Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.218893072_218893095dupCA2663174548WNT10Ac.1055_1078dup (p.Gly359_Arg360insLeuAspSerAlaGlyThrValGly)
c.562_585dup
c.1004_1027dup (p.Gly342_Arg343insLeuAspSerAlaGlyThrValGly)
c.959_982dup (p.Gly327_Arg328insLeuAspSerAlaGlyThrValGly)
c.675_698dup (p.Pro233_Pro234insGlyLeuGlyGlyHisArgGlyPro)
 gnomAD v4
2g.218893071C>ACA350590962WNT10Ac.1054C>A (p.Leu352Met)
c.561C>A
c.1003C>A (p.Leu335Met)
c.958C>A (p.Leu320Met)
c.674C>A (p.Pro225His)
 gnomAD v4
2g.218893071C>GCA350590964WNT10Ac.1054C>G (p.Leu352Val)
c.561C>G
c.1003C>G (p.Leu335Val)
c.958C>G (p.Leu320Val)
c.674C>G (p.Pro225Arg)
2g.218893071C>TCA431417228WNT10Ac.1054C>T (p.Leu352=)
c.561C>T
c.1003C>T (p.Leu335=)
c.958C>T (p.Leu320=)
c.674C>T (p.Pro225Leu)
2g.218893072T>ACA350590967WNT10Ac.1055T>A (p.Leu352Gln)
c.562T>A
c.1004T>A (p.Leu335Gln)
c.959T>A (p.Leu320Gln)
c.675T>A (p.Pro225=)
2g.218893072T>CCA350590970WNT10Ac.1055T>C (p.Leu352Pro)
c.562T>C
c.1004T>C (p.Leu335Pro)
c.959T>C (p.Leu320Pro)
c.675T>C (p.Pro225=)
 gnomAD v4
2g.218893072T>GCA350590972WNT10Ac.1055T>G (p.Leu352Arg)
c.562T>G
c.1004T>G (p.Leu335Arg)
c.959T>G (p.Leu320Arg)
c.675T>G (p.Pro225=)
 gnomAD v4
2g.218893073G>ACA431417230WNT10Ac.1056G>A (p.Leu352=)
c.563G>A
c.1005G>A (p.Leu335=)
c.960G>A (p.Leu320=)
c.676G>A (p.Gly226Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893073G>CCA431417232WNT10Ac.1056G>C (p.Leu352=)
c.563G>C
c.1005G>C (p.Leu335=)
c.960G>C (p.Leu320=)
c.676G>C (p.Gly226Arg)
2g.218893073G=CA1328965317WNT10Ac.1056G= (p.Leu352=)
c.563G=
c.1005G= (p.Leu335=)
c.960G= (p.Leu320=)
c.676G= (p.Gly226=)
2g.218893073G>TCA431417234WNT10Ac.1056G>T (p.Leu352=)
c.563G>T
c.1005G>T (p.Leu335=)
c.960G>T (p.Leu320=)
c.676G>T (p.Gly226Ter)
 gnomAD v4
2g.218893074G>ACA350590975WNT10Ac.1057G>A (p.Asp353Asn)
c.564G>A
c.1006G>A (p.Asp336Asn)
c.961G>A (p.Asp321Asn)
c.677G>A (p.Gly226Glu)
2g.218893074G>CCA65919271WNT10Ac.1057G>C (p.Asp353His)
c.564G>C
c.1006G>C (p.Asp336His)
c.961G>C (p.Asp321His)
c.677G>C (p.Gly226Ala)
 dbSNP
2g.218893074G=CA1328965319WNT10Ac.1057G= (p.Asp353=)
c.564G=
c.1006G= (p.Asp336=)
c.961G= (p.Asp321=)
c.677G= (p.Gly226=)
2g.218893074G>TCA2114102WNT10Ac.1057G>T (p.Asp353Tyr)
c.564G>T
c.1006G>T (p.Asp336Tyr)
c.961G>T (p.Asp321Tyr)
c.677G>T (p.Gly226Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893075A=CA1328965322WNT10Ac.1058A= (p.Asp353=)
c.565A=
c.1007A= (p.Asp336=)
c.962A= (p.Asp321=)
c.678A= (p.Gly226=)
2g.218893075A>CCA350590984WNT10Ac.1058A>C (p.Asp353Ala)
c.565A>C
c.1007A>C (p.Asp336Ala)
c.962A>C (p.Asp321Ala)
c.678A>C (p.Gly226=)
 COSMIC
2g.218893075A>GCA350590991WNT10Ac.1058A>G (p.Asp353Gly)
c.565A>G
c.1007A>G (p.Asp336Gly)
c.962A>G (p.Asp321Gly)
c.678A>G (p.Gly226=)
2g.218893075A>TCA2114103WNT10Ac.1058A>T (p.Asp353Val)
c.565A>T
c.1007A>T (p.Asp336Val)
c.962A>T (p.Asp321Val)
c.678A>T (p.Gly226=)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893076C>ACA350591000WNT10Ac.1059C>A (p.Asp353Glu)
c.566C>A
c.1008C>A (p.Asp336Glu)
c.963C>A (p.Asp321Glu)
c.679C>A (p.Leu227Ile)
 gnomAD v4
2g.218893076C>GCA350591007WNT10Ac.1059C>G (p.Asp353Glu)
c.566C>G
c.1008C>G (p.Asp336Glu)
c.963C>G (p.Asp321Glu)
c.679C>G (p.Leu227Val)
2g.218893076C>TCA431417240WNT10Ac.1059C>T (p.Asp353=)
c.566C>T
c.1008C>T (p.Asp336=)
c.963C>T (p.Asp321=)
c.679C>T (p.Leu227Phe)
 ClinVar gnomAD v4
2g.218893077T>ACA350591018WNT10Ac.1060T>A (p.Ser354Thr)
c.567T>A
c.1009T>A (p.Ser337Thr)
c.964T>A (p.Ser322Thr)
c.680T>A (p.Leu227His)
2g.218893077T>CCA350591015WNT10Ac.1060T>C (p.Ser354Pro)
c.567T>C
c.1009T>C (p.Ser337Pro)
c.964T>C (p.Ser322Pro)
c.680T>C (p.Leu227Pro)
2g.218893077T>GCA350591010WNT10Ac.1060T>G (p.Ser354Ala)
c.567T>G
c.1009T>G (p.Ser337Ala)
c.964T>G (p.Ser322Ala)
c.680T>G (p.Leu227Arg)
2g.218893078C>ACA350591021WNT10Ac.1061C>A (p.Ser354Ter)
c.568C>A
c.1010C>A (p.Ser337Ter)
c.965C>A (p.Ser322Ter)
c.681C>A (p.Leu227=)
2g.218893078C=CA1328965326WNT10Ac.1061C= (p.Ser354=)
c.568C=
c.1010C= (p.Ser337=)
c.965C= (p.Ser322=)
c.681C= (p.Leu227=)
2g.218893078C>GCA350591023WNT10Ac.1061C>G (p.Ser354Trp)
c.568C>G
c.1010C>G (p.Ser337Trp)
c.965C>G (p.Ser322Trp)
c.681C>G (p.Leu227=)
2g.218893078C>TCA2114104WNT10Ac.1061C>T (p.Ser354Leu)
c.568C>T
c.1010C>T (p.Ser337Leu)
c.965C>T (p.Ser322Leu)
c.681C>T (p.Leu227=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893081_218893083delCA2663174549WNT10Ac.1064_1066del (p.Ala355del)
c.571_573del
c.1013_1015del (p.Ala338del)
c.968_970del (p.Ala323del)
c.684_686del (p.Gly229del)
 gnomAD v4
2g.218893079G>ACA431417249WNT10Ac.1062G>A (p.Ser354=)
c.569G>A
c.1011G>A (p.Ser337=)
c.966G>A (p.Ser322=)
c.682G>A (p.Gly228Ser)
2g.218893079G>CCA431417250WNT10Ac.1062G>C (p.Ser354=)
c.569G>C
c.1011G>C (p.Ser337=)
c.966G>C (p.Ser322=)
c.682G>C (p.Gly228Arg)
2g.218893079G>TCA431417252WNT10Ac.1062G>T (p.Ser354=)
c.569G>T
c.1011G>T (p.Ser337=)
c.966G>T (p.Ser322=)
c.682G>T (p.Gly228Cys)
 gnomAD v4
2g.218893080delCA2573135232WNT10Ac.1063del (p.Ala355ArgfsTer?)
c.570del
c.1012del (p.Ala338ArgfsTer?)
c.967del (p.Ala323ArgfsTer?)
c.683del (p.Gly228AlafsTer?)
 ClinVar dbSNP
2g.218893082_218893094delCA2586971351WNT10Ac.1065_1077del (p.Gly356AlafsTer?)
c.572_584del
c.1014_1026del (p.Gly339AlafsTer?)
c.969_981del (p.Gly324AlafsTer?)
c.685_697del (p.Gly229ArgfsTer?)
