Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73323159_73323250del | CA619410578 | HCN4 | c.2852_2943del (p.Gly951ValfsTer21) c.1634_1725del (p.Gly545ValfsTer21) | gnomAD v2 |
15 | g.73323203_73323209delinsAGGGTGG | CA2187187699 | HCN4 | c.2884_2890delinsCCACCCT (p.Pro962=) c.1666_1672delinsCCACCCT (p.Pro556=) | |
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=) | |
15 | g.73323244C>A | CA393087310 | HCN4 | c.2849G>T (p.Gly950Val) c.1631G>T (p.Gly544Val) | gnomAD v4 |
15 | g.73323244C>G | CA393087313 | HCN4 | c.2849G>C (p.Gly950Ala) c.1631G>C (p.Gly544Ala) | |
15 | g.73323244C>T | CA393087314 | HCN4 | c.2849G>A (p.Gly950Glu) c.1631G>A (p.Gly544Glu) | COSMIC |
15 | g.73323247dup | CA2575783832 | HCN4 | c.2849dup (p.Gly951ArgfsTer21) c.1631dup (p.Gly545ArgfsTer21) | gnomAD v4 |
15 | g.73323247del | CA619410579 | HCN4 | c.2849del (p.Gly950GlufsTer?) c.1631del (p.Gly544GlufsTer?) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323246_73323247del | CA2629370559 | HCN4 | c.2848_2849del (p.Gly950ArgfsTer21) c.1630_1631del (p.Gly544ArgfsTer21) | gnomAD v4 |
15 | g.73323245C>A | CA393087317 | HCN4 | c.2848G>T (p.Gly950Ter) c.1630G>T (p.Gly544Ter) | gnomAD v4 |
15 | g.73323245C= | CA2187187796 | HCN4 | c.2848G= (p.Gly950=) c.1630G= (p.Gly544=) | |
15 | g.73323245C>G | CA393087318 | HCN4 | c.2848G>C (p.Gly950Arg) c.1630G>C (p.Gly544Arg) | |
15 | g.73323245C>T | CA393087321 | HCN4 | c.2848G>A (p.Gly950Arg) c.1630G>A (p.Gly544Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323246C>A | CA491478923 | HCN4 | c.2847G>T (p.Arg949=) c.1629G>T (p.Arg543=) | gnomAD v4 |
15 | g.73323246C>G | CA491478924 | HCN4 | c.2847G>C (p.Arg949=) c.1629G>C (p.Arg543=) | |
15 | g.73323246C>T | CA491478925 | HCN4 | c.2847G>A (p.Arg949=) c.1629G>A (p.Arg543=) | gnomAD v4 |
15 | g.73323247C>A | CA393087323 | HCN4 | c.2846G>T (p.Arg949Leu) c.1628G>T (p.Arg543Leu) | gnomAD v4 |
15 | g.73323247C= | CA2187187802 | HCN4 | c.2846G= (p.Arg949=) c.1628G= (p.Arg543=) | |
15 | g.73323247C>G | CA272664120 | HCN4 | c.2846G>C (p.Arg949Pro) c.1628G>C (p.Arg543Pro) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323247C>T | CA7648939 | HCN4 | c.2846G>A (p.Arg949Gln) c.1628G>A (p.Arg543Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323248G>A | CA7648940 | HCN4 | c.2845C>T (p.Arg949Trp) c.1627C>T (p.Arg543Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323248G>C | CA393087328 | HCN4 | c.2845C>G (p.Arg949Gly) c.1627C>G (p.Arg543Gly) | |
15 | g.73323248G= | CA2187187813 | HCN4 | c.2845C= (p.Arg949=) c.1627C= (p.Arg543=) | |
15 | g.73323248G>T | CA491478928 | HCN4 | c.2845C>A (p.Arg949=) c.1627C>A (p.Arg543=) | gnomAD v4 |
15 | g.73323250dup | CA2629370560 | HCN4 | c.2845dup (p.Arg949ProfsTer23) c.1627dup (p.Arg543ProfsTer23) | gnomAD v4 |
15 | g.73323250del | CA2629370561 | HCN4 | c.2845del (p.Arg949GlyfsTer?) c.1627del (p.Arg543GlyfsTer?) | gnomAD v4 |
15 | g.73323249G>A | CA491478929 | HCN4 | c.2844C>T (p.Ala948=) c.1626C>T (p.Ala542=) | gnomAD v4 |
