Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73323159_73323250delCA619410578HCN4c.2852_2943del (p.Gly951ValfsTer21)
c.1634_1725del (p.Gly545ValfsTer21)
 gnomAD v2
15g.73323203_73323209delinsAGGGTGGCA2187187699HCN4c.2884_2890delinsCCACCCT (p.Pro962=)
c.1666_1672delinsCCACCCT (p.Pro556=)
15g.73323206delCA2629370552HCN4c.2889del (p.Ser964HisfsTer21)
c.1671del (p.Ser558HisfsTer21)
 gnomAD v4
15g.73323210_73323215dupCA2575783831HCN4c.2884_2889dup (p.Pro963_Ser964insProPro)
c.1666_1671dup (p.Pro557_Ser558insProPro)
15g.73323210_73323215delCA7648935HCN4c.2884_2889del (p.Pro962_Pro963del)
c.1666_1671del (p.Pro556_Pro557del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323206G>ACA393087086HCN4c.2887C>T (p.Pro963Ser)
c.1669C>T (p.Pro557Ser)
 dbSNP gnomAD v4
15g.73323206G>CCA393087088HCN4c.2887C>G (p.Pro963Ala)
c.1669C>G (p.Pro557Ala)
15g.73323206G=CA2187187709HCN4c.2887C= (p.Pro963=)
c.1669C= (p.Pro557=)
15g.73323206G>TCA393087091HCN4c.2887C>A (p.Pro963Thr)
c.1669C>A (p.Pro557Thr)
 gnomAD v4
15g.73323207T>ACA491478823HCN4c.2886A>T (p.Pro962=)
c.1668A>T (p.Pro556=)
 gnomAD v4
15g.73323207T>CCA491478825HCN4c.2886A>G (p.Pro962=)
c.1668A>G (p.Pro556=)
15g.73323207T>GCA491478826HCN4c.2886A>C (p.Pro962=)
c.1668A>C (p.Pro556=)
 ClinVar dbSNP gnomAD v4
15g.73323208G>ACA393087094HCN4c.2885C>T (p.Pro962Leu)
c.1667C>T (p.Pro556Leu)
 ClinVar
15g.73323208G>CCA393087097HCN4c.2885C>G (p.Pro962Arg)
c.1667C>G (p.Pro556Arg)
15g.73323208G>TCA393087099HCN4c.2885C>A (p.Pro962Gln)
c.1667C>A (p.Pro556Gln)
 gnomAD v4
15g.73323212dupCA2629370554HCN4c.2885dup (p.Pro963ThrfsTer9)
c.1667dup (p.Pro557ThrfsTer9)
 gnomAD v4
15g.73323212delCA2629370553HCN4c.2885del (p.Pro962HisfsTer23)
c.1667del (p.Pro556HisfsTer23)
 gnomAD v4
15g.73323209G>ACA393087101HCN4c.2884C>T (p.Pro962Ser)
c.1666C>T (p.Pro556Ser)
 dbSNP gnomAD v2 gnomAD v4
15g.73323209G>CCA393087105HCN4c.2884C>G (p.Pro962Ala)
c.1666C>G (p.Pro556Ala)
15g.73323209G=CA2187187712HCN4c.2884C= (p.Pro962=)
c.1666C= (p.Pro556=)
15g.73323209G>TCA393087110HCN4c.2884C>A (p.Pro962Thr)
c.1666C>A (p.Pro556Thr)
 gnomAD v4
15g.73323210G>ACA491478831HCN4c.2883C>T (p.Pro961=)
c.1665C>T (p.Pro555=)
 dbSNP gnomAD v2 gnomAD v4
15g.73323210G>CCA491478832HCN4c.2883C>G (p.Pro961=)
c.1665C>G (p.Pro555=)
 gnomAD v4
15g.73323210G=CA2187187716HCN4c.2883C= (p.Pro961=)
c.1665C= (p.Pro555=)
15g.73323210G>TCA491478833HCN4c.2883C>A (p.Pro961=)
c.1665C>A (p.Pro555=)
 gnomAD v4
15g.73323211G>ACA393087117HCN4c.2882C>T (p.Pro961Leu)
c.1664C>T (p.Pro555Leu)
 gnomAD v4
15g.73323211G>CCA393087115HCN4c.2882C>G (p.Pro961Arg)
c.1664C>G (p.Pro555Arg)
15g.73323211G>TCA393087112HCN4c.2882C>A (p.Pro961His)
c.1664C>A (p.Pro555His)
 gnomAD v4
15g.73323212G>ACA393087120HCN4c.2881C>T (p.Pro961Ser)
c.1663C>T (p.Pro555Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323212G>CCA393087122HCN4c.2881C>G (p.Pro961Ala)
c.1663C>G (p.Pro555Ala)
15g.73323212G=CA2187187720HCN4c.2881C= (p.Pro961=)
c.1663C= (p.Pro555=)
15g.73323212G>TCA393087124HCN4c.2881C>A (p.Pro961Thr)
c.1663C>A (p.Pro555Thr)
 gnomAD v4
15g.73323213T>ACA491478834HCN4c.2880A>T (p.Pro960=)
c.1662A>T (p.Pro554=)
15g.73323213T>CCA491478835HCN4c.2880A>G (p.Pro960=)
c.1662A>G (p.Pro554=)
 ClinVar
15g.73323213T>GCA491478836HCN4c.2880A>C (p.Pro960=)
c.1662A>C (p.Pro554=)
 ClinVar dbSNP
15g.73323214G>ACA393087128HCN4c.2879C>T (p.Pro960Leu)
c.1661C>T (p.Pro554Leu)
 gnomAD v4
15g.73323214G>CCA393087130HCN4c.2879C>G (p.Pro960Arg)
c.1661C>G (p.Pro554Arg)
15g.73323214G=CA2187187724HCN4c.2879C= (p.Pro960=)
c.1661C= (p.Pro554=)
15g.73323214G>TCA393087133HCN4c.2879C>A (p.Pro960Gln)
c.1661C>A (p.Pro554Gln)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323215G>ACA393087137HCN4c.2878C>T (p.Pro960Ser)
c.1660C>T (p.Pro554Ser)
 dbSNP gnomAD v3 gnomAD v4
15g.73323215G>CCA393087140HCN4c.2878C>G (p.Pro960Ala)
c.1660C>G (p.Pro554Ala)
15g.73323215G=CA2187187727HCN4c.2878C= (p.Pro960=)
c.1660C= (p.Pro554=)
15g.73323215G>TCA393087142HCN4c.2878C>A (p.Pro960Thr)
c.1660C>A (p.Pro554Thr)
 gnomAD v4
15g.73323216C>ACA491478841HCN4c.2877G>T (p.Leu959=)
c.1659G>T (p.Leu553=)
 gnomAD v4
15g.73323216C>GCA491478842HCN4c.2877G>C (p.Leu959=)
c.1659G>C (p.Leu553=)
15g.73323216C>TCA491478843HCN4c.2877G>A (p.Leu959=)
c.1659G>A (p.Leu553=)
 gnomAD v4
15g.73323217A=CA2187187729HCN4c.2876T= (p.Leu959=)
c.1658T= (p.Leu553=)
15g.73323217A>CCA393087145HCN4c.2876T>G (p.Leu959Arg)
c.1658T>G (p.Leu553Arg)
15g.73323217A>GCA393087148HCN4c.2876T>C (p.Leu959Pro)
c.1658T>C (p.Leu553Pro)
15g.73323217A>TCA393087150HCN4c.2876T>A (p.Leu959Gln)
c.1658T>A (p.Leu553Gln)
 ClinVar dbSNP gnomAD v4
15g.73323218G>ACA491478844HCN4c.2875C>T (p.Leu959=)
c.1657C>T (p.Leu553=)
 gnomAD v4
15g.73323218G>CCA16607867HCN4c.2875C>G (p.Leu959Val)
