| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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) | |
| 15 | g.73329667A>C | CA393093743 | HCN4 | c.1496T>G (p.Met499Arg) c.278T>G (p.Met93Arg) | |
| 15 | g.73329667A>G | CA393093744 | HCN4 | c.1496T>C (p.Met499Thr) c.278T>C (p.Met93Thr) | |
| 15 | g.73329667A>T | CA393093745 | HCN4 | c.1496T>A (p.Met499Lys) c.278T>A (p.Met93Lys) | |
| 15 | g.73329668T>A | CA393093746 | HCN4 | c.1495A>T (p.Met499Leu) c.277A>T (p.Met93Leu) | |
| 15 | g.73329668T>C | CA393093747 | HCN4 | c.1495A>G (p.Met499Val) c.277A>G (p.Met93Val) | |
| 15 | g.73329668T>G | CA393093748 | HCN4 | c.1495A>C (p.Met499Leu) c.277A>C (p.Met93Leu) | |
| 15 | g.73329669G>A | CA491151559 | HCN4 | c.1494C>T (p.Ser498=) c.276C>T (p.Ser92=) | |
| 15 | g.73329669G>C | CA393093749 | HCN4 | c.1494C>G (p.Ser498Arg) c.276C>G (p.Ser92Arg) | ClinVar dbSNP |
| 15 | g.73329669G= | CA2187167500 | HCN4 | c.1494C= (p.Ser498=) c.276C= (p.Ser92=) | |
| 15 | g.73329669G>T | CA393093750 | HCN4 | c.1494C>A (p.Ser498Arg) c.276C>A (p.Ser92Arg) | ClinVar dbSNP |
| 15 | g.73329670C>A | CA393093751 | HCN4 | c.1493G>T (p.Ser498Ile) c.275G>T (p.Ser92Ile) | |
| 15 | g.73329670C>G | CA393093752 | HCN4 | c.1493G>C (p.Ser498Thr) c.275G>C (p.Ser92Thr) | |
| 15 | g.73329670C>T | CA393093753 | HCN4 | c.1493G>A (p.Ser498Asn) c.275G>A (p.Ser92Asn) | |
| 15 | g.73329671T>A | CA393093756 | HCN4 | c.1492A>T (p.Ser498Cys) c.274A>T (p.Ser92Cys) | |
| 15 | g.73329671T>C | CA393093755 | HCN4 | c.1492A>G (p.Ser498Gly) c.274A>G (p.Ser92Gly) | |
| 15 | g.73329671T>G | CA393093754 | HCN4 | c.1492A>C (p.Ser498Arg) c.274A>C (p.Ser92Arg) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329671T= | CA2187167502 | HCN4 | c.1492A= (p.Ser498=) c.274A= (p.Ser92=) | |
| 15 | g.73329672G>A | CA491151571 | HCN4 | c.1491C>T (p.Leu497=) c.273C>T (p.Leu91=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329672G>C | CA491151572 | HCN4 | c.1491C>G (p.Leu497=) c.273C>G (p.Leu91=) | |
| 15 | g.73329672G= | CA2187167506 | HCN4 | c.1491C= (p.Leu497=) c.273C= (p.Leu91=) | |
| 15 | g.73329672G>T | CA491151574 | HCN4 | c.1491C>A (p.Leu497=) c.273C>A (p.Leu91=) | |
| 15 | g.73329673A>C | CA393093757 | HCN4 | c.1490T>G (p.Leu497Arg) c.272T>G (p.Leu91Arg) | |
| 15 | g.73329673A>G | CA393093758 | HCN4 | c.1490T>C (p.Leu497Pro) c.272T>C (p.Leu91Pro) | |
| 15 | g.73329673A>T | CA393093759 | HCN4 | c.1490T>A (p.Leu497His) c.272T>A (p.Leu91His) | |
| 15 | g.73329674G>A | CA393093760 | HCN4 | c.1489C>T (p.Leu497Phe) c.271C>T (p.Leu91Phe) | |
| 15 | g.73329674G>C | CA393093761 | HCN4 | c.1489C>G (p.Leu497Val) c.271C>G (p.Leu91Val) | |
| 15 | g.73329674G>T | CA393093762 | HCN4 | c.1489C>A (p.Leu497Ile) c.271C>A (p.Leu91Ile) | |
| 15 | g.73329675C>A | CA393093763 | HCN4 | c.1488G>T (p.Met496Ile) c.270G>T (p.Met90Ile) | |
| 15 | g.73329675C>G | CA393093764 | HCN4 | c.1488G>C (p.Met496Ile) c.270G>C (p.Met90Ile) | |
| 15 | g.73329675C>T | CA393093765 | HCN4 | c.1488G>A (p.Met496Ile) c.270G>A (p.Met90Ile) | |
| 15 | g.73329676A= | CA2187167511 | HCN4 | c.1487T= (p.Met496=) c.269T= (p.Met90=) | |
| 15 | g.73329676A>C | CA393093766 | HCN4 | c.1487T>G (p.Met496Arg) c.269T>G (p.Met90Arg) | |
| 15 | g.73329676A>G | CA393093767 | HCN4 | c.1487T>C (p.Met496Thr) c.269T>C (p.Met90Thr) | dbSNP gnomAD v4 |
| 15 | g.73329676A>T | CA393093768 | HCN4 | c.1487T>A (p.Met496Lys) c.269T>A (p.Met90Lys) | |
| 15 | g.73329677T>A | CA393093770 | HCN4 | c.1486A>T (p.Met496Leu) c.268A>T (p.Met90Leu) | |
| 15 | g.73329677T>C | CA7649286 | HCN4 | c.1486A>G (p.Met496Val) c.268A>G (p.Met90Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 15 | g.73329677T>G | CA393093769 | HCN4 | c.1486A>C (p.Met496Leu) c.268A>C (p.Met90Leu) | |
| 15 | g.73329677T= | CA2187167513 | HCN4 | c.1486A= (p.Met496=) c.268A= (p.Met90=) | |
| 15 | g.73329678G>A | CA491151594 | HCN4 | c.1485C>T (p.Thr495=) c.267C>T (p.Thr89=) | |
| 15 | g.73329678G>C | CA491151596 | HCN4 | c.1485C>G (p.Thr495=) c.267C>G (p.Thr89=) | |
