Chr Mutation (hg38) CAid Gene Transcript Linkouts
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=)
2g.218893172C>ACA431417552WNT10Ac.1155C>A (p.Arg385=)
c.1104C>A (p.Arg368=)
c.1059C>A (p.Arg353=)
c.775C>A (p.Pro259Thr)
 gnomAD v4
2g.218893172C=CA1328965514WNT10Ac.1155C= (p.Arg385=)
c.1104C= (p.Arg368=)
c.1059C= (p.Arg353=)
c.775C= (p.Pro259=)
2g.218893172C>GCA431417555WNT10Ac.1155C>G (p.Arg385=)
c.1104C>G (p.Arg368=)
c.1059C>G (p.Arg353=)
c.775C>G (p.Pro259Ala)
 dbSNP
2g.218893172C>TCA431417558WNT10Ac.1155C>T (p.Arg385=)
c.1104C>T (p.Arg368=)
c.1059C>T (p.Arg353=)
c.775C>T (p.Pro259Ser)
 ClinVar
2g.218893173C>ACA350592067WNT10Ac.1156C>A (p.Gln386Lys)
c.1105C>A (p.Gln369Lys)
c.1060C>A (p.Gln354Lys)
c.776C>A (p.Pro259Gln)
2g.218893173C=CA1328965516WNT10Ac.1156C= (p.Gln386=)
c.1105C= (p.Gln369=)
c.1060C= (p.Gln354=)
c.776C= (p.Pro259=)
2g.218893173C>GCA350592069WNT10Ac.1156C>G (p.Gln386Glu)
c.1105C>G (p.Gln369Glu)
c.1060C>G (p.Gln354Glu)
c.776C>G (p.Pro259Arg)
2g.218893173C>TCA2114120WNT10Ac.1156C>T (p.Gln386Ter)
c.1105C>T (p.Gln369Ter)
c.1060C>T (p.Gln354Ter)
c.776C>T (p.Pro259Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893174A=CA1328965520WNT10Ac.1157A= (p.Gln386=)
c.1106A= (p.Gln369=)
c.1061A= (p.Gln354=)
c.777A= (p.Pro259=)
2g.218893174A>CCA350592074WNT10Ac.1157A>C (p.Gln386Pro)
c.1106A>C (p.Gln369Pro)
c.1061A>C (p.Gln354Pro)
c.777A>C (p.Pro259=)
2g.218893174A>GCA350592075WNT10Ac.1157A>G (p.Gln386Arg)
c.1106A>G (p.Gln369Arg)
c.1061A>G (p.Gln354Arg)
c.777A>G (p.Pro259=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893174A>TCA350592077WNT10Ac.1157A>T (p.Gln386Leu)
c.1106A>T (p.Gln369Leu)
c.1061A>T (p.Gln354Leu)
c.777A>T (p.Pro259=)
2g.218893175G>ACA431417564WNT10Ac.1158G>A (p.Gln386=)
c.1107G>A (p.Gln369=)
c.1062G>A (p.Gln354=)
c.778G>A (p.Asp260Asn)
 ClinVar dbSNP
2g.218893175G>CCA350592080WNT10Ac.1158G>C (p.Gln386His)
c.1107G>C (p.Gln369His)
c.1062G>C (p.Gln354His)
c.778G>C (p.Asp260His)
2g.218893175G>TCA350592084WNT10Ac.1158G>T (p.Gln386His)
c.1107G>T (p.Gln369His)
c.1062G>T (p.Gln354His)
c.778G>T (p.Asp260Tyr)
2g.218893176A>CCA350592095WNT10Ac.1159A>C (p.Thr387Pro)
c.1108A>C (p.Thr370Pro)
c.1063A>C (p.Thr355Pro)
c.779A>C (p.Asp260Ala)
2g.218893176A>GCA350592093WNT10Ac.1159A>G (p.Thr387Ala)
c.1108A>G (p.Thr370Ala)
c.1063A>G (p.Thr355Ala)
c.779A>G (p.Asp260Gly)
2g.218893176A>TCA350592089WNT10Ac.1159A>T (p.Thr387Ser)
c.1108A>T (p.Thr370Ser)
c.1063A>T (p.Thr355Ser)
c.779A>T (p.Asp260Val)
2g.218893177C>ACA2114121WNT10Ac.1160C>A (p.Thr387Lys)
c.1109C>A (p.Thr370Lys)
c.1064C>A (p.Thr355Lys)
c.780C>A (p.Asp260Glu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893177C=CA1328965523WNT10Ac.1160C= (p.Thr387=)
c.1109C= (p.Thr370=)
c.1064C= (p.Thr355=)
c.780C= (p.Asp260=)
2g.218893177C>GCA350592099WNT10Ac.1160C>G (p.Thr387Arg)
c.1109C>G (p.Thr370Arg)
c.1064C>G (p.Thr355Arg)
c.780C>G (p.Asp260Glu)
2g.218893177C>TCA350592101WNT10Ac.1160C>T (p.Thr387Met)
c.1109C>T (p.Thr370Met)
c.1064C>T (p.Thr355Met)
c.780C>T (p.Asp260=)
 gnomAD v4 COSMIC
2g.218893177_218893181delCA2577276400WNT10Ac.1160_1164del (p.Thr387LysfsTer?)
c.1109_1113del (p.Thr370LysfsTer?)
c.1064_1068del (p.Thr355LysfsTer?)
c.780_784del (p.Asp260GlufsTer?)
