Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.150958290C>ACA008681KCNH2n.1518G>T
c.685G>T (p.Glu229Ter)
c.337G>T (p.Glu113Ter)
n.908G>T
c.385G>T (p.Glu129Ter)
c.535G>T (p.Glu179Ter)
c.508G>T (p.Glu170Ter)
 ClinVar dbSNP gnomAD v4
7g.150958290C=CA1752418328KCNH2n.1518G=
c.685G= (p.Glu229=)
c.337G= (p.Glu113=)
n.908G=
c.385G= (p.Glu129=)
c.535G= (p.Glu179=)
c.508G= (p.Glu170=)
7g.150958290C>GCA369862841KCNH2n.1518G>C
c.685G>C (p.Glu229Gln)
c.337G>C (p.Glu113Gln)
n.908G>C
c.385G>C (p.Glu129Gln)
c.535G>C (p.Glu179Gln)
c.508G>C (p.Glu170Gln)
7g.150958290C>TCA369862839KCNH2n.1518G>A
c.685G>A (p.Glu229Lys)
c.337G>A (p.Glu113Lys)
n.908G>A
c.385G>A (p.Glu129Lys)
c.535G>A (p.Glu179Lys)
c.508G>A (p.Glu170Lys)
 ClinVar dbSNP gnomAD v4
7g.150958298_150958372delCA2685608128KCNH2n.1444_1518del
c.611_685del (p.Ala204_Ala228del)
c.263_337del (p.Ala88_Ala112del)
n.834_908del
c.311_385del (p.Ala104_Ala128del)
c.461_535del (p.Ala154_Ala178del)
c.434_508del (p.Ala145_Ala169del)
 gnomAD v4
7g.150958291C>ACA458872292KCNH2n.1517G>T
c.684G>T (p.Ala228=)
c.336G>T (p.Ala112=)
n.907G>T
c.384G>T (p.Ala128=)
c.534G>T (p.Ala178=)
c.507G>T (p.Ala169=)
 dbSNP gnomAD v2 gnomAD v4
7g.150958291C=CA1752418333KCNH2n.1517G=
c.684G= (p.Ala228=)
c.336G= (p.Ala112=)
n.907G=
c.384G= (p.Ala128=)
c.534G= (p.Ala178=)
c.507G= (p.Ala169=)
7g.150958291C>GCA458872293KCNH2n.1517G>C
c.684G>C (p.Ala228=)
c.336G>C (p.Ala112=)
n.907G>C
c.384G>C (p.Ala128=)
c.534G>C (p.Ala178=)
c.507G>C (p.Ala169=)
 ClinVar dbSNP gnomAD v4
7g.150958291C>TCA458872294KCNH2n.1517G>A
c.684G>A (p.Ala228=)
c.336G>A (p.Ala112=)
n.907G>A
c.384G>A (p.Ala128=)
c.534G>A (p.Ala178=)
c.507G>A (p.Ala169=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958292G>ACA369862842KCNH2n.1516C>T
c.683C>T (p.Ala228Val)
c.335C>T (p.Ala112Val)
n.906C>T
c.383C>T (p.Ala128Val)
c.533C>T (p.Ala178Val)
c.506C>T (p.Ala169Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958292G>CCA369862846KCNH2n.1516C>G
c.683C>G (p.Ala228Gly)
c.335C>G (p.Ala112Gly)
n.906C>G
c.383C>G (p.Ala128Gly)
c.533C>G (p.Ala178Gly)
c.506C>G (p.Ala169Gly)
7g.150958292G=CA1752418338KCNH2n.1516C=
c.683C= (p.Ala228=)
c.335C= (p.Ala112=)
n.906C=
c.383C= (p.Ala128=)
c.533C= (p.Ala178=)
c.506C= (p.Ala169=)
7g.150958292G>TCA369862844KCNH2n.1516C>A
c.683C>A (p.Ala228Glu)
c.335C>A (p.Ala112Glu)
n.906C>A
c.383C>A (p.Ala128Glu)
c.533C>A (p.Ala178Glu)
c.506C>A (p.Ala169Glu)
 gnomAD v4
7g.150958293C>ACA369862848KCNH2n.1515G>T
c.682G>T (p.Ala228Ser)
c.334G>T (p.Ala112Ser)
n.905G>T
c.382G>T (p.Ala128Ser)
c.532G>T (p.Ala178Ser)
c.505G>T (p.Ala169Ser)
 gnomAD v4
7g.150958293C=CA1752418341KCNH2n.1515G=
c.682G= (p.Ala228=)
c.334G= (p.Ala112=)
n.905G=
c.382G= (p.Ala128=)
c.532G= (p.Ala178=)
c.505G= (p.Ala169=)
7g.150958293C>GCA071880KCNH2n.1515G>C
c.682G>C (p.Ala228Pro)
c.334G>C (p.Ala112Pro)
n.905G>C
c.382G>C (p.Ala128Pro)
c.532G>C (p.Ala178Pro)
c.505G>C (p.Ala169Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958293C>TCA071994KCNH2n.1515G>A
c.682G>A (p.Ala228Thr)
c.334G>A (p.Ala112Thr)
n.905G>A
c.382G>A (p.Ala128Thr)
c.532G>A (p.Ala178Thr)
c.505G>A (p.Ala169Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
7g.150958294G>ACA458872303KCNH2n.1514C>T
c.681C>T (p.Pro227=)
c.333C>T (p.Pro111=)
n.904C>T
c.381C>T (p.Pro127=)
c.531C>T (p.Pro177=)
c.504C>T (p.Pro168=)
 dbSNP gnomAD v4
7g.150958294G>CCA458872304KCNH2n.1514C>G
c.681C>G (p.Pro227=)
c.333C>G (p.Pro111=)
n.904C>G
c.381C>G (p.Pro127=)
c.531C>G (p.Pro177=)
c.504C>G (p.Pro168=)
 ClinVar dbSNP gnomAD v4
7g.150958294G=CA1752418347KCNH2n.1514C=
c.681C= (p.Pro227=)
c.333C= (p.Pro111=)
n.904C=
c.381C= (p.Pro127=)
c.531C= (p.Pro177=)
c.504C= (p.Pro168=)
7g.150958294G>TCA458872307KCNH2n.1514C>A
c.681C>A (p.Pro227=)
c.333C>A (p.Pro111=)
n.904C>A
c.381C>A (p.Pro127=)
c.531C>A (p.Pro177=)
c.504C>A (p.Pro168=)
 ClinVar dbSNP gnomAD v4
7g.150958296delCA2685608157KCNH2n.1514del
c.681del (p.Ala228ArgfsTer?)
c.333del (p.Ala112ArgfsTer?)
n.904del
c.381del (p.Ala128ArgfsTer?)
c.531del (p.Ala178ArgfsTer?)
c.504del (p.Ala169ArgfsTer?)
 gnomAD v4
7g.150958295G>ACA369862851KCNH2n.1513C>T
c.680C>T (p.Pro227Leu)
c.332C>T (p.Pro111Leu)
n.903C>T
c.380C>T (p.Pro127Leu)
c.530C>T (p.Pro177Leu)
c.503C>T (p.Pro168Leu)
 dbSNP gnomAD v2 gnomAD v4
7g.150958295G>CCA369862852KCNH2n.1513C>G
c.680C>G (p.Pro227Arg)
c.332C>G (p.Pro111Arg)
n.903C>G
c.380C>G (p.Pro127Arg)
c.530C>G (p.Pro177Arg)
c.503C>G (p.Pro168Arg)
 ClinVar
7g.150958295G=CA1752418352KCNH2n.1513C=
c.680C= (p.Pro227=)
c.332C= (p.Pro111=)
n.903C=
c.380C= (p.Pro127=)
c.530C= (p.Pro177=)
c.503C= (p.Pro168=)
7g.150958295G>TCA369862854KCNH2n.1513C>A
c.680C>A (p.Pro227His)
c.332C>A (p.Pro111His)
n.903C>A
c.380C>A (p.Pro127His)
c.530C>A (p.Pro177His)
c.503C>A (p.Pro168His)
 ClinVar gnomAD v4
7g.150958296G>ACA369862857KCNH2n.1512C>T
c.679C>T (p.Pro227Ser)
c.331C>T (p.Pro111Ser)
n.902C>T
c.379C>T (p.Pro127Ser)
c.529C>T (p.Pro177Ser)
c.502C>T (p.Pro168Ser)
 gnomAD v4
7g.150958296G>CCA369862858KCNH2n.1512C>G
c.679C>G (p.Pro227Ala)
c.331C>G (p.Pro111Ala)
n.902C>G
c.379C>G (p.Pro127Ala)
c.529C>G (p.Pro177Ala)
c.502C>G (p.Pro168Ala)
 gnomAD v4
7g.150958296G=CA1752418357KCNH2n.1512C=
c.679C= (p.Pro227=)
c.331C= (p.Pro111=)
n.902C=
c.379C= (p.Pro127=)
c.529C= (p.Pro177=)
c.502C= (p.Pro168=)
7g.150958296G>TCA169081336KCNH2n.1512C>A
c.679C>A (p.Pro227Thr)
c.331C>A (p.Pro111Thr)
n.902C>A
c.379C>A (p.Pro127Thr)
c.529C>A (p.Pro177Thr)
c.502C>A (p.Pro168Thr)
 dbSNP gnomAD v4
7g.150958296_150958297delinsGCCA1752418356KCNH2n.1511_1512delinsGC
c.678_679delinsGC (p.Gly226=)
c.330_331delinsGC (p.Gly110=)
n.901_902delinsGC
c.378_379delinsGC (p.Gly126=)
c.528_529delinsGC (p.Gly176=)
c.501_502delinsGC (p.Gly167=)
7g.150958297C>ACA458872313KCNH2n.1511G>T
c.678G>T (p.Gly226=)
c.330G>T (p.Gly110=)
n.901G>T
c.378G>T (p.Gly126=)
c.528G>T (p.Gly176=)
c.501G>T (p.Gly167=)
 gnomAD v4 COSMIC COSMIC
7g.150958297C=CA1752418362KCNH2n.1511G=
c.678G= (p.Gly226=)
c.330G= (p.Gly110=)
n.901G=
c.378G= (p.Gly126=)
c.528G= (p.Gly176=)
c.501G= (p.Gly167=)
7g.150958297C>GCA458872317KCNH2n.1511G>C
c.678G>C (p.Gly226=)
c.330G>C (p.Gly110=)
n.901G>C
c.378G>C (p.Gly126=)
c.528G>C (p.Gly176=)
c.501G>C (p.Gly167=)
7g.150958297C>TCA458872318KCNH2n.1511G>A
c.678G>A (p.Gly226=)
c.330G>A (p.Gly110=)
n.901G>A
c.378G>A (p.Gly126=)
c.528G>A (p.Gly176=)
c.501G>A (p.Gly167=)
 dbSNP gnomAD v3 gnomAD v4
7g.150958299delCA008674KCNH2n.1511del
c.678del (p.Ala228ArgfsTer?)
c.330del (p.Ala112ArgfsTer?)
n.901del
c.378del (p.Ala128ArgfsTer?)
c.528del (p.Ala178ArgfsTer?)
c.501del (p.Ala169ArgfsTer?)
 ClinVar dbSNP
7g.150958298C>ACA369862862KCNH2n.1510G>T
c.677G>T (p.Gly226Val)
c.329G>T (p.Gly110Val)
n.900G>T
c.377G>T (p.Gly126Val)
c.527G>T (p.Gly176Val)
c.500G>T (p.Gly167Val)
 gnomAD v4
7g.150958298C=CA1752418365KCNH2n.1510G=
c.677G= (p.Gly226=)
c.329G= (p.Gly110=)
n.900G=
c.377G= (p.Gly126=)
c.527G= (p.Gly176=)
c.500G= (p.Gly167=)
7g.150958298C>GCA369862864KCNH2n.1510G>C
c.677G>C (p.Gly226Ala)
c.329G>C (p.Gly110Ala)
n.900G>C
c.377G>C (p.Gly126Ala)
c.527G>C (p.Gly176Ala)
c.500G>C (p.Gly167Ala)
 gnomAD v4
7g.150958298C>TCA169081346KCNH2n.1510G>A
c.677G>A (p.Gly226Glu)
c.329G>A (p.Gly110Glu)
n.900G>A
c.377G>A (p.Gly126Glu)
c.527G>A (p.Gly176Glu)
c.500G>A (p.Gly167Glu)
 dbSNP gnomAD v4
7g.150958299C>ACA369862870KCNH2n.1509G>T
c.676G>T (p.Gly226Trp)
c.328G>T (p.Gly110Trp)
n.899G>T
c.376G>T (p.Gly126Trp)
c.526G>T (p.Gly176Trp)
c.499G>T (p.Gly167Trp)
 gnomAD v4
7g.150958299C>GCA369862868KCNH2n.1509G>C
c.676G>C (p.Gly226Arg)
c.328G>C (p.Gly110Arg)
n.899G>C
c.376G>C (p.Gly126Arg)
c.526G>C (p.Gly176Arg)
c.499G>C (p.Gly167Arg)
 ClinVar gnomAD v4
7g.150958299C>TCA369862866KCNH2n.1509G>A
c.676G>A (p.Gly226Arg)
c.328G>A (p.Gly110Arg)
n.899G>A
c.376G>A (p.Gly126Arg)
c.526G>A (p.Gly176Arg)
c.499G>A (p.Gly167Arg)
 gnomAD v4
7g.150958300G>ACA040219KCNH2n.1508C>T
c.675C>T (p.Leu225=)
c.327C>T (p.Leu109=)
n.898C>T
c.375C>T (p.Leu125=)
c.525C>T (p.Leu175=)
c.498C>T (p.Leu166=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150958300G>CCA10628486KCNH2n.1508C>G
c.675C>G (p.Leu225=)
c.327C>G (p.Leu109=)
n.898C>G
c.375C>G (p.Leu125=)
c.525C>G (p.Leu175=)
c.498C>G (p.Leu166=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958300G=CA1752418369KCNH2n.1508C=
c.675C= (p.Leu225=)
c.327C= (p.Leu109=)
n.898C=
c.375C= (p.Leu125=)
c.525C= (p.Leu175=)
c.498C= (p.Leu166=)
7g.150958300G>TCA458872327KCNH2n.1508C>A
c.675C>A (p.Leu225=)
c.327C>A (p.Leu109=)
n.898C>A
c.375C>A (p.Leu125=)
c.525C>A (p.Leu175=)
c.498C>A (p.Leu166=)
 gnomAD v4
7g.150958301A>CCA369862874KCNH2n.1507T>G
c.674T>G (p.Leu225Arg)
c.326T>G (p.Leu109Arg)
n.897T>G
c.374T>G (p.Leu125Arg)
c.524T>G (p.Leu175Arg)
c.497T>G (p.Leu166Arg)
7g.150958301A>GCA369862876KCNH2n.1507T>C
c.674T>C (p.Leu225Pro)
c.326T>C (p.Leu109Pro)
n.897T>C
c.374T>C (p.Leu125Pro)
c.524T>C (p.Leu175Pro)
c.497T>C (p.Leu166Pro)
 gnomAD v4
7g.150958301A>TCA369862877KCNH2n.1507T>A
c.674T>A (p.Leu225His)
c.326T>A (p.Leu109His)
n.897T>A
c.374T>A (p.Leu125His)
c.524T>A (p.Leu175His)
c.497T>A (p.Leu166His)
 gnomAD v4
7g.150958302G>ACA369862880KCNH2n.1506C>T
c.673C>T (p.Leu225Phe)
c.325C>T (p.Leu109Phe)
n.896C>T
c.373C>T (p.Leu125Phe)
c.523C>T (p.Leu175Phe)
c.496C>T (p.Leu166Phe)
 gnomAD v4
7g.150958302G>CCA369862881KCNH2n.1506C>G
c.673C>G (p.Leu225Val)
c.325C>G (p.Leu109Val)
n.896C>G
c.373C>G (p.Leu125Val)
c.523C>G (p.Leu175Val)
c.496C>G (p.Leu166Val)
 gnomAD v4
7g.150958302G>TCA369862883KCNH2n.1506C>A
c.673C>A (p.Leu225Ile)
c.325C>A (p.Leu109Ile)
n.896C>A
c.373C>A (p.Leu125Ile)
c.523C>A (p.Leu175Ile)
c.496C>A (p.Leu166Ile)
 gnomAD v4
7g.150958303C>ACA071875KCNH2n.1505G>T
c.672G>T (p.Gly224=)
c.324G>T (p.Gly108=)
n.895G>T
c.372G>T (p.Gly124=)
c.522G>T (p.Gly174=)
c.495G>T (p.Gly165=)
 ClinVar gnomAD v4
7g.150958303C>GCA458872341KCNH2n.1505G>C
c.672G>C (p.Gly224=)
c.324G>C (p.Gly108=)
n.895G>C
c.372G>C (p.Gly124=)
c.522G>C (p.Gly174=)
c.495G>C (p.Gly165=)
 gnomAD v4
7g.150958303C>TCA071871KCNH2n.1505G>A
c.672G>A (p.Gly224=)
c.324G>A (p.Gly108=)
n.895G>A
c.372G>A (p.Gly124=)
c.522G>A (p.Gly174=)
c.495G>A (p.Gly165=)
 gnomAD v4
7g.150958304C>ACA369862885KCNH2n.1504G>T
c.671G>T (p.Gly224Val)
c.323G>T (p.Gly108Val)
n.894G>T
c.371G>T (p.Gly124Val)
c.521G>T (p.Gly174Val)
c.494G>T (p.Gly165Val)
 gnomAD v4
7g.150958304C=CA1752418376KCNH2n.1504G=
c.671G= (p.Gly224=)
c.323G= (p.Gly108=)
n.894G=
c.371G= (p.Gly124=)
c.521G= (p.Gly174=)
c.494G= (p.Gly165=)
7g.150958304C>GCA369862887KCNH2n.1504G>C
c.671G>C (p.Gly224Ala)
c.323G>C (p.Gly108Ala)
n.894G>C
c.371G>C (p.Gly124Ala)
c.521G>C (p.Gly174Ala)
c.494G>C (p.Gly165Ala)
7g.150958304C>TCA369862888KCNH2n.1504G>A
c.671G>A (p.Gly224Glu)
c.323G>A (p.Gly108Glu)
n.894G>A
c.371G>A (p.Gly124Glu)
c.521G>A (p.Gly174Glu)
c.494G>A (p.Gly165Glu)
 dbSNP gnomAD v4
7g.150958306_150958309delCA2739278349KCNH2n.1501_1504del
c.668_671del (p.Ala223GlyfsTer?)