c.1657C>G (p.Leu553Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323218G=CA2187187733HCN4c.2875C= (p.Leu959=)
c.1657C= (p.Leu553=)
15g.73323218G>TCA393087154HCN4c.2875C>A (p.Leu959Met)
c.1657C>A (p.Leu553Met)
 gnomAD v4
15g.73323219G>ACA491478846HCN4c.2874C>T (p.Phe958=)
c.1656C>T (p.Phe552=)
 dbSNP gnomAD v2
15g.73323219G>CCA393087160HCN4c.2874C>G (p.Phe958Leu)
c.1656C>G (p.Phe552Leu)
15g.73323219G=CA2187187736HCN4c.2874C= (p.Phe958=)
c.1656C= (p.Phe552=)
15g.73323219G>TCA393087163HCN4c.2874C>A (p.Phe958Leu)
c.1656C>A (p.Phe552Leu)
 gnomAD v4
15g.73323220A=CA2187187739HCN4c.2873T= (p.Phe958=)
c.1655T= (p.Phe552=)
15g.73323220A>CCA393087165HCN4c.2873T>G (p.Phe958Cys)
c.1655T>G (p.Phe552Cys)
15g.73323220A>GCA393087168HCN4c.2873T>C (p.Phe958Ser)
c.1655T>C (p.Phe552Ser)
 dbSNP
15g.73323220A>TCA393087171HCN4c.2873T>A (p.Phe958Tyr)
c.1655T>A (p.Phe552Tyr)
15g.73323221A=CA2187187742HCN4c.2872T= (p.Phe958=)
c.1654T= (p.Phe552=)
15g.73323221A>CCA393087175HCN4c.2872T>G (p.Phe958Val)
c.1654T>G (p.Phe552Val)
15g.73323221A>GCA393087176HCN4c.2872T>C (p.Phe958Leu)
c.1654T>C (p.Phe552Leu)
 gnomAD v4
15g.73323221A>TCA393087179HCN4c.2872T>A (p.Phe958Ile)
c.1654T>A (p.Phe552Ile)
 ClinVar dbSNP
15g.73323222G>ACA491478857HCN4c.2871C>T (p.His957=)
c.1653C>T (p.His551=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323222G>CCA393087184HCN4c.2871C>G (p.His957Gln)
c.1653C>G (p.His551Gln)
15g.73323222G=CA2187187744HCN4c.2871C= (p.His957=)
c.1653C= (p.His551=)
15g.73323222G>TCA393087185HCN4c.2871C>A (p.His957Gln)
c.1653C>A (p.His551Gln)
 gnomAD v4
15g.73323223T>ACA393087187HCN4c.2870A>T (p.His957Leu)
c.1652A>T (p.His551Leu)
15g.73323223T>CCA393087190HCN4c.2870A>G (p.His957Arg)
c.1652A>G (p.His551Arg)
15g.73323223T>GCA393087197HCN4c.2870A>C (p.His957Pro)
c.1652A>C (p.His551Pro)
 dbSNP
15g.73323223T=CA2187187747HCN4c.2870A= (p.His957=)
c.1652A= (p.His551=)
15g.73323224G>ACA393087206HCN4c.2869C>T (p.His957Tyr)
c.1651C>T (p.His551Tyr)
 gnomAD v4
15g.73323224G>CCA393087203HCN4c.2869C>G (p.His957Asp)
c.1651C>G (p.His551Asp)
15g.73323224G>TCA393087200HCN4c.2869C>A (p.His957Asn)
c.1651C>A (p.His551Asn)
 gnomAD v4
15g.73323225C>ACA393087212HCN4c.2868G>T (p.Glu956Asp)
c.1650G>T (p.Glu550Asp)
 gnomAD v4
15g.73323225C=CA2187187750HCN4c.2868G= (p.Glu956=)
c.1650G= (p.Glu550=)
15g.73323225C>GCA393087209HCN4c.2868G>C (p.Glu956Asp)
c.1650G>C (p.Glu550Asp)
 dbSNP gnomAD v2
15g.73323225C>TCA491478864HCN4c.2868G>A (p.Glu956=)
c.1650G>A (p.Glu550=)
 gnomAD v4
15g.73323226T>ACA393087215HCN4c.2867A>T (p.Glu956Val)
c.1649A>T (p.Glu550Val)
 gnomAD v4
15g.73323226T>CCA393087217HCN4c.2867A>G (p.Glu956Gly)
c.1649A>G (p.Glu550Gly)
 gnomAD v4
15g.73323226T>GCA393087220HCN4c.2867A>C (p.Glu956Ala)
c.1649A>C (p.Glu550Ala)
15g.73323226_73323243delinsCCCA2573151086HCN4c.2850_2867delinsGG (p.Leu952ThrfsTer28)
c.1632_1649delinsGG (p.Leu546ThrfsTer28)
 ClinVar dbSNP
15g.73323227C>ACA393087224HCN4c.2866G>T (p.Glu956Ter)
c.1648G>T (p.Glu550Ter)
 gnomAD v4
15g.73323227C=CA2187187753HCN4c.2866G= (p.Glu956=)
c.1648G= (p.Glu550=)
15g.73323227C>GCA393087226HCN4c.2866G>C (p.Glu956Gln)
c.1648G>C (p.Glu550Gln)
 gnomAD v4
15g.73323227C>TCA393087229HCN4c.2866G>A (p.Glu956Lys)
c.1648G>A (p.Glu550Lys)
 dbSNP gnomAD v3 gnomAD v4 COSMIC
15g.73323228C>ACA491478873HCN4c.2865G>T (p.Pro955=)
c.1647G>T (p.Pro549=)
 gnomAD v4
15g.73323228C=CA2187187759HCN4c.2865G= (p.Pro955=)
c.1647G= (p.Pro549=)
15g.73323228C>GCA491478874HCN4c.2865G>C (p.Pro955=)
c.1647G>C (p.Pro549=)
15g.73323228C>TCA491478875HCN4c.2865G>A (p.Pro955=)
c.1647G>A (p.Pro549=)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
15g.73323229G>ACA7648936HCN4c.2864C>T (p.Pro955Leu)
c.1646C>T (p.Pro549Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323229G>CCA393087235HCN4c.2864C>G (p.Pro955Arg)
c.1646C>G (p.Pro549Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323229G=CA2187187774HCN4c.2864C= (p.Pro955=)
c.1646C= (p.Pro549=)
15g.73323229G>TCA7648937HCN4c.2864C>A (p.Pro955Gln)
c.1646C>A (p.Pro549Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323231delCA2629370555HCN4c.2864del (p.Pro955ArgfsTer30)
c.1646del (p.Pro549ArgfsTer30)
 gnomAD v4
15g.73323230G>ACA7648938HCN4c.2863C>T (p.Pro955Ser)
c.1645C>T (p.Pro549Ser)
 ClinVar dbSNP ExAC gnomAD v4
15g.73323230G>CCA393087242HCN4c.2863C>G (p.Pro955Ala)
c.1645C>G (p.Pro549Ala)
15g.73323230G=CA2187187776HCN4c.2863C= (p.Pro955=)
c.1645C= (p.Pro549=)
15g.73323230G>TCA393087245HCN4c.2863C>A (p.Pro955Thr)
c.1645C>A (p.Pro549Thr)
 gnomAD v4
15g.73323231G>ACA491478880HCN4c.2862C>T (p.Leu954=)
c.1644C>T (p.Leu548=)
 gnomAD v4 COSMIC
15g.73323231G>CCA491478882HCN4c.2862C>G (p.Leu954=)
c.1644C>G (p.Leu548=)
15g.73323231G>TCA491478884HCN4c.2862C>A (p.Leu954=)
c.1644C>A (p.Leu548=)
 gnomAD v4
15g.73323232delCA2629370556HCN4c.2861del (p.Leu954ProfsTer?)
