Chr Mutation (hg38) CAid Gene Transcript Linkouts
15g.73322870_73322897delinsTGAGCGGGGGTGTGCCCCGGCGCTGGGGCA2187186841HCN4c.3196_3223delinsCCCCAGCGCCGGGGCACACCCCCGCTCA (p.Pro1066=)
c.1978_2005delinsCCCCAGCGCCGGGGCACACCCCCGCTCA (p.Pro660=)
15g.73322873_73322899delCA2187186847HCN4c.3196_3222del (p.Pro1066_Leu1074del)
c.1978_2004del (p.Pro660_Leu668del)
 dbSNP
15g.73322875_73322902delinsGGGGGTGTGCCCCGGCGCTGGGGGACCTCA2187186862HCN4c.3191_3218delinsAGGTCCCCCAGCGCCGGGGCACACCCCC (p.Gln1064=)
c.1973_2000delinsAGGTCCCCCAGCGCCGGGGCACACCCCC (p.Gln658=)
15g.73322882_73322908delCA7648866HCN4c.3191_3217del (p.Gln1064_Pro1072del)
c.1973_1999del (p.Gln658_Pro666del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322898delCA2575783819HCN4c.3199del (p.Gln1067SerfsTer?)
c.1981del (p.Gln661SerfsTer?)
 gnomAD v4
15g.73322895G>ACA491477931HCN4c.3198C>T (p.Pro1066=)
c.1980C>T (p.Pro660=)
 gnomAD v4
15g.73322895G>CCA491477932HCN4c.3198C>G (p.Pro1066=)
c.1980C>G (p.Pro660=)
15g.73322895G>TCA491477933HCN4c.3198C>A (p.Pro1066=)
c.1980C>A (p.Pro660=)
 gnomAD v4
15g.73322896G>ACA393086026HCN4c.3197C>T (p.Pro1066Leu)
c.1979C>T (p.Pro660Leu)
 gnomAD v4
15g.73322896G>CCA393086027HCN4c.3197C>G (p.Pro1066Arg)
c.1979C>G (p.Pro660Arg)
15g.73322896G=CA2187186921HCN4c.3197C= (p.Pro1066=)
c.1979C= (p.Pro660=)
15g.73322896G>TCA247667HCN4c.3197C>A (p.Pro1066His)
c.1979C>A (p.Pro660His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322897G>ACA393086028HCN4c.3196C>T (p.Pro1066Ser)
c.1978C>T (p.Pro660Ser)
 gnomAD v4
15g.73322897G>CCA393086029HCN4c.3196C>G (p.Pro1066Ala)
c.1978C>G (p.Pro660Ala)
15g.73322897G>TCA393086030HCN4c.3196C>A (p.Pro1066Thr)
c.1978C>A (p.Pro660Thr)
 gnomAD v4
15g.73322898G>ACA491477938HCN4c.3195C>T (p.Val1065=)
c.1977C>T (p.Val659=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322898G>CCA272663629HCN4c.3195C>G (p.Val1065=)
c.1977C>G (p.Val659=)
 dbSNP gnomAD v4
15g.73322898G=CA2187186925HCN4c.3195C= (p.Val1065=)
c.1977C= (p.Val659=)
15g.73322898G>TCA7648873HCN4c.3195C>A (p.Val1065=)
c.1977C>A (p.Val659=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322899A=CA2187186933HCN4c.3194T= (p.Val1065=)
c.1976T= (p.Val659=)
15g.73322899A>CCA393086031HCN4c.3194T>G (p.Val1065Gly)
c.1976T>G (p.Val659Gly)
 gnomAD v4
15g.73322899A>GCA393086032HCN4c.3194T>C (p.Val1065Ala)
c.1976T>C (p.Val659Ala)
 ClinVar dbSNP gnomAD v4
15g.73322899A>TCA393086033HCN4c.3194T>A (p.Val1065Asp)
c.1976T>A (p.Val659Asp)
15g.73322900C>ACA393086036HCN4c.3193G>T (p.Val1065Phe)
c.1975G>T (p.Val659Phe)
 gnomAD v4
15g.73322900C=CA2187186938HCN4c.3193G= (p.Val1065=)
c.1975G= (p.Val659=)
15g.73322900C>GCA393086035HCN4c.3193G>C (p.Val1065Leu)
c.1975G>C (p.Val659Leu)
 gnomAD v4
15g.73322900C>TCA393086034HCN4c.3193G>A (p.Val1065Ile)
c.1975G>A (p.Val659Ile)
 ClinVar dbSNP gnomAD v4
15g.73322901C>ACA393086037HCN4c.3192G>T (p.Gln1064His)
c.1974G>T (p.Gln658His)
 gnomAD v4
15g.73322901C=CA2187186943HCN4c.3192G= (p.Gln1064=)
c.1974G= (p.Gln658=)
15g.73322901C>GCA393086038HCN4c.3192G>C (p.Gln1064His)
c.1974G>C (p.Gln658His)
 ClinVar dbSNP gnomAD v4
15g.73322901C>TCA491477942HCN4c.3192G>A (p.Gln1064=)
c.1974G>A (p.Gln658=)
 dbSNP gnomAD v4
15g.73322905_73322920delCA2629370534HCN4c.3177_3192del (p.Ser1059ArgfsTer?)
c.1959_1974del (p.Ser653ArgfsTer?)
 gnomAD v4
15g.73322902T>ACA393086039HCN4c.3191A>T (p.Gln1064Leu)
c.1973A>T (p.Gln658Leu)
 gnomAD v4
15g.73322902T>CCA393086041HCN4c.3191A>G (p.Gln1064Arg)
c.1973A>G (p.Gln658Arg)
 gnomAD v4
15g.73322902T>GCA393086040HCN4c.3191A>C (p.Gln1064Pro)
c.1973A>C (p.Gln658Pro)
 dbSNP gnomAD v3 gnomAD v4
15g.73322902T=CA2187186945HCN4c.3191A= (p.Gln1064=)
c.1973A= (p.Gln658=)
15g.73322907_73322914delCA2629370535HCN4c.3184_3191del (p.Pro1062GlyfsTer?)
c.1966_1973del (p.Pro656GlyfsTer?)
 gnomAD v4
15g.73322903G>ACA393086042HCN4c.3190C>T (p.Gln1064Ter)
c.1972C>T (p.Gln658Ter)
 gnomAD v4
15g.73322903G>CCA393086043HCN4c.3190C>G (p.Gln1064Glu)
c.1972C>G (p.Gln658Glu)
 gnomAD v4
15g.73322903G=CA2187186950HCN4c.3190C= (p.Gln1064=)
c.1972C= (p.Gln658=)
15g.73322903G>TCA393086044HCN4c.3190C>A (p.Gln1064Lys)
c.1972C>A (p.Gln658Lys)
 gnomAD v4
15g.73322904_73322906dupCA2804714144HCN4c.3188_3190dup (p.Pro1063_Gln1064insPro)
c.1970_1972dup (p.Pro657_Gln658insPro)
15g.73322906delCA2575783820HCN4c.3190del (p.Gln1064ArgfsTer?)
c.1972del (p.Gln658ArgfsTer?)