c.320_323del (p.Ala107GlyfsTer?)
n.891_894del
c.368_371del (p.Ala123GlyfsTer?)
c.518_521del (p.Ala173GlyfsTer?)
c.491_494del (p.Ala164GlyfsTer?)
 ClinVar
7g.150958305C>ACA369862891KCNH2n.1503G>T
c.670G>T (p.Gly224Trp)
c.322G>T (p.Gly108Trp)
n.893G>T
c.370G>T (p.Gly124Trp)
c.520G>T (p.Gly174Trp)
c.493G>T (p.Gly165Trp)
 gnomAD v4
7g.150958305C=CA1752418382KCNH2n.1503G=
c.670G= (p.Gly224=)
c.322G= (p.Gly108=)
n.893G=
c.370G= (p.Gly124=)
c.520G= (p.Gly174=)
c.493G= (p.Gly165=)
7g.150958305C>GCA369862893KCNH2n.1503G>C
c.670G>C (p.Gly224Arg)
c.322G>C (p.Gly108Arg)
n.893G>C
c.370G>C (p.Gly124Arg)
c.520G>C (p.Gly174Arg)
c.493G>C (p.Gly165Arg)
 dbSNP
7g.150958305C>TCA008669KCNH2n.1503G>A
c.670G>A (p.Gly224Arg)
c.322G>A (p.Gly108Arg)
n.893G>A
c.370G>A (p.Gly124Arg)
c.520G>A (p.Gly174Arg)
c.493G>A (p.Gly165Arg)
 ClinVar dbSNP gnomAD v4
7g.150958305_150958310delinsCTGCCACA1752418379KCNH2n.1498_1503delinsTGGCAG
c.665_670delinsTGGCAG (p.Val222=)
c.317_322delinsTGGCAG (p.Val106=)
n.888_893delinsTGGCAG
c.365_370delinsTGGCAG (p.Val122=)
c.515_520delinsTGGCAG (p.Val172=)
c.488_493delinsTGGCAG (p.Val163=)
7g.150958306delCA2499218809KCNH2n.1502del
c.669del (p.Leu225SerfsTer?)
c.321del (p.Leu109SerfsTer?)
n.892del
c.369del (p.Leu125SerfsTer?)
c.519del (p.Leu175SerfsTer?)
c.492del (p.Leu166SerfsTer?)
 ClinVar dbSNP gnomAD v4
7g.150958306T>ACA458872353KCNH2n.1502A>T
c.669A>T (p.Ala223=)
c.321A>T (p.Ala107=)
n.892A>T
c.369A>T (p.Ala123=)
c.519A>T (p.Ala173=)
c.492A>T (p.Ala164=)
 gnomAD v4
7g.150958306T>CCA458872354KCNH2n.1502A>G
c.669A>G (p.Ala223=)
c.321A>G (p.Ala107=)
n.892A>G
c.369A>G (p.Ala123=)
c.519A>G (p.Ala173=)
c.492A>G (p.Ala164=)
 gnomAD v4
7g.150958306T>GCA458872355KCNH2n.1502A>C
c.669A>C (p.Ala223=)
c.321A>C (p.Ala107=)
n.892A>C
c.369A>C (p.Ala123=)
c.519A>C (p.Ala173=)
c.492A>C (p.Ala164=)
7g.150958306_150958310delinsGCA645294046KCNH2n.1498_1502delinsC
c.665_669delinsC (p.Val222AlafsTer?)
c.317_321delinsC (p.Val106AlafsTer?)
n.888_892delinsC
c.365_369delinsC (p.Val122AlafsTer?)
c.515_519delinsC (p.Val172AlafsTer?)
c.488_492delinsC (p.Val163AlafsTer?)
 ClinVar dbSNP
7g.150958307delCA2685608227KCNH2n.1501del
c.668del (p.Ala223GlufsTer?)
c.320del (p.Ala107GlufsTer?)
n.891del
c.368del (p.Ala123GlufsTer?)
c.518del (p.Ala173GlufsTer?)
c.491del (p.Ala164GlufsTer?)
 gnomAD v4
7g.150958307G>ACA369862895KCNH2n.1501C>T
c.668C>T (p.Ala223Val)
c.320C>T (p.Ala107Val)
n.891C>T
c.368C>T (p.Ala123Val)
c.518C>T (p.Ala173Val)
c.491C>T (p.Ala164Val)
 gnomAD v3 gnomAD v4
7g.150958307G>CCA369862896KCNH2n.1501C>G
c.668C>G (p.Ala223Gly)
c.320C>G (p.Ala107Gly)
n.891C>G
c.368C>G (p.Ala123Gly)
c.518C>G (p.Ala173Gly)
c.491C>G (p.Ala164Gly)
 gnomAD v4
7g.150958307G>TCA369862897KCNH2n.1501C>A
c.668C>A (p.Ala223Glu)
c.320C>A (p.Ala107Glu)
n.891C>A
c.368C>A (p.Ala123Glu)
c.518C>A (p.Ala173Glu)
c.491C>A (p.Ala164Glu)
 gnomAD v4
7g.150958308C>ACA369862900KCNH2n.1500G>T
c.667G>T (p.Ala223Ser)
c.319G>T (p.Ala107Ser)
n.890G>T
c.367G>T (p.Ala123Ser)
c.517G>T (p.Ala173Ser)
c.490G>T (p.Ala164Ser)
 gnomAD v4
7g.150958308C=CA1752418388KCNH2n.1500G=
c.667G= (p.Ala223=)
c.319G= (p.Ala107=)
n.890G=
c.367G= (p.Ala123=)
c.517G= (p.Ala173=)
c.490G= (p.Ala164=)
7g.150958308C>GCA040202KCNH2n.1500G>C
c.667G>C (p.Ala223Pro)
c.319G>C (p.Ala107Pro)
n.890G>C
c.367G>C (p.Ala123Pro)
c.517G>C (p.Ala173Pro)
c.490G>C (p.Ala164Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150958308C>TCA369862902KCNH2n.1500G>A
c.667G>A (p.Ala223Thr)
c.319G>A (p.Ala107Thr)
n.890G>A
c.367G>A (p.Ala123Thr)
c.517G>A (p.Ala173Thr)
c.490G>A (p.Ala164Thr)
 gnomAD v4
7g.150958309C>ACA458872357KCNH2n.1499G>T
c.666G>T (p.Val222=)
c.318G>T (p.Val106=)
n.889G>T
c.366G>T (p.Val122=)
c.516G>T (p.Val172=)
c.489G>T (p.Val163=)
 gnomAD v4
7g.150958309C>GCA458872362KCNH2n.1499G>C
c.666G>C (p.Val222=)
c.318G>C (p.Val106=)
n.889G>C
c.366G>C (p.Val122=)
c.516G>C (p.Val172=)
c.489G>C (p.Val163=)
7g.150958309C>TCA458872360KCNH2n.1499G>A
c.666G>A (p.Val222=)
c.318G>A (p.Val106=)
n.889G>A
c.366G>A (p.Val122=)
c.516G>A (p.Val172=)
c.489G>A (p.Val163=)
 gnomAD v4
7g.150958310A>CCA369862904KCNH2n.1498T>G
c.665T>G (p.Val222Gly)
c.317T>G (p.Val106Gly)
n.888T>G
c.365T>G (p.Val122Gly)
c.515T>G (p.Val172Gly)
c.488T>G (p.Val163Gly)
7g.150958310A>GCA369862906KCNH2n.1498T>C
c.665T>C (p.Val222Ala)
c.317T>C (p.Val106Ala)
n.888T>C
c.365T>C (p.Val122Ala)
c.515T>C (p.Val172Ala)
c.488T>C (p.Val163Ala)
 ClinVar dbSNP gnomAD v4
7g.150958310A>TCA369862908KCNH2n.1498T>A
c.665T>A (p.Val222Glu)
c.317T>A (p.Val106Glu)
n.888T>A
c.365T>A (p.Val122Glu)
c.515T>A (p.Val172Glu)
c.488T>A (p.Val163Glu)
7g.150958311C>ACA071906KCNH2n.1497G>T
c.664G>T (p.Val222Leu)
c.316G>T (p.Val106Leu)
n.887G>T
c.364G>T (p.Val122Leu)
c.514G>T (p.Val172Leu)
c.487G>T (p.Val163Leu)
 gnomAD v4
7g.150958311C=CA1752418391KCNH2n.1497G=
c.664G= (p.Val222=)
c.316G= (p.Val106=)
n.887G=
c.364G= (p.Val122=)
c.514G= (p.Val172=)
c.487G= (p.Val163=)
7g.150958311C>GCA369862910KCNH2n.1497G>C
c.664G>C (p.Val222Leu)
c.316G>C (p.Val106Leu)
n.887G>C
c.364G>C (p.Val122Leu)
c.514G>C (p.Val172Leu)
c.487G>C (p.Val163Leu)
 dbSNP gnomAD v2 gnomAD v4
7g.150958311C>TCA369862912KCNH2n.1497G>A
c.664G>A (p.Val222Met)
c.316G>A (p.Val106Met)
n.887G>A
c.364G>A (p.Val122Met)
c.514G>A (p.Val172Met)
c.487G>A (p.Val163Met)
 ClinVar dbSNP gnomAD v4
7g.150958312G>ACA071984KCNH2n.1496C>T
c.663C>T (p.His221=)
c.315C>T (p.His105=)
n.886C>T
c.363C>T (p.His121=)
c.513C>T (p.His171=)
c.486C>T (p.His162=)
 gnomAD v4 COSMIC COSMIC
7g.150958312G>CCA369862914KCNH2n.1496C>G
c.663C>G (p.His221Gln)
c.315C>G (p.His105Gln)
n.886C>G
c.363C>G (p.His121Gln)
c.513C>G (p.His171Gln)
c.486C>G (p.His162Gln)
 ClinVar dbSNP gnomAD v4
7g.150958312G=CA1752418394KCNH2n.1496C=
c.663C= (p.His221=)
c.315C= (p.His105=)
n.886C=
c.363C= (p.His121=)
c.513C= (p.His171=)
c.486C= (p.His162=)
7g.150958312G>TCA040187KCNH2n.1496C>A
c.663C>A (p.His221Gln)
c.315C>A (p.His105Gln)
n.886C>A
c.363C>A (p.His121Gln)
c.513C>A (p.His171Gln)
c.486C>A (p.His162Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150958313T>ACA369862916KCNH2n.1495A>T
c.662A>T (p.His221Leu)
c.314A>T (p.His105Leu)
n.885A>T
c.362A>T (p.His121Leu)
c.512A>T (p.His171Leu)
c.485A>T (p.His162Leu)
 gnomAD v4
7g.150958313T>CCA369862918KCNH2n.1495A>G
c.662A>G (p.His221Arg)
c.314A>G (p.His105Arg)
n.885A>G
c.362A>G (p.His121Arg)
c.512A>G (p.His171Arg)
c.485A>G (p.His162Arg)
 ClinVar gnomAD v4
7g.150958313T>GCA369862919KCNH2n.1495A>C
c.662A>C (p.His221Pro)
c.314A>C (p.His105Pro)
n.885A>C
c.362A>C (p.His121Pro)
c.512A>C (p.His171Pro)
c.485A>C (p.His162Pro)
7g.150958314G>ACA369862923KCNH2n.1494C>T
c.661C>T (p.His221Tyr)
c.313C>T (p.His105Tyr)
n.884C>T
c.361C>T (p.His121Tyr)
c.511C>T (p.His171Tyr)
c.484C>T (p.His162Tyr)
 gnomAD v4
7g.150958314G>CCA369862924KCNH2n.1494C>G
c.661C>G (p.His221Asp)
c.313C>G (p.His105Asp)
n.884C>G
c.361C>G (p.His121Asp)
c.511C>G (p.His171Asp)
c.484C>G (p.His162Asp)
 dbSNP gnomAD v3 gnomAD v4
7g.150958314G=CA1752418398KCNH2n.1494C=
c.661C= (p.His221=)
c.313C= (p.His105=)
n.884C=
c.361C= (p.His121=)
c.511C= (p.His171=)
c.484C= (p.His162=)
7g.150958314G>TCA369862925KCNH2n.1494C>A
c.661C>A (p.His221Asn)
c.313C>A (p.His105Asn)
n.884C>A
c.361C>A (p.His121Asn)
c.511C>A (p.His171Asn)
c.484C>A (p.His162Asn)
 gnomAD v4
7g.150958315G>ACA458872378KCNH2n.1493C>T
c.660C>T (p.Asn220=)
c.312C>T (p.Asn104=)
n.883C>T
c.360C>T (p.Asn120=)
c.510C>T (p.Asn170=)
c.483C>T (p.Asn161=)
 gnomAD v4
7g.150958315G>CCA369862927KCNH2n.1493C>G
c.660C>G (p.Asn220Lys)
c.312C>G (p.Asn104Lys)
n.883C>G
c.360C>G (p.Asn120Lys)
c.510C>G (p.Asn170Lys)
c.483C>G (p.Asn161Lys)
 gnomAD v4
7g.150958315G>TCA369862929KCNH2n.1493C>A
c.660C>A (p.Asn220Lys)
c.312C>A (p.Asn104Lys)
n.883C>A
c.360C>A (p.Asn120Lys)
c.510C>A (p.Asn170Lys)
c.483C>A (p.Asn161Lys)
 gnomAD v4
7g.150958316T>ACA369862931KCNH2n.1492A>T
c.659A>T (p.Asn220Ile)
c.311A>T (p.Asn104Ile)
n.882A>T
c.359A>T (p.Asn120Ile)
c.509A>T (p.Asn170Ile)
c.482A>T (p.Asn161Ile)
 gnomAD v4
7g.150958316T>CCA369862933KCNH2n.1492A>G
c.659A>G (p.Asn220Ser)
c.311A>G (p.Asn104Ser)
n.882A>G
c.359A>G (p.Asn120Ser)
c.509A>G (p.Asn170Ser)
c.482A>G (p.Asn161Ser)
 gnomAD v4
7g.150958316T>GCA369862935KCNH2n.1492A>C
c.659A>C (p.Asn220Thr)
c.311A>C (p.Asn104Thr)
n.882A>C
c.359A>C (p.Asn120Thr)
c.509A>C (p.Asn170Thr)
c.482A>C (p.Asn161Thr)
7g.150958317delCA2697549698KCNH2n.1492del
c.659del (p.Asn220ThrfsTer?)
