UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 15 | g.73329566G>A | CA2187167364 | HCN4 | c.1590+7C>T (n.1590+7C>T) c.372+7C>T (n.372+7C>T) | dbSNP |
| 15 | g.73329566G>C | CA915946065 | HCN4 | c.1590+7C>G (n.1590+7C>G) c.372+7C>G (n.372+7C>G) | ClinVar dbSNP |
| 15 | g.73329566G= | CA2187167363 | HCN4 | c.1590+7C= (n.1590+7C=) c.372+7C= (n.372+7C=) | |
| 15 | g.73329566G>T | CA645586814 | HCN4 | c.1590+7C>A (n.1590+7C>A) c.372+7C>A (n.372+7C>A) | COSMIC |
| 15 | g.73329567A= | CA2187167367 | HCN4 | c.1590+6T= (n.1590+6T=) c.372+6T= (n.372+6T=) | |
| 15 | g.73329567A>G | CA2730929831 | HCN4 | c.1590+6T>C (n.1590+6T>C) c.372+6T>C (n.372+6T>C) | dbSNP |
| 15 | g.73329567A>T | CA272671989 | HCN4 | c.1590+6T>A (n.1590+6T>A) c.372+6T>A (n.372+6T>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329567_73329568del | CA2629388586 | HCN4 | c.1590+5_1590+6del (n.1590+5_1590+6del) c.372+5_372+6del (n.372+5_372+6del) | gnomAD v4 |
| 15 | g.73329568C>A | CA2629388587 | HCN4 | c.1590+5G>T (n.1590+5G>T) c.372+5G>T (n.372+5G>T) | gnomAD v4 |
| 15 | g.73329569C= | CA2187167370 | HCN4 | c.1590+4G= (n.1590+4G=) c.372+4G= (n.372+4G=) | |
| 15 | g.73329569C>T | CA619410668 | HCN4 | c.1590+4G>A (n.1590+4G>A) c.372+4G>A (n.372+4G>A) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329571A>C | CA393093299 | HCN4 | c.1590+2T>G (n.1590+2T>G) c.372+2T>G (n.372+2T>G) | |
| 15 | g.73329571A>G | CA393093296 | HCN4 | c.1590+2T>C (n.1590+2T>C) c.372+2T>C (n.372+2T>C) | |
| 15 | g.73329571A>T | CA393093294 | HCN4 | c.1590+2T>A (n.1590+2T>A) c.372+2T>A (n.372+2T>A) | |
| 15 | g.73329572C>A | CA393093302 | HCN4 | c.1590+1G>T (n.1590+1G>T) c.372+1G>T (n.372+1G>T) | |
| 15 | g.73329572C>G | CA393093304 | HCN4 | c.1590+1G>C (n.1590+1G>C) c.372+1G>C (n.372+1G>C) | |
| 15 | g.73329572C>T | CA393093306 | HCN4 | c.1590+1G>A (n.1590+1G>A) c.372+1G>A (n.372+1G>A) | ClinVar |
| 15 | g.73329573C>A | CA393093309 | HCN4 | c.1590G>T (p.Lys530Asn) c.372G>T (p.Lys124Asn) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329573C= | CA2187167372 | HCN4 | c.1590G= (p.Lys530=) c.372G= (p.Lys124=) | |
| 15 | g.73329573C>G | CA393093311 | HCN4 | c.1590G>C (p.Lys530Asn) c.372G>C (p.Lys124Asn) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329573C>T | CA491151447 | HCN4 | c.1590G>A (p.Lys530=) c.372G>A (p.Lys124=) | |
| 15 | g.73329574T>A | CA393093314 | HCN4 | c.1589A>T (p.Lys530Met) c.371A>T (p.Lys124Met) | |
| 15 | g.73329574T>C | CA393093316 | HCN4 | c.1589A>G (p.Lys530Arg) c.371A>G (p.Lys124Arg) | |
| 15 | g.73329574T>G | CA393093317 | HCN4 | c.1589A>C (p.Lys530Thr) c.371A>C (p.Lys124Thr) | |
| 15 | g.73329575T>A | CA393093321 | HCN4 | c.1588A>T (p.Lys530Ter) c.370A>T (p.Lys124Ter) | |
| 15 | g.73329575T>C | CA393093322 | HCN4 | c.1588A>G (p.Lys530Glu) c.370A>G (p.Lys124Glu) | dbSNP gnomAD v4 |
| 15 | g.73329575T>G | CA393093324 | HCN4 | c.1588A>C (p.Lys530Gln) c.370A>C (p.Lys124Gln) | |
| 15 | g.73329575T= | CA2187167375 | HCN4 | c.1588A= (p.Lys530=) c.370A= (p.Lys124=) | |
| 15 | g.73329576T>A | CA393093326 | HCN4 | c.1587A>T (p.Glu529Asp) c.369A>T (p.Glu123Asp) | |
| 15 | g.73329576T>C | CA491151448 | HCN4 | c.1587A>G (p.Glu529=) c.369A>G (p.Glu123=) | |
| 15 | g.73329576T>G | CA393093328 | HCN4 | c.1587A>C (p.Glu529Asp) c.369A>C (p.Glu123Asp) | |
| 15 | g.73329577T>A | CA393093334 | HCN4 | c.1586A>T (p.Glu529Val) c.368A>T (p.Glu123Val) | |
| 15 | g.73329577T>C | CA393093330 | HCN4 | c.1586A>G (p.Glu529Gly) c.368A>G (p.Glu123Gly) | |