| 15 | g.73329678G>T | CA491151592 | HCN4 | c.1485C>A (p.Thr495=) c.267C>A (p.Thr89=) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329679G>A | CA393093771 | HCN4 | c.1484C>T (p.Thr495Ile) c.266C>T (p.Thr89Ile) | |
| 15 | g.73329679G>C | CA393093772 | HCN4 | c.1484C>G (p.Thr495Ser) c.266C>G (p.Thr89Ser) | |
| 15 | g.73329679G>T | CA393093773 | HCN4 | c.1484C>A (p.Thr495Asn) c.266C>A (p.Thr89Asn) | |
| 15 | g.73329680T>A | CA393093774 | HCN4 | c.1483A>T (p.Thr495Ser) c.265A>T (p.Thr89Ser) | |
| 15 | g.73329680T>C | CA393093775 | HCN4 | c.1483A>G (p.Thr495Ala) c.265A>G (p.Thr89Ala) | gnomAD v4 |
| 15 | g.73329680T>G | CA393093776 | HCN4 | c.1483A>C (p.Thr495Pro) c.265A>C (p.Thr89Pro) | |
| 15 | g.73329681G>A | CA272672050 | HCN4 | c.1482C>T (p.Leu494=) c.264C>T (p.Leu88=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329681G>C | CA491151603 | HCN4 | c.1482C>G (p.Leu494=) c.264C>G (p.Leu88=) | |
| 15 | g.73329681G= | CA2187167516 | HCN4 | c.1482C= (p.Leu494=) c.264C= (p.Leu88=) | |
| 15 | g.73329681G>T | CA491151605 | HCN4 | c.1482C>A (p.Leu494=) c.264C>A (p.Leu88=) | |
| 15 | g.73329682A>C | CA393093777 | HCN4 | c.1481T>G (p.Leu494Arg) c.263T>G (p.Leu88Arg) | |
| 15 | g.73329682A>G | CA393093778 | HCN4 | c.1481T>C (p.Leu494Pro) c.263T>C (p.Leu88Pro) | |
| 15 | g.73329682A>T | CA393093779 | HCN4 | c.1481T>A (p.Leu494His) c.263T>A (p.Leu88His) | |
| 15 | g.73329683G>A | CA393093780 | HCN4 | c.1480C>T (p.Leu494Phe) c.262C>T (p.Leu88Phe) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329683G>C | CA393093781 | HCN4 | c.1480C>G (p.Leu494Val) c.262C>G (p.Leu88Val) | |
| 15 | g.73329683G>T | CA393093782 | HCN4 | c.1480C>A (p.Leu494Ile) c.262C>A (p.Leu88Ile) | |
| 15 | g.73329684C>A | CA393093785 | HCN4 | c.1479G>T (p.Trp493Cys) c.261G>T (p.Trp87Cys) | gnomAD v4 |
| 15 | g.73329684C>G | CA393093784 | HCN4 | c.1479G>C (p.Trp493Cys) c.261G>C (p.Trp87Cys) | |
| 15 | g.73329684C>T | CA393093783 | HCN4 | c.1479G>A (p.Trp493Ter) c.261G>A (p.Trp87Ter) | gnomAD v4 |
| 15 | g.73329685C>A | CA393093786 | HCN4 | c.1478G>T (p.Trp493Leu) c.260G>T (p.Trp87Leu) | |
| 15 | g.73329685C>G | CA393093787 | HCN4 | c.1478G>C (p.Trp493Ser) c.260G>C (p.Trp87Ser) | |
| 15 | g.73329685C>T | CA393093788 | HCN4 | c.1478G>A (p.Trp493Ter) c.260G>A (p.Trp87Ter) | gnomAD v4 |
| 15 | g.73329686A>C | CA393093789 | HCN4 | c.1477T>G (p.Trp493Gly) c.259T>G (p.Trp87Gly) | |
| 15 | g.73329686A>G | CA393093790 | HCN4 | c.1477T>C (p.Trp493Arg) c.259T>C (p.Trp87Arg) | |
| 15 | g.73329686A>T | CA393093791 | HCN4 | c.1477T>A (p.Trp493Arg) c.259T>A (p.Trp87Arg) | |
| 15 | g.73329687G>A | CA491151625 | HCN4 | c.1476C>T (p.Val492=) c.258C>T (p.Val86=) | dbSNP |
| 15 | g.73329687G>C | CA491151627 | HCN4 | c.1476C>G (p.Val492=) c.258C>G (p.Val86=) | |
| 15 | g.73329687G= | CA2187167519 | HCN4 | c.1476C= (p.Val492=) c.258C= (p.Val86=) | |
| 15 | g.73329687G>T | CA491151629 | HCN4 | c.1476C>A (p.Val492=) c.258C>A (p.Val86=) | |
| 15 | g.73329688A>C | CA393093792 | HCN4 | c.1475T>G (p.Val492Gly) c.257T>G (p.Val86Gly) | |
| 15 | g.73329688A>G | CA393093793 | HCN4 | c.1475T>C (p.Val492Ala) c.257T>C (p.Val86Ala) | |
| 15 | g.73329688A>T | CA393093794 | HCN4 | c.1475T>A (p.Val492Asp) c.257T>A (p.Val86Asp) | |
| 15 | g.73329689C>A | CA393093795 | HCN4 | c.1474G>T (p.Val492Phe) c.256G>T (p.Val86Phe) | |
| 15 | g.73329689C= | CA2187167522 | HCN4 | c.1474G= (p.Val492=) c.256G= (p.Val86=) | |
| 15 | g.73329689C>G | CA393093796 | HCN4 | c.1474G>C (p.Val492Leu) c.256G>C (p.Val86Leu) | |
| 15 | g.73329689C>T | CA7649287 | HCN4 | c.1474G>A (p.Val492Ile) c.256G>A (p.Val86Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73329690G>A | CA7649288 | HCN4 | c.1473C>T (p.Asp491=) c.255C>T (p.Asp85=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329690G>C | CA393093798 | HCN4 | c.1473C>G (p.Asp491Glu) c.255C>G (p.Asp85Glu) | |
| 15 | g.73329690G= | CA2187167528 | HCN4 | c.1473C= (p.Asp491=) c.255C= (p.Asp85=) | |
| 15 | g.73329690G>T | CA393093797 | HCN4 | c.1473C>A (p.Asp491Glu) c.255C>A (p.Asp85Glu) | |
| 15 | g.73329691T>A | CA393093799 | HCN4 | c.1472A>T (p.Asp491Val) c.254A>T (p.Asp85Val) | |