c.311del (p.Asn104ThrfsTer?)
n.882del
c.359del (p.Asn120ThrfsTer?)
c.509del (p.Asn170ThrfsTer?)
c.482del (p.Asn161ThrfsTer?)
 ClinVar
7g.150958317T>ACA369862937KCNH2n.1491A>T
c.658A>T (p.Asn220Tyr)
c.310A>T (p.Asn104Tyr)
n.881A>T
c.358A>T (p.Asn120Tyr)
c.508A>T (p.Asn170Tyr)
c.481A>T (p.Asn161Tyr)
 COSMIC COSMIC
7g.150958317T>CCA369862939KCNH2n.1491A>G
c.658A>G (p.Asn220Asp)
c.310A>G (p.Asn104Asp)
n.881A>G
c.358A>G (p.Asn120Asp)
c.508A>G (p.Asn170Asp)
c.481A>G (p.Asn161Asp)
 gnomAD v4
7g.150958317T>GCA369862941KCNH2n.1491A>C
c.658A>C (p.Asn220His)
c.310A>C (p.Asn104His)
n.881A>C
c.358A>C (p.Asn120His)
c.508A>C (p.Asn170His)
c.481A>C (p.Asn161His)
7g.150958318delCA2685608280KCNH2n.1490del
c.657del (p.Asp219GlufsTer?)
c.309del (p.Asp103GlufsTer?)
n.880del
c.357del (p.Asp119GlufsTer?)
c.507del (p.Asp169GlufsTer?)
c.480del (p.Asp160GlufsTer?)
 gnomAD v4
7g.150958318G>ACA458872389KCNH2n.1490C>T
c.657C>T (p.Asp219=)
c.309C>T (p.Asp103=)
n.880C>T
c.357C>T (p.Asp119=)
c.507C>T (p.Asp169=)
c.480C>T (p.Asp160=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958318G>CCA369862943KCNH2n.1490C>G
c.657C>G (p.Asp219Glu)
c.309C>G (p.Asp103Glu)
n.880C>G
c.357C>G (p.Asp119Glu)
c.507C>G (p.Asp169Glu)
c.480C>G (p.Asp160Glu)
7g.150958318G=CA1752418400KCNH2n.1490C=
c.657C= (p.Asp219=)
c.309C= (p.Asp103=)
n.880C=
c.357C= (p.Asp119=)
c.507C= (p.Asp169=)
c.480C= (p.Asp160=)
7g.150958318G>TCA369862944KCNH2n.1490C>A
c.657C>A (p.Asp219Glu)
c.309C>A (p.Asp103Glu)
n.880C>A
c.357C>A (p.Asp119Glu)
c.507C>A (p.Asp169Glu)
c.480C>A (p.Asp160Glu)
 gnomAD v4
7g.150958319T>ACA008651KCNH2n.1489A>T
c.656A>T (p.Asp219Val)
c.308A>T (p.Asp103Val)
n.879A>T
c.356A>T (p.Asp119Val)
c.506A>T (p.Asp169Val)
c.479A>T (p.Asp160Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150958319T>CCA369862949KCNH2n.1489A>G
c.656A>G (p.Asp219Gly)
c.308A>G (p.Asp103Gly)
n.879A>G
c.356A>G (p.Asp119Gly)
c.506A>G (p.Asp169Gly)
c.479A>G (p.Asp160Gly)
 gnomAD v4
7g.150958319T>GCA369862947KCNH2n.1489A>C
c.656A>C (p.Asp219Ala)
c.308A>C (p.Asp103Ala)
n.879A>C
c.356A>C (p.Asp119Ala)
c.506A>C (p.Asp169Ala)
c.479A>C (p.Asp160Ala)
7g.150958319T=CA1752418404KCNH2n.1489A=
c.656A= (p.Asp219=)
c.308A= (p.Asp103=)
n.879A=
c.356A= (p.Asp119=)
c.506A= (p.Asp169=)
c.479A= (p.Asp160=)
7g.150958320C>ACA369862951KCNH2n.1488G>T
c.655G>T (p.Asp219Tyr)
c.307G>T (p.Asp103Tyr)
n.878G>T
c.355G>T (p.Asp119Tyr)
c.505G>T (p.Asp169Tyr)
c.478G>T (p.Asp160Tyr)
 gnomAD v4
7g.150958320C=CA1752418409KCNH2n.1488G=
c.655G= (p.Asp219=)
c.307G= (p.Asp103=)
n.878G=
c.355G= (p.Asp119=)
c.505G= (p.Asp169=)
c.478G= (p.Asp160=)
7g.150958320C>GCA369862953KCNH2n.1488G>C
c.655G>C (p.Asp219His)
c.307G>C (p.Asp103His)
n.878G>C
c.355G>C (p.Asp119His)
c.505G>C (p.Asp169His)
c.478G>C (p.Asp160His)
 gnomAD v4
7g.150958320C>TCA369862954KCNH2n.1488G>A
c.655G>A (p.Asp219Asn)
c.307G>A (p.Asp103Asn)
n.878G>A
c.355G>A (p.Asp119Asn)
c.505G>A (p.Asp169Asn)
c.478G>A (p.Asp160Asn)
 ClinVar dbSNP gnomAD v4
7g.150958321delCA458872397KCNH2n.1488del
c.655del (p.Asp219ThrfsTer?)
c.307del (p.Asp103ThrfsTer?)
n.878del
c.355del (p.Asp119ThrfsTer?)
c.505del (p.Asp169ThrfsTer?)
c.478del (p.Asp160ThrfsTer?)
 COSMIC
7g.150958321C>ACA369862956KCNH2n.1487G>T
c.654G>T (p.Met218Ile)
c.306G>T (p.Met102Ile)
n.877G>T
c.354G>T (p.Met118Ile)
c.504G>T (p.Met168Ile)
c.477G>T (p.Met159Ile)
 dbSNP gnomAD v2 gnomAD v4
7g.150958321C=CA1752418417KCNH2n.1487G=
c.654G= (p.Met218=)
c.306G= (p.Met102=)
n.877G=
c.354G= (p.Met118=)
c.504G= (p.Met168=)
c.477G= (p.Met159=)
7g.150958321C>GCA369862957KCNH2n.1487G>C
c.654G>C (p.Met218Ile)
c.306G>C (p.Met102Ile)
n.877G>C
c.354G>C (p.Met118Ile)
c.504G>C (p.Met168Ile)
c.477G>C (p.Met159Ile)
 gnomAD v4
7g.150958321C>TCA369862959KCNH2n.1487G>A
c.654G>A (p.Met218Ile)
c.306G>A (p.Met102Ile)
n.877G>A
c.354G>A (p.Met118Ile)
c.504G>A (p.Met168Ile)
c.477G>A (p.Met159Ile)
 gnomAD v4
7g.150958322A>CCA369862961KCNH2n.1486T>G
c.653T>G (p.Met218Arg)
c.305T>G (p.Met102Arg)
n.876T>G
c.353T>G (p.Met118Arg)
c.503T>G (p.Met168Arg)
c.476T>G (p.Met159Arg)
7g.150958322A>GCA369862962KCNH2n.1486T>C
c.653T>C (p.Met218Thr)
c.305T>C (p.Met102Thr)
n.876T>C
c.353T>C (p.Met118Thr)
c.503T>C (p.Met168Thr)
c.476T>C (p.Met159Thr)
 gnomAD v4
7g.150958322A>TCA369862963KCNH2n.1486T>A
c.653T>A (p.Met218Lys)
c.305T>A (p.Met102Lys)
n.876T>A
c.353T>A (p.Met118Lys)
c.503T>A (p.Met168Lys)
c.476T>A (p.Met159Lys)
 gnomAD v4
7g.150958323T>ACA369862965KCNH2n.1485A>T
c.652A>T (p.Met218Leu)
c.304A>T (p.Met102Leu)
n.875A>T
c.352A>T (p.Met118Leu)
c.502A>T (p.Met168Leu)
c.475A>T (p.Met159Leu)
7g.150958323T>CCA008645KCNH2n.1485A>G
c.652A>G (p.Met218Val)
c.304A>G (p.Met102Val)
n.875A>G
c.352A>G (p.Met118Val)
c.502A>G (p.Met168Val)
c.475A>G (p.Met159Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150958323T>GCA369862968KCNH2n.1485A>C
c.652A>C (p.Met218Leu)
c.304A>C (p.Met102Leu)
n.875A>C
c.352A>C (p.Met118Leu)
c.502A>C (p.Met168Leu)
c.475A>C (p.Met159Leu)
7g.150958323T=CA1752418421KCNH2n.1485A=
c.652A= (p.Met218=)
c.304A= (p.Met102=)
n.875A=
c.352A= (p.Met118=)
c.502A= (p.Met168=)
c.475A= (p.Met159=)
7g.150958324G>ACA458646519KCNH2n.1484C>T
c.651C>T (p.Ala217=)
c.303C>T (p.Ala101=)
n.874C>T
c.351C>T (p.Ala117=)
c.501C>T (p.Ala167=)
c.474C>T (p.Ala158=)
 dbSNP gnomAD v4
7g.150958324G>CCA458646521KCNH2n.1484C>G
c.651C>G (p.Ala217=)
c.303C>G (p.Ala101=)
n.874C>G
c.351C>G (p.Ala117=)
c.501C>G (p.Ala167=)
c.474C>G (p.Ala158=)
 gnomAD v4
7g.150958324G=CA1752418427KCNH2n.1484C=
c.651C= (p.Ala217=)
c.303C= (p.Ala101=)
n.874C=
c.351C= (p.Ala117=)
c.501C= (p.Ala167=)
c.474C= (p.Ala158=)
7g.150958324G>TCA458646523KCNH2n.1484C>A
c.651C>A (p.Ala217=)
c.303C>A (p.Ala101=)
n.874C>A
c.351C>A (p.Ala117=)
c.501C>A (p.Ala167=)
c.474C>A (p.Ala158=)
 gnomAD v4
7g.150958324_150958325insATCA2567370311KCNH2n.1483_1484insAT
c.650_651insAT (p.Met218SerfsTer?)
c.302_303insAT (p.Met102SerfsTer?)
n.873_874insAT
c.350_351insAT (p.Met118SerfsTer?)
c.500_501insAT (p.Met168SerfsTer?)
c.473_474insAT (p.Met159SerfsTer?)
 gnomAD v4
7g.150958325G>ACA369862970KCNH2n.1483C>T
c.650C>T (p.Ala217Val)
c.302C>T (p.Ala101Val)
n.873C>T
c.350C>T (p.Ala117Val)
c.500C>T (p.Ala167Val)
c.473C>T (p.Ala158Val)
 dbSNP gnomAD v2 gnomAD v4
7g.150958325G>CCA369862973KCNH2n.1483C>G
c.650C>G (p.Ala217Gly)
c.302C>G (p.Ala101Gly)
n.873C>G
c.350C>G (p.Ala117Gly)
c.500C>G (p.Ala167Gly)
c.473C>G (p.Ala158Gly)
 gnomAD v4
7g.150958325G=CA1752418429KCNH2n.1483C=
c.650C= (p.Ala217=)
c.302C= (p.Ala101=)
n.873C=
c.350C= (p.Ala117=)
c.500C= (p.Ala167=)
c.473C= (p.Ala158=)
7g.150958325G>TCA369862971KCNH2n.1483C>A
c.650C>A (p.Ala217Asp)
c.302C>A (p.Ala101Asp)
n.873C>A
c.350C>A (p.Ala117Asp)
c.500C>A (p.Ala167Asp)
c.473C>A (p.Ala158Asp)
 ClinVar gnomAD v4
7g.150958326C>ACA369862975KCNH2n.1482G>T
c.649G>T (p.Ala217Ser)
c.301G>T (p.Ala101Ser)
n.872G>T
c.349G>T (p.Ala117Ser)
c.499G>T (p.Ala167Ser)
c.472G>T (p.Ala158Ser)
 gnomAD v4
7g.150958326C>GCA369862976KCNH2n.1482G>C
c.649G>C (p.Ala217Pro)
c.301G>C (p.Ala101Pro)
n.872G>C
c.349G>C (p.Ala117Pro)
c.499G>C (p.Ala167Pro)
c.472G>C (p.Ala158Pro)
 gnomAD v4
7g.150958326C>TCA369862978KCNH2n.1482G>A
c.649G>A (p.Ala217Thr)
c.301G>A (p.Ala101Thr)
n.872G>A
c.349G>A (p.Ala117Thr)
c.499G>A (p.Ala167Thr)
c.472G>A (p.Ala158Thr)
 gnomAD v4
7g.150958326_150958327delCA2546923698KCNH2n.1481_1482del
c.648_649del (p.Ala217HisfsTer?)