2g.218893080G>ACA350591040WNT10Ac.1063G>A (p.Ala355Thr)
c.570G>A
c.1012G>A (p.Ala338Thr)
c.967G>A (p.Ala323Thr)
c.683G>A (p.Gly228Asp)
2g.218893080G>CCA350591044WNT10Ac.1063G>C (p.Ala355Pro)
c.570G>C
c.1012G>C (p.Ala338Pro)
c.967G>C (p.Ala323Pro)
c.683G>C (p.Gly228Ala)
2g.218893080G>TCA350591047WNT10Ac.1063G>T (p.Ala355Ser)
c.570G>T
c.1012G>T (p.Ala338Ser)
c.967G>T (p.Ala323Ser)
c.683G>T (p.Gly228Val)
 gnomAD v4
2g.218893081C>ACA350591055WNT10Ac.1064C>A (p.Ala355Glu)
c.571C>A
c.1013C>A (p.Ala338Glu)
c.968C>A (p.Ala323Glu)
c.684C>A (p.Gly228=)
 gnomAD v4
2g.218893081C=CA1328965331WNT10Ac.1064C= (p.Ala355=)
c.571C=
c.1013C= (p.Ala338=)
c.968C= (p.Ala323=)
c.684C= (p.Gly228=)
2g.218893081C>GCA350591050WNT10Ac.1064C>G (p.Ala355Gly)
c.571C>G
c.1013C>G (p.Ala338Gly)
c.968C>G (p.Ala323Gly)
c.684C>G (p.Gly228=)
2g.218893081C>TCA350591054WNT10Ac.1064C>T (p.Ala355Val)
c.571C>T
c.1013C>T (p.Ala338Val)
c.968C>T (p.Ala323Val)
c.684C>T (p.Gly228=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893082G>ACA431417258WNT10Ac.1065G>A (p.Ala355=)
c.572G>A
c.1014G>A (p.Ala338=)
c.969G>A (p.Ala323=)
c.685G>A (p.Gly229Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893082G>CCA431417259WNT10Ac.1065G>C (p.Ala355=)
c.572G>C
c.1014G>C (p.Ala338=)
c.969G>C (p.Ala323=)
c.685G>C (p.Gly229Arg)
2g.218893082G=CA1328965334WNT10Ac.1065G= (p.Ala355=)
c.572G=
c.1014G= (p.Ala338=)
c.969G= (p.Ala323=)
c.685G= (p.Gly229=)
2g.218893082G>TCA431417257WNT10Ac.1065G>T (p.Ala355=)
c.572G>T
c.1014G>T (p.Ala338=)
c.969G>T (p.Ala323=)
c.685G>T (p.Gly229Trp)
 gnomAD v4
2g.218893083G>ACA350591056WNT10Ac.1066G>A (p.Gly356Ser)
c.573G>A
c.1015G>A (p.Gly339Ser)
c.970G>A (p.Gly324Ser)
c.686G>A (p.Gly229Glu)
 ClinVar
2g.218893083G>CCA350591057WNT10Ac.1066G>C (p.Gly356Arg)
c.573G>C
c.1015G>C (p.Gly339Arg)
c.970G>C (p.Gly324Arg)
c.686G>C (p.Gly229Ala)
2g.218893083G>TCA350591059WNT10Ac.1066G>T (p.Gly356Cys)
c.573G>T
c.1015G>T (p.Gly339Cys)
c.970G>T (p.Gly324Cys)
c.686G>T (p.Gly229Val)
2g.218893084G>ACA350591064WNT10Ac.1067G>A (p.Gly356Asp)
c.574G>A
c.1016G>A (p.Gly339Asp)
c.971G>A (p.Gly324Asp)
c.687G>A (p.Gly229=)
 gnomAD v4
2g.218893084G>CCA350591067WNT10Ac.1067G>C (p.Gly356Ala)
c.574G>C
c.1016G>C (p.Gly339Ala)
c.971G>C (p.Gly324Ala)
c.687G>C (p.Gly229=)
2g.218893084G>TCA350591071WNT10Ac.1067G>T (p.Gly356Val)
c.574G>T
c.1016G>T (p.Gly339Val)
c.971G>T (p.Gly324Val)
c.687G>T (p.Gly229=)
 gnomAD v4
2g.218893085C>ACA431417273WNT10Ac.1068C>A (p.Gly356=)
c.575C>A
c.1017C>A (p.Gly339=)
c.972C>A (p.Gly324=)
c.688C>A (p.His230Asn)
2g.218893085C>GCA431417269WNT10Ac.1068C>G (p.Gly356=)
c.575C>G
c.1017C>G (p.Gly339=)
c.972C>G (p.Gly324=)
c.688C>G (p.His230Asp)
2g.218893085C>TCA431417271WNT10Ac.1068C>T (p.Gly356=)
c.575C>T
c.1017C>T (p.Gly339=)
c.972C>T (p.Gly324=)
c.688C>T (p.His230Tyr)
 gnomAD v4
2g.218893086A>CCA350591079WNT10Ac.1069A>C (p.Thr357Pro)
c.576A>C
c.1018A>C (p.Thr340Pro)
c.973A>C (p.Thr325Pro)
c.689A>C (p.His230Pro)
2g.218893086A>GCA350591082WNT10Ac.1069A>G (p.Thr357Ala)
c.576A>G
c.1018A>G (p.Thr340Ala)
c.973A>G (p.Thr325Ala)
c.689A>G (p.His230Arg)
2g.218893086A>TCA350591084WNT10Ac.1069A>T (p.Thr357Ser)
c.576A>T
c.1018A>T (p.Thr340Ser)
c.973A>T (p.Thr325Ser)
c.689A>T (p.His230Leu)
2g.218893087C>ACA350591087WNT10Ac.1070C>A (p.Thr357Asn)
c.577C>A
c.1019C>A (p.Thr340Asn)
c.974C>A (p.Thr325Asn)
c.690C>A (p.His230Gln)
2g.218893087C=CA1328965337WNT10Ac.1070C= (p.Thr357=)
c.577C=
c.1019C= (p.Thr340=)
c.974C= (p.Thr325=)
c.690C= (p.His230=)
2g.218893087C>GCA350591091WNT10Ac.1070C>G (p.Thr357Ser)
c.577C>G
c.1019C>G (p.Thr340Ser)
c.974C>G (p.Thr325Ser)
c.690C>G (p.His230Gln)
2g.218893087C>TCA2114105WNT10Ac.1070C>T (p.Thr357Ile)
c.577C>T
c.1019C>T (p.Thr340Ile)
c.974C>T (p.Thr325Ile)
c.690C>T (p.His230=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893088C>ACA431417283WNT10Ac.1071C>A (p.Thr357=)
c.578C>A
c.1020C>A (p.Thr340=)
c.975C>A (p.Thr325=)
c.691C>A (p.Arg231Ser)
 dbSNP gnomAD v2 gnomAD v4
2g.218893088C=CA1328965340WNT10Ac.1071C= (p.Thr357=)
c.578C=
c.1020C= (p.Thr340=)
c.975C= (p.Thr325=)
c.691C= (p.Arg231=)
2g.218893088C>GCA2114106WNT10Ac.1071C>G (p.Thr357=)
c.578C>G
c.1020C>G (p.Thr340=)
c.975C>G (p.Thr325=)
c.691C>G (p.Arg231Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893088C>TCA431417281WNT10Ac.1071C>T (p.Thr357=)
c.578C>T
c.1020C>T (p.Thr340=)
c.975C>T (p.Thr325=)
c.691C>T (p.Arg231Cys)
2g.218893089delCA2663174550WNT10Ac.1072del (p.Val358TrpfsTer?)
c.579del
c.1021del (p.Val341TrpfsTer?)
c.976del (p.Val326TrpfsTer?)
c.692del (p.Arg231LeufsTer?)
 gnomAD v4
2g.218893089G>ACA350591102WNT10Ac.1072G>A (p.Val358Met)
c.579G>A
c.1021G>A (p.Val341Met)
c.976G>A (p.Val326Met)
c.692G>A (p.Arg231His)
 gnomAD v4
2g.218893089G>CCA350591125WNT10Ac.1072G>C (p.Val358Leu)
c.579G>C
c.1021G>C (p.Val341Leu)
c.976G>C (p.Val326Leu)
c.692G>C (p.Arg231Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893089G=CA1328965344WNT10Ac.1072G= (p.Val358=)
c.579G=
c.1021G= (p.Val341=)
c.976G= (p.Val326=)
c.692G= (p.Arg231=)
2g.218893089G>TCA350591123WNT10Ac.1072G>T (p.Val358Leu)
c.579G>T
c.1021G>T (p.Val341Leu)
c.976G>T (p.Val326Leu)
c.692G>T (p.Arg231Leu)
 gnomAD v4
2g.218893090T>ACA350591137WNT10Ac.1073T>A (p.Val358Glu)
c.580T>A
c.1022T>A (p.Val341Glu)
c.977T>A (p.Val326Glu)
c.693T>A (p.Arg231=)
2g.218893090T>CCA350591142WNT10Ac.1073T>C (p.Val358Ala)
c.580T>C
c.1022T>C (p.Val341Ala)
c.977T>C (p.Val326Ala)
c.693T>C (p.Arg231=)
2g.218893090T>GCA350591147WNT10Ac.1073T>G (p.Val358Gly)
c.580T>G
c.1022T>G (p.Val341Gly)
c.977T>G (p.Val326Gly)
c.693T>G (p.Arg231=)
2g.218893091G>ACA431417289WNT10Ac.1074G>A (p.Val358=)
c.581G>A
c.1023G>A (p.Val341=)
c.978G>A (p.Val326=)
c.694G>A (p.Gly232Arg)
 gnomAD v4
2g.218893091G>CCA431417291WNT10Ac.1074G>C (p.Val358=)
c.581G>C
c.1023G>C (p.Val341=)
c.978G>C (p.Val326=)
c.694G>C (p.Gly232Arg)
2g.218893091G>TCA431417292WNT10Ac.1074G>T (p.Val358=)
c.581G>T
c.1023G>T (p.Val341=)
c.978G>T (p.Val326=)
c.694G>T (p.Gly232Trp)
 gnomAD v4
2g.218893092G>ACA350591151WNT10Ac.1075G>A (p.Gly359Ser)
c.582G>A
c.1024G>A (p.Gly342Ser)
c.979G>A (p.Gly327Ser)
c.695G>A (p.Gly232Glu)
2g.218893092G>CCA350591152WNT10Ac.1075G>C (p.Gly359Arg)
c.582G>C
c.1024G>C (p.Gly342Arg)
c.979G>C (p.Gly327Arg)
c.695G>C (p.Gly232Ala)
2g.218893092G>TCA350591154WNT10Ac.1075G>T (p.Gly359Cys)
c.582G>T
c.1024G>T (p.Gly342Cys)
c.979G>T (p.Gly327Cys)
c.695G>T (p.Gly232Val)
 gnomAD v4
2g.218893093G>ACA65919285WNT10Ac.1076G>A (p.Gly359Asp)
c.583G>A
c.1025G>A (p.Gly342Asp)
c.980G>A (p.Gly327Asp)
c.696G>A (p.Gly232=)
 dbSNP gnomAD v4
2g.218893093G>CCA350591194WNT10Ac.1076G>C (p.Gly359Ala)
c.583G>C
c.1025G>C (p.Gly342Ala)
c.980G>C (p.Gly327Ala)
c.696G>C (p.Gly232=)
2g.218893093G=CA1328965348WNT10Ac.1076G= (p.Gly359=)
c.583G=
c.1025G= (p.Gly342=)
c.980G= (p.Gly327=)
c.696G= (p.Gly232=)
2g.218893093G>TCA350591197WNT10Ac.1076G>T (p.Gly359Val)
c.583G>T
c.1025G>T (p.Gly342Val)
c.980G>T (p.Gly327Val)
c.696G>T (p.Gly232=)
2g.218893094C>ACA431417300WNT10Ac.1077C>A (p.Gly359=)
c.584C>A
c.1026C>A (p.Gly342=)
c.981C>A (p.Gly327=)
c.697C>A (p.Pro233Thr)
2g.218893094C>GCA431417299WNT10Ac.1077C>G (p.Gly359=)
c.584C>G
c.1026C>G (p.Gly342=)
c.981C>G (p.Gly327=)
c.697C>G (p.Pro233Ala)
2g.218893094C>TCA431417298WNT10Ac.1077C>T (p.Gly359=)