 gnomAD v4
15g.73322904G>ACA491477944HCN4c.3189C>T (p.Pro1063=)
c.1971C>T (p.Pro657=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322904G>CCA491477945HCN4c.3189C>G (p.Pro1063=)
c.1971C>G (p.Pro657=)
15g.73322904G=CA2187186953HCN4c.3189C= (p.Pro1063=)
c.1971C= (p.Pro657=)
15g.73322904G>TCA491477946HCN4c.3189C>A (p.Pro1063=)
c.1971C>A (p.Pro657=)
 dbSNP gnomAD v2 gnomAD v4
15g.73322904_73322924dupCA619410586HCN4c.3169_3189dup (p.Pro1063_Gln1064insAlaSerSerProProProPro)
c.1951_1971dup (p.Pro657_Gln658insAlaSerSerProProProPro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322905G>ACA393086045HCN4c.3188C>T (p.Pro1063Leu)
c.1970C>T (p.Pro657Leu)
 gnomAD v4
15g.73322905G>CCA393086046HCN4c.3188C>G (p.Pro1063Arg)
c.1970C>G (p.Pro657Arg)
 gnomAD v4
15g.73322905G=CA2187186957HCN4c.3188C= (p.Pro1063=)
c.1970C= (p.Pro657=)
15g.73322905G>TCA393086047HCN4c.3188C>A (p.Pro1063His)
c.1970C>A (p.Pro657His)
 dbSNP gnomAD v4
15g.73322906G>ACA393086048HCN4c.3187C>T (p.Pro1063Ser)
c.1969C>T (p.Pro657Ser)
 ClinVar gnomAD v4
15g.73322906G>CCA393086049HCN4c.3187C>G (p.Pro1063Ala)
c.1969C>G (p.Pro657Ala)
15g.73322906G=CA2187186960HCN4c.3187C= (p.Pro1063=)
c.1969C= (p.Pro657=)
15g.73322906G>TCA7648874HCN4c.3187C>A (p.Pro1063Thr)
c.1969C>A (p.Pro657Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322907T>ACA491477949HCN4c.3186A>T (p.Pro1062=)
c.1968A>T (p.Pro656=)
15g.73322907T>CCA491477950HCN4c.3186A>G (p.Pro1062=)
c.1968A>G (p.Pro656=)
 ClinVar gnomAD v4
15g.73322907T>GCA491477948HCN4c.3186A>C (p.Pro1062=)
c.1968A>C (p.Pro656=)
 dbSNP gnomAD v3 gnomAD v4
15g.73322907T=CA2187186963HCN4c.3186A= (p.Pro1062=)
c.1968A= (p.Pro656=)
15g.73322910_73322920delCA2629370536HCN4c.3176_3186del (p.Ser1059ThrfsTer?)
c.1958_1968del (p.Ser653ThrfsTer?)
 gnomAD v4
15g.73322908G>ACA393086050HCN4c.3185C>T (p.Pro1062Leu)
c.1967C>T (p.Pro656Leu)
 dbSNP gnomAD v2 gnomAD v4
15g.73322908G>CCA393086051HCN4c.3185C>G (p.Pro1062Arg)
c.1967C>G (p.Pro656Arg)
15g.73322908G=CA2187186965HCN4c.3185C= (p.Pro1062=)
c.1967C= (p.Pro656=)
15g.73322908G>TCA393086052HCN4c.3185C>A (p.Pro1062Gln)
c.1967C>A (p.Pro656Gln)
 gnomAD v4
15g.73322909delCA2575783821HCN4c.3185del (p.Pro1062HisfsTer?)
c.1967del (p.Pro656HisfsTer?)
15g.73322913_73322930delCA2629370537HCN4c.3168_3185del (p.Ala1057_Pro1062del)
c.1950_1967del (p.Ala651_Pro656del)
 gnomAD v4
15g.73322909G>ACA393086055HCN4c.3184C>T (p.Pro1062Ser)
c.1966C>T (p.Pro656Ser)
 ClinVar dbSNP gnomAD v4
15g.73322909G>CCA393086053HCN4c.3184C>G (p.Pro1062Ala)
c.1966C>G (p.Pro656Ala)
 ClinVar
15g.73322909G=CA2187186968HCN4c.3184C= (p.Pro1062=)
c.1966C= (p.Pro656=)
15g.73322909G>TCA393086054HCN4c.3184C>A (p.Pro1062Thr)
c.1966C>A (p.Pro656Thr)
 ClinVar gnomAD v4
15g.73322910T>ACA491477953HCN4c.3183A>T (p.Pro1061=)
c.1965A>T (p.Pro655=)
15g.73322910T>CCA491477957HCN4c.3183A>G (p.Pro1061=)
c.1965A>G (p.Pro655=)
 dbSNP gnomAD v2 gnomAD v4
15g.73322910T>GCA491477955HCN4c.3183A>C (p.Pro1061=)
c.1965A>C (p.Pro655=)
 dbSNP gnomAD v3 gnomAD v4
15g.73322910T=CA2187186970HCN4c.3183A= (p.Pro1061=)
c.1965A= (p.Pro655=)
15g.73322911G>ACA272663655HCN4c.3182C>T (p.Pro1061Leu)
c.1964C>T (p.Pro655Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322911G>CCA16622141HCN4c.3182C>G (p.Pro1061Arg)
c.1964C>G (p.Pro655Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322911G=CA2187186974HCN4c.3182C= (p.Pro1061=)
c.1964C= (p.Pro655=)
15g.73322911G>TCA393086056HCN4c.3182C>A (p.Pro1061Gln)
c.1964C>A (p.Pro655Gln)
 ClinVar dbSNP gnomAD v4
15g.73322916dupCA2629370538HCN4c.3182dup (p.Pro1062ThrfsTer?)
c.1964dup (p.Pro656ThrfsTer?)
 gnomAD v4
15g.73322916delCA491477958HCN4c.3182del (p.Pro1061HisfsTer?)
c.1964del (p.Pro655HisfsTer?)
 gnomAD v4 COSMIC
15g.73322915_73322916delCA2629370540HCN4c.3181_3182del (p.Pro1061ThrfsTer?)
c.1963_1964del (p.Pro655ThrfsTer?)
