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.73323474T>A | CA7648987 | HCN4 | c.2619A>T (p.Pro873=) c.1401A>T (p.Pro467=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323474T>C | CA272664527 | HCN4 | c.2619A>G (p.Pro873=) c.1401A>G (p.Pro467=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323474T>G | CA491478725 | HCN4 | c.2619A>C (p.Pro873=) c.1401A>C (p.Pro467=) | dbSNP |
| 15 | g.73323474T= | CA2187188368 | HCN4 | c.2619A= (p.Pro873=) c.1401A= (p.Pro467=) | |
| 15 | g.73323475G>A | CA393088539 | HCN4 | c.2618C>T (p.Pro873Leu) c.1400C>T (p.Pro467Leu) | gnomAD v4 COSMIC |
| 15 | g.73323475G>C | CA393088540 | HCN4 | c.2618C>G (p.Pro873Arg) c.1400C>G (p.Pro467Arg) | |
| 15 | g.73323475G>T | CA393088538 | HCN4 | c.2618C>A (p.Pro873Gln) c.1400C>A (p.Pro467Gln) | |
| 15 | g.73323476G>A | CA393088541 | HCN4 | c.2617C>T (p.Pro873Ser) c.1399C>T (p.Pro467Ser) | |
| 15 | g.73323476G>C | CA393088542 | HCN4 | c.2617C>G (p.Pro873Ala) c.1399C>G (p.Pro467Ala) | COSMIC |
| 15 | g.73323476G>T | CA393088543 | HCN4 | c.2617C>A (p.Pro873Thr) c.1399C>A (p.Pro467Thr) | gnomAD v4 |
| 15 | g.73323477G>A | CA491478729 | HCN4 | c.2616C>T (p.Ser872=) c.1398C>T (p.Ser466=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323477G>C | CA7648988 | HCN4 | c.2616C>G (p.Ser872Arg) c.1398C>G (p.Ser466Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323477G= | CA2187188375 | HCN4 | c.2616C= (p.Ser872=) c.1398C= (p.Ser466=) | |
| 15 | g.73323477G>T | CA393088544 | HCN4 | c.2616C>A (p.Ser872Arg) c.1398C>A (p.Ser466Arg) | gnomAD v4 |
| 15 | g.73323478C>A | CA393088545 | HCN4 | c.2615G>T (p.Ser872Ile) c.1397G>T (p.Ser466Ile) | |
| 15 | g.73323478C= | CA2187188383 | HCN4 | c.2615G= (p.Ser872=) c.1397G= (p.Ser466=) | |
| 15 | g.73323478C>G | CA393088546 | HCN4 | c.2615G>C (p.Ser872Thr) c.1397G>C (p.Ser466Thr) | |
| 15 | g.73323478C>T | CA393088547 | HCN4 | c.2615G>A (p.Ser872Asn) c.1397G>A (p.Ser466Asn) | ClinVar dbSNP COSMIC |
| 15 | g.73323479T>A | CA393088548 | HCN4 | c.2614A>T (p.Ser872Cys) c.1396A>T (p.Ser466Cys) | |
| 15 | g.73323479T>C | CA393088549 | HCN4 | c.2614A>G (p.Ser872Gly) c.1396A>G (p.Ser466Gly) | |
| 15 | g.73323479T>G | CA393088550 | HCN4 | c.2614A>C (p.Ser872Arg) c.1396A>C (p.Ser466Arg) | |
| 15 | g.73323480C>A | CA491478735 | HCN4 | c.2613G>T (p.Leu871=) c.1395G>T (p.Leu465=) | gnomAD v4 |
| 15 | g.73323480C= | CA2187188386 | HCN4 | c.2613G= (p.Leu871=) c.1395G= (p.Leu465=) | |
| 15 | g.73323480C>G | CA491478737 | HCN4 | c.2613G>C (p.Leu871=) c.1395G>C (p.Leu465=) | |
| 15 | g.73323480C>T | CA491478739 | HCN4 | c.2613G>A (p.Leu871=) c.1395G>A (p.Leu465=) | |
| 15 | g.73323481A>C | CA393088553 | HCN4 | c.2612T>G (p.Leu871Arg) c.1394T>G (p.Leu465Arg) | |
| 15 | g.73323481A>G | CA393088552 | HCN4 | c.2612T>C (p.Leu871Pro) c.1394T>C (p.Leu465Pro) | |
| 15 | g.73323481A>T | CA393088551 | HCN4 | c.2612T>A (p.Leu871Gln) c.1394T>A (p.Leu465Gln) | |
| 15 | g.73323482_73323499dup | CA7648989 | HCN4 | c.2595_2612dup (p.Leu871_Ser872insSerAlaProAlaGlyLeu) c.1377_1394dup (p.Leu465_Ser466insSerAlaProAlaGlyLeu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323482G>A | CA491478741 | HCN4 | c.2611C>T (p.Leu871=) c.1393C>T (p.Leu465=) | COSMIC |
| 15 | g.73323482G>C | CA393088554 | HCN4 | c.2611C>G (p.Leu871Val) c.1393C>G (p.Leu465Val) | |
| 15 | g.73323482G= | CA2187188390 | HCN4 | c.2611C= (p.Leu871=) c.1393C= (p.Leu465=) | |
| 15 | g.73323482G>T | CA393088555 | HCN4 | c.2611C>A (p.Leu871Met) c.1393C>A (p.Leu465Met) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323483T>A | CA491478745 | HCN4 | c.2610A>T (p.Gly870=) c.1392A>T (p.Gly464=) | |
| 15 | g.73323483T>C | CA491478746 | HCN4 | c.2610A>G (p.Gly870=) c.1392A>G (p.Gly464=) | gnomAD v4 |
| 15 | g.73323483T>G | CA491478748 | HCN4 | c.2610A>C (p.Gly870=) c.1392A>C (p.Gly464=) | |
| 15 | g.73323489_73323506del | CA2739269578 | HCN4 | c.2593_2610del (p.Phe865_Gly870del) c.1375_1392del (p.Phe459_Gly464del) | ClinVar |
| 15 | g.73323484C>A | CA393088556 | HCN4 | c.2609G>T (p.Gly870Val) c.1391G>T (p.Gly464Val) | gnomAD v4 |
| 15 | g.73323484C= | CA2187188393 | HCN4 | c.2609G= (p.Gly870=) c.1391G= (p.Gly464=) | |
| 15 | g.73323484C>G | CA393088557 | HCN4 | c.2609G>C (p.Gly870Ala) c.1391G>C (p.Gly464Ala) | |
| 15 | g.73323484C>T | CA7648990 | HCN4 | c.2609G>A (p.Gly870Glu) c.1391G>A (p.Gly464Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323485C>A | CA393088560 | HCN4 | c.2608G>T (p.Gly870Ter) c.1390G>T (p.Gly464Ter) | |