c.584C>T
c.1026C>T (p.Gly342=)
c.981C>T (p.Gly327=)
c.697C>T (p.Pro233Ser)
 gnomAD v4
2g.218893095C>ACA350591198WNT10Ac.1078C>A (p.Arg360Ser)
c.585C>A
c.1027C>A (p.Arg343Ser)
c.982C>A (p.Arg328Ser)
c.698C>A (p.Pro233Gln)
 COSMIC
2g.218893095C>GCA350591204WNT10Ac.1078C>G (p.Arg360Gly)
c.585C>G
c.1027C>G (p.Arg343Gly)
c.982C>G (p.Arg328Gly)
c.698C>G (p.Pro233Arg)
2g.218893095C>TCA350591211WNT10Ac.1078C>T (p.Arg360Cys)
c.585C>T
c.1027C>T (p.Arg343Cys)
c.982C>T (p.Arg328Cys)
c.698C>T (p.Pro233Leu)
 gnomAD v4
2g.218893096G>ACA350591230WNT10Ac.1079G>A (p.Arg360His)
c.586G>A
c.1028G>A (p.Arg343His)
c.983G>A (p.Arg328His)
c.699G>A (p.Pro233=)
 gnomAD v4
2g.218893096G>CCA350591216WNT10Ac.1079G>C (p.Arg360Pro)
c.586G>C
c.1028G>C (p.Arg343Pro)
c.983G>C (p.Arg328Pro)
c.699G>C (p.Pro233=)
 ClinVar dbSNP
2g.218893096G=CA1328965353WNT10Ac.1079G= (p.Arg360=)
c.586G=
c.1028G= (p.Arg343=)
c.983G= (p.Arg328=)
c.699G= (p.Pro233=)
2g.218893096G>TCA65919289WNT10Ac.1079G>T (p.Arg360Leu)
c.586G>T
c.1028G>T (p.Arg343Leu)
c.983G>T (p.Arg328Leu)
c.699G>T (p.Pro233=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893097C>ACA65919290WNT10Ac.1080C>A (p.Arg360=)
c.587C>A
c.1029C>A (p.Arg343=)
c.984C>A (p.Arg328=)
c.700C>A (p.Pro234Thr)
 ClinVar dbSNP gnomAD v4
2g.218893097C=CA1328965362WNT10Ac.1080C= (p.Arg360=)
c.587C=
c.1029C= (p.Arg343=)
c.984C= (p.Arg328=)
c.700C= (p.Pro234=)
2g.218893097C>GCA431417307WNT10Ac.1080C>G (p.Arg360=)
c.587C>G
c.1029C>G (p.Arg343=)
c.984C>G (p.Arg328=)
c.700C>G (p.Pro234Ala)
2g.218893097C>TCA431417309WNT10Ac.1080C>T (p.Arg360=)
c.587C>T
c.1029C>T (p.Arg343=)
c.984C>T (p.Arg328=)
c.700C>T (p.Pro234Ser)
 gnomAD v4
2g.218893098C>ACA350591231WNT10Ac.1081C>A (p.Leu361Met)
c.588C>A
c.1030C>A (p.Leu344Met)
c.985C>A (p.Leu329Met)
c.701C>A (p.Pro234His)
2g.218893098C=CA1328965364WNT10Ac.1081C= (p.Leu361=)
c.588C=
c.1030C= (p.Leu344=)
c.985C= (p.Leu329=)
c.701C= (p.Pro234=)
2g.218893098C>GCA350591232WNT10Ac.1081C>G (p.Leu361Val)
c.588C>G
c.1030C>G (p.Leu344Val)
c.985C>G (p.Leu329Val)
c.701C>G (p.Pro234Arg)
 gnomAD v4
2g.218893098C>TCA431417313WNT10Ac.1081C>T (p.Leu361=)
c.588C>T
c.1030C>T (p.Leu344=)
c.985C>T (p.Leu329=)
c.701C>T (p.Pro234Leu)
 ClinVar dbSNP gnomAD v4
2g.218893099T>ACA350591235WNT10Ac.1082T>A (p.Leu361Gln)
c.589T>A
c.1031T>A (p.Leu344Gln)
c.986T>A (p.Leu329Gln)
c.702T>A (p.Pro234=)
2g.218893099T>CCA350591246WNT10Ac.1082T>C (p.Leu361Pro)
c.589T>C
c.1031T>C (p.Leu344Pro)
c.986T>C (p.Leu329Pro)
c.702T>C (p.Pro234=)
 gnomAD v4
2g.218893099T>GCA350591249WNT10Ac.1082T>G (p.Leu361Arg)
c.589T>G
c.1031T>G (p.Leu344Arg)
c.986T>G (p.Leu329Arg)
c.702T>G (p.Pro234=)
2g.218893100G>ACA431417315WNT10Ac.1083G>A (p.Leu361=)
c.590G>A
c.1032G>A (p.Leu344=)
c.987G>A (p.Leu329=)
c.703G>A (p.Val235Met)
2g.218893100G>CCA431417316WNT10Ac.1083G>C (p.Leu361=)
c.590G>C
c.1032G>C (p.Leu344=)
c.987G>C (p.Leu329=)
c.703G>C (p.Val235Leu)
2g.218893100G>TCA431417317WNT10Ac.1083G>T (p.Leu361=)
c.590G>T
c.1032G>T (p.Leu344=)
c.987G>T (p.Leu329=)
c.703G>T (p.Val235Leu)
 gnomAD v4
2g.218893101T>ACA350591253WNT10Ac.1084T>A (p.Cys362Ser)
c.591T>A
c.1033T>A (p.Cys345Ser)
c.988T>A (p.Cys330Ser)
c.704T>A (p.Val235Glu)
 gnomAD v4
2g.218893101T>CCA350591255WNT10Ac.1084T>C (p.Cys362Arg)
c.591T>C
c.1033T>C (p.Cys345Arg)
c.988T>C (p.Cys330Arg)
c.704T>C (p.Val235Ala)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893101T>GCA350591258WNT10Ac.1084T>G (p.Cys362Gly)
c.591T>G
c.1033T>G (p.Cys345Gly)
c.988T>G (p.Cys330Gly)
c.704T>G (p.Val235Gly)
2g.218893101T=CA1328965369WNT10Ac.1084T= (p.Cys362=)
c.591T=
c.1033T= (p.Cys345=)
c.988T= (p.Cys330=)
c.704T= (p.Val235=)
2g.218893101_218893115delinsTGCAACAAGAGCAGCCA1328965368WNT10Ac.1084_1098delinsTGCAACAAGAGCAGC (p.Cys362=)
c.591_605delinsTGCAACAAGAGCAGC
c.1033_1047delinsTGCAACAAGAGCAGC (p.Cys345=)
c.988_1002delinsTGCAACAAGAGCAGC (p.Cys330=)
c.704_718delinsTGCAACAAGAGCAGC (p.Val235=)
2g.218893102G>ACA350591268WNT10Ac.1085G>A (p.Cys362Tyr)
c.592G>A
c.1034G>A (p.Cys345Tyr)
c.989G>A (p.Cys330Tyr)
c.705G>A (p.Val235=)
2g.218893102G>CCA350591270WNT10Ac.1085G>C (p.Cys362Ser)
c.592G>C
c.1034G>C (p.Cys345Ser)
c.989G>C (p.Cys330Ser)
c.705G>C (p.Val235=)
2g.218893102G=CA1328965376WNT10Ac.1085G= (p.Cys362=)
c.592G=
c.1034G= (p.Cys345=)
c.989G= (p.Cys330=)
c.705G= (p.Val235=)
2g.218893102G>TCA350591278WNT10Ac.1085G>T (p.Cys362Phe)
c.592G>T
c.1034G>T (p.Cys345Phe)
c.989G>T (p.Cys330Phe)
c.705G>T (p.Val235=)
 ClinVar dbSNP gnomAD v4
2g.218893104_218893117delCA2114107WNT10Ac.1087_1100del (p.Asn363ArgfsTer?)
c.594_607del
c.1036_1049del (p.Asn346ArgfsTer?)
c.991_1004del (p.Asn331ArgfsTer?)
c.707_720del (p.Gln236ProfsTer?)
 dbSNP ExAC gnomAD v2
2g.218893103C>ACA350591287WNT10Ac.1086C>A (p.Cys362Ter)
c.593C>A
c.1035C>A (p.Cys345Ter)
c.990C>A (p.Cys330Ter)
c.706C>A (p.Gln236Lys)
2g.218893103C>GCA350591290WNT10Ac.1086C>G (p.Cys362Trp)
c.593C>G
c.1035C>G (p.Cys345Trp)
c.990C>G (p.Cys330Trp)
c.706C>G (p.Gln236Glu)
2g.218893103C>TCA431417328WNT10Ac.1086C>T (p.Cys362=)
c.593C>T
c.1035C>T (p.Cys345=)
c.990C>T (p.Cys330=)
c.706C>T (p.Gln236Ter)
 gnomAD v4
2g.218893104A=CA1328965383WNT10Ac.1087A= (p.Asn363=)
c.594A=
c.1036A= (p.Asn346=)
c.991A= (p.Asn331=)
c.707A= (p.Gln236=)
2g.218893104A>CCA2114108WNT10Ac.1087A>C (p.Asn363His)
c.594A>C
c.1036A>C (p.Asn346His)
c.991A>C (p.Asn331His)
c.707A>C (p.Gln236Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893104A>GCA350591292WNT10Ac.1087A>G (p.Asn363Asp)
c.594A>G
c.1036A>G (p.Asn346Asp)
c.991A>G (p.Asn331Asp)
c.707A>G (p.Gln236Arg)
2g.218893104A>TCA350591294WNT10Ac.1087A>T (p.Asn363Tyr)
c.594A>T
c.1036A>T (p.Asn346Tyr)
c.991A>T (p.Asn331Tyr)
c.707A>T (p.Gln236Leu)
2g.218893105A>CCA350591297WNT10Ac.1088A>C (p.Asn363Thr)
c.595A>C
c.1037A>C (p.Asn346Thr)
c.992A>C (p.Asn331Thr)
c.708A>C (p.Gln236His)
2g.218893105A>GCA350591298WNT10Ac.1088A>G (p.Asn363Ser)
c.595A>G
c.1037A>G (p.Asn346Ser)
c.992A>G (p.Asn331Ser)
c.708A>G (p.Gln236=)
 gnomAD v4
2g.218893105A>TCA350591303WNT10Ac.1088A>T (p.Asn363Ile)
c.595A>T
c.1037A>T (p.Asn346Ile)
c.992A>T (p.Asn331Ile)
c.708A>T (p.Gln236His)
2g.218893106C>ACA350591307WNT10Ac.1089C>A (p.Asn363Lys)
c.596C>A
c.1038C>A (p.Asn346Lys)
c.993C>A (p.Asn331Lys)
c.709C>A (p.Gln237Lys)
 gnomAD v4
2g.218893106C>GCA350591309WNT10Ac.1089C>G (p.Asn363Lys)
c.596C>G
c.1038C>G (p.Asn346Lys)
c.993C>G (p.Asn331Lys)
c.709C>G (p.Gln237Glu)
2g.218893106C>TCA431417339WNT10Ac.1089C>T (p.Asn363=)
c.596C>T
c.1038C>T (p.Asn346=)
c.993C>T (p.Asn331=)
c.709C>T (p.Gln237Ter)
2g.218893107A=CA1328965388WNT10Ac.1090A= (p.Lys364=)
c.597A=
c.1039A= (p.Lys347=)
c.994A= (p.Lys332=)
c.710A= (p.Gln237=)
2g.218893107A>CCA350591313WNT10Ac.1090A>C (p.Lys364Gln)
c.597A>C
c.1039A>C (p.Lys347Gln)
c.994A>C (p.Lys332Gln)
c.710A>C (p.Gln237Pro)
 dbSNP gnomAD v3 gnomAD v4
2g.218893107A>GCA350591326WNT10Ac.1090A>G (p.Lys364Glu)
c.597A>G
c.1039A>G (p.Lys347Glu)
c.994A>G (p.Lys332Glu)
c.710A>G (p.Gln237Arg)
2g.218893107A>TCA350591328WNT10Ac.1090A>T (p.Lys364Ter)
c.597A>T
c.1039A>T (p.Lys347Ter)
c.994A>T (p.Lys332Ter)
c.710A>T (p.Gln237Leu)
2g.218893108dupCA2573135233WNT10Ac.1091dup (p.Ser365GlufsTer?)
c.598dup
c.1040dup (p.Ser348GlufsTer?)
c.995dup (p.Ser333GlufsTer?)
c.711dup (p.Glu238ArgfsTer?)