2g.218893178G>ACA431417572WNT10Ac.1161G>A (p.Thr387=)
c.1110G>A (p.Thr370=)
c.1065G>A (p.Thr355=)
c.781G>A (p.Ala261Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893178G>CCA431417574WNT10Ac.1161G>C (p.Thr387=)
c.1110G>C (p.Thr370=)
c.1065G>C (p.Thr355=)
c.781G>C (p.Ala261Pro)
2g.218893178G=CA1328965527WNT10Ac.1161G= (p.Thr387=)
c.1110G= (p.Thr370=)
c.1065G= (p.Thr355=)
c.781G= (p.Ala261=)
2g.218893178G>TCA431417577WNT10Ac.1161G>T (p.Thr387=)
c.1110G>T (p.Thr370=)
c.1065G>T (p.Thr355=)
c.781G>T (p.Ala261Ser)
 ClinVar dbSNP gnomAD v4
2g.218893179C>ACA350592119WNT10Ac.1162C>A (p.Arg388Ser)
c.1111C>A (p.Arg371Ser)
c.1066C>A (p.Arg356Ser)
c.782C>A (p.Ala261Glu)
 dbSNP gnomAD v4
2g.218893179C=CA1328965530WNT10Ac.1162C= (p.Arg388=)
c.1111C= (p.Arg371=)
c.1066C= (p.Arg356=)
c.782C= (p.Ala261=)
2g.218893179C>GCA350592122WNT10Ac.1162C>G (p.Arg388Gly)
c.1111C>G (p.Arg371Gly)
c.1066C>G (p.Arg356Gly)
c.782C>G (p.Ala261Gly)
2g.218893179C>TCA350592125WNT10Ac.1162C>T (p.Arg388Cys)
c.1111C>T (p.Arg371Cys)
c.1066C>T (p.Arg356Cys)
c.782C>T (p.Ala261Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893180G>ACA350592141WNT10Ac.1163G>A (p.Arg388His)
c.1112G>A (p.Arg371His)
c.1067G>A (p.Arg356His)
c.783G>A (p.Ala261=)
 gnomAD v4
2g.218893180G>CCA350592147WNT10Ac.1163G>C (p.Arg388Pro)
c.1112G>C (p.Arg371Pro)
c.1067G>C (p.Arg356Pro)
c.783G>C (p.Ala261=)
2g.218893180G=CA1328965533WNT10Ac.1163G= (p.Arg388=)
c.1112G= (p.Arg371=)
c.1067G= (p.Arg356=)
c.783G= (p.Ala261=)
2g.218893180G>TCA350592148WNT10Ac.1163G>T (p.Arg388Leu)
c.1112G>T (p.Arg371Leu)
c.1067G>T (p.Arg356Leu)
c.783G>T (p.Ala261=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893181C>ACA431417582WNT10Ac.1164C>A (p.Arg388=)
c.1113C>A (p.Arg371=)
c.1068C>A (p.Arg356=)
c.784C>A (p.Gln262Lys)
2g.218893181C>GCA431417583WNT10Ac.1164C>G (p.Arg388=)
c.1113C>G (p.Arg371=)
c.1068C>G (p.Arg356=)
c.784C>G (p.Gln262Glu)
2g.218893181C>TCA431417584WNT10Ac.1164C>T (p.Arg388=)
c.1113C>T (p.Arg371=)
c.1068C>T (p.Arg356=)
c.784C>T (p.Gln262Ter)
 ClinVar dbSNP
2g.218893181_218893195delinsCAGCGAGCGCTGCCACA1328965537WNT10Ac.1164_1178delinsCAGCGAGCGCTGCCA (p.Arg388=)
c.1113_1127delinsCAGCGAGCGCTGCCA (p.Arg371=)
c.1068_1082delinsCAGCGAGCGCTGCCA (p.Arg356=)
c.784_798delinsCAGCGAGCGCTGCCA (p.Gln262=)
2g.218893182A>CCA350592151WNT10Ac.1165A>C (p.Ser389Arg)
c.1114A>C (p.Ser372Arg)
c.1069A>C (p.Ser357Arg)
c.785A>C (p.Gln262Pro)
 gnomAD v4
2g.218893182A>GCA350592154WNT10Ac.1165A>G (p.Ser389Gly)
c.1114A>G (p.Ser372Gly)
c.1069A>G (p.Ser357Gly)
c.785A>G (p.Gln262Arg)
 gnomAD v4
2g.218893182A>TCA350592155WNT10Ac.1165A>T (p.Ser389Cys)
c.1114A>T (p.Ser372Cys)
c.1069A>T (p.Ser357Cys)
c.785A>T (p.Gln262Leu)
 gnomAD v4
2g.218893182dupCA2663174554WNT10Ac.1165dup (p.Ser389LysfsTer?)
c.1114dup (p.Ser372LysfsTer?)
c.1069dup (p.Ser357LysfsTer?)
c.785dup (p.Arg263AlafsTer?)
 gnomAD v4
2g.218893182_218893195delinsTTCCAGCACAACATCCA1139657705WNT10Ac.1165_1178delinsTTCCAGCACAACATC (p.Ser389PhefsTer?)
c.1114_1127delinsTTCCAGCACAACATC (p.Ser372PhefsTer?)
c.1069_1082delinsTTCCAGCACAACATC (p.Ser357PhefsTer?)
c.785_798delinsTTCCAGCACAACATC (p.Gln262LeufsTer?)
 ClinVar dbSNP
2g.218893183G>ACA350592161WNT10Ac.1166G>A (p.Ser389Asn)
c.1115G>A (p.Ser372Asn)
c.1070G>A (p.Ser357Asn)
c.786G>A (p.Gln262=)
 dbSNP gnomAD v3 gnomAD v4
2g.218893183G>CCA350592160WNT10Ac.1166G>C (p.Ser389Thr)
c.1115G>C (p.Ser372Thr)
c.1070G>C (p.Ser357Thr)
c.786G>C (p.Gln262His)
2g.218893183G=CA1328965541WNT10Ac.1166G= (p.Ser389=)
c.1115G= (p.Ser372=)
c.1070G= (p.Ser357=)
c.786G= (p.Gln262=)
2g.218893183G>TCA350592159WNT10Ac.1166G>T (p.Ser389Ile)
c.1115G>T (p.Ser372Ile)
c.1070G>T (p.Ser357Ile)
c.786G>T (p.Gln262His)
2g.218893184C>ACA350592164WNT10Ac.1167C>A (p.Ser389Arg)
c.1116C>A (p.Ser372Arg)
c.1071C>A (p.Ser357Arg)
c.787C>A (p.Arg263=)
 gnomAD v4
2g.218893184C=CA1328965543WNT10Ac.1167C= (p.Ser389=)
c.1116C= (p.Ser372=)
c.1071C= (p.Ser357=)
c.787C= (p.Arg263=)
2g.218893184C>GCA2114122WNT10Ac.1167C>G (p.Ser389Arg)
c.1116C>G (p.Ser372Arg)
c.1071C>G (p.Ser357Arg)
c.787C>G (p.Arg263Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893184C>TCA431417591WNT10Ac.1167C>T (p.Ser389=)
c.1116C>T (p.Ser372=)
c.1071C>T (p.Ser357=)
c.787C>T (p.Arg263Ter)
 ClinVar gnomAD v4
2g.218893185G>ACA350592168WNT10Ac.1168G>A (p.Glu390Lys)
c.1117G>A (p.Glu373Lys)
c.1072G>A (p.Glu358Lys)
c.788G>A (p.Arg263Gln)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893185G>CCA350592170WNT10Ac.1168G>C (p.Glu390Gln)