15 | g.73323249G>C | CA491478931 | HCN4 | c.2844C>G (p.Ala948=) c.1626C>G (p.Ala542=) | |
15 | g.73323249G>T | CA491478933 | HCN4 | c.2844C>A (p.Ala948=) c.1626C>A (p.Ala542=) | gnomAD v4 |
15 | g.73323250G>A | CA393087331 | HCN4 | c.2843C>T (p.Ala948Val) c.1625C>T (p.Ala542Val) | dbSNP gnomAD v4 |
15 | g.73323250G>C | CA393087333 | HCN4 | c.2843C>G (p.Ala948Gly) c.1625C>G (p.Ala542Gly) | |
15 | g.73323250G= | CA2187187819 | HCN4 | c.2843C= (p.Ala948=) c.1625C= (p.Ala542=) | |
15 | g.73323250G>T | CA393087334 | HCN4 | c.2843C>A (p.Ala948Asp) c.1625C>A (p.Ala542Asp) | gnomAD v4 |
15 | g.73323250_73323251delinsGC | CA2187187818 | HCN4 | c.2842_2843delinsGC (p.Ala948=) c.1624_1625delinsGC (p.Ala542=) | |
15 | g.73323251C>A | CA393087335 | HCN4 | c.2842G>T (p.Ala948Ser) c.1624G>T (p.Ala542Ser) | dbSNP gnomAD v4 |
15 | g.73323251C= | CA2187187826 | HCN4 | c.2842G= (p.Ala948=) c.1624G= (p.Ala542=) | |
15 | g.73323251C>G | CA393087337 | HCN4 | c.2842G>C (p.Ala948Pro) c.1624G>C (p.Ala542Pro) | |
15 | g.73323251C>T | CA7648941 | HCN4 | c.2842G>A (p.Ala948Thr) c.1624G>A (p.Ala542Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323254del | CA619410580 | HCN4 | c.2842del (p.Ala948ProfsTer?) c.1624del (p.Ala542ProfsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323252C>A | CA491478940 | HCN4 | c.2841G>T (p.Gly947=) c.1623G>T (p.Gly541=) | gnomAD v4 |
15 | g.73323252C>G | CA491478941 | HCN4 | c.2841G>C (p.Gly947=) c.1623G>C (p.Gly541=) | |
15 | g.73323252C>T | CA491478942 | HCN4 | c.2841G>A (p.Gly947=) c.1623G>A (p.Gly541=) | gnomAD v4 |
15 | g.73323252_73323258del | CA2629370562 | HCN4 | c.2835_2841del (p.Ala948GlufsTer?) c.1617_1623del (p.Ala542GlufsTer?) | gnomAD v4 |
15 | g.73323253C>A | CA393087341 | HCN4 | c.2840G>T (p.Gly947Val) c.1622G>T (p.Gly541Val) | |
15 | g.73323253C= | CA2187187833 | HCN4 | c.2840G= (p.Gly947=) c.1622G= (p.Gly541=) | |
15 | g.73323253C>G | CA393087342 | HCN4 | c.2840G>C (p.Gly947Ala) c.1622G>C (p.Gly541Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323253C>T | CA393087344 | HCN4 | c.2840G>A (p.Gly947Glu) c.1622G>A (p.Gly541Glu) | gnomAD v4 |
15 | g.73323254C>A | CA393087347 | HCN4 | c.2839G>T (p.Gly947Trp) c.1621G>T (p.Gly541Trp) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323254C= | CA2187187838 | HCN4 | c.2839G= (p.Gly947=) c.1621G= (p.Gly541=) | |
15 | g.73323254C>G | CA393087349 | HCN4 | c.2839G>C (p.Gly947Arg) c.1621G>C (p.Gly541Arg) | gnomAD v4 |
15 | g.73323254C>T | CA7648942 | HCN4 | c.2839G>A (p.Gly947Arg) c.1621G>A (p.Gly541Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323254_73323255insCGGCAGC | CA2509381855 | HCN4 | c.2839_2840insCTGCCGG (p.Gly947AlafsTer27) c.1621_1622insCTGCCGG (p.Gly541AlafsTer27) | |
15 | g.73323255G>A | CA7648943 | HCN4 | c.2838C>T (p.Pro946=) c.1620C>T (p.Pro540=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323255G>C | CA491478950 | HCN4 | c.2838C>G (p.Pro946=) c.1620C>G (p.Pro540=) | |
15 | g.73323255G= | CA2187187843 | HCN4 | c.2838C= (p.Pro946=) c.1620C= (p.Pro540=) | |
