Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323143G>A | CA491478668 | HCN4 | c.2950C>T (p.Leu984=) c.1732C>T (p.Leu578=) | gnomAD v4 |
15 | g.73323143G>C | CA393086721 | HCN4 | c.2950C>G (p.Leu984Val) c.1732C>G (p.Leu578Val) | ClinVar dbSNP |
15 | g.73323143G>T | CA393086724 | HCN4 | c.2950C>A (p.Leu984Ile) c.1732C>A (p.Leu578Ile) | gnomAD v4 |
15 | g.73323143_73323144insT | CA2804714152 | HCN4 | c.2949_2950insA (p.Leu984ThrfsTer19) c.1731_1732insA (p.Leu578ThrfsTer19) | |
15 | g.73323144G>A | CA272664002 | HCN4 | c.2949C>T (p.Ser983=) c.1731C>T (p.Ser577=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323144G>C | CA491478673 | HCN4 | c.2949C>G (p.Ser983=) c.1731C>G (p.Ser577=) | |
15 | g.73323144G= | CA2187187574 | HCN4 | c.2949C= (p.Ser983=) c.1731C= (p.Ser577=) | |
15 | g.73323144G>T | CA491478675 | HCN4 | c.2949C>A (p.Ser983=) c.1731C>A (p.Ser577=) | gnomAD v4 |
15 | g.73323145G>A | CA7648917 | HCN4 | c.2948C>T (p.Ser983Phe) c.1730C>T (p.Ser577Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323145G>C | CA393086731 | HCN4 | c.2948C>G (p.Ser983Cys) c.1730C>G (p.Ser577Cys) | |
15 | g.73323145G= | CA2187187576 | HCN4 | c.2948C= (p.Ser983=) c.1730C= (p.Ser577=) | |
15 | g.73323145G>T | CA393086734 | HCN4 | c.2948C>A (p.Ser983Tyr) c.1730C>A (p.Ser577Tyr) | gnomAD v4 |
15 | g.73323146A>C | CA393086736 | HCN4 | c.2947T>G (p.Ser983Ala) c.1729T>G (p.Ser577Ala) | |
15 | g.73323146A>G | CA393086741 | HCN4 | c.2947T>C (p.Ser983Pro) c.1729T>C (p.Ser577Pro) | |
15 | g.73323146A>T | CA393086739 | HCN4 | c.2947T>A (p.Ser983Thr) c.1729T>A (p.Ser577Thr) | gnomAD v4 |
15 | g.73323147C>A | CA393086744 | HCN4 | c.2946G>T (p.Leu982Phe) c.1728G>T (p.Leu576Phe) | gnomAD v4 |
15 | g.73323147C= | CA2187187581 | HCN4 | c.2946G= (p.Leu982=) c.1728G= (p.Leu576=) | |
15 | g.73323147C>G | CA393086747 | HCN4 | c.2946G>C (p.Leu982Phe) c.1728G>C (p.Leu576Phe) | |
15 | g.73323147C>T | CA16607136 | HCN4 | c.2946G>A (p.Leu982=) c.1728G>A (p.Leu576=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323148A>C | CA393086749 | HCN4 | c.2945T>G (p.Leu982Trp) c.1727T>G (p.Leu576Trp) | |
15 | g.73323148A>G | CA393086751 | HCN4 | c.2945T>C (p.Leu982Ser) c.1727T>C (p.Leu576Ser) | gnomAD v4 |
15 | g.73323148A>T | CA393086753 | HCN4 | c.2945T>A (p.Leu982Ter) c.1727T>A (p.Leu576Ter) | |
15 | g.73323149A>C | CA393086755 | HCN4 | c.2944T>G (p.Leu982Val) c.1726T>G (p.Leu576Val) | |
15 | g.73323149A>G | CA491478682 | HCN4 | c.2944T>C (p.Leu982=) c.1726T>C (p.Leu576=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323149A>T | CA393086758 | HCN4 | c.2944T>A (p.Leu982Met) c.1726T>A (p.Leu576Met) | |
15 | g.73323150C>A | CA393086760 | HCN4 | c.2943G>T (p.Glu981Asp) c.1725G>T (p.Glu575Asp) | gnomAD v4 |
15 | g.73323150C>G | CA393086762 | HCN4 | c.2943G>C (p.Glu981Asp) c.1725G>C (p.Glu575Asp) | gnomAD v4 COSMIC |
15 | g.73323150C>T | CA491478684 | HCN4 | c.2943G>A (p.Glu981=) c.1725G>A (p.Glu575=) | gnomAD v4 |
15 | g.73323159_73323250del | CA619410578 | HCN4 | c.2852_2943del (p.Gly951ValfsTer21) c.1634_1725del (p.Gly545ValfsTer21) | gnomAD v2 |
15 | g.73323151T>A | CA393086766 | HCN4 | c.2942A>T (p.Glu981Val) c.1724A>T (p.Glu575Val) | |
15 | g.73323151T>C | CA393086769 | HCN4 | c.2942A>G (p.Glu981Gly) c.1724A>G (p.Glu575Gly) | gnomAD v4 |
15 | g.73323151T>G | CA393086771 | HCN4 | c.2942A>C (p.Glu981Ala) c.1724A>C (p.Glu575Ala) | |
15 | g.73323152C>A | CA393086774 | HCN4 | c.2941G>T (p.Glu981Ter) c.1723G>T (p.Glu575Ter) | ClinVar dbSNP gnomAD v4 |
15 | g.73323152C= | CA2187187584 | HCN4 | c.2941G= (p.Glu981=) c.1723G= (p.Glu575=) | |
15 | g.73323152C>G | CA393086778 | HCN4 | c.2941G>C (p.Glu981Gln) c.1723G>C (p.Glu575Gln) | |
15 | g.73323152C>T | CA393086776 | HCN4 | c.2941G>A (p.Glu981Lys) c.1723G>A (p.Glu575Lys) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323155del | CA2629370546 | HCN4 | c.2941del (p.Glu981SerfsTer4) c.1723del (p.Glu575SerfsTer4) | gnomAD v4 |
15 | g.73323153C>A | CA491478692 | HCN4 | c.2940G>T (p.Gly980=) c.1722G>T (p.Gly574=) | gnomAD v4 |
15 | g.73323153C>G | CA491478694 | HCN4 | c.2940G>C (p.Gly980=) c.1722G>C (p.Gly574=) | ClinVar |
15 | g.73323153C>T | CA491478693 | HCN4 | c.2940G>A (p.Gly980=) c.1722G>A (p.Gly574=) | gnomAD v4 COSMIC |
15 | g.73323154C>A | CA393086782 | HCN4 | c.2939G>T (p.Gly980Val) c.1721G>T (p.Gly574Val) | |
15 | g.73323154C= | CA2187187591 | HCN4 | c.2939G= (p.Gly980=) c.1721G= (p.Gly574=) | |
15 | g.73323154C>G | CA7648918 | HCN4 | c.2939G>C (p.Gly980Ala) c.1721G>C (p.Gly574Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323154C>T | CA393086786 | HCN4 | c.2939G>A (p.Gly980Glu) c.1721G>A (p.Gly574Glu) | ClinVar gnomAD v4 |
15 | g.73323155C>A | CA393086790 | HCN4 | c.2938G>T (p.Gly980Trp) c.1720G>T (p.Gly574Trp) | gnomAD v4 COSMIC |
15 | g.73323155C= | CA2187187599 | HCN4 | c.2938G= (p.Gly980=) c.1720G= (p.Gly574=) | |
15 | g.73323155C>G | CA393086791 | HCN4 | c.2938G>C (p.Gly980Arg) c.1720G>C (p.Gly574Arg) | ClinVar dbSNP gnomAD v4 |