c.300_301del (p.Ala101HisfsTer?)
n.871_872del
c.348_349del (p.Ala117HisfsTer?)
c.498_499del (p.Ala167HisfsTer?)
c.471_472del (p.Ala158HisfsTer?)
 gnomAD v4
7g.150958327delCA2685608307KCNH2n.1481del
c.648del (p.Ala217ProfsTer?)
c.300del (p.Ala101ProfsTer?)
n.871del
c.348del (p.Ala117ProfsTer?)
c.498del (p.Ala167ProfsTer?)
c.471del (p.Ala158ProfsTer?)
 gnomAD v4
7g.150958327T>ACA458646529KCNH2n.1481A>T
c.648A>T (p.Thr216=)
c.300A>T (p.Thr100=)
n.871A>T
c.348A>T (p.Thr116=)
c.498A>T (p.Thr166=)
c.471A>T (p.Thr157=)
7g.150958327T>CCA458646531KCNH2n.1481A>G
c.648A>G (p.Thr216=)
c.300A>G (p.Thr100=)
n.871A>G
c.348A>G (p.Thr116=)
c.498A>G (p.Thr166=)
c.471A>G (p.Thr157=)
 gnomAD v4
7g.150958327T>GCA458646532KCNH2n.1481A>C
c.648A>C (p.Thr216=)
c.300A>C (p.Thr100=)
n.871A>C
c.348A>C (p.Thr116=)
c.498A>C (p.Thr166=)
c.471A>C (p.Thr157=)
 gnomAD v4
7g.150958328G>ACA369862979KCNH2n.1480C>T
c.647C>T (p.Thr216Ile)
c.299C>T (p.Thr100Ile)
n.870C>T
c.347C>T (p.Thr116Ile)
c.497C>T (p.Thr166Ile)
c.470C>T (p.Thr157Ile)
 ClinVar dbSNP gnomAD v4
7g.150958328G>CCA369862981KCNH2n.1480C>G
c.647C>G (p.Thr216Arg)
c.299C>G (p.Thr100Arg)
n.870C>G
c.347C>G (p.Thr116Arg)
c.497C>G (p.Thr166Arg)
c.470C>G (p.Thr157Arg)
7g.150958328G=CA1752418432KCNH2n.1480C=
c.647C= (p.Thr216=)
c.299C= (p.Thr100=)
n.870C=
c.347C= (p.Thr116=)
c.497C= (p.Thr166=)
c.470C= (p.Thr157=)
7g.150958328G>TCA369862983KCNH2n.1480C>A
c.647C>A (p.Thr216Lys)
c.299C>A (p.Thr100Lys)
n.870C>A
c.347C>A (p.Thr116Lys)
c.497C>A (p.Thr166Lys)
c.470C>A (p.Thr157Lys)
 dbSNP gnomAD v4
7g.150958329T>ACA369862984KCNH2n.1479A>T
c.646A>T (p.Thr216Ser)
c.298A>T (p.Thr100Ser)
n.869A>T
c.346A>T (p.Thr116Ser)
c.496A>T (p.Thr166Ser)
c.469A>T (p.Thr157Ser)
 gnomAD v4
7g.150958329T>CCA369862986KCNH2n.1479A>G
c.646A>G (p.Thr216Ala)
c.298A>G (p.Thr100Ala)
n.869A>G
c.346A>G (p.Thr116Ala)
c.496A>G (p.Thr166Ala)
c.469A>G (p.Thr157Ala)
 dbSNP gnomAD v2 gnomAD v4
7g.150958329T>GCA369862988KCNH2n.1479A>C
c.646A>C (p.Thr216Pro)
c.298A>C (p.Thr100Pro)
n.869A>C
c.346A>C (p.Thr116Pro)
c.496A>C (p.Thr166Pro)
c.469A>C (p.Thr157Pro)
7g.150958329T=CA1752418436KCNH2n.1479A=
c.646A= (p.Thr216=)
c.298A= (p.Thr100=)
n.869A=
c.346A= (p.Thr116=)
c.496A= (p.Thr166=)
c.469A= (p.Thr157=)
7g.150958330C>ACA458646538KCNH2n.1478G>T
c.645G>T (p.Val215=)
c.297G>T (p.Val99=)
n.868G>T
c.345G>T (p.Val115=)
c.495G>T (p.Val165=)
c.468G>T (p.Val156=)
 gnomAD v4
7g.150958330C>GCA458646541KCNH2n.1478G>C
c.645G>C (p.Val215=)
c.297G>C (p.Val99=)
n.868G>C
c.345G>C (p.Val115=)
c.495G>C (p.Val165=)
c.468G>C (p.Val156=)
7g.150958330C>TCA458646540KCNH2n.1478G>A
c.645G>A (p.Val215=)
c.297G>A (p.Val99=)
n.868G>A
c.345G>A (p.Val115=)
c.495G>A (p.Val165=)
c.468G>A (p.Val156=)
 gnomAD v4
7g.150958331A=CA1752418439KCNH2n.1477T=
c.644T= (p.Val215=)
c.296T= (p.Val99=)
n.867T=
c.344T= (p.Val115=)
c.494T= (p.Val165=)
c.467T= (p.Val156=)
7g.150958331A>CCA008637KCNH2n.1477T>G
c.644T>G (p.Val215Gly)
c.296T>G (p.Val99Gly)
n.867T>G
c.344T>G (p.Val115Gly)
c.494T>G (p.Val165Gly)
c.467T>G (p.Val156Gly)
 ClinVar dbSNP
7g.150958331A>GCA369862993KCNH2n.1477T>C
c.644T>C (p.Val215Ala)
c.296T>C (p.Val99Ala)
n.867T>C
c.344T>C (p.Val115Ala)
c.494T>C (p.Val165Ala)
c.467T>C (p.Val156Ala)
 gnomAD v4
7g.150958331A>TCA369862990KCNH2n.1477T>A
c.644T>A (p.Val215Glu)
c.296T>A (p.Val99Glu)
n.867T>A
c.344T>A (p.Val115Glu)
c.494T>A (p.Val165Glu)
c.467T>A (p.Val156Glu)
 gnomAD v4
7g.150958332C>ACA369862994KCNH2n.1476G>T
c.643G>T (p.Val215Leu)
c.295G>T (p.Val99Leu)
n.866G>T
c.343G>T (p.Val115Leu)
c.493G>T (p.Val165Leu)
c.466G>T (p.Val156Leu)
 gnomAD v4
7g.150958332C>GCA369862996KCNH2n.1476G>C
c.643G>C (p.Val215Leu)
c.295G>C (p.Val99Leu)
n.866G>C
c.343G>C (p.Val115Leu)
c.493G>C (p.Val165Leu)
c.466G>C (p.Val156Leu)
7g.150958332C>TCA369862997KCNH2n.1476G>A
c.643G>A (p.Val215Met)
c.295G>A (p.Val99Met)
n.866G>A
c.343G>A (p.Val115Met)
c.493G>A (p.Val165Met)
c.466G>A (p.Val156Met)
 gnomAD v4
7g.150958333T>ACA369862999KCNH2n.1475A>T
c.642A>T (p.Glu214Asp)
c.294A>T (p.Glu98Asp)
n.865A>T
c.342A>T (p.Glu114Asp)
c.492A>T (p.Glu164Asp)
c.465A>T (p.Glu155Asp)
 gnomAD v4
7g.150958333T>CCA458646547KCNH2n.1475A>G
c.642A>G (p.Glu214=)
c.294A>G (p.Glu98=)
n.865A>G
c.342A>G (p.Glu114=)
c.492A>G (p.Glu164=)
c.465A>G (p.Glu155=)
 dbSNP gnomAD v4
7g.150958333T>GCA369863000KCNH2n.1475A>C
c.642A>C (p.Glu214Asp)
c.294A>C (p.Glu98Asp)
n.865A>C
c.342A>C (p.Glu114Asp)
c.492A>C (p.Glu164Asp)
c.465A>C (p.Glu155Asp)
7g.150958333T=CA1752418443KCNH2n.1475A=
c.642A= (p.Glu214=)
c.294A= (p.Glu98=)
n.865A=
c.342A= (p.Glu114=)
c.492A= (p.Glu164=)
c.465A= (p.Glu155=)
7g.150958334T>ACA369863002KCNH2n.1474A>T
c.641A>T (p.Glu214Val)
c.293A>T (p.Glu98Val)
n.864A>T
c.341A>T (p.Glu114Val)
c.491A>T (p.Glu164Val)
c.464A>T (p.Glu155Val)
7g.150958334T>CCA369863004KCNH2n.1474A>G
c.641A>G (p.Glu214Gly)
c.293A>G (p.Glu98Gly)
n.864A>G
c.341A>G (p.Glu114Gly)
c.491A>G (p.Glu164Gly)
c.464A>G (p.Glu155Gly)
 gnomAD v4
7g.150958334T>GCA369863005KCNH2n.1474A>C
c.641A>C (p.Glu214Ala)
c.293A>C (p.Glu98Ala)
n.864A>C
c.341A>C (p.Glu114Ala)
c.491A>C (p.Glu164Ala)
c.464A>C (p.Glu155Ala)
7g.150958335C>ACA369863008KCNH2n.1473G>T
c.640G>T (p.Glu214Ter)
c.292G>T (p.Glu98Ter)
n.863G>T
c.340G>T (p.Glu114Ter)
c.490G>T (p.Glu164Ter)
c.463G>T (p.Glu155Ter)
 ClinVar gnomAD v4
7g.150958335C=CA1752418447KCNH2n.1473G=
c.640G= (p.Glu214=)
c.292G= (p.Glu98=)
n.863G=
c.340G= (p.Glu114=)
c.490G= (p.Glu164=)
c.463G= (p.Glu155=)
7g.150958335C>GCA369863009KCNH2n.1473G>C
c.640G>C (p.Glu214Gln)
c.292G>C (p.Glu98Gln)
n.863G>C
c.340G>C (p.Glu114Gln)
c.490G>C (p.Glu164Gln)
c.463G>C (p.Glu155Gln)
7g.150958335C>TCA040168KCNH2n.1473G>A
c.640G>A (p.Glu214Lys)
c.292G>A (p.Glu98Lys)
n.863G>A
c.340G>A (p.Glu114Lys)
c.490G>A (p.Glu164Lys)
c.463G>A (p.Glu155Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150958336G>ACA458646554KCNH2n.1472C>T
c.639C>T (p.Asp213=)
c.291C>T (p.Asp97=)
n.862C>T
c.339C>T (p.Asp113=)
c.489C>T (p.Asp163=)
c.462C>T (p.Asp154=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958336G>CCA369863012KCNH2n.1472C>G
c.639C>G (p.Asp213Glu)
c.291C>G (p.Asp97Glu)
n.862C>G
c.339C>G (p.Asp113Glu)
c.489C>G (p.Asp163Glu)
c.462C>G (p.Asp154Glu)
7g.150958336G=CA1752418450KCNH2n.1472C=
c.639C= (p.Asp213=)
c.291C= (p.Asp97=)
n.862C=
c.339C= (p.Asp113=)
c.489C= (p.Asp163=)
c.462C= (p.Asp154=)
7g.150958336G>TCA369863014KCNH2n.1472C>A
c.639C>A (p.Asp213Glu)
c.291C>A (p.Asp97Glu)
n.862C>A
c.339C>A (p.Asp113Glu)
c.489C>A (p.Asp163Glu)
c.462C>A (p.Asp154Glu)
 gnomAD v4
7g.150958337T>ACA369863019KCNH2n.1471A>T
c.638A>T (p.Asp213Val)
c.290A>T (p.Asp97Val)
n.861A>T
c.338A>T (p.Asp113Val)
c.488A>T (p.Asp163Val)
c.461A>T (p.Asp154Val)
 gnomAD v4
7g.150958337T>CCA040150KCNH2n.1471A>G
c.638A>G (p.Asp213Gly)
c.290A>G (p.Asp97Gly)
n.861A>G
c.338A>G (p.Asp113Gly)
c.488A>G (p.Asp163Gly)
c.461A>G (p.Asp154Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150958337T>GCA369863016KCNH2n.1471A>C
c.638A>C (p.Asp213Ala)
c.290A>C (p.Asp97Ala)
n.861A>C
c.338A>C (p.Asp113Ala)
c.488A>C (p.Asp163Ala)
c.461A>C (p.Asp154Ala)
7g.150958337T=CA1752418456KCNH2n.1471A=
c.638A= (p.Asp213=)
c.290A= (p.Asp97=)
n.861A=
c.338A= (p.Asp113=)
c.488A= (p.Asp163=)
c.461A= (p.Asp154=)
7g.150958338C>ACA369863020KCNH2n.1470G>T
c.637G>T (p.Asp213Tyr)
c.289G>T (p.Asp97Tyr)
n.860G>T
c.337G>T (p.Asp113Tyr)
c.487G>T (p.Asp163Tyr)
c.460G>T (p.Asp154Tyr)
 gnomAD v4
7g.150958338C=CA1752418462KCNH2n.1470G=
c.637G= (p.Asp213=)
c.289G= (p.Asp97=)
n.860G=
c.337G= (p.Asp113=)
c.487G= (p.Asp163=)
c.460G= (p.Asp154=)
7g.150958338C>GCA369863022KCNH2n.1470G>C
c.637G>C (p.Asp213His)
c.289G>C (p.Asp97His)
n.860G>C
c.337G>C (p.Asp113His)
c.487G>C (p.Asp163His)
c.460G>C (p.Asp154His)
 gnomAD v4
7g.150958338C>TCA369863023KCNH2n.1470G>A
c.637G>A (p.Asp213Asn)
c.289G>A (p.Asp97Asn)
n.860G>A
c.337G>A (p.Asp113Asn)
c.487G>A (p.Asp163Asn)
c.460G>A (p.Asp154Asn)
 dbSNP gnomAD v4
7g.150958339delCA2685608358KCNH2n.1470del
c.637del (p.Asp213ThrfsTer3)
c.289del (p.Asp97ThrfsTer3)
n.860del
c.337del (p.Asp113ThrfsTer3)
c.487del (p.Asp163ThrfsTer3)
c.460del (p.Asp154ThrfsTer3)
 gnomAD v4
7g.150958339C>ACA458646564KCNH2n.1469G>T
c.636G>T (p.Leu212=)
c.288G>T (p.Leu96=)
n.859G>T
c.336G>T (p.Leu112=)
c.486G>T (p.Leu162=)
c.459G>T (p.Leu153=)
 gnomAD v4
7g.150958339C=CA1752418464KCNH2n.1469G=
c.636G= (p.Leu212=)
c.288G= (p.Leu96=)
n.859G=
c.336G= (p.Leu112=)
c.486G= (p.Leu162=)
c.459G= (p.Leu153=)
7g.150958339C>GCA040142KCNH2n.1469G>C
c.636G>C (p.Leu212=)
c.288G>C (p.Leu96=)
n.859G>C
c.336G>C (p.Leu112=)
c.486G>C (p.Leu162=)
c.459G>C (p.Leu153=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150958339C>TCA458646561KCNH2n.1469G>A
c.636G>A (p.Leu212=)
c.288G>A (p.Leu96=)
n.859G>A
c.336G>A (p.Leu112=)
c.486G>A (p.Leu162=)
c.459G>A (p.Leu153=)
 gnomAD v4
7g.150958340delCA071918KCNH2n.1468del
c.635del (p.Leu212ArgfsTer4)
c.287del (p.Leu96ArgfsTer4)
n.858del
c.335del (p.Leu112ArgfsTer4)
c.485del (p.Leu162ArgfsTer4)
c.458del (p.Leu153ArgfsTer4)
7g.150958340A=CA1752418471KCNH2n.1468T=
c.635T= (p.Leu212=)
c.287T= (p.Leu96=)
n.858T=
c.335T= (p.Leu112=)
c.485T= (p.Leu162=)
c.458T= (p.Leu153=)
7g.150958340A>CCA369863026KCNH2n.1468T>G