15 | g.73323255G>T | CA491478949 | HCN4 | c.2838C>A (p.Pro946=) c.1620C>A (p.Pro540=) | gnomAD v4 |
15 | g.73323257del | CA971394656 | HCN4 | c.2838del (p.Ala948ProfsTer?) c.1620del (p.Ala542ProfsTer?) | gnomAD v3 gnomAD v4 |
15 | g.73323256G>A | CA393087356 | HCN4 | c.2837C>T (p.Pro946Leu) c.1619C>T (p.Pro540Leu) | gnomAD v4 |
15 | g.73323256G>C | CA393087357 | HCN4 | c.2837C>G (p.Pro946Arg) c.1619C>G (p.Pro540Arg) | |
15 | g.73323256G>T | CA393087354 | HCN4 | c.2837C>A (p.Pro946His) c.1619C>A (p.Pro540His) | gnomAD v4 |
15 | g.73323257G>A | CA393087360 | HCN4 | c.2836C>T (p.Pro946Ser) c.1618C>T (p.Pro540Ser) | gnomAD v4 |
15 | g.73323257G>C | CA393087362 | HCN4 | c.2836C>G (p.Pro946Ala) c.1618C>G (p.Pro540Ala) | |
15 | g.73323257G>T | CA393087361 | HCN4 | c.2836C>A (p.Pro946Thr) c.1618C>A (p.Pro540Thr) | gnomAD v4 |
15 | g.73323258T>A | CA491478960 | HCN4 | c.2835A>T (p.Pro945=) c.1617A>T (p.Pro539=) | |
15 | g.73323258T>C | CA491478958 | HCN4 | c.2835A>G (p.Pro945=) c.1617A>G (p.Pro539=) | |
15 | g.73323258T>G | CA491478956 | HCN4 | c.2835A>C (p.Pro945=) c.1617A>C (p.Pro539=) | |
15 | g.73323258_73323259insCAGCA | CA2629370563 | HCN4 | c.2834_2835insTGCTG (p.Pro946AlafsTer?) c.1616_1617insTGCTG (p.Pro540AlafsTer?) | gnomAD v4 |
15 | g.73323259G>A | CA393087364 | HCN4 | c.2834C>T (p.Pro945Leu) c.1616C>T (p.Pro539Leu) | gnomAD v4 |
15 | g.73323259G>C | CA393087367 | HCN4 | c.2834C>G (p.Pro945Arg) c.1616C>G (p.Pro539Arg) | |
15 | g.73323259G>T | CA393087366 | HCN4 | c.2834C>A (p.Pro945Gln) c.1616C>A (p.Pro539Gln) | gnomAD v4 |
15 | g.73323260G>A | CA7648944 | HCN4 | c.2833C>T (p.Pro945Ser) c.1615C>T (p.Pro539Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323260G>C | CA393087370 | HCN4 | c.2833C>G (p.Pro945Ala) c.1615C>G (p.Pro539Ala) | gnomAD v4 |
15 | g.73323260G= | CA2187187848 | HCN4 | c.2833C= (p.Pro945=) c.1615C= (p.Pro539=) | |
15 | g.73323260G>T | CA393087372 | HCN4 | c.2833C>A (p.Pro945Thr) c.1615C>A (p.Pro539Thr) | gnomAD v4 |
15 | g.73323261C>A | CA491478967 | HCN4 | c.2832G>T (p.Ala944=) c.1614G>T (p.Ala538=) | gnomAD v4 |
15 | g.73323261C= | CA2187187854 | HCN4 | c.2832G= (p.Ala944=) c.1614G= (p.Ala538=) | |
15 | g.73323261C>G | CA491478971 | HCN4 | c.2832G>C (p.Ala944=) c.1614G>C (p.Ala538=) | |
15 | g.73323261C>T | CA7648945 | HCN4 | c.2832G>A (p.Ala944=) c.1614G>A (p.Ala538=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323262G>A | CA199743 | HCN4 | c.2831C>T (p.Ala944Val) c.1613C>T (p.Ala538Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323262G>C | CA393087376 | HCN4 | c.2831C>G (p.Ala944Gly) c.1613C>G (p.Ala538Gly) | |
15 | g.73323262G= | CA2187187856 | HCN4 | c.2831C= (p.Ala944=) c.1613C= (p.Ala538=) | |
15 | g.73323262G>T | CA393087378 | HCN4 | c.2831C>A (p.Ala944Glu) c.1613C>A (p.Ala538Glu) | gnomAD v4 |
15 | g.73323263C>A | CA7648947 | HCN4 | c.2830G>T (p.Ala944Ser) c.1612G>T (p.Ala538Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
15 | g.73323263C= | CA2187187863 | HCN4 | c.2830G= (p.Ala944=) c.1612G= (p.Ala538=) | |