| 15 | g.73329691T>C | CA393093800 | HCN4 | c.1472A>G (p.Asp491Gly) c.254A>G (p.Asp85Gly) | |
| 15 | g.73329691T>G | CA393093801 | HCN4 | c.1472A>C (p.Asp491Ala) c.254A>C (p.Asp85Ala) | |
| 15 | g.73329692C>A | CA393093802 | HCN4 | c.1471G>T (p.Asp491Tyr) c.253G>T (p.Asp85Tyr) | |
| 15 | g.73329692C= | CA2187167535 | HCN4 | c.1471G= (p.Asp491=) c.253G= (p.Asp85=) | |
| 15 | g.73329692C>G | CA393093803 | HCN4 | c.1471G>C (p.Asp491His) c.253G>C (p.Asp85His) | ClinVar dbSNP |
| 15 | g.73329692C>T | CA16614921 | HCN4 | c.1471G>A (p.Asp491Asn) c.253G>A (p.Asp85Asn) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73329693G>A | CA7649289 | HCN4 | c.1470C>T (p.Ser490=) c.252C>T (p.Ser84=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329693G>C | CA491151649 | HCN4 | c.1470C>G (p.Ser490=) c.252C>G (p.Ser84=) | |
| 15 | g.73329693G= | CA2187167541 | HCN4 | c.1470C= (p.Ser490=) c.252C= (p.Ser84=) | |
| 15 | g.73329693G>T | CA491151651 | HCN4 | c.1470C>A (p.Ser490=) c.252C>A (p.Ser84=) | |
| 15 | g.73329694G>A | CA393093806 | HCN4 | c.1469C>T (p.Ser490Phe) c.251C>T (p.Ser84Phe) | |
| 15 | g.73329694G>C | CA393093804 | HCN4 | c.1469C>G (p.Ser490Cys) c.251C>G (p.Ser84Cys) | |
| 15 | g.73329694G>T | CA393093805 | HCN4 | c.1469C>A (p.Ser490Tyr) c.251C>A (p.Ser84Tyr) | |
| 15 | g.73329695A>C | CA393093807 | HCN4 | c.1468T>G (p.Ser490Ala) c.250T>G (p.Ser84Ala) | |
| 15 | g.73329695A>G | CA393093808 | HCN4 | c.1468T>C (p.Ser490Pro) c.250T>C (p.Ser84Pro) | |
| 15 | g.73329695A>T | CA393093810 | HCN4 | c.1468T>A (p.Ser490Thr) c.250T>A (p.Ser84Thr) | |
| 15 | g.73329696C>A | CA393093812 | HCN4 | c.1467G>T (p.Met489Ile) c.249G>T (p.Met83Ile) | |
| 15 | g.73329696C= | CA2187167544 | HCN4 | c.1467G= (p.Met489=) c.249G= (p.Met83=) | |
| 15 | g.73329696C>G | CA393093814 | HCN4 | c.1467G>C (p.Met489Ile) c.249G>C (p.Met83Ile) | |
| 15 | g.73329696C>T | CA7649290 | HCN4 | c.1467G>A (p.Met489Ile) c.249G>A (p.Met83Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329697A>C | CA393093817 | HCN4 | c.1466T>G (p.Met489Arg) c.248T>G (p.Met83Arg) | |
| 15 | g.73329697A>G | CA393093821 | HCN4 | c.1466T>C (p.Met489Thr) c.248T>C (p.Met83Thr) | gnomAD v4 |
| 15 | g.73329697A>T | CA393093819 | HCN4 | c.1466T>A (p.Met489Lys) c.248T>A (p.Met83Lys) | |
| 15 | g.73329698T>A | CA393093823 | HCN4 | c.1465A>T (p.Met489Leu) c.247A>T (p.Met83Leu) | |
| 15 | g.73329698T>C | CA393093825 | HCN4 | c.1465A>G (p.Met489Val) c.247A>G (p.Met83Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329698T>G | CA393093827 | HCN4 | c.1465A>C (p.Met489Leu) c.247A>C (p.Met83Leu) | |
| 15 | g.73329698T= | CA2187167548 | HCN4 | c.1465A= (p.Met489=) c.247A= (p.Met83=) | |
| 15 | g.73329699G>A | CA491151671 | HCN4 | c.1464C>T (p.Gly488=) c.246C>T (p.Gly82=) | |
| 15 | g.73329699G>C | CA491151669 | HCN4 | c.1464C>G (p.Gly488=) c.246C>G (p.Gly82=) | |
| 15 | g.73329699G>T | CA491151668 | HCN4 | c.1464C>A (p.Gly488=) c.246C>A (p.Gly82=) | |
| 15 | g.73329700C>A | CA393093829 | HCN4 | c.1463G>T (p.Gly488Val) c.245G>T (p.Gly82Val) | |
| 15 | g.73329700C>G | CA393093831 | HCN4 | c.1463G>C (p.Gly488Ala) c.245G>C (p.Gly82Ala) | |
| 15 | g.73329700C>T | CA393093833 | HCN4 | c.1463G>A (p.Gly488Asp) c.245G>A (p.Gly82Asp) | gnomAD v4 |
| 15 | g.73329701C>A | CA393093835 | HCN4 | c.1462G>T (p.Gly488Cys) c.244G>T (p.Gly82Cys) | |
| 15 | g.73329701C= | CA2187167554 | HCN4 | c.1462G= (p.Gly488=) c.244G= (p.Gly82=) | |
| 15 | g.73329701C>G | CA393093836 | HCN4 | c.1462G>C (p.Gly488Arg) c.244G>C (p.Gly82Arg) | |
| 15 | g.73329701C>T | CA10604722 | HCN4 | c.1462G>A (p.Gly488Ser) c.244G>A (p.Gly82Ser) | ClinVar dbSNP |
| 15 | g.73329702C>A | CA491151679 | HCN4 | c.1461G>T (p.Val487=) c.243G>T (p.Val81=) | |
| 15 | g.73329702C>G | CA491151681 | HCN4 | c.1461G>C (p.Val487=) c.243G>C (p.Val81=) | |
| 15 | g.73329702C>T | CA491151683 | HCN4 | c.1461G>A (p.Val487=) c.243G>A (p.Val81=) | gnomAD v4 |
| 15 | g.73329703A>C | CA393093840 | HCN4 | c.1460T>G (p.Val487Gly) c.242T>G (p.Val81Gly) | |
| 15 | g.73329703A>G | CA393093842 | HCN4 | c.1460T>C (p.Val487Ala) c.242T>C (p.Val81Ala) | |