c.1117G>C (p.Glu373Gln)
c.1072G>C (p.Glu358Gln)
c.788G>C (p.Arg263Pro)
2g.218893185G=CA1328965550WNT10Ac.1168G= (p.Glu390=)
c.1117G= (p.Glu373=)
c.1072G= (p.Glu358=)
c.788G= (p.Arg263=)
2g.218893185G>TCA2114123WNT10Ac.1168G>T (p.Glu390Ter)
c.1117G>T (p.Glu373Ter)
c.1072G>T (p.Glu358Ter)
c.788G>T (p.Arg263Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893186A>CCA350592173WNT10Ac.1169A>C (p.Glu390Ala)
c.1118A>C (p.Glu373Ala)
c.1073A>C (p.Glu358Ala)
c.789A>C (p.Arg263=)
2g.218893186A>GCA350592175WNT10Ac.1169A>G (p.Glu390Gly)
c.1118A>G (p.Glu373Gly)
c.1073A>G (p.Glu358Gly)
c.789A>G (p.Arg263=)
2g.218893186A>TCA350592182WNT10Ac.1169A>T (p.Glu390Val)
c.1118A>T (p.Glu373Val)
c.1073A>T (p.Glu358Val)
c.789A>T (p.Arg263=)
2g.218893187G>ACA431234828WNT10Ac.1170G>A (p.Glu390=)
c.1119G>A (p.Glu373=)
c.1074G>A (p.Glu358=)
c.790G>A (p.Ala264Thr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.218893187G>CCA350592184WNT10Ac.1170G>C (p.Glu390Asp)
c.1119G>C (p.Glu373Asp)
c.1074G>C (p.Glu358Asp)
c.790G>C (p.Ala264Pro)
2g.218893187G=CA1328965553WNT10Ac.1170G= (p.Glu390=)
c.1119G= (p.Glu373=)
c.1074G= (p.Glu358=)
c.790G= (p.Ala264=)
2g.218893187G>TCA350592202WNT10Ac.1170G>T (p.Glu390Asp)
c.1119G>T (p.Glu373Asp)
c.1074G>T (p.Glu358Asp)
c.790G>T (p.Ala264Ser)
 dbSNP gnomAD v4
2g.218893188C>ACA350592206WNT10Ac.1171C>A (p.Arg391Ser)
c.1120C>A (p.Arg374Ser)
c.1075C>A (p.Arg359Ser)
c.791C>A (p.Ala264Glu)
 gnomAD v4
2g.218893188C>GCA350592207WNT10Ac.1171C>G (p.Arg391Gly)
c.1120C>G (p.Arg374Gly)
c.1075C>G (p.Arg359Gly)
c.791C>G (p.Ala264Gly)
 gnomAD v4
2g.218893188C>TCA350592208WNT10Ac.1171C>T (p.Arg391Cys)
c.1120C>T (p.Arg374Cys)
c.1075C>T (p.Arg359Cys)
c.791C>T (p.Ala264Val)
 gnomAD v4
2g.218893189G>ACA350592215WNT10Ac.1172G>A (p.Arg391His)
c.1121G>A (p.Arg374His)
c.1076G>A (p.Arg359His)
c.792G>A (p.Ala264=)
 gnomAD v4
2g.218893189G>CCA350592209WNT10Ac.1172G>C (p.Arg391Pro)
c.1121G>C (p.Arg374Pro)
c.1076G>C (p.Arg359Pro)
c.792G>C (p.Ala264=)
2g.218893189G>TCA350592211WNT10Ac.1172G>T (p.Arg391Leu)
c.1121G>T (p.Arg374Leu)
c.1076G>T (p.Arg359Leu)
c.792G>T (p.Ala264=)
2g.218893190C>ACA431234829WNT10Ac.1173C>A (p.Arg391=)
c.1122C>A (p.Arg374=)
c.1077C>A (p.Arg359=)
c.793C>A (p.Leu265Met)
2g.218893190C=CA1328965561WNT10Ac.1173C= (p.Arg391=)
c.1122C= (p.Arg374=)
c.1077C= (p.Arg359=)
c.793C= (p.Leu265=)
2g.218893190C>GCA431234830WNT10Ac.1173C>G (p.Arg391=)
c.1122C>G (p.Arg374=)
c.1077C>G (p.Arg359=)
c.793C>G (p.Leu265Val)
2g.218893190C>TCA431234831WNT10Ac.1173C>T (p.Arg391=)
c.1122C>T (p.Arg374=)
c.1077C>T (p.Arg359=)
c.793C>T (p.Leu265=)
 ClinVar dbSNP
2g.218893191T>ACA350592223WNT10Ac.1174T>A (p.Cys392Ser)
c.1123T>A (p.Cys375Ser)
c.1078T>A (p.Cys360Ser)
c.794T>A (p.Leu265Gln)
2g.218893191T>CCA350592227WNT10Ac.1174T>C (p.Cys392Arg)
c.1123T>C (p.Cys375Arg)
c.1078T>C (p.Cys360Arg)
c.794T>C (p.Leu265Pro)
 dbSNP gnomAD v4
2g.218893191T>GCA350592233WNT10Ac.1174T>G (p.Cys392Gly)
c.1123T>G (p.Cys375Gly)
c.1078T>G (p.Cys360Gly)
c.794T>G (p.Leu265Arg)
2g.218893191T=CA1328965565WNT10Ac.1174T= (p.Cys392=)
c.1123T= (p.Cys375=)
c.1078T= (p.Cys360=)
c.794T= (p.Leu265=)
2g.218893192G>ACA350592236WNT10Ac.1175G>A (p.Cys392Tyr)
c.1124G>A (p.Cys375Tyr)
c.1079G>A (p.Cys360Tyr)
c.795G>A (p.Leu265=)
 gnomAD v4
2g.218893192G>CCA350592238WNT10Ac.1175G>C (p.Cys392Ser)
c.1124G>C (p.Cys375Ser)
c.1079G>C (p.Cys360Ser)
c.795G>C (p.Leu265=)
2g.218893192G=CA1328965569WNT10Ac.1175G= (p.Cys392=)
c.1124G= (p.Cys375=)
c.1079G= (p.Cys360=)
c.795G= (p.Leu265=)
2g.218893192G>TCA350592243WNT10Ac.1175G>T (p.Cys392Phe)
c.1124G>T (p.Cys375Phe)
c.1079G>T (p.Cys360Phe)
c.795G>T (p.Leu265=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893193C>ACA350592246WNT10Ac.1176C>A (p.Cys392Ter)
c.1125C>A (p.Cys375Ter)
c.1080C>A (p.Cys360Ter)
c.796C>A (p.Pro266Thr)
 ClinVar dbSNP gnomAD v4
2g.218893193C=CA1328965574WNT10Ac.1176C= (p.Cys392=)
c.1125C= (p.Cys375=)
c.1080C= (p.Cys360=)
c.796C= (p.Pro266=)
2g.218893193C>GCA350592248WNT10Ac.1176C>G (p.Cys392Trp)
c.1125C>G (p.Cys375Trp)
c.1080C>G (p.Cys360Trp)
c.796C>G (p.Pro266Ala)
2g.218893193C>TCA431234832WNT10Ac.1176C>T (p.Cys392=)
c.1125C>T (p.Cys375=)
c.1080C>T (p.Cys360=)
c.796C>T (p.Pro266Ser)
 gnomAD v4
2g.218893199_218893210dupCA2577276401WNT10Ac.1182_1193dup (p.His397_Trp398insCysArgPheHis)
c.1131_1142dup (p.His380_Trp381insCysArgPheHis)
c.1086_1097dup (p.His365_Trp366insCysArgPheHis)
c.802_813dup (p.Leu271_Val272insProLeuProLeu)
2g.218893194C>ACA350592251WNT10Ac.1177C>A (p.His393Asn)