15 | g.73323263C>G | CA393087380 | HCN4 | c.2830G>C (p.Ala944Pro) c.1612G>C (p.Ala538Pro) | |
15 | g.73323263C>T | CA7648946 | HCN4 | c.2830G>A (p.Ala944Thr) c.1612G>A (p.Ala538Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323264G>A | CA491478975 | HCN4 | c.2829C>T (p.Pro943=) c.1611C>T (p.Pro537=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323264G>C | CA491478976 | HCN4 | c.2829C>G (p.Pro943=) c.1611C>G (p.Pro537=) | gnomAD v4 |
15 | g.73323264G= | CA2187187868 | HCN4 | c.2829C= (p.Pro943=) c.1611C= (p.Pro537=) | |
15 | g.73323264G>T | CA491478977 | HCN4 | c.2829C>A (p.Pro943=) c.1611C>A (p.Pro537=) | gnomAD v4 |
15 | g.73323265G>A | CA393087383 | HCN4 | c.2828C>T (p.Pro943Leu) c.1610C>T (p.Pro537Leu) | gnomAD v4 |
15 | g.73323265G>C | CA393087385 | HCN4 | c.2828C>G (p.Pro943Arg) c.1610C>G (p.Pro537Arg) | dbSNP gnomAD v4 |
15 | g.73323265G= | CA2187187874 | HCN4 | c.2828C= (p.Pro943=) c.1610C= (p.Pro537=) | |
15 | g.73323265G>T | CA393087387 | HCN4 | c.2828C>A (p.Pro943His) c.1610C>A (p.Pro537His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323266G>A | CA393087389 | HCN4 | c.2827C>T (p.Pro943Ser) c.1609C>T (p.Pro537Ser) | dbSNP |
15 | g.73323266G>C | CA393087393 | HCN4 | c.2827C>G (p.Pro943Ala) c.1609C>G (p.Pro537Ala) | |
15 | g.73323266G= | CA2187187877 | HCN4 | c.2827C= (p.Pro943=) c.1609C= (p.Pro537=) | |
15 | g.73323266G>T | CA393087391 | HCN4 | c.2827C>A (p.Pro943Thr) c.1609C>A (p.Pro537Thr) | |
15 | g.73323267A>C | CA491478981 | HCN4 | c.2826T>G (p.Ser942=) c.1608T>G (p.Ser536=) | |
15 | g.73323267A>G | CA491478983 | HCN4 | c.2826T>C (p.Ser942=) c.1608T>C (p.Ser536=) | |
15 | g.73323267A>T | CA491478984 | HCN4 | c.2826T>A (p.Ser942=) c.1608T>A (p.Ser536=) | |
15 | g.73323268G>A | CA393087395 | HCN4 | c.2825C>T (p.Ser942Phe) c.1607C>T (p.Ser536Phe) | gnomAD v4 |
15 | g.73323268G>C | CA393087396 | HCN4 | c.2825C>G (p.Ser942Cys) c.1607C>G (p.Ser536Cys) | |
15 | g.73323268G>T | CA393087399 | HCN4 | c.2825C>A (p.Ser942Tyr) c.1607C>A (p.Ser536Tyr) | gnomAD v4 |
15 | g.73323269A>C | CA393087400 | HCN4 | c.2824T>G (p.Ser942Ala) c.1606T>G (p.Ser536Ala) | |
15 | g.73323269A>G | CA393087401 | HCN4 | c.2824T>C (p.Ser942Pro) c.1606T>C (p.Ser536Pro) | dbSNP |
15 | g.73323269A>T | CA393087403 | HCN4 | c.2824T>A (p.Ser942Thr) c.1606T>A (p.Ser536Thr) | |
15 | g.73323270T>A | CA491478989 | HCN4 | c.2823A>T (p.Pro941=) c.1605A>T (p.Pro535=) | |
15 | g.73323270T>C | CA491478990 | HCN4 | c.2823A>G (p.Pro941=) c.1605A>G (p.Pro535=) | gnomAD v4 |
15 | g.73323270T>G | CA491478991 | HCN4 | c.2823A>C (p.Pro941=) c.1605A>C (p.Pro535=) | |
15 | g.73323271G>A | CA393087406 | HCN4 | c.2822C>T (p.Pro941Leu) c.1604C>T (p.Pro535Leu) | |
15 | g.73323271G>C | CA393087407 | HCN4 | c.2822C>G (p.Pro941Arg) c.1604C>G (p.Pro535Arg) | |
15 | g.73323271G>T | CA393087410 | HCN4 | c.2822C>A (p.Pro941Gln) c.1604C>A (p.Pro535Gln) | |
15 | g.73323272G>A | CA393087416 | HCN4 | c.2821C>T (p.Pro941Ser) c.1603C>T (p.Pro535Ser) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323272G>C | CA393087415 | HCN4 | c.2821C>G (p.Pro941Ala) c.1603C>G (p.Pro535Ala) | |
