| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73323441G>A | CA7648980 | HCN4 | c.2652C>T (p.Pro884=) c.1434C>T (p.Pro478=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323441G>C | CA491478630 | HCN4 | c.2652C>G (p.Pro884=) c.1434C>G (p.Pro478=) | |
| 15 | g.73323441G= | CA2187188297 | HCN4 | c.2652C= (p.Pro884=) c.1434C= (p.Pro478=) | |
| 15 | g.73323441G>T | CA491478631 | HCN4 | c.2652C>A (p.Pro884=) c.1434C>A (p.Pro478=) | gnomAD v4 |
| 15 | g.73323446dup | CA619410590 | HCN4 | c.2652dup (p.Gly885ArgfsTer?) c.1434dup (p.Gly479ArgfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323446del | CA2629370567 | HCN4 | c.2652del (p.Ala886ProfsTer14) c.1434del (p.Ala480ProfsTer14) | gnomAD v4 |
| 15 | g.73323442G>A | CA393088478 | HCN4 | c.2651C>T (p.Pro884Leu) c.1433C>T (p.Pro478Leu) | gnomAD v4 |
| 15 | g.73323442G>C | CA393088479 | HCN4 | c.2651C>G (p.Pro884Arg) c.1433C>G (p.Pro478Arg) | |
| 15 | g.73323442G>T | CA393088480 | HCN4 | c.2651C>A (p.Pro884His) c.1433C>A (p.Pro478His) | |
| 15 | g.73323443G>A | CA7648981 | HCN4 | c.2650C>T (p.Pro884Ser) c.1432C>T (p.Pro478Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323443G>C | CA272664429 | HCN4 | c.2650C>G (p.Pro884Ala) c.1432C>G (p.Pro478Ala) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323443G= | CA2187188302 | HCN4 | c.2650C= (p.Pro884=) c.1432C= (p.Pro478=) | |
| 15 | g.73323443G>T | CA272664436 | HCN4 | c.2650C>A (p.Pro884Thr) c.1432C>A (p.Pro478Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323444G>A | CA491478639 | HCN4 | c.2649C>T (p.Pro883=) c.1431C>T (p.Pro477=) | |
| 15 | g.73323444G>C | CA491478641 | HCN4 | c.2649C>G (p.Pro883=) c.1431C>G (p.Pro477=) | dbSNP gnomAD v4 |
| 15 | g.73323444G= | CA2187188305 | HCN4 | c.2649C= (p.Pro883=) c.1431C= (p.Pro477=) | |
| 15 | g.73323444G>T | CA491478640 | HCN4 | c.2649C>A (p.Pro883=) c.1431C>A (p.Pro477=) | gnomAD v4 |
| 15 | g.73323445G>A | CA393088481 | HCN4 | c.2648C>T (p.Pro883Leu) c.1430C>T (p.Pro477Leu) | |
| 15 | g.73323445G>C | CA163178 | HCN4 | c.2648C>G (p.Pro883Arg) c.1430C>G (p.Pro477Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323445G= | CA2187188311 | HCN4 | c.2648C= (p.Pro883=) c.1430C= (p.Pro477=) | |
| 15 | g.73323445G>T | CA393088482 | HCN4 | c.2648C>A (p.Pro883His) c.1430C>A (p.Pro477His) | gnomAD v4 |
| 15 | g.73323446G>A | CA7648982 | HCN4 | c.2647C>T (p.Pro883Ser) c.1429C>T (p.Pro477Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73323446G>C | CA393088483 | HCN4 | c.2647C>G (p.Pro883Ala) c.1429C>G (p.Pro477Ala) | |
| 15 | g.73323446G= | CA2187188315 | HCN4 | c.2647C= (p.Pro883=) c.1429C= (p.Pro477=) | |