c.1126C>A (p.His376Asn)
c.1081C>A (p.His361Asn)
c.797C>A (p.Pro266Gln)
 gnomAD v4
2g.218893194C>GCA350592254WNT10Ac.1177C>G (p.His393Asp)
c.1126C>G (p.His376Asp)
c.1081C>G (p.His361Asp)
c.797C>G (p.Pro266Arg)
2g.218893194C>TCA350592257WNT10Ac.1177C>T (p.His393Tyr)
c.1126C>T (p.His376Tyr)
c.1081C>T (p.His361Tyr)
c.797C>T (p.Pro266Leu)
 gnomAD v4
2g.218893195A=CA1328965581WNT10Ac.1178A= (p.His393=)
c.1127A= (p.His376=)
c.1082A= (p.His361=)
c.798A= (p.Pro266=)
2g.218893195A>CCA350592262WNT10Ac.1178A>C (p.His393Pro)
c.1127A>C (p.His376Pro)
c.1082A>C (p.His361Pro)
c.798A>C (p.Pro266=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893195A>GCA350592266WNT10Ac.1178A>G (p.His393Arg)
c.1127A>G (p.His376Arg)
c.1082A>G (p.His361Arg)
c.798A>G (p.Pro266=)
 gnomAD v4
2g.218893195A>TCA350592261WNT10Ac.1178A>T (p.His393Leu)
c.1127A>T (p.His376Leu)
c.1082A>T (p.His361Leu)
c.798A>T (p.Pro266=)
2g.218893196C>ACA350592272WNT10Ac.1179C>A (p.His393Gln)
c.1128C>A (p.His376Gln)
c.1083C>A (p.His361Gln)
c.799C>A (p.Leu267Met)
 gnomAD v4
2g.218893196C>GCA350592280WNT10Ac.1179C>G (p.His393Gln)
c.1128C>G (p.His376Gln)
c.1083C>G (p.His361Gln)
c.799C>G (p.Leu267Val)
2g.218893196C>TCA431234833WNT10Ac.1179C>T (p.His393=)
c.1128C>T (p.His376=)
c.1083C>T (p.His361=)
c.799C>T (p.Leu267=)
 ClinVar gnomAD v4
2g.218893197T>ACA350592284WNT10Ac.1180T>A (p.Cys394Ser)
c.1129T>A (p.Cys377Ser)
c.1084T>A (p.Cys362Ser)
c.800T>A (p.Leu267Gln)
2g.218893197T>CCA350592290WNT10Ac.1180T>C (p.Cys394Arg)
c.1129T>C (p.Cys377Arg)
c.1084T>C (p.Cys362Arg)
c.800T>C (p.Leu267Pro)
 dbSNP gnomAD v4
2g.218893197T>GCA350592292WNT10Ac.1180T>G (p.Cys394Gly)
c.1129T>G (p.Cys377Gly)
c.1084T>G (p.Cys362Gly)
c.800T>G (p.Leu267Arg)
2g.218893197T=CA1328965583WNT10Ac.1180T= (p.Cys394=)
c.1129T= (p.Cys377=)
c.1084T= (p.Cys362=)
c.800T= (p.Leu267=)
2g.218893198G>ACA350592314WNT10Ac.1181G>A (p.Cys394Tyr)
c.1130G>A (p.Cys377Tyr)
c.1085G>A (p.Cys362Tyr)
c.801G>A (p.Leu267=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893198G>CCA350592295WNT10Ac.1181G>C (p.Cys394Ser)
c.1130G>C (p.Cys377Ser)
c.1085G>C (p.Cys362Ser)
c.801G>C (p.Leu267=)
2g.218893198G=CA1328965584WNT10Ac.1181G= (p.Cys394=)
c.1130G= (p.Cys377=)
c.1085G= (p.Cys362=)
c.801G= (p.Leu267=)
2g.218893198G>TCA350592312WNT10Ac.1181G>T (p.Cys394Phe)
c.1130G>T (p.Cys377Phe)
c.1085G>T (p.Cys362Phe)
c.801G>T (p.Leu267=)
 gnomAD v4
2g.218893199C>ACA350592316WNT10Ac.1182C>A (p.Cys394Ter)
c.1131C>A (p.Cys377Ter)
c.1086C>A (p.Cys362Ter)
c.802C>A (p.Pro268Thr)
 gnomAD v4
2g.218893199C>GCA350592318WNT10Ac.1182C>G (p.Cys394Trp)
c.1131C>G (p.Cys377Trp)
c.1086C>G (p.Cys362Trp)
c.802C>G (p.Pro268Ala)
2g.218893199C>TCA431234834WNT10Ac.1182C>T (p.Cys394=)
c.1131C>T (p.Cys377=)
c.1086C>T (p.Cys362=)
c.802C>T (p.Pro268Ser)
 gnomAD v4
2g.218893200delCA2663174555WNT10Ac.1183del (p.Arg395AlafsTer?)
c.1132del (p.Arg378AlafsTer?)
c.1087del (p.Arg363AlafsTer?)
c.803del (p.Pro268ArgfsTer24)
 gnomAD v4
2g.218893201_218893206delCA2663174556WNT10Ac.1184_1189del (p.Arg395_Phe396del)
c.1133_1138del (p.Arg378_Phe379del)
c.1088_1093del (p.Arg363_Phe364del)
c.804_809del (p.Leu269_Pro270del)
 gnomAD v4
2g.218893200C>ACA350592319WNT10Ac.1183C>A (p.Arg395Ser)
c.1132C>A (p.Arg378Ser)
c.1087C>A (p.Arg363Ser)
c.803C>A (p.Pro268Gln)
 gnomAD v4
2g.218893200C=CA1328965587WNT10Ac.1183C= (p.Arg395=)
c.1132C= (p.Arg378=)
c.1087C= (p.Arg363=)
c.803C= (p.Pro268=)
2g.218893200C>GCA350592322WNT10Ac.1183C>G (p.Arg395Gly)
c.1132C>G (p.Arg378Gly)
c.1087C>G (p.Arg363Gly)
c.803C>G (p.Pro268Arg)
2g.218893200C>TCA2114124WNT10Ac.1183C>T (p.Arg395Cys)
c.1132C>T (p.Arg378Cys)
c.1087C>T (p.Arg363Cys)
c.803C>T (p.Pro268Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893201G>ACA2114125WNT10Ac.1184G>A (p.Arg395His)
c.1133G>A (p.Arg378His)
c.1088G>A (p.Arg363His)
c.804G>A (p.Pro268=)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893201G>CCA350592331WNT10Ac.1184G>C (p.Arg395Pro)
c.1133G>C (p.Arg378Pro)
c.1088G>C (p.Arg363Pro)
c.804G>C (p.Pro268=)
2g.218893201G=CA1328965593WNT10Ac.1184G= (p.Arg395=)
c.1133G= (p.Arg378=)
c.1088G= (p.Arg363=)
c.804G= (p.Pro268=)
2g.218893201G>TCA65919428WNT10Ac.1184G>T (p.Arg395Leu)
c.1133G>T (p.Arg378Leu)
c.1088G>T (p.Arg363Leu)
c.804G>T (p.Pro268=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893202C>ACA431234835WNT10Ac.1185C>A (p.Arg395=)
c.1134C>A (p.Arg378=)
c.1089C>A (p.Arg363=)
c.805C>A (p.Leu269Ile)
 gnomAD v4
2g.218893202C=CA1328965595WNT10Ac.1185C= (p.Arg395=)
c.1134C= (p.Arg378=)