15 | g.73323272G= | CA2187187882 | HCN4 | c.2821C= (p.Pro941=) c.1603C= (p.Pro535=) | |
15 | g.73323272G>T | CA393087413 | HCN4 | c.2821C>A (p.Pro941Thr) c.1603C>A (p.Pro535Thr) | gnomAD v4 |
15 | g.73323273C>A | CA393087827 | HCN4 | c.2820G>T (p.Gln940His) c.1602G>T (p.Gln534His) | gnomAD v4 |
15 | g.73323273C>G | CA393087830 | HCN4 | c.2820G>C (p.Gln940His) c.1602G>C (p.Gln534His) | |
15 | g.73323273C>T | CA491478170 | HCN4 | c.2820G>A (p.Gln940=) c.1602G>A (p.Gln534=) | gnomAD v4 |
15 | g.73323274T>A | CA393087832 | HCN4 | c.2819A>T (p.Gln940Leu) c.1601A>T (p.Gln534Leu) | |
15 | g.73323274T>C | CA393087835 | HCN4 | c.2819A>G (p.Gln940Arg) c.1601A>G (p.Gln534Arg) | |
15 | g.73323274T>G | CA393087838 | HCN4 | c.2819A>C (p.Gln940Pro) c.1601A>C (p.Gln534Pro) | |
15 | g.73323275G>A | CA393087840 | HCN4 | c.2818C>T (p.Gln940Ter) c.1600C>T (p.Gln534Ter) | |
15 | g.73323275G>C | CA393087843 | HCN4 | c.2818C>G (p.Gln940Glu) c.1600C>G (p.Gln534Glu) | |
15 | g.73323275G>T | CA393087846 | HCN4 | c.2818C>A (p.Gln940Lys) c.1600C>A (p.Gln534Lys) | gnomAD v4 |
15 | g.73323276G>A | CA491478173 | HCN4 | c.2817C>T (p.Ala939=) c.1599C>T (p.Ala533=) | |
15 | g.73323276G>C | CA491478172 | HCN4 | c.2817C>G (p.Ala939=) c.1599C>G (p.Ala533=) | |
15 | g.73323276G>T | CA491478171 | HCN4 | c.2817C>A (p.Ala939=) c.1599C>A (p.Ala533=) | gnomAD v4 |
15 | g.73323277G>A | CA393087849 | HCN4 | c.2816C>T (p.Ala939Val) c.1598C>T (p.Ala533Val) | gnomAD v4 |
15 | g.73323277G>C | CA393087851 | HCN4 | c.2816C>G (p.Ala939Gly) c.1598C>G (p.Ala533Gly) | |
15 | g.73323277G>T | CA393087854 | HCN4 | c.2816C>A (p.Ala939Asp) c.1598C>A (p.Ala533Asp) | gnomAD v4 |
15 | g.73323278C>A | CA393087862 | HCN4 | c.2815G>T (p.Ala939Ser) c.1597G>T (p.Ala533Ser) | gnomAD v4 |
15 | g.73323278C>G | CA393087861 | HCN4 | c.2815G>C (p.Ala939Pro) c.1597G>C (p.Ala533Pro) | |
15 | g.73323278C>T | CA393087857 | HCN4 | c.2815G>A (p.Ala939Thr) c.1597G>A (p.Ala533Thr) | gnomAD v4 |
15 | g.73323279A>C | CA491478174 | HCN4 | c.2814T>G (p.Ala938=) c.1596T>G (p.Ala532=) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323279A>G | CA491478175 | HCN4 | c.2814T>C (p.Ala938=) c.1596T>C (p.Ala532=) | gnomAD v4 |
15 | g.73323279A>T | CA491478176 | HCN4 | c.2814T>A (p.Ala938=) c.1596T>A (p.Ala532=) | |
15 | g.73323280G>A | CA393087865 | HCN4 | c.2813C>T (p.Ala938Val) c.1595C>T (p.Ala532Val) | gnomAD v4 |
15 | g.73323280G>C | CA393087867 | HCN4 | c.2813C>G (p.Ala938Gly) c.1595C>G (p.Ala532Gly) | |
15 | g.73323280G>T | CA393087871 | HCN4 | c.2813C>A (p.Ala938Asp) c.1595C>A (p.Ala532Asp) | gnomAD v4 |
15 | g.73323280_73323281delinsGC | CA2187187886 | HCN4 | c.2812_2813delinsGC (p.Ala938=) c.1594_1595delinsGC (p.Ala532=) | |
15 | g.73323281C>A | CA393087874 | HCN4 | c.2812G>T (p.Ala938Ser) c.1594G>T (p.Ala532Ser) | gnomAD v4 |
15 | g.73323281C>G | CA393087875 | HCN4 | c.2812G>C (p.Ala938Pro) c.1594G>C (p.Ala532Pro) | |
15 | g.73323281C>T | CA393087878 | HCN4 | c.2812G>A (p.Ala938Thr) c.1594G>A (p.Ala532Thr) | gnomAD v4 |