 ClinVar dbSNP
2g.218893108A=CA1328965390WNT10Ac.1091A= (p.Lys364=)
c.598A=
c.1040A= (p.Lys347=)
c.995A= (p.Lys332=)
c.711A= (p.Gln237=)
2g.218893108A>CCA350591331WNT10Ac.1091A>C (p.Lys364Thr)
c.598A>C
c.1040A>C (p.Lys347Thr)
c.995A>C (p.Lys332Thr)
c.711A>C (p.Gln237His)
 dbSNP
2g.218893108A>GCA350591332WNT10Ac.1091A>G (p.Lys364Arg)
c.598A>G
c.1040A>G (p.Lys347Arg)
c.995A>G (p.Lys332Arg)
c.711A>G (p.Gln237=)
 gnomAD v4
2g.218893108A>TCA350591333WNT10Ac.1091A>T (p.Lys364Met)
c.598A>T
c.1040A>T (p.Lys347Met)
c.995A>T (p.Lys332Met)
c.711A>T (p.Gln237His)
2g.218893109G>ACA431417347WNT10Ac.1092G>A (p.Lys364=)
c.599G>A
c.1041G>A (p.Lys347=)
c.996G>A (p.Lys332=)
c.712G>A (p.Glu238Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893109G>CCA350591345WNT10Ac.1092G>C (p.Lys364Asn)
c.599G>C
c.1041G>C (p.Lys347Asn)
c.996G>C (p.Lys332Asn)
c.712G>C (p.Glu238Gln)
2g.218893109G=CA1328965392WNT10Ac.1092G= (p.Lys364=)
c.599G=
c.1041G= (p.Lys347=)
c.996G= (p.Lys332=)
c.712G= (p.Glu238=)
2g.218893109G>TCA350591338WNT10Ac.1092G>T (p.Lys364Asn)
c.599G>T
c.1041G>T (p.Lys347Asn)
c.996G>T (p.Lys332Asn)
c.712G>T (p.Glu238Ter)
2g.218893110A>CCA350591350WNT10Ac.1093A>C (p.Ser365Arg)
c.600A>C
c.1042A>C (p.Ser348Arg)
c.997A>C (p.Ser333Arg)
c.713A>C (p.Glu238Ala)
2g.218893110A>GCA350591355WNT10Ac.1093A>G (p.Ser365Gly)
c.600A>G
c.1042A>G (p.Ser348Gly)
c.997A>G (p.Ser333Gly)
c.713A>G (p.Glu238Gly)
 gnomAD v4
2g.218893110A>TCA350591367WNT10Ac.1093A>T (p.Ser365Cys)
c.600A>T
c.1042A>T (p.Ser348Cys)
c.997A>T (p.Ser333Cys)
c.713A>T (p.Glu238Val)
2g.218893111G>ACA350591388WNT10Ac.1094G>A (p.Ser365Asn)
c.601G>A
c.1043G>A (p.Ser348Asn)
c.998G>A (p.Ser333Asn)
c.714G>A (p.Glu238=)
2g.218893111G>CCA350591390WNT10Ac.1094G>C (p.Ser365Thr)
c.601G>C
c.1043G>C (p.Ser348Thr)
c.998G>C (p.Ser333Thr)
c.714G>C (p.Glu238Asp)
2g.218893111G>TCA350591400WNT10Ac.1094G>T (p.Ser365Ile)
c.601G>T
c.1043G>T (p.Ser348Ile)
c.998G>T (p.Ser333Ile)
c.714G>T (p.Glu238Asp)
 gnomAD v4
2g.218893112C>ACA350591414WNT10Ac.1095C>A (p.Ser365Arg)
c.602C>A
c.1044C>A (p.Ser348Arg)
c.999C>A (p.Ser333Arg)
c.715C>A (p.Gln239Lys)
2g.218893112C>GCA350591404WNT10Ac.1095C>G (p.Ser365Arg)
c.602C>G
c.1044C>G (p.Ser348Arg)
c.999C>G (p.Ser333Arg)
c.715C>G (p.Gln239Glu)
2g.218893112C>TCA431417350WNT10Ac.1095C>T (p.Ser365=)
c.602C>T
c.1044C>T (p.Ser348=)
c.999C>T (p.Ser333=)
c.715C>T (p.Gln239Ter)
2g.218893113A=CA1328965397WNT10Ac.1096A= (p.Ser366=)
c.603A=
c.1045A= (p.Ser349=)
c.1000A= (p.Ser334=)
c.716A= (p.Gln239=)
2g.218893113A>CCA350591420WNT10Ac.1096A>C (p.Ser366Arg)
c.603A>C
c.1045A>C (p.Ser349Arg)
c.1000A>C (p.Ser334Arg)
c.716A>C (p.Gln239Pro)
2g.218893113A>GCA350591424WNT10Ac.1096A>G (p.Ser366Gly)
c.603A>G
c.1045A>G (p.Ser349Gly)
c.1000A>G (p.Ser334Gly)
c.716A>G (p.Gln239Arg)
2g.218893113A>TCA350591429WNT10Ac.1096A>T (p.Ser366Cys)
c.603A>T
c.1045A>T (p.Ser349Cys)
c.1000A>T (p.Ser334Cys)
c.716A>T (p.Gln239Leu)
 dbSNP gnomAD v3 gnomAD v4
2g.218893114G>ACA350591432WNT10Ac.1097G>A (p.Ser366Asn)
c.604G>A
c.1046G>A (p.Ser349Asn)
c.1001G>A (p.Ser334Asn)
c.717G>A (p.Gln239=)
 dbSNP gnomAD v4
2g.218893114G>CCA350591435WNT10Ac.1097G>C (p.Ser366Thr)
c.604G>C
c.1046G>C (p.Ser349Thr)
c.1001G>C (p.Ser334Thr)
c.717G>C (p.Gln239His)
2g.218893114G=CA1328965400WNT10Ac.1097G= (p.Ser366=)
c.604G=
c.1046G= (p.Ser349=)
c.1001G= (p.Ser334=)
c.717G= (p.Gln239=)
2g.218893114G>TCA350591441WNT10Ac.1097G>T (p.Ser366Ile)
c.604G>T
c.1046G>T (p.Ser349Ile)
c.1001G>T (p.Ser334Ile)
c.717G>T (p.Gln239His)
2g.218893115C>ACA350591471WNT10Ac.1098C>A (p.Ser366Arg)
c.605C>A
c.1047C>A (p.Ser349Arg)
c.1002C>A (p.Ser334Arg)
c.718C>A (p.Arg240Ser)
 dbSNP gnomAD v4
2g.218893115C=CA1328965403WNT10Ac.1098C= (p.Ser366=)
c.605C=
c.1047C= (p.Ser349=)
c.1002C= (p.Ser334=)
c.718C= (p.Arg240=)
2g.218893115C>GCA350591452WNT10Ac.1098C>G (p.Ser366Arg)
c.605C>G
c.1047C>G (p.Ser349Arg)
c.1002C>G (p.Ser334Arg)
c.718C>G (p.Arg240Gly)
2g.218893115C>TCA2114109WNT10Ac.1098C>T (p.Ser366=)
c.605C>T
c.1047C>T (p.Ser349=)
c.1002C>T (p.Ser334=)
c.718C>T (p.Arg240Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893116G>ACA350591475WNT10Ac.1099G>A (p.Ala367Thr)
c.606G>A
c.1048G>A (p.Ala350Thr)
c.1003G>A (p.Ala335Thr)
c.719G>A (p.Arg240His)
 gnomAD v4
2g.218893116G>CCA350591479WNT10Ac.1099G>C (p.Ala367Pro)
c.606G>C
c.1048G>C (p.Ala350Pro)
c.1003G>C (p.Ala335Pro)
c.719G>C (p.Arg240Pro)
2g.218893116G>TCA350591484WNT10Ac.1099G>T (p.Ala367Ser)
c.606G>T
c.1048G>T (p.Ala350Ser)
c.1003G>T (p.Ala335Ser)
c.719G>T (p.Arg240Leu)
 gnomAD v4
2g.218893117C>ACA350591494WNT10Ac.1100C>A (p.Ala367Asp)
c.607C>A
c.1049C>A (p.Ala350Asp)
c.1004C>A (p.Ala335Asp)
c.720C>A (p.Arg240=)
2g.218893117C>GCA350591497WNT10Ac.1100C>G (p.Ala367Gly)
c.607C>G
c.1049C>G (p.Ala350Gly)
c.1004C>G (p.Ala335Gly)
c.720C>G (p.Arg240=)
 gnomAD v4
2g.218893117C>TCA350591501WNT10Ac.1100C>T (p.Ala367Val)
c.607C>T
c.1049C>T (p.Ala350Val)
c.1004C>T (p.Ala335Val)
c.720C>T (p.Arg240=)
 gnomAD v4
2g.218893118C>ACA431417369WNT10Ac.1101C>A (p.Ala367=)
c.608C>A
c.1050C>A (p.Ala350=)
c.1005C>A (p.Ala335=)
c.721C>A (p.Arg241=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893118C=CA1328965407WNT10Ac.1101C= (p.Ala367=)
c.608C=
c.1050C= (p.Ala350=)
c.1005C= (p.Ala335=)
c.721C= (p.Arg241=)
2g.218893118C>GCA431417373WNT10Ac.1101C>G (p.Ala367=)
c.608C>G
c.1050C>G (p.Ala350=)
c.1005C>G (p.Ala335=)
c.721C>G (p.Arg241Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893118C>TCA431417376WNT10Ac.1101C>T (p.Ala367=)
c.608C>T
c.1050C>T (p.Ala350=)
c.1005C>T (p.Ala335=)
c.721C>T (p.Arg241Trp)
 gnomAD v4
2g.218893119G>ACA350591504WNT10Ac.1102G>A (p.Gly368Ser)
c.609G>A
c.1051G>A (p.Gly351Ser)
c.1006G>A (p.Gly336Ser)
c.722G>A (p.Arg241Gln)
 dbSNP gnomAD v4
2g.218893119G>CCA350591503WNT10Ac.1102G>C (p.Gly368Arg)
c.609G>C
c.1051G>C (p.Gly351Arg)
c.1006G>C (p.Gly336Arg)
c.722G>C (p.Arg241Pro)
2g.218893119G=CA1328965410WNT10Ac.1102G= (p.Gly368=)
c.609G=
c.1051G= (p.Gly351=)
c.1006G= (p.Gly336=)
c.722G= (p.Arg241=)
2g.218893119G>TCA350591502WNT10Ac.1102G>T (p.Gly368Cys)
c.609G>T
c.1051G>T (p.Gly351Cys)
c.1006G>T (p.Gly336Cys)
c.722G>T (p.Arg241Leu)
2g.218893120G>ACA350591506WNT10Ac.1103G>A (p.Gly368Asp)
c.610G>A
c.1052G>A (p.Gly351Asp)
c.1007G>A (p.Gly336Asp)
c.723G>A (p.Arg241=)
 dbSNP gnomAD v4
2g.218893120G>CCA350591530WNT10Ac.1103G>C (p.Gly368Ala)
c.610G>C
c.1052G>C (p.Gly351Ala)
c.1007G>C (p.Gly336Ala)
c.723G>C (p.Arg241=)
2g.218893120G=CA1328965412WNT10Ac.1103G= (p.Gly368=)
c.610G=
c.1052G= (p.Gly351=)
c.1007G= (p.Gly336=)
c.723G= (p.Arg241=)
2g.218893120G>TCA350591532WNT10Ac.1103G>T (p.Gly368Val)