 gnomAD v4
15g.73322914_73322916delCA2629370539HCN4c.3180_3182del (p.Pro1061del)
c.1962_1964del (p.Pro655del)
 gnomAD v4
15g.73322912G>ACA393086057HCN4c.3181C>T (p.Pro1061Ser)
c.1963C>T (p.Pro655Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322912G>CCA393086058HCN4c.3181C>G (p.Pro1061Ala)
c.1963C>G (p.Pro655Ala)
15g.73322912G=CA2187186976HCN4c.3181C= (p.Pro1061=)
c.1963C= (p.Pro655=)
15g.73322912G>TCA393086059HCN4c.3181C>A (p.Pro1061Thr)
c.1963C>A (p.Pro655Thr)
 gnomAD v4
15g.73322913G>ACA491477962HCN4c.3180C>T (p.Pro1060=)
c.1962C>T (p.Pro654=)
 gnomAD v4 COSMIC
15g.73322913G>CCA491477963HCN4c.3180C>G (p.Pro1060=)
c.1962C>G (p.Pro654=)
 gnomAD v4
15g.73322913G>TCA491477964HCN4c.3180C>A (p.Pro1060=)
c.1962C>A (p.Pro654=)
 gnomAD v4
15g.73322914G>ACA393086060HCN4c.3179C>T (p.Pro1060Leu)
c.1961C>T (p.Pro654Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322914G>CCA272663662HCN4c.3179C>G (p.Pro1060Arg)
c.1961C>G (p.Pro654Arg)
 ClinVar dbSNP gnomAD v4
15g.73322914G=CA2187186980HCN4c.3179C= (p.Pro1060=)
c.1961C= (p.Pro654=)
15g.73322914G>TCA7648875HCN4c.3179C>A (p.Pro1060His)
c.1961C>A (p.Pro654His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322915G>ACA393086061HCN4c.3178C>T (p.Pro1060Ser)
c.1960C>T (p.Pro654Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322915G>CCA393086062HCN4c.3178C>G (p.Pro1060Ala)
c.1960C>G (p.Pro654Ala)
 gnomAD v4
15g.73322915G=CA2187186985HCN4c.3178C= (p.Pro1060=)
c.1960C= (p.Pro654=)
15g.73322915G>TCA393086063HCN4c.3178C>A (p.Pro1060Thr)
c.1960C>A (p.Pro654Thr)
 gnomAD v4
15g.73322916G>ACA491477969HCN4c.3177C>T (p.Ser1059=)
c.1959C>T (p.Ser653=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322916G>CCA393086064HCN4c.3177C>G (p.Ser1059Arg)
c.1959C>G (p.Ser653Arg)
15g.73322916G=CA2187186988HCN4c.3177C= (p.Ser1059=)
c.1959C= (p.Ser653=)
15g.73322916G>TCA393086065HCN4c.3177C>A (p.Ser1059Arg)
c.1959C>A (p.Ser653Arg)
 gnomAD v4
15g.73322917C>ACA393086066HCN4c.3176G>T (p.Ser1059Ile)
c.1958G>T (p.Ser653Ile)
 gnomAD v4
15g.73322917C>GCA393086067HCN4c.3176G>C (p.Ser1059Thr)
c.1958G>C (p.Ser653Thr)
 gnomAD v4
15g.73322917C>TCA393086068HCN4c.3176G>A (p.Ser1059Asn)
c.1958G>A (p.Ser653Asn)
 gnomAD v4
15g.73322918T>ACA393086069HCN4c.3175A>T (p.Ser1059Cys)
c.1957A>T (p.Ser653Cys)
15g.73322918T>CCA393086070HCN4c.3175A>G (p.Ser1059Gly)
c.1957A>G (p.Ser653Gly)
 gnomAD v4
15g.73322918T>GCA393086071HCN4c.3175A>C (p.Ser1059Arg)
c.1957A>C (p.Ser653Arg)
 gnomAD v3 gnomAD v4
15g.73322919G>ACA491477974HCN4c.3174C>T (p.Ser1058=)
c.1956C>T (p.Ser652=)
 ClinVar dbSNP gnomAD v4
15g.73322919G>CCA491477975HCN4c.3174C>G (p.Ser1058=)
c.1956C>G (p.Ser652=)
15g.73322919G>TCA491477976HCN4c.3174C>A (p.Ser1058=)
c.1956C>A (p.Ser652=)
 gnomAD v4
15g.73322920delCA2575783822HCN4c.3174del (p.Ser1059AlafsTer?)
c.1956del (p.Ser653AlafsTer?)
15g.73322920G>ACA393086072HCN4c.3173C>T (p.Ser1058Phe)
c.1955C>T (p.Ser652Phe)
 gnomAD v4
15g.73322920G>CCA393086073HCN4c.3173C>G (p.Ser1058Cys)
c.1955C>G (p.Ser652Cys)
15g.73322920G>TCA393086074HCN4c.3173C>A (p.Ser1058Tyr)
c.1955C>A (p.Ser652Tyr)
 gnomAD v4
15g.73322921A=CA2187186995HCN4c.3172T= (p.Ser1058=)
c.1954T= (p.Ser652=)
15g.73322921A>CCA16620005HCN4c.3172T>G (p.Ser1058Ala)
c.1954T>G (p.Ser652Ala)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322921A>GCA393086075HCN4c.3172T>C (p.Ser1058Pro)
c.1954T>C (p.Ser652Pro)
 gnomAD v4
15g.73322921A>TCA393086076HCN4c.3172T>A (p.Ser1058Thr)
c.1954T>A (p.Ser652Thr)
15g.73322922T>ACA491477980HCN4c.3171A>T (p.Ala1057=)
c.1953A>T (p.Ala651=)
15g.73322922T>CCA491477981HCN4c.3171A>G (p.Ala1057=)
c.1953A>G (p.Ala651=)
 ClinVar dbSNP gnomAD v4
15g.73322922T>GCA16607864HCN4c.3171A>C (p.Ala1057=)
c.1953A>C (p.Ala651=)
 ClinVar dbSNP
15g.73322922T=CA2187186999HCN4c.3171A= (p.Ala1057=)
c.1953A= (p.Ala651=)
15g.73322922dupCA2575783823HCN4c.3171dup (p.Ser1058IlefsTer?)
c.1953dup (p.Ser652IlefsTer?)
15g.73322923G>ACA393086079HCN4c.3170C>T (p.Ala1057Val)
c.1952C>T (p.Ala651Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322923G>CCA393086078HCN4c.3170C>G (p.Ala1057Gly)
c.1952C>G (p.Ala651Gly)
15g.73322923G=CA2187187005HCN4c.3170C= (p.Ala1057=)
c.1952C= (p.Ala651=)
15g.73322923G>TCA393086077HCN4c.3170C>A (p.Ala1057Glu)
c.1952C>A (p.Ala651Glu)
 gnomAD v4
15g.73322924C>ACA393086080HCN4c.3169G>T (p.Ala1057Ser)
c.1951G>T (p.Ala651Ser)
 gnomAD v4
15g.73322924C>GCA393086081HCN4c.3169G>C (p.Ala1057Pro)
c.1951G>C (p.Ala651Pro)
 gnomAD v4
15g.73322924C>TCA393086082HCN4c.3169G>A (p.Ala1057Thr)
c.1951G>A (p.Ala651Thr)
 gnomAD v4
15g.73322925A=CA2187187007HCN4c.3168T= (p.Pro1056=)
c.1950T= (p.Pro650=)
15g.73322925A>CCA491477982HCN4c.3168T>G (p.Pro1056=)
c.1950T>G (p.Pro650=)