15 | g.73323282del | CA272664172 | HCN4 | c.2812del (p.Ala938LeufsTer?) c.1594del (p.Ala532LeufsTer?) | dbSNP |
15 | g.73323282C>A | CA393087881 | HCN4 | c.2811G>T (p.Gln937His) c.1593G>T (p.Gln531His) | gnomAD v4 |
15 | g.73323282C>G | CA393087883 | HCN4 | c.2811G>C (p.Gln937His) c.1593G>C (p.Gln531His) | |
15 | g.73323282C>T | CA491478177 | HCN4 | c.2811G>A (p.Gln937=) c.1593G>A (p.Gln531=) | |
15 | g.73323283T>A | CA7648948 | HCN4 | c.2810A>T (p.Gln937Leu) c.1592A>T (p.Gln531Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323283T>C | CA393087889 | HCN4 | c.2810A>G (p.Gln937Arg) c.1592A>G (p.Gln531Arg) | gnomAD v4 |
15 | g.73323283T>G | CA393087890 | HCN4 | c.2810A>C (p.Gln937Pro) c.1592A>C (p.Gln531Pro) | |
15 | g.73323283T= | CA2187187893 | HCN4 | c.2810A= (p.Gln937=) c.1592A= (p.Gln531=) | |
15 | g.73323284G>A | CA7648949 | HCN4 | c.2809C>T (p.Gln937Ter) c.1591C>T (p.Gln531Ter) | ClinVar dbSNP ExAC gnomAD v4 |
15 | g.73323284G>C | CA393087897 | HCN4 | c.2809C>G (p.Gln937Glu) c.1591C>G (p.Gln531Glu) | |
15 | g.73323284G= | CA2187187900 | HCN4 | c.2809C= (p.Gln937=) c.1591C= (p.Gln531=) | |
15 | g.73323284G>T | CA393087894 | HCN4 | c.2809C>A (p.Gln937Lys) c.1591C>A (p.Gln531Lys) | gnomAD v4 |
15 | g.73323285C>A | CA272664207 | HCN4 | c.2808G>T (p.Pro936=) c.1590G>T (p.Pro530=) | dbSNP gnomAD v4 |
15 | g.73323285C= | CA2187187905 | HCN4 | c.2808G= (p.Pro936=) c.1590G= (p.Pro530=) | |
15 | g.73323285C>G | CA491478178 | HCN4 | c.2808G>C (p.Pro936=) c.1590G>C (p.Pro530=) | |
15 | g.73323285C>T | CA7648950 | HCN4 | c.2808G>A (p.Pro936=) c.1590G>A (p.Pro530=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323286G>A | CA7648951 | HCN4 | c.2807C>T (p.Pro936Leu) c.1589C>T (p.Pro530Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73323286G>C | CA393087906 | HCN4 | c.2807C>G (p.Pro936Arg) c.1589C>G (p.Pro530Arg) | |
15 | g.73323286G= | CA2187187915 | HCN4 | c.2807C= (p.Pro936=) c.1589C= (p.Pro530=) | |
15 | g.73323286G>T | CA393087908 | HCN4 | c.2807C>A (p.Pro936Gln) c.1589C>A (p.Pro530Gln) | dbSNP gnomAD v2 gnomAD v4 COSMIC |
15 | g.73323287G>A | CA393087912 | HCN4 | c.2806C>T (p.Pro936Ser) c.1588C>T (p.Pro530Ser) | dbSNP gnomAD v4 |
15 | g.73323287G>C | CA393087915 | HCN4 | c.2806C>G (p.Pro936Ala) c.1588C>G (p.Pro530Ala) | |
15 | g.73323287G= | CA2187187924 | HCN4 | c.2806C= (p.Pro936=) c.1588C= (p.Pro530=) | |
15 | g.73323287G>T | CA393087916 | HCN4 | c.2806C>A (p.Pro936Thr) c.1588C>A (p.Pro530Thr) | gnomAD v4 |
15 | g.73323288G>A | CA491478179 | HCN4 | c.2805C>T (p.Ser935=) c.1587C>T (p.Ser529=) | gnomAD v4 |
15 | g.73323288G>C | CA491478181 | HCN4 | c.2805C>G (p.Ser935=) c.1587C>G (p.Ser529=) | |
15 | g.73323288G>T | CA491478180 | HCN4 | c.2805C>A (p.Ser935=) c.1587C>A (p.Ser529=) | gnomAD v4 |
15 | g.73323288_73323289delinsTA | CA2573151087 | HCN4 | c.2804_2805delinsTA (p.Ser935Leu) c.1586_1587delinsTA (p.Ser529Leu) | ClinVar dbSNP |