| 15 | g.73323485C= | CA2187188395 | HCN4 | c.2608G= (p.Gly870=) c.1390G= (p.Gly464=) | |
| 15 | g.73323485C>G | CA393088558 | HCN4 | c.2608G>C (p.Gly870Arg) c.1390G>C (p.Gly464Arg) | |
| 15 | g.73323485C>T | CA393088559 | HCN4 | c.2608G>A (p.Gly870Arg) c.1390G>A (p.Gly464Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323486A>C | CA491478757 | HCN4 | c.2607T>G (p.Ala869=) c.1389T>G (p.Ala463=) | |
| 15 | g.73323486A>G | CA491478756 | HCN4 | c.2607T>C (p.Ala869=) c.1389T>C (p.Ala463=) | ClinVar |
| 15 | g.73323486A>T | CA491478755 | HCN4 | c.2607T>A (p.Ala869=) c.1389T>A (p.Ala463=) | gnomAD v4 |
| 15 | g.73323487G>A | CA7648991 | HCN4 | c.2606C>T (p.Ala869Val) c.1388C>T (p.Ala463Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323487G>C | CA393088561 | HCN4 | c.2606C>G (p.Ala869Gly) c.1388C>G (p.Ala463Gly) | |
| 15 | g.73323487G= | CA2187188399 | HCN4 | c.2606C= (p.Ala869=) c.1388C= (p.Ala463=) | |
| 15 | g.73323487G>T | CA393088562 | HCN4 | c.2606C>A (p.Ala869Asp) c.1388C>A (p.Ala463Asp) | |
| 15 | g.73323488C>A | CA393088563 | HCN4 | c.2605G>T (p.Ala869Ser) c.1387G>T (p.Ala463Ser) | |
| 15 | g.73323488C= | CA2187188405 | HCN4 | c.2605G= (p.Ala869=) c.1387G= (p.Ala463=) | |
| 15 | g.73323488C>G | CA7648992 | HCN4 | c.2605G>C (p.Ala869Pro) c.1387G>C (p.Ala463Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323488C>T | CA7648993 | HCN4 | c.2605G>A (p.Ala869Thr) c.1387G>A (p.Ala463Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323489G>A | CA7648995 | HCN4 | c.2604C>T (p.Pro868=) c.1386C>T (p.Pro462=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323489G>C | CA7648994 | HCN4 | c.2604C>G (p.Pro868=) c.1386C>G (p.Pro462=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323489G= | CA2187188415 | HCN4 | c.2604C= (p.Pro868=) c.1386C= (p.Pro462=) | |
| 15 | g.73323489G>T | CA491478768 | HCN4 | c.2604C>A (p.Pro868=) c.1386C>A (p.Pro462=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323493del | CA2575783834 | HCN4 | c.2604del (p.Ala869LeufsTer3) c.1386del (p.Ala463LeufsTer3) | gnomAD v4 |
| 15 | g.73323490G>A | CA393088564 | HCN4 | c.2603C>T (p.Pro868Leu) c.1385C>T (p.Pro462Leu) | |
| 15 | g.73323490G>C | CA393088565 | HCN4 | c.2603C>G (p.Pro868Arg) c.1385C>G (p.Pro462Arg) | |
| 15 | g.73323490G>T | CA393088566 | HCN4 | c.2603C>A (p.Pro868His) c.1385C>A (p.Pro462His) | gnomAD v4 |
| 15 | g.73323491G>A | CA393088567 | HCN4 | c.2602C>T (p.Pro868Ser) c.1384C>T (p.Pro462Ser) | dbSNP gnomAD v4 |
| 15 | g.73323491G>C | CA393088568 | HCN4 | c.2602C>G (p.Pro868Ala) c.1384C>G (p.Pro462Ala) | |
| 15 | g.73323491G= | CA2187188419 | HCN4 | c.2602C= (p.Pro868=) c.1384C= (p.Pro462=) | |
| 15 | g.73323491G>T | CA393088569 | HCN4 | c.2602C>A (p.Pro868Thr) c.1384C>A (p.Pro462Thr) | |
| 15 | g.73323492G>A | CA491478778 | HCN4 | c.2601C>T (p.Ala867=) c.1383C>T (p.Ala461=) | gnomAD v3 gnomAD v4 |
| 15 | g.73323492G>C | CA491478779 | HCN4 | c.2601C>G (p.Ala867=) c.1383C>G (p.Ala461=) | |
| 15 | g.73323492G= | CA2187188422 | HCN4 | c.2601C= (p.Ala867=) c.1383C= (p.Ala461=) | |
| 15 | g.73323492G>T | CA203633 | HCN4 | c.2601C>A (p.Ala867=) c.1383C>A (p.Ala461=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323493G>A | CA393088570 | HCN4 | c.2600C>T (p.Ala867Val) c.1382C>T (p.Ala461Val) | |
| 15 | g.73323493G>C | CA393088571 | HCN4 | c.2600C>G (p.Ala867Gly) c.1382C>G (p.Ala461Gly) | |
| 15 | g.73323493G>T | CA393088572 | HCN4 | c.2600C>A (p.Ala867Asp) c.1382C>A (p.Ala461Asp) | ClinVar |
| 15 | g.73323494C>A | CA393088573 | HCN4 | c.2599G>T (p.Ala867Ser) c.1381G>T (p.Ala461Ser) | |
| 15 | g.73323494C>G | CA393088574 | HCN4 | c.2599G>C (p.Ala867Pro) c.1381G>C (p.Ala461Pro) | |
| 15 | g.73323494C>T | CA393088575 | HCN4 | c.2599G>A (p.Ala867Thr) c.1381G>A (p.Ala461Thr) | |
| 15 | g.73323495A>C | CA491478783 | HCN4 | c.2598T>G (p.Ser866=) c.1380T>G (p.Ser460=) | |
| 15 | g.73323495A>G | CA491478785 | HCN4 | c.2598T>C (p.Ser866=) c.1380T>C (p.Ser460=) | gnomAD v4 |
| 15 | g.73323495A>T | CA491478788 | HCN4 | c.2598T>A (p.Ser866=) c.1380T>A (p.Ser460=) | |
| 15 | g.73323496G>A | CA393088578 | HCN4 | c.2597C>T (p.Ser866Phe) c.1379C>T (p.Ser460Phe) | |
| 15 | g.73323496G>C | CA393088577 | HCN4 | c.2597C>G (p.Ser866Cys) c.1379C>G (p.Ser460Cys) | |
| 15 | g.73323496G>T | CA393088576 | HCN4 | c.2597C>A (p.Ser866Tyr) c.1379C>A (p.Ser460Tyr) | |
| 15 | g.73323497A>C | CA393088579 | HCN4 | c.2596T>G (p.Ser866Ala) c.1378T>G (p.Ser460Ala) | |
| 15 | g.73323497A>G | CA393088580 | HCN4 | c.2596T>C (p.Ser866Pro) c.1378T>C (p.Ser460Pro) | |