15g.73322925A>GCA491477983HCN4c.3168T>C (p.Pro1056=)
c.1950T>C (p.Pro650=)
 dbSNP gnomAD v4
15g.73322925A>TCA491477985HCN4c.3168T>A (p.Pro1056=)
c.1950T>A (p.Pro650=)
 gnomAD v4
15g.73322925_73322927delinsGGGTGGTGGGGGGCTGGATGCAGTCA2580089971HCN4c.3166_3168delinsACTGCATCCAGCCCCCCACCACCC (p.Pro1055_Pro1056insThrAlaSerSerProProPro)
c.1948_1950delinsACTGCATCCAGCCCCCCACCACCC (p.Pro649_Pro650insThrAlaSerSerProProPro)
 ClinVar
15g.73322926G>ACA393086083HCN4c.3167C>T (p.Pro1056Leu)
c.1949C>T (p.Pro650Leu)
 gnomAD v4
15g.73322926G>CCA393086084HCN4c.3167C>G (p.Pro1056Arg)
c.1949C>G (p.Pro650Arg)
 dbSNP
15g.73322926G=CA2187187010HCN4c.3167C= (p.Pro1056=)
c.1949C= (p.Pro650=)
15g.73322926G>TCA393086085HCN4c.3167C>A (p.Pro1056His)
c.1949C>A (p.Pro650His)
 gnomAD v4
15g.73322927G>ACA393086086HCN4c.3166C>T (p.Pro1056Ser)
c.1948C>T (p.Pro650Ser)
 gnomAD v4
15g.73322927G>CCA393086087HCN4c.3166C>G (p.Pro1056Ala)
c.1948C>G (p.Pro650Ala)
 ClinVar gnomAD v4
15g.73322927G=CA2187187014HCN4c.3166C= (p.Pro1056=)
c.1948C= (p.Pro650=)
15g.73322927G>TCA272663675HCN4c.3166C>A (p.Pro1056Thr)
c.1948C>A (p.Pro650Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322928T>ACA491477991HCN4c.3165A>T (p.Pro1055=)
c.1947A>T (p.Pro649=)
 gnomAD v4
15g.73322928T>CCA491477990HCN4c.3165A>G (p.Pro1055=)
c.1947A>G (p.Pro649=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322928T>GCA491477989HCN4c.3165A>C (p.Pro1055=)
c.1947A>C (p.Pro649=)
 gnomAD v4
15g.73322928T=CA2187187018HCN4c.3165A= (p.Pro1055=)
c.1947A= (p.Pro649=)
15g.73322929G>ACA393086088HCN4c.3164C>T (p.Pro1055Leu)
c.1946C>T (p.Pro649Leu)
 gnomAD v4
15g.73322929G>CCA393086089HCN4c.3164C>G (p.Pro1055Arg)
c.1946C>G (p.Pro649Arg)
15g.73322929G>TCA393086090HCN4c.3164C>A (p.Pro1055Gln)
c.1946C>A (p.Pro649Gln)
 gnomAD v4
15g.73322930G>ACA393086093HCN4c.3163C>T (p.Pro1055Ser)
c.1945C>T (p.Pro649Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322930G>CCA393086092HCN4c.3163C>G (p.Pro1055Ala)
c.1945C>G (p.Pro649Ala)
15g.73322930G=CA2187187020HCN4c.3163C= (p.Pro1055=)
c.1945C= (p.Pro649=)
15g.73322930G>TCA393086091HCN4c.3163C>A (p.Pro1055Thr)
c.1945C>A (p.Pro649Thr)
 gnomAD v4
15g.73322931C>ACA491477995HCN4c.3162G>T (p.Leu1054=)
c.1944G>T (p.Leu648=)
 gnomAD v4
15g.73322931C>GCA491477996HCN4c.3162G>C (p.Leu1054=)
c.1944G>C (p.Leu648=)
 gnomAD v4
15g.73322931C>TCA491477997HCN4c.3162G>A (p.Leu1054=)
c.1944G>A (p.Leu648=)
 gnomAD v4
15g.73322932A>CCA393086094HCN4c.3161T>G (p.Leu1054Arg)
c.1943T>G (p.Leu648Arg)
15g.73322932A>GCA393086096HCN4c.3161T>C (p.Leu1054Pro)
c.1943T>C (p.Leu648Pro)
 gnomAD v4
15g.73322932A>TCA393086095HCN4c.3161T>A (p.Leu1054Gln)
c.1943T>A (p.Leu648Gln)
 gnomAD v4
15g.73322933G>ACA491478001HCN4c.3160C>T (p.Leu1054=)
c.1942C>T (p.Leu648=)
 gnomAD v4
15g.73322933G>CCA393086097HCN4c.3160C>G (p.Leu1054Val)
c.1942C>G (p.Leu648Val)
15g.73322933G>TCA393086098HCN4c.3160C>A (p.Leu1054Met)
c.1942C>A (p.Leu648Met)
 gnomAD v4
15g.73322934G>ACA491478002HCN4c.3159C>T (p.Leu1053=)
c.1941C>T (p.Leu647=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322934G>CCA491478004HCN4c.3159C>G (p.Leu1053=)
c.1941C>G (p.Leu647=)
15g.73322934G=CA2187187022HCN4c.3159C= (p.Leu1053=)
c.1941C= (p.Leu647=)
15g.73322934G>TCA491478003HCN4c.3159C>A (p.Leu1053=)
c.1941C>A (p.Leu647=)
 gnomAD v4
15g.73322935A=CA2187187027HCN4c.3158T= (p.Leu1053=)
c.1940T= (p.Leu647=)
15g.73322935A>CCA393086099HCN4c.3158T>G (p.Leu1053Arg)
c.1940T>G (p.Leu647Arg)
15g.73322935A>GCA393086100HCN4c.3158T>C (p.Leu1053Pro)
c.1940T>C (p.Leu647Pro)
 ClinVar dbSNP gnomAD v4
15g.73322935A>TCA393086101HCN4c.3158T>A (p.Leu1053His)
c.1940T>A (p.Leu647His)
 gnomAD v4
15g.73322936G>ACA393086102HCN4c.3157C>T (p.Leu1053Phe)
c.1939C>T (p.Leu647Phe)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322936G>CCA393086103HCN4c.3157C>G (p.Leu1053Val)
c.1939C>G (p.Leu647Val)
 gnomAD v4
15g.73322936G=CA2187187029HCN4c.3157C= (p.Leu1053=)
c.1939C= (p.Leu647=)
15g.73322936G>TCA393086104HCN4c.3157C>A (p.Leu1053Ile)
c.1939C>A (p.Leu647Ile)
 gnomAD v4
15g.73322937C>ACA393086105HCN4c.3156G>T (p.Leu1052Phe)
c.1938G>T (p.Leu646Phe)
 dbSNP gnomAD v4
15g.73322937C=CA2187187033HCN4c.3156G= (p.Leu1052=)
c.1938G= (p.Leu646=)
15g.73322937C>GCA393086106HCN4c.3156G>C (p.Leu1052Phe)
c.1938G>C (p.Leu646Phe)
15g.73322937C>TCA491478008HCN4c.3156G>A (p.Leu1052=)
c.1938G>A (p.Leu646=)
 gnomAD v4
15g.73322938A>CCA393086109HCN4c.3155T>G (p.Leu1052Trp)
c.1937T>G (p.Leu646Trp)
15g.73322938A>GCA393086108HCN4c.3155T>C (p.Leu1052Ser)
c.1937T>C (p.Leu646Ser)
15g.73322938A>TCA393086107HCN4c.3155T>A (p.Leu1052Ter)
c.1937T>A (p.Leu646Ter)
 gnomAD v4
15g.73322939A>CCA393086110HCN4c.3154T>G (p.Leu1052Val)
c.1936T>G (p.Leu646Val)