c.1643del (p.Leu548ProfsTer?)
 gnomAD v4
15g.73323232A>CCA393087253HCN4c.2861T>G (p.Leu954Arg)
c.1643T>G (p.Leu548Arg)
15g.73323232A>GCA393087251HCN4c.2861T>C (p.Leu954Pro)
c.1643T>C (p.Leu548Pro)
15g.73323232A>TCA393087248HCN4c.2861T>A (p.Leu954His)
c.1643T>A (p.Leu548His)
15g.73323233G>ACA393087256HCN4c.2860C>T (p.Leu954Phe)
c.1642C>T (p.Leu548Phe)
 dbSNP gnomAD v2 gnomAD v4
15g.73323233G>CCA393087259HCN4c.2860C>G (p.Leu954Val)
c.1642C>G (p.Leu548Val)
 COSMIC
15g.73323233G=CA2187187778HCN4c.2860C= (p.Leu954=)
c.1642C= (p.Leu548=)
15g.73323233G>TCA393087262HCN4c.2860C>A (p.Leu954Ile)
c.1642C>A (p.Leu548Ile)
 gnomAD v4
15g.73323234T>ACA491478891HCN4c.2859A>T (p.Gly953=)
c.1641A>T (p.Gly547=)
15g.73323234T>CCA491478892HCN4c.2859A>G (p.Gly953=)
c.1641A>G (p.Gly547=)
15g.73323234T>GCA491478890HCN4c.2859A>C (p.Gly953=)
c.1641A>C (p.Gly547=)
15g.73323235C>ACA393087265HCN4c.2858G>T (p.Gly953Val)
c.1640G>T (p.Gly547Val)
 gnomAD v4
15g.73323235C=CA2187187782HCN4c.2858G= (p.Gly953=)
c.1640G= (p.Gly547=)
15g.73323235C>GCA393087268HCN4c.2858G>C (p.Gly953Ala)
c.1640G>C (p.Gly547Ala)
15g.73323235C>TCA393087270HCN4c.2858G>A (p.Gly953Glu)
c.1640G>A (p.Gly547Glu)
 ClinVar dbSNP gnomAD v4
15g.73323237delCA2629370557HCN4c.2858del (p.Gly953AspfsTer?)
c.1640del (p.Gly547AspfsTer?)
 ClinVar gnomAD v4
15g.73323236_73323237delCA2629370558HCN4c.2857_2858del (p.Gly953ThrfsTer18)
c.1639_1640del (p.Gly547ThrfsTer18)
 gnomAD v4
15g.73323236C>ACA393087275HCN4c.2857G>T (p.Gly953Ter)
c.1639G>T (p.Gly547Ter)
 gnomAD v4
15g.73323236C>GCA393087277HCN4c.2857G>C (p.Gly953Arg)
c.1639G>C (p.Gly547Arg)
15g.73323236C>TCA393087280HCN4c.2857G>A (p.Gly953Arg)
c.1639G>A (p.Gly547Arg)
 gnomAD v4
15g.73323237C>ACA491478901HCN4c.2856G>T (p.Leu952=)
c.1638G>T (p.Leu546=)
 gnomAD v4
15g.73323237C>GCA491478904HCN4c.2856G>C (p.Leu952=)
c.1638G>C (p.Leu546=)
15g.73323237C>TCA491478907HCN4c.2856G>A (p.Leu952=)
c.1638G>A (p.Leu546=)
 ClinVar dbSNP gnomAD v4
15g.73323238A>CCA393087283HCN4c.2855T>G (p.Leu952Arg)
c.1637T>G (p.Leu546Arg)
15g.73323238A>GCA393087285HCN4c.2855T>C (p.Leu952Pro)
c.1637T>C (p.Leu546Pro)
 gnomAD v4
15g.73323238A>TCA393087287HCN4c.2855T>A (p.Leu952Gln)
c.1637T>A (p.Leu546Gln)
 gnomAD v4
15g.73323239G>ACA491478908HCN4c.2854C>T (p.Leu952=)
c.1636C>T (p.Leu546=)
15g.73323239G>CCA393087289HCN4c.2854C>G (p.Leu952Val)
c.1636C>G (p.Leu546Val)
15g.73323239G>TCA393087291HCN4c.2854C>A (p.Leu952Met)
c.1636C>A (p.Leu546Met)
 gnomAD v4
15g.73323240G>ACA491478913HCN4c.2853C>T (p.Gly951=)
c.1635C>T (p.Gly545=)
 gnomAD v4
15g.73323240G>CCA491478912HCN4c.2853C>G (p.Gly951=)
c.1635C>G (p.Gly545=)
15g.73323240G>TCA491478911HCN4c.2853C>A (p.Gly951=)
c.1635C>A (p.Gly545=)
 gnomAD v4
15g.73323241C>ACA393087297HCN4c.2852G>T (p.Gly951Val)
c.1634G>T (p.Gly545Val)
 gnomAD v4
15g.73323241C=CA2187187784HCN4c.2852G= (p.Gly951=)
c.1634G= (p.Gly545=)
15g.73323241C>GCA393087300HCN4c.2852G>C (p.Gly951Ala)
c.1634G>C (p.Gly545Ala)
15g.73323241C>TCA393087295HCN4c.2852G>A (p.Gly951Asp)
c.1634G>A (p.Gly545Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323242C>ACA393087304HCN4c.2851G>T (p.Gly951Cys)
c.1633G>T (p.Gly545Cys)
 gnomAD v4 COSMIC
15g.73323242C=CA2187187787HCN4c.2851G= (p.Gly951=)
c.1633G= (p.Gly545=)
15g.73323242C>GCA393087305HCN4c.2851G>C (p.Gly951Arg)
c.1633G>C (p.Gly545Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323242C>TCA393087307HCN4c.2851G>A (p.Gly951Ser)
c.1633G>A (p.Gly545Ser)
 gnomAD v4
15g.73323243T>ACA491478917HCN4c.2850A>T (p.Gly950=)
c.1632A>T (p.Gly544=)
15g.73323243T>CCA491478918HCN4c.2850A>G (p.Gly950=)
c.1632A>G (p.Gly544=)
 ClinVar dbSNP gnomAD v4
15g.73323243T>GCA491478919HCN4c.2850A>C (p.Gly950=)
c.1632A>C (p.Gly544=)
15g.73323243_73323244delinsTCCA2187187790HCN4c.2849_2850delinsGA (p.Gly950=)
c.1631_1632delinsGA (p.Gly544=)
15g.73323244C>ACA393087310HCN4c.2849G>T (p.Gly950Val)
c.1631G>T (p.Gly544Val)
 gnomAD v4
15g.73323244C>GCA393087313HCN4c.2849G>C (p.Gly950Ala)
c.1631G>C (p.Gly544Ala)
15g.73323244C>TCA393087314HCN4c.2849G>A (p.Gly950Glu)
c.1631G>A (p.Gly544Glu)
 COSMIC
15g.73323247dupCA2575783832HCN4c.2849dup (p.Gly951ArgfsTer21)
c.1631dup (p.Gly545ArgfsTer21)
 gnomAD v4
15g.73323247delCA619410579HCN4c.2849del (p.Gly950GlufsTer?)