| 15 | g.73329577T>G | CA393093332 | HCN4 | c.1586A>C (p.Glu529Ala) c.368A>C (p.Glu123Ala) | |
| 15 | g.73329578C>A | CA393093336 | HCN4 | c.1585G>T (p.Glu529Ter) c.367G>T (p.Glu123Ter) | |
| 15 | g.73329578C>G | CA393093337 | HCN4 | c.1585G>C (p.Glu529Gln) c.367G>C (p.Glu123Gln) | |
| 15 | g.73329578C>T | CA393093339 | HCN4 | c.1585G>A (p.Glu529Lys) c.367G>A (p.Glu123Lys) | |
| 15 | g.73329579C>A | CA393093342 | HCN4 | c.1584G>T (p.Gln528His) c.366G>T (p.Gln122His) | |
| 15 | g.73329579C>G | CA393093345 | HCN4 | c.1584G>C (p.Gln528His) c.366G>C (p.Gln122His) | gnomAD v4 |
| 15 | g.73329579C>T | CA491151449 | HCN4 | c.1584G>A (p.Gln528=) c.366G>A (p.Gln122=) | |
| 15 | g.73329579_73329580delinsCT | CA2187167378 | HCN4 | c.1583_1584delinsAG (p.Gln528=) c.365_366delinsAG (p.Gln122=) | |
| 15 | g.73329580del | CA7649276 | HCN4 | c.1583del (p.Gln528ArgfsTer?) c.365del (p.Gln122ArgfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73329580T>A | CA393093347 | HCN4 | c.1583A>T (p.Gln528Leu) c.365A>T (p.Gln122Leu) | |
| 15 | g.73329580T>C | CA393093348 | HCN4 | c.1583A>G (p.Gln528Arg) c.365A>G (p.Gln122Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329580T>G | CA393093350 | HCN4 | c.1583A>C (p.Gln528Pro) c.365A>C (p.Gln122Pro) | |
| 15 | g.73329580T= | CA2187167381 | HCN4 | c.1583A= (p.Gln528=) c.365A= (p.Gln122=) | |
| 15 | g.73329581G>A | CA393093353 | HCN4 | c.1582C>T (p.Gln528Ter) c.364C>T (p.Gln122Ter) | |
| 15 | g.73329581G>C | CA393093355 | HCN4 | c.1582C>G (p.Gln528Glu) c.364C>G (p.Gln122Glu) | |
| 15 | g.73329581G>T | CA393093357 | HCN4 | c.1582C>A (p.Gln528Lys) c.364C>A (p.Gln122Lys) | |
| 15 | g.73329582G>A | CA7649277 | HCN4 | c.1581C>T (p.Tyr527=) c.363C>T (p.Tyr121=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73329582G>C | CA393093363 | HCN4 | c.1581C>G (p.Tyr527Ter) c.363C>G (p.Tyr121Ter) | |
| 15 | g.73329582G= | CA2187167384 | HCN4 | c.1581C= (p.Tyr527=) c.363C= (p.Tyr121=) | |
| 15 | g.73329582G>T | CA393093361 | HCN4 | c.1581C>A (p.Tyr527Ter) c.363C>A (p.Tyr121Ter) | |
| 15 | g.73329583T>A | CA393093365 | HCN4 | c.1580A>T (p.Tyr527Phe) c.362A>T (p.Tyr121Phe) | |
| 15 | g.73329583T>C | CA393093369 | HCN4 | c.1580A>G (p.Tyr527Cys) c.362A>G (p.Tyr121Cys) | |
| 15 | g.73329583T>G | CA393093367 | HCN4 | c.1580A>C (p.Tyr527Ser) c.362A>C (p.Tyr121Ser) | |
| 15 | g.73329584A= | CA2187167386 | HCN4 | c.1579T= (p.Tyr527=) c.361T= (p.Tyr121=) | |
| 15 | g.73329584A>C | CA393093371 | HCN4 | c.1579T>G (p.Tyr527Asp) c.361T>G (p.Tyr121Asp) | |
| 15 | g.73329584A>G | CA393093372 | HCN4 | c.1579T>C (p.Tyr527His) c.361T>C (p.Tyr121His) | dbSNP |
| 15 | g.73329584A>T | CA393093374 | HCN4 | c.1579T>A (p.Tyr527Asn) c.361T>A (p.Tyr121Asn) | |
| 15 | g.73329585C>A | CA393093376 | HCN4 | c.1578G>T (p.Gln526His) c.360G>T (p.Gln120His) | |
| 15 | g.73329585C>G | CA393093378 | HCN4 | c.1578G>C (p.Gln526His) c.360G>C (p.Gln120His) | |
| 15 | g.73329585C>T | CA491151450 | HCN4 | c.1578G>A (p.Gln526=) c.360G>A (p.Gln120=) | |
| 15 | g.73329586T>A | CA393093380 | HCN4 | c.1577A>T (p.Gln526Leu) c.359A>T (p.Gln120Leu) | |
| 15 | g.73329586T>C | CA393093382 | HCN4 | c.1577A>G (p.Gln526Arg) c.359A>G (p.Gln120Arg) | gnomAD v4 |
| 15 | g.73329586T>G | CA393093384 | HCN4 | c.1577A>C (p.Gln526Pro) c.359A>C (p.Gln120Pro) | |
| 15 | g.73329587G>A | CA393093386 | HCN4 | c.1576C>T (p.Gln526Ter) c.358C>T (p.Gln120Ter) | COSMIC |