| 15 | g.73323497A>T | CA393088581 | HCN4 | c.2596T>A (p.Ser866Thr) c.1378T>A (p.Ser460Thr) | |
| 15 | g.73323498G>A | CA272664566 | HCN4 | c.2595C>T (p.Phe865=) c.1377C>T (p.Phe459=) | ClinVar dbSNP COSMIC |
| 15 | g.73323498G>C | CA393088582 | HCN4 | c.2595C>G (p.Phe865Leu) c.1377C>G (p.Phe459Leu) | |
| 15 | g.73323498G= | CA2187188426 | HCN4 | c.2595C= (p.Phe865=) c.1377C= (p.Phe459=) | |
| 15 | g.73323498G>T | CA393088583 | HCN4 | c.2595C>A (p.Phe865Leu) c.1377C>A (p.Phe459Leu) | |
| 15 | g.73323499A>C | CA393088584 | HCN4 | c.2594T>G (p.Phe865Cys) c.1376T>G (p.Phe459Cys) | |
| 15 | g.73323499A>G | CA393088585 | HCN4 | c.2594T>C (p.Phe865Ser) c.1376T>C (p.Phe459Ser) | |
| 15 | g.73323499A>T | CA393088586 | HCN4 | c.2594T>A (p.Phe865Tyr) c.1376T>A (p.Phe459Tyr) | |
| 15 | g.73323500A>C | CA393088587 | HCN4 | c.2593T>G (p.Phe865Val) c.1375T>G (p.Phe459Val) | |
| 15 | g.73323500A>G | CA393088588 | HCN4 | c.2593T>C (p.Phe865Leu) c.1375T>C (p.Phe459Leu) | |
| 15 | g.73323500A>T | CA393088589 | HCN4 | c.2593T>A (p.Phe865Ile) c.1375T>A (p.Phe459Ile) | |
| 15 | g.73323501T>A | CA491478791 | HCN4 | c.2592A>T (p.Gly864=) c.1374A>T (p.Gly458=) | |
| 15 | g.73323501T>C | CA491478793 | HCN4 | c.2592A>G (p.Gly864=) c.1374A>G (p.Gly458=) | |
| 15 | g.73323501T>G | CA491478794 | HCN4 | c.2592A>C (p.Gly864=) c.1374A>C (p.Gly458=) | |
| 15 | g.73323501_73323502delinsAA | CA272664570 | HCN4 | c.2591_2592delinsTT (p.Gly864Val) c.1373_1374delinsTT (p.Gly458Val) | dbSNP |
| 15 | g.73323501_73323502delinsTC | CA2187188430 | HCN4 | c.2591_2592delinsGA (p.Gly864=) c.1373_1374delinsGA (p.Gly458=) | |
| 15 | g.73323502C>A | CA393088590 | HCN4 | c.2591G>T (p.Gly864Val) c.1373G>T (p.Gly458Val) | |
| 15 | g.73323502C= | CA2187188432 | HCN4 | c.2591G= (p.Gly864=) c.1373G= (p.Gly458=) | |
| 15 | g.73323502C>G | CA393088591 | HCN4 | c.2591G>C (p.Gly864Ala) c.1373G>C (p.Gly458Ala) | |
| 15 | g.73323502C>T | CA393088592 | HCN4 | c.2591G>A (p.Gly864Glu) c.1373G>A (p.Gly458Glu) | dbSNP |
| 15 | g.73323503C>A | CA393088595 | HCN4 | c.2590G>T (p.Gly864Ter) c.1372G>T (p.Gly458Ter) | |
| 15 | g.73323503C= | CA2187188435 | HCN4 | c.2590G= (p.Gly864=) c.1372G= (p.Gly458=) | |
| 15 | g.73323503C>G | CA393088594 | HCN4 | c.2590G>C (p.Gly864Arg) c.1372G>C (p.Gly458Arg) | |
| 15 | g.73323503C>T | CA393088593 | HCN4 | c.2590G>A (p.Gly864Arg) c.1372G>A (p.Gly458Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323504A>C | CA491478799 | HCN4 | c.2589T>G (p.Ala863=) c.1371T>G (p.Ala457=) | |
| 15 | g.73323504A>G | CA491478800 | HCN4 | c.2589T>C (p.Ala863=) c.1371T>C (p.Ala457=) | |
| 15 | g.73323504A>T | CA491478801 | HCN4 | c.2589T>A (p.Ala863=) c.1371T>A (p.Ala457=) | |
| 15 | g.73323505G>A | CA393088596 | HCN4 | c.2588C>T (p.Ala863Val) c.1370C>T (p.Ala457Val) | gnomAD v4 |
| 15 | g.73323505G>C | CA393088597 | HCN4 | c.2588C>G (p.Ala863Gly) c.1370C>G (p.Ala457Gly) | |
| 15 | g.73323505G>T | CA393088598 | HCN4 | c.2588C>A (p.Ala863Asp) c.1370C>A (p.Ala457Asp) | gnomAD v4 |
| 15 | g.73323506C>A | CA272664581 | HCN4 | c.2587G>T (p.Ala863Ser) c.1369G>T (p.Ala457Ser) | ClinVar dbSNP |
| 15 | g.73323506C= | CA2187188443 | HCN4 | c.2587G= (p.Ala863=) c.1369G= (p.Ala457=) | |
| 15 | g.73323506C>G | CA393088599 | HCN4 | c.2587G>C (p.Ala863Pro) c.1369G>C (p.Ala457Pro) | |
| 15 | g.73323506C>T | CA7648996 | HCN4 | c.2587G>A (p.Ala863Thr) c.1369G>A (p.Ala457Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323507C>A | CA491478814 | HCN4 | c.2586G>T (p.Leu862=) c.1368G>T (p.Leu456=) | |
| 15 | g.73323507C>G | CA491478816 | HCN4 | c.2586G>C (p.Leu862=) c.1368G>C (p.Leu456=) | |
| 15 | g.73323507C>T | CA491478813 | HCN4 | c.2586G>A (p.Leu862=) c.1368G>A (p.Leu456=) | |
| 15 | g.73323508A= | CA2187188453 | HCN4 | c.2585T= (p.Leu862=) c.1367T= (p.Leu456=) | |
| 15 | g.73323508A>C | CA393088600 | HCN4 | c.2585T>G (p.Leu862Arg) c.1367T>G (p.Leu456Arg) | |
| 15 | g.73323508A>G | CA393088601 | HCN4 | c.2585T>C (p.Leu862Pro) c.1367T>C (p.Leu456Pro) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323508A>T | CA393088602 | HCN4 | c.2585T>A (p.Leu862Gln) c.1367T>A (p.Leu456Gln) | |
| 15 | g.73323509G>A | CA491478827 | HCN4 | c.2584C>T (p.Leu862=) c.1366C>T (p.Leu456=) | |
| 15 | g.73323509G>C | CA393088603 | HCN4 | c.2584C>G (p.Leu862Val) c.1366C>G (p.Leu456Val) | |
| 15 | g.73323509G>T | CA393088604 | HCN4 | c.2584C>A (p.Leu862Met) c.1366C>A (p.Leu456Met) | |
| 15 | g.73323510C>A | CA393088605 | HCN4 | c.2583G>T (p.Gln861His) c.1365G>T (p.Gln455His) | |
| 15 | g.73323510C>G | CA393088606 | HCN4 | c.2583G>C (p.Gln861His) c.1365G>C (p.Gln455His) | |