c.635T>G (p.Leu212Arg)
c.287T>G (p.Leu96Arg)
n.858T>G
c.335T>G (p.Leu112Arg)
c.485T>G (p.Leu162Arg)
c.458T>G (p.Leu153Arg)
7g.150958340A>GCA369863027KCNH2n.1468T>C
c.635T>C (p.Leu212Pro)
c.287T>C (p.Leu96Pro)
n.858T>C
c.335T>C (p.Leu112Pro)
c.485T>C (p.Leu162Pro)
c.458T>C (p.Leu153Pro)
 dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
7g.150958340A>TCA369863028KCNH2n.1468T>A
c.635T>A (p.Leu212Gln)
c.287T>A (p.Leu96Gln)
n.858T>A
c.335T>A (p.Leu112Gln)
c.485T>A (p.Leu162Gln)
c.458T>A (p.Leu153Gln)
 gnomAD v4
7g.150958341G>ACA458646568KCNH2n.1467C>T
c.634C>T (p.Leu212=)
c.286C>T (p.Leu96=)
n.857C>T
c.334C>T (p.Leu112=)
c.484C>T (p.Leu162=)
c.457C>T (p.Leu153=)
 dbSNP gnomAD v4
7g.150958341G>CCA369863029KCNH2n.1467C>G
c.634C>G (p.Leu212Val)
c.286C>G (p.Leu96Val)
n.857C>G
c.334C>G (p.Leu112Val)
c.484C>G (p.Leu162Val)
c.457C>G (p.Leu153Val)
7g.150958341G=CA1752418475KCNH2n.1467C=
c.634C= (p.Leu212=)
c.286C= (p.Leu96=)
n.857C=
c.334C= (p.Leu112=)
c.484C= (p.Leu162=)
c.457C= (p.Leu153=)
7g.150958341G>TCA369863031KCNH2n.1467C>A
c.634C>A (p.Leu212Met)
c.286C>A (p.Leu96Met)
n.857C>A
c.334C>A (p.Leu112Met)
c.484C>A (p.Leu162Met)
c.457C>A (p.Leu153Met)
 gnomAD v4
7g.150958343delCA2685608374KCNH2n.1467del
c.634del (p.Leu212TrpfsTer4)
c.286del (p.Leu96TrpfsTer4)
n.857del
c.334del (p.Leu112TrpfsTer4)
c.484del (p.Leu162TrpfsTer4)
c.457del (p.Leu153TrpfsTer4)
 gnomAD v4
7g.150958342G>ACA040124KCNH2n.1466C>T
c.633C>T (p.Ala211=)
c.285C>T (p.Ala95=)
n.856C>T
c.333C>T (p.Ala111=)
c.483C>T (p.Ala161=)
c.456C>T (p.Ala152=)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150958342G>CCA458646572KCNH2n.1466C>G
c.633C>G (p.Ala211=)
c.285C>G (p.Ala95=)
n.856C>G
c.333C>G (p.Ala111=)
c.483C>G (p.Ala161=)
c.456C>G (p.Ala152=)
 gnomAD v4
7g.150958342G=CA1752418477KCNH2n.1466C=
c.633C= (p.Ala211=)
c.285C= (p.Ala95=)
n.856C=
c.333C= (p.Ala111=)
c.483C= (p.Ala161=)
c.456C= (p.Ala152=)
7g.150958342G>TCA458646573KCNH2n.1466C>A
c.633C>A (p.Ala211=)
c.285C>A (p.Ala95=)
n.856C>A
c.333C>A (p.Ala111=)
c.483C>A (p.Ala161=)
c.456C>A (p.Ala152=)
 gnomAD v4
7g.150958343G>ACA369863034KCNH2n.1465C>T
c.632C>T (p.Ala211Val)
c.284C>T (p.Ala95Val)
n.855C>T
c.332C>T (p.Ala111Val)
c.482C>T (p.Ala161Val)
c.455C>T (p.Ala152Val)
 ClinVar gnomAD v4
7g.150958343G>CCA369863036KCNH2n.1465C>G
c.632C>G (p.Ala211Gly)
c.284C>G (p.Ala95Gly)
n.855C>G
c.332C>G (p.Ala111Gly)
c.482C>G (p.Ala161Gly)
c.455C>G (p.Ala152Gly)
 gnomAD v4
7g.150958343G=CA1752418480KCNH2n.1465C=
c.632C= (p.Ala211=)
c.284C= (p.Ala95=)
n.855C=
c.332C= (p.Ala111=)
c.482C= (p.Ala161=)
c.455C= (p.Ala152=)
7g.150958343G>TCA169081387KCNH2n.1465C>A
c.632C>A (p.Ala211Asp)
c.284C>A (p.Ala95Asp)
n.855C>A
c.332C>A (p.Ala111Asp)
c.482C>A (p.Ala161Asp)
c.455C>A (p.Ala152Asp)
 dbSNP gnomAD v4
7g.150958344C>ACA169081388KCNH2n.1464G>T
c.631G>T (p.Ala211Ser)
c.283G>T (p.Ala95Ser)
n.854G>T
c.331G>T (p.Ala111Ser)
c.481G>T (p.Ala161Ser)
c.454G>T (p.Ala152Ser)
 dbSNP gnomAD v4
7g.150958344C=CA1752418482KCNH2n.1464G=
c.631G= (p.Ala211=)
c.283G= (p.Ala95=)
n.854G=
c.331G= (p.Ala111=)
c.481G= (p.Ala161=)
c.454G= (p.Ala152=)
7g.150958344C>GCA369863040KCNH2n.1464G>C
c.631G>C (p.Ala211Pro)
c.283G>C (p.Ala95Pro)
n.854G>C
c.331G>C (p.Ala111Pro)
c.481G>C (p.Ala161Pro)
c.454G>C (p.Ala152Pro)
7g.150958344C>TCA071854KCNH2n.1464G>A
c.631G>A (p.Ala211Thr)
c.283G>A (p.Ala95Thr)
n.854G>A
c.331G>A (p.Ala111Thr)
c.481G>A (p.Ala161Thr)
c.454G>A (p.Ala152Thr)
 gnomAD v4
7g.150958345delCA2685608398KCNH2n.1464del
c.631del (p.Ala211ProfsTer5)
c.283del (p.Ala95ProfsTer5)
n.854del
c.331del (p.Ala111ProfsTer5)
c.481del (p.Ala161ProfsTer5)
c.454del (p.Ala152ProfsTer5)
 gnomAD v4
7g.150958345C>ACA458646580KCNH2n.1463G>T
c.630G>T (p.Leu210=)
c.282G>T (p.Leu94=)
n.853G>T
c.330G>T (p.Leu110=)
c.480G>T (p.Leu160=)
c.453G>T (p.Leu151=)
 dbSNP gnomAD v4
7g.150958345C=CA1752418484KCNH2n.1463G=
c.630G= (p.Leu210=)
c.282G= (p.Leu94=)
n.853G=
c.330G= (p.Leu110=)
c.480G= (p.Leu160=)
c.453G= (p.Leu151=)
7g.150958345C>GCA458646581KCNH2n.1463G>C
c.630G>C (p.Leu210=)
c.282G>C (p.Leu94=)
n.853G>C
c.330G>C (p.Leu110=)
c.480G>C (p.Leu160=)
c.453G>C (p.Leu151=)
 dbSNP gnomAD v2 gnomAD v4
7g.150958345C>TCA458646582KCNH2n.1463G>A
c.630G>A (p.Leu210=)
c.282G>A (p.Leu94=)
n.853G>A
c.330G>A (p.Leu110=)
c.480G>A (p.Leu160=)
c.453G>A (p.Leu151=)
 gnomAD v4
7g.150958346A=CA1752418488KCNH2n.1462T=
c.629T= (p.Leu210=)
c.281T= (p.Leu94=)
n.852T=
c.329T= (p.Leu110=)
c.479T= (p.Leu160=)
c.452T= (p.Leu151=)
7g.150958346A>CCA369863044KCNH2n.1462T>G
c.629T>G (p.Leu210Arg)
c.281T>G (p.Leu94Arg)
n.852T>G
c.329T>G (p.Leu110Arg)
c.479T>G (p.Leu160Arg)
c.452T>G (p.Leu151Arg)
7g.150958346A>GCA369863042KCNH2n.1462T>C
c.629T>C (p.Leu210Pro)
c.281T>C (p.Leu94Pro)
n.852T>C
c.329T>C (p.Leu110Pro)
c.479T>C (p.Leu160Pro)
c.452T>C (p.Leu151Pro)
 ClinVar dbSNP gnomAD v4
7g.150958346A>TCA369863046KCNH2n.1462T>A
c.629T>A (p.Leu210Gln)
c.281T>A (p.Leu94Gln)
n.852T>A
c.329T>A (p.Leu110Gln)
c.479T>A (p.Leu160Gln)
c.452T>A (p.Leu151Gln)
 ClinVar dbSNP gnomAD v4
7g.150958347G>ACA458646586KCNH2n.1461C>T
c.628C>T (p.Leu210=)
c.280C>T (p.Leu94=)
n.851C>T
c.328C>T (p.Leu110=)
c.478C>T (p.Leu160=)
c.451C>T (p.Leu151=)
 gnomAD v4
7g.150958347G>CCA369863048KCNH2n.1461C>G
c.628C>G (p.Leu210Val)
c.280C>G (p.Leu94Val)
n.851C>G
c.328C>G (p.Leu110Val)
c.478C>G (p.Leu160Val)
c.451C>G (p.Leu151Val)
 gnomAD v4
7g.150958347G>TCA369863049KCNH2n.1461C>A
c.628C>A (p.Leu210Met)
c.280C>A (p.Leu94Met)
n.851C>A
c.328C>A (p.Leu110Met)
c.478C>A (p.Leu160Met)
c.451C>A (p.Leu151Met)
 gnomAD v4
7g.150958348C>ACA169081389KCNH2n.1460G>T
c.627G>T (p.Ser209=)
c.279G>T (p.Ser93=)
n.850G>T
c.327G>T (p.Ser109=)
c.477G>T (p.Ser159=)
c.450G>T (p.Ser150=)
 ClinVar dbSNP gnomAD v4
7g.150958348C=CA1752418492KCNH2n.1460G=
c.627G= (p.Ser209=)
c.279G= (p.Ser93=)
n.850G=
c.327G= (p.Ser109=)
c.477G= (p.Ser159=)
c.450G= (p.Ser150=)
7g.150958348C>GCA458646590KCNH2n.1460G>C
c.627G>C (p.Ser209=)
c.279G>C (p.Ser93=)
n.850G>C
c.327G>C (p.Ser109=)
c.477G>C (p.Ser159=)
c.450G>C (p.Ser150=)
 gnomAD v4
7g.150958348C>TCA458646592KCNH2n.1460G>A
c.627G>A (p.Ser209=)
c.279G>A (p.Ser93=)
n.850G>A
c.327G>A (p.Ser109=)
c.477G>A (p.Ser159=)
c.450G>A (p.Ser150=)
 gnomAD v4
7g.150958349G>ACA071932KCNH2n.1459C>T
c.626C>T (p.Ser209Leu)
c.278C>T (p.Ser93Leu)
n.849C>T
c.326C>T (p.Ser109Leu)
c.476C>T (p.Ser159Leu)
c.449C>T (p.Ser150Leu)
 dbSNP gnomAD v4
7g.150958349G>CCA369863052KCNH2n.1459C>G
c.626C>G (p.Ser209Trp)
c.278C>G (p.Ser93Trp)
n.849C>G
c.326C>G (p.Ser109Trp)
c.476C>G (p.Ser159Trp)
c.449C>G (p.Ser150Trp)
7g.150958349G=CA1752418494KCNH2n.1459C=
c.626C= (p.Ser209=)
c.278C= (p.Ser93=)
n.849C=
c.326C= (p.Ser109=)
c.476C= (p.Ser159=)
c.449C= (p.Ser150=)
7g.150958349G>TCA369863054KCNH2n.1459C>A
c.626C>A (p.Ser209Ter)
c.278C>A (p.Ser93Ter)
n.849C>A
c.326C>A (p.Ser109Ter)
c.476C>A (p.Ser159Ter)
c.449C>A (p.Ser150Ter)
 gnomAD v4
7g.150958350A>CCA369863057KCNH2n.1458T>G
c.625T>G (p.Ser209Ala)
c.277T>G (p.Ser93Ala)
n.848T>G
c.325T>G (p.Ser109Ala)
c.475T>G (p.Ser159Ala)
c.448T>G (p.Ser150Ala)
7g.150958350A>GCA369863058KCNH2n.1458T>C
c.625T>C (p.Ser209Pro)
c.277T>C (p.Ser93Pro)
n.848T>C
c.325T>C (p.Ser109Pro)
c.475T>C (p.Ser159Pro)
c.448T>C (p.Ser150Pro)
 gnomAD v4
7g.150958350A>TCA369863059KCNH2n.1458T>A
c.625T>A (p.Ser209Thr)
c.277T>A (p.Ser93Thr)
n.848T>A
c.325T>A (p.Ser109Thr)
c.475T>A (p.Ser159Thr)
c.448T>A (p.Ser150Thr)
 gnomAD v4
7g.150958351C>ACA369863062KCNH2n.1457G>T
c.624G>T (p.Glu208Asp)
c.276G>T (p.Glu92Asp)
n.847G>T
c.324G>T (p.Glu108Asp)
c.474G>T (p.Glu158Asp)
c.447G>T (p.Glu149Asp)
 gnomAD v4
7g.150958351C>GCA369863064KCNH2n.1457G>C
c.624G>C (p.Glu208Asp)
c.276G>C (p.Glu92Asp)
n.847G>C
c.324G>C (p.Glu108Asp)
c.474G>C (p.Glu158Asp)
c.447G>C (p.Glu149Asp)
7g.150958351C>TCA458646597KCNH2n.1457G>A
c.624G>A (p.Glu208=)
c.276G>A (p.Glu92=)
n.847G>A
c.324G>A (p.Glu108=)
c.474G>A (p.Glu158=)
c.447G>A (p.Glu149=)
 ClinVar gnomAD v4
7g.150958352T>ACA369863066KCNH2n.1456A>T
c.623A>T (p.Glu208Val)
c.275A>T (p.Glu92Val)
n.846A>T
c.323A>T (p.Glu108Val)
c.473A>T (p.Glu158Val)
c.446A>T (p.Glu149Val)
 gnomAD v4
7g.150958352T>CCA369863068KCNH2n.1456A>G
c.623A>G (p.Glu208Gly)
c.275A>G (p.Glu92Gly)
n.846A>G
c.323A>G (p.Glu108Gly)
c.473A>G (p.Glu158Gly)
c.446A>G (p.Glu149Gly)
 gnomAD v4
7g.150958352T>GCA369863070KCNH2n.1456A>C
c.623A>C (p.Glu208Ala)
c.275A>C (p.Glu92Ala)
n.846A>C
c.323A>C (p.Glu108Ala)
c.473A>C (p.Glu158Ala)
c.446A>C (p.Glu149Ala)
7g.150958353C>ACA369863074KCNH2n.1455G>T
c.622G>T (p.Glu208Ter)
c.274G>T (p.Glu92Ter)
n.845G>T
c.322G>T (p.Glu108Ter)
c.472G>T (p.Glu158Ter)
c.445G>T (p.Glu149Ter)
 gnomAD v4
7g.150958353C=CA1752418496KCNH2n.1455G=
c.622G= (p.Glu208=)
c.274G= (p.Glu92=)
n.845G=
c.322G= (p.Glu108=)
c.472G= (p.Glu158=)
c.445G= (p.Glu149=)
7g.150958353C>GCA369863071KCNH2n.1455G>C
c.622G>C (p.Glu208Gln)
c.274G>C (p.Glu92Gln)
n.845G>C
c.322G>C (p.Glu108Gln)
c.472G>C (p.Glu158Gln)
c.445G>C (p.Glu149Gln)
 gnomAD v4
7g.150958353C>TCA369863072KCNH2n.1455G>A
c.622G>A (p.Glu208Lys)
c.274G>A (p.Glu92Lys)
n.845G>A
c.322G>A (p.Glu108Lys)
c.472G>A (p.Glu158Lys)
c.445G>A (p.Glu149Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958354_150958355dupCA2695208640KCNH2n.1454_1455dup