| 15 | g.73329703A>T | CA393093843 | HCN4 | c.1460T>A (p.Val487Glu) c.242T>A (p.Val81Glu) | |
| 15 | g.73329704C>A | CA393093845 | HCN4 | c.1459G>T (p.Val487Leu) c.241G>T (p.Val81Leu) | |
| 15 | g.73329704C= | CA2187167560 | HCN4 | c.1459G= (p.Val487=) c.241G= (p.Val81=) | |
| 15 | g.73329704C>G | CA393093848 | HCN4 | c.1459G>C (p.Val487Leu) c.241G>C (p.Val81Leu) | |
| 15 | g.73329704C>T | CA234114 | HCN4 | c.1459G>A (p.Val487Met) c.241G>A (p.Val81Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329705G>A | CA7649291 | HCN4 | c.1458C>T (p.Pro486=) c.240C>T (p.Pro80=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329705G>C | CA491151694 | HCN4 | c.1458C>G (p.Pro486=) c.240C>G (p.Pro80=) | gnomAD v4 |
| 15 | g.73329705G= | CA2187167569 | HCN4 | c.1458C= (p.Pro486=) c.240C= (p.Pro80=) | |
| 15 | g.73329705G>T | CA491151695 | HCN4 | c.1458C>A (p.Pro486=) c.240C>A (p.Pro80=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329706G>A | CA393093852 | HCN4 | c.1457C>T (p.Pro486Leu) c.239C>T (p.Pro80Leu) | gnomAD v4 |
| 15 | g.73329706G>C | CA393093853 | HCN4 | c.1457C>G (p.Pro486Arg) c.239C>G (p.Pro80Arg) | |
| 15 | g.73329706G>T | CA393093855 | HCN4 | c.1457C>A (p.Pro486His) c.239C>A (p.Pro80His) | |
| 15 | g.73329707G>A | CA393093858 | HCN4 | c.1456C>T (p.Pro486Ser) c.238C>T (p.Pro80Ser) | ClinVar dbSNP |
| 15 | g.73329707G>C | CA393093860 | HCN4 | c.1456C>G (p.Pro486Ala) c.238C>G (p.Pro80Ala) | |
| 15 | g.73329707G>T | CA393093862 | HCN4 | c.1456C>A (p.Pro486Thr) c.238C>A (p.Pro80Thr) | |
| 15 | g.73329708C>A | CA491151703 | HCN4 | c.1455G>T (p.Ala485=) c.237G>T (p.Ala79=) | ClinVar dbSNP |
| 15 | g.73329708C= | CA2187167577 | HCN4 | c.1455G= (p.Ala485=) c.237G= (p.Ala79=) | |
| 15 | g.73329708C>G | CA491151704 | HCN4 | c.1455G>C (p.Ala485=) c.237G>C (p.Ala79=) | COSMIC |
| 15 | g.73329708C>T | CA7649292 | HCN4 | c.1455G>A (p.Ala485=) c.237G>A (p.Ala79=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73329709G>A | CA393093865 | HCN4 | c.1454C>T (p.Ala485Val) c.236C>T (p.Ala79Val) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73329709G>C | CA393093867 | HCN4 | c.1454C>G (p.Ala485Gly) c.236C>G (p.Ala79Gly) | gnomAD v4 |
| 15 | g.73329709G= | CA2187167582 | HCN4 | c.1454C= (p.Ala485=) c.236C= (p.Ala79=) | |
| 15 | g.73329709G>T | CA393093869 | HCN4 | c.1454C>A (p.Ala485Glu) c.236C>A (p.Ala79Glu) | |
| 15 | g.73329710C>A | CA393093870 | HCN4 | c.1453G>T (p.Ala485Ser) c.235G>T (p.Ala79Ser) | |
| 15 | g.73329710C>G | CA393093872 | HCN4 | c.1453G>C (p.Ala485Pro) c.235G>C (p.Ala79Pro) | COSMIC |
| 15 | g.73329710C>T | CA393093873 | HCN4 | c.1453G>A (p.Ala485Thr) c.235G>A (p.Ala79Thr) | |
| 15 | g.73329711C>A | CA393093876 | HCN4 | c.1452G>T (p.Gln484His) c.234G>T (p.Gln78His) | |
| 15 | g.73329711C>G | CA393093878 | HCN4 | c.1452G>C (p.Gln484His) c.234G>C (p.Gln78His) | |
| 15 | g.73329711C>T | CA491151717 | HCN4 | c.1452G>A (p.Gln484=) c.234G>A (p.Gln78=) | |
| 15 | g.73329711_73329727delinsCTGCCGCCCGTAGCCGA | CA2187167585 | HCN4 | c.1436_1452delinsTCGGCTACGGGCGGCAG (p.Ile479=) c.218_234delinsTCGGCTACGGGCGGCAG (p.Ile73=) | |
| 15 | g.73329712T>A | CA393093880 | HCN4 | c.1451A>T (p.Gln484Leu) c.233A>T (p.Gln78Leu) | |
| 15 | g.73329712T>C | CA393093882 | HCN4 | c.1451A>G (p.Gln484Arg) c.233A>G (p.Gln78Arg) | |
| 15 | g.73329712T>G | CA393093884 | HCN4 | c.1451A>C (p.Gln484Pro) c.233A>C (p.Gln78Pro) | |
| 15 | g.73329715_73329730del | CA619410697 | HCN4 | c.1436_1451del (p.Ile479ArgfsTer16) c.218_233del (p.Ile73ArgfsTer16) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329713G>A | CA393093886 | HCN4 | c.1450C>T (p.Gln484Ter) c.232C>T (p.Gln78Ter) | |
| 15 | g.73329713G>C | CA393093888 | HCN4 | c.1450C>G (p.Gln484Glu) c.232C>G (p.Gln78Glu) | dbSNP |
| 15 | g.73329713G= | CA2187167590 | HCN4 | c.1450C= (p.Gln484=) c.232C= (p.Gln78=) | |
| 15 | g.73329713G>T | CA393093890 | HCN4 | c.1450C>A (p.Gln484Lys) c.232C>A (p.Gln78Lys) | |
| 15 | g.73329714C>A | CA491151725 | HCN4 | c.1449G>T (p.Arg483=) c.231G>T (p.Arg77=) | gnomAD v4 |
| 15 | g.73329714C= | CA2187167592 | HCN4 | c.1449G= (p.Arg483=) c.231G= (p.Arg77=) | |
