Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.111787039C>A | CA341660764 | KCND3 | c.1174G>T (p.Val392Phe) | |
1 | g.111787039C= | CA1189065703 | KCND3 | c.1174G= (p.Val392=) | |
1 | g.111787039C>G | CA341660766 | KCND3 | c.1174G>C (p.Val392Leu) | |
1 | g.111787039C>T | CA200132 | KCND3 | c.1174G>A (p.Val392Ile) | ClinVar dbSNP |
1 | g.111787040G>A | CA1007500 | KCND3 | c.1173C>T (p.Gly391=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.111787040G>C | CA419530154 | KCND3 | c.1173C>G (p.Gly391=) | |
1 | g.111787040G= | CA1144687146 | KCND3 | c.1173C= (p.Gly391=) | |
1 | g.111787040G>T | CA419530155 | KCND3 | c.1173C>A (p.Gly391=) | ClinVar dbSNP gnomAD v4 |
1 | g.111787041C>A | CA341660775 | KCND3 | c.1172G>T (p.Gly391Val) | |
1 | g.111787041C>G | CA341660773 | KCND3 | c.1172G>C (p.Gly391Ala) | |
1 | g.111787041C>T | CA341660771 | KCND3 | c.1172G>A (p.Gly391Asp) | |
1 | g.111787042C>A | CA341660777 | KCND3 | c.1171G>T (p.Gly391Cys) | |
1 | g.111787042C>G | CA341660780 | KCND3 | c.1171G>C (p.Gly391Arg) | |
1 | g.111787042C>T | CA341660781 | KCND3 | c.1171G>A (p.Gly391Ser) | |
1 | g.111787043A>C | CA341660783 | KCND3 | c.1170T>G (p.Ser390Arg) | |
1 | g.111787043A>G | CA419530156 | KCND3 | c.1170T>C (p.Ser390=) | |
1 | g.111787043A>T | CA341660785 | KCND3 | c.1170T>A (p.Ser390Arg) | |
1 | g.111787044C>A | CA341660786 | KCND3 | c.1169G>T (p.Ser390Ile) | |
1 | g.111787044C= | CA1144228930 | KCND3 | c.1169G= (p.Ser390=) | |
1 | g.111787044C>G | CA341660788 | KCND3 | c.1169G>C (p.Ser390Thr) | |
1 | g.111787044C>T | CA144862 | KCND3 | c.1169G>A (p.Ser390Asn) | ClinVar dbSNP |
1 | g.111787045T>A | CA341660790 | KCND3 | c.1168A>T (p.Ser390Cys) | |
1 | g.111787045T>C | CA341660793 | KCND3 | c.1168A>G (p.Ser390Gly) | |
1 | g.111787045T>G | CA341660795 | KCND3 | c.1168A>C (p.Ser390Arg) | |
1 | g.111787046C>A | CA341660797 | KCND3 | c.1167G>T (p.Leu389Phe) | |
1 | g.111787046C= | CA1189065704 | KCND3 | c.1167G= (p.Leu389=) | |
1 | g.111787046C>G | CA341660799 | KCND3 | c.1167G>C (p.Leu389Phe) | |
1 | g.111787046C>T | CA419530157 | KCND3 | c.1167G>A (p.Leu389=) | ClinVar dbSNP |
1 | g.111787047A>C | CA341660803 | KCND3 | c.1166T>G (p.Leu389Trp) | |
1 | g.111787047A>G | CA341660804 | KCND3 | c.1166T>C (p.Leu389Ser) | |
1 | g.111787047A>T | CA341660801 | KCND3 | c.1166T>A (p.Leu389Ter) | |
1 | g.111787048A>C | CA341660807 | KCND3 | c.1165T>G (p.Leu389Val) | |
1 | g.111787048A>G | CA419530158 | KCND3 | c.1165T>C (p.Leu389=) | |
1 | g.111787048A>T | CA341660808 | KCND3 | c.1165T>A (p.Leu389Met) | |
1 | g.111787049G>A | CA1007501 | KCND3 | c.1164C>T (p.Ser388=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.111787049G>C | CA419530159 | KCND3 | c.1164C>G (p.Ser388=) | |
1 | g.111787049G= | CA1189065705 | KCND3 | c.1164C= (p.Ser388=) | |
1 | g.111787049G>T | CA419530160 | KCND3 | c.1164C>A (p.Ser388=) | |
1 | g.111787050G>A | CA341660811 | KCND3 | c.1163C>T (p.Ser388Phe) | |
1 | g.111787050G>C | CA341660813 | KCND3 | c.1163C>G (p.Ser388Cys) | |
1 | g.111787050G>T | CA341660815 | KCND3 | c.1163C>A (p.Ser388Tyr) | |
1 | g.111787051A>C | CA341660817 | KCND3 | c.1162T>G (p.Ser388Ala) | |
1 | g.111787051A>G | CA341660818 | KCND3 | c.1162T>C (p.Ser388Pro) | |
1 | g.111787051A>T | CA341660821 | KCND3 | c.1162T>A (p.Ser388Thr) | |
1 | g.111787052G>A | CA28905233 | KCND3 | c.1161C>T (p.Cys387=) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.111787052G>C | CA341660824 | KCND3 | c.1161C>G (p.Cys387Trp) | |
1 | g.111787052G= | CA1144068748 | KCND3 | c.1161C= (p.Cys387=) | |
1 | g.111787052G>T | CA341660825 | KCND3 | c.1161C>A (p.Cys387Ter) | |
1 | g.111787053C>A | CA341660831 | KCND3 | c.1160G>T (p.Cys387Phe) | |
1 | g.111787053C>G | CA341660828 | KCND3 | c.1160G>C (p.Cys387Ser) |