| 15 | g.73329587G>C | CA393093388 | HCN4 | c.1576C>G (p.Gln526Glu) c.358C>G (p.Gln120Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329587G= | CA2187167389 | HCN4 | c.1576C= (p.Gln526=) c.358C= (p.Gln120=) | |
| 15 | g.73329587G>T | CA393093390 | HCN4 | c.1576C>A (p.Gln526Lys) c.358C>A (p.Gln120Lys) | |
| 15 | g.73329588G>A | CA491151451 | HCN4 | c.1575C>T (p.Arg525=) c.357C>T (p.Arg119=) | |
| 15 | g.73329588G>C | CA491151452 | HCN4 | c.1575C>G (p.Arg525=) c.357C>G (p.Arg119=) | |
| 15 | g.73329588G>T | CA491151453 | HCN4 | c.1575C>A (p.Arg525=) c.357C>A (p.Arg119=) | |
| 15 | g.73329589C>A | CA393093394 | HCN4 | c.1574G>T (p.Arg525Leu) c.356G>T (p.Arg119Leu) | |
| 15 | g.73329589C= | CA2187167392 | HCN4 | c.1574G= (p.Arg525=) c.356G= (p.Arg119=) | |
| 15 | g.73329589C>G | CA393093392 | HCN4 | c.1574G>C (p.Arg525Pro) c.356G>C (p.Arg119Pro) | |
| 15 | g.73329589C>T | CA7649278 | HCN4 | c.1574G>A (p.Arg525His) c.356G>A (p.Arg119His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73329590G>A | CA393093397 | HCN4 | c.1573C>T (p.Arg525Cys) c.355C>T (p.Arg119Cys) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 15 | g.73329590G>C | CA393093399 | HCN4 | c.1573C>G (p.Arg525Gly) c.355C>G (p.Arg119Gly) | |
| 15 | g.73329590G= | CA2187167395 | HCN4 | c.1573C= (p.Arg525=) c.355C= (p.Arg119=) | |
| 15 | g.73329590G>T | CA393093401 | HCN4 | c.1573C>A (p.Arg525Ser) c.355C>A (p.Arg119Ser) | dbSNP gnomAD v2 |
| 15 | g.73329591C>A | CA491151454 | HCN4 | c.1572G>T (p.Arg524=) c.354G>T (p.Arg118=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329591C>G | CA491151455 | HCN4 | c.1572G>C (p.Arg524=) c.354G>C (p.Arg118=) | |
| 15 | g.73329591C>T | CA491151456 | HCN4 | c.1572G>A (p.Arg524=) c.354G>A (p.Arg118=) | |
| 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=) | |
| 15 | g.73329606G= | CA2187167428 | HCN4 | c.1557C= (p.Ser519=) c.339C= (p.Ser113=) | |
| 15 | g.73329606G>T | CA491151467 | HCN4 | c.1557C>A (p.Ser519=) c.339C>A (p.Ser113=) | |
| 15 | g.73329607G>A | CA393093466 | HCN4 | c.1556C>T (p.Ser519Phe) c.338C>T (p.Ser113Phe) | |
| 15 | g.73329607G>C | CA393093467 | HCN4 | c.1556C>G (p.Ser519Cys) c.338C>G (p.Ser113Cys) | COSMIC |
| 15 | g.73329607G>T | CA393093469 | HCN4 | c.1556C>A (p.Ser519Tyr) c.338C>A (p.Ser113Tyr) | |
| 15 | g.73329608A>C | CA393093472 | HCN4 | c.1555T>G (p.Ser519Ala) c.337T>G (p.Ser113Ala) | |
| 15 | g.73329608A>G | CA393093473 | HCN4 | c.1555T>C (p.Ser519Pro) c.337T>C (p.Ser113Pro) | |
| 15 | g.73329608A>T | CA393093475 | HCN4 | c.1555T>A (p.Ser519Thr) c.337T>A (p.Ser113Thr) | |
| 15 | g.73329609C>A | CA393093477 | HCN4 | c.1554G>T (p.Gln518His) c.336G>T (p.Gln112His) | |
| 15 | g.73329609C>G | CA393093479 | HCN4 | c.1554G>C (p.Gln518His) c.336G>C (p.Gln112His) | |
| 15 | g.73329609C>T | CA491151468 | HCN4 | c.1554G>A (p.Gln518=) c.336G>A (p.Gln112=) | |
| 15 | g.73329610T>A | CA393093484 | HCN4 | c.1553A>T (p.Gln518Leu) c.335A>T (p.Gln112Leu) | |
| 15 | g.73329610T>C | CA393093486 | HCN4 | c.1553A>G (p.Gln518Arg) c.335A>G (p.Gln112Arg) | gnomAD v4 |
| 15 | g.73329610T>G | CA393093482 | HCN4 | c.1553A>C (p.Gln518Pro) c.335A>C (p.Gln112Pro) | |
| 15 | g.73329611G>A | CA393093489 | HCN4 | c.1552C>T (p.Gln518Ter) c.334C>T (p.Gln112Ter) | |
| 15 | g.73329611G>C | CA393093492 | HCN4 | c.1552C>G (p.Gln518Glu) c.334C>G (p.Gln112Glu) | |
| 15 | g.73329611G>T | CA393093491 | HCN4 | c.1552C>A (p.Gln518Lys) c.334C>A (p.Gln112Lys) | |
| 15 | g.73329612G>A | CA491151469 | HCN4 | c.1551C>T (p.Ile517=) c.333C>T (p.Ile111=) | ClinVar |
| 15 | g.73329612G>C | CA393093495 | HCN4 | c.1551C>G (p.Ile517Met) c.333C>G (p.Ile111Met) | |