c.1631del (p.Gly544GlufsTer?)
 dbSNP gnomAD v2 gnomAD v4
15g.73323246_73323247delCA2629370559HCN4c.2848_2849del (p.Gly950ArgfsTer21)
c.1630_1631del (p.Gly544ArgfsTer21)
 gnomAD v4
15g.73323245C>ACA393087317HCN4c.2848G>T (p.Gly950Ter)
c.1630G>T (p.Gly544Ter)
 gnomAD v4
15g.73323245C=CA2187187796HCN4c.2848G= (p.Gly950=)
c.1630G= (p.Gly544=)
15g.73323245C>GCA393087318HCN4c.2848G>C (p.Gly950Arg)
c.1630G>C (p.Gly544Arg)
15g.73323245C>TCA393087321HCN4c.2848G>A (p.Gly950Arg)
c.1630G>A (p.Gly544Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323246C>ACA491478923HCN4c.2847G>T (p.Arg949=)
c.1629G>T (p.Arg543=)
 gnomAD v4
15g.73323246C>GCA491478924HCN4c.2847G>C (p.Arg949=)
c.1629G>C (p.Arg543=)
15g.73323246C>TCA491478925HCN4c.2847G>A (p.Arg949=)
c.1629G>A (p.Arg543=)
 gnomAD v4
15g.73323247C>ACA393087323HCN4c.2846G>T (p.Arg949Leu)
c.1628G>T (p.Arg543Leu)
 gnomAD v4
15g.73323247C=CA2187187802HCN4c.2846G= (p.Arg949=)
c.1628G= (p.Arg543=)
15g.73323247C>GCA272664120HCN4c.2846G>C (p.Arg949Pro)
c.1628G>C (p.Arg543Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323247C>TCA7648939HCN4c.2846G>A (p.Arg949Gln)
c.1628G>A (p.Arg543Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323248G>ACA7648940HCN4c.2845C>T (p.Arg949Trp)
c.1627C>T (p.Arg543Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323248G>CCA393087328HCN4c.2845C>G (p.Arg949Gly)
c.1627C>G (p.Arg543Gly)
15g.73323248G=CA2187187813HCN4c.2845C= (p.Arg949=)
c.1627C= (p.Arg543=)
15g.73323248G>TCA491478928HCN4c.2845C>A (p.Arg949=)
c.1627C>A (p.Arg543=)
 gnomAD v4
15g.73323250dupCA2629370560HCN4c.2845dup (p.Arg949ProfsTer23)
c.1627dup (p.Arg543ProfsTer23)
 gnomAD v4
15g.73323250delCA2629370561HCN4c.2845del (p.Arg949GlyfsTer?)
c.1627del (p.Arg543GlyfsTer?)
 gnomAD v4
15g.73323249G>ACA491478929HCN4c.2844C>T (p.Ala948=)
c.1626C>T (p.Ala542=)
 gnomAD v4
15g.73323249G>CCA491478931HCN4c.2844C>G (p.Ala948=)
c.1626C>G (p.Ala542=)
15g.73323249G>TCA491478933HCN4c.2844C>A (p.Ala948=)
c.1626C>A (p.Ala542=)
 gnomAD v4
15g.73323250G>ACA393087331HCN4c.2843C>T (p.Ala948Val)
c.1625C>T (p.Ala542Val)
 dbSNP gnomAD v4
15g.73323250G>CCA393087333HCN4c.2843C>G (p.Ala948Gly)
c.1625C>G (p.Ala542Gly)
15g.73323250G=CA2187187819HCN4c.2843C= (p.Ala948=)
c.1625C= (p.Ala542=)
15g.73323250G>TCA393087334HCN4c.2843C>A (p.Ala948Asp)
c.1625C>A (p.Ala542Asp)
 gnomAD v4
15g.73323250_73323251delinsGCCA2187187818HCN4c.2842_2843delinsGC (p.Ala948=)
c.1624_1625delinsGC (p.Ala542=)
15g.73323251C>ACA393087335HCN4c.2842G>T (p.Ala948Ser)
c.1624G>T (p.Ala542Ser)
 dbSNP gnomAD v4
15g.73323251C=CA2187187826HCN4c.2842G= (p.Ala948=)
c.1624G= (p.Ala542=)
15g.73323251C>GCA393087337HCN4c.2842G>C (p.Ala948Pro)
c.1624G>C (p.Ala542Pro)
15g.73323251C>TCA7648941HCN4c.2842G>A (p.Ala948Thr)
c.1624G>A (p.Ala542Thr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323254delCA619410580HCN4c.2842del (p.Ala948ProfsTer?)
c.1624del (p.Ala542ProfsTer?)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323252C>ACA491478940HCN4c.2841G>T (p.Gly947=)
c.1623G>T (p.Gly541=)
 gnomAD v4
15g.73323252C>GCA491478941HCN4c.2841G>C (p.Gly947=)
c.1623G>C (p.Gly541=)
15g.73323252C>TCA491478942HCN4c.2841G>A (p.Gly947=)
c.1623G>A (p.Gly541=)
 gnomAD v4
15g.73323252_73323258delCA2629370562HCN4c.2835_2841del (p.Ala948GlufsTer?)