c.621_622dup (p.Glu208AlafsTer9)
c.273_274dup (p.Glu92AlafsTer9)
n.844_845dup
c.321_322dup (p.Glu108AlafsTer9)
c.471_472dup (p.Glu158AlafsTer9)
c.444_445dup (p.Glu149AlafsTer9)
7g.150958354G>ACA040109KCNH2n.1454C>T
c.621C>T (p.Ser207=)
c.273C>T (p.Ser91=)
n.844C>T
c.321C>T (p.Ser107=)
c.471C>T (p.Ser157=)
c.444C>T (p.Ser148=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150958354G>CCA369863077KCNH2n.1454C>G
c.621C>G (p.Ser207Arg)
c.273C>G (p.Ser91Arg)
n.844C>G
c.321C>G (p.Ser107Arg)
c.471C>G (p.Ser157Arg)
c.444C>G (p.Ser148Arg)
 gnomAD v4
7g.150958354G=CA1752418499KCNH2n.1454C=
c.621C= (p.Ser207=)
c.273C= (p.Ser91=)
n.844C=
c.321C= (p.Ser107=)
c.471C= (p.Ser157=)
c.444C= (p.Ser148=)
7g.150958354G>TCA169081394KCNH2n.1454C>A
c.621C>A (p.Ser207Arg)
c.273C>A (p.Ser91Arg)
n.844C>A
c.321C>A (p.Ser107Arg)
c.471C>A (p.Ser157Arg)
c.444C>A (p.Ser148Arg)
 dbSNP gnomAD v4
7g.150958355C>ACA369863080KCNH2n.1453G>T
c.620G>T (p.Ser207Ile)
c.272G>T (p.Ser91Ile)
n.843G>T
c.320G>T (p.Ser107Ile)
c.470G>T (p.Ser157Ile)
c.443G>T (p.Ser148Ile)
 gnomAD v4
7g.150958355C>GCA369863082KCNH2n.1453G>C
c.620G>C (p.Ser207Thr)
c.272G>C (p.Ser91Thr)
n.843G>C
c.320G>C (p.Ser107Thr)
c.470G>C (p.Ser157Thr)
c.443G>C (p.Ser148Thr)
 gnomAD v4
7g.150958355C>TCA369863084KCNH2n.1453G>A
c.620G>A (p.Ser207Asn)
c.272G>A (p.Ser91Asn)
n.843G>A
c.320G>A (p.Ser107Asn)
c.470G>A (p.Ser157Asn)
c.443G>A (p.Ser148Asn)
 gnomAD v4
7g.150958356delCA2695208641KCNH2n.1452del
c.619del (p.Ser207AlafsTer9)
c.271del (p.Ser91AlafsTer9)
n.842del
c.319del (p.Ser107AlafsTer9)
c.469del (p.Ser157AlafsTer9)
c.442del (p.Ser148AlafsTer9)
7g.150958356T>ACA369863086KCNH2n.1452A>T
c.619A>T (p.Ser207Cys)
c.271A>T (p.Ser91Cys)
n.842A>T
c.319A>T (p.Ser107Cys)
c.469A>T (p.Ser157Cys)
c.442A>T (p.Ser148Cys)
7g.150958356T>CCA369863088KCNH2n.1452A>G
c.619A>G (p.Ser207Gly)
c.271A>G (p.Ser91Gly)
n.842A>G
c.319A>G (p.Ser107Gly)
c.469A>G (p.Ser157Gly)
c.442A>G (p.Ser148Gly)
 gnomAD v4
7g.150958356T>GCA369863089KCNH2n.1452A>C
c.619A>C (p.Ser207Arg)
c.271A>C (p.Ser91Arg)
n.842A>C
c.319A>C (p.Ser107Arg)
c.469A>C (p.Ser157Arg)
c.442A>C (p.Ser148Arg)
7g.150958357G>ACA458646607KCNH2n.1451C>T
c.618C>T (p.Ser206=)
c.270C>T (p.Ser90=)
n.841C>T
c.318C>T (p.Ser106=)
c.468C>T (p.Ser156=)
c.441C>T (p.Ser147=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958357G>CCA369863091KCNH2n.1451C>G
c.618C>G (p.Ser206Arg)
c.270C>G (p.Ser90Arg)
n.841C>G
c.318C>G (p.Ser106Arg)
c.468C>G (p.Ser156Arg)
c.441C>G (p.Ser147Arg)
 gnomAD v4
7g.150958357G=CA1752418504KCNH2n.1451C=
c.618C= (p.Ser206=)
c.270C= (p.Ser90=)
n.841C=
c.318C= (p.Ser106=)
c.468C= (p.Ser156=)
c.441C= (p.Ser147=)
7g.150958357G>TCA369863093KCNH2n.1451C>A
c.618C>A (p.Ser206Arg)
c.270C>A (p.Ser90Arg)
n.841C>A
c.318C>A (p.Ser106Arg)
c.468C>A (p.Ser156Arg)
c.441C>A (p.Ser147Arg)
 gnomAD v4
7g.150958357_150958358delinsAACA16612050KCNH2n.1450_1451delinsTT
c.617_618delinsTT (p.Ser206Ile)
c.269_270delinsTT (p.Ser90Ile)
n.840_841delinsTT
c.317_318delinsTT (p.Ser106Ile)
c.467_468delinsTT (p.Ser156Ile)
c.440_441delinsTT (p.Ser147Ile)
 ClinVar dbSNP
7g.150958357_150958358delinsGCCA1752418506KCNH2n.1450_1451delinsGC
c.617_618delinsGC (p.Ser206=)
c.269_270delinsGC (p.Ser90=)
n.840_841delinsGC
c.317_318delinsGC (p.Ser106=)
c.467_468delinsGC (p.Ser156=)
c.440_441delinsGC (p.Ser147=)
7g.150958358C>ACA369863097KCNH2n.1450G>T
c.617G>T (p.Ser206Ile)
c.269G>T (p.Ser90Ile)
n.840G>T
c.317G>T (p.Ser106Ile)
c.467G>T (p.Ser156Ile)
c.440G>T (p.Ser147Ile)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958358C=CA1752418509KCNH2n.1450G=
c.617G= (p.Ser206=)
c.269G= (p.Ser90=)
n.840G=
c.317G= (p.Ser106=)
c.467G= (p.Ser156=)
c.440G= (p.Ser147=)
7g.150958358C>GCA369863099KCNH2n.1450G>C
c.617G>C (p.Ser206Thr)
c.269G>C (p.Ser90Thr)
n.840G>C
c.317G>C (p.Ser106Thr)
c.467G>C (p.Ser156Thr)
c.440G>C (p.Ser147Thr)
7g.150958358C>TCA369863095KCNH2n.1450G>A
c.617G>A (p.Ser206Asn)
c.269G>A (p.Ser90Asn)
n.840G>A
c.317G>A (p.Ser106Asn)
c.467G>A (p.Ser156Asn)
c.440G>A (p.Ser147Asn)
 gnomAD v4
7g.150958359T>ACA369863101KCNH2n.1449A>T
c.616A>T (p.Ser206Cys)
c.268A>T (p.Ser90Cys)
n.839A>T
c.316A>T (p.Ser106Cys)
c.466A>T (p.Ser156Cys)
c.439A>T (p.Ser147Cys)
 gnomAD v4
7g.150958359T>CCA369863103KCNH2n.1449A>G
c.616A>G (p.Ser206Gly)
c.268A>G (p.Ser90Gly)
n.839A>G
c.316A>G (p.Ser106Gly)
c.466A>G (p.Ser156Gly)
c.439A>G (p.Ser147Gly)
 gnomAD v4
7g.150958359T>GCA369863104KCNH2n.1449A>C
c.616A>C (p.Ser206Arg)
c.268A>C (p.Ser90Arg)
n.839A>C
c.316A>C (p.Ser106Arg)
c.466A>C (p.Ser156Arg)
c.439A>C (p.Ser147Arg)
7g.150958360G>ACA458646615KCNH2n.1448C>T
c.615C>T (p.Pro205=)
c.267C>T (p.Pro89=)
n.838C>T
c.315C>T (p.Pro105=)
c.465C>T (p.Pro155=)
c.438C>T (p.Pro146=)
 gnomAD v4
7g.150958360G>CCA071815KCNH2n.1448C>G
c.615C>G (p.Pro205=)
c.267C>G (p.Pro89=)
n.838C>G
c.315C>G (p.Pro105=)
c.465C>G (p.Pro155=)
c.438C>G (p.Pro146=)
 gnomAD v4
7g.150958360G>TCA458646616KCNH2n.1448C>A
c.615C>A (p.Pro205=)
c.267C>A (p.Pro89=)
n.838C>A
c.315C>A (p.Pro105=)
c.465C>A (p.Pro155=)
c.438C>A (p.Pro146=)
 gnomAD v4
7g.150958361G>ACA369863107KCNH2n.1447C>T
c.614C>T (p.Pro205Leu)
c.266C>T (p.Pro89Leu)
n.837C>T
c.314C>T (p.Pro105Leu)
c.464C>T (p.Pro155Leu)
c.437C>T (p.Pro146Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958361G>CCA071810KCNH2n.1447C>G
c.614C>G (p.Pro205Arg)
c.266C>G (p.Pro89Arg)
n.837C>G
c.314C>G (p.Pro105Arg)
c.464C>G (p.Pro155Arg)
c.437C>G (p.Pro146Arg)
7g.150958361G=CA1752418513KCNH2n.1447C=
c.614C= (p.Pro205=)
c.266C= (p.Pro89=)
n.837C=
c.314C= (p.Pro105=)
c.464C= (p.Pro155=)
c.437C= (p.Pro146=)
7g.150958361G>TCA369863109KCNH2n.1447C>A
c.614C>A (p.Pro205His)
c.266C>A (p.Pro89His)
n.837C>A
c.314C>A (p.Pro105His)
c.464C>A (p.Pro155His)
c.437C>A (p.Pro146His)
 gnomAD v4
7g.150958362G>ACA169081399KCNH2n.1446C>T
c.613C>T (p.Pro205Ser)
c.265C>T (p.Pro89Ser)
n.836C>T
c.313C>T (p.Pro105Ser)
c.463C>T (p.Pro155Ser)
c.436C>T (p.Pro146Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.150958362G>CCA071950KCNH2n.1446C>G
c.613C>G (p.Pro205Ala)
c.265C>G (p.Pro89Ala)
n.836C>G
c.313C>G (p.Pro105Ala)
c.463C>G (p.Pro155Ala)
c.436C>G (p.Pro146Ala)
 gnomAD v4
7g.150958362G=CA1752418516KCNH2n.1446C=
c.613C= (p.Pro205=)
c.265C= (p.Pro89=)
n.836C=
c.313C= (p.Pro105=)
c.463C= (p.Pro155=)
c.436C= (p.Pro146=)
7g.150958362G>TCA169081404KCNH2n.1446C>A
c.613C>A (p.Pro205Thr)
c.265C>A (p.Pro89Thr)
n.836C>A
c.313C>A (p.Pro105Thr)
c.463C>A (p.Pro155Thr)
c.436C>A (p.Pro146Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958363T>ACA458646623KCNH2n.1445A>T
c.612A>T (p.Ala204=)
c.264A>T (p.Ala88=)
n.835A>T
c.312A>T (p.Ala104=)
c.462A>T (p.Ala154=)
c.435A>T (p.Ala145=)
 gnomAD v4
7g.150958363T>CCA458646624KCNH2n.1445A>G
c.612A>G (p.Ala204=)
c.264A>G (p.Ala88=)
n.835A>G
c.312A>G (p.Ala104=)
c.462A>G (p.Ala154=)
c.435A>G (p.Ala145=)
 gnomAD v4
7g.150958363T>GCA458646626KCNH2n.1445A>C
c.612A>C (p.Ala204=)
c.264A>C (p.Ala88=)
n.835A>C
c.312A>C (p.Ala104=)
c.462A>C (p.Ala154=)
c.435A>C (p.Ala145=)
 dbSNP
7g.150958363T=CA1752418518KCNH2n.1445A=
c.612A= (p.Ala204=)
c.264A= (p.Ala88=)
n.835A=
c.312A= (p.Ala104=)
c.462A= (p.Ala154=)
c.435A= (p.Ala145=)
7g.150958364G>ACA369863113KCNH2n.1444C>T
c.611C>T (p.Ala204Val)
c.263C>T (p.Ala88Val)
n.834C>T
c.311C>T (p.Ala104Val)
c.461C>T (p.Ala154Val)
c.434C>T (p.Ala145Val)
 gnomAD v4
7g.150958364G>CCA369863115KCNH2n.1444C>G
c.611C>G (p.Ala204Gly)
c.263C>G (p.Ala88Gly)
n.834C>G
c.311C>G (p.Ala104Gly)
c.461C>G (p.Ala154Gly)
c.434C>G (p.Ala145Gly)
7g.150958364G>TCA369863117KCNH2n.1444C>A
c.611C>A (p.Ala204Glu)
c.263C>A (p.Ala88Glu)
n.834C>A
c.311C>A (p.Ala104Glu)
c.461C>A (p.Ala154Glu)
c.434C>A (p.Ala145Glu)
 gnomAD v4
7g.150958365C>ACA369863121KCNH2n.1443G>T
c.610G>T (p.Ala204Ser)
c.262G>T (p.Ala88Ser)
n.833G>T
c.310G>T (p.Ala104Ser)
c.460G>T (p.Ala154Ser)
c.433G>T (p.Ala145Ser)
 gnomAD v4
7g.150958365C=CA1752418521KCNH2n.1443G=
c.610G= (p.Ala204=)
c.262G= (p.Ala88=)
n.833G=
c.310G= (p.Ala104=)
c.460G= (p.Ala154=)
c.433G= (p.Ala145=)
7g.150958365C>GCA369863119KCNH2n.1443G>C
c.610G>C (p.Ala204Pro)
c.262G>C (p.Ala88Pro)
n.833G>C
c.310G>C (p.Ala104Pro)
c.460G>C (p.Ala154Pro)
c.433G>C (p.Ala145Pro)
 gnomAD v4
7g.150958365C>TCA169081407KCNH2n.1443G>A
c.610G>A (p.Ala204Thr)
c.262G>A (p.Ala88Thr)
n.833G>A
c.310G>A (p.Ala104Thr)
c.460G>A (p.Ala154Thr)
c.433G>A (p.Ala145Thr)
 dbSNP gnomAD v2 gnomAD v4
7g.150958366delCA2716208800KCNH2n.1443del
c.610del (p.Ala204HisfsTer12)
c.262del (p.Ala88HisfsTer12)
n.833del
c.310del (p.Ala104HisfsTer12)
c.460del (p.Ala154HisfsTer12)
c.433del (p.Ala145HisfsTer12)
 dbSNP
7g.150958366C>ACA458646631KCNH2n.1442G>T
c.609G>T (p.Ala203=)
c.261G>T (p.Ala87=)
n.832G>T
c.309G>T (p.Ala103=)
c.459G>T (p.Ala153=)
c.432G>T (p.Ala144=)
 dbSNP gnomAD v4
7g.150958366C>GCA458646633KCNH2n.1442G>C
c.609G>C (p.Ala203=)
c.261G>C (p.Ala87=)
n.832G>C
c.309G>C (p.Ala103=)
c.459G>C (p.Ala153=)
c.432G>C (p.Ala144=)
7g.150958366C>TCA458646635KCNH2n.1442G>A
c.609G>A (p.Ala203=)
c.261G>A (p.Ala87=)
n.832G>A
c.309G>A (p.Ala103=)
c.459G>A (p.Ala153=)
c.432G>A (p.Ala144=)
 gnomAD v4
7g.150958368_150958369delCA2716208801KCNH2n.1441_1442del
c.608_609del (p.Ala203GlyfsTer?)