| 15 | g.73323510C>T | CA491478829 | HCN4 | c.2583G>A (p.Gln861=) c.1365G>A (p.Gln455=) | |
| 15 | g.73323511T>A | CA393088609 | HCN4 | c.2582A>T (p.Gln861Leu) c.1364A>T (p.Gln455Leu) | |
| 15 | g.73323511T>C | CA393088608 | HCN4 | c.2582A>G (p.Gln861Arg) c.1364A>G (p.Gln455Arg) | gnomAD v4 |
| 15 | g.73323511T>G | CA393088607 | HCN4 | c.2582A>C (p.Gln861Pro) c.1364A>C (p.Gln455Pro) | |
| 15 | g.73323512G>A | CA393088610 | HCN4 | c.2581C>T (p.Gln861Ter) c.1363C>T (p.Gln455Ter) | |
| 15 | g.73323512G>C | CA393088611 | HCN4 | c.2581C>G (p.Gln861Glu) c.1363C>G (p.Gln455Glu) | |
| 15 | g.73323512G>T | CA393088612 | HCN4 | c.2581C>A (p.Gln861Lys) c.1363C>A (p.Gln455Lys) | |
| 15 | g.73323513T>A | CA393088613 | HCN4 | c.2580A>T (p.Gln860His) c.1362A>T (p.Gln454His) | |
| 15 | g.73323513T>C | CA7648997 | HCN4 | c.2580A>G (p.Gln860=) c.1362A>G (p.Gln454=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323513T>G | CA393088614 | HCN4 | c.2580A>C (p.Gln860His) c.1362A>C (p.Gln454His) | |
| 15 | g.73323513T= | CA2187188455 | HCN4 | c.2580A= (p.Gln860=) c.1362A= (p.Gln454=) | |
| 15 | g.73323514T>A | CA393088615 | HCN4 | c.2579A>T (p.Gln860Leu) c.1361A>T (p.Gln454Leu) | |
| 15 | g.73323514T>C | CA393088616 | HCN4 | c.2579A>G (p.Gln860Arg) c.1361A>G (p.Gln454Arg) | |
| 15 | g.73323514T>G | CA393088617 | HCN4 | c.2579A>C (p.Gln860Pro) c.1361A>C (p.Gln454Pro) | |
| 15 | g.73323515G>A | CA393088618 | HCN4 | c.2578C>T (p.Gln860Ter) c.1360C>T (p.Gln454Ter) | |
| 15 | g.73323515G>C | CA393088619 | HCN4 | c.2578C>G (p.Gln860Glu) c.1360C>G (p.Gln454Glu) | |
| 15 | g.73323515G>T | CA393088620 | HCN4 | c.2578C>A (p.Gln860Lys) c.1360C>A (p.Gln454Lys) | |
| 15 | g.73323516G>A | CA491478837 | HCN4 | c.2577C>T (p.Ile859=) c.1359C>T (p.Ile453=) | |
| 15 | g.73323516G>C | CA393088621 | HCN4 | c.2577C>G (p.Ile859Met) c.1359C>G (p.Ile453Met) | gnomAD v4 COSMIC |
| 15 | g.73323516G>T | CA491478839 | HCN4 | c.2577C>A (p.Ile859=) c.1359C>A (p.Ile453=) | |
| 15 | g.73323517A>C | CA393088623 | HCN4 | c.2576T>G (p.Ile859Ser) c.1358T>G (p.Ile453Ser) | |
| 15 | g.73323517A>G | CA393088624 | HCN4 | c.2576T>C (p.Ile859Thr) c.1358T>C (p.Ile453Thr) | |
| 15 | g.73323517A>T | CA393088622 | HCN4 | c.2576T>A (p.Ile859Asn) c.1358T>A (p.Ile453Asn) | |
| 15 | g.73323518T>A | CA393088625 | HCN4 | c.2575A>T (p.Ile859Phe) c.1357A>T (p.Ile453Phe) | |
| 15 | g.73323518T>C | CA393088627 | HCN4 | c.2575A>G (p.Ile859Val) c.1357A>G (p.Ile453Val) | |
| 15 | g.73323518T>G | CA393088626 | HCN4 | c.2575A>C (p.Ile859Leu) c.1357A>C (p.Ile453Leu) | |
| 15 | g.73323519G>A | CA491478845 | HCN4 | c.2574C>T (p.His858=) c.1356C>T (p.His452=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323519G>C | CA393088628 | HCN4 | c.2574C>G (p.His858Gln) c.1356C>G (p.His452Gln) | |
| 15 | g.73323519G= | CA2187188458 | HCN4 | c.2574C= (p.His858=) c.1356C= (p.His452=) | |
| 15 | g.73323519G>T | CA393088629 | HCN4 | c.2574C>A (p.His858Gln) c.1356C>A (p.His452Gln) | |
| 15 | g.73323520T>A | CA393088630 | HCN4 | c.2573A>T (p.His858Leu) c.1355A>T (p.His452Leu) | |
| 15 | g.73323520T>C | CA393088631 | HCN4 | c.2573A>G (p.His858Arg) c.1355A>G (p.His452Arg) | gnomAD v4 |
| 15 | g.73323520T>G | CA393088632 | HCN4 | c.2573A>C (p.His858Pro) c.1355A>C (p.His452Pro) | |
| 15 | g.73323521G>A | CA393088633 | HCN4 | c.2572C>T (p.His858Tyr) c.1354C>T (p.His452Tyr) | gnomAD v4 |
| 15 | g.73323521G>C | CA393088634 | HCN4 | c.2572C>G (p.His858Asp) c.1354C>G (p.His452Asp) | |
| 15 | g.73323521G>T | CA393088635 | HCN4 | c.2572C>A (p.His858Asn) c.1354C>A (p.His452Asn) | gnomAD v4 |
| 15 | g.73323522G>A | CA491478855 | HCN4 | c.2571C>T (p.Phe857=) c.1353C>T (p.Phe451=) | |
| 15 | g.73323522G>C | CA7648998 | HCN4 | c.2571C>G (p.Phe857Leu) c.1353C>G (p.Phe451Leu) | ClinVar dbSNP ExAC gnomAD v4 |
| 15 | g.73323522G= | CA2187188461 | HCN4 | c.2571C= (p.Phe857=) c.1353C= (p.Phe451=) | |
| 15 | g.73323522G>T | CA393088636 | HCN4 | c.2571C>A (p.Phe857Leu) c.1353C>A (p.Phe451Leu) | |
| 15 | g.73323523A>C | CA393088639 | HCN4 | c.2570T>G (p.Phe857Cys) c.1352T>G (p.Phe451Cys) | |
| 15 | g.73323523A>G | CA393088638 | HCN4 | c.2570T>C (p.Phe857Ser) c.1352T>C (p.Phe451Ser) | gnomAD v4 |
| 15 | g.73323523A>T | CA393088637 | HCN4 | c.2570T>A (p.Phe857Tyr) c.1352T>A (p.Phe451Tyr) | |
| 15 | g.73323524A>C | CA393088640 | HCN4 | c.2569T>G (p.Phe857Val) c.1351T>G (p.Phe451Val) | |
| 15 | g.73323524A>G | CA393088641 | HCN4 | c.2569T>C (p.Phe857Leu) c.1351T>C (p.Phe451Leu) | |