| 15 | g.73329612G>T | CA491151470 | HCN4 | c.1551C>A (p.Ile517=) c.333C>A (p.Ile111=) | |
| 15 | g.73329613A>C | CA393093498 | HCN4 | c.1550T>G (p.Ile517Ser) c.332T>G (p.Ile111Ser) | |
| 15 | g.73329613A>G | CA393093500 | HCN4 | c.1550T>C (p.Ile517Thr) c.332T>C (p.Ile111Thr) | |
| 15 | g.73329613A>T | CA393093501 | HCN4 | c.1550T>A (p.Ile517Asn) c.332T>A (p.Ile111Asn) | |
| 15 | g.73329614T>A | CA393093503 | HCN4 | c.1549A>T (p.Ile517Phe) c.331A>T (p.Ile111Phe) | |
| 15 | g.73329614T>C | CA393093505 | HCN4 | c.1549A>G (p.Ile517Val) c.331A>G (p.Ile111Val) | dbSNP gnomAD v4 |
| 15 | g.73329614T>G | CA393093506 | HCN4 | c.1549A>C (p.Ile517Leu) c.331A>C (p.Ile111Leu) | |
| 15 | g.73329614T= | CA2187167432 | HCN4 | c.1549A= (p.Ile517=) c.331A= (p.Ile111=) | |
| 15 | g.73329615G>A | CA16614561 | HCN4 | c.1548C>T (p.Leu516=) c.330C>T (p.Leu110=) | ClinVar dbSNP |
| 15 | g.73329615G>C | CA491151472 | HCN4 | c.1548C>G (p.Leu516=) c.330C>G (p.Leu110=) | |
| 15 | g.73329615G= | CA2187167435 | HCN4 | c.1548C= (p.Leu516=) c.330C= (p.Leu110=) | |
| 15 | g.73329615G>T | CA491151471 | HCN4 | c.1548C>A (p.Leu516=) c.330C>A (p.Leu110=) | |
| 15 | g.73329616A>C | CA393093509 | HCN4 | c.1547T>G (p.Leu516Arg) c.329T>G (p.Leu110Arg) | |
| 15 | g.73329616A>G | CA393093510 | HCN4 | c.1547T>C (p.Leu516Pro) c.329T>C (p.Leu110Pro) | |
| 15 | g.73329616A>T | CA393093512 | HCN4 | c.1547T>A (p.Leu516His) c.329T>A (p.Leu110His) | |
| 15 | g.73329617G>A | CA393093514 | HCN4 | c.1546C>T (p.Leu516Phe) c.328C>T (p.Leu110Phe) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329617G>C | CA393093516 | HCN4 | c.1546C>G (p.Leu516Val) c.328C>G (p.Leu110Val) | |
| 15 | g.73329617G= | CA2187167439 | HCN4 | c.1546C= (p.Leu516=) c.328C= (p.Leu110=) | |
| 15 | g.73329617G>T | CA393093518 | HCN4 | c.1546C>A (p.Leu516Ile) c.328C>A (p.Leu110Ile) | |
| 15 | g.73329618G>A | CA491151473 | HCN4 | c.1545C>T (p.Ala515=) c.327C>T (p.Ala109=) | |
| 15 | g.73329618G>C | CA491151474 | HCN4 | c.1545C>G (p.Ala515=) c.327C>G (p.Ala109=) | dbSNP |
| 15 | g.73329618G= | CA2187167443 | HCN4 | c.1545C= (p.Ala515=) c.327C= (p.Ala109=) | |
| 15 | g.73329618G>T | CA491151475 | HCN4 | c.1545C>A (p.Ala515=) c.327C>A (p.Ala109=) | |
| 15 | g.73329619G>A | CA393093521 | HCN4 | c.1544C>T (p.Ala515Val) c.326C>T (p.Ala109Val) | |
| 15 | g.73329619G>C | CA393093524 | HCN4 | c.1544C>G (p.Ala515Gly) c.326C>G (p.Ala109Gly) | |
| 15 | g.73329619G>T | CA393093522 | HCN4 | c.1544C>A (p.Ala515Asp) c.326C>A (p.Ala109Asp) | |
| 15 | g.73329620C>A | CA393093527 | HCN4 | c.1543G>T (p.Ala515Ser) c.325G>T (p.Ala109Ser) | |
| 15 | g.73329620C>G | CA393093529 | HCN4 | c.1543G>C (p.Ala515Pro) c.325G>C (p.Ala109Pro) | |
| 15 | g.73329620C>T | CA393093531 | HCN4 | c.1543G>A (p.Ala515Thr) c.325G>A (p.Ala109Thr) | |
| 15 | g.73329621A>C | CA491151476 | HCN4 | c.1542T>G (p.Thr514=) c.324T>G (p.Thr108=) | |
| 15 | g.73329621A>G | CA491151478 | HCN4 | c.1542T>C (p.Thr514=) c.324T>C (p.Thr108=) | |
| 15 | g.73329621A>T | CA491151477 | HCN4 | c.1542T>A (p.Thr514=) c.324T>A (p.Thr108=) | |
| 15 | g.73329622G>A | CA393093533 | HCN4 | c.1541C>T (p.Thr514Ile) c.323C>T (p.Thr108Ile) | |
| 15 | g.73329622G>C | CA393093534 | HCN4 | c.1541C>G (p.Thr514Ser) c.323C>G (p.Thr108Ser) | |
| 15 | g.73329622G>T | CA393093536 | HCN4 | c.1541C>A (p.Thr514Asn) c.323C>A (p.Thr108Asn) | |
| 15 | g.73329623T>A | CA393093538 | HCN4 | c.1540A>T (p.Thr514Ser) c.322A>T (p.Thr108Ser) | |