c.1617_1623del (p.Ala542GlufsTer?)
 gnomAD v4
15g.73323253C>ACA393087341HCN4c.2840G>T (p.Gly947Val)
c.1622G>T (p.Gly541Val)
15g.73323253C=CA2187187833HCN4c.2840G= (p.Gly947=)
c.1622G= (p.Gly541=)
15g.73323253C>GCA393087342HCN4c.2840G>C (p.Gly947Ala)
c.1622G>C (p.Gly541Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323253C>TCA393087344HCN4c.2840G>A (p.Gly947Glu)
c.1622G>A (p.Gly541Glu)
 gnomAD v4
15g.73323254C>ACA393087347HCN4c.2839G>T (p.Gly947Trp)
c.1621G>T (p.Gly541Trp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323254C=CA2187187838HCN4c.2839G= (p.Gly947=)
c.1621G= (p.Gly541=)
15g.73323254C>GCA393087349HCN4c.2839G>C (p.Gly947Arg)
c.1621G>C (p.Gly541Arg)
 gnomAD v4
15g.73323254C>TCA7648942HCN4c.2839G>A (p.Gly947Arg)
c.1621G>A (p.Gly541Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323254_73323255insCGGCAGCCA2509381855HCN4c.2839_2840insCTGCCGG (p.Gly947AlafsTer27)
c.1621_1622insCTGCCGG (p.Gly541AlafsTer27)
15g.73323255G>ACA7648943HCN4c.2838C>T (p.Pro946=)
c.1620C>T (p.Pro540=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323255G>CCA491478950HCN4c.2838C>G (p.Pro946=)
c.1620C>G (p.Pro540=)
15g.73323255G=CA2187187843HCN4c.2838C= (p.Pro946=)
c.1620C= (p.Pro540=)
15g.73323255G>TCA491478949HCN4c.2838C>A (p.Pro946=)
c.1620C>A (p.Pro540=)
 gnomAD v4
15g.73323257delCA971394656HCN4c.2838del (p.Ala948ProfsTer?)
c.1620del (p.Ala542ProfsTer?)
 gnomAD v3 gnomAD v4
15g.73323256G>ACA393087356HCN4c.2837C>T (p.Pro946Leu)
c.1619C>T (p.Pro540Leu)
 gnomAD v4
15g.73323256G>CCA393087357HCN4c.2837C>G (p.Pro946Arg)
c.1619C>G (p.Pro540Arg)
15g.73323256G>TCA393087354HCN4c.2837C>A (p.Pro946His)
c.1619C>A (p.Pro540His)
 gnomAD v4
15g.73323257G>ACA393087360HCN4c.2836C>T (p.Pro946Ser)
c.1618C>T (p.Pro540Ser)
 gnomAD v4
15g.73323257G>CCA393087362HCN4c.2836C>G (p.Pro946Ala)
c.1618C>G (p.Pro540Ala)
15g.73323257G>TCA393087361HCN4c.2836C>A (p.Pro946Thr)
c.1618C>A (p.Pro540Thr)
 gnomAD v4
15g.73323258T>ACA491478960HCN4c.2835A>T (p.Pro945=)
c.1617A>T (p.Pro539=)
15g.73323258T>CCA491478958HCN4c.2835A>G (p.Pro945=)
c.1617A>G (p.Pro539=)
15g.73323258T>GCA491478956HCN4c.2835A>C (p.Pro945=)
c.1617A>C (p.Pro539=)
15g.73323258_73323259insCAGCACA2629370563HCN4c.2834_2835insTGCTG (p.Pro946AlafsTer?)
c.1616_1617insTGCTG (p.Pro540AlafsTer?)
 gnomAD v4
15g.73323259G>ACA393087364HCN4c.2834C>T (p.Pro945Leu)
c.1616C>T (p.Pro539Leu)
 gnomAD v4
15g.73323259G>CCA393087367HCN4c.2834C>G (p.Pro945Arg)
c.1616C>G (p.Pro539Arg)
15g.73323259G>TCA393087366HCN4c.2834C>A (p.Pro945Gln)
c.1616C>A (p.Pro539Gln)
 gnomAD v4
15g.73323260G>ACA7648944HCN4c.2833C>T (p.Pro945Ser)
c.1615C>T (p.Pro539Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323260G>CCA393087370HCN4c.2833C>G (p.Pro945Ala)
c.1615C>G (p.Pro539Ala)
 gnomAD v4
15g.73323260G=CA2187187848HCN4c.2833C= (p.Pro945=)
c.1615C= (p.Pro539=)
15g.73323260G>TCA393087372HCN4c.2833C>A (p.Pro945Thr)
c.1615C>A (p.Pro539Thr)
 gnomAD v4
15g.73323261C>ACA491478967HCN4c.2832G>T (p.Ala944=)
c.1614G>T (p.Ala538=)
 gnomAD v4
15g.73323261C=CA2187187854HCN4c.2832G= (p.Ala944=)
c.1614G= (p.Ala538=)
15g.73323261C>GCA491478971HCN4c.2832G>C (p.Ala944=)
c.1614G>C (p.Ala538=)
15g.73323261C>TCA7648945HCN4c.2832G>A (p.Ala944=)
c.1614G>A (p.Ala538=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323262G>ACA199743HCN4c.2831C>T (p.Ala944Val)
c.1613C>T (p.Ala538Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323262G>CCA393087376HCN4c.2831C>G (p.Ala944Gly)
c.1613C>G (p.Ala538Gly)
15g.73323262G=CA2187187856HCN4c.2831C= (p.Ala944=)
c.1613C= (p.Ala538=)
15g.73323262G>TCA393087378HCN4c.2831C>A (p.Ala944Glu)
c.1613C>A (p.Ala538Glu)
 gnomAD v4
15g.73323263C>ACA7648947HCN4c.2830G>T (p.Ala944Ser)
c.1612G>T (p.Ala538Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323263C=CA2187187863HCN4c.2830G= (p.Ala944=)
c.1612G= (p.Ala538=)
15g.73323263C>GCA393087380HCN4c.2830G>C (p.Ala944Pro)
c.1612G>C (p.Ala538Pro)
15g.73323263C>TCA7648946HCN4c.2830G>A (p.Ala944Thr)
c.1612G>A (p.Ala538Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323264G>ACA491478975HCN4c.2829C>T (p.Pro943=)
c.1611C>T (p.Pro537=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323264G>CCA491478976HCN4c.2829C>G (p.Pro943=)
c.1611C>G (p.Pro537=)
 gnomAD v4
15g.73323264G=CA2187187868HCN4c.2829C= (p.Pro943=)
c.1611C= (p.Pro537=)
15g.73323264G>TCA491478977HCN4c.2829C>A (p.Pro943=)
c.1611C>A (p.Pro537=)
 gnomAD v4
15g.73323265G>ACA393087383HCN4c.2828C>T (p.Pro943Leu)
c.1610C>T (p.Pro537Leu)
 gnomAD v4
15g.73323265G>CCA393087385HCN4c.2828C>G (p.Pro943Arg)