15 | g.73323289G>A | CA301966 | HCN4 | c.2804C>T (p.Ser935Phe) c.1586C>T (p.Ser529Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323289G>C | CA393087921 | HCN4 | c.2804C>G (p.Ser935Cys) c.1586C>G (p.Ser529Cys) | ClinVar |
15 | g.73323289G= | CA2187187930 | HCN4 | c.2804C= (p.Ser935=) c.1586C= (p.Ser529=) | |
15 | g.73323289G>T | CA7648952 | HCN4 | c.2804C>A (p.Ser935Tyr) c.1586C>A (p.Ser529Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323290A>C | CA393087925 | HCN4 | c.2803T>G (p.Ser935Ala) c.1585T>G (p.Ser529Ala) | |
15 | g.73323290A>G | CA393087928 | HCN4 | c.2803T>C (p.Ser935Pro) c.1585T>C (p.Ser529Pro) | gnomAD v4 |
15 | g.73323290A>T | CA393087930 | HCN4 | c.2803T>A (p.Ser935Thr) c.1585T>A (p.Ser529Thr) | |
15 | g.73323291G>A | CA491478185 | HCN4 | c.2802C>T (p.Arg934=) c.1584C>T (p.Arg528=) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73323291G>C | CA491478186 | HCN4 | c.2802C>G (p.Arg934=) c.1584C>G (p.Arg528=) | gnomAD v4 |
15 | g.73323291G= | CA2187187934 | HCN4 | c.2802C= (p.Arg934=) c.1584C= (p.Arg528=) | |
15 | g.73323291G>T | CA491478189 | HCN4 | c.2802C>A (p.Arg934=) c.1584C>A (p.Arg528=) | gnomAD v4 |
15 | g.73323292C>A | CA393087934 | HCN4 | c.2801G>T (p.Arg934Leu) c.1583G>T (p.Arg528Leu) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323292C= | CA2187187937 | HCN4 | c.2801G= (p.Arg934=) c.1583G= (p.Arg528=) | |
15 | g.73323292C>G | CA393087932 | HCN4 | c.2801G>C (p.Arg934Pro) c.1583G>C (p.Arg528Pro) | |
15 | g.73323292C>T | CA247655 | HCN4 | c.2801G>A (p.Arg934His) c.1583G>A (p.Arg528His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323293G>A | CA301952 | HCN4 | c.2800C>T (p.Arg934Cys) c.1582C>T (p.Arg528Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323293G>C | CA393087938 | HCN4 | c.2800C>G (p.Arg934Gly) c.1582C>G (p.Arg528Gly) | |
15 | g.73323293G= | CA2187187945 | HCN4 | c.2800C= (p.Arg934=) c.1582C= (p.Arg528=) | |
15 | g.73323293G>T | CA393087939 | HCN4 | c.2800C>A (p.Arg934Ser) c.1582C>A (p.Arg528Ser) | gnomAD v4 |
15 | g.73323294G>A | CA491478193 | HCN4 | c.2799C>T (p.Ala933=) c.1581C>T (p.Ala527=) | COSMIC |
15 | g.73323294G>C | CA491478194 | HCN4 | c.2799C>G (p.Ala933=) c.1581C>G (p.Ala527=) | |
15 | g.73323294G>T | CA491478195 | HCN4 | c.2799C>A (p.Ala933=) c.1581C>A (p.Ala527=) | |
15 | g.73323295G>A | CA393087942 | HCN4 | c.2798C>T (p.Ala933Val) c.1580C>T (p.Ala527Val) | dbSNP gnomAD v2 gnomAD v4 |
15 | g.73323295G>C | CA393087943 | HCN4 | c.2798C>G (p.Ala933Gly) c.1580C>G (p.Ala527Gly) | COSMIC |
15 | g.73323295G= | CA2187187949 | HCN4 | c.2798C= (p.Ala933=) c.1580C= (p.Ala527=) | |
15 | g.73323295G>T | CA393087945 | HCN4 | c.2798C>A (p.Ala933Asp) c.1580C>A (p.Ala527Asp) | |
15 | g.73323296C>A | CA10581185 | HCN4 | c.2797G>T (p.Ala933Ser) c.1579G>T (p.Ala527Ser) | ClinVar dbSNP gnomAD v4 |
15 | g.73323296C= | CA2187187955 | HCN4 | c.2797G= (p.Ala933=) c.1579G= (p.Ala527=) | |
15 | g.73323296C>G | CA393087950 | HCN4 | c.2797G>C (p.Ala933Pro) c.1579G>C (p.Ala527Pro) | |