| 15 | g.73329623T>C | CA393093541 | HCN4 | c.1540A>G (p.Thr514Ala) c.322A>G (p.Thr108Ala) | COSMIC |
| 15 | g.73329623T>G | CA393093543 | HCN4 | c.1540A>C (p.Thr514Pro) c.322A>C (p.Thr108Pro) | |
| 15 | g.73329624G>A | CA491151479 | HCN4 | c.1539C>T (p.Ala513=) c.321C>T (p.Ala107=) | |
| 15 | g.73329624G>C | CA491151480 | HCN4 | c.1539C>G (p.Ala513=) c.321C>G (p.Ala107=) | |
| 15 | g.73329624G>T | CA491151481 | HCN4 | c.1539C>A (p.Ala513=) c.321C>A (p.Ala107=) | |
| 15 | g.73329625G>A | CA393093549 | HCN4 | c.1538C>T (p.Ala513Val) c.320C>T (p.Ala107Val) | |
| 15 | g.73329625G>C | CA393093547 | HCN4 | c.1538C>G (p.Ala513Gly) c.320C>G (p.Ala107Gly) | |
| 15 | g.73329625G>T | CA393093545 | HCN4 | c.1538C>A (p.Ala513Asp) c.320C>A (p.Ala107Asp) | |
| 15 | g.73329626C>A | CA393093552 | HCN4 | c.1537G>T (p.Ala513Ser) c.319G>T (p.Ala107Ser) | |
| 15 | g.73329626C= | CA2187167446 | HCN4 | c.1537G= (p.Ala513=) c.319G= (p.Ala107=) | |
| 15 | g.73329626C>G | CA393093553 | HCN4 | c.1537G>C (p.Ala513Pro) c.319G>C (p.Ala107Pro) | |
| 15 | g.73329626C>T | CA393093555 | HCN4 | c.1537G>A (p.Ala513Thr) c.319G>A (p.Ala107Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329627G>A | CA7649283 | HCN4 | c.1536C>T (p.His512=) c.318C>T (p.His106=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73329627G>C | CA393093558 | HCN4 | c.1536C>G (p.His512Gln) c.318C>G (p.His106Gln) | |
| 15 | g.73329627G= | CA2187167452 | HCN4 | c.1536C= (p.His512=) c.318C= (p.His106=) | |
| 15 | g.73329627G>T | CA393093560 | HCN4 | c.1536C>A (p.His512Gln) c.318C>A (p.His106Gln) | |
| 15 | g.73329628T>A | CA393093562 | HCN4 | c.1535A>T (p.His512Leu) c.317A>T (p.His106Leu) | |
| 15 | g.73329628T>C | CA393093564 | HCN4 | c.1535A>G (p.His512Arg) c.317A>G (p.His106Arg) | |
| 15 | g.73329628T>G | CA393093566 | HCN4 | c.1535A>C (p.His512Pro) c.317A>C (p.His106Pro) | |
| 15 | g.73329629G>A | CA393093568 | HCN4 | c.1534C>T (p.His512Tyr) c.316C>T (p.His106Tyr) | |
| 15 | g.73329629G>C | CA393093570 | HCN4 | c.1534C>G (p.His512Asp) c.316C>G (p.His106Asp) | |
| 15 | g.73329629G>T | CA393093572 | HCN4 | c.1534C>A (p.His512Asn) c.316C>A (p.His106Asn) | |
| 15 | g.73329630G>A | CA491151484 | HCN4 | c.1533C>T (p.Gly511=) c.315C>T (p.Gly105=) | gnomAD v4 |
| 15 | g.73329630G>C | CA491151482 | HCN4 | c.1533C>G (p.Gly511=) c.315C>G (p.Gly105=) | |
| 15 | g.73329630G>T | CA491151483 | HCN4 | c.1533C>A (p.Gly511=) c.315C>A (p.Gly105=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329631C>A | CA393093579 | HCN4 | c.1532G>T (p.Gly511Val) c.314G>T (p.Gly105Val) | |
| 15 | g.73329631C>G | CA393093576 | HCN4 | c.1532G>C (p.Gly511Ala) c.314G>C (p.Gly105Ala) | gnomAD v4 |
| 15 | g.73329631C>T | CA393093574 | HCN4 | c.1532G>A (p.Gly511Asp) c.314G>A (p.Gly105Asp) | |
| 15 | g.73329632C>A | CA393093581 | HCN4 | c.1531G>T (p.Gly511Cys) c.313G>T (p.Gly105Cys) | |
| 15 | g.73329632C>G | CA393093582 | HCN4 | c.1531G>C (p.Gly511Arg) c.313G>C (p.Gly105Arg) | |
| 15 | g.73329632C>T | CA393093584 | HCN4 | c.1531G>A (p.Gly511Ser) c.313G>A (p.Gly105Ser) | |
| 15 | g.73329633A>C | CA393093586 | HCN4 | c.1530T>G (p.Ile510Met) c.312T>G (p.Ile104Met) | |
| 15 | g.73329633A>G | CA491151485 | HCN4 | c.1530T>C (p.Ile510=) c.312T>C (p.Ile104=) | |
| 15 | g.73329633A>T | CA491151486 | HCN4 | c.1530T>A (p.Ile510=) c.312T>A (p.Ile104=) | |
| 15 | g.73329634A>C | CA393093589 | HCN4 | c.1529T>G (p.Ile510Ser) c.311T>G (p.Ile104Ser) | |
| 15 | g.73329634A>G | CA393093591 | HCN4 | c.1529T>C (p.Ile510Thr) c.311T>C (p.Ile104Thr) | |
