| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73323883T>A | CA393089408 | HCN4 | c.2210A>T (p.Gln737Leu) c.992A>T (p.Gln331Leu) | |
| 15 | g.73323883T>C | CA7649076 | HCN4 | c.2210A>G (p.Gln737Arg) c.992A>G (p.Gln331Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323883T>G | CA393089406 | HCN4 | c.2210A>C (p.Gln737Pro) c.992A>C (p.Gln331Pro) | |
| 15 | g.73323883T= | CA2187188750 | HCN4 | c.2210A= (p.Gln737=) c.992A= (p.Gln331=) | |
| 15 | g.73323884G>A | CA393089414 | HCN4 | c.2209C>T (p.Gln737Ter) c.991C>T (p.Gln331Ter) | |
| 15 | g.73323884G>C | CA393089411 | HCN4 | c.2209C>G (p.Gln737Glu) c.991C>G (p.Gln331Glu) | |
| 15 | g.73323884G>T | CA393089412 | HCN4 | c.2209C>A (p.Gln737Lys) c.991C>A (p.Gln331Lys) | gnomAD v4 |
| 15 | g.73323885G>A | CA7649077 | HCN4 | c.2208C>T (p.Tyr736=) c.990C>T (p.Tyr330=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323885G>C | CA393089416 | HCN4 | c.2208C>G (p.Tyr736Ter) c.990C>G (p.Tyr330Ter) | |
| 15 | g.73323885G= | CA2187188753 | HCN4 | c.2208C= (p.Tyr736=) c.990C= (p.Tyr330=) | |
| 15 | g.73323885G>T | CA393089418 | HCN4 | c.2208C>A (p.Tyr736Ter) c.990C>A (p.Tyr330Ter) | gnomAD v4 |
| 15 | g.73323886T>A | CA393089420 | HCN4 | c.2207A>T (p.Tyr736Phe) c.989A>T (p.Tyr330Phe) | |
| 15 | g.73323886T>C | CA393089421 | HCN4 | c.2207A>G (p.Tyr736Cys) c.989A>G (p.Tyr330Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323886T>G | CA393089423 | HCN4 | c.2207A>C (p.Tyr736Ser) c.989A>C (p.Tyr330Ser) | |
| 15 | g.73323886T= | CA2187188757 | HCN4 | c.2207A= (p.Tyr736=) c.989A= (p.Tyr330=) | |
| 15 | g.73323887A= | CA2187188760 | HCN4 | c.2206T= (p.Tyr736=) c.988T= (p.Tyr330=) | |
| 15 | g.73323887A>C | CA393089424 | HCN4 | c.2206T>G (p.Tyr736Asp) c.988T>G (p.Tyr330Asp) | |
| 15 | g.73323887A>G | CA272665111 | HCN4 | c.2206T>C (p.Tyr736His) c.988T>C (p.Tyr330His) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323887A>T | CA393089426 | HCN4 | c.2206T>A (p.Tyr736Asn) c.988T>A (p.Tyr330Asn) | |
| 15 | g.73323888G>A | CA491478659 | HCN4 | c.2205C>T (p.Asn735=) c.987C>T (p.Asn329=) | |
| 15 | g.73323888G>C | CA393089428 | HCN4 | c.2205C>G (p.Asn735Lys) c.987C>G (p.Asn329Lys) | |
| 15 | g.73323888G>T | CA393089430 | HCN4 | c.2205C>A (p.Asn735Lys) c.987C>A (p.Asn329Lys) | |
| 15 | g.73323889T>A | CA393089434 | HCN4 | c.2204A>T (p.Asn735Ile) c.986A>T (p.Asn329Ile) | |
| 15 | g.73323889T>C | CA393089432 | HCN4 | c.2204A>G (p.Asn735Ser) c.986A>G (p.Asn329Ser) | dbSNP gnomAD v4 |
| 15 | g.73323889T>G | CA393089431 | HCN4 | c.2204A>C (p.Asn735Thr) c.986A>C (p.Asn329Thr) | gnomAD v4 |