| 15 | g.73329714C>G | CA491151727 | HCN4 | c.1449G>C (p.Arg483=) c.231G>C (p.Arg77=) | |
| 15 | g.73329714C>T | CA491151729 | HCN4 | c.1449G>A (p.Arg483=) c.231G>A (p.Arg77=) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329715C>A | CA393093892 | HCN4 | c.1448G>T (p.Arg483Leu) c.230G>T (p.Arg77Leu) | |
| 15 | g.73329715C= | CA2187167596 | HCN4 | c.1448G= (p.Arg483=) c.230G= (p.Arg77=) | |
| 15 | g.73329715C>G | CA393093894 | HCN4 | c.1448G>C (p.Arg483Pro) c.230G>C (p.Arg77Pro) | |
| 15 | g.73329715C>T | CA272672089 | HCN4 | c.1448G>A (p.Arg483Gln) c.230G>A (p.Arg77Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73329716G>A | CA393093899 | HCN4 | c.1447C>T (p.Arg483Trp) c.229C>T (p.Arg77Trp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329716G>C | CA393093900 | HCN4 | c.1447C>G (p.Arg483Gly) c.229C>G (p.Arg77Gly) | |
| 15 | g.73329716G= | CA2187167600 | HCN4 | c.1447C= (p.Arg483=) c.229C= (p.Arg77=) | |
| 15 | g.73329716G>T | CA491151736 | HCN4 | c.1447C>A (p.Arg483=) c.229C>A (p.Arg77=) | |
| 15 | g.73329717C>A | CA491151738 | HCN4 | c.1446G>T (p.Gly482=) c.228G>T (p.Gly76=) | |
| 15 | g.73329717C>G | CA491151740 | HCN4 | c.1446G>C (p.Gly482=) c.228G>C (p.Gly76=) | |
| 15 | g.73329717C>T | CA491151742 | HCN4 | c.1446G>A (p.Gly482=) c.228G>A (p.Gly76=) | |
| 15 | g.73329718C>A | CA393093903 | HCN4 | c.1445G>T (p.Gly482Val) c.227G>T (p.Gly76Val) | |
| 15 | g.73329718C>G | CA393093906 | HCN4 | c.1445G>C (p.Gly482Ala) c.227G>C (p.Gly76Ala) | |
| 15 | g.73329718C>T | CA393093905 | HCN4 | c.1445G>A (p.Gly482Glu) c.227G>A (p.Gly76Glu) | ClinVar dbSNP |
| 15 | g.73329719C>A | CA393093909 | HCN4 | c.1444G>T (p.Gly482Trp) c.226G>T (p.Gly76Trp) | |
| 15 | g.73329719C= | CA2187167606 | HCN4 | c.1444G= (p.Gly482=) c.226G= (p.Gly76=) | |
| 15 | g.73329719C>G | CA16043942 | HCN4 | c.1444G>C (p.Gly482Arg) c.226G>C (p.Gly76Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329719C>T | CA202778 | HCN4 | c.1444G>A (p.Gly482Arg) c.226G>A (p.Gly76Arg) | ClinVar dbSNP |
| 15 | g.73329720G>A | CA7649293 | HCN4 | c.1443C>T (p.Tyr481=) c.225C>T (p.Tyr75=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329720G>C | CA393093913 | HCN4 | c.1443C>G (p.Tyr481Ter) c.225C>G (p.Tyr75Ter) | |
| 15 | g.73329720G= | CA2187167618 | HCN4 | c.1443C= (p.Tyr481=) c.225C= (p.Tyr75=) | |
| 15 | g.73329720G>T | CA393093915 | HCN4 | c.1443C>A (p.Tyr481Ter) c.225C>A (p.Tyr75Ter) | dbSNP gnomAD v2 gnomAD v4 |
| 15 | g.73329720_73329721delinsCA | CA2580089965 | HCN4 | c.1442_1443delinsTG (p.Tyr481Leu) c.224_225delinsTG (p.Tyr75Leu) | ClinVar |
| 15 | g.73329721T>A | CA393093917 | HCN4 | c.1442A>T (p.Tyr481Phe) c.224A>T (p.Tyr75Phe) | |
| 15 | g.73329721T>C | CA393093919 | HCN4 | c.1442A>G (p.Tyr481Cys) c.224A>G (p.Tyr75Cys) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329721T>G | CA393093921 | HCN4 | c.1442A>C (p.Tyr481Ser) c.224A>C (p.Tyr75Ser) | |
| 15 | g.73329722A= | CA2187167624 | HCN4 | c.1441T= (p.Tyr481=) c.223T= (p.Tyr75=) | |
| 15 | g.73329722A>C | CA393093923 | HCN4 | c.1441T>G (p.Tyr481Asp) c.223T>G (p.Tyr75Asp) | |
| 15 | g.73329722A>G | CA16043943 | HCN4 | c.1441T>C (p.Tyr481His) c.223T>C (p.Tyr75His) | ClinVar dbSNP |
| 15 | g.73329722A>T | CA393093925 | HCN4 | c.1441T>A (p.Tyr481Asn) c.223T>A (p.Tyr75Asn) | |
| 15 | g.73329723G>A | CA491151767 | HCN4 | c.1440C>T (p.Gly480=) c.222C>T (p.Gly74=) | |
| 15 | g.73329723G>C | CA491151763 | HCN4 | c.1440C>G (p.Gly480=) c.222C>G (p.Gly74=) | |
| 15 | g.73329723G>T | CA491151765 | HCN4 | c.1440C>A (p.Gly480=) c.222C>A (p.Gly74=) | gnomAD v4 |
| 15 | g.73329724C>A | CA16614737 | HCN4 | c.1439G>T (p.Gly480Val) c.221G>T (p.Gly74Val) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329724C= | CA2187167629 | HCN4 | c.1439G= (p.Gly480=) c.221G= (p.Gly74=) | |
| 15 | g.73329724C>G | CA393093928 | HCN4 | c.1439G>C (p.Gly480Ala) c.221G>C (p.Gly74Ala) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329724C>T | CA393093930 | HCN4 | c.1439G>A (p.Gly480Asp) c.221G>A (p.Gly74Asp) | |