15g.73322939A>GCA491478010HCN4c.3154T>C (p.Leu1052=)
c.1936T>C (p.Leu646=)
 gnomAD v4
15g.73322939A>TCA393086111HCN4c.3154T>A (p.Leu1052Met)
c.1936T>A (p.Leu646Met)
15g.73322940G>ACA491478011HCN4c.3153C>T (p.Ser1051=)
c.1935C>T (p.Ser645=)
 gnomAD v4 COSMIC
15g.73322940G>CCA491478012HCN4c.3153C>G (p.Ser1051=)
c.1935C>G (p.Ser645=)
15g.73322940G>TCA491478013HCN4c.3153C>A (p.Ser1051=)
c.1935C>A (p.Ser645=)
 gnomAD v4
15g.73322941G>ACA393086112HCN4c.3152C>T (p.Ser1051Phe)
c.1934C>T (p.Ser645Phe)
15g.73322941G>CCA393086113HCN4c.3152C>G (p.Ser1051Cys)
c.1934C>G (p.Ser645Cys)
 ClinVar dbSNP
15g.73322941G>TCA393086114HCN4c.3152C>A (p.Ser1051Tyr)
c.1934C>A (p.Ser645Tyr)
 gnomAD v4
15g.73322942A>CCA393086115HCN4c.3151T>G (p.Ser1051Ala)
c.1933T>G (p.Ser645Ala)
15g.73322942A>GCA393086116HCN4c.3151T>C (p.Ser1051Pro)
c.1933T>C (p.Ser645Pro)
 gnomAD v4
15g.73322942A>TCA393086117HCN4c.3151T>A (p.Ser1051Thr)
c.1933T>A (p.Ser645Thr)
 gnomAD v4
15g.73322943T>ACA491478015HCN4c.3150A>T (p.Gly1050=)
c.1932A>T (p.Gly644=)
15g.73322943T>CCA491478016HCN4c.3150A>G (p.Gly1050=)
c.1932A>G (p.Gly644=)
15g.73322943T>GCA7648876HCN4c.3150A>C (p.Gly1050=)
c.1932A>C (p.Gly644=)
 dbSNP ExAC gnomAD v4
15g.73322943T=CA2187187035HCN4c.3150A= (p.Gly1050=)
c.1932A= (p.Gly644=)
15g.73322944C>ACA393086118HCN4c.3149G>T (p.Gly1050Val)
c.1931G>T (p.Gly644Val)
 gnomAD v4
15g.73322944C>GCA393086119HCN4c.3149G>C (p.Gly1050Ala)
c.1931G>C (p.Gly644Ala)
15g.73322944C>TCA393086120HCN4c.3149G>A (p.Gly1050Glu)
c.1931G>A (p.Gly644Glu)
 gnomAD v4
15g.73322945C>ACA393086122HCN4c.3148G>T (p.Gly1050Ter)
c.1930G>T (p.Gly644Ter)
 gnomAD v4
15g.73322945C=CA2187187038HCN4c.3148G= (p.Gly1050=)
c.1930G= (p.Gly644=)
15g.73322945C>GCA393086123HCN4c.3148G>C (p.Gly1050Arg)
c.1930G>C (p.Gly644Arg)
15g.73322945C>TCA393086121HCN4c.3148G>A (p.Gly1050Arg)
c.1930G>A (p.Gly644Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322946G>ACA7648877HCN4c.3147C>T (p.His1049=)
c.1929C>T (p.His643=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322946G>CCA393086124HCN4c.3147C>G (p.His1049Gln)
c.1929C>G (p.His643Gln)
15g.73322946G=CA2187187045HCN4c.3147C= (p.His1049=)
c.1929C= (p.His643=)
15g.73322946G>TCA393086125HCN4c.3147C>A (p.His1049Gln)
c.1929C>A (p.His643Gln)
 gnomAD v4
15g.73322947T>ACA393086126HCN4c.3146A>T (p.His1049Leu)
c.1928A>T (p.His643Leu)
15g.73322947T>CCA393086127HCN4c.3146A>G (p.His1049Arg)
c.1928A>G (p.His643Arg)
15g.73322947T>GCA393086128HCN4c.3146A>C (p.His1049Pro)
c.1928A>C (p.His643Pro)
 gnomAD v4
15g.73322948G>ACA393086129HCN4c.3145C>T (p.His1049Tyr)
c.1927C>T (p.His643Tyr)
 gnomAD v4
15g.73322948G>CCA393086130HCN4c.3145C>G (p.His1049Asp)
c.1927C>G (p.His643Asp)
 dbSNP gnomAD v3 gnomAD v4
15g.73322948G=CA2187187048HCN4c.3145C= (p.His1049=)
c.1927C= (p.His643=)
15g.73322948G>TCA393086131HCN4c.3145C>A (p.His1049Asn)
c.1927C>A (p.His643Asn)
 gnomAD v4
15g.73322950delCA2575783824HCN4c.3145del (p.His1049ThrfsTer?)
c.1927del (p.His643ThrfsTer?)
 gnomAD v4
15g.73322949G>ACA491478025HCN4c.3144C>T (p.Ser1048=)
c.1926C>T (p.Ser642=)
 ClinVar dbSNP gnomAD v4
15g.73322949G>CCA491478027HCN4c.3144C>G (p.Ser1048=)
c.1926C>G (p.Ser642=)
15g.73322949G>TCA491478029HCN4c.3144C>A (p.Ser1048=)
c.1926C>A (p.Ser642=)
 gnomAD v4
15g.73322950G>ACA393086132HCN4c.3143C>T (p.Ser1048Phe)
c.1925C>T (p.Ser642Phe)
 gnomAD v4
15g.73322950G>CCA393086133HCN4c.3143C>G (p.Ser1048Cys)
c.1925C>G (p.Ser642Cys)
15g.73322950G>TCA393086134HCN4c.3143C>A (p.Ser1048Tyr)
c.1925C>A (p.Ser642Tyr)
 gnomAD v4
15g.73322951A>CCA393086136HCN4c.3142T>G (p.Ser1048Ala)
c.1924T>G (p.Ser642Ala)
15g.73322951A>GCA393086137HCN4c.3142T>C (p.Ser1048Pro)
c.1924T>C (p.Ser642Pro)
 gnomAD v4
15g.73322951A>TCA393086135HCN4c.3142T>A (p.Ser1048Thr)
c.1924T>A (p.Ser642Thr)
 gnomAD v4
15g.73322952G>ACA491478033HCN4c.3141C>T (p.Gly1047=)
c.1923C>T (p.Gly641=)
 gnomAD v4
15g.73322952G>CCA491478034HCN4c.3141C>G (p.Gly1047=)
c.1923C>G (p.Gly641=)
15g.73322952G>TCA491478036HCN4c.3141C>A (p.Gly1047=)
c.1923C>A (p.Gly641=)
 gnomAD v4
15g.73322953C>ACA393086138HCN4c.3140G>T (p.Gly1047Val)
c.1922G>T (p.Gly641Val)
 gnomAD v4
15g.73322953C>GCA393086139HCN4c.3140G>C (p.Gly1047Ala)
c.1922G>C (p.Gly641Ala)
15g.73322953C>TCA393086140HCN4c.3140G>A (p.Gly1047Asp)
c.1922G>A (p.Gly641Asp)
 gnomAD v4
15g.73322954C>ACA393086141HCN4c.3139G>T (p.Gly1047Cys)
c.1921G>T (p.Gly641Cys)
 gnomAD v4
15g.73322954C>GCA393086142HCN4c.3139G>C (p.Gly1047Arg)
c.1921G>C (p.Gly641Arg)
15g.73322954C>TCA393086143HCN4c.3139G>A (p.Gly1047Ser)
c.1921G>A (p.Gly641Ser)
 gnomAD v4 COSMIC
15g.73322955A>CCA491478041HCN4c.3138T>G (p.Ser1046=)
c.1920T>G (p.Ser640=)
15g.73322955A>GCA491478042HCN4c.3138T>C (p.Ser1046=)