| 15 | g.73323524A>T | CA393088642 | HCN4 | c.2569T>A (p.Phe857Ile) c.1351T>A (p.Phe451Ile) | |
| 15 | g.73323525G>A | CA491478860 | HCN4 | c.2568C>T (p.Ser856=) c.1350C>T (p.Ser450=) | gnomAD v4 |
| 15 | g.73323525G>C | CA491478861 | HCN4 | c.2568C>G (p.Ser856=) c.1350C>G (p.Ser450=) | |
| 15 | g.73323525G>T | CA491478863 | HCN4 | c.2568C>A (p.Ser856=) c.1350C>A (p.Ser450=) | |
| 15 | g.73323526G>A | CA393088643 | HCN4 | c.2567C>T (p.Ser856Phe) c.1349C>T (p.Ser450Phe) | ClinVar gnomAD v4 COSMIC |
| 15 | g.73323526G>C | CA393088644 | HCN4 | c.2567C>G (p.Ser856Cys) c.1349C>G (p.Ser450Cys) | |
| 15 | g.73323526G>T | CA393088645 | HCN4 | c.2567C>A (p.Ser856Tyr) c.1349C>A (p.Ser450Tyr) | |
| 15 | g.73323527A>C | CA393088646 | HCN4 | c.2566T>G (p.Ser856Ala) c.1348T>G (p.Ser450Ala) | gnomAD v4 |
| 15 | g.73323527A>G | CA393088647 | HCN4 | c.2566T>C (p.Ser856Pro) c.1348T>C (p.Ser450Pro) | |
| 15 | g.73323527A>T | CA393088648 | HCN4 | c.2566T>A (p.Ser856Thr) c.1348T>A (p.Ser450Thr) | |
| 15 | g.73323528G>A | CA491478879 | HCN4 | c.2565C>T (p.Ser855=) c.1347C>T (p.Ser449=) | |
| 15 | g.73323528G>C | CA491478878 | HCN4 | c.2565C>G (p.Ser855=) c.1347C>G (p.Ser449=) | gnomAD v4 |
| 15 | g.73323528G>T | CA491478877 | HCN4 | c.2565C>A (p.Ser855=) c.1347C>A (p.Ser449=) | gnomAD v4 |
| 15 | g.73323529G>A | CA393088649 | HCN4 | c.2564C>T (p.Ser855Phe) c.1346C>T (p.Ser449Phe) | COSMIC |
| 15 | g.73323529G>C | CA393088650 | HCN4 | c.2564C>G (p.Ser855Cys) c.1346C>G (p.Ser449Cys) | |
| 15 | g.73323529G>T | CA393088651 | HCN4 | c.2564C>A (p.Ser855Tyr) c.1346C>A (p.Ser449Tyr) | gnomAD v4 COSMIC |
| 15 | g.73323530A= | CA2187188465 | HCN4 | c.2563T= (p.Ser855=) c.1345T= (p.Ser449=) | |
| 15 | g.73323530A>C | CA393088653 | HCN4 | c.2563T>G (p.Ser855Ala) c.1345T>G (p.Ser449Ala) | |
| 15 | g.73323530A>G | CA7648999 | HCN4 | c.2563T>C (p.Ser855Pro) c.1345T>C (p.Ser449Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323530A>T | CA393088652 | HCN4 | c.2563T>A (p.Ser855Thr) c.1345T>A (p.Ser449Thr) | |
| 15 | g.73323531T>A | CA491478182 | HCN4 | c.2562A>T (p.Ser854=) c.1344A>T (p.Ser448=) | |
| 15 | g.73323531T>C | CA491478183 | HCN4 | c.2562A>G (p.Ser854=) c.1344A>G (p.Ser448=) | |
| 15 | g.73323531T>G | CA491478184 | HCN4 | c.2562A>C (p.Ser854=) c.1344A>C (p.Ser448=) | |
| 15 | g.73323532G>A | CA393088654 | HCN4 | c.2561C>T (p.Ser854Leu) c.1343C>T (p.Ser448Leu) | COSMIC |
| 15 | g.73323532G>C | CA393088655 | HCN4 | c.2561C>G (p.Ser854Ter) c.1343C>G (p.Ser448Ter) | |
| 15 | g.73323532G>T | CA393088656 | HCN4 | c.2561C>A (p.Ser854Ter) c.1343C>A (p.Ser448Ter) | gnomAD v4 |
| 15 | g.73323533A= | CA2187188469 | HCN4 | c.2560T= (p.Ser854=) c.1342T= (p.Ser448=) | |
| 15 | g.73323533A>C | CA393088657 | HCN4 | c.2560T>G (p.Ser854Ala) c.1342T>G (p.Ser448Ala) | |
| 15 | g.73323533A>G | CA7649000 | HCN4 | c.2560T>C (p.Ser854Pro) c.1342T>C (p.Ser448Pro) | ClinVar dbSNP ExAC gnomAD v2 |
| 15 | g.73323533A>T | CA393088658 | HCN4 | c.2560T>A (p.Ser854Thr) c.1342T>A (p.Ser448Thr) | |
| 15 | g.73323534A>C | CA491478187 | HCN4 | c.2559T>G (p.Ser853=) c.1341T>G (p.Ser447=) | |
| 15 | g.73323534A>G | CA491478188 | HCN4 | c.2559T>C (p.Ser853=) c.1341T>C (p.Ser447=) | |
| 15 | g.73323534A>T | CA491478190 | HCN4 | c.2559T>A (p.Ser853=) c.1341T>A (p.Ser447=) | |
| 15 | g.73323535G>A | CA393088659 | HCN4 | c.2558C>T (p.Ser853Phe) c.1340C>T (p.Ser447Phe) | gnomAD v4 |
| 15 | g.73323535G>C | CA393088660 | HCN4 | c.2558C>G (p.Ser853Cys) c.1340C>G (p.Ser447Cys) | |
| 15 | g.73323535G>T | CA393088661 | HCN4 | c.2558C>A (p.Ser853Tyr) c.1340C>A (p.Ser447Tyr) | |
| 15 | g.73323536A>C | CA393088662 | HCN4 | c.2557T>G (p.Ser853Ala) c.1339T>G (p.Ser447Ala) | |
| 15 | g.73323536A>G | CA393088663 | HCN4 | c.2557T>C (p.Ser853Pro) c.1339T>C (p.Ser447Pro) | gnomAD v4 |
| 15 | g.73323536A>T | CA393088664 | HCN4 | c.2557T>A (p.Ser853Thr) c.1339T>A (p.Ser447Thr) | |
| 15 | g.73323537C>A | CA491478191 | HCN4 | c.2556G>T (p.Pro852=) c.1338G>T (p.Pro446=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323537C= | CA2187188476 | HCN4 | c.2556G= (p.Pro852=) c.1338G= (p.Pro446=) | |
| 15 | g.73323537C>G | CA491478192 | HCN4 | c.2556G>C (p.Pro852=) c.1338G>C (p.Pro446=) | |
| 15 | g.73323537C>T | CA148386 | HCN4 | c.2556G>A (p.Pro852=) c.1338G>A (p.Pro446=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323538G>A | CA7649001 | HCN4 | c.2555C>T (p.Pro852Leu) c.1337C>T (p.Pro446Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323538G>C | CA393088666 | HCN4 | c.2555C>G (p.Pro852Arg) c.1337C>G (p.Pro446Arg) | |
