061",null,54,92,"A","ENSG00000077616","ENST00000534061","intron_variant","intron_variant","-/3600","-/2223","-/740"]
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["POLR2B",5431,"WUGSC","GRCh38","chr4",56986366,56986366,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.32A>T","ENST00000314595",42791,136,273,"T","ENSG00000047315","ENST00000314595","missense_variant","missense_variant","75/3748","32/3525","11/1174","D/V","gAt/gTt"]
["NDST3",9348,"WUGSC","GRCh38","chr4",118255634,118255634,"+","Silent","SNP","G","G","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.2544G>T","ENST00000296499","14/14",110,151,"T","ENSG00000164100","ENST00000296499","synonymous_variant","synonymous_variant","2947/5961","2544/2622","848/873","V","gtG/gtT"]
["PAPD7",11044,"WUGSC","GRCh38","chr5",6739740,6739740,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.146A>G","ENST00000230859",42838,72,74,"G","ENSG00000112941","ENST00000230859","missense_variant","missense_variant","275/3861","146/1629","49/542","D/G","gAc/gGc"]
["KDM3B",51780,"WUGSC","GRCh38","chr5",138386301,138386301,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1060A>T","ENST00000314358",42940,243,229,"T","ENSG00000120733","ENST00000314358","missense_variant","missense_variant","1260/6813","1060/5286","354/1761","I/F","Att/Ttt"]
["PCDHB10",56126,"WUGSC","GRCh38","chr5",141194076,141194076,"+","Silent","SNP","G","G","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1524G>T","ENST00000239446",42736,40,73,"T","ENSG00000120324","ENST00000239446","synonymous_variant","synonymous_variant","1724/3290","1524/2403","508/800","A","gcG/gcT"]
["DUSP22",56940,"WUGSC","GRCh38","chr6",350772,350772,"+","Intron","SNP","C","C","T","rs777641099",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.509-50C>T","ENST00000344450",null,90,263,"T","ENSG00000112679","ENST00000344450","intron_variant","intron_variant","-/1485","-/555","-/184"]
["GABRR1",2569,"WUGSC","GRCh38","chr6",89198099,89198099,"+","Missense_Mutation","SNP","G","G","A","rs185436805","by1000G;byCluster;byFrequency","TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.493C>T","ENST00000454853",42865,193,357,"A","ENSG00000146276","ENST00000454853","missense_variant","missense_variant","604/2820","493/1440","165/479","R/C","Cgc/Tgc"]
["CASP8AP2",9994,"WUGSC","GRCh38","chr6",89863590,89863590,"+","Silent","SNP","C","C","T","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1881C>T","ENST00000551025",42925,76,137,"T","ENSG00000118412","ENST00000551025","synonymous_variant","synonymous_variant","2116/6151","1881/5916","627/1972","T","acC/acT"]
["RFX6",222546,"WUGSC","GRCh38","chr6",116918059,116918059,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.995C>T","ENST00000332958",43027,134,241,"T","ENSG00000185002","ENST00000332958","missense_variant","missense_variant","1011/3460","995/2787","332/928","P/L","cCt/cTt"]
["ENPP1",5167,"WUGSC","GRCh38","chr6",131879879,131879879,"+","Splice_Site","SNP","G","G","C",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1946-1G>C","ENST00000360971",null,493,166,"C","ENSG00000197594","ENST00000360971","splice_acceptor_variant","splice_acceptor_variant","-/7442","1946/2778","649/925"]
["CALN1",83698,"WUGSC","GRCh38","chr7",72403383,72403383,"+","5'UTR","SNP","C","C","T","rs778012748",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.-14G>A","ENST00000395275",42773,93,64,"T","ENSG00000183166","ENST00000395275","5_prime_UTR_variant","5_prime_UTR_variant","376/9459","-/786","-/261"]
["TNPO3",23534,"WUGSC","GRCh38","chr7",128970199,128970199,"+","Silent","SNP","G","G","A","rs775545486","byFrequency","TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.2547C>T","ENST00000265388","20/23",107,120,"A","ENSG00000064419","ENST00000265388","synonymous_variant","synonymous_variant","2691/4153","2547/2772","849/923","T","acC/acT"]
["GIMAP1",170575,"WUGSC","GRCh38","chr7",150720549,150720549,"+","Missense_Mutation","SNP","G","G","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.545G>T","ENST00000307194",42797,57,45,"T","ENSG00000213203","ENST00000307194","missense_variant","missense_variant","685/4420","545/921","182/306","G/V","gGg/gTg"]