15 | g.73323155C>T | CA7648919 | HCN4 | c.2938G>A (p.Gly980Arg) c.1720G>A (p.Gly574Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323156G>A | CA7648920 | HCN4 | c.2937C>T (p.Pro979=) c.1719C>T (p.Pro573=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323156G>C | CA491478702 | HCN4 | c.2937C>G (p.Pro979=) c.1719C>G (p.Pro573=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323156G= | CA2187187605 | HCN4 | c.2937C= (p.Pro979=) c.1719C= (p.Pro573=) | |
15 | g.73323156G>T | CA7648921 | HCN4 | c.2937C>A (p.Pro979=) c.1719C>A (p.Pro573=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323158del | CA2629370547 | HCN4 | c.2937del (p.Glu981SerfsTer4) c.1719del (p.Glu575SerfsTer4) | gnomAD v4 |
15 | g.73323157G>A | CA393086799 | HCN4 | c.2936C>T (p.Pro979Leu) c.1718C>T (p.Pro573Leu) | gnomAD v4 |
15 | g.73323157G>C | CA393086801 | HCN4 | c.2936C>G (p.Pro979Arg) c.1718C>G (p.Pro573Arg) | |
15 | g.73323157G>T | CA393086804 | HCN4 | c.2936C>A (p.Pro979His) c.1718C>A (p.Pro573His) | |
15 | g.73323158G>A | CA393086808 | HCN4 | c.2935C>T (p.Pro979Ser) c.1717C>T (p.Pro573Ser) | gnomAD v4 |
15 | g.73323158G>C | CA393086811 | HCN4 | c.2935C>G (p.Pro979Ala) c.1717C>G (p.Pro573Ala) | |
15 | g.73323158G>T | CA393086813 | HCN4 | c.2935C>A (p.Pro979Thr) c.1717C>A (p.Pro573Thr) | gnomAD v4 |
15 | g.73323159A>C | CA491478709 | HCN4 | c.2934T>G (p.Pro978=) c.1716T>G (p.Pro572=) | |
15 | g.73323159A>G | CA491478710 | HCN4 | c.2934T>C (p.Pro978=) c.1716T>C (p.Pro572=) | gnomAD v4 |
15 | g.73323159A>T | CA491478711 | HCN4 | c.2934T>A (p.Pro978=) c.1716T>A (p.Pro572=) | |
15 | g.73323160G>A | CA393086817 | HCN4 | c.2933C>T (p.Pro978Leu) c.1715C>T (p.Pro572Leu) | |
15 | g.73323160G>C | CA393086823 | HCN4 | c.2933C>G (p.Pro978Arg) c.1715C>G (p.Pro572Arg) | |
15 | g.73323160G>T | CA393086819 | HCN4 | c.2933C>A (p.Pro978His) c.1715C>A (p.Pro572His) | gnomAD v4 |
15 | g.73323161G>A | CA393086826 | HCN4 | c.2932C>T (p.Pro978Ser) c.1714C>T (p.Pro572Ser) | gnomAD v4 |
15 | g.73323161G>C | CA393086829 | HCN4 | c.2932C>G (p.Pro978Ala) c.1714C>G (p.Pro572Ala) | |
15 | g.73323161G= | CA2187187614 | HCN4 | c.2932C= (p.Pro978=) c.1714C= (p.Pro572=) | |
15 | g.73323161G>T | CA393086830 | HCN4 | c.2932C>A (p.Pro978Thr) c.1714C>A (p.Pro572Thr) | dbSNP gnomAD v4 |
15 | g.73323162C>A | CA393086832 | HCN4 | c.2931G>T (p.Gln977His) c.1713G>T (p.Gln571His) | dbSNP gnomAD v4 |
15 | g.73323162C= | CA2187187618 | HCN4 | c.2931G= (p.Gln977=) c.1713G= (p.Gln571=) | |
15 | g.73323162C>G | CA393086836 | HCN4 | c.2931G>C (p.Gln977His) c.1713G>C (p.Gln571His) | |
15 | g.73323162C>T | CA491478717 | HCN4 | c.2931G>A (p.Gln977=) c.1713G>A (p.Gln571=) | gnomAD v4 |
15 | g.73323163T>A | CA393086839 | HCN4 | c.2930A>T (p.Gln977Leu) c.1712A>T (p.Gln571Leu) | |
15 | g.73323163T>C | CA393086841 | HCN4 | c.2930A>G (p.Gln977Arg) c.1712A>G (p.Gln571Arg) | gnomAD v4 |
15 | g.73323163T>G | CA393086844 | HCN4 | c.2930A>C (p.Gln977Pro) c.1712A>C (p.Gln571Pro) | |
15 | g.73323164G>A | CA393086848 | HCN4 | c.2929C>T (p.Gln977Ter) c.1711C>T (p.Gln571Ter) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323164G>C | CA393086850 | HCN4 | c.2929C>G (p.Gln977Glu) c.1711C>G (p.Gln571Glu) | |
15 | g.73323164G= | CA2187187620 | HCN4 | c.2929C= (p.Gln977=) c.1711C= (p.Gln571=) | |
15 | g.73323164G>T | CA393086853 | HCN4 | c.2929C>A (p.Gln977Lys) c.1711C>A (p.Gln571Lys) | ClinVar dbSNP gnomAD v4 |
15 | g.73323165G>A | CA491478722 | HCN4 | c.2928C>T (p.Gly976=) c.1710C>T (p.Gly570=) | gnomAD v4 |
15 | g.73323165G>C | CA491478723 | HCN4 | c.2928C>G (p.Gly976=) c.1710C>G (p.Gly570=) | |
15 | g.73323165G>T | CA491478724 | HCN4 | c.2928C>A (p.Gly976=) c.1710C>A (p.Gly570=) | gnomAD v4 |
15 | g.73323166C>A | CA393086857 | HCN4 | c.2927G>T (p.Gly976Val) c.1709G>T (p.Gly570Val) | gnomAD v4 |
15 | g.73323166C>G | CA393086863 | HCN4 | c.2927G>C (p.Gly976Ala) c.1709G>C (p.Gly570Ala) | |
15 | g.73323166C>T | CA393086859 | HCN4 | c.2927G>A (p.Gly976Asp) c.1709G>A (p.Gly570Asp) | gnomAD v4 |
15 | g.73323168del | CA2629370548 | HCN4 | c.2927del (p.Gly976AlafsTer9) c.1709del (p.Gly570AlafsTer9) | gnomAD v4 |
15 | g.73323167C>A | CA393086868 | HCN4 | c.2926G>T (p.Gly976Cys) c.1708G>T (p.Gly570Cys) | gnomAD v4 |
15 | g.73323167C>G | CA393086873 | HCN4 | c.2926G>C (p.Gly976Arg) c.1708G>C (p.Gly570Arg) | |
15 | g.73323167C>T | CA393086870 | HCN4 | c.2926G>A (p.Gly976Ser) c.1708G>A (p.Gly570Ser) | |
15 | g.73323168C>A | CA491478726 | HCN4 | c.2925G>T (p.Leu975=) c.1707G>T (p.Leu569=) | gnomAD v4 |
15 | g.73323168C>G | CA491478727 | HCN4 | c.2925G>C (p.Leu975=) c.1707G>C (p.Leu569=) | |
15 | g.73323168C>T | CA491478728 | HCN4 | c.2925G>A (p.Leu975=) c.1707G>A (p.Leu569=) | |
15 | g.73323169A>C | CA393086875 | HCN4 | c.2924T>G (p.Leu975Arg) c.1706T>G (p.Leu569Arg) | gnomAD v4 |
15 | g.73323169A>G | CA393086877 | HCN4 | c.2924T>C (p.Leu975Pro) c.1706T>C (p.Leu569Pro) | gnomAD v4 |