| 15 | g.73323538G= | CA2187188480 | HCN4 | c.2555C= (p.Pro852=) c.1337C= (p.Pro446=) | |
| 15 | g.73323538G>T | CA393088665 | HCN4 | c.2555C>A (p.Pro852Gln) c.1337C>A (p.Pro446Gln) | dbSNP |
| 15 | g.73323539G>A | CA393088667 | HCN4 | c.2554C>T (p.Pro852Ser) c.1336C>T (p.Pro446Ser) | |
| 15 | g.73323539G>C | CA393088668 | HCN4 | c.2554C>G (p.Pro852Ala) c.1336C>G (p.Pro446Ala) | gnomAD v4 |
| 15 | g.73323539G>T | CA393088669 | HCN4 | c.2554C>A (p.Pro852Thr) c.1336C>A (p.Pro446Thr) | |
| 15 | g.73323539_73323540insCGT | CA2629370568 | HCN4 | c.2553_2554insACG (p.Thr851_Pro852insThr) c.1335_1336insACG (p.Thr445_Pro446insThr) | gnomAD v4 |
| 15 | g.73323540T>A | CA491478197 | HCN4 | c.2553A>T (p.Thr851=) c.1335A>T (p.Thr445=) | |
| 15 | g.73323540T>C | CA247659 | HCN4 | c.2553A>G (p.Thr851=) c.1335A>G (p.Thr445=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323540T>G | CA491478196 | HCN4 | c.2553A>C (p.Thr851=) c.1335A>C (p.Thr445=) | |
| 15 | g.73323540T= | CA2187188487 | HCN4 | c.2553A= (p.Thr851=) c.1335A= (p.Thr445=) | |
| 15 | g.73323541G>A | CA393088670 | HCN4 | c.2552C>T (p.Thr851Ile) c.1334C>T (p.Thr445Ile) | |
| 15 | g.73323541G>C | CA393088671 | HCN4 | c.2552C>G (p.Thr851Arg) c.1334C>G (p.Thr445Arg) | |
| 15 | g.73323541G>T | CA393088672 | HCN4 | c.2552C>A (p.Thr851Lys) c.1334C>A (p.Thr445Lys) | |
| 15 | g.73323542T>A | CA393088673 | HCN4 | c.2551A>T (p.Thr851Ser) c.1333A>T (p.Thr445Ser) | |
| 15 | g.73323542T>C | CA393088674 | HCN4 | c.2551A>G (p.Thr851Ala) c.1333A>G (p.Thr445Ala) | ClinVar dbSNP |
| 15 | g.73323542T>G | CA393088675 | HCN4 | c.2551A>C (p.Thr851Pro) c.1333A>C (p.Thr445Pro) | ClinVar |
| 15 | g.73323542T= | CA2187188496 | HCN4 | c.2551A= (p.Thr851=) c.1333A= (p.Thr445=) | |
| 15 | g.73323543G>A | CA491478198 | HCN4 | c.2550C>T (p.Asp850=) c.1332C>T (p.Asp444=) | dbSNP |
| 15 | g.73323543G>C | CA393088676 | HCN4 | c.2550C>G (p.Asp850Glu) c.1332C>G (p.Asp444Glu) | |
| 15 | g.73323543G= | CA2187188499 | HCN4 | c.2550C= (p.Asp850=) c.1332C= (p.Asp444=) | |
| 15 | g.73323543G>T | CA393088677 | HCN4 | c.2550C>A (p.Asp850Glu) c.1332C>A (p.Asp444Glu) | gnomAD v4 |
| 15 | g.73323544T>A | CA393088680 | HCN4 | c.2549A>T (p.Asp850Val) c.1331A>T (p.Asp444Val) | |
| 15 | g.73323544T>C | CA393088679 | HCN4 | c.2549A>G (p.Asp850Gly) c.1331A>G (p.Asp444Gly) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323544T>G | CA393088678 | HCN4 | c.2549A>C (p.Asp850Ala) c.1331A>C (p.Asp444Ala) | |
| 15 | g.73323544T= | CA2187188503 | HCN4 | c.2549A= (p.Asp850=) c.1331A= (p.Asp444=) | |
| 15 | g.73323545C>A | CA393088681 | HCN4 | c.2548G>T (p.Asp850Tyr) c.1330G>T (p.Asp444Tyr) | |
| 15 | g.73323545C= | CA2187188506 | HCN4 | c.2548G= (p.Asp850=) c.1330G= (p.Asp444=) | |
| 15 | g.73323545C>G | CA393088682 | HCN4 | c.2548G>C (p.Asp850His) c.1330G>C (p.Asp444His) | |
| 15 | g.73323545C>T | CA272664617 | HCN4 | c.2548G>A (p.Asp850Asn) c.1330G>A (p.Asp444Asn) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323546C>A | CA491478201 | HCN4 | c.2547G>T (p.Val849=) c.1329G>T (p.Val443=) | |
| 15 | g.73323546C= | CA2187188511 | HCN4 | c.2547G= (p.Val849=) c.1329G= (p.Val443=) | |
| 15 | g.73323546C>G | CA491478200 | HCN4 | c.2547G>C (p.Val849=) c.1329G>C (p.Val443=) | |
| 15 | g.73323546C>T | CA272664618 | HCN4 | c.2547G>A (p.Val849=) c.1329G>A (p.Val443=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323547A>C | CA393088684 | HCN4 | c.2546T>G (p.Val849Gly) c.1328T>G (p.Val443Gly) | |
| 15 | g.73323547A>G | CA393088683 | HCN4 | c.2546T>C (p.Val849Ala) c.1328T>C (p.Val443Ala) | |
| 15 | g.73323547A>T | CA393088685 | HCN4 | c.2546T>A (p.Val849Glu) c.1328T>A (p.Val443Glu) | |
| 15 | g.73323547_73323548delinsAC | CA2187188513 | HCN4 | c.2545_2546delinsGT (p.Val849=) c.1327_1328delinsGT (p.Val443=) | |
| 15 | g.73323548C>A | CA236699 | HCN4 | c.2545G>T (p.Val849Leu) c.1327G>T (p.Val443Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323548C= | CA2187188516 | HCN4 | c.2545G= (p.Val849=) c.1327G= (p.Val443=) | |
| 15 | g.73323548C>G | CA393088686 | HCN4 | c.2545G>C (p.Val849Leu) c.1327G>C (p.Val443Leu) | |
| 15 | g.73323548C>T | CA393088687 | HCN4 | c.2545G>A (p.Val849Met) c.1327G>A (p.Val443Met) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323549del | CA7649002 | HCN4 | c.2545del (p.Val849TrpfsTer23) c.1327del (p.Val443TrpfsTer23) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323549C>A | CA393088688 | HCN4 | c.2544G>T (p.Gln848His) c.1326G>T (p.Gln442His) | |