c.1920T>C (p.Ser640=)
 gnomAD v4
15g.73322955A>TCA491478039HCN4c.3138T>A (p.Ser1046=)
c.1920T>A (p.Ser640=)
 gnomAD v4
15g.73322956G>ACA393086146HCN4c.3137C>T (p.Ser1046Phe)
c.1919C>T (p.Ser640Phe)
15g.73322956G>CCA393086144HCN4c.3137C>G (p.Ser1046Cys)
c.1919C>G (p.Ser640Cys)
 gnomAD v4
15g.73322956G>TCA393086145HCN4c.3137C>A (p.Ser1046Tyr)
c.1919C>A (p.Ser640Tyr)
 gnomAD v4 COSMIC
15g.73322957A>CCA393086147HCN4c.3136T>G (p.Ser1046Ala)
c.1918T>G (p.Ser640Ala)
15g.73322957A>GCA393086148HCN4c.3136T>C (p.Ser1046Pro)
c.1918T>C (p.Ser640Pro)
 gnomAD v4
15g.73322957A>TCA393086149HCN4c.3136T>A (p.Ser1046Thr)
c.1918T>A (p.Ser640Thr)
 gnomAD v4
15g.73322958G>ACA491478045HCN4c.3135C>T (p.Ala1045=)
c.1917C>T (p.Ala639=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322958G>CCA491478044HCN4c.3135C>G (p.Ala1045=)
c.1917C>G (p.Ala639=)
15g.73322958G=CA2187187051HCN4c.3135C= (p.Ala1045=)
c.1917C= (p.Ala639=)
15g.73322958G>TCA491478043HCN4c.3135C>A (p.Ala1045=)
c.1917C>A (p.Ala639=)
 gnomAD v4
15g.73322959G>ACA272663688HCN4c.3134C>T (p.Ala1045Val)
c.1916C>T (p.Ala639Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322959G>CCA393086150HCN4c.3134C>G (p.Ala1045Gly)
c.1916C>G (p.Ala639Gly)
15g.73322959G=CA2187187055HCN4c.3134C= (p.Ala1045=)
c.1916C= (p.Ala639=)
15g.73322959G>TCA393086151HCN4c.3134C>A (p.Ala1045Asp)
c.1916C>A (p.Ala639Asp)
 gnomAD v4
15g.73322960C>ACA393086152HCN4c.3133G>T (p.Ala1045Ser)
c.1915G>T (p.Ala639Ser)
 gnomAD v4
15g.73322960C=CA2187187061HCN4c.3133G= (p.Ala1045=)
c.1915G= (p.Ala639=)
15g.73322960C>GCA393086153HCN4c.3133G>C (p.Ala1045Pro)
c.1915G>C (p.Ala639Pro)
15g.73322960C>TCA7648878HCN4c.3133G>A (p.Ala1045Thr)
c.1915G>A (p.Ala639Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73322961C>ACA491478047HCN4c.3132G>T (p.Arg1044=)
c.1914G>T (p.Arg638=)
 gnomAD v4
15g.73322961C>GCA491478049HCN4c.3132G>C (p.Arg1044=)
c.1914G>C (p.Arg638=)
15g.73322961C>TCA491478048HCN4c.3132G>A (p.Arg1044=)
c.1914G>A (p.Arg638=)
 gnomAD v4
15g.73322962C>ACA393086155HCN4c.3131G>T (p.Arg1044Leu)
c.1913G>T (p.Arg638Leu)
 gnomAD v4
15g.73322962C=CA2187187064HCN4c.3131G= (p.Arg1044=)
c.1913G= (p.Arg638=)
15g.73322962C>GCA393086154HCN4c.3131G>C (p.Arg1044Pro)
c.1913G>C (p.Arg638Pro)
 gnomAD v4
15g.73322962C>TCA247663HCN4c.3131G>A (p.Arg1044Gln)
c.1913G>A (p.Arg638Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322963G>ACA7648879HCN4c.3130C>T (p.Arg1044Trp)
c.1912C>T (p.Arg638Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322963G>CCA393086156HCN4c.3130C>G (p.Arg1044Gly)
c.1912C>G (p.Arg638Gly)
 gnomAD v4
15g.73322963G=CA2187187070HCN4c.3130C= (p.Arg1044=)
c.1912C= (p.Arg638=)
15g.73322963G>TCA491478053HCN4c.3130C>A (p.Arg1044=)
c.1912C>A (p.Arg638=)
 gnomAD v4
15g.73322966delCA2629370541HCN4c.3130del (p.Arg1044GlyfsTer?)
c.1912del (p.Arg638GlyfsTer?)
 gnomAD v4
15g.73322964G>ACA491478054HCN4c.3129C>T (p.Pro1043=)
c.1911C>T (p.Pro637=)
 ClinVar gnomAD v4
15g.73322964G>CCA491478055HCN4c.3129C>G (p.Pro1043=)
c.1911C>G (p.Pro637=)
 gnomAD v4
15g.73322964G>TCA491478056HCN4c.3129C>A (p.Pro1043=)
c.1911C>A (p.Pro637=)
 gnomAD v4
15g.73322965G>ACA393086157HCN4c.3128C>T (p.Pro1043Leu)
c.1910C>T (p.Pro637Leu)
 gnomAD v4
15g.73322965G>CCA393086158HCN4c.3128C>G (p.Pro1043Arg)
c.1910C>G (p.Pro637Arg)
15g.73322965G>TCA393086159HCN4c.3128C>A (p.Pro1043His)
c.1910C>A (p.Pro637His)
 gnomAD v4
15g.73322966G>ACA393086160HCN4c.3127C>T (p.Pro1043Ser)
c.1909C>T (p.Pro637Ser)
15g.73322966G>CCA393086161HCN4c.3127C>G (p.Pro1043Ala)
c.1909C>G (p.Pro637Ala)
15g.73322966G=CA2187187075HCN4c.3127C= (p.Pro1043=)
c.1909C= (p.Pro637=)
15g.73322966G>TCA393086162HCN4c.3127C>A (p.Pro1043Thr)
c.1909C>A (p.Pro637Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322967C>ACA491478059HCN4c.3126G>T (p.Pro1042=)
c.1908G>T (p.Pro636=)
 gnomAD v4
15g.73322967C=CA2187187078HCN4c.3126G= (p.Pro1042=)
c.1908G= (p.Pro636=)
15g.73322967C>GCA491478060HCN4c.3126G>C (p.Pro1042=)
c.1908G>C (p.Pro636=)
 gnomAD v4
15g.73322967C>TCA16606777HCN4c.3126G>A (p.Pro1042=)
c.1908G>A (p.Pro636=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322968G>ACA393086163HCN4c.3125C>T (p.Pro1042Leu)
c.1907C>T (p.Pro636Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322968G>CCA393086164HCN4c.3125C>G (p.Pro1042Arg)
c.1907C>G (p.Pro636Arg)
 gnomAD v4
15g.73322968G=CA2187187085HCN4c.3125C= (p.Pro1042=)
c.1907C= (p.Pro636=)
15g.73322968G>TCA393086165HCN4c.3125C>A (p.Pro1042Gln)
c.1907C>A (p.Pro636Gln)
 gnomAD v4
15g.73322971delCA2575783825HCN4c.3125del (p.Pro1042ArgfsTer?)
c.1907del (p.Pro636ArgfsTer?)
 gnomAD v4
15g.73322970_73322971delCA2575783826HCN4c.3124_3125del (p.Pro1042AlafsTer?)
c.1906_1907del (p.Pro636AlafsTer?)