c.1089C= (p.Arg363=)
c.805C= (p.Leu269=)
2g.218893202C>GCA431234836WNT10Ac.1185C>G (p.Arg395=)
c.1134C>G (p.Arg378=)
c.1089C>G (p.Arg363=)
c.805C>G (p.Leu269Val)
 gnomAD v4
2g.218893202C>TCA2114126WNT10Ac.1185C>T (p.Arg395=)
c.1134C>T (p.Arg378=)
c.1089C>T (p.Arg363=)
c.805C>T (p.Leu269Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893203T>ACA350592339WNT10Ac.1186T>A (p.Phe396Ile)
c.1135T>A (p.Phe379Ile)
c.1090T>A (p.Phe364Ile)
c.806T>A (p.Leu269His)
2g.218893203T>CCA350592346WNT10Ac.1186T>C (p.Phe396Leu)
c.1135T>C (p.Phe379Leu)
c.1090T>C (p.Phe364Leu)
c.806T>C (p.Leu269Pro)
 gnomAD v4
2g.218893203T>GCA350592359WNT10Ac.1186T>G (p.Phe396Val)
c.1135T>G (p.Phe379Val)
c.1090T>G (p.Phe364Val)
c.806T>G (p.Leu269Arg)
 gnomAD v4
2g.218893204T>ACA350592381WNT10Ac.1187T>A (p.Phe396Tyr)
c.1136T>A (p.Phe379Tyr)
c.1091T>A (p.Phe364Tyr)
c.807T>A (p.Leu269=)
2g.218893204T>CCA350592382WNT10Ac.1187T>C (p.Phe396Ser)
c.1136T>C (p.Phe379Ser)
c.1091T>C (p.Phe364Ser)
c.807T>C (p.Leu269=)
2g.218893204T>GCA350592383WNT10Ac.1187T>G (p.Phe396Cys)
c.1136T>G (p.Phe379Cys)
c.1091T>G (p.Phe364Cys)
c.807T>G (p.Leu269=)
2g.218893205C>ACA350592384WNT10Ac.1188C>A (p.Phe396Leu)
c.1137C>A (p.Phe379Leu)
c.1092C>A (p.Phe364Leu)
c.808C>A (p.Pro270Thr)
 gnomAD v4
2g.218893205C=CA1328965598WNT10Ac.1188C= (p.Phe396=)
c.1137C= (p.Phe379=)
c.1092C= (p.Phe364=)
c.808C= (p.Pro270=)
2g.218893205C>GCA350592386WNT10Ac.1188C>G (p.Phe396Leu)
c.1137C>G (p.Phe379Leu)
c.1092C>G (p.Phe364Leu)
c.808C>G (p.Pro270Ala)
 dbSNP gnomAD v4
2g.218893205C>TCA431234837WNT10Ac.1188C>T (p.Phe396=)
c.1137C>T (p.Phe379=)
c.1092C>T (p.Phe364=)
c.808C>T (p.Pro270Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893206C>ACA350592389WNT10Ac.1189C>A (p.His397Asn)
c.1138C>A (p.His380Asn)
c.1093C>A (p.His365Asn)
c.809C>A (p.Pro270Gln)
 gnomAD v4
2g.218893206C>GCA350592393WNT10Ac.1189C>G (p.His397Asp)
c.1138C>G (p.His380Asp)
c.1093C>G (p.His365Asp)
c.809C>G (p.Pro270Arg)
2g.218893206C>TCA350592394WNT10Ac.1189C>T (p.His397Tyr)
c.1138C>T (p.His380Tyr)
c.1093C>T (p.His365Tyr)
c.809C>T (p.Pro270Leu)
2g.218893206_218893207insGAACA2754311150WNT10Ac.1189_1190insGAA (p.His397delinsArgAsn)
c.1138_1139insGAA (p.His380delinsArgAsn)
c.1093_1094insGAA (p.His365delinsArgAsn)
c.809_810insGAA (p.Pro270_Leu271insLys)
2g.218893207A>CCA350592396WNT10Ac.1190A>C (p.His397Pro)
c.1139A>C (p.His380Pro)
c.1094A>C (p.His365Pro)
c.810A>C (p.Pro270=)
2g.218893207A>GCA350592398WNT10Ac.1190A>G (p.His397Arg)
c.1139A>G (p.His380Arg)
c.1094A>G (p.His365Arg)
c.810A>G (p.Pro270=)
2g.218893207A>TCA350592395WNT10Ac.1190A>T (p.His397Leu)
c.1139A>T (p.His380Leu)
c.1094A>T (p.His365Leu)
c.810A>T (p.Pro270=)
2g.218893208C>ACA350592415WNT10Ac.1191C>A (p.His397Gln)
c.1140C>A (p.His380Gln)
c.1095C>A (p.His365Gln)
c.811C>A (p.Leu271Met)
 gnomAD v4
2g.218893208C=CA1328965600WNT10Ac.1191C= (p.His397=)
c.1140C= (p.His380=)
c.1095C= (p.His365=)
c.811C= (p.Leu271=)
2g.218893208C>GCA350592405WNT10Ac.1191C>G (p.His397Gln)
c.1140C>G (p.His380Gln)
c.1095C>G (p.His365Gln)
c.811C>G (p.Leu271Val)
2g.218893208C>TCA431234838WNT10Ac.1191C>T (p.His397=)
c.1140C>T (p.His380=)
c.1095C>T (p.His365=)
c.811C>T (p.Leu271=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893209T>ACA350592446WNT10Ac.1192T>A (p.Trp398Arg)
c.1141T>A (p.Trp381Arg)
c.1096T>A (p.Trp366Arg)
c.812T>A (p.Leu271Gln)
 gnomAD v4
2g.218893209T>CCA350592428WNT10Ac.1192T>C (p.Trp398Arg)
c.1141T>C (p.Trp381Arg)
c.1096T>C (p.Trp366Arg)
c.812T>C (p.Leu271Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893209T>GCA350592443WNT10Ac.1192T>G (p.Trp398Gly)
c.1141T>G (p.Trp381Gly)
c.1096T>G (p.Trp366Gly)
c.812T>G (p.Leu271Arg)
 gnomAD v4
2g.218893209T=CA1328965604WNT10Ac.1192T= (p.Trp398=)
c.1141T= (p.Trp381=)
c.1096T= (p.Trp366=)
c.812T= (p.Leu271=)
2g.218893210G>ACA350592453WNT10Ac.1193G>A (p.Trp398Ter)
c.1142G>A (p.Trp381Ter)
c.1097G>A (p.Trp366Ter)
c.813G>A (p.Leu271=)
 gnomAD v4
2g.218893210G>CCA350592459WNT10Ac.1193G>C (p.Trp398Ser)
c.1142G>C (p.Trp381Ser)
c.1097G>C (p.Trp366Ser)
c.813G>C (p.Leu271=)
2g.218893210G>TCA350592462WNT10Ac.1193G>T (p.Trp398Leu)
c.1142G>T (p.Trp381Leu)
c.1097G>T (p.Trp366Leu)
c.813G>T (p.Leu271=)
 gnomAD v4
2g.218893211G>ACA350592463WNT10Ac.1194G>A (p.Trp398Ter)
c.1143G>A (p.Trp381Ter)
c.1098G>A (p.Trp366Ter)
c.814G>A (p.Val272Met)
 dbSNP gnomAD v2 gnomAD v4
2g.218893211G>CCA350592464WNT10Ac.1194G>C (p.Trp398Cys)
c.1143G>C (p.Trp381Cys)
c.1098G>C (p.Trp366Cys)
c.814G>C (p.Val272Leu)