c.260_261del (p.Ala87GlyfsTer?)
n.831_832del
c.308_309del (p.Ala103GlyfsTer?)
c.458_459del (p.Ala153GlyfsTer?)
c.431_432del (p.Ala144GlyfsTer?)
 dbSNP
7g.150958367G>ACA071954KCNH2n.1441C>T
c.608C>T (p.Ala203Val)
c.260C>T (p.Ala87Val)
n.831C>T
c.308C>T (p.Ala103Val)
c.458C>T (p.Ala153Val)
c.431C>T (p.Ala144Val)
 gnomAD v4
7g.150958367G>CCA369863124KCNH2n.1441C>G
c.608C>G (p.Ala203Gly)
c.260C>G (p.Ala87Gly)
n.831C>G
c.308C>G (p.Ala103Gly)
c.458C>G (p.Ala153Gly)
c.431C>G (p.Ala144Gly)
 gnomAD v4
7g.150958367G>TCA369863126KCNH2n.1441C>A
c.608C>A (p.Ala203Glu)
c.260C>A (p.Ala87Glu)
n.831C>A
c.308C>A (p.Ala103Glu)
c.458C>A (p.Ala153Glu)
c.431C>A (p.Ala144Glu)
 gnomAD v4
7g.150958368C>ACA369863128KCNH2n.1440G>T
c.607G>T (p.Ala203Ser)
c.259G>T (p.Ala87Ser)
n.830G>T
c.307G>T (p.Ala103Ser)
c.457G>T (p.Ala153Ser)
c.430G>T (p.Ala144Ser)
 gnomAD v4
7g.150958368C=CA1752418523KCNH2n.1440G=
c.607G= (p.Ala203=)
c.259G= (p.Ala87=)
n.830G=
c.307G= (p.Ala103=)
c.457G= (p.Ala153=)
c.430G= (p.Ala144=)
7g.150958368C>GCA369863130KCNH2n.1440G>C
c.607G>C (p.Ala203Pro)
c.259G>C (p.Ala87Pro)
n.830G>C
c.307G>C (p.Ala103Pro)
c.457G>C (p.Ala153Pro)
c.430G>C (p.Ala144Pro)
7g.150958368C>TCA008631KCNH2n.1440G>A
c.607G>A (p.Ala203Thr)
c.259G>A (p.Ala87Thr)
n.830G>A
c.307G>A (p.Ala103Thr)
c.457G>A (p.Ala153Thr)
c.430G>A (p.Ala144Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958369G>ACA458646640KCNH2n.1439C>T
c.606C>T (p.Pro202=)
c.258C>T (p.Pro86=)
n.829C>T
c.306C>T (p.Pro102=)
c.456C>T (p.Pro152=)
c.429C>T (p.Pro143=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958369G>CCA458646641KCNH2n.1439C>G
c.606C>G (p.Pro202=)
c.258C>G (p.Pro86=)
n.829C>G
c.306C>G (p.Pro102=)
c.456C>G (p.Pro152=)
c.429C>G (p.Pro143=)
 gnomAD v4
7g.150958369G=CA1752418527KCNH2n.1439C=
c.606C= (p.Pro202=)
c.258C= (p.Pro86=)
n.829C=
c.306C= (p.Pro102=)
c.456C= (p.Pro152=)
c.429C= (p.Pro143=)
7g.150958369G>TCA458646643KCNH2n.1439C>A
c.606C>A (p.Pro202=)
c.258C>A (p.Pro86=)
n.829C>A
c.306C>A (p.Pro102=)
c.456C>A (p.Pro152=)
c.429C>A (p.Pro143=)
 gnomAD v4
7g.150958371delCA2685608471KCNH2n.1439del
c.606del (p.Ala203ArgfsTer13)
c.258del (p.Ala87ArgfsTer13)
n.829del
c.306del (p.Ala103ArgfsTer13)
c.456del (p.Ala153ArgfsTer13)
c.429del (p.Ala144ArgfsTer13)
 gnomAD v4
7g.150958370G>ACA369863133KCNH2n.1438C>T
c.605C>T (p.Pro202Leu)
c.257C>T (p.Pro86Leu)
n.828C>T
c.305C>T (p.Pro102Leu)
c.455C>T (p.Pro152Leu)
c.428C>T (p.Pro143Leu)
 gnomAD v4
7g.150958370G>CCA369863134KCNH2n.1438C>G
c.605C>G (p.Pro202Arg)
c.257C>G (p.Pro86Arg)
n.828C>G
c.305C>G (p.Pro102Arg)
c.455C>G (p.Pro152Arg)
c.428C>G (p.Pro143Arg)
7g.150958370G>TCA369863136KCNH2n.1438C>A
c.605C>A (p.Pro202His)
c.257C>A (p.Pro86His)
n.828C>A
c.305C>A (p.Pro102His)
c.455C>A (p.Pro152His)
c.428C>A (p.Pro143His)
 gnomAD v4
7g.150958371G>ACA071797KCNH2n.1437C>T
c.604C>T (p.Pro202Ser)
c.256C>T (p.Pro86Ser)
n.827C>T
c.304C>T (p.Pro102Ser)
c.454C>T (p.Pro152Ser)
c.427C>T (p.Pro143Ser)
 gnomAD v4
7g.150958371G>CCA369863139KCNH2n.1437C>G
c.604C>G (p.Pro202Ala)
c.256C>G (p.Pro86Ala)
n.827C>G
c.304C>G (p.Pro102Ala)
c.454C>G (p.Pro152Ala)
c.427C>G (p.Pro143Ala)
7g.150958371G=CA1752418530KCNH2n.1437C=
c.604C= (p.Pro202=)
c.256C= (p.Pro86=)
n.827C=
c.304C= (p.Pro102=)
c.454C= (p.Pro152=)
c.427C= (p.Pro143=)
7g.150958371G>TCA369863140KCNH2n.1437C>A
c.604C>A (p.Pro202Thr)
c.256C>A (p.Pro86Thr)
n.827C>A
c.304C>A (p.Pro102Thr)
c.454C>A (p.Pro152Thr)
c.427C>A (p.Pro143Thr)
 dbSNP gnomAD v2 gnomAD v4
7g.150958372C>ACA458646649KCNH2n.1436G>T
c.603G>T (p.Thr201=)
c.255G>T (p.Thr85=)
n.826G>T
c.303G>T (p.Thr101=)
c.453G>T (p.Thr151=)
c.426G>T (p.Thr142=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958372C=CA1752418534KCNH2n.1436G=
c.603G= (p.Thr201=)
c.255G= (p.Thr85=)
n.826G=
c.303G= (p.Thr101=)
c.453G= (p.Thr151=)
c.426G= (p.Thr142=)
7g.150958372C>GCA458646650KCNH2n.1436G>C
c.603G>C (p.Thr201=)
c.255G>C (p.Thr85=)
n.826G>C
c.303G>C (p.Thr101=)
c.453G>C (p.Thr151=)
c.426G>C (p.Thr142=)
 gnomAD v4
7g.150958372C>TCA040086KCNH2n.1436G>A
c.603G>A (p.Thr201=)
c.255G>A (p.Thr85=)
n.826G>A
c.303G>A (p.Thr101=)
c.453G>A (p.Thr151=)
c.426G>A (p.Thr142=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.150958373G>ACA008625KCNH2n.1435C>T
c.602C>T (p.Thr201Met)
c.254C>T (p.Thr85Met)
n.825C>T
c.302C>T (p.Thr101Met)
c.452C>T (p.Thr151Met)
c.425C>T (p.Thr142Met)
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.150958373G>CCA369863146KCNH2n.1435C>G
c.602C>G (p.Thr201Arg)
c.254C>G (p.Thr85Arg)
n.825C>G
c.302C>G (p.Thr101Arg)
c.452C>G (p.Thr151Arg)
c.425C>G (p.Thr142Arg)
 gnomAD v4
7g.150958373G=CA1752418539KCNH2n.1435C=
c.602C= (p.Thr201=)
c.254C= (p.Thr85=)
n.825C=
c.302C= (p.Thr101=)
c.452C= (p.Thr151=)
c.425C= (p.Thr142=)
7g.150958373G>TCA369863143KCNH2n.1435C>A
c.602C>A (p.Thr201Lys)
c.254C>A (p.Thr85Lys)
n.825C>A
c.302C>A (p.Thr101Lys)
c.452C>A (p.Thr151Lys)
c.425C>A (p.Thr142Lys)
 ClinVar gnomAD v4
7g.150958374T>ACA369863148KCNH2n.1434A>T
c.601A>T (p.Thr201Ser)
c.253A>T (p.Thr85Ser)
n.824A>T
c.301A>T (p.Thr101Ser)
c.451A>T (p.Thr151Ser)
c.424A>T (p.Thr142Ser)
7g.150958374T>CCA369863150KCNH2n.1434A>G
c.601A>G (p.Thr201Ala)
c.253A>G (p.Thr85Ala)
n.824A>G
c.301A>G (p.Thr101Ala)
c.451A>G (p.Thr151Ala)
c.424A>G (p.Thr142Ala)
 gnomAD v4
7g.150958374T>GCA369863152KCNH2n.1434A>C
c.601A>C (p.Thr201Pro)
c.253A>C (p.Thr85Pro)
n.824A>C
c.301A>C (p.Thr101Pro)
c.451A>C (p.Thr151Pro)
c.424A>C (p.Thr142Pro)
 gnomAD v4
7g.150958375C>ACA458646657KCNH2n.1433G>T
c.600G>T (p.Leu200=)
c.252G>T (p.Leu84=)
n.823G>T
c.300G>T (p.Leu100=)
c.450G>T (p.Leu150=)
c.423G>T (p.Leu141=)
 gnomAD v4
7g.150958375C>GCA458646659KCNH2n.1433G>C
c.600G>C (p.Leu200=)
c.252G>C (p.Leu84=)
n.823G>C
c.300G>C (p.Leu100=)
c.450G>C (p.Leu150=)
c.423G>C (p.Leu141=)
7g.150958375C>TCA071784KCNH2n.1433G>A
c.600G>A (p.Leu200=)
c.252G>A (p.Leu84=)
n.823G>A
c.300G>A (p.Leu100=)
c.450G>A (p.Leu150=)
c.423G>A (p.Leu141=)
 ClinVar dbSNP gnomAD v4
7g.150958376A=CA1752418542KCNH2n.1432T=
c.599T= (p.Leu200=)
c.251T= (p.Leu84=)
n.822T=
c.299T= (p.Leu100=)
c.449T= (p.Leu150=)
c.422T= (p.Leu141=)
7g.150958376A>CCA369863154KCNH2n.1432T>G
c.599T>G (p.Leu200Arg)
c.251T>G (p.Leu84Arg)
n.822T>G
c.299T>G (p.Leu100Arg)
c.449T>G (p.Leu150Arg)
c.422T>G (p.Leu141Arg)
7g.150958376A>GCA369863156KCNH2n.1432T>C
c.599T>C (p.Leu200Pro)
c.251T>C (p.Leu84Pro)
n.822T>C
c.299T>C (p.Leu100Pro)
c.449T>C (p.Leu150Pro)
c.422T>C (p.Leu141Pro)
 gnomAD v4
7g.150958376A>TCA040069KCNH2n.1432T>A
c.599T>A (p.Leu200Gln)
c.251T>A (p.Leu84Gln)
n.822T>A
c.299T>A (p.Leu100Gln)
c.449T>A (p.Leu150Gln)
c.422T>A (p.Leu141Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150958377G>ACA16605175KCNH2n.1431C>T
c.598C>T (p.Leu200=)
c.250C>T (p.Leu84=)
n.821C>T
c.298C>T (p.Leu100=)
c.448C>T (p.Leu150=)
c.421C>T (p.Leu141=)
 ClinVar dbSNP gnomAD v4
7g.150958377G>CCA369863159KCNH2n.1431C>G
c.598C>G (p.Leu200Val)
c.250C>G (p.Leu84Val)
n.821C>G
c.298C>G (p.Leu100Val)
c.448C>G (p.Leu150Val)
c.421C>G (p.Leu141Val)
 ClinVar dbSNP gnomAD v4
7g.150958377G=CA1752418545KCNH2n.1431C=
c.598C= (p.Leu200=)
c.250C= (p.Leu84=)
n.821C=
c.298C= (p.Leu100=)
c.448C= (p.Leu150=)
c.421C= (p.Leu141=)
7g.150958377G>TCA369863161KCNH2n.1431C>A
c.598C>A (p.Leu200Met)
c.250C>A (p.Leu84Met)
n.821C>A
c.298C>A (p.Leu100Met)
c.448C>A (p.Leu150Met)
c.421C>A (p.Leu141Met)
 gnomAD v4
7g.150958378G>ACA458646664KCNH2n.1430C>T
c.597C>T (p.Asp199=)
c.249C>T (p.Asp83=)
n.820C>T
c.297C>T (p.Asp99=)
c.447C>T (p.Asp149=)
c.420C>T (p.Asp140=)