15g.73322969G>ACA393086167HCN4c.3124C>T (p.Pro1042Ser)
c.1906C>T (p.Pro636Ser)
 gnomAD v4
15g.73322969G>CCA393086168HCN4c.3124C>G (p.Pro1042Ala)
c.1906C>G (p.Pro636Ala)
 dbSNP
15g.73322969G=CA2187187088HCN4c.3124C= (p.Pro1042=)
c.1906C= (p.Pro636=)
15g.73322969G>TCA393086166HCN4c.3124C>A (p.Pro1042Thr)
c.1906C>A (p.Pro636Thr)
 gnomAD v4
15g.73322970G>ACA491478063HCN4c.3123C>T (p.Ala1041=)
c.1905C>T (p.Ala635=)
 gnomAD v4
15g.73322970G>CCA491478064HCN4c.3123C>G (p.Ala1041=)
c.1905C>G (p.Ala635=)
15g.73322970G>TCA491478065HCN4c.3123C>A (p.Ala1041=)
c.1905C>A (p.Ala635=)
 gnomAD v4
15g.73322971G>ACA393086169HCN4c.3122C>T (p.Ala1041Val)
c.1904C>T (p.Ala635Val)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322971G>CCA393086170HCN4c.3122C>G (p.Ala1041Gly)
c.1904C>G (p.Ala635Gly)
15g.73322971G=CA2187187092HCN4c.3122C= (p.Ala1041=)
c.1904C= (p.Ala635=)
15g.73322971G>TCA393086171HCN4c.3122C>A (p.Ala1041Asp)
c.1904C>A (p.Ala635Asp)
 gnomAD v4
15g.73322972C>ACA393086172HCN4c.3121G>T (p.Ala1041Ser)
c.1903G>T (p.Ala635Ser)
 gnomAD v4
15g.73322972C=CA2187187100HCN4c.3121G= (p.Ala1041=)
c.1903G= (p.Ala635=)
15g.73322972C>GCA393086173HCN4c.3121G>C (p.Ala1041Pro)
c.1903G>C (p.Ala635Pro)
15g.73322972C>TCA7648880HCN4c.3121G>A (p.Ala1041Thr)
c.1903G>A (p.Ala635Thr)
 dbSNP ExAC gnomAD v4
15g.73322973A>CCA393086174HCN4c.3120T>G (p.Ser1040Arg)
c.1902T>G (p.Ser634Arg)
15g.73322973A>GCA491478069HCN4c.3120T>C (p.Ser1040=)
c.1902T>C (p.Ser634=)
 gnomAD v4
15g.73322973A>TCA393086175HCN4c.3120T>A (p.Ser1040Arg)
c.1902T>A (p.Ser634Arg)
 COSMIC
15g.73322974C>ACA393086176HCN4c.3119G>T (p.Ser1040Ile)
c.1901G>T (p.Ser634Ile)
 dbSNP gnomAD v3 gnomAD v4
15g.73322974C=CA2187187103HCN4c.3119G= (p.Ser1040=)
c.1901G= (p.Ser634=)
15g.73322974C>GCA393086177HCN4c.3119G>C (p.Ser1040Thr)
c.1901G>C (p.Ser634Thr)
15g.73322974C>TCA393086178HCN4c.3119G>A (p.Ser1040Asn)
c.1901G>A (p.Ser634Asn)
15g.73322975T>ACA393086179HCN4c.3118A>T (p.Ser1040Cys)
c.1900A>T (p.Ser634Cys)
 dbSNP gnomAD v3 gnomAD v4
15g.73322975T>CCA393086180HCN4c.3118A>G (p.Ser1040Gly)
c.1900A>G (p.Ser634Gly)
 gnomAD v4
15g.73322975T>GCA393086181HCN4c.3118A>C (p.Ser1040Arg)
c.1900A>C (p.Ser634Arg)
15g.73322975T=CA2187187106HCN4c.3118A= (p.Ser1040=)
c.1900A= (p.Ser634=)
15g.73322976C>ACA491478073HCN4c.3117G>T (p.Pro1039=)
c.1899G>T (p.Pro633=)
 gnomAD v4
15g.73322976C=CA2187187110HCN4c.3117G= (p.Pro1039=)
c.1899G= (p.Pro633=)
15g.73322976C>GCA491478074HCN4c.3117G>C (p.Pro1039=)
c.1899G>C (p.Pro633=)
 gnomAD v4
15g.73322976C>TCA7648881HCN4c.3117G>A (p.Pro1039=)
c.1899G>A (p.Pro633=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322977G>ACA7648882HCN4c.3116C>T (p.Pro1039Leu)
c.1898C>T (p.Pro633Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322977G>CCA393086182HCN4c.3116C>G (p.Pro1039Arg)
c.1898C>G (p.Pro633Arg)
 ClinVar dbSNP
15g.73322977G=CA2187187118HCN4c.3116C= (p.Pro1039=)
c.1898C= (p.Pro633=)
15g.73322977G>TCA393086183HCN4c.3116C>A (p.Pro1039Gln)
c.1898C>A (p.Pro633Gln)
 gnomAD v4
15g.73322978_73322979delCA2575783827HCN4c.3115_3116del (p.Pro1039GlufsTer?)
c.1897_1898del (p.Pro633GlufsTer?)
15g.73322978G>ACA393086184HCN4c.3115C>T (p.Pro1039Ser)
c.1897C>T (p.Pro633Ser)
 gnomAD v4 COSMIC
15g.73322978G>CCA393086185HCN4c.3115C>G (p.Pro1039Ala)
c.1897C>G (p.Pro633Ala)
15g.73322978G>TCA393086186HCN4c.3115C>A (p.Pro1039Thr)
c.1897C>A (p.Pro633Thr)
 gnomAD v4
15g.73322979G>ACA491478076HCN4c.3114C>T (p.Phe1038=)
c.1896C>T (p.Phe632=)
15g.73322979G>CCA393086187HCN4c.3114C>G (p.Phe1038Leu)
c.1896C>G (p.Phe632Leu)
15g.73322979G=CA2187187131HCN4c.3114C= (p.Phe1038=)
c.1896C= (p.Phe632=)
15g.73322979G>TCA393086188HCN4c.3114C>A (p.Phe1038Leu)
c.1896C>A (p.Phe632Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322980A>CCA393086189HCN4c.3113T>G (p.Phe1038Cys)
c.1895T>G (p.Phe632Cys)
15g.73322980A>GCA393086190HCN4c.3113T>C (p.Phe1038Ser)
c.1895T>C (p.Phe632Ser)
15g.73322980A>TCA393086191HCN4c.3113T>A (p.Phe1038Tyr)
c.1895T>A (p.Phe632Tyr)
15g.73322981A=CA2187187135HCN4c.3112T= (p.Phe1038=)
c.1894T= (p.Phe632=)
15g.73322981A>CCA393086192HCN4c.3112T>G (p.Phe1038Val)
c.1894T>G (p.Phe632Val)
15g.73322981A>GCA393086193HCN4c.3112T>C (p.Phe1038Leu)
c.1894T>C (p.Phe632Leu)
 dbSNP gnomAD v4
15g.73322981A>TCA393086194HCN4c.3112T>A (p.Phe1038Ile)
c.1894T>A (p.Phe632Ile)
15g.73322982G>ACA491478079HCN4c.3111C>T (p.Thr1037=)
c.1893C>T (p.Thr631=)
 gnomAD v4
15g.73322982G>CCA491478080HCN4c.3111C>G (p.Thr1037=)
c.1893C>G (p.Thr631=)
15g.73322982G>TCA491478081HCN4c.3111C>A (p.Thr1037=)