2g.218893211G=CA1328965609WNT10Ac.1194G= (p.Trp398=)
c.1143G= (p.Trp381=)
c.1098G= (p.Trp366=)
c.814G= (p.Val272=)
2g.218893211G>TCA350592466WNT10Ac.1194G>T (p.Trp398Cys)
c.1143G>T (p.Trp381Cys)
c.1098G>T (p.Trp366Cys)
c.814G>T (p.Val272Leu)
 gnomAD v4
2g.218893212T>ACA350592468WNT10Ac.1195T>A (p.Cys399Ser)
c.1144T>A (p.Cys382Ser)
c.1099T>A (p.Cys367Ser)
c.815T>A (p.Val272Glu)
2g.218893212T>CCA350592476WNT10Ac.1195T>C (p.Cys399Arg)
c.1144T>C (p.Cys382Arg)
c.1099T>C (p.Cys367Arg)
c.815T>C (p.Val272Ala)
2g.218893212T>GCA350592479WNT10Ac.1195T>G (p.Cys399Gly)
c.1144T>G (p.Cys382Gly)
c.1099T>G (p.Cys367Gly)
c.815T>G (p.Val272Gly)
2g.218893213G>ACA350592486WNT10Ac.1196G>A (p.Cys399Tyr)
c.1145G>A (p.Cys382Tyr)
c.1100G>A (p.Cys367Tyr)
c.816G>A (p.Val272=)
2g.218893213G>CCA350592488WNT10Ac.1196G>C (p.Cys399Ser)
c.1145G>C (p.Cys382Ser)
c.1100G>C (p.Cys367Ser)
c.816G>C (p.Val272=)
2g.218893213G>TCA350592493WNT10Ac.1196G>T (p.Cys399Phe)
c.1145G>T (p.Cys382Phe)
c.1100G>T (p.Cys367Phe)
c.816G>T (p.Val272=)
 gnomAD v4
2g.218893214C>ACA350592495WNT10Ac.1197C>A (p.Cys399Ter)
c.1146C>A (p.Cys382Ter)
c.1101C>A (p.Cys367Ter)
c.817C>A (p.Leu273Met)
 gnomAD v4
2g.218893214C>GCA350592498WNT10Ac.1197C>G (p.Cys399Trp)
c.1146C>G (p.Cys382Trp)
c.1101C>G (p.Cys367Trp)
c.817C>G (p.Leu273Val)
2g.218893214C>TCA431234839WNT10Ac.1197C>T (p.Cys399=)
c.1146C>T (p.Cys382=)
c.1101C>T (p.Cys367=)
c.817C>T (p.Leu273=)
 ClinVar gnomAD v4
2g.218893215T>ACA350592503WNT10Ac.1198T>A (p.Cys400Ser)
c.1147T>A (p.Cys383Ser)
c.1102T>A (p.Cys368Ser)
c.818T>A (p.Leu273Gln)
2g.218893215T>CCA350592507WNT10Ac.1198T>C (p.Cys400Arg)
c.1147T>C (p.Cys383Arg)
c.1102T>C (p.Cys368Arg)
c.818T>C (p.Leu273Pro)
2g.218893215T>GCA350592509WNT10Ac.1198T>G (p.Cys400Gly)
c.1147T>G (p.Cys383Gly)
c.1102T>G (p.Cys368Gly)
c.818T>G (p.Leu273Arg)
2g.218893216G>ACA350592511WNT10Ac.1199G>A (p.Cys400Tyr)
c.1148G>A (p.Cys383Tyr)
c.1103G>A (p.Cys368Tyr)
c.819G>A (p.Leu273=)
 ClinVar dbSNP gnomAD v4
2g.218893216G>CCA350592514WNT10Ac.1199G>C (p.Cys400Ser)
c.1148G>C (p.Cys383Ser)
c.1103G>C (p.Cys368Ser)
c.819G>C (p.Leu273=)
 ClinVar dbSNP gnomAD v4
2g.218893216G=CA1328965615WNT10Ac.1199G= (p.Cys400=)
c.1148G= (p.Cys383=)
c.1103G= (p.Cys368=)
c.819G= (p.Leu273=)
2g.218893216G>TCA350592515WNT10Ac.1199G>T (p.Cys400Phe)
c.1148G>T (p.Cys383Phe)
c.1103G>T (p.Cys368Phe)
c.819G>T (p.Leu273=)
 gnomAD v4
2g.218893217T>ACA350592519WNT10Ac.1200T>A (p.Cys400Ter)
c.1149T>A (p.Cys383Ter)
c.1104T>A (p.Cys368Ter)
c.820T>A (p.Phe274Ile)
2g.218893217T>CCA431234840WNT10Ac.1200T>C (p.Cys400=)
c.1149T>C (p.Cys383=)
c.1104T>C (p.Cys368=)
c.820T>C (p.Phe274Leu)
 dbSNP gnomAD v2 gnomAD v4
2g.218893217T>GCA350592523WNT10Ac.1200T>G (p.Cys400Trp)
c.1149T>G (p.Cys383Trp)
c.1104T>G (p.Cys368Trp)
c.820T>G (p.Phe274Val)
2g.218893217T=CA1328965621WNT10Ac.1200T= (p.Cys400=)
c.1149T= (p.Cys383=)
c.1104T= (p.Cys368=)
c.820T= (p.Phe274=)
2g.218893218T>ACA350592528WNT10Ac.1201T>A (p.Phe401Ile)
c.1150T>A (p.Phe384Ile)
c.1105T>A (p.Phe369Ile)
c.821T>A (p.Phe274Tyr)
 gnomAD v4
2g.218893218T>CCA350592529WNT10Ac.1201T>C (p.Phe401Leu)
c.1150T>C (p.Phe384Leu)
c.1105T>C (p.Phe369Leu)
c.821T>C (p.Phe274Ser)
 gnomAD v4
2g.218893218T>GCA350592530WNT10Ac.1201T>G (p.Phe401Val)
c.1150T>G (p.Phe384Val)
c.1105T>G (p.Phe369Val)
c.821T>G (p.Phe274Cys)
2g.218893219T>ACA350592535WNT10Ac.1202T>A (p.Phe401Tyr)
c.1151T>A (p.Phe384Tyr)
c.1106T>A (p.Phe369Tyr)
c.822T>A (p.Phe274Leu)
2g.218893219T>CCA350592533WNT10Ac.1202T>C (p.Phe401Ser)
c.1151T>C (p.Phe384Ser)
c.1106T>C (p.Phe369Ser)
c.822T>C (p.Phe274=)
 gnomAD v4
2g.218893219T>GCA350592531WNT10Ac.1202T>G (p.Phe401Cys)
c.1151T>G (p.Phe384Cys)
c.1106T>G (p.Phe369Cys)
c.822T>G (p.Phe274Leu)
 dbSNP gnomAD v3 gnomAD v4
2g.218893219T=CA1328965624WNT10Ac.1202T= (p.Phe401=)
c.1151T= (p.Phe384=)
c.1106T= (p.Phe369=)
c.822T= (p.Phe274=)
2g.218893220C>ACA350592537WNT10Ac.1203C>A (p.Phe401Leu)
c.1152C>A (p.Phe384Leu)
c.1107C>A (p.Phe369Leu)
c.823C>A (p.Arg275Ser)
 gnomAD v4
2g.218893220C=CA1328965626WNT10Ac.1203C= (p.Phe401=)
c.1152C= (p.Phe384=)
c.1107C= (p.Phe369=)
c.823C= (p.Arg275=)
2g.218893220C>GCA350592539WNT10Ac.1203C>G (p.Phe401Leu)
c.1152C>G (p.Phe384Leu)
c.1107C>G (p.Phe369Leu)
c.823C>G (p.Arg275Gly)
 gnomAD v4
2g.218893220C>TCA431234841WNT10Ac.1203C>T (p.Phe401=)
c.1152C>T (p.Phe384=)
c.1107C>T (p.Phe369=)
c.823C>T (p.Arg275Cys)
 dbSNP gnomAD v2 gnomAD v4
2g.218893221G>ACA350592543WNT10Ac.1204G>A (p.Val402Met)
n.1G>A
c.1153G>A (p.Val385Met)
c.1108G>A (p.Val370Met)