c.610G>T
c.1052G>T (p.Gly351Val)
c.1007G>T (p.Gly336Val)
c.723G>T (p.Arg241=)
 gnomAD v4
2g.218893121C>ACA431417381WNT10Ac.1104C>A (p.Gly368=)
c.611C>A
c.1053C>A (p.Gly351=)
c.1008C>A (p.Gly336=)
c.724C>A (p.Leu242Ile)
2g.218893121C>GCA431417386WNT10Ac.1104C>G (p.Gly368=)
c.611C>G
c.1053C>G (p.Gly351=)
c.1008C>G (p.Gly336=)
c.724C>G (p.Leu242Val)
2g.218893121C>TCA431417387WNT10Ac.1104C>T (p.Gly368=)
c.611C>T
c.1053C>T (p.Gly351=)
c.1008C>T (p.Gly336=)
c.724C>T (p.Leu242Phe)
 dbSNP
2g.218893122T>ACA350591534WNT10Ac.1105T>A (p.Ser369Thr)
c.612T>A
c.1054T>A (p.Ser352Thr)
c.1009T>A (p.Ser337Thr)
c.725T>A (p.Leu242His)
2g.218893122T>CCA350591536WNT10Ac.1105T>C (p.Ser369Pro)
c.612T>C
c.1054T>C (p.Ser352Pro)
c.1009T>C (p.Ser337Pro)
c.725T>C (p.Leu242Pro)
2g.218893122T>GCA350591538WNT10Ac.1105T>G (p.Ser369Ala)
c.612T>G
c.1054T>G (p.Ser352Ala)
c.1009T>G (p.Ser337Ala)
c.725T>G (p.Leu242Arg)
2g.218893123C>ACA350591543WNT10Ac.1106C>A (p.Ser369Ter)
c.613C>A
c.1055C>A (p.Ser352Ter)
c.1010C>A (p.Ser337Ter)
c.726C>A (p.Leu242=)
2g.218893123C=CA1328965415WNT10Ac.1106C= (p.Ser369=)
c.613C=
c.1055C= (p.Ser352=)
c.1010C= (p.Ser337=)
c.726C= (p.Leu242=)
2g.218893123C>GCA2114110WNT10Ac.1106C>G (p.Ser369Trp)
c.613C>G
c.1055C>G (p.Ser352Trp)
c.1010C>G (p.Ser337Trp)
c.726C>G (p.Leu242=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893123C>TCA2114111WNT10Ac.1106C>T (p.Ser369Leu)
c.613C>T
c.1055C>T (p.Ser352Leu)
c.1010C>T (p.Ser337Leu)
c.726C>T (p.Leu242=)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893124G>ACA431417396WNT10Ac.1107G>A (p.Ser369=)
c.614G>A
c.1056G>A (p.Ser352=)
c.1011G>A (p.Ser337=)
c.727G>A (p.Gly243Arg)
 ClinVar dbSNP gnomAD v4
2g.218893124G>CCA431417399WNT10Ac.1107G>C (p.Ser369=)
c.614G>C
c.1056G>C (p.Ser352=)
c.1011G>C (p.Ser337=)
c.727G>C (p.Gly243Arg)
2g.218893124G=CA1328965420WNT10Ac.1107G= (p.Ser369=)
c.614G=
c.1056G= (p.Ser352=)
c.1011G= (p.Ser337=)
c.727G= (p.Gly243=)
2g.218893124G>TCA431417402WNT10Ac.1107G>T (p.Ser369=)
c.614G>T
c.1056G>T (p.Ser352=)
c.1011G>T (p.Ser337=)
c.727G>T (p.Gly243Ter)
 ClinVar dbSNP gnomAD v4
2g.218893125G>ACA350591555WNT10Ac.1108G>A (p.Asp370Asn)
c.615G>A
c.1057G>A (p.Asp353Asn)
c.1012G>A (p.Asp338Asn)
c.728G>A (p.Gly243Glu)
 gnomAD v4 COSMIC
2g.218893125G>CCA350591559WNT10Ac.1108G>C (p.Asp370His)
c.615G>C
c.1057G>C (p.Asp353His)
c.1012G>C (p.Asp338His)
c.728G>C (p.Gly243Ala)
2g.218893125G>TCA350591562WNT10Ac.1108G>T (p.Asp370Tyr)
c.615G>T
c.1057G>T (p.Asp353Tyr)
c.1012G>T (p.Asp338Tyr)
c.728G>T (p.Gly243Val)
2g.218893126A=CA1328965423WNT10Ac.1109A= (p.Asp370=)
c.616A=
c.1058A= (p.Asp353=)
c.1013A= (p.Asp338=)
c.729A= (p.Gly243=)
2g.218893126A>CCA350591565WNT10Ac.1109A>C (p.Asp370Ala)
c.616A>C
c.1058A>C (p.Asp353Ala)
c.1013A>C (p.Asp338Ala)
c.729A>C (p.Gly243=)
 dbSNP gnomAD v3 gnomAD v4
2g.218893126A>GCA350591570WNT10Ac.1109A>G (p.Asp370Gly)
c.616A>G
c.1058A>G (p.Asp353Gly)
c.1013A>G (p.Asp338Gly)
c.729A>G (p.Gly243=)
2g.218893126A>TCA350591571WNT10Ac.1109A>T (p.Asp370Val)
c.616A>T
c.1058A>T (p.Asp353Val)
c.1013A>T (p.Asp338Val)
c.729A>T (p.Gly243=)
2g.218893127T>ACA350591574WNT10Ac.1110T>A (p.Asp370Glu)
c.617T>A
c.1059T>A (p.Asp353Glu)
c.1014T>A (p.Asp338Glu)
c.730T>A (p.Trp244Arg)
2g.218893127T>CCA431417410WNT10Ac.1110T>C (p.Asp370=)
c.617T>C
c.1059T>C (p.Asp353=)
c.1014T>C (p.Asp338=)
c.730T>C (p.Trp244Arg)
 ClinVar dbSNP gnomAD v4
2g.218893127T>GCA350591576WNT10Ac.1110T>G (p.Asp370Glu)
c.617T>G
c.1059T>G (p.Asp353Glu)
c.1014T>G (p.Asp338Glu)
c.730T>G (p.Trp244Gly)
2g.218893127T=CA1328965426WNT10Ac.1110T= (p.Asp370=)
c.617T=
c.1059T= (p.Asp353=)
c.1014T= (p.Asp338=)
c.730T= (p.Trp244=)
2g.218893128G>ACA350591579WNT10Ac.1111G>A (p.Gly371Ser)
c.618G>A
c.1060G>A (p.Gly354Ser)
c.1015G>A (p.Gly339Ser)
c.731G>A (p.Trp244Ter)
2g.218893128G>CCA350591596WNT10Ac.1111G>C (p.Gly371Arg)
c.618G>C
c.1060G>C (p.Gly354Arg)
c.1015G>C (p.Gly339Arg)
c.731G>C (p.Trp244Ser)
2g.218893128G=CA1328965427WNT10Ac.1111G= (p.Gly371=)
c.618G=
c.1060G= (p.Gly354=)
c.1015G= (p.Gly339=)
c.731G= (p.Trp244=)
2g.218893128G>TCA350591600WNT10Ac.1111G>T (p.Gly371Cys)
c.618G>T
c.1060G>T (p.Gly354Cys)
c.1015G>T (p.Gly339Cys)
c.731G>T (p.Trp244Leu)
 gnomAD v4
2g.218893129G>ACA350591604WNT10Ac.1112G>A (p.Gly371Asp)
c.619G>A
c.1061G>A (p.Gly354Asp)
c.1016G>A (p.Gly339Asp)
c.732G>A (p.Trp244Ter)
 gnomAD v4
2g.218893129G>CCA350591615WNT10Ac.1112G>C (p.Gly371Ala)
c.619G>C
c.1061G>C (p.Gly354Ala)
c.1016G>C (p.Gly339Ala)
c.732G>C (p.Trp244Cys)
2g.218893129G>TCA350591614WNT10Ac.1112G>T (p.Gly371Val)
c.619G>T
c.1061G>T (p.Gly354Val)
c.1016G>T (p.Gly339Val)
c.732G>T (p.Trp244Cys)
 gnomAD v4
2g.218893137_218893151dupCA539840853WNT10Ac.1120_1134dup (p.Gly378_Arg379insSerMetCysCysGly)
c.1069_1083dup (p.Gly361_Arg362insSerMetCysCysGly)
c.1024_1038dup (p.Gly346_Arg347insSerMetCysCysGly)
c.740_754dup (p.Arg251_Pro252insGlnHisValLeuArg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893130C>ACA431417416WNT10Ac.1113C>A (p.Gly371=)
c.620C>A
c.1062C>A (p.Gly354=)
c.1017C>A (p.Gly339=)
c.733C>A (p.Leu245Met)
2g.218893130C>GCA431417415WNT10Ac.1113C>G (p.Gly371=)
c.620C>G
c.1062C>G (p.Gly354=)
c.1017C>G (p.Gly339=)
c.733C>G (p.Leu245Val)
2g.218893130C>TCA431417414WNT10Ac.1113C>T (p.Gly371=)
c.620C>T
c.1062C>T (p.Gly354=)
c.1017C>T (p.Gly339=)
c.733C>T (p.Leu245=)
 gnomAD v4
2g.218893131T>ACA350591616WNT10Ac.1114T>A (p.Cys372Ser)
c.621T>A
c.1063T>A (p.Cys355Ser)
c.1018T>A (p.Cys340Ser)
c.734T>A (p.Leu245Gln)
2g.218893131T>CCA350591637WNT10Ac.1114T>C (p.Cys372Arg)
c.621T>C
c.1063T>C (p.Cys355Arg)
c.1018T>C (p.Cys340Arg)
c.734T>C (p.Leu245Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893131T>GCA350591634WNT10Ac.1114T>G (p.Cys372Gly)
c.621T>G
c.1063T>G (p.Cys355Gly)
c.1018T>G (p.Cys340Gly)
c.734T>G (p.Leu245Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893131T=CA1328965434WNT10Ac.1114T= (p.Cys372=)
c.621T=
c.1063T= (p.Cys355=)
c.1018T= (p.Cys340=)
c.734T= (p.Leu245=)
2g.218893132G>ACA350591640WNT10Ac.1115G>A (p.Cys372Tyr)
c.622G>A
c.1064G>A (p.Cys355Tyr)
c.1019G>A (p.Cys340Tyr)
c.735G>A (p.Leu245=)
2g.218893132G>CCA350591641WNT10Ac.1115G>C (p.Cys372Ser)
c.622G>C
c.1064G>C (p.Cys355Ser)
c.1019G>C (p.Cys340Ser)
c.735G>C (p.Leu245=)
2g.218893132G>TCA350591642WNT10Ac.1115G>T (p.Cys372Phe)
c.622G>T
c.1064G>T (p.Cys355Phe)
c.1019G>T (p.Cys340Phe)
c.735G>T (p.Leu245=)
 gnomAD v4
2g.218893133C>ACA350591644WNT10Ac.1116C>A (p.Cys372Ter)
c.623C>A
c.1065C>A (p.Cys355Ter)
c.1020C>A (p.Cys340Ter)
c.736C>A (p.Arg246=)
2g.218893133C=CA1328965438WNT10Ac.1116C= (p.Cys372=)
c.623C=
c.1065C= (p.Cys355=)