15 | g.73323169A>T | CA393086878 | HCN4 | c.2924T>A (p.Leu975Gln) c.1706T>A (p.Leu569Gln) | |
15 | g.73323170G>A | CA7648922 | HCN4 | c.2923C>T (p.Leu975=) c.1705C>T (p.Leu569=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323170G>C | CA393086882 | HCN4 | c.2923C>G (p.Leu975Val) c.1705C>G (p.Leu569Val) | |
15 | g.73323170G= | CA2187187624 | HCN4 | c.2923C= (p.Leu975=) c.1705C= (p.Leu569=) | |
15 | g.73323170G>T | CA393086885 | HCN4 | c.2923C>A (p.Leu975Met) c.1705C>A (p.Leu569Met) | gnomAD v4 |
15 | g.73323171C>A | CA393086889 | HCN4 | c.2922G>T (p.Gln974His) c.1704G>T (p.Gln568His) | gnomAD v4 |
15 | g.73323171C>G | CA393086892 | HCN4 | c.2922G>C (p.Gln974His) c.1704G>C (p.Gln568His) | |
15 | g.73323171C>T | CA491478731 | HCN4 | c.2922G>A (p.Gln974=) c.1704G>A (p.Gln568=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323172T>A | CA393086896 | HCN4 | c.2921A>T (p.Gln974Leu) c.1703A>T (p.Gln568Leu) | |
15 | g.73323172T>C | CA393086901 | HCN4 | c.2921A>G (p.Gln974Arg) c.1703A>G (p.Gln568Arg) | dbSNP |
15 | g.73323172T>G | CA393086904 | HCN4 | c.2921A>C (p.Gln974Pro) c.1703A>C (p.Gln568Pro) | |
15 | g.73323172T= | CA2187187627 | HCN4 | c.2921A= (p.Gln974=) c.1703A= (p.Gln568=) | |
15 | g.73323173G>A | CA393086910 | HCN4 | c.2920C>T (p.Gln974Ter) c.1702C>T (p.Gln568Ter) | gnomAD v4 |
15 | g.73323173G>C | CA393086906 | HCN4 | c.2920C>G (p.Gln974Glu) c.1702C>G (p.Gln568Glu) | |
15 | g.73323173G>T | CA393086907 | HCN4 | c.2920C>A (p.Gln974Lys) c.1702C>A (p.Gln568Lys) | gnomAD v4 |
15 | g.73323174C>A | CA491478736 | HCN4 | c.2919G>T (p.Gly973=) c.1701G>T (p.Gly567=) | gnomAD v4 |
15 | g.73323174C>G | CA491478738 | HCN4 | c.2919G>C (p.Gly973=) c.1701G>C (p.Gly567=) | |
15 | g.73323174C>T | CA491478740 | HCN4 | c.2919G>A (p.Gly973=) c.1701G>A (p.Gly567=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323175C>A | CA393086911 | HCN4 | c.2918G>T (p.Gly973Val) c.1700G>T (p.Gly567Val) | gnomAD v4 |
15 | g.73323175C= | CA2187187632 | HCN4 | c.2918G= (p.Gly973=) c.1700G= (p.Gly567=) | |
15 | g.73323175C>G | CA393086914 | HCN4 | c.2918G>C (p.Gly973Ala) c.1700G>C (p.Gly567Ala) | |
15 | g.73323175C>T | CA7648923 | HCN4 | c.2918G>A (p.Gly973Glu) c.1700G>A (p.Gly567Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323176C>A | CA7648925 | HCN4 | c.2917G>T (p.Gly973Trp) c.1699G>T (p.Gly567Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323176C= | CA2187187636 | HCN4 | c.2917G= (p.Gly973=) c.1699G= (p.Gly567=) | |
15 | g.73323176C>G | CA393086921 | HCN4 | c.2917G>C (p.Gly973Arg) c.1699G>C (p.Gly567Arg) | gnomAD v4 |
15 | g.73323176C>T | CA7648924 | HCN4 | c.2917G>A (p.Gly973Arg) c.1699G>A (p.Gly567Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323176_73323177insA | CA2629370550 | HCN4 | c.2916_2917insT (p.Gly973TrpfsTer30) c.1698_1699insT (p.Gly567TrpfsTer30) | gnomAD v4 |
15 | g.73323177G>A | CA7648926 | HCN4 | c.2916C>T (p.Pro972=) c.1698C>T (p.Pro566=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323177G>C | CA491478743 | HCN4 | c.2916C>G (p.Pro972=) c.1698C>G (p.Pro566=) | gnomAD v4 |
15 | g.73323177G= | CA2187187641 | HCN4 | c.2916C= (p.Pro972=) c.1698C= (p.Pro566=) | |
15 | g.73323177G>T | CA491478744 | HCN4 | c.2916C>A (p.Pro972=) c.1698C>A (p.Pro566=) | dbSNP gnomAD v4 |
15 | g.73323180del | CA2629370549 | HCN4 | c.2916del (p.Gln974SerfsTer11) c.1698del (p.Gln568SerfsTer11) | gnomAD v4 |
15 | g.73323178G>A | CA393086926 | HCN4 | c.2915C>T (p.Pro972Leu) c.1697C>T (p.Pro566Leu) | gnomAD v4 |
15 | g.73323178G>C | CA393086928 | HCN4 | c.2915C>G (p.Pro972Arg) c.1697C>G (p.Pro566Arg) | |
15 | g.73323178G>T | CA393086930 | HCN4 | c.2915C>A (p.Pro972His) c.1697C>A (p.Pro566His) | gnomAD v4 |
15 | g.73323179G>A | CA7648927 | HCN4 | c.2914C>T (p.Pro972Ser) c.1696C>T (p.Pro566Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323179G>C | CA393086937 | HCN4 | c.2914C>G (p.Pro972Ala) c.1696C>G (p.Pro566Ala) | |
15 | g.73323179G= | CA2187187647 | HCN4 | c.2914C= (p.Pro972=) c.1696C= (p.Pro566=) | |
15 | g.73323179G>T | CA393086932 | HCN4 | c.2914C>A (p.Pro972Thr) c.1696C>A (p.Pro566Thr) | gnomAD v4 |
15 | g.73323180G>A | CA491478751 | HCN4 | c.2913C>T (p.Ser971=) c.1695C>T (p.Ser565=) | gnomAD v4 |
15 | g.73323180G>C | CA393086940 | HCN4 | c.2913C>G (p.Ser971Arg) c.1695C>G (p.Ser565Arg) | |
15 | g.73323180G>T | CA393086941 | HCN4 | c.2913C>A (p.Ser971Arg) c.1695C>A (p.Ser565Arg) | gnomAD v4 |
15 | g.73323181C>A | CA393086944 | HCN4 | c.2912G>T (p.Ser971Ile) c.1694G>T (p.Ser565Ile) | gnomAD v4 |
15 | g.73323181C= | CA2187187650 | HCN4 | c.2912G= (p.Ser971=) c.1694G= (p.Ser565=) | |
15 | g.73323181C>G | CA393086948 | HCN4 | c.2912G>C (p.Ser971Thr) c.1694G>C (p.Ser565Thr) | gnomAD v4 |
15 | g.73323181C>T | CA393086951 | HCN4 | c.2912G>A (p.Ser971Asn) c.1694G>A (p.Ser565Asn) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323182T>A | CA393086953 | HCN4 | c.2911A>T (p.Ser971Cys) c.1693A>T (p.Ser565Cys) | |