| 15 | g.73329634A>T | CA393093593 | HCN4 | c.1529T>A (p.Ile510Asn) c.311T>A (p.Ile104Asn) | |
| 15 | g.73329635T>A | CA393093596 | HCN4 | c.1528A>T (p.Ile510Phe) c.310A>T (p.Ile104Phe) | |
| 15 | g.73329635T>C | CA393093598 | HCN4 | c.1528A>G (p.Ile510Val) c.310A>G (p.Ile104Val) | |
| 15 | g.73329635T>G | CA393093600 | HCN4 | c.1528A>C (p.Ile510Leu) c.310A>C (p.Ile104Leu) | |
| 15 | g.73329636G>A | CA491151487 | HCN4 | c.1527C>T (p.Phe509=) c.309C>T (p.Phe103=) | |
| 15 | g.73329636G>C | CA393093602 | HCN4 | c.1527C>G (p.Phe509Leu) c.309C>G (p.Phe103Leu) | |
| 15 | g.73329636G>T | CA393093604 | HCN4 | c.1527C>A (p.Phe509Leu) c.309C>A (p.Phe103Leu) | |
| 15 | g.73329637A>C | CA393093606 | HCN4 | c.1526T>G (p.Phe509Cys) c.308T>G (p.Phe103Cys) | |
| 15 | g.73329637A>G | CA393093610 | HCN4 | c.1526T>C (p.Phe509Ser) c.308T>C (p.Phe103Ser) | |
| 15 | g.73329637A>T | CA393093608 | HCN4 | c.1526T>A (p.Phe509Tyr) c.308T>A (p.Phe103Tyr) | |
| 15 | g.73329638A>C | CA393093612 | HCN4 | c.1525T>G (p.Phe509Val) c.307T>G (p.Phe103Val) | |
| 15 | g.73329638A>G | CA393093615 | HCN4 | c.1525T>C (p.Phe509Leu) c.307T>C (p.Phe103Leu) | gnomAD v4 |
| 15 | g.73329638A>T | CA393093613 | HCN4 | c.1525T>A (p.Phe509Ile) c.307T>A (p.Phe103Ile) | |
| 15 | g.73329639C>A | CA393093618 | HCN4 | c.1524G>T (p.Met508Ile) c.306G>T (p.Met102Ile) | |
| 15 | g.73329639C>G | CA393093622 | HCN4 | c.1524G>C (p.Met508Ile) c.306G>C (p.Met102Ile) | |
| 15 | g.73329639C>T | CA393093619 | HCN4 | c.1524G>A (p.Met508Ile) c.306G>A (p.Met102Ile) | |
| 15 | g.73329640A>C | CA393093623 | HCN4 | c.1523T>G (p.Met508Arg) c.305T>G (p.Met102Arg) | |
| 15 | g.73329640A>G | CA393093625 | HCN4 | c.1523T>C (p.Met508Thr) c.305T>C (p.Met102Thr) | gnomAD v4 |
| 15 | g.73329640A>T | CA393093627 | HCN4 | c.1523T>A (p.Met508Lys) c.305T>A (p.Met102Lys) | |
| 15 | g.73329641T>A | CA393093630 | HCN4 | c.1522A>T (p.Met508Leu) c.304A>T (p.Met102Leu) | |
| 15 | g.73329641T>C | CA272672022 | HCN4 | c.1522A>G (p.Met508Val) c.304A>G (p.Met102Val) | ClinVar dbSNP |
| 15 | g.73329641T>G | CA393093633 | HCN4 | c.1522A>C (p.Met508Leu) c.304A>C (p.Met102Leu) | |
| 15 | g.73329641T= | CA2187167457 | HCN4 | c.1522A= (p.Met508=) c.304A= (p.Met102=) | |
| 15 | g.73329641dup | CA2695220988 | HCN4 | c.1522dup (p.Met508AsnfsTer?) c.304dup (p.Met102AsnfsTer?) | |
| 15 | g.73329642G>A | CA272672032 | HCN4 | c.1521C>T (p.Ala507=) c.303C>T (p.Ala101=) | ClinVar dbSNP |
| 15 | g.73329642G>C | CA491151488 | HCN4 | c.1521C>G (p.Ala507=) c.303C>G (p.Ala101=) | |
| 15 | g.73329642G= | CA2187167461 | HCN4 | c.1521C= (p.Ala507=) c.303C= (p.Ala101=) | |
| 15 | g.73329642G>T | CA491151489 | HCN4 | c.1521C>A (p.Ala507=) c.303C>A (p.Ala101=) | |
| 15 | g.73329643G>A | CA393093636 | HCN4 | c.1520C>T (p.Ala507Val) c.302C>T (p.Ala101Val) | |
| 15 | g.73329643G>C | CA393093638 | HCN4 | c.1520C>G (p.Ala507Gly) c.302C>G (p.Ala101Gly) | |
| 15 | g.73329643G>T | CA393093639 | HCN4 | c.1520C>A (p.Ala507Asp) c.302C>A (p.Ala101Asp) | |
| 15 | g.73329644C>A | CA393093642 | HCN4 | c.1519G>T (p.Ala507Ser) c.301G>T (p.Ala101Ser) | COSMIC |
| 15 | g.73329644C= | CA2187167464 | HCN4 | c.1519G= (p.Ala507=) c.301G= (p.Ala101=) | |
| 15 | g.73329644C>G | CA393093644 | HCN4 | c.1519G>C (p.Ala507Pro) c.301G>C (p.Ala101Pro) | |
| 15 | g.73329644C>T | CA393093645 | HCN4 | c.1519G>A (p.Ala507Thr) c.301G>A (p.Ala101Thr) | dbSNP gnomAD v4 |