["CSMD1",64478,"WUGSC","GRCh38","chr8",3110174,3110174,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.6595G>A","ENST00000520002","44/71",71,225,"T","ENSG00000183117","ENST00000520002","missense_variant","missense_variant","7151/11740","6595/10698","2199/3565","D/N","Gat/Aat"]
["PNMA2",10687,"WUGSC","GRCh38","chr8",26508440,26508440,"+","Silent","SNP","A","A","G",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.316T>C","ENST00000522362",42797,72,167,"G","ENSG00000240694","ENST00000522362","synonymous_variant","synonymous_variant","1211/4965","316/1095","106/364","L","Ttg/Ctg"]
["TEX15",56154,"WUGSC","GRCh38","chr8",30837687,30837687,"+","Missense_Mutation","SNP","T","T","A","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.7448A>T","ENST00000256246",42798,43,57,"A","ENSG00000133863","ENST00000256246","missense_variant","missense_variant","7523/10187","7448/8370","2483/2789","N/I","aAt/aTt"]
["ALDOB",229,"WUGSC","GRCh38","chr9",101421861,101421861,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1043C>T","ENST00000374855",42987,410,211,"A","ENSG00000136872","ENST00000374855","missense_variant","missense_variant","1168/2451","1043/1095","348/364","S/F","tCt/tTt"]
["RNF20",56254,"WUGSC","GRCh38","chr9",101552392,101552392,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1540C>T","ENST00000389120","13/20",177,158,"T","ENSG00000155827","ENST00000389120","missense_variant","missense_variant","1630/3940","1540/2928","514/975","R/C","Cgt/Tgt"]
["UPF2",26019,"WUGSC","GRCh38","chr10",11936708,11936708,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.3383G>A","ENST00000356352","18/21",287,119,"T","ENSG00000151461","ENST00000356352","missense_variant","missense_variant","3857/5569","3383/3819","1128/1272","R/Q","cGa/cAa"]
["RCN1",5954,"WUGSC","GRCh38","chr11",32103475,32103475,"+","Missense_Mutation","SNP","A","A","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.883A>T","ENST00000054950",42861,131,127,"T","ENSG00000049449","ENST00000054950","missense_variant","missense_variant","1176/2572","883/996","295/331","N/Y","Aac/Tac"]
["MYO7A",4647,"WUGSC","GRCh38","chr11",77213860,77213860,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.6439G>A","ENST00000409709","48/49",81,187,"A","ENSG00000137474","ENST00000409709","missense_variant","missense_variant;splice_region_variant","6711/7462","6439/6648","2147/2215","D/N","Gat/Aat"]
["CD4",920,"WUGSC","GRCh38","chr12",6817269,6817269,"+","Silent","SNP","G","G","A","rs782116340",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1095G>A","ENST00000011653",42926,1196,217,"A","ENSG00000010610","ENST00000011653","synonymous_variant","synonymous_variant","1353/3114","1095/1377","365/458","A","gcG/gcA"]
["KMT2D",8085,"WUGSC","GRCh38","chr12",49033829,49033829,"+","Missense_Mutation","SNP","G","G","A","rs766696812",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.10876C>T","ENST00000301067","39/54",28,26,"A","ENSG00000167548","ENST00000301067","missense_variant","missense_variant","10876/19419","10876/16614","3626/5537","R/W","Cgg/Tgg"]
["FMNL3",91010,"WUGSC","GRCh38","chr12",49656831,49656831,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.783G>C","ENST00000335154",42973,556,515,"G","ENSG00000161791","ENST00000335154","missense_variant","missense_variant","1017/12634","783/3084","261/1027","K/N","aaG/aaC"]
["ORMDL2",29095,"WUGSC","GRCh38","chr12",55820514,55820514,"+","3'UTR","SNP","C","C","T","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.*119C>T","ENST00000243045",42829,218,79,"T","ENSG00000123353","ENST00000243045","3_prime_UTR_variant","3_prime_UTR_variant","776/2141","-/462","-/153"]
["FBXO21",23014,"WUGSC","GRCh38","chr12",117186558,117186558,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.389G>A","ENST00000330622",42806,150,292,"T","ENSG00000135108","ENST00000330622","missense_variant","missense_variant","389/2906","389/1887","130/628","G/D","gGc/gAc"]
["TMEM132B",114795,"WUGSC","GRCh38","chr12",125350220,125350220,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.821C>A","ENST00000299308",42775,184,163,"A","ENSG00000139364","ENST00000299308","missense_variant","missense_variant","829/10906","821/3237","274/1078","S/Y","tCc/tAc"]