15 | g.73323296C>T | CA7648953 | HCN4 | c.2797G>A (p.Ala933Thr) c.1579G>A (p.Ala527Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323297G>A | CA7648954 | HCN4 | c.2796C>T (p.Gly932=) c.1578C>T (p.Gly526=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323297G>C | CA272664238 | HCN4 | c.2796C>G (p.Gly932=) c.1578C>G (p.Gly526=) | ClinVar dbSNP gnomAD v4 |
15 | g.73323297G= | CA2187187965 | HCN4 | c.2796C= (p.Gly932=) c.1578C= (p.Gly526=) | |
15 | g.73323297G>T | CA491478199 | HCN4 | c.2796C>A (p.Gly932=) c.1578C>A (p.Gly526=) | gnomAD v4 |
15 | g.73323298C>A | CA393087957 | HCN4 | c.2795G>T (p.Gly932Val) c.1577G>T (p.Gly526Val) | |
15 | g.73323298C= | CA2187187972 | HCN4 | c.2795G= (p.Gly932=) c.1577G= (p.Gly526=) | |
15 | g.73323298C>G | CA393087960 | HCN4 | c.2795G>C (p.Gly932Ala) c.1577G>C (p.Gly526Ala) | |
15 | g.73323298C>T | CA393087963 | HCN4 | c.2795G>A (p.Gly932Asp) c.1577G>A (p.Gly526Asp) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73323299C>A | CA393087966 | HCN4 | c.2794G>T (p.Gly932Cys) c.1576G>T (p.Gly526Cys) | gnomAD v4 |
15 | g.73323299C>G | CA393087968 | HCN4 | c.2794G>C (p.Gly932Arg) c.1576G>C (p.Gly526Arg) | |
15 | g.73323299C>T | CA393087965 | HCN4 | c.2794G>A (p.Gly932Ser) c.1576G>A (p.Gly526Ser) | gnomAD v4 |
15 | g.73323300T>A | CA491478202 | HCN4 | c.2793A>T (p.Pro931=) c.1575A>T (p.Pro525=) | |
15 | g.73323300T>C | CA491478203 | HCN4 | c.2793A>G (p.Pro931=) c.1575A>G (p.Pro525=) | gnomAD v4 |
15 | g.73323300T>G | CA491478204 | HCN4 | c.2793A>C (p.Pro931=) c.1575A>C (p.Pro525=) | |
15 | g.73323301G>A | CA393087970 | HCN4 | c.2792C>T (p.Pro931Leu) c.1574C>T (p.Pro525Leu) | gnomAD v4 |
15 | g.73323301G>C | CA393087972 | HCN4 | c.2792C>G (p.Pro931Arg) c.1574C>G (p.Pro525Arg) | |
15 | g.73323301G>T | CA393087974 | HCN4 | c.2792C>A (p.Pro931Gln) c.1574C>A (p.Pro525Gln) | gnomAD v4 |
15 | g.73323302G>A | CA393087977 | HCN4 | c.2791C>T (p.Pro931Ser) c.1573C>T (p.Pro525Ser) | gnomAD v4 |
15 | g.73323302G>C | CA393087978 | HCN4 | c.2791C>G (p.Pro931Ala) c.1573C>G (p.Pro525Ala) | |
15 | g.73323302G>T | CA393087981 | HCN4 | c.2791C>A (p.Pro931Thr) c.1573C>A (p.Pro525Thr) | gnomAD v4 |
15 | g.73323303C>A | CA393087983 | HCN4 | c.2790G>T (p.Gln930His) c.1572G>T (p.Gln524His) | gnomAD v4 |
15 | g.73323303C>G | CA393087986 | HCN4 | c.2790G>C (p.Gln930His) c.1572G>C (p.Gln524His) | |
15 | g.73323303C>T | CA491478206 | HCN4 | c.2790G>A (p.Gln930=) c.1572G>A (p.Gln524=) | gnomAD v4 |
15 | g.73323304T>A | CA393087990 | HCN4 | c.2789A>T (p.Gln930Leu) c.1571A>T (p.Gln524Leu) | |
15 | g.73323304T>C | CA393087991 | HCN4 | c.2789A>G (p.Gln930Arg) c.1571A>G (p.Gln524Arg) | gnomAD v4 |
15 | g.73323304T>G | CA393087993 | HCN4 | c.2789A>C (p.Gln930Pro) c.1571A>C (p.Gln524Pro) | |
15 | g.73323305G>A | CA393088001 | HCN4 | c.2788C>T (p.Gln930Ter) c.1570C>T (p.Gln524Ter) | ClinVar dbSNP gnomAD v4 |
15 | g.73323305G>C | CA393087999 | HCN4 | c.2788C>G (p.Gln930Glu) c.1570C>G (p.Gln524Glu) | |
15 | g.73323305G= | CA2187187978 | HCN4 | c.2788C= (p.Gln930=) c.1570C= (p.Gln524=) | |
15 | g.73323305G>T | CA393087997 | HCN4 | c.2788C>A (p.Gln930Lys) c.1570C>A (p.Gln524Lys) | gnomAD v4 COSMIC |