c.1893C>A (p.Thr631=)
 ClinVar gnomAD v4
15g.73322983G>ACA393086196HCN4c.3110C>T (p.Thr1037Ile)
c.1892C>T (p.Thr631Ile)
15g.73322983G>CCA393086197HCN4c.3110C>G (p.Thr1037Ser)
c.1892C>G (p.Thr631Ser)
15g.73322983G>TCA393086195HCN4c.3110C>A (p.Thr1037Asn)
c.1892C>A (p.Thr631Asn)
 ClinVar gnomAD v4
15g.73322984T>ACA393086198HCN4c.3109A>T (p.Thr1037Ser)
c.1891A>T (p.Thr631Ser)
15g.73322984T>CCA393086199HCN4c.3109A>G (p.Thr1037Ala)
c.1891A>G (p.Thr631Ala)
 gnomAD v4
15g.73322984T>GCA393086200HCN4c.3109A>C (p.Thr1037Pro)
c.1891A>C (p.Thr631Pro)
15g.73322985T>ACA393086201HCN4c.3108A>T (p.Arg1036Ser)
c.1890A>T (p.Arg630Ser)
 ClinVar
15g.73322985T>CCA491478084HCN4c.3108A>G (p.Arg1036=)
c.1890A>G (p.Arg630=)
15g.73322985T>GCA393086202HCN4c.3108A>C (p.Arg1036Ser)
c.1890A>C (p.Arg630Ser)
15g.73322986C>ACA393086205HCN4c.3107G>T (p.Arg1036Ile)
c.1889G>T (p.Arg630Ile)
 gnomAD v4
15g.73322986C>GCA393086203HCN4c.3107G>C (p.Arg1036Thr)
c.1889G>C (p.Arg630Thr)
15g.73322986C>TCA393086204HCN4c.3107G>A (p.Arg1036Lys)
c.1889G>A (p.Arg630Lys)
15g.73322987T>ACA393086206HCN4c.3106A>T (p.Arg1036Ter)
c.1888A>T (p.Arg630Ter)
15g.73322987T>CCA393086207HCN4c.3106A>G (p.Arg1036Gly)
c.1888A>G (p.Arg630Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
15g.73322987T>GCA491478088HCN4c.3106A>C (p.Arg1036=)
c.1888A>C (p.Arg630=)
15g.73322987T=CA2187187138HCN4c.3106A= (p.Arg1036=)
c.1888A= (p.Arg630=)
15g.73322988T>ACA491478089HCN4c.3105A>T (p.Pro1035=)
c.1887A>T (p.Pro629=)
15g.73322988T>CCA491478090HCN4c.3105A>G (p.Pro1035=)
c.1887A>G (p.Pro629=)
 gnomAD v4
15g.73322988T>GCA491478092HCN4c.3105A>C (p.Pro1035=)
c.1887A>C (p.Pro629=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
15g.73322988T=CA2187187144HCN4c.3105A= (p.Pro1035=)
c.1887A= (p.Pro629=)
15g.73322989G>ACA393086208HCN4c.3104C>T (p.Pro1035Leu)
c.1886C>T (p.Pro629Leu)
 gnomAD v4 COSMIC
15g.73322989G>CCA393086209HCN4c.3104C>G (p.Pro1035Arg)
c.1886C>G (p.Pro629Arg)
15g.73322989G>TCA393086210HCN4c.3104C>A (p.Pro1035Gln)
c.1886C>A (p.Pro629Gln)
 gnomAD v4
15g.73322994dupCA619410589HCN4c.3104dup (p.Arg1036LysfsTer?)
c.1886dup (p.Arg630LysfsTer?)
 dbSNP gnomAD v2 gnomAD v4
15g.73322994delCA2629370542HCN4c.3104del (p.Pro1035GlnfsTer?)
c.1886del (p.Pro629GlnfsTer?)
 gnomAD v4
15g.73322990G>ACA393086212HCN4c.3103C>T (p.Pro1035Ser)
c.1885C>T (p.Pro629Ser)
 gnomAD v4
15g.73322990G>CCA7648883HCN4c.3103C>G (p.Pro1035Ala)
c.1885C>G (p.Pro629Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
15g.73322990G=CA2187187155HCN4c.3103C= (p.Pro1035=)
c.1885C= (p.Pro629=)
15g.73322990G>TCA393086211HCN4c.3103C>A (p.Pro1035Thr)
c.1885C>A (p.Pro629Thr)
 gnomAD v4
15g.73322991G>ACA491478095HCN4c.3102C>T (p.Pro1034=)
c.1884C>T (p.Pro628=)
 gnomAD v4 COSMIC
15g.73322991G>CCA491478096HCN4c.3102C>G (p.Pro1034=)
c.1884C>G (p.Pro628=)
15g.73322991G>TCA491478097HCN4c.3102C>A (p.Pro1034=)
c.1884C>A (p.Pro628=)
 gnomAD v4
15g.73322992G>ACA393086213HCN4c.3101C>T (p.Pro1034Leu)
c.1883C>T (p.Pro628Leu)
 ClinVar gnomAD v4
15g.73322992G>CCA272663736HCN4c.3101C>G (p.Pro1034Arg)
c.1883C>G (p.Pro628Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322992G=CA2187187164HCN4c.3101C= (p.Pro1034=)
c.1883C= (p.Pro628=)
15g.73322992G>TCA393086214HCN4c.3101C>A (p.Pro1034His)
c.1883C>A (p.Pro628His)
 gnomAD v4
15g.73322993G>ACA393086215HCN4c.3100C>T (p.Pro1034Ser)
c.1882C>T (p.Pro628Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322993G>CCA393086216HCN4c.3100C>G (p.Pro1034Ala)
c.1882C>G (p.Pro628Ala)
15g.73322993G=CA2187187173HCN4c.3100C= (p.Pro1034=)
c.1882C= (p.Pro628=)
15g.73322993G>TCA393086217HCN4c.3100C>A (p.Pro1034Thr)
c.1882C>A (p.Pro628Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
15g.73322994G>ACA7648884HCN4c.3099C>T (p.Gly1033=)
c.1881C>T (p.Gly627=)
 dbSNP ExAC gnomAD v2 gnomAD v4
15g.73322994G>CCA491478100HCN4c.3099C>G (p.Gly1033=)
c.1881C>G (p.Gly627=)
 dbSNP gnomAD v4
15g.73322994G=CA2187187181HCN4c.3099C= (p.Gly1033=)
c.1881C= (p.Gly627=)
15g.73322994G>TCA491478101HCN4c.3099C>A (p.Gly1033=)
c.1881C>A (p.Gly627=)
 dbSNP gnomAD v4
15g.73322995C>ACA393086218HCN4c.3098G>T (p.Gly1033Val)
c.1880G>T (p.Gly627Val)
 gnomAD v4
15g.73322995C=CA2187187186HCN4c.3098G= (p.Gly1033=)
c.1880G= (p.Gly627=)
15g.73322995C>GCA393086219HCN4c.3098G>C (p.Gly1033Ala)
c.1880G>C (p.Gly627Ala)
 gnomAD v4
15g.73322995C>TCA393086220HCN4c.3098G>A (p.Gly1033Asp)
c.1880G>A (p.Gly627Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4

Number of alleles fetched