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[{"$nulls":3},"CTNNA1 variants identified in DGC cases in the current study"]
["N","Variant’s reference","Exon / Intron","Frequency Hm (%)","Frequency Hz (%)","Genomic position","Sequence variation","Clinvar","ACMG Classification","Frequency 1000 Genome","Protein Change","Type"]
[1,"rs11552054","Exon5",0,"5,88 (2/34)",138812254,"c.540A>C","B","B","0.018","p.180L=","S"]
[]
[]
[2,"rs28363395","Exon5",null,"5,88(2/34)",138812260,"c.546T>G","B","LB",null,"p.182P="]
[]
[{"$nulls":3},0,{"$nulls":5},"0.011",null,"S"]
[3,"rs1223706415","Exon6",0,"2,94(1/34)",138160227,"c.597A>G","NI","LB","3.98356e-06","p.199K=","S"]
[]
[]
[4,"rs1345755897","Intron6",null,"2,94(1/34)",138160503,"c.585+15G>T","NI",null,null,"NA"]
[{"$nulls":3},0,{"$nulls":5},"4.00998e-06 (gnomAD)"]
[{"$nulls":8},"VUS",null,null,"I"]
[5,"rs1402504955","Exon6",0,"11,76(4/34)",138160473,"c.843A>G","NI","LB","7.96400e-06 (TOPMed)","p.281A=","S"]
[]
[]
[6,"rs1361845780","Intron7",null,0,138221831,"c.1063-70C>G","NI",null,null,"NA"]
[]
[{"$nulls":9},"7.96400e-06 (TOPMed)"]
[{"$nulls":3},"2,94 (1/34)",{"$nulls":4},"B",null,null,"I"]
[7,"rs288028","Intron8",0,"26,47(9/34)",13822989,"c.1143+8G>C","NI","B","0.186","NA","SR"]
[]
[]
[8,"rs61736921","Exon9",null,"2,94(1/34)",138887513,"c.1167C>T","B","LB",null,"p.389H="]
[]
[{"$nulls":3},0,{"$nulls":5},"0.002",null,"S"]
[9,"rs28363461","Intron10","5,88(2/34)",0,138253420,"c.1390-11A>G","NI","LB","0.009","NA","I"]
[]
[10,"rs28363462","Exon11",null,"5,88(2/34)",138917757,"c.1405C>T","B","LB",null,"p. 469L="]
[]
[{"$nulls":3},0,{"$nulls":5},"0.009",null,"S"]
[11,"rs543204283","Intron15",0,"8,82(3/34)",138266485,"c.2193-34A>G","NI","LB","0.000199680511182109","NA","I"]
[]
[]
[]
[null,"Novel","Intron16",null,0,138266451,"c.2193-68C>T","NR",null,null,"NA"]
[12]
[]
[]
[{"$nulls":3},"5,88(2/34)",{"$nulls":4},"VUS","NA",null,"I"]
[13,"rs1059110","Exon16","11,76(4/34)","29,41(10/34)",138930857,"c.2220G>A","B","B","0.249","P.740S=","S"]
[]
[14,"rs11552052",{"$nulls":3},138930863,"c.2226 C>G","B","LB",null,"p.742V=","S"]
[null,null,"Exon16",0,"2,94(1/34)",{"$nulls":4},"0.009"]
[15,"rs1032311542","Intron17",0,"5,88(2/34)",138268454,"c.2433+53 C>G","NI","VUS","3.48962e-05","NA","I"]
[]
[{"$nulls":4},"B : Benign ;P : Pathogenic ; VUS : Variant of Uncertain Significance ; NR : Not Reported ;NI : Non Indicated;  Hz: Heterozygous status; S:Synonymous Variant; M:Missense Variant,I : Intronic Variant, SR : Splice Region Variant"]

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