c.1610C>G (p.Pro537Arg)
 dbSNP gnomAD v4
15g.73323265G=CA2187187874HCN4c.2828C= (p.Pro943=)
c.1610C= (p.Pro537=)
15g.73323265G>TCA393087387HCN4c.2828C>A (p.Pro943His)
c.1610C>A (p.Pro537His)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323266G>ACA393087389HCN4c.2827C>T (p.Pro943Ser)
c.1609C>T (p.Pro537Ser)
 dbSNP
15g.73323266G>CCA393087393HCN4c.2827C>G (p.Pro943Ala)
c.1609C>G (p.Pro537Ala)
15g.73323266G=CA2187187877HCN4c.2827C= (p.Pro943=)
c.1609C= (p.Pro537=)
15g.73323266G>TCA393087391HCN4c.2827C>A (p.Pro943Thr)
c.1609C>A (p.Pro537Thr)
15g.73323267A>CCA491478981HCN4c.2826T>G (p.Ser942=)
c.1608T>G (p.Ser536=)
15g.73323267A>GCA491478983HCN4c.2826T>C (p.Ser942=)
c.1608T>C (p.Ser536=)
15g.73323267A>TCA491478984HCN4c.2826T>A (p.Ser942=)
c.1608T>A (p.Ser536=)
15g.73323268G>ACA393087395HCN4c.2825C>T (p.Ser942Phe)
c.1607C>T (p.Ser536Phe)
 gnomAD v4
15g.73323268G>CCA393087396HCN4c.2825C>G (p.Ser942Cys)
c.1607C>G (p.Ser536Cys)
15g.73323268G>TCA393087399HCN4c.2825C>A (p.Ser942Tyr)
c.1607C>A (p.Ser536Tyr)
 gnomAD v4
15g.73323269A>CCA393087400HCN4c.2824T>G (p.Ser942Ala)
c.1606T>G (p.Ser536Ala)
15g.73323269A>GCA393087401HCN4c.2824T>C (p.Ser942Pro)
c.1606T>C (p.Ser536Pro)
 dbSNP
15g.73323269A>TCA393087403HCN4c.2824T>A (p.Ser942Thr)
c.1606T>A (p.Ser536Thr)
15g.73323270T>ACA491478989HCN4c.2823A>T (p.Pro941=)
c.1605A>T (p.Pro535=)
15g.73323270T>CCA491478990HCN4c.2823A>G (p.Pro941=)
c.1605A>G (p.Pro535=)
 gnomAD v4
15g.73323270T>GCA491478991HCN4c.2823A>C (p.Pro941=)
c.1605A>C (p.Pro535=)
15g.73323271G>ACA393087406HCN4c.2822C>T (p.Pro941Leu)
c.1604C>T (p.Pro535Leu)
15g.73323271G>CCA393087407HCN4c.2822C>G (p.Pro941Arg)
c.1604C>G (p.Pro535Arg)
15g.73323271G>TCA393087410HCN4c.2822C>A (p.Pro941Gln)
c.1604C>A (p.Pro535Gln)
15g.73323272G>ACA393087416HCN4c.2821C>T (p.Pro941Ser)
c.1603C>T (p.Pro535Ser)
 dbSNP gnomAD v2 gnomAD v4
15g.73323272G>CCA393087415HCN4c.2821C>G (p.Pro941Ala)
c.1603C>G (p.Pro535Ala)
15g.73323272G=CA2187187882HCN4c.2821C= (p.Pro941=)
c.1603C= (p.Pro535=)
15g.73323272G>TCA393087413HCN4c.2821C>A (p.Pro941Thr)
c.1603C>A (p.Pro535Thr)
 gnomAD v4
15g.73323273C>ACA393087827HCN4c.2820G>T (p.Gln940His)
c.1602G>T (p.Gln534His)
 gnomAD v4
15g.73323273C>GCA393087830HCN4c.2820G>C (p.Gln940His)
c.1602G>C (p.Gln534His)
15g.73323273C>TCA491478170HCN4c.2820G>A (p.Gln940=)
c.1602G>A (p.Gln534=)
 gnomAD v4
15g.73323274T>ACA393087832HCN4c.2819A>T (p.Gln940Leu)
c.1601A>T (p.Gln534Leu)
15g.73323274T>CCA393087835HCN4c.2819A>G (p.Gln940Arg)
c.1601A>G (p.Gln534Arg)
15g.73323274T>GCA393087838HCN4c.2819A>C (p.Gln940Pro)
c.1601A>C (p.Gln534Pro)
15g.73323275G>ACA393087840HCN4c.2818C>T (p.Gln940Ter)
c.1600C>T (p.Gln534Ter)
15g.73323275G>CCA393087843HCN4c.2818C>G (p.Gln940Glu)
c.1600C>G (p.Gln534Glu)
15g.73323275G>TCA393087846HCN4c.2818C>A (p.Gln940Lys)
c.1600C>A (p.Gln534Lys)
 gnomAD v4
15g.73323276G>ACA491478173HCN4c.2817C>T (p.Ala939=)
c.1599C>T (p.Ala533=)
15g.73323276G>CCA491478172HCN4c.2817C>G (p.Ala939=)
c.1599C>G (p.Ala533=)
15g.73323276G>TCA491478171HCN4c.2817C>A (p.Ala939=)
c.1599C>A (p.Ala533=)
 gnomAD v4
15g.73323277G>ACA393087849HCN4c.2816C>T (p.Ala939Val)
c.1598C>T (p.Ala533Val)
 gnomAD v4
15g.73323277G>CCA393087851HCN4c.2816C>G (p.Ala939Gly)
c.1598C>G (p.Ala533Gly)
15g.73323277G>TCA393087854HCN4c.2816C>A (p.Ala939Asp)
c.1598C>A (p.Ala533Asp)
 gnomAD v4
15g.73323278C>ACA393087862HCN4c.2815G>T (p.Ala939Ser)
c.1597G>T (p.Ala533Ser)
 gnomAD v4
15g.73323278C>GCA393087861HCN4c.2815G>C (p.Ala939Pro)
c.1597G>C (p.Ala533Pro)
15g.73323278C>TCA393087857HCN4c.2815G>A (p.Ala939Thr)
c.1597G>A (p.Ala533Thr)
 gnomAD v4
15g.73323279A>CCA491478174HCN4c.2814T>G (p.Ala938=)
c.1596T>G (p.Ala532=)
 dbSNP gnomAD v3 gnomAD v4
15g.73323279A>GCA491478175HCN4c.2814T>C (p.Ala938=)
c.1596T>C (p.Ala532=)
 gnomAD v4
15g.73323279A>TCA491478176HCN4c.2814T>A (p.Ala938=)
c.1596T>A (p.Ala532=)
15g.73323280G>ACA393087865HCN4c.2813C>T (p.Ala938Val)
c.1595C>T (p.Ala532Val)
 gnomAD v4
15g.73323280G>CCA393087867HCN4c.2813C>G (p.Ala938Gly)
c.1595C>G (p.Ala532Gly)
15g.73323280G>TCA393087871HCN4c.2813C>A (p.Ala938Asp)
c.1595C>A (p.Ala532Asp)
 gnomAD v4
15g.73323280_73323281delinsGCCA2187187886HCN4c.2812_2813delinsGC (p.Ala938=)
c.1594_1595delinsGC (p.Ala532=)
15g.73323281C>ACA393087874HCN4c.2812G>T (p.Ala938Ser)
c.1594G>T (p.Ala532Ser)
 gnomAD v4
15g.73323281C>GCA393087875HCN4c.2812G>C (p.Ala938Pro)
c.1594G>C (p.Ala532Pro)
15g.73323281C>TCA393087878HCN4c.2812G>A (p.Ala938Thr)
c.1594G>A (p.Ala532Thr)
 gnomAD v4
15g.73323282delCA272664172HCN4c.2812del (p.Ala938LeufsTer?)