| 15 | g.73323446G>T | CA393088484 | HCN4 | c.2647C>A (p.Pro883Thr) c.1429C>A (p.Pro477Thr) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323447T>A | CA491478648 | HCN4 | c.2646A>T (p.Pro882=) c.1428A>T (p.Pro476=) | |
| 15 | g.73323447T>C | CA491478650 | HCN4 | c.2646A>G (p.Pro882=) c.1428A>G (p.Pro476=) | gnomAD v4 |
| 15 | g.73323447T>G | CA491478649 | HCN4 | c.2646A>C (p.Pro882=) c.1428A>C (p.Pro476=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323447T= | CA2187188318 | HCN4 | c.2646A= (p.Pro882=) c.1428A= (p.Pro476=) | |
| 15 | g.73323448G>A | CA393088486 | HCN4 | c.2645C>T (p.Pro882Leu) c.1427C>T (p.Pro476Leu) | gnomAD v4 |
| 15 | g.73323448G>C | CA393088487 | HCN4 | c.2645C>G (p.Pro882Arg) c.1427C>G (p.Pro476Arg) | |
| 15 | g.73323448G>T | CA393088485 | HCN4 | c.2645C>A (p.Pro882Gln) c.1427C>A (p.Pro476Gln) | gnomAD v4 |
| 15 | g.73323449G>A | CA393088488 | HCN4 | c.2644C>T (p.Pro882Ser) c.1426C>T (p.Pro476Ser) | |
| 15 | g.73323449G>C | CA393088489 | HCN4 | c.2644C>G (p.Pro882Ala) c.1426C>G (p.Pro476Ala) | |
| 15 | g.73323449G>T | CA393088490 | HCN4 | c.2644C>A (p.Pro882Thr) c.1426C>A (p.Pro476Thr) | COSMIC |
| 15 | g.73323450G>A | CA491478660 | HCN4 | c.2643C>T (p.Ser881=) c.1425C>T (p.Ser475=) | dbSNP gnomAD v2 |
| 15 | g.73323450G>C | CA491478661 | HCN4 | c.2643C>G (p.Ser881=) c.1425C>G (p.Ser475=) | |
| 15 | g.73323450G= | CA2187188320 | HCN4 | c.2643C= (p.Ser881=) c.1425C= (p.Ser475=) | |
| 15 | g.73323450G>T | CA491478662 | HCN4 | c.2643C>A (p.Ser881=) c.1425C>A (p.Ser475=) | |
| 15 | g.73323451G>A | CA393088491 | HCN4 | c.2642C>T (p.Ser881Phe) c.1424C>T (p.Ser475Phe) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323451G>C | CA393088492 | HCN4 | c.2642C>G (p.Ser881Cys) c.1424C>G (p.Ser475Cys) | |
| 15 | g.73323451G>T | CA393088493 | HCN4 | c.2642C>A (p.Ser881Tyr) c.1424C>A (p.Ser475Tyr) | gnomAD v4 |
| 15 | g.73323452A= | CA2187188322 | HCN4 | c.2641T= (p.Ser881=) c.1423T= (p.Ser475=) | |
| 15 | g.73323452A>C | CA393088494 | HCN4 | c.2641T>G (p.Ser881Ala) c.1423T>G (p.Ser475Ala) | |
| 15 | g.73323452A>G | CA7648983 | HCN4 | c.2641T>C (p.Ser881Pro) c.1423T>C (p.Ser475Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323452A>T | CA393088495 | HCN4 | c.2641T>A (p.Ser881Thr) c.1423T>A (p.Ser475Thr) | |
| 15 | g.73323453G>A | CA491478674 | HCN4 | c.2640C>T (p.Ser880=) c.1422C>T (p.Ser474=) | |
| 15 | g.73323453G>C | CA491478676 | HCN4 | c.2640C>G (p.Ser880=) c.1422C>G (p.Ser474=) | |
| 15 | g.73323453G>T | CA491478677 | HCN4 | c.2640C>A (p.Ser880=) c.1422C>A (p.Ser474=) | gnomAD v4 |
| 15 | g.73323454G>A | CA393088496 | HCN4 | c.2639C>T (p.Ser880Phe) c.1421C>T (p.Ser474Phe) | gnomAD v4 |