Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323104del | CA491478535 | HCN4 | c.2993del (p.Pro998HisfsTer20) c.1775del (p.Pro592HisfsTer20) | gnomAD v4 COSMIC |
15 | g.73323101G>A | CA393086536 | HCN4 | c.2992C>T (p.Pro998Ser) c.1774C>T (p.Pro592Ser) | gnomAD v4 |
15 | g.73323101G>C | CA7648910 | HCN4 | c.2992C>G (p.Pro998Ala) c.1774C>G (p.Pro592Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323101G= | CA2187187504 | HCN4 | c.2992C= (p.Pro998=) c.1774C= (p.Pro592=) | |
15 | g.73323101G>T | CA393086534 | HCN4 | c.2992C>A (p.Pro998Thr) c.1774C>A (p.Pro592Thr) | gnomAD v4 |
15 | g.73323102G>A | CA491478537 | HCN4 | c.2991C>T (p.Pro997=) c.1773C>T (p.Pro591=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323102G>C | CA491478539 | HCN4 | c.2991C>G (p.Pro997=) c.1773C>G (p.Pro591=) | gnomAD v4 |
15 | g.73323102G= | CA2187187506 | HCN4 | c.2991C= (p.Pro997=) c.1773C= (p.Pro591=) | |
15 | g.73323102G>T | CA491478540 | HCN4 | c.2991C>A (p.Pro997=) c.1773C>A (p.Pro591=) | |
15 | g.73323103G>A | CA393086539 | HCN4 | c.2990C>T (p.Pro997Leu) c.1772C>T (p.Pro591Leu) | gnomAD v4 |
15 | g.73323103G>C | CA393086541 | HCN4 | c.2990C>G (p.Pro997Arg) c.1772C>G (p.Pro591Arg) | |
15 | g.73323103G= | CA2187187511 | HCN4 | c.2990C= (p.Pro997=) c.1772C= (p.Pro591=) | |
15 | g.73323103G>T | CA272663982 | HCN4 | c.2990C>A (p.Pro997His) c.1772C>A (p.Pro591His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323104G>A | CA393086551 | HCN4 | c.2989C>T (p.Pro997Ser) c.1771C>T (p.Pro591Ser) | gnomAD v4 |
15 | g.73323104G>C | CA393086554 | HCN4 | c.2989C>G (p.Pro997Ala) c.1771C>G (p.Pro591Ala) | |
15 | g.73323104G= | CA2187187516 | HCN4 | c.2989C= (p.Pro997=) c.1771C= (p.Pro591=) | |
15 | g.73323104G>T | CA7648911 | HCN4 | c.2989C>A (p.Pro997Thr) c.1771C>A (p.Pro591Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323105T>A | CA491478550 | HCN4 | c.2988A>T (p.Thr996=) c.1770A>T (p.Thr590=) | dbSNP |
15 | g.73323105T>C | CA491478551 | HCN4 | c.2988A>G (p.Thr996=) c.1770A>G (p.Thr590=) | gnomAD v4 |
15 | g.73323105T>G | CA491478553 | HCN4 | c.2988A>C (p.Thr996=) c.1770A>C (p.Thr590=) | ClinVar |
15 | g.73323105T= | CA2187187520 | HCN4 | c.2988A= (p.Thr996=) c.1770A= (p.Thr590=) | |
15 | g.73323106G>A | CA393086559 | HCN4 | c.2987C>T (p.Thr996Ile) c.1769C>T (p.Thr590Ile) | gnomAD v4 |
15 | g.73323106G>C | CA393086561 | HCN4 | c.2987C>G (p.Thr996Arg) c.1769C>G (p.Thr590Arg) | |
15 | g.73323106G>T | CA393086563 | HCN4 | c.2987C>A (p.Thr996Lys) c.1769C>A (p.Thr590Lys) | gnomAD v4 |