c.1594del (p.Ala532LeufsTer?)
 dbSNP
15g.73323282C>ACA393087881HCN4c.2811G>T (p.Gln937His)
c.1593G>T (p.Gln531His)
 gnomAD v4
15g.73323282C>GCA393087883HCN4c.2811G>C (p.Gln937His)
c.1593G>C (p.Gln531His)
15g.73323282C>TCA491478177HCN4c.2811G>A (p.Gln937=)
c.1593G>A (p.Gln531=)
15g.73323283T>ACA7648948HCN4c.2810A>T (p.Gln937Leu)
c.1592A>T (p.Gln531Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323283T>CCA393087889HCN4c.2810A>G (p.Gln937Arg)
c.1592A>G (p.Gln531Arg)
 gnomAD v4
15g.73323283T>GCA393087890HCN4c.2810A>C (p.Gln937Pro)
c.1592A>C (p.Gln531Pro)
15g.73323283T=CA2187187893HCN4c.2810A= (p.Gln937=)
c.1592A= (p.Gln531=)
15g.73323284G>ACA7648949HCN4c.2809C>T (p.Gln937Ter)
c.1591C>T (p.Gln531Ter)
 ClinVar dbSNP ExAC gnomAD v4
15g.73323284G>CCA393087897HCN4c.2809C>G (p.Gln937Glu)
c.1591C>G (p.Gln531Glu)
15g.73323284G=CA2187187900HCN4c.2809C= (p.Gln937=)
c.1591C= (p.Gln531=)
15g.73323284G>TCA393087894HCN4c.2809C>A (p.Gln937Lys)
c.1591C>A (p.Gln531Lys)
 gnomAD v4
15g.73323285C>ACA272664207HCN4c.2808G>T (p.Pro936=)
c.1590G>T (p.Pro530=)
 dbSNP gnomAD v4
15g.73323285C=CA2187187905HCN4c.2808G= (p.Pro936=)
c.1590G= (p.Pro530=)
15g.73323285C>GCA491478178HCN4c.2808G>C (p.Pro936=)
c.1590G>C (p.Pro530=)
15g.73323285C>TCA7648950HCN4c.2808G>A (p.Pro936=)
c.1590G>A (p.Pro530=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323286G>ACA7648951HCN4c.2807C>T (p.Pro936Leu)
c.1589C>T (p.Pro530Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73323286G>CCA393087906HCN4c.2807C>G (p.Pro936Arg)
c.1589C>G (p.Pro530Arg)
15g.73323286G=CA2187187915HCN4c.2807C= (p.Pro936=)
c.1589C= (p.Pro530=)
15g.73323286G>TCA393087908HCN4c.2807C>A (p.Pro936Gln)
c.1589C>A (p.Pro530Gln)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
15g.73323287G>ACA393087912HCN4c.2806C>T (p.Pro936Ser)
c.1588C>T (p.Pro530Ser)
 dbSNP gnomAD v4
15g.73323287G>CCA393087915HCN4c.2806C>G (p.Pro936Ala)
c.1588C>G (p.Pro530Ala)
15g.73323287G=CA2187187924HCN4c.2806C= (p.Pro936=)
c.1588C= (p.Pro530=)
15g.73323287G>TCA393087916HCN4c.2806C>A (p.Pro936Thr)
c.1588C>A (p.Pro530Thr)
 gnomAD v4
15g.73323288G>ACA491478179HCN4c.2805C>T (p.Ser935=)
c.1587C>T (p.Ser529=)
 gnomAD v4
15g.73323288G>CCA491478181HCN4c.2805C>G (p.Ser935=)
c.1587C>G (p.Ser529=)
15g.73323288G>TCA491478180HCN4c.2805C>A (p.Ser935=)
c.1587C>A (p.Ser529=)
 gnomAD v4
15g.73323288_73323289delinsTACA2573151087HCN4c.2804_2805delinsTA (p.Ser935Leu)
c.1586_1587delinsTA (p.Ser529Leu)
 ClinVar dbSNP
15g.73323289G>ACA301966HCN4c.2804C>T (p.Ser935Phe)
c.1586C>T (p.Ser529Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323289G>CCA393087921HCN4c.2804C>G (p.Ser935Cys)
c.1586C>G (p.Ser529Cys)
 ClinVar
15g.73323289G=CA2187187930HCN4c.2804C= (p.Ser935=)
c.1586C= (p.Ser529=)
15g.73323289G>TCA7648952HCN4c.2804C>A (p.Ser935Tyr)
c.1586C>A (p.Ser529Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323290A>CCA393087925HCN4c.2803T>G (p.Ser935Ala)
c.1585T>G (p.Ser529Ala)
15g.73323290A>GCA393087928HCN4c.2803T>C (p.Ser935Pro)
c.1585T>C (p.Ser529Pro)
 gnomAD v4
15g.73323290A>TCA393087930HCN4c.2803T>A (p.Ser935Thr)
c.1585T>A (p.Ser529Thr)
15g.73323291G>ACA491478185HCN4c.2802C>T (p.Arg934=)
c.1584C>T (p.Arg528=)
 dbSNP gnomAD v3 gnomAD v4
15g.73323291G>CCA491478186HCN4c.2802C>G (p.Arg934=)
c.1584C>G (p.Arg528=)
 gnomAD v4
15g.73323291G=CA2187187934HCN4c.2802C= (p.Arg934=)
c.1584C= (p.Arg528=)
15g.73323291G>TCA491478189HCN4c.2802C>A (p.Arg934=)
c.1584C>A (p.Arg528=)
 gnomAD v4
15g.73323292C>ACA393087934HCN4c.2801G>T (p.Arg934Leu)
c.1583G>T (p.Arg528Leu)
 dbSNP gnomAD v2 gnomAD v4
15g.73323292C=CA2187187937HCN4c.2801G= (p.Arg934=)
c.1583G= (p.Arg528=)
15g.73323292C>GCA393087932HCN4c.2801G>C (p.Arg934Pro)
c.1583G>C (p.Arg528Pro)
15g.73323292C>TCA247655HCN4c.2801G>A (p.Arg934His)
c.1583G>A (p.Arg528His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323293G>ACA301952HCN4c.2800C>T (p.Arg934Cys)
c.1582C>T (p.Arg528Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323293G>CCA393087938HCN4c.2800C>G (p.Arg934Gly)
c.1582C>G (p.Arg528Gly)
15g.73323293G=CA2187187945HCN4c.2800C= (p.Arg934=)
c.1582C= (p.Arg528=)
15g.73323293G>TCA393087939HCN4c.2800C>A (p.Arg934Ser)
c.1582C>A (p.Arg528Ser)
 gnomAD v4
15g.73323294G>ACA491478193HCN4c.2799C>T (p.Ala933=)
c.1581C>T (p.Ala527=)
 COSMIC
15g.73323294G>CCA491478194HCN4c.2799C>G (p.Ala933=)
c.1581C>G (p.Ala527=)
15g.73323294G>TCA491478195HCN4c.2799C>A (p.Ala933=)
c.1581C>A (p.Ala527=)
15g.73323295G>ACA393087942HCN4c.2798C>T (p.Ala933Val)
c.1580C>T (p.Ala527Val)
 dbSNP gnomAD v2 gnomAD v4
15g.73323295G>CCA393087943HCN4c.2798C>G (p.Ala933Gly)
c.1580C>G (p.Ala527Gly)
 COSMIC
15g.73323295G=CA2187187949HCN4c.2798C= (p.Ala933=)
c.1580C= (p.Ala527=)
15g.73323295G>TCA393087945HCN4c.2798C>A (p.Ala933Asp)
c.1580C>A (p.Ala527Asp)
15g.73323296C>ACA10581185HCN4c.2797G>T (p.Ala933Ser)
c.1579G>T (p.Ala527Ser)
 ClinVar dbSNP gnomAD v4
15g.73323296C=CA2187187955HCN4c.2797G= (p.Ala933=)
c.1579G= (p.Ala527=)
15g.73323296C>GCA393087950HCN4c.2797G>C (p.Ala933Pro)
c.1579G>C (p.Ala527Pro)
15g.73323296C>TCA7648953HCN4c.2797G>A (p.Ala933Thr)
c.1579G>A (p.Ala527Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323297G>ACA7648954HCN4c.2796C>T (p.Gly932=)
c.1578C>T (p.Gly526=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323297G>CCA272664238HCN4c.2796C>G (p.Gly932=)
c.1578C>G (p.Gly526=)
 ClinVar dbSNP gnomAD v4
15g.73323297G=CA2187187965HCN4c.2796C= (p.Gly932=)
c.1578C= (p.Gly526=)
15g.73323297G>TCA491478199HCN4c.2796C>A (p.Gly932=)
c.1578C>A (p.Gly526=)
 gnomAD v4
15g.73323298C>ACA393087957HCN4c.2795G>T (p.Gly932Val)
c.1577G>T (p.Gly526Val)
15g.73323298C=CA2187187972HCN4c.2795G= (p.Gly932=)
c.1577G= (p.Gly526=)
15g.73323298C>GCA393087960HCN4c.2795G>C (p.Gly932Ala)
c.1577G>C (p.Gly526Ala)
15g.73323298C>TCA393087963HCN4c.2795G>A (p.Gly932Asp)
c.1577G>A (p.Gly526Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323299C>ACA393087966HCN4c.2794G>T (p.Gly932Cys)
c.1576G>T (p.Gly526Cys)
 gnomAD v4
15g.73323299C>GCA393087968HCN4c.2794G>C (p.Gly932Arg)
c.1576G>C (p.Gly526Arg)
15g.73323299C>TCA393087965HCN4c.2794G>A (p.Gly932Ser)
c.1576G>A (p.Gly526Ser)
 gnomAD v4
15g.73323300T>ACA491478202HCN4c.2793A>T (p.Pro931=)
c.1575A>T (p.Pro525=)
15g.73323300T>CCA491478203HCN4c.2793A>G (p.Pro931=)
c.1575A>G (p.Pro525=)
 gnomAD v4
15g.73323300T>GCA491478204HCN4c.2793A>C (p.Pro931=)
c.1575A>C (p.Pro525=)
15g.73323301G>ACA393087970HCN4c.2792C>T (p.Pro931Leu)
c.1574C>T (p.Pro525Leu)
 gnomAD v4
15g.73323301G>CCA393087972HCN4c.2792C>G (p.Pro931Arg)
c.1574C>G (p.Pro525Arg)
15g.73323301G>TCA393087974HCN4c.2792C>A (p.Pro931Gln)
c.1574C>A (p.Pro525Gln)
 gnomAD v4
15g.73323302G>ACA393087977HCN4c.2791C>T (p.Pro931Ser)
c.1573C>T (p.Pro525Ser)
 gnomAD v4
15g.73323302G>CCA393087978HCN4c.2791C>G (p.Pro931Ala)
c.1573C>G (p.Pro525Ala)
15g.73323302G>TCA393087981HCN4c.2791C>A (p.Pro931Thr)
c.1573C>A (p.Pro525Thr)
 gnomAD v4
15g.73323303C>ACA393087983HCN4c.2790G>T (p.Gln930His)
c.1572G>T (p.Gln524His)
 gnomAD v4
15g.73323303C>GCA393087986HCN4c.2790G>C (p.Gln930His)
c.1572G>C (p.Gln524His)
15g.73323303C>TCA491478206HCN4c.2790G>A (p.Gln930=)
c.1572G>A (p.Gln524=)
 gnomAD v4
15g.73323304T>ACA393087990HCN4c.2789A>T (p.Gln930Leu)
c.1571A>T (p.Gln524Leu)
15g.73323304T>CCA393087991HCN4c.2789A>G (p.Gln930Arg)
c.1571A>G (p.Gln524Arg)
 gnomAD v4
15g.73323304T>GCA393087993HCN4c.2789A>C (p.Gln930Pro)
c.1571A>C (p.Gln524Pro)
15g.73323305G>ACA393088001HCN4c.2788C>T (p.Gln930Ter)
c.1570C>T (p.Gln524Ter)
 ClinVar dbSNP gnomAD v4
15g.73323305G>CCA393087999HCN4c.2788C>G (p.Gln930Glu)
c.1570C>G (p.Gln524Glu)
15g.73323305G=CA2187187978HCN4c.2788C= (p.Gln930=)
c.1570C= (p.Gln524=)
15g.73323305G>TCA393087997HCN4c.2788C>A (p.Gln930Lys)
c.1570C>A (p.Gln524Lys)
 gnomAD v4 COSMIC
15g.73323306C>ACA491478210HCN4c.2787G>T (p.Leu929=)
c.1569G>T (p.Leu523=)
 gnomAD v4
15g.73323306C>GCA491478212HCN4c.2787G>C (p.Leu929=)
c.1569G>C (p.Leu523=)
15g.73323306C>TCA491478213HCN4c.2787G>A (p.Leu929=)
c.1569G>A (p.Leu523=)
 gnomAD v4

Number of alleles fetched