| 15 | g.73329725C>A | CA393093937 | HCN4 | c.1438G>T (p.Gly480Cys) c.220G>T (p.Gly74Cys) | COSMIC |
| 15 | g.73329725C= | CA2187167635 | HCN4 | c.1438G= (p.Gly480=) c.220G= (p.Gly74=) | |
| 15 | g.73329725C>G | CA117313 | HCN4 | c.1438G>C (p.Gly480Arg) c.220G>C (p.Gly74Arg) | ClinVar dbSNP |
| 15 | g.73329725C>T | CA393093935 | HCN4 | c.1438G>A (p.Gly480Ser) c.220G>A (p.Gly74Ser) | ClinVar dbSNP gnomAD v4 COSMIC |
| 15 | g.73329726G>A | CA7649294 | HCN4 | c.1437C>T (p.Ile479=) c.219C>T (p.Ile73=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329726G>C | CA393093940 | HCN4 | c.1437C>G (p.Ile479Met) c.219C>G (p.Ile73Met) | |
| 15 | g.73329726G= | CA2187167641 | HCN4 | c.1437C= (p.Ile479=) c.219C= (p.Ile73=) | |
| 15 | g.73329726G>T | CA491151777 | HCN4 | c.1437C>A (p.Ile479=) c.219C>A (p.Ile73=) | |
| 15 | g.73329727A>C | CA393093943 | HCN4 | c.1436T>G (p.Ile479Ser) c.218T>G (p.Ile73Ser) | |
| 15 | g.73329727A>G | CA393093945 | HCN4 | c.1436T>C (p.Ile479Thr) c.218T>C (p.Ile73Thr) | |
| 15 | g.73329727A>T | CA393093947 | HCN4 | c.1436T>A (p.Ile479Asn) c.218T>A (p.Ile73Asn) | |
| 15 | g.73329728T>A | CA393093949 | HCN4 | c.1435A>T (p.Ile479Phe) c.217A>T (p.Ile73Phe) | |
| 15 | g.73329728T>C | CA393093950 | HCN4 | c.1435A>G (p.Ile479Val) c.217A>G (p.Ile73Val) | gnomAD v4 |
| 15 | g.73329728T>G | CA393093951 | HCN4 | c.1435A>C (p.Ile479Leu) c.217A>C (p.Ile73Leu) | ClinVar dbSNP |
| 15 | g.73329728T= | CA2187167646 | HCN4 | c.1435A= (p.Ile479=) c.217A= (p.Ile73=) | |
| 15 | g.73329729G>A | CA272672110 | HCN4 | c.1434C>T (p.Cys478=) c.216C>T (p.Cys72=) | dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329729G>C | CA393093952 | HCN4 | c.1434C>G (p.Cys478Trp) c.216C>G (p.Cys72Trp) | |
| 15 | g.73329729G= | CA2187167649 | HCN4 | c.1434C= (p.Cys478=) c.216C= (p.Cys72=) | |
| 15 | g.73329729G>T | CA393093954 | HCN4 | c.1434C>A (p.Cys478Ter) c.216C>A (p.Cys72Ter) | |
| 15 | g.73329730C>A | CA393093961 | HCN4 | c.1433G>T (p.Cys478Phe) c.215G>T (p.Cys72Phe) | |
| 15 | g.73329730C>G | CA393093959 | HCN4 | c.1433G>C (p.Cys478Ser) c.215G>C (p.Cys72Ser) | |
| 15 | g.73329730C>T | CA393093957 | HCN4 | c.1433G>A (p.Cys478Tyr) c.215G>A (p.Cys72Tyr) | ClinVar |
| 15 | g.73329731A>C | CA393093962 | HCN4 | c.1432T>G (p.Cys478Gly) c.214T>G (p.Cys72Gly) | |
| 15 | g.73329731A>G | CA393093964 | HCN4 | c.1432T>C (p.Cys478Arg) c.214T>C (p.Cys72Arg) | |
| 15 | g.73329731A>T | CA393093967 | HCN4 | c.1432T>A (p.Cys478Ser) c.214T>A (p.Cys72Ser) | gnomAD v4 |
| 15 | g.73329732C>A | CA491151797 | HCN4 | c.1431G>T (p.Leu477=) c.213G>T (p.Leu71=) | |
| 15 | g.73329732C>G | CA491151799 | HCN4 | c.1431G>C (p.Leu477=) c.213G>C (p.Leu71=) | |
| 15 | g.73329732C>T | CA491151801 | HCN4 | c.1431G>A (p.Leu477=) c.213G>A (p.Leu71=) | gnomAD v4 |
| 15 | g.73329733A>C | CA393093969 | HCN4 | c.1430T>G (p.Leu477Arg) c.212T>G (p.Leu71Arg) | |
| 15 | g.73329733A>G | CA393093971 | HCN4 | c.1430T>C (p.Leu477Pro) c.212T>C (p.Leu71Pro) | ClinVar |
| 15 | g.73329733A>T | CA393093973 | HCN4 | c.1430T>A (p.Leu477Gln) c.212T>A (p.Leu71Gln) | |
| 15 | g.73329734G>A | CA491151808 | HCN4 | c.1429C>T (p.Leu477=) c.211C>T (p.Leu71=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 15 | g.73329734G>C | CA393093977 | HCN4 | c.1429C>G (p.Leu477Val) c.211C>G (p.Leu71Val) | |
| 15 | g.73329734G= | CA2187167653 | HCN4 | c.1429C= (p.Leu477=) c.211C= (p.Leu71=) | |
| 15 | g.73329734G>T | CA393093975 | HCN4 | c.1429C>A (p.Leu477Met) c.211C>A (p.Leu71Met) | |
| 15 | g.73329735C>A | CA393093980 | HCN4 | c.1428G>T (p.Met476Ile) c.210G>T (p.Met70Ile) | |
| 15 | g.73329735C>G | CA393093982 | HCN4 | c.1428G>C (p.Met476Ile) c.210G>C (p.Met70Ile) | |
| 15 | g.73329735C>T | CA393093983 | HCN4 | c.1428G>A (p.Met476Ile) c.210G>A (p.Met70Ile) | |
| 15 | g.73329736A>C | CA393093985 | HCN4 | c.1427T>G (p.Met476Arg) c.209T>G (p.Met70Arg) | |
| 15 | g.73329736A>G | CA393093987 | HCN4 | c.1427T>C (p.Met476Thr) c.209T>C (p.Met70Thr) | ClinVar |
| 15 | g.73329736A>T | CA393093990 | HCN4 | c.1427T>A (p.Met476Lys) c.209T>A (p.Met70Lys) | |
| 15 | g.73329737T>A | CA393093992 | HCN4 | c.1426A>T (p.Met476Leu) c.208A>T (p.Met70Leu) | |