| 15 | g.73329645G>A | CA202780 | HCN4 | c.1518C>T (p.Tyr506=) c.300C>T (p.Tyr100=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329645G>C | CA393093651 | HCN4 | c.1518C>G (p.Tyr506Ter) c.300C>G (p.Tyr100Ter) | |
| 15 | g.73329645G= | CA2187167471 | HCN4 | c.1518C= (p.Tyr506=) c.300C= (p.Tyr100=) | |
| 15 | g.73329645G>T | CA393093650 | HCN4 | c.1518C>A (p.Tyr506Ter) c.300C>A (p.Tyr100Ter) | |
| 15 | g.73329646T>A | CA393093653 | HCN4 | c.1517A>T (p.Tyr506Phe) c.299A>T (p.Tyr100Phe) | |
| 15 | g.73329646T>C | CA393093655 | HCN4 | c.1517A>G (p.Tyr506Cys) c.299A>G (p.Tyr100Cys) | |
| 15 | g.73329646T>G | CA393093657 | HCN4 | c.1517A>C (p.Tyr506Ser) c.299A>C (p.Tyr100Ser) | |
| 15 | g.73329647A>C | CA393093659 | HCN4 | c.1516T>G (p.Tyr506Asp) c.298T>G (p.Tyr100Asp) | |
| 15 | g.73329647A>G | CA393093661 | HCN4 | c.1516T>C (p.Tyr506His) c.298T>C (p.Tyr100His) | |
| 15 | g.73329647A>T | CA393093663 | HCN4 | c.1516T>A (p.Tyr506Asn) c.298T>A (p.Tyr100Asn) | |
| 15 | g.73329648G>A | CA491151490 | HCN4 | c.1515C>T (p.Cys505=) c.297C>T (p.Cys99=) | |
| 15 | g.73329648G>C | CA393093665 | HCN4 | c.1515C>G (p.Cys505Trp) c.297C>G (p.Cys99Trp) | |
| 15 | g.73329648G>T | CA393093667 | HCN4 | c.1515C>A (p.Cys505Ter) c.297C>A (p.Cys99Ter) | |
| 15 | g.73329649C>A | CA393093670 | HCN4 | c.1514G>T (p.Cys505Phe) c.296G>T (p.Cys99Phe) | gnomAD v4 |
| 15 | g.73329649C>G | CA393093672 | HCN4 | c.1514G>C (p.Cys505Ser) c.296G>C (p.Cys99Ser) | |
| 15 | g.73329649C>T | CA393093674 | HCN4 | c.1514G>A (p.Cys505Tyr) c.296G>A (p.Cys99Tyr) | ClinVar |
| 15 | g.73329650A>C | CA393093680 | HCN4 | c.1513T>G (p.Cys505Gly) c.295T>G (p.Cys99Gly) | |
| 15 | g.73329650A>G | CA393093678 | HCN4 | c.1513T>C (p.Cys505Arg) c.295T>C (p.Cys99Arg) | |
| 15 | g.73329650A>T | CA393093675 | HCN4 | c.1513T>A (p.Cys505Ser) c.295T>A (p.Cys99Ser) | |
| 15 | g.73329651G>A | CA7649284 | HCN4 | c.1512C>T (p.Thr504=) c.294C>T (p.Thr98=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329651G>C | CA491151494 | HCN4 | c.1512C>G (p.Thr504=) c.294C>G (p.Thr98=) | |
| 15 | g.73329651G= | CA2187167473 | HCN4 | c.1512C= (p.Thr504=) c.294C= (p.Thr98=) | |
| 15 | g.73329651G>T | CA491151496 | HCN4 | c.1512C>A (p.Thr504=) c.294C>A (p.Thr98=) | |
| 15 | g.73329652G>A | CA393093682 | HCN4 | c.1511C>T (p.Thr504Ile) c.293C>T (p.Thr98Ile) | |
| 15 | g.73329652G>C | CA393093684 | HCN4 | c.1511C>G (p.Thr504Ser) c.293C>G (p.Thr98Ser) | |
| 15 | g.73329652G= | CA2187167477 | HCN4 | c.1511C= (p.Thr504=) c.293C= (p.Thr98=) | |
| 15 | g.73329652G>T | CA393093686 | HCN4 | c.1511C>A (p.Thr504Asn) c.293C>A (p.Thr98Asn) | ClinVar dbSNP |
| 15 | g.73329653T>A | CA393093689 | HCN4 | c.1510A>T (p.Thr504Ser) c.292A>T (p.Thr98Ser) | |
| 15 | g.73329653T>C | CA393093690 | HCN4 | c.1510A>G (p.Thr504Ala) c.292A>G (p.Thr98Ala) | |
| 15 | g.73329653T>G | CA393093692 | HCN4 | c.1510A>C (p.Thr504Pro) c.292A>C (p.Thr98Pro) | dbSNP |
| 15 | g.73329653T= | CA2187167481 | HCN4 | c.1510A= (p.Thr504=) c.292A= (p.Thr98=) | |
| 15 | g.73329654G>A | CA16614505 | HCN4 | c.1509C>T (p.Ala503=) c.291C>T (p.Ala97=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329654G>C | CA491151506 | HCN4 | c.1509C>G (p.Ala503=) c.291C>G (p.Ala97=) | |
| 15 | g.73329654G= | CA2187167486 | HCN4 | c.1509C= (p.Ala503=) c.291C= (p.Ala97=) | |
| 15 | g.73329654G>T | CA491151508 | HCN4 | c.1509C>A (p.Ala503=) c.291C>A (p.Ala97=) | |
| 15 | g.73329655G>A | CA393093695 | HCN4 | c.1508C>T (p.Ala503Val) c.290C>T (p.Ala97Val) | gnomAD v4 |
| 15 | g.73329655G>C | CA393093698 | HCN4 | c.1508C>G (p.Ala503Gly) c.290C>G (p.Ala97Gly) | |