c.1020C= (p.Cys340=)
c.736C= (p.Arg246=)
2g.218893133C>GCA350591646WNT10Ac.1116C>G (p.Cys372Trp)
c.623C>G
c.1065C>G (p.Cys355Trp)
c.1020C>G (p.Cys340Trp)
c.736C>G (p.Arg246Gly)
2g.218893133C>TCA2114112WNT10Ac.1116C>T (p.Cys372=)
c.623C>T
c.1065C>T (p.Cys355=)
c.1020C>T (p.Cys340=)
c.736C>T (p.Arg246Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893134G>ACA2114113WNT10Ac.1117G>A (p.Gly373Ser)
c.624G>A
c.1066G>A (p.Gly356Ser)
c.1021G>A (p.Gly341Ser)
c.737G>A (p.Arg246Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893134G>CCA350591654WNT10Ac.1117G>C (p.Gly373Arg)
c.624G>C
c.1066G>C (p.Gly356Arg)
c.1021G>C (p.Gly341Arg)
c.737G>C (p.Arg246Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893134G=CA1328965441WNT10Ac.1117G= (p.Gly373=)
c.624G=
c.1066G= (p.Gly356=)
c.1021G= (p.Gly341=)
c.737G= (p.Arg246=)
2g.218893134G>TCA350591657WNT10Ac.1117G>T (p.Gly373Cys)
c.624G>T
c.1066G>T (p.Gly356Cys)
c.1021G>T (p.Gly341Cys)
c.737G>T (p.Arg246Leu)
2g.218893135G>ACA350591660WNT10Ac.1118G>A (p.Gly373Asp)
c.625G>A
c.1067G>A (p.Gly356Asp)
c.1022G>A (p.Gly341Asp)
c.738G>A (p.Arg246=)
 gnomAD v4
2g.218893135G>CCA350591663WNT10Ac.1118G>C (p.Gly373Ala)
c.625G>C
c.1067G>C (p.Gly356Ala)
c.1022G>C (p.Gly341Ala)
c.738G>C (p.Arg246=)
2g.218893135G>TCA350591678WNT10Ac.1118G>T (p.Gly373Val)
c.625G>T
c.1067G>T (p.Gly356Val)
c.1022G>T (p.Gly341Val)
c.738G>T (p.Arg246=)
2g.218893136C>ACA431417441WNT10Ac.1119C>A (p.Gly373=)
c.626C>A
c.1068C>A (p.Gly356=)
c.1023C>A (p.Gly341=)
c.739C>A (p.Gln247Lys)
 gnomAD v4
2g.218893136C>GCA431417437WNT10Ac.1119C>G (p.Gly373=)
c.626C>G
c.1068C>G (p.Gly356=)
c.1023C>G (p.Gly341=)
c.739C>G (p.Gln247Glu)
2g.218893136C>TCA431417439WNT10Ac.1119C>T (p.Gly373=)
c.626C>T
c.1068C>T (p.Gly356=)
c.1023C>T (p.Gly341=)
c.739C>T (p.Gln247Ter)
 gnomAD v4
2g.218893137A>CCA350591690WNT10Ac.1120A>C (p.Ser374Arg)
c.627A>C
c.1069A>C (p.Ser357Arg)
c.1024A>C (p.Ser342Arg)
c.740A>C (p.Gln247Pro)
2g.218893137A>GCA350591683WNT10Ac.1120A>G (p.Ser374Gly)
c.627A>G
c.1069A>G (p.Ser357Gly)
c.1024A>G (p.Ser342Gly)
c.740A>G (p.Gln247Arg)
2g.218893137A>TCA350591687WNT10Ac.1120A>T (p.Ser374Cys)
c.627A>T
c.1069A>T (p.Ser357Cys)
c.1024A>T (p.Ser342Cys)
c.740A>T (p.Gln247Leu)
2g.218893138G>ACA350591696WNT10Ac.1121G>A (p.Ser374Asn)
c.628G>A
c.1070G>A (p.Ser357Asn)
c.1025G>A (p.Ser342Asn)
c.741G>A (p.Gln247=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893138G>CCA350591698WNT10Ac.1121G>C (p.Ser374Thr)
c.628G>C
c.1070G>C (p.Ser357Thr)
c.1025G>C (p.Ser342Thr)
c.741G>C (p.Gln247His)
 gnomAD v4
2g.218893138G=CA1328965443WNT10Ac.1121G= (p.Ser374=)
c.628G=
c.1070G= (p.Ser357=)
c.1025G= (p.Ser342=)
c.741G= (p.Gln247=)
2g.218893138G>TCA350591701WNT10Ac.1121G>T (p.Ser374Ile)
c.628G>T
c.1070G>T (p.Ser357Ile)
c.1025G>T (p.Ser342Ile)
c.741G>T (p.Gln247His)
 gnomAD v4
2g.218893140_218893154delCA2663174551WNT10Ac.1123_1137del (p.Met375_Arg379del)
c.1072_1086del (p.Met358_Arg362del)
c.1027_1041del (p.Met343_Arg347del)
c.743_757del (p.His248_Pro252del)
 gnomAD v4
2g.218893139C>ACA350591705WNT10Ac.1122C>A (p.Ser374Arg)
c.629C>A
c.1071C>A (p.Ser357Arg)
c.1026C>A (p.Ser342Arg)
c.742C>A (p.His248Asn)
2g.218893139C>GCA350591711WNT10Ac.1122C>G (p.Ser374Arg)
c.629C>G
c.1071C>G (p.Ser357Arg)
c.1026C>G (p.Ser342Arg)
c.742C>G (p.His248Asp)
2g.218893139C>TCA431417456WNT10Ac.1122C>T (p.Ser374=)
c.629C>T
c.1071C>T (p.Ser357=)
c.1026C>T (p.Ser342=)
c.742C>T (p.His248Tyr)
 gnomAD v4
2g.218893140A>CCA350591721WNT10Ac.1123A>C (p.Met375Leu)
c.630A>C
c.1072A>C (p.Met358Leu)
c.1027A>C (p.Met343Leu)
c.743A>C (p.His248Pro)
2g.218893140A>GCA350591728WNT10Ac.1123A>G (p.Met375Val)
c.630A>G
c.1072A>G (p.Met358Val)
c.1027A>G (p.Met343Val)
c.743A>G (p.His248Arg)
 gnomAD v4
2g.218893140A>TCA350591729WNT10Ac.1123A>T (p.Met375Leu)
c.630A>T
c.1072A>T (p.Met358Leu)
c.1027A>T (p.Met343Leu)
c.743A>T (p.His248Leu)
2g.218893141T>ACA2114114WNT10Ac.1124T>A (p.Met375Lys)
c.631T>A
c.1073T>A (p.Met358Lys)
c.1028T>A (p.Met343Lys)
c.744T>A (p.His248Gln)
 dbSNP ExAC
2g.218893141T>CCA350591740WNT10Ac.1124T>C (p.Met375Thr)
c.631T>C
c.1073T>C (p.Met358Thr)
c.1028T>C (p.Met343Thr)
c.744T>C (p.His248=)
 ClinVar gnomAD v4
2g.218893141T>GCA350591743WNT10Ac.1124T>G (p.Met375Arg)
c.631T>G
c.1073T>G (p.Met358Arg)
c.1028T>G (p.Met343Arg)
c.744T>G (p.His248Gln)
 ClinVar dbSNP gnomAD v4
2g.218893141T=CA1328965447WNT10Ac.1124T= (p.Met375=)
c.631T=
c.1073T= (p.Met358=)
c.1028T= (p.Met343=)
c.744T= (p.His248=)
2g.218893142G>ACA350591755WNT10Ac.1125G>A (p.Met375Ile)
c.632G>A
c.1074G>A (p.Met358Ile)
c.1029G>A (p.Met343Ile)
c.745G>A (p.Val249Met)
 gnomAD v4
2g.218893142G>CCA350591751WNT10Ac.1125G>C (p.Met375Ile)
c.632G>C
c.1074G>C (p.Met358Ile)
c.1029G>C (p.Met343Ile)
c.745G>C (p.Val249Leu)
2g.218893142G>TCA350591747WNT10Ac.1125G>T (p.Met375Ile)
c.632G>T
c.1074G>T (p.Met358Ile)
c.1029G>T (p.Met343Ile)
c.745G>T (p.Val249Leu)
 gnomAD v4
2g.218893143T>ACA350591759WNT10Ac.1126T>A (p.Cys376Ser)
c.633T>A
c.1075T>A (p.Cys359Ser)
c.1030T>A (p.Cys344Ser)
c.746T>A (p.Val249Glu)
2g.218893143T>CCA350591761WNT10Ac.1126T>C (p.Cys376Arg)
c.633T>C
c.1075T>C (p.Cys359Arg)
c.1030T>C (p.Cys344Arg)
c.746T>C (p.Val249Ala)
2g.218893143T>GCA350591764WNT10Ac.1126T>G (p.Cys376Gly)
c.633T>G
c.1075T>G (p.Cys359Gly)
c.1030T>G (p.Cys344Gly)
c.746T>G (p.Val249Gly)
 gnomAD v4
2g.218893144G>ACA350591766WNT10Ac.1127G>A (p.Cys376Tyr)
c.634G>A
c.1076G>A (p.Cys359Tyr)
c.1031G>A (p.Cys344Tyr)
c.747G>A (p.Val249=)
 gnomAD v4
2g.218893144G>CCA350591778WNT10Ac.1127G>C (p.Cys376Ser)
c.634G>C
c.1076G>C (p.Cys359Ser)
c.1031G>C (p.Cys344Ser)
c.747G>C (p.Val249=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893144G=CA1328965452WNT10Ac.1127G= (p.Cys376=)
c.634G=
c.1076G= (p.Cys359=)
c.1031G= (p.Cys344=)
c.747G= (p.Val249=)
2g.218893144G>TCA350591782WNT10Ac.1127G>T (p.Cys376Phe)
c.634G>T
c.1076G>T (p.Cys359Phe)
c.1031G>T (p.Cys344Phe)
c.747G>T (p.Val249=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893145C>ACA116869WNT10Ac.1128C>A (p.Cys376Ter)
c.635C>A
c.1077C>A (p.Cys359Ter)
c.1032C>A (p.Cys344Ter)
c.748C>A (p.Leu250Met)
 ClinVar dbSNP
2g.218893145C=CA1328965455WNT10Ac.1128C= (p.Cys376=)
c.635C=
c.1077C= (p.Cys359=)
c.1032C= (p.Cys344=)
c.748C= (p.Leu250=)
2g.218893145C>GCA350591785WNT10Ac.1128C>G (p.Cys376Trp)
c.635C>G
c.1077C>G (p.Cys359Trp)
c.1032C>G (p.Cys344Trp)
c.748C>G (p.Leu250Val)
 dbSNP
2g.218893145C>TCA431417476WNT10Ac.1128C>T (p.Cys376=)
c.635C>T
c.1077C>T (p.Cys359=)
c.1032C>T (p.Cys344=)
c.748C>T (p.Leu250=)
 ClinVar dbSNP
2g.218893146T>ACA350591788WNT10Ac.1129T>A (p.Cys377Ser)
c.636T>A