15 | g.73323182T>C | CA393086955 | HCN4 | c.2911A>G (p.Ser971Gly) c.1693A>G (p.Ser565Gly) | |
15 | g.73323182T>G | CA393086957 | HCN4 | c.2911A>C (p.Ser971Arg) c.1693A>C (p.Ser565Arg) | |
15 | g.73323183_73323186dup | CA2575783830 | HCN4 | c.2908_2911dup (p.Ser971IlefsTer2) c.1690_1693dup (p.Ser565IlefsTer2) | |
15 | g.73323183A>C | CA491478764 | HCN4 | c.2910T>G (p.Ser970=) c.1692T>G (p.Ser564=) | gnomAD v4 |
15 | g.73323183A>G | CA491478760 | HCN4 | c.2910T>C (p.Ser970=) c.1692T>C (p.Ser564=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323183A>T | CA491478762 | HCN4 | c.2910T>A (p.Ser970=) c.1692T>A (p.Ser564=) | gnomAD v4 |
15 | g.73323183_73323186delinsAGAT | CA2187187652 | HCN4 | c.2907_2910delinsATCT (p.Ser969=) c.1689_1692delinsATCT (p.Ser563=) | |
15 | g.73323184G>A | CA393086960 | HCN4 | c.2909C>T (p.Ser970Phe) c.1691C>T (p.Ser564Phe) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323184G>C | CA393086963 | HCN4 | c.2909C>G (p.Ser970Cys) c.1691C>G (p.Ser564Cys) | |
15 | g.73323184G= | CA2187187656 | HCN4 | c.2909C= (p.Ser970=) c.1691C= (p.Ser564=) | |
15 | g.73323184G>T | CA393086965 | HCN4 | c.2909C>A (p.Ser970Tyr) c.1691C>A (p.Ser564Tyr) | gnomAD v4 |
15 | g.73323186_73323188del | CA2187187654 | HCN4 | c.2907_2909del (p.Ser970del) c.1689_1691del (p.Ser564del) | dbSNP |
15 | g.73323185A>C | CA393086967 | HCN4 | c.2908T>G (p.Ser970Ala) c.1690T>G (p.Ser564Ala) | |
15 | g.73323185A>G | CA393086969 | HCN4 | c.2908T>C (p.Ser970Pro) c.1690T>C (p.Ser564Pro) | ClinVar gnomAD v4 |
15 | g.73323185A>T | CA393086972 | HCN4 | c.2908T>A (p.Ser970Thr) c.1690T>A (p.Ser564Thr) | |
15 | g.73323186T>A | CA491478769 | HCN4 | c.2907A>T (p.Ser969=) c.1689A>T (p.Ser563=) | |
15 | g.73323186T>C | CA7648928 | HCN4 | c.2907A>G (p.Ser969=) c.1689A>G (p.Ser563=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323186T>G | CA491478772 | HCN4 | c.2907A>C (p.Ser969=) c.1689A>C (p.Ser563=) | |
15 | g.73323186T= | CA2187187658 | HCN4 | c.2907A= (p.Ser969=) c.1689A= (p.Ser563=) | |
15 | g.73323187G>A | CA393086978 | HCN4 | c.2906C>T (p.Ser969Leu) c.1688C>T (p.Ser563Leu) | gnomAD v4 |
15 | g.73323187G>C | CA393086980 | HCN4 | c.2906C>G (p.Ser969Ter) c.1688C>G (p.Ser563Ter) | |
15 | g.73323187G>T | CA393086983 | HCN4 | c.2906C>A (p.Ser969Ter) c.1688C>A (p.Ser563Ter) | gnomAD v4 |
15 | g.73323188A>C | CA393086987 | HCN4 | c.2905T>G (p.Ser969Ala) c.1687T>G (p.Ser563Ala) | |
15 | g.73323188A>G | CA393086990 | HCN4 | c.2905T>C (p.Ser969Pro) c.1687T>C (p.Ser563Pro) | gnomAD v4 |
15 | g.73323188A>T | CA393086992 | HCN4 | c.2905T>A (p.Ser969Thr) c.1687T>A (p.Ser563Thr) | gnomAD v4 |
15 | g.73323189C>A | CA491478777 | HCN4 | c.2904G>T (p.Pro968=) c.1686G>T (p.Pro562=) | gnomAD v4 |
15 | g.73323189C= | CA2187187662 | HCN4 | c.2904G= (p.Pro968=) c.1686G= (p.Pro562=) | |
15 | g.73323189C>G | CA491478781 | HCN4 | c.2904G>C (p.Pro968=) c.1686G>C (p.Pro562=) | |
15 | g.73323189C>T | CA7648929 | HCN4 | c.2904G>A (p.Pro968=) c.1686G>A (p.Pro562=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323190G>A | CA7648930 | HCN4 | c.2903C>T (p.Pro968Leu) c.1685C>T (p.Pro562Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323190G>C | CA7648931 | HCN4 | c.2903C>G (p.Pro968Arg) c.1685C>G (p.Pro562Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323190G= | CA2187187670 | HCN4 | c.2903C= (p.Pro968=) c.1685C= (p.Pro562=) | |
15 | g.73323190G>T | CA393087002 | HCN4 | c.2903C>A (p.Pro968Gln) c.1685C>A (p.Pro562Gln) | gnomAD v4 |
15 | g.73323193del | CA2629370551 | HCN4 | c.2903del (p.Pro968ArgfsTer17) c.1685del (p.Pro562ArgfsTer17) | gnomAD v4 |
15 | g.73323191G>A | CA7648932 | HCN4 | c.2902C>T (p.Pro968Ser) c.1684C>T (p.Pro562Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323191G>C | CA393087008 | HCN4 | c.2902C>G (p.Pro968Ala) c.1684C>G (p.Pro562Ala) | |
15 | g.73323191G= | CA2187187673 | HCN4 | c.2902C= (p.Pro968=) c.1684C= (p.Pro562=) | |
15 | g.73323191G>T | CA393087010 | HCN4 | c.2902C>A (p.Pro968Thr) c.1684C>A (p.Pro562Thr) | gnomAD v4 |
15 | g.73323192G>A | CA7648933 | HCN4 | c.2901C>T (p.Ser967=) c.1683C>T (p.Ser561=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323192G>C | CA491478789 | HCN4 | c.2901C>G (p.Ser967=) c.1683C>G (p.Ser561=) | |
15 | g.73323192G= | CA2187187675 | HCN4 | c.2901C= (p.Ser967=) c.1683C= (p.Ser561=) | |
15 | g.73323192G>T | CA491478787 | HCN4 | c.2901C>A (p.Ser967=) c.1683C>A (p.Ser561=) | |
15 | g.73323193G>A | CA393087019 | HCN4 | c.2900C>T (p.Ser967Phe) c.1682C>T (p.Ser561Phe) | gnomAD v4 |
15 | g.73323193G>C | CA393087016 | HCN4 | c.2900C>G (p.Ser967Cys) c.1682C>G (p.Ser561Cys) | gnomAD v4 |
15 | g.73323193G>T | CA393087014 | HCN4 | c.2900C>A (p.Ser967Tyr) c.1682C>A (p.Ser561Tyr) | gnomAD v4 |
15 | g.73323194A= | CA2187187681 | HCN4 | c.2899T= (p.Ser967=) c.1681T= (p.Ser561=) | |
15 | g.73323194A>C | CA393087025 | HCN4 | c.2899T>G (p.Ser967Ala) c.1681T>G (p.Ser561Ala) | |