| 15 | g.73323549C= | CA2187188527 | HCN4 | c.2544G= (p.Gln848=) c.1326G= (p.Gln442=) | |
| 15 | g.73323549C>G | CA393088689 | HCN4 | c.2544G>C (p.Gln848His) c.1326G>C (p.Gln442His) | |
| 15 | g.73323549C>T | CA491478205 | HCN4 | c.2544G>A (p.Gln848=) c.1326G>A (p.Gln442=) | dbSNP gnomAD v4 |
| 15 | g.73323550T>A | CA393088690 | HCN4 | c.2543A>T (p.Gln848Leu) c.1325A>T (p.Gln442Leu) | |
| 15 | g.73323550T>C | CA393088691 | HCN4 | c.2543A>G (p.Gln848Arg) c.1325A>G (p.Gln442Arg) | |
| 15 | g.73323550T>G | CA393088692 | HCN4 | c.2543A>C (p.Gln848Pro) c.1325A>C (p.Gln442Pro) | |
| 15 | g.73323551G>A | CA393088693 | HCN4 | c.2542C>T (p.Gln848Ter) c.1324C>T (p.Gln442Ter) | dbSNP gnomAD v2 |
| 15 | g.73323551G>C | CA393088694 | HCN4 | c.2542C>G (p.Gln848Glu) c.1324C>G (p.Gln442Glu) | |
| 15 | g.73323551G= | CA2187188530 | HCN4 | c.2542C= (p.Gln848=) c.1324C= (p.Gln442=) | |
| 15 | g.73323551G>T | CA393088695 | HCN4 | c.2542C>A (p.Gln848Lys) c.1324C>A (p.Gln442Lys) | |
| 15 | g.73323552G>A | CA7649003 | HCN4 | c.2541C>T (p.Ser847=) c.1323C>T (p.Ser441=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323552G>C | CA491478207 | HCN4 | c.2541C>G (p.Ser847=) c.1323C>G (p.Ser441=) | ClinVar dbSNP |
| 15 | g.73323552G= | CA2187188534 | HCN4 | c.2541C= (p.Ser847=) c.1323C= (p.Ser441=) | |
| 15 | g.73323552G>T | CA491478208 | HCN4 | c.2541C>A (p.Ser847=) c.1323C>A (p.Ser441=) | gnomAD v4 |
| 15 | g.73323553G>A | CA393088696 | HCN4 | c.2540C>T (p.Ser847Phe) c.1322C>T (p.Ser441Phe) | |
| 15 | g.73323553G>C | CA393088698 | HCN4 | c.2540C>G (p.Ser847Cys) c.1322C>G (p.Ser441Cys) | |
| 15 | g.73323553G>T | CA393088697 | HCN4 | c.2540C>A (p.Ser847Tyr) c.1322C>A (p.Ser441Tyr) | COSMIC |
| 15 | g.73323554A>C | CA393088699 | HCN4 | c.2539T>G (p.Ser847Ala) c.1321T>G (p.Ser441Ala) | |
| 15 | g.73323554A>G | CA393088700 | HCN4 | c.2539T>C (p.Ser847Pro) c.1321T>C (p.Ser441Pro) | |
| 15 | g.73323554A>T | CA393088701 | HCN4 | c.2539T>A (p.Ser847Thr) c.1321T>A (p.Ser441Thr) | |
| 15 | g.73323555C>A | CA491478209 | HCN4 | c.2538G>T (p.Pro846=) c.1320G>T (p.Pro440=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323555C= | CA2187188536 | HCN4 | c.2538G= (p.Pro846=) c.1320G= (p.Pro440=) | |
| 15 | g.73323555C>G | CA491478211 | HCN4 | c.2538G>C (p.Pro846=) c.1320G>C (p.Pro440=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73323555C>T | CA7649004 | HCN4 | c.2538G>A (p.Pro846=) c.1320G>A (p.Pro440=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323556G>A | CA7649005 | HCN4 | c.2537C>T (p.Pro846Leu) c.1319C>T (p.Pro440Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323556G>C | CA393088702 | HCN4 | c.2537C>G (p.Pro846Arg) c.1319C>G (p.Pro440Arg) | gnomAD v4 |
| 15 | g.73323556G= | CA2187188537 | HCN4 | c.2537C= (p.Pro846=) c.1319C= (p.Pro440=) | |
| 15 | g.73323556G>T | CA393088703 | HCN4 | c.2537C>A (p.Pro846Gln) c.1319C>A (p.Pro440Gln) | |
| 15 | g.73323557G>A | CA393088704 | HCN4 | c.2536C>T (p.Pro846Ser) c.1318C>T (p.Pro440Ser) | COSMIC |
| 15 | g.73323557G>C | CA393088705 | HCN4 | c.2536C>G (p.Pro846Ala) c.1318C>G (p.Pro440Ala) | ClinVar |
| 15 | g.73323557G>T | CA393088706 | HCN4 | c.2536C>A (p.Pro846Thr) c.1318C>A (p.Pro440Thr) | gnomAD v4 |
| 15 | g.73323558G>A | CA491478214 | HCN4 | c.2535C>T (p.Ser845=) c.1317C>T (p.Ser439=) | |
| 15 | g.73323558G>C | CA393088708 | HCN4 | c.2535C>G (p.Ser845Arg) c.1317C>G (p.Ser439Arg) | |
| 15 | g.73323558G>T | CA393088707 | HCN4 | c.2535C>A (p.Ser845Arg) c.1317C>A (p.Ser439Arg) | gnomAD v4 |
| 15 | g.73323559C>A | CA393088709 | HCN4 | c.2534G>T (p.Ser845Ile) c.1316G>T (p.Ser439Ile) | gnomAD v4 |
| 15 | g.73323559C= | CA2187188538 | HCN4 | c.2534G= (p.Ser845=) c.1316G= (p.Ser439=) | |
| 15 | g.73323559C>G | CA393088710 | HCN4 | c.2534G>C (p.Ser845Thr) c.1316G>C (p.Ser439Thr) | ClinVar dbSNP |
| 15 | g.73323559C>T | CA393088711 | HCN4 | c.2534G>A (p.Ser845Asn) c.1316G>A (p.Ser439Asn) | gnomAD v4 |
| 15 | g.73323560T>A | CA393088712 | HCN4 | c.2533A>T (p.Ser845Cys) c.1315A>T (p.Ser439Cys) | |
| 15 | g.73323560T>C | CA393088713 | HCN4 | c.2533A>G (p.Ser845Gly) c.1315A>G (p.Ser439Gly) | |
| 15 | g.73323560T>G | CA393088714 | HCN4 | c.2533A>C (p.Ser845Arg) c.1315A>C (p.Ser439Arg) | |
| 15 | g.73323561G>A | CA491478218 | HCN4 | c.2532C>T (p.Ser844=) c.1314C>T (p.Ser438=) | gnomAD v4 |
| 15 | g.73323561G>C | CA393088716 | HCN4 | c.2532C>G (p.Ser844Arg) c.1314C>G (p.Ser438Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323561G= | CA2187188539 | HCN4 | c.2532C= (p.Ser844=) c.1314C= (p.Ser438=) | |