c.1078T>A (p.Cys360Ser)
c.1033T>A (p.Cys345Ser)
c.749T>A (p.Leu250Gln)
2g.218893146T>CCA350591790WNT10Ac.1129T>C (p.Cys377Arg)
c.636T>C
c.1078T>C (p.Cys360Arg)
c.1033T>C (p.Cys345Arg)
c.749T>C (p.Leu250Pro)
2g.218893146T>GCA350591793WNT10Ac.1129T>G (p.Cys377Gly)
c.636T>G
c.1078T>G (p.Cys360Gly)
c.1033T>G (p.Cys345Gly)
c.749T>G (p.Leu250Arg)
 dbSNP gnomAD v4
2g.218893147G>ACA350591795WNT10Ac.1130G>A (p.Cys377Tyr)
c.1079G>A (p.Cys360Tyr)
c.1034G>A (p.Cys345Tyr)
c.750G>A (p.Leu250=)
 gnomAD v4
2g.218893147G>CCA350591798WNT10Ac.1130G>C (p.Cys377Ser)
c.1079G>C (p.Cys360Ser)
c.1034G>C (p.Cys345Ser)
c.750G>C (p.Leu250=)
2g.218893147G>TCA350591811WNT10Ac.1130G>T (p.Cys377Phe)
c.1079G>T (p.Cys360Phe)
c.1034G>T (p.Cys345Phe)
c.750G>T (p.Leu250=)
2g.218893153_218893158dupCA2663174552WNT10Ac.1136_1141dup (p.Gly380_His381insArgGly)
c.1085_1090dup (p.Gly363_His364insArgGly)
c.1040_1045dup (p.Gly348_His349insArgGly)
c.756_761dup (p.Pro254_Gln255insArgPro)
 gnomAD v4
2g.218893148C>ACA350591814WNT10Ac.1131C>A (p.Cys377Ter)
c.1080C>A (p.Cys360Ter)
c.1035C>A (p.Cys345Ter)
c.751C>A (p.Arg251=)
2g.218893148C=CA1328965461WNT10Ac.1131C= (p.Cys377=)
c.1080C= (p.Cys360=)
c.1035C= (p.Cys345=)
c.751C= (p.Arg251=)
2g.218893148C>GCA350591825WNT10Ac.1131C>G (p.Cys377Trp)
c.1080C>G (p.Cys360Trp)
c.1035C>G (p.Cys345Trp)
c.751C>G (p.Arg251Gly)
2g.218893148C>TCA2114115WNT10Ac.1131C>T (p.Cys377=)
c.1080C>T (p.Cys360=)
c.1035C>T (p.Cys345=)
c.751C>T (p.Arg251Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893149G>ACA350591828WNT10Ac.1132G>A (p.Gly378Ser)
c.1081G>A (p.Gly361Ser)
c.1036G>A (p.Gly346Ser)
c.752G>A (p.Arg251Gln)
 dbSNP
2g.218893149G>CCA350591830WNT10Ac.1132G>C (p.Gly378Arg)
c.1081G>C (p.Gly361Arg)
c.1036G>C (p.Gly346Arg)
c.752G>C (p.Arg251Pro)
2g.218893149G=CA1328965463WNT10Ac.1132G= (p.Gly378=)
c.1081G= (p.Gly361=)
c.1036G= (p.Gly346=)
c.752G= (p.Arg251=)
2g.218893149G>TCA350591834WNT10Ac.1132G>T (p.Gly378Cys)
c.1081G>T (p.Gly361Cys)
c.1036G>T (p.Gly346Cys)
c.752G>T (p.Arg251Leu)
2g.218893150delCA2663174553WNT10Ac.1133del (p.Gly378AlafsTer?)
c.1082del (p.Gly361AlafsTer?)
c.1037del (p.Gly346AlafsTer?)
c.753del (p.Pro252ArgfsTer?)
 gnomAD v4
2g.218893150G>ACA2114116WNT10Ac.1133G>A (p.Gly378Asp)
c.1082G>A (p.Gly361Asp)
c.1037G>A (p.Gly346Asp)
c.753G>A (p.Arg251=)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893150G>CCA350591839WNT10Ac.1133G>C (p.Gly378Ala)
c.1082G>C (p.Gly361Ala)
c.1037G>C (p.Gly346Ala)
c.753G>C (p.Arg251=)
2g.218893150G=CA1328965465WNT10Ac.1133G= (p.Gly378=)
c.1082G= (p.Gly361=)
c.1037G= (p.Gly346=)
c.753G= (p.Arg251=)
2g.218893150G>TCA350591844WNT10Ac.1133G>T (p.Gly378Val)
c.1082G>T (p.Gly361Val)
c.1037G>T (p.Gly346Val)
c.753G>T (p.Arg251=)
2g.218893151C>ACA431417489WNT10Ac.1134C>A (p.Gly378=)
c.1083C>A (p.Gly361=)
c.1038C>A (p.Gly346=)
c.754C>A (p.Pro252Thr)
2g.218893151C=CA1328965468WNT10Ac.1134C= (p.Gly378=)
c.1083C= (p.Gly361=)
c.1038C= (p.Gly346=)
c.754C= (p.Pro252=)
2g.218893151C>GCA431417491WNT10Ac.1134C>G (p.Gly378=)
c.1083C>G (p.Gly361=)
c.1038C>G (p.Gly346=)
c.754C>G (p.Pro252Ala)
2g.218893151C>TCA10614356WNT10Ac.1134C>T (p.Gly378=)
c.1083C>T (p.Gly361=)
c.1038C>T (p.Gly346=)
c.754C>T (p.Pro252Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893152C>ACA350591847WNT10Ac.1135C>A (p.Arg379Ser)
c.1084C>A (p.Arg362Ser)
c.1039C>A (p.Arg347Ser)
c.755C>A (p.Pro252Gln)
 gnomAD v4
2g.218893152C=CA1328965474WNT10Ac.1135C= (p.Arg379=)
c.1084C= (p.Arg362=)
c.1039C= (p.Arg347=)
c.755C= (p.Pro252=)
2g.218893152C>GCA350591849WNT10Ac.1135C>G (p.Arg379Gly)
c.1084C>G (p.Arg362Gly)
c.1039C>G (p.Arg347Gly)
c.755C>G (p.Pro252Arg)
 gnomAD v4
2g.218893152C>TCA350591851WNT10Ac.1135C>T (p.Arg379Cys)
c.1084C>T (p.Arg362Cys)
c.1039C>T (p.Arg347Cys)
c.755C>T (p.Pro252Leu)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893153G>ACA350591860WNT10Ac.1136G>A (p.Arg379His)
c.1085G>A (p.Arg362His)
c.1040G>A (p.Arg347His)
c.756G>A (p.Pro252=)
 gnomAD v4
2g.218893153G>CCA350591859WNT10Ac.1136G>C (p.Arg379Pro)
c.1085G>C (p.Arg362Pro)
c.1040G>C (p.Arg347Pro)
c.756G>C (p.Pro252=)
2g.218893153G>TCA350591854WNT10Ac.1136G>T (p.Arg379Leu)
c.1085G>T (p.Arg362Leu)
c.1040G>T (p.Arg347Leu)
c.756G>T (p.Pro252=)
2g.218893154C>ACA431417498WNT10Ac.1137C>A (p.Arg379=)
c.1086C>A (p.Arg362=)
c.1041C>A (p.Arg347=)
c.757C>A (p.Arg253=)
 gnomAD v4
2g.218893154C>GCA431417500WNT10Ac.1137C>G (p.Arg379=)
c.1086C>G (p.Arg362=)
c.1041C>G (p.Arg347=)
c.757C>G (p.Arg253Gly)
2g.218893154C>TCA431417502WNT10Ac.1137C>T (p.Arg379=)
c.1086C>T (p.Arg362=)
c.1041C>T (p.Arg347=)
c.757C>T (p.Arg253Trp)
 ClinVar
2g.218893155G>ACA350591861WNT10Ac.1138G>A (p.Gly380Ser)
c.1087G>A (p.Gly363Ser)
c.1042G>A (p.Gly348Ser)
c.758G>A (p.Arg253Gln)
 gnomAD v4
2g.218893155G>CCA350591863WNT10Ac.1138G>C (p.Gly380Arg)
c.1087G>C (p.Gly363Arg)
c.1042G>C (p.Gly348Arg)
c.758G>C (p.Arg253Pro)
 dbSNP
2g.218893155G=CA1328965477WNT10Ac.1138G= (p.Gly380=)
c.1087G= (p.Gly363=)
c.1042G= (p.Gly348=)
c.758G= (p.Arg253=)
2g.218893155G>TCA350591862WNT10Ac.1138G>T (p.Gly380Cys)
c.1087G>T (p.Gly363Cys)
c.1042G>T (p.Gly348Cys)
c.758G>T (p.Arg253Leu)
2g.218893156G>ACA350591866WNT10Ac.1139G>A (p.Gly380Asp)
c.1088G>A (p.Gly363Asp)
c.1043G>A (p.Gly348Asp)
c.759G>A (p.Arg253=)
 gnomAD v4
2g.218893156G>CCA350591884WNT10Ac.1139G>C (p.Gly380Ala)
c.1088G>C (p.Gly363Ala)
c.1043G>C (p.Gly348Ala)
c.759G>C (p.Arg253=)
2g.218893156G>TCA350591873WNT10Ac.1139G>T (p.Gly380Val)
c.1088G>T (p.Gly363Val)
c.1043G>T (p.Gly348Val)
c.759G>T (p.Arg253=)
 gnomAD v4
2g.218893157C>ACA431417511WNT10Ac.1140C>A (p.Gly380=)
c.1089C>A (p.Gly363=)
c.1044C>A (p.Gly348=)
c.760C>A (p.Pro254Thr)
 gnomAD v4
2g.218893157C=CA1328965481WNT10Ac.1140C= (p.Gly380=)
c.1089C= (p.Gly363=)
c.1044C= (p.Gly348=)
c.760C= (p.Pro254=)
2g.218893157C>GCA431417514WNT10Ac.1140C>G (p.Gly380=)
c.1089C>G (p.Gly363=)
c.1044C>G (p.Gly348=)
c.760C>G (p.Pro254Ala)
2g.218893157C>TCA2114117WNT10Ac.1140C>T (p.Gly380=)
c.1089C>T (p.Gly363=)
c.1044C>T (p.Gly348=)
c.760C>T (p.Pro254Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893157_218893158insGCGGCCCA2580617930WNT10Ac.1140_1141insGCGGCC (p.Gly380_His381insAlaAla)
c.1089_1090insGCGGCC (p.Gly363_His364insAlaAla)
c.1044_1045insGCGGCC (p.Gly348_His349insAlaAla)
c.760_761insGCGGCC (p.Arg253_Pro254insArgGly)
2g.218893158C>ACA350591898WNT10Ac.1141C>A (p.His381Asn)
c.1090C>A (p.His364Asn)
c.1045C>A (p.His349Asn)
c.761C>A (p.Pro254Gln)
 gnomAD v4
2g.218893158C=CA1328965485WNT10Ac.1141C= (p.His381=)
c.1090C= (p.His364=)
c.1045C= (p.His349=)
c.761C= (p.Pro254=)
2g.218893158C>GCA350591894WNT10Ac.1141C>G (p.His381Asp)