| 15 | g.73329737T>C | CA393093996 | HCN4 | c.1426A>G (p.Met476Val) c.208A>G (p.Met70Val) | |
| 15 | g.73329737T>G | CA393093994 | HCN4 | c.1426A>C (p.Met476Leu) c.208A>C (p.Met70Leu) | |
| 15 | g.73329738G>A | CA491151823 | HCN4 | c.1425C>T (p.His475=) c.207C>T (p.His69=) | |
| 15 | g.73329738G>C | CA393093998 | HCN4 | c.1425C>G (p.His475Gln) c.207C>G (p.His69Gln) | |
| 15 | g.73329738G>T | CA393094000 | HCN4 | c.1425C>A (p.His475Gln) c.207C>A (p.His69Gln) | |
| 15 | g.73329739T>A | CA393094001 | HCN4 | c.1424A>T (p.His475Leu) c.206A>T (p.His69Leu) | |
| 15 | g.73329739T>C | CA393094002 | HCN4 | c.1424A>G (p.His475Arg) c.206A>G (p.His69Arg) | ClinVar dbSNP |
| 15 | g.73329739T>G | CA393094003 | HCN4 | c.1424A>C (p.His475Pro) c.206A>C (p.His69Pro) | |
| 15 | g.73329739T= | CA2187167657 | HCN4 | c.1424A= (p.His475=) c.206A= (p.His69=) | |
| 15 | g.73329740G>A | CA393094004 | HCN4 | c.1423C>T (p.His475Tyr) c.205C>T (p.His69Tyr) | |
| 15 | g.73329740G>C | CA393094006 | HCN4 | c.1423C>G (p.His475Asp) c.205C>G (p.His69Asp) | |
| 15 | g.73329740G>T | CA393094008 | HCN4 | c.1423C>A (p.His475Asn) c.205C>A (p.His69Asn) | |
| 15 | g.73329741G>A | CA491151835 | HCN4 | c.1422C>T (p.Ser474=) c.204C>T (p.Ser68=) | |
| 15 | g.73329741G>C | CA393094010 | HCN4 | c.1422C>G (p.Ser474Arg) c.204C>G (p.Ser68Arg) | |
| 15 | g.73329741G>T | CA393094012 | HCN4 | c.1422C>A (p.Ser474Arg) c.204C>A (p.Ser68Arg) | |
| 15 | g.73329742C>A | CA393094017 | HCN4 | c.1421G>T (p.Ser474Ile) c.203G>T (p.Ser68Ile) | |
| 15 | g.73329742C>G | CA393094016 | HCN4 | c.1421G>C (p.Ser474Thr) c.203G>C (p.Ser68Thr) | |
| 15 | g.73329742C>T | CA393094015 | HCN4 | c.1421G>A (p.Ser474Asn) c.203G>A (p.Ser68Asn) | ClinVar dbSNP |
| 15 | g.73329743T>A | CA393094019 | HCN4 | c.1420A>T (p.Ser474Cys) c.202A>T (p.Ser68Cys) | |
| 15 | g.73329743T>C | CA393094021 | HCN4 | c.1420A>G (p.Ser474Gly) c.202A>G (p.Ser68Gly) | |
| 15 | g.73329743T>G | CA393094020 | HCN4 | c.1420A>C (p.Ser474Arg) c.202A>C (p.Ser68Arg) | |
| 15 | g.73329744C>A | CA393094023 | HCN4 | c.1419G>T (p.Met473Ile) c.201G>T (p.Met67Ile) | |
| 15 | g.73329744C= | CA2187167662 | HCN4 | c.1419G= (p.Met473=) c.201G= (p.Met67=) | |
| 15 | g.73329744C>G | CA393094025 | HCN4 | c.1419G>C (p.Met473Ile) c.201G>C (p.Met67Ile) | |
| 15 | g.73329744C>T | CA16614922 | HCN4 | c.1419G>A (p.Met473Ile) c.201G>A (p.Met67Ile) | ClinVar dbSNP gnomAD v4 |
| 15 | g.73329745A= | CA2187167665 | HCN4 | c.1418T= (p.Met473=) c.200T= (p.Met67=) | |
| 15 | g.73329745A>C | CA393094027 | HCN4 | c.1418T>G (p.Met473Arg) c.200T>G (p.Met67Arg) | |
| 15 | g.73329745A>G | CA393094029 | HCN4 | c.1418T>C (p.Met473Thr) c.200T>C (p.Met67Thr) | ClinVar dbSNP |
| 15 | g.73329745A>T | CA393094031 | HCN4 | c.1418T>A (p.Met473Lys) c.200T>A (p.Met67Lys) | |
| 15 | g.73329746T>A | CA393094034 | HCN4 | c.1417A>T (p.Met473Leu) c.199A>T (p.Met67Leu) | |
| 15 | g.73329746T>C | CA393094033 | HCN4 | c.1417A>G (p.Met473Val) c.199A>G (p.Met67Val) | ClinVar gnomAD v4 |
| 15 | g.73329746T>G | CA393094032 | HCN4 | c.1417A>C (p.Met473Leu) c.199A>C (p.Met67Leu) | |
| 15 | g.73329747G>A | CA491151859 | HCN4 | c.1416C>T (p.Ala472=) c.198C>T (p.Ala66=) | |
| 15 | g.73329747G>C | CA491151855 | HCN4 | c.1416C>G (p.Ala472=) c.198C>G (p.Ala66=) | |
| 15 | g.73329747G>T | CA491151857 | HCN4 | c.1416C>A (p.Ala472=) c.198C>A (p.Ala66=) | |
| 15 | g.73329748G>A | CA393094035 | HCN4 | c.1415C>T (p.Ala472Val) c.197C>T (p.Ala66Val) | gnomAD v4 |
| 15 | g.73329748G>C | CA393094036 | HCN4 | c.1415C>G (p.Ala472Gly) c.197C>G (p.Ala66Gly) | |
| 15 | g.73329748G>T | CA393094037 | HCN4 | c.1415C>A (p.Ala472Asp) c.197C>A (p.Ala66Asp) | |
| 15 | g.73329749C>A | CA393094043 | HCN4 | c.1414G>T (p.Ala472Ser) c.196G>T (p.Ala66Ser) | |
| 15 | g.73329749C>G | CA393094045 | HCN4 | c.1414G>C (p.Ala472Pro) c.196G>C (p.Ala66Pro) | |
| 15 | g.73329749C>T | CA393094046 | HCN4 | c.1414G>A (p.Ala472Thr) c.196G>A (p.Ala66Thr) | ClinVar |
| 15 | g.73329750C>A | CA393094048 | HCN4 | c.1413G>T (p.Lys471Asn) c.195G>T (p.Lys65Asn) | COSMIC |