c.824G>A (p.Arg275His)
 ClinVar gnomAD v4
2g.218893221G>CCA350592545WNT10Ac.1204G>C (p.Val402Leu)
n.1G>C
c.1153G>C (p.Val385Leu)
c.1108G>C (p.Val370Leu)
c.824G>C (p.Arg275Pro)
2g.218893221G>TCA350592548WNT10Ac.1204G>T (p.Val402Leu)
n.1G>T
c.1153G>T (p.Val385Leu)
c.1108G>T (p.Val370Leu)
c.824G>T (p.Arg275Leu)
2g.218893222T>ACA350592553WNT10Ac.1205T>A (p.Val402Glu)
n.2T>A
c.1154T>A (p.Val385Glu)
c.1109T>A (p.Val370Glu)
c.825T>A (p.Arg275=)
2g.218893222T>CCA350592551WNT10Ac.1205T>C (p.Val402Ala)
n.2T>C
c.1154T>C (p.Val385Ala)
c.1109T>C (p.Val370Ala)
c.825T>C (p.Arg275=)
 gnomAD v4
2g.218893222T>GCA350592550WNT10Ac.1205T>G (p.Val402Gly)
n.2T>G
c.1154T>G (p.Val385Gly)
c.1109T>G (p.Val370Gly)
c.825T>G (p.Arg275=)
2g.218893223G>ACA431234842WNT10Ac.1206G>A (p.Val402=)
n.3G>A
c.1155G>A (p.Val385=)
c.1110G>A (p.Val370=)
c.826G>A (p.Gly276Ser)
 gnomAD v4
2g.218893223G>CCA431234843WNT10Ac.1206G>C (p.Val402=)
n.3G>C
c.1155G>C (p.Val385=)
c.1110G>C (p.Val370=)
c.826G>C (p.Gly276Arg)
 ClinVar
2g.218893223G>TCA431234844WNT10Ac.1206G>T (p.Val402=)
n.3G>T
c.1155G>T (p.Val385=)
c.1110G>T (p.Val370=)
c.826G>T (p.Gly276Cys)
 gnomAD v4
2g.218893224G>ACA350592556WNT10Ac.1207G>A (p.Val403Ile)
n.4G>A
c.1156G>A (p.Val386Ile)
c.1111G>A (p.Val371Ile)
c.827G>A (p.Gly276Asp)
2g.218893224G>CCA350592560WNT10Ac.1207G>C (p.Val403Leu)
n.4G>C
c.1156G>C (p.Val386Leu)
c.1111G>C (p.Val371Leu)
c.827G>C (p.Gly276Ala)
2g.218893224G>TCA350592563WNT10Ac.1207G>T (p.Val403Phe)
n.4G>T
c.1156G>T (p.Val386Phe)
c.1111G>T (p.Val371Phe)
c.827G>T (p.Gly276Val)
 gnomAD v4
2g.218893225T>ACA350592571WNT10Ac.1208T>A (p.Val403Asp)
n.5T>A
c.1157T>A (p.Val386Asp)
c.1112T>A (p.Val371Asp)
c.828T>A (p.Gly276=)
2g.218893225T>CCA350592574WNT10Ac.1208T>C (p.Val403Ala)
n.5T>C
c.1157T>C (p.Val386Ala)
c.1112T>C (p.Val371Ala)
c.828T>C (p.Gly276=)
2g.218893225T>GCA350592580WNT10Ac.1208T>G (p.Val403Gly)
n.5T>G
c.1157T>G (p.Val386Gly)
c.1112T>G (p.Val371Gly)
c.828T>G (p.Gly276=)
2g.218893226C>ACA431234845WNT10Ac.1209C>A (p.Val403=)
n.6C>A
c.1158C>A (p.Val386=)
c.1113C>A (p.Val371=)
c.829C>A (p.Leu277Met)
 gnomAD v4
2g.218893226C>GCA431234846WNT10Ac.1209C>G (p.Val403=)
n.6C>G
c.1158C>G (p.Val386=)
c.1113C>G (p.Val371=)
c.829C>G (p.Leu277Val)
2g.218893226C>TCA431234847WNT10Ac.1209C>T (p.Val403=)
n.6C>T
c.1158C>T (p.Val386=)
c.1113C>T (p.Val371=)
c.829C>T (p.Leu277=)
 gnomAD v4
2g.218893227T>ACA2114127WNT10Ac.1210T>A (p.Cys404Ser)
n.7T>A
c.1159T>A (p.Cys387Ser)
c.1114T>A (p.Cys372Ser)
c.830T>A (p.Leu277Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.218893227T>CCA350592601WNT10Ac.1210T>C (p.Cys404Arg)
n.7T>C
c.1159T>C (p.Cys387Arg)
c.1114T>C (p.Cys372Arg)
c.830T>C (p.Leu277Pro)
2g.218893227T>GCA350592599WNT10Ac.1210T>G (p.Cys404Gly)
n.7T>G
c.1159T>G (p.Cys387Gly)
c.1114T>G (p.Cys372Gly)
c.830T>G (p.Leu277Arg)
2g.218893227T=CA1328965630WNT10Ac.1210T= (p.Cys404=)
n.7T=
c.1159T= (p.Cys387=)
c.1114T= (p.Cys372=)
c.830T= (p.Leu277=)
2g.218893228G>ACA350592606WNT10Ac.1211G>A (p.Cys404Tyr)
n.8G>A
c.1160G>A (p.Cys387Tyr)
c.1115G>A (p.Cys372Tyr)
c.831G>A (p.Leu277=)
 gnomAD v4
2g.218893228G>CCA350592610WNT10Ac.1211G>C (p.Cys404Ser)
n.8G>C
c.1160G>C (p.Cys387Ser)
c.1115G>C (p.Cys372Ser)
c.831G>C (p.Leu277=)
2g.218893228G>TCA350592618WNT10Ac.1211G>T (p.Cys404Phe)
n.8G>T
c.1160G>T (p.Cys387Phe)
c.1115G>T (p.Cys372Phe)
c.831G>T (p.Leu277=)
 gnomAD v4
2g.218893229C>ACA350592621WNT10Ac.1212C>A (p.Cys404Ter)
n.9C>A
c.1161C>A (p.Cys387Ter)
c.1116C>A (p.Cys372Ter)
c.832C>A (p.Arg278=)
 gnomAD v4
2g.218893229C=CA1328965633WNT10Ac.1212C= (p.Cys404=)
n.9C=
c.1161C= (p.Cys387=)
c.1116C= (p.Cys372=)
c.832C= (p.Arg278=)
2g.218893229C>GCA350592627WNT10Ac.1212C>G (p.Cys404Trp)
n.9C>G
c.1161C>G (p.Cys387Trp)
c.1116C>G (p.Cys372Trp)
c.832C>G (p.Arg278Gly)
 ClinVar dbSNP gnomAD v4
2g.218893229C>TCA431234848WNT10Ac.1212C>T (p.Cys404=)
n.9C>T
c.1161C>T (p.Cys387=)
c.1116C>T (p.Cys372=)
c.832C>T (p.Arg278Ter)
 ClinVar gnomAD v4
2g.218893230G>ACA350592631WNT10Ac.1213G>A (p.Glu405Lys)
n.10G>A
c.1162G>A (p.Glu388Lys)
c.1117G>A (p.Glu373Lys)
c.833G>A (p.Arg278Gln)
 gnomAD v4
2g.218893230G>CCA350592633WNT10Ac.1213G>C (p.Glu405Gln)
n.10G>C
c.1162G>C (p.Glu388Gln)
c.1117G>C (p.Glu373Gln)
c.833G>C (p.Arg278Pro)
2g.218893230G>TCA350592635WNT10Ac.1213G>T (p.Glu405Ter)
n.10G>T
c.1162G>T (p.Glu388Ter)
c.1117G>T (p.Glu373Ter)
c.833G>T (p.Arg278Leu)
 gnomAD v4
2g.218893231A>CCA350592638WNT10Ac.1214A>C (p.Glu405Ala)
n.11A>C
c.1163A>C (p.Glu388Ala)
c.1118A>C (p.Glu373Ala)