c.1090C>G (p.His364Asp)
c.1045C>G (p.His349Asp)
c.761C>G (p.Pro254Arg)
2g.218893158C>TCA350591903WNT10Ac.1141C>T (p.His381Tyr)
c.1090C>T (p.His364Tyr)
c.1045C>T (p.His349Tyr)
c.761C>T (p.Pro254Leu)
 dbSNP gnomAD v2
2g.218893158_218893161delinsCACACA1328965487WNT10Ac.1141_1144delinsCACA (p.His381=)
c.1090_1093delinsCACA (p.His364=)
c.1045_1048delinsCACA (p.His349=)
c.761_764delinsCACA (p.Pro254=)
2g.218893159A>CCA350591912WNT10Ac.1142A>C (p.His381Pro)
c.1091A>C (p.His364Pro)
c.1046A>C (p.His349Pro)
c.762A>C (p.Pro254=)
2g.218893159A>GCA350591915WNT10Ac.1142A>G (p.His381Arg)
c.1091A>G (p.His364Arg)
c.1046A>G (p.His349Arg)
c.762A>G (p.Pro254=)
2g.218893159A>TCA350591916WNT10Ac.1142A>T (p.His381Leu)
c.1091A>T (p.His364Leu)
c.1046A>T (p.His349Leu)
c.762A>T (p.Pro254=)
2g.218893162_218893164delCA1328965489WNT10Ac.1145_1147del (p.Asn382del)
c.1094_1096del (p.Asn365del)
c.1049_1051del (p.Asn350del)
c.765_767del (p.Gln255del)
 dbSNP gnomAD v4
2g.218893160C>ACA350591919WNT10Ac.1143C>A (p.His381Gln)
c.1092C>A (p.His364Gln)
c.1047C>A (p.His349Gln)
c.763C>A (p.Gln255Lys)
2g.218893160C=CA1328965492WNT10Ac.1143C= (p.His381=)
c.1092C= (p.His364=)
c.1047C= (p.His349=)
c.763C= (p.Gln255=)
2g.218893160C>GCA350591922WNT10Ac.1143C>G (p.His381Gln)
c.1092C>G (p.His364Gln)
c.1047C>G (p.His349Gln)
c.763C>G (p.Gln255Glu)
2g.218893160C>TCA431417519WNT10Ac.1143C>T (p.His381=)
c.1092C>T (p.His364=)
c.1047C>T (p.His349=)
c.763C>T (p.Gln255Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893161A>CCA350591924WNT10Ac.1144A>C (p.Asn382His)
c.1093A>C (p.Asn365His)
c.1048A>C (p.Asn350His)
c.764A>C (p.Gln255Pro)
2g.218893161A>GCA350591926WNT10Ac.1144A>G (p.Asn382Asp)
c.1093A>G (p.Asn365Asp)
c.1048A>G (p.Asn350Asp)
c.764A>G (p.Gln255Arg)
2g.218893161A>TCA350591928WNT10Ac.1144A>T (p.Asn382Tyr)
c.1093A>T (p.Asn365Tyr)
c.1048A>T (p.Asn350Tyr)
c.764A>T (p.Gln255Leu)
2g.218893162A=CA1328965496WNT10Ac.1145A= (p.Asn382=)
c.1094A= (p.Asn365=)
c.1049A= (p.Asn350=)
c.765A= (p.Gln255=)
2g.218893162A>CCA350591933WNT10Ac.1145A>C (p.Asn382Thr)
c.1094A>C (p.Asn365Thr)
c.1049A>C (p.Asn350Thr)
c.765A>C (p.Gln255His)
2g.218893162A>GCA350591938WNT10Ac.1145A>G (p.Asn382Ser)
c.1094A>G (p.Asn365Ser)
c.1049A>G (p.Asn350Ser)
c.765A>G (p.Gln255=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893162A>TCA350591941WNT10Ac.1145A>T (p.Asn382Ile)
c.1094A>T (p.Asn365Ile)
c.1049A>T (p.Asn350Ile)
c.765A>T (p.Gln255His)
2g.218893163C>ACA350591954WNT10Ac.1146C>A (p.Asn382Lys)
c.1095C>A (p.Asn365Lys)
c.1050C>A (p.Asn350Lys)
c.766C>A (p.His256Asn)
2g.218893163C=CA1328965499WNT10Ac.1146C= (p.Asn382=)
c.1095C= (p.Asn365=)
c.1050C= (p.Asn350=)
c.766C= (p.His256=)
2g.218893163C>GCA350591948WNT10Ac.1146C>G (p.Asn382Lys)
c.1095C>G (p.Asn365Lys)
c.1050C>G (p.Asn350Lys)
c.766C>G (p.His256Asp)
 dbSNP gnomAD v2 gnomAD v4
2g.218893163C>TCA2114118WNT10Ac.1146C>T (p.Asn382=)
c.1095C>T (p.Asn365=)
c.1050C>T (p.Asn350=)
c.766C>T (p.His256Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893164A>CCA350591966WNT10Ac.1147A>C (p.Ile383Leu)
c.1096A>C (p.Ile366Leu)
c.1051A>C (p.Ile351Leu)
c.767A>C (p.His256Pro)
2g.218893164A>GCA350591973WNT10Ac.1147A>G (p.Ile383Val)
c.1096A>G (p.Ile366Val)
c.1051A>G (p.Ile351Val)
c.767A>G (p.His256Arg)
2g.218893164A>TCA350591976WNT10Ac.1147A>T (p.Ile383Phe)
c.1096A>T (p.Ile366Phe)
c.1051A>T (p.Ile351Phe)
c.767A>T (p.His256Leu)
2g.218893165T>ACA350591982WNT10Ac.1148T>A (p.Ile383Asn)
c.1097T>A (p.Ile366Asn)
c.1052T>A (p.Ile351Asn)
c.768T>A (p.His256Gln)
2g.218893165T>CCA350591991WNT10Ac.1148T>C (p.Ile383Thr)
c.1097T>C (p.Ile366Thr)
c.1052T>C (p.Ile351Thr)
c.768T>C (p.His256=)
2g.218893165T>GCA350591999WNT10Ac.1148T>G (p.Ile383Ser)
c.1097T>G (p.Ile366Ser)
c.1052T>G (p.Ile351Ser)
c.768T>G (p.His256Gln)
 dbSNP gnomAD v2 gnomAD v4
2g.218893165T=CA1328965505WNT10Ac.1148T= (p.Ile383=)
c.1097T= (p.Ile366=)
c.1052T= (p.Ile351=)
c.768T= (p.His256=)
2g.218893166C>ACA431417533WNT10Ac.1149C>A (p.Ile383=)
c.1098C>A (p.Ile366=)
c.1053C>A (p.Ile351=)
c.769C>A (p.Pro257Thr)
2g.218893166C>GCA350592001WNT10Ac.1149C>G (p.Ile383Met)
c.1098C>G (p.Ile366Met)
c.1053C>G (p.Ile351Met)
c.769C>G (p.Pro257Ala)
2g.218893166C>TCA431417536WNT10Ac.1149C>T (p.Ile383=)
c.1098C>T (p.Ile366=)
c.1053C>T (p.Ile351=)
c.769C>T (p.Pro257Ser)
 ClinVar dbSNP gnomAD v4
2g.218893167C>ACA350592011WNT10Ac.1150C>A (p.Leu384Met)
c.1099C>A (p.Leu367Met)
c.1054C>A (p.Leu352Met)
c.770C>A (p.Pro257His)
2g.218893167C>GCA350592016WNT10Ac.1150C>G (p.Leu384Val)
c.1099C>G (p.Leu367Val)
c.1054C>G (p.Leu352Val)
c.770C>G (p.Pro257Arg)
2g.218893167C>TCA431417539WNT10Ac.1150C>T (p.Leu384=)
c.1099C>T (p.Leu367=)
c.1054C>T (p.Leu352=)
c.770C>T (p.Pro257Leu)
 gnomAD v4
2g.218893168T>ACA350592029WNT10Ac.1151T>A (p.Leu384Gln)
c.1100T>A (p.Leu367Gln)
c.1055T>A (p.Leu352Gln)
c.771T>A (p.Pro257=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893168T>CCA350592046WNT10Ac.1151T>C (p.Leu384Pro)
c.1100T>C (p.Leu367Pro)
c.1055T>C (p.Leu352Pro)
c.771T>C (p.Pro257=)
2g.218893168T>GCA350592047WNT10Ac.1151T>G (p.Leu384Arg)
c.1100T>G (p.Leu367Arg)
c.1055T>G (p.Leu352Arg)
c.771T>G (p.Pro257=)
2g.218893168T=CA1328965508WNT10Ac.1151T= (p.Leu384=)
c.1100T= (p.Leu367=)
c.1055T= (p.Leu352=)
c.771T= (p.Pro257=)
2g.218893169G>ACA431417544WNT10Ac.1152G>A (p.Leu384=)
c.1101G>A (p.Leu367=)
c.1056G>A (p.Leu352=)
c.772G>A (p.Ala258Thr)
 gnomAD v4
2g.218893169G>CCA431417545WNT10Ac.1152G>C (p.Leu384=)
c.1101G>C (p.Leu367=)
c.1056G>C (p.Leu352=)
c.772G>C (p.Ala258Pro)
2g.218893169G>TCA431417549WNT10Ac.1152G>T (p.Leu384=)
c.1101G>T (p.Leu367=)
c.1056G>T (p.Leu352=)
c.772G>T (p.Ala258Ser)
2g.218893170C>ACA350592055WNT10Ac.1153C>A (p.Arg385Ser)
c.1102C>A (p.Arg368Ser)
c.1057C>A (p.Arg353Ser)
c.773C>A (p.Ala258Glu)
2g.218893170C>GCA350592051WNT10Ac.1153C>G (p.Arg385Gly)
c.1102C>G (p.Arg368Gly)
c.1057C>G (p.Arg353Gly)
c.773C>G (p.Ala258Gly)
2g.218893170C>TCA350592049WNT10Ac.1153C>T (p.Arg385Cys)
c.1102C>T (p.Arg368Cys)
c.1057C>T (p.Arg353Cys)
c.773C>T (p.Ala258Val)
2g.218893171G>ACA2114119WNT10Ac.1154G>A (p.Arg385His)
c.1103G>A (p.Arg368His)
c.1058G>A (p.Arg353His)
c.774G>A (p.Ala258=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893171G>CCA350592059WNT10Ac.1154G>C (p.Arg385Pro)
c.1103G>C (p.Arg368Pro)
c.1058G>C (p.Arg353Pro)
c.774G>C (p.Ala258=)
2g.218893171G=CA1328965512WNT10Ac.1154G= (p.Arg385=)
c.1103G= (p.Arg368=)
c.1058G= (p.Arg353=)
c.774G= (p.Ala258=)
2g.218893171G>TCA350592064WNT10Ac.1154G>T (p.Arg385Leu)
c.1103G>T (p.Arg368Leu)
c.1058G>T (p.Arg353Leu)
c.774G>T (p.Ala258=)

Number of alleles fetched