15 | g.73323107T>A | CA393086567 | HCN4 | c.2986A>T (p.Thr996Ser) c.1768A>T (p.Thr590Ser) | dbSNP |
15 | g.73323107T>C | CA393086568 | HCN4 | c.2986A>G (p.Thr996Ala) c.1768A>G (p.Thr590Ala) | gnomAD v4 |
15 | g.73323107T>G | CA393086570 | HCN4 | c.2986A>C (p.Thr996Pro) c.1768A>C (p.Thr590Pro) | |
15 | g.73323107T= | CA2187187523 | HCN4 | c.2986A= (p.Thr996=) c.1768A= (p.Thr590=) | |
15 | g.73323108C>A | CA393086573 | HCN4 | c.2985G>T (p.Glu995Asp) c.1767G>T (p.Glu589Asp) | gnomAD v4 |
15 | g.73323108C>G | CA393086575 | HCN4 | c.2985G>C (p.Glu995Asp) c.1767G>C (p.Glu589Asp) | ClinVar gnomAD v4 |
15 | g.73323108C>T | CA491478563 | HCN4 | c.2985G>A (p.Glu995=) c.1767G>A (p.Glu589=) | gnomAD v4 |
15 | g.73323109T>A | CA393086579 | HCN4 | c.2984A>T (p.Glu995Val) c.1766A>T (p.Glu589Val) | |
15 | g.73323109T>C | CA393086583 | HCN4 | c.2984A>G (p.Glu995Gly) c.1766A>G (p.Glu589Gly) | gnomAD v4 |
15 | g.73323109T>G | CA393086581 | HCN4 | c.2984A>C (p.Glu995Ala) c.1766A>C (p.Glu589Ala) | |
15 | g.73323110C>A | CA393086587 | HCN4 | c.2983G>T (p.Glu995Ter) c.1765G>T (p.Glu589Ter) | gnomAD v4 |
15 | g.73323110C>G | CA393086590 | HCN4 | c.2983G>C (p.Glu995Gln) c.1765G>C (p.Glu589Gln) | |
15 | g.73323110C>T | CA393086591 | HCN4 | c.2983G>A (p.Glu995Lys) c.1765G>A (p.Glu589Lys) | |
15 | g.73323111T>A | CA491478567 | HCN4 | c.2982A>T (p.Pro994=) c.1764A>T (p.Pro588=) | |
15 | g.73323111T>C | CA491478570 | HCN4 | c.2982A>G (p.Pro994=) c.1764A>G (p.Pro588=) | dbSNP |
15 | g.73323111T>G | CA491478573 | HCN4 | c.2982A>C (p.Pro994=) c.1764A>C (p.Pro588=) | |
15 | g.73323111T= | CA2187187525 | HCN4 | c.2982A= (p.Pro994=) c.1764A= (p.Pro588=) | |
15 | g.73323112G>A | CA393086595 | HCN4 | c.2981C>T (p.Pro994Leu) c.1763C>T (p.Pro588Leu) | gnomAD v4 |
15 | g.73323112G>C | CA393086597 | HCN4 | c.2981C>G (p.Pro994Arg) c.1763C>G (p.Pro588Arg) | |
15 | g.73323112G>T | CA393086599 | HCN4 | c.2981C>A (p.Pro994Gln) c.1763C>A (p.Pro588Gln) | gnomAD v4 |
15 | g.73323113G>A | CA393086602 | HCN4 | c.2980C>T (p.Pro994Ser) c.1762C>T (p.Pro588Ser) | gnomAD v4 |
15 | g.73323113G>C | CA393086603 | HCN4 | c.2980C>G (p.Pro994Ala) c.1762C>G (p.Pro588Ala) | |
15 | g.73323113G>T | CA393086606 | HCN4 | c.2980C>A (p.Pro994Thr) c.1762C>A (p.Pro588Thr) | |
15 | g.73323114C>A | CA491478585 | HCN4 | c.2979G>T (p.Thr993=) c.1761G>T (p.Thr587=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323114C= | CA2187187528 | HCN4 | c.2979G= (p.Thr993=) c.1761G= (p.Thr587=) | |
15 | g.73323114C>G | CA491478584 | HCN4 | c.2979G>C (p.Thr993=) c.1761G>C (p.Thr587=) | ClinVar |