15 | g.73323194A>G | CA393087023 | HCN4 | c.2899T>C (p.Ser967Pro) c.1681T>C (p.Ser561Pro) | dbSNP |
15 | g.73323194A>T | CA393087027 | HCN4 | c.2899T>A (p.Ser967Thr) c.1681T>A (p.Ser561Thr) | |
15 | g.73323195T>A | CA393087030 | HCN4 | c.2898A>T (p.Arg966Ser) c.1680A>T (p.Arg560Ser) | |
15 | g.73323195T>C | CA491478790 | HCN4 | c.2898A>G (p.Arg966=) c.1680A>G (p.Arg560=) | |
15 | g.73323195T>G | CA393087031 | HCN4 | c.2898A>C (p.Arg966Ser) c.1680A>C (p.Arg560Ser) | gnomAD v4 |
15 | g.73323196C>A | CA393087035 | HCN4 | c.2897G>T (p.Arg966Ile) c.1679G>T (p.Arg560Ile) | gnomAD v4 |
15 | g.73323196C>G | CA393087039 | HCN4 | c.2897G>C (p.Arg966Thr) c.1679G>C (p.Arg560Thr) | |
15 | g.73323196C>T | CA393087038 | HCN4 | c.2897G>A (p.Arg966Lys) c.1679G>A (p.Arg560Lys) | |
15 | g.73323196_73323197delinsCT | CA2187187685 | HCN4 | c.2896_2897delinsAG (p.Arg966=) c.1678_1679delinsAG (p.Arg560=) | |
15 | g.73323197del | CA7648934 | HCN4 | c.2896del (p.Arg966AspfsTer19) c.1678del (p.Arg560AspfsTer19) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323197T>A | CA393087041 | HCN4 | c.2896A>T (p.Arg966Ter) c.1678A>T (p.Arg560Ter) | gnomAD v4 |
15 | g.73323197T>C | CA393087046 | HCN4 | c.2896A>G (p.Arg966Gly) c.1678A>G (p.Arg560Gly) | gnomAD v4 |
15 | g.73323197T>G | CA491478792 | HCN4 | c.2896A>C (p.Arg966=) c.1678A>C (p.Arg560=) | ClinVar |
15 | g.73323198G>A | CA491478795 | HCN4 | c.2895C>T (p.Ser965=) c.1677C>T (p.Ser559=) | dbSNP gnomAD v4 |
15 | g.73323198G>C | CA491478797 | HCN4 | c.2895C>G (p.Ser965=) c.1677C>G (p.Ser559=) | |
15 | g.73323198G= | CA2187187690 | HCN4 | c.2895C= (p.Ser965=) c.1677C= (p.Ser559=) | |
15 | g.73323198G>T | CA491478798 | HCN4 | c.2895C>A (p.Ser965=) c.1677C>A (p.Ser559=) | ClinVar gnomAD v4 |
15 | g.73323199G>A | CA393087050 | HCN4 | c.2894C>T (p.Ser965Phe) c.1676C>T (p.Ser559Phe) | gnomAD v4 |
15 | g.73323199G>C | CA393087052 | HCN4 | c.2894C>G (p.Ser965Cys) c.1676C>G (p.Ser559Cys) | |
15 | g.73323199G>T | CA393087054 | HCN4 | c.2894C>A (p.Ser965Tyr) c.1676C>A (p.Ser559Tyr) | gnomAD v4 |
15 | g.73323200A>C | CA393087055 | HCN4 | c.2893T>G (p.Ser965Ala) c.1675T>G (p.Ser559Ala) | |
15 | g.73323200A>G | CA393087057 | HCN4 | c.2893T>C (p.Ser965Pro) c.1675T>C (p.Ser559Pro) | gnomAD v4 |
15 | g.73323200A>T | CA393087060 | HCN4 | c.2893T>A (p.Ser965Thr) c.1675T>A (p.Ser559Thr) | |
15 | g.73323201T>A | CA491478802 | HCN4 | c.2892A>T (p.Ser964=) c.1674A>T (p.Ser558=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323201T>C | CA491478804 | HCN4 | c.2892A>G (p.Ser964=) c.1674A>G (p.Ser558=) | |
15 | g.73323201T>G | CA491478805 | HCN4 | c.2892A>C (p.Ser964=) c.1674A>C (p.Ser558=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323201T= | CA2187187692 | HCN4 | c.2892A= (p.Ser964=) c.1674A= (p.Ser558=) | |
15 | g.73323202G>A | CA393087064 | HCN4 | c.2891C>T (p.Ser964Leu) c.1673C>T (p.Ser558Leu) | dbSNP gnomAD v4 |
15 | g.73323202G>C | CA393087065 | HCN4 | c.2891C>G (p.Ser964Ter) c.1673C>G (p.Ser558Ter) | |
15 | g.73323202G= | CA2187187695 | HCN4 | c.2891C= (p.Ser964=) c.1673C= (p.Ser558=) | |
15 | g.73323202G>T | CA393087068 | HCN4 | c.2891C>A (p.Ser964Ter) c.1673C>A (p.Ser558Ter) | |
15 | g.73323203A>C | CA393087070 | HCN4 | c.2890T>G (p.Ser964Ala) c.1672T>G (p.Ser558Ala) | dbSNP |
15 | g.73323203A>G | CA393087074 | HCN4 | c.2890T>C (p.Ser964Pro) c.1672T>C (p.Ser558Pro) | gnomAD v4 |
15 | g.73323203A>T | CA393087075 | HCN4 | c.2890T>A (p.Ser964Thr) c.1672T>A (p.Ser558Thr) | gnomAD v4 |
15 | g.73323203_73323209delinsAGGGTGG | CA2187187699 | HCN4 | c.2884_2890delinsCCACCCT (p.Pro962=) c.1666_1672delinsCCACCCT (p.Pro556=) | |
15 | g.73323204G>A | CA491478818 | HCN4 | c.2889C>T (p.Pro963=) c.1671C>T (p.Pro557=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323204G>C | CA491478815 | HCN4 | c.2889C>G (p.Pro963=) c.1671C>G (p.Pro557=) | |
15 | g.73323204G= | CA2187187704 | HCN4 | c.2889C= (p.Pro963=) c.1671C= (p.Pro557=) | |
15 | g.73323204G>T | CA491478812 | HCN4 | c.2889C>A (p.Pro963=) c.1671C>A (p.Pro557=) | gnomAD v4 |
15 | g.73323206del | CA2629370552 | HCN4 | c.2889del (p.Ser964HisfsTer21) c.1671del (p.Ser558HisfsTer21) | gnomAD v4 |
15 | g.73323210_73323215dup | CA2575783831 | HCN4 | c.2884_2889dup (p.Pro963_Ser964insProPro) c.1666_1671dup (p.Pro557_Ser558insProPro) | |
15 | g.73323210_73323215del | CA7648935 | HCN4 | c.2884_2889del (p.Pro962_Pro963del) c.1666_1671del (p.Pro556_Pro557del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323205G>A | CA393087078 | HCN4 | c.2888C>T (p.Pro963Leu) c.1670C>T (p.Pro557Leu) | ClinVar gnomAD v4 |
15 | g.73323205G>C | CA393087082 | HCN4 | c.2888C>G (p.Pro963Arg) c.1670C>G (p.Pro557Arg) | |
15 | g.73323205G>T | CA393087079 | HCN4 | c.2888C>A (p.Pro963His) c.1670C>A (p.Pro557His) | gnomAD v4 |
15 | g.73323206G>A | CA393087086 | HCN4 | c.2887C>T (p.Pro963Ser) c.1669C>T (p.Pro557Ser) | dbSNP gnomAD v4 |