| 15 | g.73329750C= | CA2187167667 | HCN4 | c.1413G= (p.Lys471=) c.195G= (p.Lys65=) | |
| 15 | g.73329750C>G | CA393094050 | HCN4 | c.1413G>C (p.Lys471Asn) c.195G>C (p.Lys65Asn) | gnomAD v4 |
| 15 | g.73329750C>T | CA7649295 | HCN4 | c.1413G>A (p.Lys471=) c.195G>A (p.Lys65=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329751T>A | CA393094051 | HCN4 | c.1412A>T (p.Lys471Met) c.194A>T (p.Lys65Met) | dbSNP |
| 15 | g.73329751T>C | CA393094052 | HCN4 | c.1412A>G (p.Lys471Arg) c.194A>G (p.Lys65Arg) | |
| 15 | g.73329751T>G | CA272672130 | HCN4 | c.1412A>C (p.Lys471Thr) c.194A>C (p.Lys65Thr) | dbSNP |
| 15 | g.73329751T= | CA2187167668 | HCN4 | c.1412A= (p.Lys471=) c.194A= (p.Lys65=) | |
| 15 | g.73329752T>A | CA393094054 | HCN4 | c.1411A>T (p.Lys471Ter) c.193A>T (p.Lys65Ter) | |
| 15 | g.73329752T>C | CA393094056 | HCN4 | c.1411A>G (p.Lys471Glu) c.193A>G (p.Lys65Glu) | |
| 15 | g.73329752T>G | CA393094058 | HCN4 | c.1411A>C (p.Lys471Gln) c.193A>C (p.Lys65Gln) | |
| 15 | g.73329753G>A | CA491151878 | HCN4 | c.1410C>T (p.Phe470=) c.192C>T (p.Phe64=) | gnomAD v4 |
| 15 | g.73329753G>C | CA393094059 | HCN4 | c.1410C>G (p.Phe470Leu) c.192C>G (p.Phe64Leu) | |
| 15 | g.73329753G>T | CA393094061 | HCN4 | c.1410C>A (p.Phe470Leu) c.192C>A (p.Phe64Leu) | |
| 15 | g.73329754A>C | CA393094063 | HCN4 | c.1409T>G (p.Phe470Cys) c.191T>G (p.Phe64Cys) | |
| 15 | g.73329754A>G | CA393094065 | HCN4 | c.1409T>C (p.Phe470Ser) c.191T>C (p.Phe64Ser) | |
| 15 | g.73329754A>T | CA393094067 | HCN4 | c.1409T>A (p.Phe470Tyr) c.191T>A (p.Phe64Tyr) | |
| 15 | g.73329755A>C | CA393094070 | HCN4 | c.1408T>G (p.Phe470Val) c.190T>G (p.Phe64Val) | |
| 15 | g.73329755A>G | CA393094073 | HCN4 | c.1408T>C (p.Phe470Leu) c.190T>C (p.Phe64Leu) | |
| 15 | g.73329755A>T | CA393094071 | HCN4 | c.1408T>A (p.Phe470Ile) c.190T>A (p.Phe64Ile) | |
| 15 | g.73329756G>A | CA491151886 | HCN4 | c.1407C>T (p.Leu469=) c.189C>T (p.Leu63=) | gnomAD v4 |
| 15 | g.73329756G>C | CA491151888 | HCN4 | c.1407C>G (p.Leu469=) c.189C>G (p.Leu63=) | ClinVar dbSNP |
| 15 | g.73329756G>T | CA491151890 | HCN4 | c.1407C>A (p.Leu469=) c.189C>A (p.Leu63=) | |
| 15 | g.73329757A>C | CA393094075 | HCN4 | c.1406T>G (p.Leu469Arg) c.188T>G (p.Leu63Arg) | |
| 15 | g.73329757A>G | CA393094076 | HCN4 | c.1406T>C (p.Leu469Pro) c.188T>C (p.Leu63Pro) | |
| 15 | g.73329757A>T | CA393094078 | HCN4 | c.1406T>A (p.Leu469His) c.188T>A (p.Leu63His) | |
| 15 | g.73329758G>A | CA393094081 | HCN4 | c.1405C>T (p.Leu469Phe) c.187C>T (p.Leu63Phe) | |
| 15 | g.73329758G>C | CA393094082 | HCN4 | c.1405C>G (p.Leu469Val) c.187C>G (p.Leu63Val) | |
| 15 | g.73329758G>T | CA393094083 | HCN4 | c.1405C>A (p.Leu469Ile) c.187C>A (p.Leu63Ile) | |
| 15 | g.73329759C>A | CA491151900 | HCN4 | c.1404G>T (p.Ala468=) c.186G>T (p.Ala62=) | |
| 15 | g.73329759C= | CA2187167671 | HCN4 | c.1404G= (p.Ala468=) c.186G= (p.Ala62=) | |
| 15 | g.73329759C>G | CA491151902 | HCN4 | c.1404G>C (p.Ala468=) c.186G>C (p.Ala62=) | |
| 15 | g.73329759C>T | CA7649296 | HCN4 | c.1404G>A (p.Ala468=) c.186G>A (p.Ala62=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 15 | g.73329759_73329760insAG | CA2804727105 | HCN4 | c.1403_1404insCT (p.Leu469CysfsTer6) c.185_186insCT (p.Leu63CysfsTer6) | |
| 15 | g.73329760G>A | CA7649297 | HCN4 | c.1403C>T (p.Ala468Val) c.185C>T (p.Ala62Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 15 | g.73329760G>C | CA393094087 | HCN4 | c.1403C>G (p.Ala468Gly) c.185C>G (p.Ala62Gly) | |
| 15 | g.73329760G= | CA2187167674 | HCN4 | c.1403C= (p.Ala468=) c.185C= (p.Ala62=) | |
| 15 | g.73329760G>T | CA393094089 | HCN4 | c.1403C>A (p.Ala468Glu) c.185C>A (p.Ala62Glu) | |
| 15 | g.73329761C>A | CA393094091 | HCN4 | c.1402G>T (p.Ala468Ser) c.184G>T (p.Ala62Ser) | gnomAD v4 |
| 15 | g.73329761C= | CA2187167680 | HCN4 | c.1402G= (p.Ala468=) c.184G= (p.Ala62=) | |
| 15 | g.73329761C>G | CA393094092 | HCN4 | c.1402G>C (p.Ala468Pro) c.184G>C (p.Ala62Pro) | |
| 15 | g.73329761C>T | CA7649298 | HCN4 | c.1402G>A (p.Ala468Thr) c.184G>A (p.Ala62Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |