| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73323708G>A | CA10583261 | HCN4 | c.2385C>T (p.Leu795=) c.1167C>T (p.Leu389=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323708G>C | CA491478522 | HCN4 | c.2385C>G (p.Leu795=) c.1167C>G (p.Leu389=) | dbSNP |
| 15 | g.73323708G= | CA2187188614 | HCN4 | c.2385C= (p.Leu795=) c.1167C= (p.Leu389=) | |
| 15 | g.73323708G>T | CA491478523 | HCN4 | c.2385C>A (p.Leu795=) c.1167C>A (p.Leu389=) | gnomAD v4 |
| 15 | g.73323709A>C | CA393088995 | HCN4 | c.2384T>G (p.Leu795Arg) c.1166T>G (p.Leu389Arg) | |
| 15 | g.73323709A>G | CA393088996 | HCN4 | c.2384T>C (p.Leu795Pro) c.1166T>C (p.Leu389Pro) | gnomAD v4 |
| 15 | g.73323709A>T | CA393088997 | HCN4 | c.2384T>A (p.Leu795His) c.1166T>A (p.Leu389His) | |
| 15 | g.73323710G>A | CA393088998 | HCN4 | c.2383C>T (p.Leu795Phe) c.1165C>T (p.Leu389Phe) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323710G>C | CA393088999 | HCN4 | c.2383C>G (p.Leu795Val) c.1165C>G (p.Leu389Val) | |
| 15 | g.73323710G= | CA2187188615 | HCN4 | c.2383C= (p.Leu795=) c.1165C= (p.Leu389=) | |
| 15 | g.73323710G>T | CA393089000 | HCN4 | c.2383C>A (p.Leu795Ile) c.1165C>A (p.Leu389Ile) | dbSNP gnomAD v4 |
| 15 | g.73323711G>A | CA491478529 | HCN4 | c.2382C>T (p.Ala794=) c.1164C>T (p.Ala388=) | gnomAD v4 |
| 15 | g.73323711G>C | CA491478532 | HCN4 | c.2382C>G (p.Ala794=) c.1164C>G (p.Ala388=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323711G= | CA2187188616 | HCN4 | c.2382C= (p.Ala794=) c.1164C= (p.Ala388=) | |
| 15 | g.73323711G>T | CA491478530 | HCN4 | c.2382C>A (p.Ala794=) c.1164C>A (p.Ala388=) | gnomAD v4 COSMIC |
| 15 | g.73323712G>A | CA393089001 | HCN4 | c.2381C>T (p.Ala794Val) c.1163C>T (p.Ala388Val) | gnomAD v4 |
| 15 | g.73323712G>C | CA393089003 | HCN4 | c.2381C>G (p.Ala794Gly) c.1163C>G (p.Ala388Gly) | |
| 15 | g.73323712G>T | CA393089002 | HCN4 | c.2381C>A (p.Ala794Asp) c.1163C>A (p.Ala388Asp) | ClinVar gnomAD v4 |
| 15 | g.73323713C>A | CA393089004 | HCN4 | c.2380G>T (p.Ala794Ser) c.1162G>T (p.Ala388Ser) | gnomAD v4 |
| 15 | g.73323713C= | CA2187188617 | HCN4 | c.2380G= (p.Ala794=) c.1162G= (p.Ala388=) | |
| 15 | g.73323713C>G | CA393089005 | HCN4 | c.2380G>C (p.Ala794Pro) c.1162G>C (p.Ala388Pro) | |
| 15 | g.73323713C>T | CA272664854 | HCN4 | c.2380G>A (p.Ala794Thr) c.1162G>A (p.Ala388Thr) | dbSNP |
| 15 | g.73323714T>A | CA491478536 | HCN4 | c.2379A>T (p.Ile793=) c.1161A>T (p.Ile387=) | gnomAD v4 |
| 15 | g.73323714T>C | CA393089006 | HCN4 | c.2379A>G (p.Ile793Met) c.1161A>G (p.Ile387Met) | gnomAD v4 |
| 15 | g.73323714T>G | CA491478538 | HCN4 | c.2379A>C (p.Ile793=) c.1161A>C (p.Ile387=) | |
| 15 | g.73323715A>C | CA393089007 | HCN4 | c.2378T>G (p.Ile793Arg) c.1160T>G (p.Ile387Arg) | |
| 15 | g.73323715A>G | CA393089009 | HCN4 | c.2378T>C (p.Ile793Thr) c.1160T>C (p.Ile387Thr) | COSMIC |
| 15 | g.73323715A>T | CA393089008 | HCN4 | c.2378T>A (p.Ile793Lys) c.1160T>A (p.Ile387Lys) | |
| 15 | g.73323716T>A | CA393089010 | HCN4 | c.2377A>T (p.Ile793Leu) c.1159A>T (p.Ile387Leu) | |
| 15 | g.73323716T>C | CA393089011 | HCN4 | c.2377A>G (p.Ile793Val) c.1159A>G (p.Ile387Val) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73323716T>G | CA393089012 | HCN4 | c.2377A>C (p.Ile793Leu) c.1159A>C (p.Ile387Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323716T= | CA2187188618 | HCN4 | c.2377A= (p.Ile793=) c.1159A= (p.Ile387=) | |
| 15 | g.73323717G>A | CA491478544 | HCN4 | c.2376C>T (p.Ala792=) c.1158C>T (p.Ala386=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323717G>C | CA491478545 | HCN4 | c.2376C>G (p.Ala792=) c.1158C>G (p.Ala386=) | ClinVar dbSNP |
| 15 | g.73323717G= | CA2187188619 | HCN4 | c.2376C= (p.Ala792=) c.1158C= (p.Ala386=) | |
| 15 | g.73323717G>T | CA491478546 | HCN4 | c.2376C>A (p.Ala792=) c.1158C>A (p.Ala386=) | gnomAD v4 |
| 15 | g.73323717_73323718delinsAC | CA645586811 | HCN4 | c.2375_2376delinsGT (p.Ala792Gly) c.1157_1158delinsGT (p.Ala386Gly) | COSMIC |
| 15 | g.73323718G>A | CA393089013 | HCN4 | c.2375C>T (p.Ala792Val) c.1157C>T (p.Ala386Val) | gnomAD v4 |
| 15 | g.73323718G>C | CA393089014 | HCN4 | c.2375C>G (p.Ala792Gly) c.1157C>G (p.Ala386Gly) | |
| 15 | g.73323718G>T | CA393089015 | HCN4 | c.2375C>A (p.Ala792Asp) c.1157C>A (p.Ala386Asp) | gnomAD v4 |
| 15 | g.73323719C>A | CA7649038 | HCN4 | c.2374G>T (p.Ala792Ser) c.1156G>T (p.Ala386Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323719C= | CA2187188620 | HCN4 | c.2374G= (p.Ala792=) c.1156G= (p.Ala386=) | |
| 15 | g.73323719C>G | CA393089016 | HCN4 | c.2374G>C (p.Ala792Pro) c.1156G>C (p.Ala386Pro) | |
| 15 | g.73323719C>T | CA393089017 | HCN4 | c.2374G>A (p.Ala792Thr) c.1156G>A (p.Ala386Thr) | gnomAD v4 |
| 15 | g.73323720C>A | CA7649039 | HCN4 | c.2373G>T (p.Val791=) c.1155G>T (p.Val385=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323720C= | CA2187188621 | HCN4 | c.2373G= (p.Val791=) c.1155G= (p.Val385=) | |
| 15 | g.73323720C>G | CA491478554 | HCN4 | c.2373G>C (p.Val791=) c.1155G>C (p.Val385=) | |
| 15 | g.73323720C>T | CA491478555 | HCN4 | c.2373G>A (p.Val791=) c.1155G>A (p.Val385=) | |
| 15 | g.73323721A>C | CA393089018 | HCN4 | c.2372T>G (p.Val791Gly) c.1154T>G (p.Val385Gly) | |
| 15 | g.73323721A>G | CA393089020 | HCN4 | c.2372T>C (p.Val791Ala) c.1154T>C (p.Val385Ala) |