15 | g.73323206G>C | CA393087088 | HCN4 | c.2887C>G (p.Pro963Ala) c.1669C>G (p.Pro557Ala) | |
15 | g.73323206G= | CA2187187709 | HCN4 | c.2887C= (p.Pro963=) c.1669C= (p.Pro557=) | |
15 | g.73323206G>T | CA393087091 | HCN4 | c.2887C>A (p.Pro963Thr) c.1669C>A (p.Pro557Thr) | gnomAD v4 |
15 | g.73323207T>A | CA491478823 | HCN4 | c.2886A>T (p.Pro962=) c.1668A>T (p.Pro556=) | gnomAD v4 |
15 | g.73323207T>C | CA491478825 | HCN4 | c.2886A>G (p.Pro962=) c.1668A>G (p.Pro556=) | |
15 | g.73323207T>G | CA491478826 | HCN4 | c.2886A>C (p.Pro962=) c.1668A>C (p.Pro556=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323208G>A | CA393087094 | HCN4 | c.2885C>T (p.Pro962Leu) c.1667C>T (p.Pro556Leu) | ClinVar |
15 | g.73323208G>C | CA393087097 | HCN4 | c.2885C>G (p.Pro962Arg) c.1667C>G (p.Pro556Arg) | |
15 | g.73323208G>T | CA393087099 | HCN4 | c.2885C>A (p.Pro962Gln) c.1667C>A (p.Pro556Gln) | gnomAD v4 |
15 | g.73323212dup | CA2629370554 | HCN4 | c.2885dup (p.Pro963ThrfsTer9) c.1667dup (p.Pro557ThrfsTer9) | gnomAD v4 |
15 | g.73323212del | CA2629370553 | HCN4 | c.2885del (p.Pro962HisfsTer23) c.1667del (p.Pro556HisfsTer23) | gnomAD v4 |
15 | g.73323209G>A | CA393087101 | HCN4 | c.2884C>T (p.Pro962Ser) c.1666C>T (p.Pro556Ser) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323209G>C | CA393087105 | HCN4 | c.2884C>G (p.Pro962Ala) c.1666C>G (p.Pro556Ala) | |
15 | g.73323209G= | CA2187187712 | HCN4 | c.2884C= (p.Pro962=) c.1666C= (p.Pro556=) | |
15 | g.73323209G>T | CA393087110 | HCN4 | c.2884C>A (p.Pro962Thr) c.1666C>A (p.Pro556Thr) | gnomAD v4 |
15 | g.73323210G>A | CA491478831 | HCN4 | c.2883C>T (p.Pro961=) c.1665C>T (p.Pro555=) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323210G>C | CA491478832 | HCN4 | c.2883C>G (p.Pro961=) c.1665C>G (p.Pro555=) | gnomAD v4 |
15 | g.73323210G= | CA2187187716 | HCN4 | c.2883C= (p.Pro961=) c.1665C= (p.Pro555=) | |
15 | g.73323210G>T | CA491478833 | HCN4 | c.2883C>A (p.Pro961=) c.1665C>A (p.Pro555=) | gnomAD v4 |
15 | g.73323211G>A | CA393087117 | HCN4 | c.2882C>T (p.Pro961Leu) c.1664C>T (p.Pro555Leu) | gnomAD v4 |
15 | g.73323211G>C | CA393087115 | HCN4 | c.2882C>G (p.Pro961Arg) c.1664C>G (p.Pro555Arg) | |
15 | g.73323211G>T | CA393087112 | HCN4 | c.2882C>A (p.Pro961His) c.1664C>A (p.Pro555His) | gnomAD v4 |
15 | g.73323212G>A | CA393087120 | HCN4 | c.2881C>T (p.Pro961Ser) c.1663C>T (p.Pro555Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323212G>C | CA393087122 | HCN4 | c.2881C>G (p.Pro961Ala) c.1663C>G (p.Pro555Ala) | |
15 | g.73323212G= | CA2187187720 | HCN4 | c.2881C= (p.Pro961=) c.1663C= (p.Pro555=) | |
15 | g.73323212G>T | CA393087124 | HCN4 | c.2881C>A (p.Pro961Thr) c.1663C>A (p.Pro555Thr) | gnomAD v4 |
15 | g.73323213T>A | CA491478834 | HCN4 | c.2880A>T (p.Pro960=) c.1662A>T (p.Pro554=) | |
15 | g.73323213T>C | CA491478835 | HCN4 | c.2880A>G (p.Pro960=) c.1662A>G (p.Pro554=) | ClinVar |
15 | g.73323213T>G | CA491478836 | HCN4 | c.2880A>C (p.Pro960=) c.1662A>C (p.Pro554=) | ClinVar dbSNP |
15 | g.73323214G>A | CA393087128 | HCN4 | c.2879C>T (p.Pro960Leu) c.1661C>T (p.Pro554Leu) | gnomAD v4 |
15 | g.73323214G>C | CA393087130 | HCN4 | c.2879C>G (p.Pro960Arg) c.1661C>G (p.Pro554Arg) | |
15 | g.73323214G= | CA2187187724 | HCN4 | c.2879C= (p.Pro960=) c.1661C= (p.Pro554=) | |
15 | g.73323214G>T | CA393087133 | HCN4 | c.2879C>A (p.Pro960Gln) c.1661C>A (p.Pro554Gln) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323215G>A | CA393087137 | HCN4 | c.2878C>T (p.Pro960Ser) c.1660C>T (p.Pro554Ser) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323215G>C | CA393087140 | HCN4 | c.2878C>G (p.Pro960Ala) c.1660C>G (p.Pro554Ala) | |
15 | g.73323215G= | CA2187187727 | HCN4 | c.2878C= (p.Pro960=) c.1660C= (p.Pro554=) | |
15 | g.73323215G>T | CA393087142 | HCN4 | c.2878C>A (p.Pro960Thr) c.1660C>A (p.Pro554Thr) | gnomAD v4 |
15 | g.73323216C>A | CA491478841 | HCN4 | c.2877G>T (p.Leu959=) c.1659G>T (p.Leu553=) | gnomAD v4 |
15 | g.73323216C>G | CA491478842 | HCN4 | c.2877G>C (p.Leu959=) c.1659G>C (p.Leu553=) | |
15 | g.73323216C>T | CA491478843 | HCN4 | c.2877G>A (p.Leu959=) c.1659G>A (p.Leu553=) | gnomAD v4 |
15 | g.73323217A= | CA2187187729 | HCN4 | c.2876T= (p.Leu959=) c.1658T= (p.Leu553=) | |
15 | g.73323217A>C | CA393087145 | HCN4 | c.2876T>G (p.Leu959Arg) c.1658T>G (p.Leu553Arg) | |
15 | g.73323217A>G | CA393087148 | HCN4 | c.2876T>C (p.Leu959Pro) c.1658T>C (p.Leu553Pro) | |
15 | g.73323217A>T | CA393087150 | HCN4 | c.2876T>A (p.Leu959Gln) c.1658T>A (p.Leu553Gln) | ClinVar dbSNP gnomAD v4 |
15 | g.73323218G>A | CA491478844 | HCN4 | c.2875C>T (p.Leu959=) c.1657C>T (p.Leu553=) | gnomAD v4 |
15 | g.73323218G>C | CA16607867 | HCN4 | c.2875C>G (p.Leu959Val) c.1657C>G (p.Leu553Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323218G= | CA2187187733 | HCN4 | c.2875C= (p.Leu959=) c.1657C= (p.Leu553=) | |
15 | g.73323218G>T | CA393087154 | HCN4 | c.2875C>A (p.Leu959Met) c.1657C>A (p.Leu553Met) | gnomAD v4 |