 gnomAD v4
7g.150958378G>CCA369863163KCNH2n.1430C>G
c.597C>G (p.Asp199Glu)
c.249C>G (p.Asp83Glu)
n.820C>G
c.297C>G (p.Asp99Glu)
c.447C>G (p.Asp149Glu)
c.420C>G (p.Asp140Glu)
 ClinVar
7g.150958378G>TCA369863164KCNH2n.1430C>A
c.597C>A (p.Asp199Glu)
c.249C>A (p.Asp83Glu)
n.820C>A
c.297C>A (p.Asp99Glu)
c.447C>A (p.Asp149Glu)
c.420C>A (p.Asp140Glu)
 gnomAD v4
7g.150958379T>ACA369863167KCNH2n.1429A>T
c.596A>T (p.Asp199Val)
c.248A>T (p.Asp83Val)
n.819A>T
c.296A>T (p.Asp99Val)
c.446A>T (p.Asp149Val)
c.419A>T (p.Asp140Val)
7g.150958379T>CCA369863168KCNH2n.1429A>G
c.596A>G (p.Asp199Gly)
c.248A>G (p.Asp83Gly)
n.819A>G
c.296A>G (p.Asp99Gly)
c.446A>G (p.Asp149Gly)
c.419A>G (p.Asp140Gly)
 gnomAD v4
7g.150958379T>GCA040055KCNH2n.1429A>C
c.596A>C (p.Asp199Ala)
c.248A>C (p.Asp83Ala)
n.819A>C
c.296A>C (p.Asp99Ala)
c.446A>C (p.Asp149Ala)
c.419A>C (p.Asp140Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.150958379T=CA1752418549KCNH2n.1429A=
c.596A= (p.Asp199=)
c.248A= (p.Asp83=)
n.819A=
c.296A= (p.Asp99=)
c.446A= (p.Asp149=)
c.419A= (p.Asp140=)
7g.150958380C>ACA369863173KCNH2n.1428G>T
c.595G>T (p.Asp199Tyr)
c.247G>T (p.Asp83Tyr)
n.818G>T
c.295G>T (p.Asp99Tyr)
c.445G>T (p.Asp149Tyr)
c.418G>T (p.Asp140Tyr)
 gnomAD v4
7g.150958380C>GCA071979KCNH2n.1428G>C
c.595G>C (p.Asp199His)
c.247G>C (p.Asp83His)
n.818G>C
c.295G>C (p.Asp99His)
c.445G>C (p.Asp149His)
c.418G>C (p.Asp140His)
7g.150958380C>TCA071975KCNH2n.1428G>A
c.595G>A (p.Asp199Asn)
c.247G>A (p.Asp83Asn)
n.818G>A
c.295G>A (p.Asp99Asn)
c.445G>A (p.Asp149Asn)
c.418G>A (p.Asp140Asn)
 gnomAD v4
7g.150958381C>ACA458646670KCNH2n.1427G>T
c.594G>T (p.Val198=)
c.246G>T (p.Val82=)
n.817G>T
c.294G>T (p.Val98=)
c.444G>T (p.Val148=)
c.417G>T (p.Val139=)
 gnomAD v4
7g.150958381C>GCA458646673KCNH2n.1427G>C
c.594G>C (p.Val198=)
c.246G>C (p.Val82=)
n.817G>C
c.294G>C (p.Val98=)
c.444G>C (p.Val148=)
c.417G>C (p.Val139=)
7g.150958381C>TCA458646671KCNH2n.1427G>A
c.594G>A (p.Val198=)
c.246G>A (p.Val82=)
n.817G>A
c.294G>A (p.Val98=)
c.444G>A (p.Val148=)
c.417G>A (p.Val139=)
 gnomAD v4
7g.150958382A>CCA369863174KCNH2n.1426T>G
c.593T>G (p.Val198Gly)
c.245T>G (p.Val82Gly)
n.816T>G
c.293T>G (p.Val98Gly)
c.443T>G (p.Val148Gly)
c.416T>G (p.Val139Gly)
7g.150958382A>GCA369863176KCNH2n.1426T>C
c.593T>C (p.Val198Ala)
c.245T>C (p.Val82Ala)
n.816T>C
c.293T>C (p.Val98Ala)
c.443T>C (p.Val148Ala)
c.416T>C (p.Val139Ala)
 gnomAD v4
7g.150958382A>TCA369863178KCNH2n.1426T>A
c.593T>A (p.Val198Glu)
c.245T>A (p.Val82Glu)
n.816T>A
c.293T>A (p.Val98Glu)
c.443T>A (p.Val148Glu)
c.416T>A (p.Val139Glu)
 gnomAD v4
7g.150958383C>ACA369863180KCNH2n.1425G>T
c.592G>T (p.Val198Leu)
c.244G>T (p.Val82Leu)
n.815G>T
c.292G>T (p.Val98Leu)
c.442G>T (p.Val148Leu)
c.415G>T (p.Val139Leu)
 dbSNP gnomAD v4
7g.150958383C=CA1752418553KCNH2n.1425G=
c.592G= (p.Val198=)
c.244G= (p.Val82=)
n.815G=
c.292G= (p.Val98=)
c.442G= (p.Val148=)
c.415G= (p.Val139=)
7g.150958383C>GCA040043KCNH2n.1425G>C
c.592G>C (p.Val198Leu)
c.244G>C (p.Val82Leu)
n.815G>C
c.292G>C (p.Val98Leu)
c.442G>C (p.Val148Leu)
c.415G>C (p.Val139Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.150958383C>TCA369863183KCNH2n.1425G>A
c.592G>A (p.Val198Met)
c.244G>A (p.Val82Met)
n.815G>A
c.292G>A (p.Val98Met)
c.442G>A (p.Val148Met)
c.415G>A (p.Val139Met)
 gnomAD v4
7g.150958384G>ACA458646678KCNH2n.1424C>T
c.591C>T (p.Asp197=)
c.243C>T (p.Asp81=)
n.814C>T
c.291C>T (p.Asp97=)
c.441C>T (p.Asp147=)
c.414C>T (p.Asp138=)
 gnomAD v4 COSMIC COSMIC
7g.150958384G>CCA369863185KCNH2n.1424C>G
c.591C>G (p.Asp197Glu)
c.243C>G (p.Asp81Glu)
n.814C>G
c.291C>G (p.Asp97Glu)
c.441C>G (p.Asp147Glu)
c.414C>G (p.Asp138Glu)
 gnomAD v4
7g.150958384G>TCA369863187KCNH2n.1424C>A
c.591C>A (p.Asp197Glu)
c.243C>A (p.Asp81Glu)
n.814C>A
c.291C>A (p.Asp97Glu)
c.441C>A (p.Asp147Glu)
c.414C>A (p.Asp138Glu)
 gnomAD v4
7g.150958385T>ACA369863189KCNH2n.1423A>T
c.590A>T (p.Asp197Val)
c.242A>T (p.Asp81Val)
n.813A>T
c.290A>T (p.Asp97Val)
c.440A>T (p.Asp147Val)
c.413A>T (p.Asp138Val)
 gnomAD v4
7g.150958385T>CCA369863190KCNH2n.1423A>G
c.590A>G (p.Asp197Gly)
c.242A>G (p.Asp81Gly)
n.813A>G
c.290A>G (p.Asp97Gly)
c.440A>G (p.Asp147Gly)
c.413A>G (p.Asp138Gly)
 gnomAD v4
7g.150958385T>GCA369863191KCNH2n.1423A>C
c.590A>C (p.Asp197Ala)
c.242A>C (p.Asp81Ala)
n.813A>C
c.290A>C (p.Asp97Ala)
c.440A>C (p.Asp147Ala)
c.413A>C (p.Asp138Ala)
7g.150958386C>ACA369863194KCNH2n.1422G>T
c.589G>T (p.Asp197Tyr)
c.241G>T (p.Asp81Tyr)
n.812G>T
c.289G>T (p.Asp97Tyr)
c.439G>T (p.Asp147Tyr)
c.412G>T (p.Asp138Tyr)
 gnomAD v4
7g.150958386C=CA1752418557KCNH2n.1422G=
c.589G= (p.Asp197=)
c.241G= (p.Asp81=)
n.812G=
c.289G= (p.Asp97=)
c.439G= (p.Asp147=)
c.412G= (p.Asp138=)
7g.150958386C>GCA369863196KCNH2n.1422G>C
c.589G>C (p.Asp197His)
c.241G>C (p.Asp81His)
n.812G>C
c.289G>C (p.Asp97His)
c.439G>C (p.Asp147His)
c.412G>C (p.Asp138His)
7g.150958386C>TCA369863197KCNH2n.1422G>A
c.589G>A (p.Asp197Asn)
c.241G>A (p.Asp81Asn)
n.812G>A
c.289G>A (p.Asp97Asn)
c.439G>A (p.Asp147Asn)
c.412G>A (p.Asp138Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.150958386_150958387delCA2685608539KCNH2n.1421_1422del
c.588_589del (p.Asp197ArgfsTer?)
c.240_241del (p.Asp81ArgfsTer?)
n.811_812del
c.288_289del (p.Asp97ArgfsTer?)
c.438_439del (p.Asp147ArgfsTer?)
c.411_412del (p.Asp138ArgfsTer?)
 gnomAD v4
7g.150958387C>ACA458646685KCNH2n.1421G>T
c.588G>T (p.Val196=)
c.240G>T (p.Val80=)
n.811G>T
c.288G>T (p.Val96=)
c.438G>T (p.Val146=)
c.411G>T (p.Val137=)
 gnomAD v4
7g.150958387C>GCA458646687KCNH2n.1421G>C
c.588G>C (p.Val196=)
c.240G>C (p.Val80=)
n.811G>C
c.288G>C (p.Val96=)
c.438G>C (p.Val146=)
c.411G>C (p.Val137=)
7g.150958387C>TCA458646689KCNH2n.1421G>A
c.588G>A (p.Val196=)
c.240G>A (p.Val80=)
n.811G>A
c.288G>A (p.Val96=)
c.438G>A (p.Val146=)
c.411G>A (p.Val137=)
 gnomAD v4
7g.150958388A=CA1752418560KCNH2n.1420T=
c.587T= (p.Val196=)
c.239T= (p.Val80=)
n.810T=
c.287T= (p.Val96=)
c.437T= (p.Val146=)
c.410T= (p.Val137=)
7g.150958388A>CCA369863200KCNH2n.1420T>G
c.587T>G (p.Val196Gly)
c.239T>G (p.Val80Gly)
n.810T>G
c.287T>G (p.Val96Gly)
c.437T>G (p.Val146Gly)
c.410T>G (p.Val137Gly)
7g.150958388A>GCA369863202KCNH2n.1420T>C
c.587T>C (p.Val196Ala)
c.239T>C (p.Val80Ala)
n.810T>C
c.287T>C (p.Val96Ala)
c.437T>C (p.Val146Ala)
c.410T>C (p.Val137Ala)
7g.150958388A>TCA369863199KCNH2n.1420T>A
c.587T>A (p.Val196Glu)
c.239T>A (p.Val80Glu)
n.810T>A
c.287T>A (p.Val96Glu)
c.437T>A (p.Val146Glu)
c.410T>A (p.Val137Glu)
 dbSNP gnomAD v2
7g.150958389C>ACA369863204KCNH2n.1419G>T
c.586G>T (p.Val196Leu)
c.238G>T (p.Val80Leu)
n.809G>T
c.286G>T (p.Val96Leu)
c.436G>T (p.Val146Leu)
c.409G>T (p.Val137Leu)
 gnomAD v4
7g.150958389C>GCA369863205KCNH2n.1419G>C
c.586G>C (p.Val196Leu)
c.238G>C (p.Val80Leu)
n.809G>C
c.286G>C (p.Val96Leu)
c.436G>C (p.Val146Leu)
c.409G>C (p.Val137Leu)
7g.150958389C>TCA369863207KCNH2n.1419G>A
c.586G>A (p.Val196Met)
c.238G>A (p.Val80Met)
n.809G>A
c.286G>A (p.Val96Met)
c.436G>A (p.Val146Met)
c.409G>A (p.Val137Met)
 gnomAD v4
7g.150958390C>ACA458646694KCNH2n.1418G>T
c.585G>T (p.Val195=)
c.237G>T (p.Val79=)
n.808G>T
c.285G>T (p.Val95=)
c.435G>T (p.Val145=)
c.408G>T (p.Val136=)
 gnomAD v4
7g.150958390C>GCA458646696KCNH2n.1418G>C
c.585G>C (p.Val195=)
c.237G>C (p.Val79=)
n.808G>C
c.285G>C (p.Val95=)
c.435G>C (p.Val145=)
c.408G>C (p.Val136=)
 gnomAD v4
7g.150958390C>TCA458646697KCNH2n.1418G>A
c.585G>A (p.Val195=)
c.237G>A (p.Val79=)
n.808G>A
c.285G>A (p.Val95=)
c.435G>A (p.Val145=)
c.408G>A (p.Val136=)
 ClinVar dbSNP gnomAD v4

Number of alleles fetched