| 15 | g.73323561G>T | CA393088715 | HCN4 | c.2532C>A (p.Ser844Arg) c.1314C>A (p.Ser438Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73323562C>A | CA393088717 | HCN4 | c.2531G>T (p.Ser844Ile) c.1313G>T (p.Ser438Ile) | |
| 15 | g.73323562C>G | CA393088718 | HCN4 | c.2531G>C (p.Ser844Thr) c.1313G>C (p.Ser438Thr) | |
| 15 | g.73323562C>T | CA393088719 | HCN4 | c.2531G>A (p.Ser844Asn) c.1313G>A (p.Ser438Asn) | |
| 15 | g.73323563T>A | CA393088720 | HCN4 | c.2530A>T (p.Ser844Cys) c.1312A>T (p.Ser438Cys) | |
| 15 | g.73323563T>C | CA393088721 | HCN4 | c.2530A>G (p.Ser844Gly) c.1312A>G (p.Ser438Gly) | ClinVar |
| 15 | g.73323563T>G | CA393088722 | HCN4 | c.2530A>C (p.Ser844Arg) c.1312A>C (p.Ser438Arg) | |
| 15 | g.73323564G>A | CA491478219 | HCN4 | c.2529C>T (p.Ala843=) c.1311C>T (p.Ala437=) | |
| 15 | g.73323564G>C | CA491478220 | HCN4 | c.2529C>G (p.Ala843=) c.1311C>G (p.Ala437=) | |
| 15 | g.73323564G>T | CA491478221 | HCN4 | c.2529C>A (p.Ala843=) c.1311C>A (p.Ala437=) | |
| 15 | g.73323565G>A | CA393088723 | HCN4 | c.2528C>T (p.Ala843Val) c.1310C>T (p.Ala437Val) | |
| 15 | g.73323565G>C | CA393088724 | HCN4 | c.2528C>G (p.Ala843Gly) c.1310C>G (p.Ala437Gly) | |
| 15 | g.73323565G= | CA2187188540 | HCN4 | c.2528C= (p.Ala843=) c.1310C= (p.Ala437=) | |
| 15 | g.73323565G>T | CA7649006 | HCN4 | c.2528C>A (p.Ala843Asp) c.1310C>A (p.Ala437Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73323566C>A | CA393088725 | HCN4 | c.2527G>T (p.Ala843Ser) c.1309G>T (p.Ala437Ser) | gnomAD v4 |
| 15 | g.73323566C= | CA2187188541 | HCN4 | c.2527G= (p.Ala843=) c.1309G= (p.Ala437=) | |
| 15 | g.73323566C>G | CA393088726 | HCN4 | c.2527G>C (p.Ala843Pro) c.1309G>C (p.Ala437Pro) | |
| 15 | g.73323566C>T | CA301964 | HCN4 | c.2527G>A (p.Ala843Thr) c.1309G>A (p.Ala437Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73323567G>A | CA7649007 | HCN4 | c.2526C>T (p.Pro842=) c.1308C>T (p.Pro436=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323567G>C | CA491478226 | HCN4 | c.2526C>G (p.Pro842=) c.1308C>G (p.Pro436=) | |
| 15 | g.73323567G= | CA2187188542 | HCN4 | c.2526C= (p.Pro842=) c.1308C= (p.Pro436=) | |
| 15 | g.73323567G>T | CA491478225 | HCN4 | c.2526C>A (p.Pro842=) c.1308C>A (p.Pro436=) | gnomAD v4 |
| 15 | g.73323568G>A | CA393088727 | HCN4 | c.2525C>T (p.Pro842Leu) c.1307C>T (p.Pro436Leu) | |
| 15 | g.73323568G>C | CA393088728 | HCN4 | c.2525C>G (p.Pro842Arg) c.1307C>G (p.Pro436Arg) | |
| 15 | g.73323568G>T | CA393088729 | HCN4 | c.2525C>A (p.Pro842His) c.1307C>A (p.Pro436His) | |
| 15 | g.73323569G>A | CA393088730 | HCN4 | c.2524C>T (p.Pro842Ser) c.1306C>T (p.Pro436Ser) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73323569G>C | CA393088731 | HCN4 | c.2524C>G (p.Pro842Ala) c.1306C>G (p.Pro436Ala) | |
| 15 | g.73323569G>T | CA393088732 | HCN4 | c.2524C>A (p.Pro842Thr) c.1306C>A (p.Pro436Thr) | |
| 15 | g.73323570C>A | CA491478227 | HCN4 | c.2523G>T (p.Ser841=) c.1305G>T (p.Ser435=) | ClinVar dbSNP |
| 15 | g.73323570C= | CA2187188543 | HCN4 | c.2523G= (p.Ser841=) c.1305G= (p.Ser435=) | |
| 15 | g.73323570C>G | CA491478228 | HCN4 | c.2523G>C (p.Ser841=) c.1305G>C (p.Ser435=) | |
| 15 | g.73323570C>T | CA247657 | HCN4 | c.2523G>A (p.Ser841=) c.1305G>A (p.Ser435=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323571G>A | CA235703 | HCN4 | c.2522C>T (p.Ser841Leu) c.1304C>T (p.Ser435Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73323571G>C | CA393088734 | HCN4 | c.2522C>G (p.Ser841Trp) c.1304C>G (p.Ser435Trp) | |
| 15 | g.73323571G= | CA2187188544 | HCN4 | c.2522C= (p.Ser841=) c.1304C= (p.Ser435=) | |
| 15 | g.73323571G>T | CA393088733 | HCN4 | c.2522C>A (p.Ser841Ter) c.1304C>A (p.Ser435Ter) | |
| 15 | g.73323572A>C | CA393088735 | HCN4 | c.2521T>G (p.Ser841Ala) c.1303T>G (p.Ser435Ala) | |
| 15 | g.73323572A>G | CA393088736 | HCN4 | c.2521T>C (p.Ser841Pro) c.1303T>C (p.Ser435Pro) | |
| 15 | g.73323572A>T | CA393088737 | HCN4 | c.2521T>A (p.Ser841Thr) c.1303T>A (p.Ser435Thr) | |
| 15 | g.73323573G>A | CA491478232 | HCN4 | c.2520C>T (p.Ala840=) c.1302C>T (p.Ala434=) | |
| 15 | g.73323573G>C | CA491478234 | HCN4 | c.2520C>G (p.Ala840=) c.1302C>G (p.Ala434=) | |
| 15 | g.73323573G>T | CA491478233 | HCN4 | c.2520C>A (p.Ala840=) c.1302C>A (p.Ala434=) | |
| 15 | g.73323574G>A | CA393088738 | HCN4 | c.2519C>T (p.Ala840Val) c.1301C>T (p.Ala434Val) | |
| 15 | g.73323574G>C | CA393088739 | HCN4 | c.2519C>G (p.Ala840Gly) c.1301C>G (p.Ala434Gly) | |
| 15 | g.73323574G>T | CA393088740 | HCN4 | c.2519C>A (p.Ala840Asp) c.1301C>A (p.Ala434Asp) |