["PUS1",80324,"WUGSC","GRCh38","chr12",131941478,131941478,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.731A>G","ENST00000376649",42861,33,130,"G","ENSG00000177192","ENST00000376649","missense_variant","missense_variant","1231/4094","731/1284","244/427","N/S","aAc/aGc"]
["PCDH9",5101,"WUGSC","GRCh38","chr13",67226886,67226886,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1555C>T","ENST00000377865",42771,88,182,"A","ENSG00000184226","ENST00000377865","stop_gained","stop_gained","1729/5709","1555/3714","519/1237","R/*","Cga/Tga"]
["MTHFD1",4522,"WUGSC","GRCh38","chr14",64412471,64412471,"+","Splice_Site","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.187-1G>A","ENST00000216605",null,330,544,"A","ENSG00000100714","ENST00000216605","splice_acceptor_variant","splice_acceptor_variant","-/3136","187/2808","63/935"]
["IGHV3-16",28447,"WUGSC","GRCh38","chr14",106165473,106165473,"+","Missense_Mutation","SNP","C","C","T","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.83G>A","ENST00000390604",42768,260,273,"T","ENSG00000211944","ENST00000390604","missense_variant","missense_variant","157/425","83/351","28/117","G/E","gGa/gAa"]
["PIF1",80119,"WUGSC","GRCh38","chr15",64816071,64816071,"+","3'UTR","SNP","C","C","A","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.*227G>T","ENST00000268043","13/13",10,14,"A","ENSG00000140451","ENST00000268043","3_prime_UTR_variant","3_prime_UTR_variant","2248/2687","-/1926","-/641"]
["KAT8",84148,"WUGSC","GRCh38","chr16",31120228,31120228,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.254G>A","ENST00000219797",42777,149,223,"A","ENSG00000103510","ENST00000219797","missense_variant","missense_variant","272/1525","254/1377","85/458","G/D","gGc/gAc"]
["ZNF232",7775,"WUGSC","GRCh38","chr17",5106023,5106023,"+","Missense_Mutation","SNP","C","C","A","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1136G>T","ENST00000250076",42860,100,276,"A","ENSG00000167840","ENST00000250076","missense_variant","missense_variant","1791/2179","1136/1335","379/444","R/M","aGg/aTg"]
["TP53",7157,"WUGSC","GRCh38","chr17",7675076,7675076,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.536A>G","ENST00000269305",42866,147,103,"C","ENSG00000141510","ENST00000269305","missense_variant","missense_variant","726/2579","536/1182","179/393","H/R","cAt/cGt"]
["GRIN2C",2905,"WUGSC","GRCh38","chr17",74852505,74852505,"+","Missense_Mutation","SNP","G","C","C",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.506C>G","ENST00000293190",42807,12,13,"C","ENSG00000161509","ENST00000293190","missense_variant","missense_variant","653/4261","506/3702","169/1233","T/S","aCc/aGc"]
["ARHGAP28",79822,"WUGSC","GRCh38","chr18",6859847,6859847,"+","Missense_Mutation","SNP","G","G","A","rs147162571","byCluster","TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.676G>A","ENST00000383472",42873,408,414,"A","ENSG00000088756","ENST00000383472","missense_variant","missense_variant","780/2295","676/2190","226/729","A/T","Gca/Aca"]
["TRAPPC8",22878,"WUGSC","GRCh38","chr18",31874475,31874475,"+","Splice_Region","SNP","G","G","A","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1953+5C>T","ENST00000283351",null,111,155,"A","ENSG00000153339","ENST00000283351","splice_region_variant","splice_region_variant;intron_variant","-/6226","-/4308","-/1435"]
["CFAP53",220136,"WUGSC","GRCh38","chr18",50243064,50243064,"+","Missense_Mutation","SNP","C","C","T","rs371352284","byCluster;byFrequency","TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1049G>A","ENST00000398545",42894,131,298,"T","ENSG00000172361","ENST00000398545","missense_variant","missense_variant","1167/1851","1049/1545","350/514","R/H","cGt/cAt"]
["DCC",1630,"WUGSC","GRCh38","chr18",53205317,53205317,"+","Missense_Mutation","SNP","C","C","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1675C>A","ENST00000442544",43037,294,350,"A","ENSG00000187323","ENST00000442544","missense_variant","missense_variant","2291/10206","1675/4344","559/1447","Q/K","Caa/Aaa"]