15 | g.73323219G>A | CA491478846 | HCN4 | c.2874C>T (p.Phe958=) c.1656C>T (p.Phe552=) | dbSNP gnomAD v2 |
15 | g.73323219G>C | CA393087160 | HCN4 | c.2874C>G (p.Phe958Leu) c.1656C>G (p.Phe552Leu) | |
15 | g.73323219G= | CA2187187736 | HCN4 | c.2874C= (p.Phe958=) c.1656C= (p.Phe552=) | |
15 | g.73323219G>T | CA393087163 | HCN4 | c.2874C>A (p.Phe958Leu) c.1656C>A (p.Phe552Leu) | gnomAD v4 |
15 | g.73323220A= | CA2187187739 | HCN4 | c.2873T= (p.Phe958=) c.1655T= (p.Phe552=) | |
15 | g.73323220A>C | CA393087165 | HCN4 | c.2873T>G (p.Phe958Cys) c.1655T>G (p.Phe552Cys) | |
15 | g.73323220A>G | CA393087168 | HCN4 | c.2873T>C (p.Phe958Ser) c.1655T>C (p.Phe552Ser) | dbSNP |
15 | g.73323220A>T | CA393087171 | HCN4 | c.2873T>A (p.Phe958Tyr) c.1655T>A (p.Phe552Tyr) | |
15 | g.73323221A= | CA2187187742 | HCN4 | c.2872T= (p.Phe958=) c.1654T= (p.Phe552=) | |
15 | g.73323221A>C | CA393087175 | HCN4 | c.2872T>G (p.Phe958Val) c.1654T>G (p.Phe552Val) | |
15 | g.73323221A>G | CA393087176 | HCN4 | c.2872T>C (p.Phe958Leu) c.1654T>C (p.Phe552Leu) | gnomAD v4 |
15 | g.73323221A>T | CA393087179 | HCN4 | c.2872T>A (p.Phe958Ile) c.1654T>A (p.Phe552Ile) | ClinVar dbSNP |
15 | g.73323222G>A | CA491478857 | HCN4 | c.2871C>T (p.His957=) c.1653C>T (p.His551=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323222G>C | CA393087184 | HCN4 | c.2871C>G (p.His957Gln) c.1653C>G (p.His551Gln) | |
15 | g.73323222G= | CA2187187744 | HCN4 | c.2871C= (p.His957=) c.1653C= (p.His551=) | |
15 | g.73323222G>T | CA393087185 | HCN4 | c.2871C>A (p.His957Gln) c.1653C>A (p.His551Gln) | gnomAD v4 |
15 | g.73323223T>A | CA393087187 | HCN4 | c.2870A>T (p.His957Leu) c.1652A>T (p.His551Leu) | |
15 | g.73323223T>C | CA393087190 | HCN4 | c.2870A>G (p.His957Arg) c.1652A>G (p.His551Arg) | |
15 | g.73323223T>G | CA393087197 | HCN4 | c.2870A>C (p.His957Pro) c.1652A>C (p.His551Pro) | dbSNP |
15 | g.73323223T= | CA2187187747 | HCN4 | c.2870A= (p.His957=) c.1652A= (p.His551=) | |
15 | g.73323224G>A | CA393087206 | HCN4 | c.2869C>T (p.His957Tyr) c.1651C>T (p.His551Tyr) | gnomAD v4 |
15 | g.73323224G>C | CA393087203 | HCN4 | c.2869C>G (p.His957Asp) c.1651C>G (p.His551Asp) | |
15 | g.73323224G>T | CA393087200 | HCN4 | c.2869C>A (p.His957Asn) c.1651C>A (p.His551Asn) | gnomAD v4 |
15 | g.73323225C>A | CA393087212 | HCN4 | c.2868G>T (p.Glu956Asp) c.1650G>T (p.Glu550Asp) | gnomAD v4 |
15 | g.73323225C= | CA2187187750 | HCN4 | c.2868G= (p.Glu956=) c.1650G= (p.Glu550=) | |
15 | g.73323225C>G | CA393087209 | HCN4 | c.2868G>C (p.Glu956Asp) c.1650G>C (p.Glu550Asp) | dbSNP gnomAD v2 |
15 | g.73323225C>T | CA491478864 | HCN4 | c.2868G>A (p.Glu956=) c.1650G>A (p.Glu550=) | gnomAD v4 |
15 | g.73323226T>A | CA393087215 | HCN4 | c.2867A>T (p.Glu956Val) c.1649A>T (p.Glu550Val) | gnomAD v4 |
15 | g.73323226T>C | CA393087217 | HCN4 | c.2867A>G (p.Glu956Gly) c.1649A>G (p.Glu550Gly) | gnomAD v4 |
15 | g.73323226T>G | CA393087220 | HCN4 | c.2867A>C (p.Glu956Ala) c.1649A>C (p.Glu550Ala) | |
15 | g.73323226_73323243delinsCC | CA2573151086 | HCN4 | c.2850_2867delinsGG (p.Leu952ThrfsTer28) c.1632_1649delinsGG (p.Leu546ThrfsTer28) | ClinVar dbSNP |
15 | g.73323227C>A | CA393087224 | HCN4 | c.2866G>T (p.Glu956Ter) c.1648G>T (p.Glu550Ter) | gnomAD v4 |
15 | g.73323227C= | CA2187187753 | HCN4 | c.2866G= (p.Glu956=) c.1648G= (p.Glu550=) | |
15 | g.73323227C>G | CA393087226 | HCN4 | c.2866G>C (p.Glu956Gln) c.1648G>C (p.Glu550Gln) | gnomAD v4 |
15 | g.73323227C>T | CA393087229 | HCN4 | c.2866G>A (p.Glu956Lys) c.1648G>A (p.Glu550Lys) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
15 | g.73323228C>A | CA491478873 | HCN4 | c.2865G>T (p.Pro955=) c.1647G>T (p.Pro549=) | gnomAD v4 |
15 | g.73323228C= | CA2187187759 | HCN4 | c.2865G= (p.Pro955=) c.1647G= (p.Pro549=) | |
15 | g.73323228C>G | CA491478874 | HCN4 | c.2865G>C (p.Pro955=) c.1647G>C (p.Pro549=) | |
15 | g.73323228C>T | CA491478875 | HCN4 | c.2865G>A (p.Pro955=) c.1647G>A (p.Pro549=) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73323229G>A | CA7648936 | HCN4 | c.2864C>T (p.Pro955Leu) c.1646C>T (p.Pro549Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323229G>C | CA393087235 | HCN4 | c.2864C>G (p.Pro955Arg) c.1646C>G (p.Pro549Arg) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323229G= | CA2187187774 | HCN4 | c.2864C= (p.Pro955=) c.1646C= (p.Pro549=) | |
15 | g.73323229G>T | CA7648937 | HCN4 | c.2864C>A (p.Pro955Gln) c.1646C>A (p.Pro549Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323231del | CA2629370555 | HCN4 | c.2864del (p.Pro955ArgfsTer30) c.1646del (p.Pro549ArgfsTer30) | gnomAD v4 |
15 | g.73323230G>A | CA7648938 | HCN4 | c.2863C>T (p.Pro955Ser) c.1645C>T (p.Pro549Ser) | ClinVar dbSNP ExAC gnomAD v4 |
15 | g.73323230G>C | CA393087242 | HCN4 | c.2863C>G (p.Pro955Ala) c.1645C>G (p.Pro549Ala) | |
15 | g.73323230G= | CA2187187776 | HCN4 | c.2863C= (p.Pro955=) c.1645C= (p.Pro549=) | |
