| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73329592C>A | CA393093403 | HCN4 | c.1571G>T (p.Arg524Leu) c.353G>T (p.Arg118Leu) | |
| 15 | g.73329592C= | CA2187167401 | HCN4 | c.1571G= (p.Arg524=) c.353G= (p.Arg118=) | |
| 15 | g.73329592C>G | CA393093405 | HCN4 | c.1571G>C (p.Arg524Pro) c.353G>C (p.Arg118Pro) | |
| 15 | g.73329592C>T | CA7649279 | HCN4 | c.1571G>A (p.Arg524Gln) c.353G>A (p.Arg118Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329593G>A | CA393093408 | HCN4 | c.1570C>T (p.Arg524Trp) c.352C>T (p.Arg118Trp) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329593G>C | CA393093410 | HCN4 | c.1570C>G (p.Arg524Gly) c.352C>G (p.Arg118Gly) | |
| 15 | g.73329593G= | CA2187167406 | HCN4 | c.1570C= (p.Arg524=) c.352C= (p.Arg118=) | |
| 15 | g.73329593G>T | CA7649280 | HCN4 | c.1570C>A (p.Arg524=) c.352C>A (p.Arg118=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329594G>A | CA491151457 | HCN4 | c.1569C>T (p.Ser523=) c.351C>T (p.Ser117=) | |
| 15 | g.73329594G>C | CA491151459 | HCN4 | c.1569C>G (p.Ser523=) c.351C>G (p.Ser117=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329594G= | CA2187167410 | HCN4 | c.1569C= (p.Ser523=) c.351C= (p.Ser117=) | |
| 15 | g.73329594G>T | CA491151458 | HCN4 | c.1569C>A (p.Ser523=) c.351C>A (p.Ser117=) | |
| 15 | g.73329595G>A | CA393093413 | HCN4 | c.1568C>T (p.Ser523Phe) c.350C>T (p.Ser117Phe) | |
| 15 | g.73329595G>C | CA393093415 | HCN4 | c.1568C>G (p.Ser523Cys) c.350C>G (p.Ser117Cys) | |
| 15 | g.73329595G>T | CA393093416 | HCN4 | c.1568C>A (p.Ser523Tyr) c.350C>A (p.Ser117Tyr) | |
| 15 | g.73329596A>C | CA393093422 | HCN4 | c.1567T>G (p.Ser523Ala) c.349T>G (p.Ser117Ala) | |
| 15 | g.73329596A>G | CA393093420 | HCN4 | c.1567T>C (p.Ser523Pro) c.349T>C (p.Ser117Pro) | |
| 15 | g.73329596A>T | CA393093418 | HCN4 | c.1567T>A (p.Ser523Thr) c.349T>A (p.Ser117Thr) | |
| 15 | g.73329597G>A | CA491151460 | HCN4 | c.1566C>T (p.Ser522=) c.348C>T (p.Ser116=) | |
| 15 | g.73329597G>C | CA491151461 | HCN4 | c.1566C>G (p.Ser522=) c.348C>G (p.Ser116=) | |
| 15 | g.73329597G>T | CA491151462 | HCN4 | c.1566C>A (p.Ser522=) c.348C>A (p.Ser116=) | |
| 15 | g.73329598G>A | CA393093428 | HCN4 | c.1565C>T (p.Ser522Phe) c.347C>T (p.Ser116Phe) | gnomAD v4 |
| 15 | g.73329598G>C | CA393093424 | HCN4 | c.1565C>G (p.Ser522Cys) c.347C>G (p.Ser116Cys) | |
| 15 | g.73329598G>T | CA393093426 | HCN4 | c.1565C>A (p.Ser522Tyr) c.347C>A (p.Ser116Tyr) | |
| 15 | g.73329599A>C | CA393093431 | HCN4 | c.1564T>G (p.Ser522Ala) c.346T>G (p.Ser116Ala) | |
| 15 | g.73329599A>G | CA393093433 | HCN4 | c.1564T>C (p.Ser522Pro) c.346T>C (p.Ser116Pro) | |
| 15 | g.73329599A>T | CA393093435 | HCN4 | c.1564T>A (p.Ser522Thr) c.346T>A (p.Ser116Thr) | |
| 15 | g.73329600G>A | CA7649281 | HCN4 | c.1563C>T (p.Asp521=) c.345C>T (p.Asp115=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329600G>C | CA393093439 | HCN4 | c.1563C>G (p.Asp521Glu) c.345C>G (p.Asp115Glu) | |
| 15 | g.73329600G= | CA2187167414 | HCN4 | c.1563C= (p.Asp521=) c.345C= (p.Asp115=) | |
| 15 | g.73329600G>T | CA393093441 | HCN4 | c.1563C>A (p.Asp521Glu) c.345C>A (p.Asp115Glu) | |
| 15 | g.73329601T>A | CA393093442 | HCN4 | c.1562A>T (p.Asp521Val) c.344A>T (p.Asp115Val) | |
| 15 | g.73329601T>C | CA393093444 | HCN4 | c.1562A>G (p.Asp521Gly) c.344A>G (p.Asp115Gly) | |
| 15 | g.73329601T>G | CA393093447 | HCN4 | c.1562A>C (p.Asp521Ala) c.344A>C (p.Asp115Ala) | |
| 15 | g.73329602C>A | CA393093449 | HCN4 | c.1561G>T (p.Asp521Tyr) c.343G>T (p.Asp115Tyr) | |
| 15 | g.73329602C>G | CA393093451 | HCN4 | c.1561G>C (p.Asp521His) c.343G>C (p.Asp115His) | |
| 15 | g.73329602C>T | CA393093453 | HCN4 | c.1561G>A (p.Asp521Asn) c.343G>A (p.Asp115Asn) | |
| 15 | g.73329603C>A | CA491151463 | HCN4 | c.1560G>T (p.Leu520=) c.342G>T (p.Leu114=) | |
| 15 | g.73329603C= | CA2187167419 | HCN4 | c.1560G= (p.Leu520=) c.342G= (p.Leu114=) | |
| 15 | g.73329603C>G | CA491151464 | HCN4 | c.1560G>C (p.Leu520=) c.342G>C (p.Leu114=) | |
| 15 | g.73329603C>T | CA7649282 | HCN4 | c.1560G>A (p.Leu520=) c.342G>A (p.Leu114=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329604A>C | CA393093456 | HCN4 | c.1559T>G (p.Leu520Arg) c.341T>G (p.Leu114Arg) | |
| 15 | g.73329604A>G | CA393093458 | HCN4 | c.1559T>C (p.Leu520Pro) c.341T>C (p.Leu114Pro) | |
| 15 | g.73329604A>T | CA393093460 | HCN4 | c.1559T>A (p.Leu520Gln) c.341T>A (p.Leu114Gln) | |
| 15 | g.73329605G>A | CA291166 | HCN4 | c.1558C>T (p.Leu520=) c.340C>T (p.Leu114=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329605G>C | CA393093464 | HCN4 | c.1558C>G (p.Leu520Val) c.340C>G (p.Leu114Val) | |
| 15 | g.73329605G= | CA2187167423 | HCN4 | c.1558C= (p.Leu520=) c.340C= (p.Leu114=) | |
| 15 | g.73329605G>T | CA393093465 | HCN4 | c.1558C>A (p.Leu520Met) c.340C>A (p.Leu114Met) | |
| 15 | g.73329606G>A | CA491151465 | HCN4 | c.1557C>T (p.Ser519=) c.339C>T (p.Ser113=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329606G>C | CA491151466 | HCN4 | c.1557C>G (p.Ser519=) c.339C>G (p.Ser113=) |