| 15 | g.73329655G>T | CA393093699 | HCN4 | c.1508C>A (p.Ala503Asp) c.290C>A (p.Ala97Asp) | |
| 15 | g.73329656C>A | CA393093700 | HCN4 | c.1507G>T (p.Ala503Ser) c.289G>T (p.Ala97Ser) | |
| 15 | g.73329656C>G | CA393093702 | HCN4 | c.1507G>C (p.Ala503Pro) c.289G>C (p.Ala97Pro) | |
| 15 | g.73329656C>T | CA393093704 | HCN4 | c.1507G>A (p.Ala503Thr) c.289G>A (p.Ala97Thr) | |
| 15 | g.73329657A>C | CA491151517 | HCN4 | c.1506T>G (p.Gly502=) c.288T>G (p.Gly96=) | |
| 15 | g.73329657A>G | CA491151516 | HCN4 | c.1506T>C (p.Gly502=) c.288T>C (p.Gly96=) | |
| 15 | g.73329657A>T | CA491151519 | HCN4 | c.1506T>A (p.Gly502=) c.288T>A (p.Gly96=) | |
| 15 | g.73329658C>A | CA393093709 | HCN4 | c.1505G>T (p.Gly502Val) c.287G>T (p.Gly96Val) | |
| 15 | g.73329658C>G | CA393093710 | HCN4 | c.1505G>C (p.Gly502Ala) c.287G>C (p.Gly96Ala) | |
| 15 | g.73329658C>T | CA393093707 | HCN4 | c.1505G>A (p.Gly502Asp) c.287G>A (p.Gly96Asp) | |
| 15 | g.73329659C>A | CA393093713 | HCN4 | c.1504G>T (p.Gly502Cys) c.286G>T (p.Gly96Cys) | |
| 15 | g.73329659C>G | CA393093714 | HCN4 | c.1504G>C (p.Gly502Arg) c.286G>C (p.Gly96Arg) | |
| 15 | g.73329659C>T | CA393093716 | HCN4 | c.1504G>A (p.Gly502Ser) c.286G>A (p.Gly96Ser) | |
| 15 | g.73329660C>A | CA491151527 | HCN4 | c.1503G>T (p.Val501=) c.285G>T (p.Val95=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329660C= | CA2187167492 | HCN4 | c.1503G= (p.Val501=) c.285G= (p.Val95=) | |
| 15 | g.73329660C>G | CA491151529 | HCN4 | c.1503G>C (p.Val501=) c.285G>C (p.Val95=) | |
| 15 | g.73329660C>T | CA491151531 | HCN4 | c.1503G>A (p.Val501=) c.285G>A (p.Val95=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329661A>C | CA393093718 | HCN4 | c.1502T>G (p.Val501Gly) c.284T>G (p.Val95Gly) | |
| 15 | g.73329661A>G | CA393093719 | HCN4 | c.1502T>C (p.Val501Ala) c.284T>C (p.Val95Ala) | |
| 15 | g.73329661A>T | CA393093721 | HCN4 | c.1502T>A (p.Val501Glu) c.284T>A (p.Val95Glu) | |
| 15 | g.73329662C>A | CA393093723 | HCN4 | c.1501G>T (p.Val501Leu) c.283G>T (p.Val95Leu) | |
| 15 | g.73329662C>G | CA393093726 | HCN4 | c.1501G>C (p.Val501Leu) c.283G>C (p.Val95Leu) | |
| 15 | g.73329662C>T | CA393093725 | HCN4 | c.1501G>A (p.Val501Met) c.283G>A (p.Val95Met) | COSMIC |
| 15 | g.73329663G>A | CA7649285 | HCN4 | c.1500C>T (p.Ile500=) c.282C>T (p.Ile94=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73329663G>C | CA393093729 | HCN4 | c.1500C>G (p.Ile500Met) c.282C>G (p.Ile94Met) | |
| 15 | g.73329663G= | CA2187167495 | HCN4 | c.1500C= (p.Ile500=) c.282C= (p.Ile94=) | |
| 15 | g.73329663G>T | CA491151543 | HCN4 | c.1500C>A (p.Ile500=) c.282C>A (p.Ile94=) | |
| 15 | g.73329664A>C | CA393093731 | HCN4 | c.1499T>G (p.Ile500Ser) c.281T>G (p.Ile94Ser) | |
| 15 | g.73329664A>G | CA393093732 | HCN4 | c.1499T>C (p.Ile500Thr) c.281T>C (p.Ile94Thr) | |
| 15 | g.73329664A>T | CA393093735 | HCN4 | c.1499T>A (p.Ile500Asn) c.281T>A (p.Ile94Asn) | |
| 15 | g.73329665T>A | CA393093738 | HCN4 | c.1498A>T (p.Ile500Phe) c.280A>T (p.Ile94Phe) | |
| 15 | g.73329665T>C | CA393093739 | HCN4 | c.1498A>G (p.Ile500Val) c.280A>G (p.Ile94Val) | |
| 15 | g.73329665T>G | CA393093737 | HCN4 | c.1498A>C (p.Ile500Leu) c.280A>C (p.Ile94Leu) | |
| 15 | g.73329666C>A | CA393093740 | HCN4 | c.1497G>T (p.Met499Ile) c.279G>T (p.Met93Ile) | |
| 15 | g.73329666C>G | CA393093742 | HCN4 | c.1497G>C (p.Met499Ile) c.279G>C (p.Met93Ile) | |
| 15 | g.73329666C>T | CA393093741 | HCN4 | c.1497G>A (p.Met499Ile) c.279G>A (p.Met93Ile) |