15 | g.73323230G>T | CA393087245 | HCN4 | c.2863C>A (p.Pro955Thr) c.1645C>A (p.Pro549Thr) | gnomAD v4 |
15 | g.73323231G>A | CA491478880 | HCN4 | c.2862C>T (p.Leu954=) c.1644C>T (p.Leu548=) | gnomAD v4 COSMIC |
15 | g.73323231G>C | CA491478882 | HCN4 | c.2862C>G (p.Leu954=) c.1644C>G (p.Leu548=) | |
15 | g.73323231G>T | CA491478884 | HCN4 | c.2862C>A (p.Leu954=) c.1644C>A (p.Leu548=) | gnomAD v4 |
15 | g.73323232del | CA2629370556 | HCN4 | c.2861del (p.Leu954ProfsTer?) c.1643del (p.Leu548ProfsTer?) | gnomAD v4 |
15 | g.73323232A>C | CA393087253 | HCN4 | c.2861T>G (p.Leu954Arg) c.1643T>G (p.Leu548Arg) | |
15 | g.73323232A>G | CA393087251 | HCN4 | c.2861T>C (p.Leu954Pro) c.1643T>C (p.Leu548Pro) | |
15 | g.73323232A>T | CA393087248 | HCN4 | c.2861T>A (p.Leu954His) c.1643T>A (p.Leu548His) | |
15 | g.73323233G>A | CA393087256 | HCN4 | c.2860C>T (p.Leu954Phe) c.1642C>T (p.Leu548Phe) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323233G>C | CA393087259 | HCN4 | c.2860C>G (p.Leu954Val) c.1642C>G (p.Leu548Val) | COSMIC |
15 | g.73323233G= | CA2187187778 | HCN4 | c.2860C= (p.Leu954=) c.1642C= (p.Leu548=) | |
15 | g.73323233G>T | CA393087262 | HCN4 | c.2860C>A (p.Leu954Ile) c.1642C>A (p.Leu548Ile) | gnomAD v4 |
15 | g.73323234T>A | CA491478891 | HCN4 | c.2859A>T (p.Gly953=) c.1641A>T (p.Gly547=) | |
15 | g.73323234T>C | CA491478892 | HCN4 | c.2859A>G (p.Gly953=) c.1641A>G (p.Gly547=) | |
15 | g.73323234T>G | CA491478890 | HCN4 | c.2859A>C (p.Gly953=) c.1641A>C (p.Gly547=) | |
15 | g.73323235C>A | CA393087265 | HCN4 | c.2858G>T (p.Gly953Val) c.1640G>T (p.Gly547Val) | gnomAD v4 |
15 | g.73323235C= | CA2187187782 | HCN4 | c.2858G= (p.Gly953=) c.1640G= (p.Gly547=) | |
15 | g.73323235C>G | CA393087268 | HCN4 | c.2858G>C (p.Gly953Ala) c.1640G>C (p.Gly547Ala) | |
15 | g.73323235C>T | CA393087270 | HCN4 | c.2858G>A (p.Gly953Glu) c.1640G>A (p.Gly547Glu) | ClinVar dbSNP gnomAD v4 |
15 | g.73323237del | CA2629370557 | HCN4 | c.2858del (p.Gly953AspfsTer?) c.1640del (p.Gly547AspfsTer?) | ClinVar gnomAD v4 |
15 | g.73323236_73323237del | CA2629370558 | HCN4 | c.2857_2858del (p.Gly953ThrfsTer18) c.1639_1640del (p.Gly547ThrfsTer18) | gnomAD v4 |
15 | g.73323236C>A | CA393087275 | HCN4 | c.2857G>T (p.Gly953Ter) c.1639G>T (p.Gly547Ter) | gnomAD v4 |
15 | g.73323236C>G | CA393087277 | HCN4 | c.2857G>C (p.Gly953Arg) c.1639G>C (p.Gly547Arg) | |
15 | g.73323236C>T | CA393087280 | HCN4 | c.2857G>A (p.Gly953Arg) c.1639G>A (p.Gly547Arg) | gnomAD v4 |
15 | g.73323237C>A | CA491478901 | HCN4 | c.2856G>T (p.Leu952=) c.1638G>T (p.Leu546=) | gnomAD v4 |
15 | g.73323237C>G | CA491478904 | HCN4 | c.2856G>C (p.Leu952=) c.1638G>C (p.Leu546=) | |
15 | g.73323237C>T | CA491478907 | HCN4 | c.2856G>A (p.Leu952=) c.1638G>A (p.Leu546=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323238A>C | CA393087283 | HCN4 | c.2855T>G (p.Leu952Arg) c.1637T>G (p.Leu546Arg) | |
15 | g.73323238A>G | CA393087285 | HCN4 | c.2855T>C (p.Leu952Pro) c.1637T>C (p.Leu546Pro) | gnomAD v4 |
15 | g.73323238A>T | CA393087287 | HCN4 | c.2855T>A (p.Leu952Gln) c.1637T>A (p.Leu546Gln) | gnomAD v4 |
15 | g.73323239G>A | CA491478908 | HCN4 | c.2854C>T (p.Leu952=) c.1636C>T (p.Leu546=) | |
15 | g.73323239G>C | CA393087289 | HCN4 | c.2854C>G (p.Leu952Val) c.1636C>G (p.Leu546Val) | |
15 | g.73323239G>T | CA393087291 | HCN4 | c.2854C>A (p.Leu952Met) c.1636C>A (p.Leu546Met) | gnomAD v4 |
15 | g.73323240G>A | CA491478913 | HCN4 | c.2853C>T (p.Gly951=) c.1635C>T (p.Gly545=) | gnomAD v4 |
15 | g.73323240G>C | CA491478912 | HCN4 | c.2853C>G (p.Gly951=) c.1635C>G (p.Gly545=) | |
15 | g.73323240G>T | CA491478911 | HCN4 | c.2853C>A (p.Gly951=) c.1635C>A (p.Gly545=) | gnomAD v4 |
15 | g.73323241C>A | CA393087297 | HCN4 | c.2852G>T (p.Gly951Val) c.1634G>T (p.Gly545Val) | gnomAD v4 |
15 | g.73323241C= | CA2187187784 | HCN4 | c.2852G= (p.Gly951=) c.1634G= (p.Gly545=) | |
15 | g.73323241C>G | CA393087300 | HCN4 | c.2852G>C (p.Gly951Ala) c.1634G>C (p.Gly545Ala) | |
15 | g.73323241C>T | CA393087295 | HCN4 | c.2852G>A (p.Gly951Asp) c.1634G>A (p.Gly545Asp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323242C>A | CA393087304 | HCN4 | c.2851G>T (p.Gly951Cys) c.1633G>T (p.Gly545Cys) | gnomAD v4 COSMIC |
15 | g.73323242C= | CA2187187787 | HCN4 | c.2851G= (p.Gly951=) c.1633G= (p.Gly545=) | |
15 | g.73323242C>G | CA393087305 | HCN4 | c.2851G>C (p.Gly951Arg) c.1633G>C (p.Gly545Arg) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323242C>T | CA393087307 | HCN4 | c.2851G>A (p.Gly951Ser) c.1633G>A (p.Gly545Ser) | gnomAD v4 |
15 | g.73323243T>A | CA491478917 | HCN4 | c.2850A>T (p.Gly950=) c.1632A>T (p.Gly544=) | |
15 | g.73323243T>C | CA491478918 | HCN4 | c.2850A>G (p.Gly950=) c.1632A>G (p.Gly544=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323243T>G | CA491478919 | HCN4 | c.2850A>C (p.Gly950=) c.1632A>C (p.Gly544=) | |
15 | g.73323243_73323244delinsTC | CA2187187790 | HCN4 | c.2849_2850delinsGA (p.Gly950=) c.1631_1632delinsGA (p.Gly544=) |