| 15 | g.73323889T= | CA2187188764 | HCN4 | c.2204A= (p.Asn735=) c.986A= (p.Asn329=) | |
| 15 | g.73323890T>A | CA393089435 | HCN4 | c.2203A>T (p.Asn735Tyr) c.985A>T (p.Asn329Tyr) | |
| 15 | g.73323890T>C | CA393089437 | HCN4 | c.2203A>G (p.Asn735Asp) c.985A>G (p.Asn329Asp) | |
| 15 | g.73323890T>G | CA393089438 | HCN4 | c.2203A>C (p.Asn735His) c.985A>C (p.Asn329His) | |
| 15 | g.73323891G>A | CA491478669 | HCN4 | c.2202C>T (p.Phe734=) c.984C>T (p.Phe328=) | gnomAD v4 |
| 15 | g.73323891G>C | CA393089440 | HCN4 | c.2202C>G (p.Phe734Leu) c.984C>G (p.Phe328Leu) | |
| 15 | g.73323891G>T | CA393089442 | HCN4 | c.2202C>A (p.Phe734Leu) c.984C>A (p.Phe328Leu) | gnomAD v4 |
| 15 | g.73323892A>C | CA393089444 | HCN4 | c.2201T>G (p.Phe734Cys) c.983T>G (p.Phe328Cys) | |
| 15 | g.73323892A>G | CA393089445 | HCN4 | c.2201T>C (p.Phe734Ser) c.983T>C (p.Phe328Ser) | |
| 15 | g.73323892A>T | CA393089446 | HCN4 | c.2201T>A (p.Phe734Tyr) c.983T>A (p.Phe328Tyr) | |
| 15 | g.73323893A>C | CA393089448 | HCN4 | c.2200T>G (p.Phe734Val) c.982T>G (p.Phe328Val) | |
| 15 | g.73323893A>G | CA393089449 | HCN4 | c.2200T>C (p.Phe734Leu) c.982T>C (p.Phe328Leu) | |
| 15 | g.73323893A>T | CA393089451 | HCN4 | c.2200T>A (p.Phe734Ile) c.982T>A (p.Phe328Ile) | |
| 15 | g.73323894G>A | CA491478678 | HCN4 | c.2199C>T (p.Val733=) c.981C>T (p.Val327=) | |
| 15 | g.73323894G>C | CA491478679 | HCN4 | c.2199C>G (p.Val733=) c.981C>G (p.Val327=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323894G= | CA2187188768 | HCN4 | c.2199C= (p.Val733=) c.981C= (p.Val327=) | |
| 15 | g.73323894G>T | CA491478680 | HCN4 | c.2199C>A (p.Val733=) c.981C>A (p.Val327=) | |
| 15 | g.73323895A= | CA2187188773 | HCN4 | c.2198T= (p.Val733=) c.980T= (p.Val327=) | |
| 15 | g.73323895A>C | CA393089452 | HCN4 | c.2198T>G (p.Val733Gly) c.980T>G (p.Val327Gly) | |
| 15 | g.73323895A>G | CA393089454 | HCN4 | c.2198T>C (p.Val733Ala) c.980T>C (p.Val327Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323895A>T | CA393089455 | HCN4 | c.2198T>A (p.Val733Asp) c.980T>A (p.Val327Asp) | |
| 15 | g.73323896C>A | CA393089459 | HCN4 | c.2197G>T (p.Val733Phe) c.979G>T (p.Val327Phe) | |
| 15 | g.73323896C= | CA2187188785 | HCN4 | c.2197G= (p.Val733=) c.979G= (p.Val327=) | |
| 15 | g.73323896C>G | CA393089457 | HCN4 | c.2197G>C (p.Val733Leu) c.979G>C (p.Val327Leu) | |
| 15 | g.73323896C>T | CA068221 | HCN4 | c.2197G>A (p.Val733Ile) c.979G>A (p.Val327Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |