Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73323084C>ACA491478491HCN4c.3009G>T (p.Pro1003=)
c.1791G>T (p.Pro597=)
 gnomAD v4
15g.73323084C=CA2187187456HCN4c.3009G= (p.Pro1003=)
c.1791G= (p.Pro597=)
15g.73323084C>GCA491478492HCN4c.3009G>C (p.Pro1003=)
c.1791G>C (p.Pro597=)
15g.73323084C>TCA7648906HCN4c.3009G>A (p.Pro1003=)
c.1791G>A (p.Pro597=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73323085G>ACA393086462HCN4c.3008C>T (p.Pro1003Leu)
c.1790C>T (p.Pro597Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323085G>CCA393086464HCN4c.3008C>G (p.Pro1003Arg)
c.1790C>G (p.Pro597Arg)
15g.73323085G=CA2187187458HCN4c.3008C= (p.Pro1003=)
c.1790C= (p.Pro597=)
15g.73323085G>TCA393086466HCN4c.3008C>A (p.Pro1003Gln)
c.1790C>A (p.Pro597Gln)
 gnomAD v4
15g.73323086G>ACA393086467HCN4c.3007C>T (p.Pro1003Ser)
c.1789C>T (p.Pro597Ser)
 gnomAD v4
15g.73323086G>CCA393086469HCN4c.3007C>G (p.Pro1003Ala)
c.1789C>G (p.Pro597Ala)
15g.73323086G>TCA393086471HCN4c.3007C>A (p.Pro1003Thr)
c.1789C>A (p.Pro597Thr)
 gnomAD v4
15g.73323087C>ACA393086473HCN4c.3006G>T (p.Glu1002Asp)
c.1788G>T (p.Glu596Asp)
 gnomAD v4
15g.73323087C>GCA393086474HCN4c.3006G>C (p.Glu1002Asp)
c.1788G>C (p.Glu596Asp)
15g.73323087C>TCA491478498HCN4c.3006G>A (p.Glu1002=)
c.1788G>A (p.Glu596=)
15g.73323088T>ACA393086479HCN4c.3005A>T (p.Glu1002Val)
c.1787A>T (p.Glu596Val)
15g.73323088T>CCA393086477HCN4c.3005A>G (p.Glu1002Gly)
c.1787A>G (p.Glu596Gly)
 gnomAD v4
15g.73323088T>GCA393086478HCN4c.3005A>C (p.Glu1002Ala)
c.1787A>C (p.Glu596Ala)
15g.73323089C>ACA393086481HCN4c.3004G>T (p.Glu1002Ter)
c.1786G>T (p.Glu596Ter)
 gnomAD v4
15g.73323089C=CA2187187464HCN4c.3004G= (p.Glu1002=)
c.1786G= (p.Glu596=)
15g.73323089C>GCA16614917HCN4c.3004G>C (p.Glu1002Gln)
c.1786G>C (p.Glu596Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323089C>TCA393086483HCN4c.3004G>A (p.Glu1002Lys)
c.1786G>A (p.Glu596Lys)
 ClinVar dbSNP gnomAD v4
15g.73323090A>CCA491478503HCN4c.3003T>G (p.Pro1001=)
c.1785T>G (p.Pro595=)
15g.73323090A>GCA491478504HCN4c.3003T>C (p.Pro1001=)
c.1785T>C (p.Pro595=)
 gnomAD v4
15g.73323090A>TCA491478505HCN4c.3003T>A (p.Pro1001=)
c.1785T>A (p.Pro595=)
 gnomAD v4
15g.73323091G>ACA393086485HCN4c.3002C>T (p.Pro1001Leu)
c.1784C>T (p.Pro595Leu)
15g.73323091G>CCA393086486HCN4c.3002C>G (p.Pro1001Arg)
c.1784C>G (p.Pro595Arg)
15g.73323091G=CA2187187469HCN4c.3002C= (p.Pro1001=)
c.1784C= (p.Pro595=)
15g.73323091G>TCA272663955HCN4c.3002C>A (p.Pro1001His)
c.1784C>A (p.Pro595His)
 dbSNP gnomAD v4
15g.73323092G>ACA393086489HCN4c.3001C>T (p.Pro1001Ser)
c.1783C>T (p.Pro595Ser)
 gnomAD v4
15g.73323092G>CCA393086491HCN4c.3001C>G (p.Pro1001Ala)
c.1783C>G (p.Pro595Ala)
15g.73323092G>TCA393086492HCN4c.3001C>A (p.Pro1001Thr)
c.1783C>A (p.Pro595Thr)
 ClinVar gnomAD v4
15g.73323093C>ACA393086494HCN4c.3000G>T (p.Gln1000His)
c.1782G>T (p.Gln594His)
 gnomAD v4
15g.73323093C>GCA393086495HCN4c.3000G>C (p.Gln1000His)
c.1782G>C (p.Gln594His)
15g.73323093C>TCA491478508HCN4c.3000G>A (p.Gln1000=)
c.1782G>A (p.Gln594=)
 gnomAD v4
15g.73323094T>ACA393086500HCN4c.2999A>T (p.Gln1000Leu)
c.1781A>T (p.Gln594Leu)
15g.73323094T>CCA393086499HCN4c.2999A>G (p.Gln1000Arg)
c.1781A>G (p.Gln594Arg)
15g.73323094T>GCA393086497HCN4c.2999A>C (p.Gln1000Pro)
c.1781A>C (p.Gln594Pro)
15g.73323095G>ACA393086502HCN4c.2998C>T (p.Gln1000Ter)
c.1780C>T (p.Gln594Ter)
 gnomAD v4
15g.73323095G>CCA393086504HCN4c.2998C>G (p.Gln1000Glu)
c.1780C>G (p.Gln594Glu)
15g.73323095G=CA2187187474HCN4c.2998C= (p.Gln1000=)
c.1780C= (p.Gln594=)
15g.73323095G>TCA393086506HCN4c.2998C>A (p.Gln1000Lys)
c.1780C>A (p.Gln594Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323096C>ACA491478517HCN4c.2997G>T (p.Arg999=)
c.1779G>T (p.Arg593=)
 gnomAD v4
15g.73323096C=CA2187187481HCN4c.2997G= (p.Arg999=)
c.1779G= (p.Arg593=)
15g.73323096C>GCA7648907HCN4c.2997G>C (p.Arg999=)
c.1779G>C (p.Arg593=)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323096C>TCA7648908HCN4c.2997G>A (p.Arg999=)
c.1779G>A (p.Arg593=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323097C>ACA393086514HCN4c.2996G>T (p.Arg999Leu)
c.1778G>T (p.Arg593Leu)
 gnomAD v4
15g.73323097C=CA2187187487HCN4c.2996G= (p.Arg999=)
c.1778G= (p.Arg593=)
15g.73323097C>GCA393086516HCN4c.2996G>C (p.Arg999Pro)
c.1778G>C (p.Arg593Pro)
15g.73323097C>TCA393086517HCN4c.2996G>A (p.Arg999Gln)
c.1778G>A (p.Arg593Gln)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323098G>ACA272663979HCN4c.2995C>T (p.Arg999Trp)
c.1777C>T (p.Arg593Trp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
15g.73323098G>CCA393086522HCN4c.2995C>G (p.Arg999Gly)
c.1777C>G (p.Arg593Gly)
15g.73323098G=CA2187187494HCN4c.2995C= (p.Arg999=)
c.1777C= (p.Arg593=)
15g.73323098G>TCA491478524HCN4c.2995C>A (p.Arg999=)
c.1777C>A (p.Arg593=)
 gnomAD v4
15g.73323099T>ACA491478526HCN4c.2994A>T (p.Pro998=)
c.1776A>T (p.Pro592=)
15g.73323099T>CCA491478527HCN4c.2994A>G (p.Pro998=)
c.1776A>G (p.Pro592=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323099T>GCA491478528HCN4c.2994A>C (p.Pro998=)
c.1776A>C (p.Pro592=)
15g.73323099T=CA2187187499HCN4c.2994A= (p.Pro998=)
c.1776A= (p.Pro592=)
15g.73323100G>ACA7648909HCN4c.2993C>T (p.Pro998Leu)
c.1775C>T (p.Pro592Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323100G>CCA393086525HCN4c.2993C>G (p.Pro998Arg)
c.1775C>G (p.Pro592Arg)
15g.73323100G=CA2187187502HCN4c.2993C= (p.Pro998=)
c.1775C= (p.Pro592=)
15g.73323100G>TCA393086528HCN4c.2993C>A (p.Pro998Gln)
c.1775C>A (p.Pro592Gln)
 gnomAD v4
15g.73323104delCA491478535HCN4c.2993del (p.Pro998HisfsTer20)
c.1775del (p.Pro592HisfsTer20)
 gnomAD v4 COSMIC
15g.73323101G>ACA393086536HCN4c.2992C>T (p.Pro998Ser)
c.1774C>T (p.Pro592Ser)
 gnomAD v4
15g.73323101G>CCA7648910HCN4c.2992C>G (p.Pro998Ala)
c.1774C>G (p.Pro592Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323101G=CA2187187504HCN4c.2992C= (p.Pro998=)
c.1774C= (p.Pro592=)
15g.73323101G>TCA393086534HCN4c.2992C>A (p.Pro998Thr)
c.1774C>A (p.Pro592Thr)
 gnomAD v4
15g.73323102G>ACA491478537HCN4c.2991C>T (p.Pro997=)
c.1773C>T (p.Pro591=)
 dbSNP gnomAD v2 gnomAD v4
15g.73323102G>CCA491478539HCN4c.2991C>G (p.Pro997=)
c.1773C>G (p.Pro591=)
 gnomAD v4
15g.73323102G=CA2187187506HCN4c.2991C= (p.Pro997=)
c.1773C= (p.Pro591=)
15g.73323102G>TCA491478540HCN4c.2991C>A (p.Pro997=)
c.1773C>A (p.Pro591=)
15g.73323103G>ACA393086539HCN4c.2990C>T (p.Pro997Leu)
c.1772C>T (p.Pro591Leu)
 gnomAD v4
15g.73323103G>CCA393086541HCN4c.2990C>G (p.Pro997Arg)
c.1772C>G (p.Pro591Arg)
15g.73323103G=CA2187187511HCN4c.2990C= (p.Pro997=)
c.1772C= (p.Pro591=)
15g.73323103G>TCA272663982HCN4c.2990C>A (p.Pro997His)
c.1772C>A (p.Pro591His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323104G>ACA393086551HCN4c.2989C>T (p.Pro997Ser)
c.1771C>T (p.Pro591Ser)
 gnomAD v4
15g.73323104G>CCA393086554HCN4c.2989C>G (p.Pro997Ala)
c.1771C>G (p.Pro591Ala)
15g.73323104G=CA2187187516HCN4c.2989C= (p.Pro997=)
c.1771C= (p.Pro591=)
15g.73323104G>TCA7648911HCN4c.2989C>A (p.Pro997Thr)
c.1771C>A (p.Pro591Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323105T>ACA491478550HCN4c.2988A>T (p.Thr996=)
c.1770A>T (p.Thr590=)
 dbSNP
15g.73323105T>CCA491478551HCN4c.2988A>G (p.Thr996=)
c.1770A>G (p.Thr590=)
 gnomAD v4
15g.73323105T>GCA491478553HCN4c.2988A>C (p.Thr996=)
c.1770A>C (p.Thr590=)
 ClinVar
15g.73323105T=CA2187187520HCN4c.2988A= (p.Thr996=)
c.1770A= (p.Thr590=)
15g.73323106G>ACA393086559HCN4c.2987C>T (p.Thr996Ile)
c.1769C>T (p.Thr590Ile)
 gnomAD v4
15g.73323106G>CCA393086561HCN4c.2987C>G (p.Thr996Arg)
c.1769C>G (p.Thr590Arg)
15g.73323106G>TCA393086563HCN4c.2987C>A (p.Thr996Lys)
c.1769C>A (p.Thr590Lys)
 gnomAD v4
15g.73323107T>ACA393086567HCN4c.2986A>T (p.Thr996Ser)
c.1768A>T (p.Thr590Ser)
 dbSNP
15g.73323107T>CCA393086568HCN4c.2986A>G (p.Thr996Ala)
c.1768A>G (p.Thr590Ala)
 gnomAD v4
15g.73323107T>GCA393086570HCN4c.2986A>C (p.Thr996Pro)
c.1768A>C (p.Thr590Pro)
15g.73323107T=CA2187187523HCN4c.2986A= (p.Thr996=)
c.1768A= (p.Thr590=)
15g.73323108C>ACA393086573HCN4c.2985G>T (p.Glu995Asp)
c.1767G>T (p.Glu589Asp)
 gnomAD v4
15g.73323108C>GCA393086575HCN4c.2985G>C (p.Glu995Asp)
c.1767G>C (p.Glu589Asp)
 ClinVar gnomAD v4
15g.73323108C>TCA491478563HCN4c.2985G>A (p.Glu995=)
c.1767G>A (p.Glu589=)
 gnomAD v4
15g.73323109T>ACA393086579HCN4c.2984A>T (p.Glu995Val)
c.1766A>T (p.Glu589Val)
15g.73323109T>CCA393086583HCN4c.2984A>G (p.Glu995Gly)
c.1766A>G (p.Glu589Gly)
 gnomAD v4
15g.73323109T>GCA393086581HCN4c.2984A>C (p.Glu995Ala)
c.1766A>C (p.Glu589Ala)
15g.73323110C>ACA393086587HCN4c.2983G>T (p.Glu995Ter)
c.1765G>T (p.Glu589Ter)
 gnomAD v4
15g.73323110C>GCA393086590HCN4c.2983G>C (p.Glu995Gln)
c.1765G>C (p.Glu589Gln)
15g.73323110C>TCA393086591HCN4c.2983G>A (p.Glu995Lys)
c.1765G>A (p.Glu589Lys)
15g.73323111T>ACA491478567HCN4c.2982A>T (p.Pro994=)
c.1764A>T (p.Pro588=)
15g.73323111T>CCA491478570HCN4c.2982A>G (p.Pro994=)
c.1764A>G (p.Pro588=)
 dbSNP
15g.73323111T>GCA491478573HCN4c.2982A>C (p.Pro994=)
c.1764A>C (p.Pro588=)
15g.73323111T=CA2187187525HCN4c.2982A= (p.Pro994=)
c.1764A= (p.Pro588=)
15g.73323112G>ACA393086595HCN4c.2981C>T (p.Pro994Leu)
c.1763C>T (p.Pro588Leu)
 gnomAD v4
15g.73323112G>CCA393086597HCN4c.2981C>G (p.Pro994Arg)
c.1763C>G (p.Pro588Arg)
15g.73323112G>TCA393086599HCN4c.2981C>A (p.Pro994Gln)
c.1763C>A (p.Pro588Gln)
 gnomAD v4
15g.73323113G>ACA393086602HCN4c.2980C>T (p.Pro994Ser)
c.1762C>T (p.Pro588Ser)
 gnomAD v4
15g.73323113G>CCA393086603HCN4c.2980C>G (p.Pro994Ala)
c.1762C>G (p.Pro588Ala)
15g.73323113G>TCA393086606HCN4c.2980C>A (p.Pro994Thr)
c.1762C>A (p.Pro588Thr)
15g.73323114C>ACA491478585HCN4c.2979G>T (p.Thr993=)
c.1761G>T (p.Thr587=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73323114C=CA2187187528HCN4c.2979G= (p.Thr993=)
c.1761G= (p.Thr587=)
15g.73323114C>GCA491478584HCN4c.2979G>C (p.Thr993=)
c.1761G>C (p.Thr587=)
 ClinVar
15g.73323114C>TCA203637HCN4c.2979G>A (p.Thr993=)
c.1761G>A (p.Thr587=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323115G>ACA7648912HCN4c.2978C>T (p.Thr993Met)
c.1760C>T (p.Thr587Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323115G>CCA393086610HCN4c.2978C>G (p.Thr993Arg)
c.1760C>G (p.Thr587Arg)
 gnomAD v4
15g.73323115G=CA2187187536HCN4c.2978C= (p.Thr993=)
c.1760C= (p.Thr587=)
15g.73323115G>TCA393086609HCN4c.2978C>A (p.Thr993Lys)
c.1760C>A (p.Thr587Lys)
 COSMIC
15g.73323116T>ACA393086614HCN4c.2977A>T (p.Thr993Ser)
c.1759A>T (p.Thr587Ser)
 dbSNP
15g.73323116T>CCA393086615HCN4c.2977A>G (p.Thr993Ala)
c.1759A>G (p.Thr587Ala)
 gnomAD v4
15g.73323116T>GCA393086617HCN4c.2977A>C (p.Thr993Pro)
c.1759A>C (p.Thr587Pro)
15g.73323116T=CA2187187541HCN4c.2977A= (p.Thr993=)
c.1759A= (p.Thr587=)
15g.73323117G>ACA7648913HCN4c.2976C>T (p.Ser992=)
c.1758C>T (p.Ser586=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323117G>CCA393086619HCN4c.2976C>G (p.Ser992Arg)
c.1758C>G (p.Ser586Arg)
15g.73323117G=CA2187187543HCN4c.2976C= (p.Ser992=)
c.1758C= (p.Ser586=)
15g.73323117G>TCA393086620HCN4c.2976C>A (p.Ser992Arg)
c.1758C>A (p.Ser586Arg)
 gnomAD v4
15g.73323118C>ACA7648914HCN4c.2975G>T (p.Ser992Ile)
c.1757G>T (p.Ser586Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323118C=CA2187187548HCN4c.2975G= (p.Ser992=)
c.1757G= (p.Ser586=)
15g.73323118C>GCA393086622HCN4c.2975G>C (p.Ser992Thr)
c.1757G>C (p.Ser586Thr)
15g.73323118C>TCA393086623HCN4c.2975G>A (p.Ser992Asn)
c.1757G>A (p.Ser586Asn)
 gnomAD v4
15g.73323119T>ACA393086625HCN4c.2974A>T (p.Ser992Cys)
c.1756A>T (p.Ser586Cys)
15g.73323119T>CCA393086627HCN4c.2974A>G (p.Ser992Gly)
c.1756A>G (p.Ser586Gly)
 gnomAD v4
15g.73323119T>GCA393086628HCN4c.2974A>C (p.Ser992Arg)
c.1756A>C (p.Ser586Arg)
15g.73323120C>ACA491478598HCN4c.2973G>T (p.Leu991=)
c.1755G>T (p.Leu585=)
 gnomAD v4
15g.73323120C=CA2187187551HCN4c.2973G= (p.Leu991=)
c.1755G= (p.Leu585=)
15g.73323120C>GCA491478601HCN4c.2973G>C (p.Leu991=)
c.1755G>C (p.Leu585=)
15g.73323120C>TCA491478600HCN4c.2973G>A (p.Leu991=)
c.1755G>A (p.Leu585=)
 dbSNP
15g.73323121A=CA2187187553HCN4c.2972T= (p.Leu991=)
c.1754T= (p.Leu585=)
15g.73323121A>CCA393086631HCN4c.2972T>G (p.Leu991Arg)
c.1754T>G (p.Leu585Arg)
15g.73323121A>GCA272663993HCN4c.2972T>C (p.Leu991Pro)
c.1754T>C (p.Leu585Pro)
 dbSNP gnomAD v2 gnomAD v4
15g.73323121A>TCA393086629HCN4c.2972T>A (p.Leu991Gln)
c.1754T>A (p.Leu585Gln)
15g.73323122G>ACA491478607HCN4c.2971C>T (p.Leu991=)
c.1753C>T (p.Leu585=)
 gnomAD v4
15g.73323122G>CCA393086633HCN4c.2971C>G (p.Leu991Val)
c.1753C>G (p.Leu585Val)
15g.73323122G>TCA393086634HCN4c.2971C>A (p.Leu991Met)
c.1753C>A (p.Leu585Met)
 gnomAD v4 COSMIC
15g.73323123T>ACA491478609HCN4c.2970A>T (p.Pro990=)
c.1752A>T (p.Pro584=)
 gnomAD v4
15g.73323123T>CCA491478611HCN4c.2970A>G (p.Pro990=)
c.1752A>G (p.Pro584=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323123T>GCA491478613HCN4c.2970A>C (p.Pro990=)
c.1752A>C (p.Pro584=)
15g.73323123T=CA2187187556HCN4c.2970A= (p.Pro990=)
c.1752A= (p.Pro584=)
15g.73323124G>ACA7648915HCN4c.2969C>T (p.Pro990Leu)
c.1751C>T (p.Pro584Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323124G>CCA393086637HCN4c.2969C>G (p.Pro990Arg)
c.1751C>G (p.Pro584Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323124G=CA2187187559HCN4c.2969C= (p.Pro990=)
c.1751C= (p.Pro584=)
15g.73323124G>TCA393086639HCN4c.2969C>A (p.Pro990Gln)
c.1751C>A (p.Pro584Gln)
 gnomAD v4
15g.73323125G>ACA393086643HCN4c.2968C>T (p.Pro990Ser)
c.1750C>T (p.Pro584Ser)
 gnomAD v4
15g.73323125G>CCA393086642HCN4c.2968C>G (p.Pro990Ala)
c.1750C>G (p.Pro584Ala)
 ClinVar dbSNP
15g.73323125G>TCA393086640HCN4c.2968C>A (p.Pro990Thr)
c.1750C>A (p.Pro584Thr)
 gnomAD v4
15g.73323126G>ACA491478615HCN4c.2967C>T (p.Gly989=)
c.1749C>T (p.Gly583=)
 gnomAD v4
15g.73323126G>CCA491478617HCN4c.2967C>G (p.Gly989=)
c.1749C>G (p.Gly583=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323126G=CA2187187563HCN4c.2967C= (p.Gly989=)
c.1749C= (p.Gly583=)
15g.73323126G>TCA491478620HCN4c.2967C>A (p.Gly989=)
c.1749C>A (p.Gly583=)
 gnomAD v4
15g.73323127C>ACA393086645HCN4c.2966G>T (p.Gly989Val)
c.1748G>T (p.Gly583Val)
 gnomAD v4
15g.73323127C>GCA393086646HCN4c.2966G>C (p.Gly989Ala)
c.1748G>C (p.Gly583Ala)
15g.73323127C>TCA393086648HCN4c.2966G>A (p.Gly989Asp)
c.1748G>A (p.Gly583Asp)
 gnomAD v4
15g.73323128C>ACA393086650HCN4c.2965G>T (p.Gly989Cys)
c.1747G>T (p.Gly583Cys)
 gnomAD v4
15g.73323128C>GCA393086651HCN4c.2965G>C (p.Gly989Arg)
c.1747G>C (p.Gly583Arg)
15g.73323128C>TCA393086653HCN4c.2965G>A (p.Gly989Ser)
c.1747G>A (p.Gly583Ser)
 gnomAD v4
15g.73323129A=CA2187187566HCN4c.2964T= (p.Thr988=)
c.1746T= (p.Thr582=)
15g.73323129A>CCA491478623HCN4c.2964T>G (p.Thr988=)
c.1746T>G (p.Thr582=)
15g.73323129A>GCA491478625HCN4c.2964T>C (p.Thr988=)
c.1746T>C (p.Thr582=)
 ClinVar dbSNP gnomAD v4
15g.73323129A>TCA491478629HCN4c.2964T>A (p.Thr988=)
c.1746T>A (p.Thr582=)
 gnomAD v4
15g.73323130G>ACA393086654HCN4c.2963C>T (p.Thr988Ile)
c.1745C>T (p.Thr582Ile)
 gnomAD v4
15g.73323130G>CCA393086656HCN4c.2963C>G (p.Thr988Ser)
c.1745C>G (p.Thr582Ser)
15g.73323130G>TCA393086655HCN4c.2963C>A (p.Thr988Asn)
c.1745C>A (p.Thr582Asn)
 gnomAD v4
15g.73323131T>ACA393086658HCN4c.2962A>T (p.Thr988Ser)
c.1744A>T (p.Thr582Ser)
 gnomAD v4
15g.73323131T>CCA393086660HCN4c.2962A>G (p.Thr988Ala)
c.1744A>G (p.Thr582Ala)
15g.73323131T>GCA393086661HCN4c.2962A>C (p.Thr988Pro)
c.1744A>C (p.Thr582Pro)
15g.73323132G>ACA491478635HCN4c.2961C>T (p.Ala987=)
c.1743C>T (p.Ala581=)
 gnomAD v4
15g.73323132G>CCA491478636HCN4c.2961C>G (p.Ala987=)
c.1743C>G (p.Ala581=)
15g.73323132G>TCA491478638HCN4c.2961C>A (p.Ala987=)
c.1743C>A (p.Ala581=)
 gnomAD v4
15g.73323133G>ACA393086663HCN4c.2960C>T (p.Ala987Val)
c.1742C>T (p.Ala581Val)
 gnomAD v4
15g.73323133G>CCA393086665HCN4c.2960C>G (p.Ala987Gly)
c.1742C>G (p.Ala581Gly)
15g.73323133G>TCA393086666HCN4c.2960C>A (p.Ala987Asp)
c.1742C>A (p.Ala581Asp)
 gnomAD v4
15g.73323134C>ACA393086669HCN4c.2959G>T (p.Ala987Ser)
c.1741G>T (p.Ala581Ser)
 gnomAD v4
15g.73323134C>GCA393086672HCN4c.2959G>C (p.Ala987Pro)
c.1741G>C (p.Ala581Pro)
15g.73323134C>TCA393086674HCN4c.2959G>A (p.Ala987Thr)
c.1741G>A (p.Ala581Thr)
 gnomAD v4
15g.73323135C>ACA491478644HCN4c.2958G>T (p.Leu986=)
c.1740G>T (p.Leu580=)
 gnomAD v4
15g.73323135C>GCA491478645HCN4c.2958G>C (p.Leu986=)
c.1740G>C (p.Leu580=)
15g.73323135C>TCA491478647HCN4c.2958G>A (p.Leu986=)
c.1740G>A (p.Leu580=)
 gnomAD v4
15g.73323136A>CCA393086677HCN4c.2957T>G (p.Leu986Arg)
c.1739T>G (p.Leu580Arg)
15g.73323136A>GCA393086680HCN4c.2957T>C (p.Leu986Pro)
c.1739T>C (p.Leu580Pro)
 gnomAD v4
15g.73323136A>TCA393086682HCN4c.2957T>A (p.Leu986Gln)
c.1739T>A (p.Leu580Gln)
 gnomAD v4
15g.73323137G>ACA491478651HCN4c.2956C>T (p.Leu986=)
c.1738C>T (p.Leu580=)
 gnomAD v4
15g.73323137G>CCA393086685HCN4c.2956C>G (p.Leu986Val)
c.1738C>G (p.Leu580Val)
15g.73323137G>TCA393086687HCN4c.2956C>A (p.Leu986Met)
c.1738C>A (p.Leu580Met)
 gnomAD v4
15g.73323138A=CA2187187569HCN4c.2955T= (p.Gly985=)
c.1737T= (p.Gly579=)
15g.73323138A>CCA491478655HCN4c.2955T>G (p.Gly985=)
c.1737T>G (p.Gly579=)
15g.73323138A>GCA491478656HCN4c.2955T>C (p.Gly985=)
c.1737T>C (p.Gly579=)
 dbSNP gnomAD v4
15g.73323138A>TCA491478657HCN4c.2955T>A (p.Gly985=)
c.1737T>A (p.Gly579=)
15g.73323139C>ACA393086690HCN4c.2954G>T (p.Gly985Val)
c.1736G>T (p.Gly579Val)
 gnomAD v4
15g.73323139C>GCA393086693HCN4c.2954G>C (p.Gly985Ala)
c.1736G>C (p.Gly579Ala)
15g.73323139C>TCA393086696HCN4c.2954G>A (p.Gly985Asp)
c.1736G>A (p.Gly579Asp)
15g.73323140C>ACA393086698HCN4c.2953G>T (p.Gly985Cys)
c.1735G>T (p.Gly579Cys)
 gnomAD v4
15g.73323140C>GCA393086706HCN4c.2953G>C (p.Gly985Arg)
c.1735G>C (p.Gly579Arg)
15g.73323140C>TCA393086709HCN4c.2953G>A (p.Gly985Ser)
c.1735G>A (p.Gly579Ser)
 gnomAD v4
15g.73323141T>ACA491478667HCN4c.2952A>T (p.Leu984=)
c.1734A>T (p.Leu578=)
 gnomAD v4
15g.73323141T>CCA7648916HCN4c.2952A>G (p.Leu984=)
c.1734A>G (p.Leu578=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323141T>GCA491478666HCN4c.2952A>C (p.Leu984=)
c.1734A>C (p.Leu578=)
15g.73323141T=CA2187187571HCN4c.2952A= (p.Leu984=)
c.1734A= (p.Leu578=)
15g.73323142A>CCA393086718HCN4c.2951T>G (p.Leu984Arg)
c.1733T>G (p.Leu578Arg)
15g.73323142A>GCA393086713HCN4c.2951T>C (p.Leu984Pro)
c.1733T>C (p.Leu578Pro)
 gnomAD v4
15g.73323142A>TCA393086714HCN4c.2951T>A (p.Leu984Gln)
c.1733T>A (p.Leu578Gln)
15g.73323143G>ACA491478668HCN4c.2950C>T (p.Leu984=)
c.1732C>T (p.Leu578=)
 gnomAD v4
15g.73323143G>CCA393086721HCN4c.2950C>G (p.Leu984Val)
c.1732C>G (p.Leu578Val)
 ClinVar dbSNP
15g.73323143G>TCA393086724HCN4c.2950C>A (p.Leu984Ile)
c.1732C>A (p.Leu578Ile)
 gnomAD v4
15g.73323143_73323144insTCA2804714152HCN4c.2949_2950insA (p.Leu984ThrfsTer19)
c.1731_1732insA (p.Leu578ThrfsTer19)
15g.73323144G>ACA272664002HCN4c.2949C>T (p.Ser983=)
c.1731C>T (p.Ser577=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323144G>CCA491478673HCN4c.2949C>G (p.Ser983=)
c.1731C>G (p.Ser577=)
15g.73323144G=CA2187187574HCN4c.2949C= (p.Ser983=)
c.1731C= (p.Ser577=)
15g.73323144G>TCA491478675HCN4c.2949C>A (p.Ser983=)
c.1731C>A (p.Ser577=)
 gnomAD v4
15g.73323145G>ACA7648917HCN4c.2948C>T (p.Ser983Phe)
c.1730C>T (p.Ser577Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323145G>CCA393086731HCN4c.2948C>G (p.Ser983Cys)
c.1730C>G (p.Ser577Cys)
15g.73323145G=CA2187187576HCN4c.2948C= (p.Ser983=)
c.1730C= (p.Ser577=)
15g.73323145G>TCA393086734HCN4c.2948C>A (p.Ser983Tyr)
c.1730C>A (p.Ser577Tyr)
 gnomAD v4
15g.73323146A>CCA393086736HCN4c.2947T>G (p.Ser983Ala)
c.1729T>G (p.Ser577Ala)
15g.73323146A>GCA393086741HCN4c.2947T>C (p.Ser983Pro)
c.1729T>C (p.Ser577Pro)
15g.73323146A>TCA393086739HCN4c.2947T>A (p.Ser983Thr)
c.1729T>A (p.Ser577Thr)
 gnomAD v4
15g.73323147C>ACA393086744HCN4c.2946G>T (p.Leu982Phe)
c.1728G>T (p.Leu576Phe)
 gnomAD v4
15g.73323147C=CA2187187581HCN4c.2946G= (p.Leu982=)
c.1728G= (p.Leu576=)
15g.73323147C>GCA393086747HCN4c.2946G>C (p.Leu982Phe)
c.1728G>C (p.Leu576Phe)
15g.73323147C>TCA16607136HCN4c.2946G>A (p.Leu982=)
c.1728G>A (p.Leu576=)
 ClinVar dbSNP gnomAD v4
15g.73323148A>CCA393086749HCN4c.2945T>G (p.Leu982Trp)
c.1727T>G (p.Leu576Trp)
15g.73323148A>GCA393086751HCN4c.2945T>C (p.Leu982Ser)
c.1727T>C (p.Leu576Ser)
 gnomAD v4
15g.73323148A>TCA393086753HCN4c.2945T>A (p.Leu982Ter)
c.1727T>A (p.Leu576Ter)
15g.73323149A>CCA393086755HCN4c.2944T>G (p.Leu982Val)
c.1726T>G (p.Leu576Val)
15g.73323149A>GCA491478682HCN4c.2944T>C (p.Leu982=)
c.1726T>C (p.Leu576=)
 ClinVar dbSNP gnomAD v4
15g.73323149A>TCA393086758HCN4c.2944T>A (p.Leu982Met)
c.1726T>A (p.Leu576Met)
15g.73323150C>ACA393086760HCN4c.2943G>T (p.Glu981Asp)
c.1725G>T (p.Glu575Asp)
 gnomAD v4
15g.73323150C>GCA393086762HCN4c.2943G>C (p.Glu981Asp)
c.1725G>C (p.Glu575Asp)
 gnomAD v4 COSMIC
15g.73323150C>TCA491478684HCN4c.2943G>A (p.Glu981=)
c.1725G>A (p.Glu575=)
 gnomAD v4
15g.73323159_73323250delCA619410578HCN4c.2852_2943del (p.Gly951ValfsTer21)
c.1634_1725del (p.Gly545ValfsTer21)
 gnomAD v2
15g.73323151T>ACA393086766HCN4c.2942A>T (p.Glu981Val)
c.1724A>T (p.Glu575Val)
15g.73323151T>CCA393086769HCN4c.2942A>G (p.Glu981Gly)
c.1724A>G (p.Glu575Gly)
 gnomAD v4
15g.73323151T>GCA393086771HCN4c.2942A>C (p.Glu981Ala)
c.1724A>C (p.Glu575Ala)
15g.73323152C>ACA393086774HCN4c.2941G>T (p.Glu981Ter)
c.1723G>T (p.Glu575Ter)
 ClinVar dbSNP gnomAD v4
15g.73323152C=CA2187187584HCN4c.2941G= (p.Glu981=)
c.1723G= (p.Glu575=)
15g.73323152C>GCA393086778HCN4c.2941G>C (p.Glu981Gln)
c.1723G>C (p.Glu575Gln)
15g.73323152C>TCA393086776HCN4c.2941G>A (p.Glu981Lys)
c.1723G>A (p.Glu575Lys)
 dbSNP gnomAD v2 gnomAD v4
15g.73323155delCA2629370546HCN4c.2941del (p.Glu981SerfsTer4)
c.1723del (p.Glu575SerfsTer4)
 gnomAD v4
15g.73323153C>ACA491478692HCN4c.2940G>T (p.Gly980=)
c.1722G>T (p.Gly574=)
 gnomAD v4
15g.73323153C>GCA491478694HCN4c.2940G>C (p.Gly980=)
c.1722G>C (p.Gly574=)
 ClinVar
15g.73323153C>TCA491478693HCN4c.2940G>A (p.Gly980=)
c.1722G>A (p.Gly574=)
 gnomAD v4 COSMIC
15g.73323154C>ACA393086782HCN4c.2939G>T (p.Gly980Val)
c.1721G>T (p.Gly574Val)
15g.73323154C=CA2187187591HCN4c.2939G= (p.Gly980=)
c.1721G= (p.Gly574=)
15g.73323154C>GCA7648918HCN4c.2939G>C (p.Gly980Ala)
c.1721G>C (p.Gly574Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323154C>TCA393086786HCN4c.2939G>A (p.Gly980Glu)
c.1721G>A (p.Gly574Glu)
 ClinVar gnomAD v4
15g.73323155C>ACA393086790HCN4c.2938G>T (p.Gly980Trp)
c.1720G>T (p.Gly574Trp)
 gnomAD v4 COSMIC
15g.73323155C=CA2187187599HCN4c.2938G= (p.Gly980=)
c.1720G= (p.Gly574=)
15g.73323155C>GCA393086791HCN4c.2938G>C (p.Gly980Arg)
c.1720G>C (p.Gly574Arg)
 ClinVar dbSNP gnomAD v4
15g.73323155C>TCA7648919HCN4c.2938G>A (p.Gly980Arg)
c.1720G>A (p.Gly574Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323156G>ACA7648920HCN4c.2937C>T (p.Pro979=)
c.1719C>T (p.Pro573=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323156G>CCA491478702HCN4c.2937C>G (p.Pro979=)
c.1719C>G (p.Pro573=)
 ClinVar dbSNP gnomAD v4
15g.73323156G=CA2187187605HCN4c.2937C= (p.Pro979=)
c.1719C= (p.Pro573=)
15g.73323156G>TCA7648921HCN4c.2937C>A (p.Pro979=)
c.1719C>A (p.Pro573=)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323158delCA2629370547HCN4c.2937del (p.Glu981SerfsTer4)
c.1719del (p.Glu575SerfsTer4)
 gnomAD v4
15g.73323157G>ACA393086799HCN4c.2936C>T (p.Pro979Leu)
c.1718C>T (p.Pro573Leu)
 gnomAD v4
15g.73323157G>CCA393086801HCN4c.2936C>G (p.Pro979Arg)
c.1718C>G (p.Pro573Arg)
15g.73323157G>TCA393086804HCN4c.2936C>A (p.Pro979His)
c.1718C>A (p.Pro573His)
15g.73323158G>ACA393086808HCN4c.2935C>T (p.Pro979Ser)
c.1717C>T (p.Pro573Ser)
 gnomAD v4
15g.73323158G>CCA393086811HCN4c.2935C>G (p.Pro979Ala)
c.1717C>G (p.Pro573Ala)
15g.73323158G>TCA393086813HCN4c.2935C>A (p.Pro979Thr)
c.1717C>A (p.Pro573Thr)
 gnomAD v4
15g.73323159A>CCA491478709HCN4c.2934T>G (p.Pro978=)
c.1716T>G (p.Pro572=)
15g.73323159A>GCA491478710HCN4c.2934T>C (p.Pro978=)
c.1716T>C (p.Pro572=)
 gnomAD v4
15g.73323159A>TCA491478711HCN4c.2934T>A (p.Pro978=)
c.1716T>A (p.Pro572=)
15g.73323160G>ACA393086817HCN4c.2933C>T (p.Pro978Leu)
c.1715C>T (p.Pro572Leu)
15g.73323160G>CCA393086823HCN4c.2933C>G (p.Pro978Arg)
c.1715C>G (p.Pro572Arg)
15g.73323160G>TCA393086819HCN4c.2933C>A (p.Pro978His)
c.1715C>A (p.Pro572His)
 gnomAD v4
15g.73323161G>ACA393086826HCN4c.2932C>T (p.Pro978Ser)
c.1714C>T (p.Pro572Ser)
 gnomAD v4
15g.73323161G>CCA393086829HCN4c.2932C>G (p.Pro978Ala)
c.1714C>G (p.Pro572Ala)
15g.73323161G=CA2187187614HCN4c.2932C= (p.Pro978=)
c.1714C= (p.Pro572=)
15g.73323161G>TCA393086830HCN4c.2932C>A (p.Pro978Thr)
c.1714C>A (p.Pro572Thr)
 dbSNP gnomAD v4
15g.73323162C>ACA393086832HCN4c.2931G>T (p.Gln977His)
c.1713G>T (p.Gln571His)
 dbSNP gnomAD v4
15g.73323162C=CA2187187618HCN4c.2931G= (p.Gln977=)
c.1713G= (p.Gln571=)
15g.73323162C>GCA393086836HCN4c.2931G>C (p.Gln977His)
c.1713G>C (p.Gln571His)
15g.73323162C>TCA491478717HCN4c.2931G>A (p.Gln977=)
c.1713G>A (p.Gln571=)
 gnomAD v4
15g.73323163T>ACA393086839HCN4c.2930A>T (p.Gln977Leu)
c.1712A>T (p.Gln571Leu)
15g.73323163T>CCA393086841HCN4c.2930A>G (p.Gln977Arg)
c.1712A>G (p.Gln571Arg)
 gnomAD v4
15g.73323163T>GCA393086844HCN4c.2930A>C (p.Gln977Pro)
c.1712A>C (p.Gln571Pro)
15g.73323164G>ACA393086848HCN4c.2929C>T (p.Gln977Ter)
c.1711C>T (p.Gln571Ter)
 dbSNP gnomAD v2 gnomAD v4
15g.73323164G>CCA393086850HCN4c.2929C>G (p.Gln977Glu)
c.1711C>G (p.Gln571Glu)
15g.73323164G=CA2187187620HCN4c.2929C= (p.Gln977=)
c.1711C= (p.Gln571=)
15g.73323164G>TCA393086853HCN4c.2929C>A (p.Gln977Lys)
c.1711C>A (p.Gln571Lys)
 ClinVar dbSNP gnomAD v4
15g.73323165G>ACA491478722HCN4c.2928C>T (p.Gly976=)
c.1710C>T (p.Gly570=)
 gnomAD v4
15g.73323165G>CCA491478723HCN4c.2928C>G (p.Gly976=)
c.1710C>G (p.Gly570=)
15g.73323165G>TCA491478724HCN4c.2928C>A (p.Gly976=)
c.1710C>A (p.Gly570=)
 gnomAD v4
15g.73323166C>ACA393086857HCN4c.2927G>T (p.Gly976Val)
c.1709G>T (p.Gly570Val)
 gnomAD v4
15g.73323166C>GCA393086863HCN4c.2927G>C (p.Gly976Ala)
c.1709G>C (p.Gly570Ala)
15g.73323166C>TCA393086859HCN4c.2927G>A (p.Gly976Asp)
c.1709G>A (p.Gly570Asp)
 gnomAD v4
15g.73323168delCA2629370548HCN4c.2927del (p.Gly976AlafsTer9)
c.1709del (p.Gly570AlafsTer9)
 gnomAD v4
15g.73323167C>ACA393086868HCN4c.2926G>T (p.Gly976Cys)
c.1708G>T (p.Gly570Cys)
 gnomAD v4
15g.73323167C>GCA393086873HCN4c.2926G>C (p.Gly976Arg)
c.1708G>C (p.Gly570Arg)
15g.73323167C>TCA393086870HCN4c.2926G>A (p.Gly976Ser)
c.1708G>A (p.Gly570Ser)
15g.73323168C>ACA491478726HCN4c.2925G>T (p.Leu975=)
c.1707G>T (p.Leu569=)
 gnomAD v4
15g.73323168C>GCA491478727HCN4c.2925G>C (p.Leu975=)
c.1707G>C (p.Leu569=)
15g.73323168C>TCA491478728HCN4c.2925G>A (p.Leu975=)
c.1707G>A (p.Leu569=)
15g.73323169A>CCA393086875HCN4c.2924T>G (p.Leu975Arg)
c.1706T>G (p.Leu569Arg)
 gnomAD v4
15g.73323169A>GCA393086877HCN4c.2924T>C (p.Leu975Pro)
c.1706T>C (p.Leu569Pro)
 gnomAD v4
15g.73323169A>TCA393086878HCN4c.2924T>A (p.Leu975Gln)
c.1706T>A (p.Leu569Gln)
15g.73323170G>ACA7648922HCN4c.2923C>T (p.Leu975=)
c.1705C>T (p.Leu569=)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323170G>CCA393086882HCN4c.2923C>G (p.Leu975Val)
c.1705C>G (p.Leu569Val)
15g.73323170G=CA2187187624HCN4c.2923C= (p.Leu975=)
c.1705C= (p.Leu569=)
15g.73323170G>TCA393086885HCN4c.2923C>A (p.Leu975Met)
c.1705C>A (p.Leu569Met)
 gnomAD v4
15g.73323171C>ACA393086889HCN4c.2922G>T (p.Gln974His)
c.1704G>T (p.Gln568His)
 gnomAD v4
15g.73323171C>GCA393086892HCN4c.2922G>C (p.Gln974His)
c.1704G>C (p.Gln568His)
15g.73323171C>TCA491478731HCN4c.2922G>A (p.Gln974=)
c.1704G>A (p.Gln568=)
 ClinVar dbSNP gnomAD v4
15g.73323172T>ACA393086896HCN4c.2921A>T (p.Gln974Leu)
c.1703A>T (p.Gln568Leu)
15g.73323172T>CCA393086901HCN4c.2921A>G (p.Gln974Arg)
c.1703A>G (p.Gln568Arg)
 dbSNP
15g.73323172T>GCA393086904HCN4c.2921A>C (p.Gln974Pro)
c.1703A>C (p.Gln568Pro)
15g.73323172T=CA2187187627HCN4c.2921A= (p.Gln974=)
c.1703A= (p.Gln568=)
15g.73323173G>ACA393086910HCN4c.2920C>T (p.Gln974Ter)
c.1702C>T (p.Gln568Ter)
 gnomAD v4
15g.73323173G>CCA393086906HCN4c.2920C>G (p.Gln974Glu)
c.1702C>G (p.Gln568Glu)
15g.73323173G>TCA393086907HCN4c.2920C>A (p.Gln974Lys)
c.1702C>A (p.Gln568Lys)
 gnomAD v4
15g.73323174C>ACA491478736HCN4c.2919G>T (p.Gly973=)
c.1701G>T (p.Gly567=)
 gnomAD v4
15g.73323174C>GCA491478738HCN4c.2919G>C (p.Gly973=)
c.1701G>C (p.Gly567=)
15g.73323174C>TCA491478740HCN4c.2919G>A (p.Gly973=)
c.1701G>A (p.Gly567=)
 ClinVar dbSNP gnomAD v4
15g.73323175C>ACA393086911HCN4c.2918G>T (p.Gly973Val)
c.1700G>T (p.Gly567Val)
 gnomAD v4
15g.73323175C=CA2187187632HCN4c.2918G= (p.Gly973=)
c.1700G= (p.Gly567=)
15g.73323175C>GCA393086914HCN4c.2918G>C (p.Gly973Ala)
c.1700G>C (p.Gly567Ala)
15g.73323175C>TCA7648923HCN4c.2918G>A (p.Gly973Glu)
c.1700G>A (p.Gly567Glu)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323176C>ACA7648925HCN4c.2917G>T (p.Gly973Trp)
c.1699G>T (p.Gly567Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323176C=CA2187187636HCN4c.2917G= (p.Gly973=)
c.1699G= (p.Gly567=)
15g.73323176C>GCA393086921HCN4c.2917G>C (p.Gly973Arg)
c.1699G>C (p.Gly567Arg)
 gnomAD v4
15g.73323176C>TCA7648924HCN4c.2917G>A (p.Gly973Arg)
c.1699G>A (p.Gly567Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323176_73323177insACA2629370550HCN4c.2916_2917insT (p.Gly973TrpfsTer30)
c.1698_1699insT (p.Gly567TrpfsTer30)
 gnomAD v4
15g.73323177G>ACA7648926HCN4c.2916C>T (p.Pro972=)
c.1698C>T (p.Pro566=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73323177G>CCA491478743HCN4c.2916C>G (p.Pro972=)
c.1698C>G (p.Pro566=)
 gnomAD v4
15g.73323177G=CA2187187641HCN4c.2916C= (p.Pro972=)
c.1698C= (p.Pro566=)
15g.73323177G>TCA491478744HCN4c.2916C>A (p.Pro972=)
c.1698C>A (p.Pro566=)
 dbSNP gnomAD v4
15g.73323180delCA2629370549HCN4c.2916del (p.Gln974SerfsTer11)
c.1698del (p.Gln568SerfsTer11)
 gnomAD v4
15g.73323178G>ACA393086926HCN4c.2915C>T (p.Pro972Leu)
c.1697C>T (p.Pro566Leu)
 gnomAD v4
15g.73323178G>CCA393086928HCN4c.2915C>G (p.Pro972Arg)
c.1697C>G (p.Pro566Arg)
15g.73323178G>TCA393086930HCN4c.2915C>A (p.Pro972His)
c.1697C>A (p.Pro566His)
 gnomAD v4
15g.73323179G>ACA7648927HCN4c.2914C>T (p.Pro972Ser)
c.1696C>T (p.Pro566Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
15g.73323179G>CCA393086937HCN4c.2914C>G (p.Pro972Ala)
c.1696C>G (p.Pro566Ala)
15g.73323179G=CA2187187647HCN4c.2914C= (p.Pro972=)
c.1696C= (p.Pro566=)
15g.73323179G>TCA393086932HCN4c.2914C>A (p.Pro972Thr)
c.1696C>A (p.Pro566Thr)
 gnomAD v4
15g.73323180G>ACA491478751HCN4c.2913C>T (p.Ser971=)
c.1695C>T (p.Ser565=)
 gnomAD v4
15g.73323180G>CCA393086940HCN4c.2913C>G (p.Ser971Arg)
c.1695C>G (p.Ser565Arg)
15g.73323180G>TCA393086941HCN4c.2913C>A (p.Ser971Arg)
c.1695C>A (p.Ser565Arg)
 gnomAD v4
15g.73323181C>ACA393086944HCN4c.2912G>T (p.Ser971Ile)
c.1694G>T (p.Ser565Ile)
 gnomAD v4
15g.73323181C=CA2187187650HCN4c.2912G= (p.Ser971=)
c.1694G= (p.Ser565=)
15g.73323181C>GCA393086948HCN4c.2912G>C (p.Ser971Thr)
c.1694G>C (p.Ser565Thr)
 gnomAD v4
15g.73323181C>TCA393086951HCN4c.2912G>A (p.Ser971Asn)
c.1694G>A (p.Ser565Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73323182T>ACA393086953HCN4c.2911A>T (p.Ser971Cys)
c.1693A>T (p.Ser565Cys)
15g.73323182T>CCA393086955HCN4c.2911A>G (p.Ser971Gly)
c.1693A>G (p.Ser565Gly)
15g.73323182T>GCA393086957HCN4c.2911A>C (p.Ser971Arg)
c.1693A>C (p.Ser565Arg)
15g.73323183_73323186dupCA2575783830HCN4c.2908_2911dup (p.Ser971IlefsTer2)
c.1690_1693dup (p.Ser565IlefsTer2)
15g.73323183A>CCA491478764HCN4c.2910T>G (p.Ser970=)
c.1692T>G (p.Ser564=)
 gnomAD v4
15g.73323183A>GCA491478760HCN4c.2910T>C (p.Ser970=)
c.1692T>C (p.Ser564=)
 ClinVar dbSNP gnomAD v4
15g.73323183A>TCA491478762HCN4c.2910T>A (p.Ser970=)
c.1692T>A (p.Ser564=)
 gnomAD v4
15g.73323183_73323186delinsAGATCA2187187652HCN4c.2907_2910delinsATCT (p.Ser969=)
c.1689_1692delinsATCT (p.Ser563=)
15g.73323184G>ACA393086960HCN4c.2909C>T (p.Ser970Phe)
c.1691C>T (p.Ser564Phe)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73323184G>CCA393086963HCN4c.2909C>G (p.Ser970Cys)
c.1691C>G (p.Ser564Cys)
15g.73323184G=CA2187187656HCN4c.2909C= (p.Ser970=)
c.1691C= (p.Ser564=)
15g.73323184G>TCA393086965HCN4c.2909C>A (p.Ser970Tyr)
c.1691C>A (p.Ser564Tyr)
 gnomAD v4
15g.73323186_73323188delCA2187187654HCN4c.2907_2909del (p.Ser970del)
c.1689_1691del (p.Ser564del)
 dbSNP

Number of alleles fetched