["GRIK5",2901,"WUGSC","GRCh38","chr19",42053859,42053859,"+","Missense_Mutation","SNP","C","C","T","rs778914367","byFrequency","TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1127G>A","ENST00000262895",42997,111,167,"T","ENSG00000105737","ENST00000262895","missense_variant","missense_variant","1127/3493","1127/2943","376/980","R/H","cGc/cAc"]
["RPL13A",23521,"WUGSC","GRCh38","chr19",49490252,49490252,"+","Missense_Mutation","SNP","C","C","G",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.109C>G","ENST00000391857",42802,109,76,"G","ENSG00000142541","ENST00000391857","missense_variant","missense_variant","185/1181","109/612","37/203","R/G","Cgc/Ggc"]
["DNAAF3",352909,"WUGSC","GRCh38","chr19",55166563,55166563,"+","5'Flank","SNP","C","C","T","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2",null,"ENST00000524407",null,77,131,"T","ENSG00000167646","ENST00000524407","upstream_gene_variant","upstream_gene_variant","-/2059","-/1626","-/541"]
["KCNB1",3745,"WUGSC","GRCh38","chr20",49373542,49373542,"+","Missense_Mutation","SNP","T","T","C",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.2018A>G","ENST00000371741",42768,76,61,"C","ENSG00000158445","ENST00000371741","missense_variant","missense_variant","2185/11850","2018/2577","673/858","K/R","aAa/aGa"]
["BCAS1",8537,"WUGSC","GRCh38","chr20",54028452,54028452,"+","Missense_Mutation","SNP","T","T","G",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.663A>C","ENST00000395961",42837,450,298,"G","ENSG00000064787","ENST00000395961","missense_variant","missense_variant","830/3303","663/1755","221/584","Q/H","caA/caC"]
["TRAPPC10",7109,"WUGSC","GRCh38","chr21",44082788,44082788,"+","Missense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1724G>A","ENST00000291574","14/23",89,158,"A","ENSG00000160218","ENST00000291574","missense_variant","missense_variant;splice_region_variant","1899/6976","1724/3780","575/1259","G/D","gGt/gAt"]
["FAM9C",171484,"WUGSC","GRCh38","chrX",13038390,13038390,"+","3'UTR","SNP","G","G","T","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.*51C>A","ENST00000333995",42923,643,408,"T","ENSG00000187268","ENST00000333995","3_prime_UTR_variant","3_prime_UTR_variant","683/3361","-/501","-/166"]
["KCND1",3750,"WUGSC","GRCh38","chrX",48970024,48970024,"+","Missense_Mutation","SNP","A","A","C",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.248T>G","ENST00000218176",42741,30,47,"C","ENSG00000102057","ENST00000218176","missense_variant","missense_variant","1546/4437","248/1944","83/647","F/C","tTc/tGc"]
["SSX8",280659,"WUGSC","GRCh38","chrX",52630278,52630278,"+","RNA","SNP","C","C","G","novel",null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","n.345C>G","ENST00000506270",42861,390,511,"G","ENSG00000157965","ENST00000506270","non_coding_transcript_exon_variant","non_coding_transcript_exon_variant;non_coding_transcript_variant","345/579"]
["ARR3",407,"WUGSC","GRCh38","chrX",70281707,70281707,"+","Missense_Mutation","SNP","C","C","T",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.1108C>T","ENST00000307959","17/17",469,255,"T","ENSG00000120500","ENST00000307959","missense_variant","missense_variant","1159/1292","1108/1167","370/388","R/W","Cgg/Tgg"]
["CXCR3",2833,"WUGSC","GRCh38","chrX",71616598,71616598,"+","Nonsense_Mutation","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.874C>T","ENST00000373693",42768,39,45,"A","ENSG00000186810","ENST00000373693","stop_gained","stop_gained","942/1624","874/1107","292/368","R/*","Cga/Tga"]
["DOCK11",139818,"WUGSC","GRCh38","chrX",118608297,118608297,"+","Missense_Mutation","SNP","A","A","G",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.2818A>G","ENST00000276202","26/53",262,135,"G","ENSG00000147251","ENST00000276202","missense_variant","missense_variant","2881/6625","2818/6222","940/2073","T/A","Acg/Gcg"]
["GPC4",2239,"WUGSC","GRCh38","chrX",133324193,133324193,"+","Silent","SNP","G","G","A",null,null,"TCGA-AN-A04C-01A-21W-A050-09","TCGA-AN-A04C-10A-01D-A047-09",null,null,"Somatic","Illumina HiSeq 2000","c1302f79-cc50-487a-9db5-016df85e67d7","e0036635-4a4e-485d-8e5d-810964be64a2","c.663C>T","ENST00000370828",42803,249,137,"A","ENSG00000076716","ENST00000370828","synonymous_variant","synonymous_variant","1188/4960","663/1671","221/556","F","ttC/ttT"]