c.834A>C (p.Arg278=)
2g.218893231A>GCA350592639WNT10Ac.1214A>G (p.Glu405Gly)
n.11A>G
c.1163A>G (p.Glu388Gly)
c.1118A>G (p.Glu373Gly)
c.834A>G (p.Arg278=)
 gnomAD v4
2g.218893231A>TCA350592646WNT10Ac.1214A>T (p.Glu405Val)
n.11A>T
c.1163A>T (p.Glu388Val)
c.1118A>T (p.Glu373Val)
c.834A>T (p.Arg278=)
2g.218893232A>CCA350592657WNT10Ac.1215A>C (p.Glu405Asp)
n.12A>C
c.1164A>C (p.Glu388Asp)
c.1119A>C (p.Glu373Asp)
c.835A>C (p.Arg279=)
2g.218893232A>GCA431234849WNT10Ac.1215A>G (p.Glu405=)
n.12A>G
c.1164A>G (p.Glu388=)
c.1119A>G (p.Glu373=)
c.835A>G (p.Arg279Gly)
 gnomAD v4
2g.218893232A>TCA350592650WNT10Ac.1215A>T (p.Glu405Asp)
n.12A>T
c.1164A>T (p.Glu388Asp)
c.1119A>T (p.Glu373Asp)
c.835A>T (p.Arg279Ter)
2g.218893233G>ACA350592660WNT10Ac.1216G>A (p.Glu406Lys)
n.13G>A
c.1165G>A (p.Glu389Lys)
c.1120G>A (p.Glu374Lys)
c.836G>A (p.Arg279Lys)
 dbSNP gnomAD v2
2g.218893233G>CCA350592663WNT10Ac.1216G>C (p.Glu406Gln)
n.13G>C
c.1165G>C (p.Glu389Gln)
c.1120G>C (p.Glu374Gln)
c.836G>C (p.Arg279Thr)
2g.218893233G=CA1328965638WNT10Ac.1216G= (p.Glu406=)
n.13G=
c.1165G= (p.Glu389=)
c.1120G= (p.Glu374=)
c.836G= (p.Arg279=)
2g.218893233G>TCA350592662WNT10Ac.1216G>T (p.Glu406Ter)
n.13G>T
c.1165G>T (p.Glu389Ter)
c.1120G>T (p.Glu374Ter)
c.836G>T (p.Arg279Ile)
 gnomAD v4
2g.218893234A>CCA350592666WNT10Ac.1217A>C (p.Glu406Ala)
n.14A>C
c.1166A>C (p.Glu389Ala)
c.1121A>C (p.Glu374Ala)
c.837A>C (p.Arg279Ser)
2g.218893234A>GCA350592670WNT10Ac.1217A>G (p.Glu406Gly)
n.14A>G
c.1166A>G (p.Glu389Gly)
c.1121A>G (p.Glu374Gly)
c.837A>G (p.Arg279=)
2g.218893234A>TCA350592672WNT10Ac.1217A>T (p.Glu406Val)
n.14A>T
c.1166A>T (p.Glu389Val)
c.1121A>T (p.Glu374Val)
c.837A>T (p.Arg279Ser)
2g.218893235G>ACA431234850WNT10Ac.1218G>A (p.Glu406=)
n.15G>A
c.1167G>A (p.Glu389=)
c.1122G>A (p.Glu374=)
c.838G>A (p.Val280Met)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.218893235G>CCA350592674WNT10Ac.1218G>C (p.Glu406Asp)
n.15G>C
c.1167G>C (p.Glu389Asp)
c.1122G>C (p.Glu374Asp)
c.838G>C (p.Val280Leu)
 gnomAD v4
2g.218893235G=CA1328965640WNT10Ac.1218G= (p.Glu406=)
n.15G=
c.1167G= (p.Glu389=)
c.1122G= (p.Glu374=)
c.838G= (p.Val280=)
2g.218893235G>TCA350592676WNT10Ac.1218G>T (p.Glu406Asp)
n.15G>T
c.1167G>T (p.Glu389Asp)
c.1122G>T (p.Glu374Asp)
c.838G>T (p.Val280Leu)
 gnomAD v4
2g.218893236T>ACA350592680WNT10Ac.1219T>A (p.Cys407Ser)
n.16T>A
c.1168T>A (p.Cys390Ser)
c.1123T>A (p.Cys375Ser)
c.839T>A (p.Val280Glu)
2g.218893236T>CCA350592694WNT10Ac.1219T>C (p.Cys407Arg)
n.16T>C
c.1168T>C (p.Cys390Arg)
c.1123T>C (p.Cys375Arg)
c.839T>C (p.Val280Ala)
2g.218893236T>GCA350592696WNT10Ac.1219T>G (p.Cys407Gly)
n.16T>G
c.1168T>G (p.Cys390Gly)
c.1123T>G (p.Cys375Gly)
c.839T>G (p.Val280Gly)
2g.218893237G>ACA350592699WNT10Ac.1220G>A (p.Cys407Tyr)
n.17G>A
c.1169G>A (p.Cys390Tyr)
c.1124G>A (p.Cys375Tyr)
c.840G>A (p.Val280=)
 gnomAD v4
2g.218893237G>CCA350592707WNT10Ac.1220G>C (p.Cys407Ser)
n.17G>C
c.1169G>C (p.Cys390Ser)
c.1124G>C (p.Cys375Ser)
c.840G>C (p.Val280=)
2g.218893237G>TCA350592708WNT10Ac.1220G>T (p.Cys407Phe)
n.17G>T
c.1169G>T (p.Cys390Phe)
c.1124G>T (p.Cys375Phe)
c.840G>T (p.Val280=)
 gnomAD v4
2g.218893238C>ACA350592711WNT10Ac.1221C>A (p.Cys407Ter)
n.18C>A
c.1170C>A (p.Cys390Ter)
c.1125C>A (p.Cys375Ter)
c.841C>A (p.Pro281Thr)
 dbSNP gnomAD v3 gnomAD v4
2g.218893238C=CA1328965642WNT10Ac.1221C= (p.Cys407=)
n.18C=
c.1170C= (p.Cys390=)
c.1125C= (p.Cys375=)
c.841C= (p.Pro281=)
2g.218893238C>GCA350592715WNT10Ac.1221C>G (p.Cys407Trp)
n.18C>G
c.1170C>G (p.Cys390Trp)
c.1125C>G (p.Cys375Trp)
c.841C>G (p.Pro281Ala)
2g.218893238C>TCA431234851WNT10Ac.1221C>T (p.Cys407=)
n.18C>T
c.1170C>T (p.Cys390=)
c.1125C>T (p.Cys375=)
c.841C>T (p.Pro281Ser)
 ClinVar dbSNP gnomAD v4
2g.218893239C>ACA350592718WNT10Ac.1222C>A (p.Arg408Ser)
n.19C>A
c.1171C>A (p.Arg391Ser)
c.1126C>A (p.Arg376Ser)
c.842C>A (p.Pro281Gln)
 dbSNP gnomAD v2 gnomAD v4
2g.218893239C=CA1328965644WNT10Ac.1222C= (p.Arg408=)
n.19C=
c.1171C= (p.Arg391=)
c.1126C= (p.Arg376=)
c.842C= (p.Pro281=)
2g.218893239C>GCA350592723WNT10Ac.1222C>G (p.Arg408Gly)
n.19C>G
c.1171C>G (p.Arg391Gly)
c.1126C>G (p.Arg376Gly)
c.842C>G (p.Pro281Arg)
2g.218893239C>TCA350592721WNT10Ac.1222C>T (p.Arg408Cys)
n.19C>T
c.1171C>T (p.Arg391Cys)
c.1126C>T (p.Arg376Cys)
c.842C>T (p.Pro281Leu)
 dbSNP gnomAD v2 gnomAD v4
2g.218893240G>ACA65919439WNT10Ac.1223G>A (p.Arg408His)
n.20G>A
c.1172G>A (p.Arg391His)
c.1127G>A (p.Arg376His)
c.843G>A (p.Pro281=)
 ClinVar dbSNP gnomAD v4
2g.218893240G>CCA350592728WNT10Ac.1223G>C (p.Arg408Pro)
n.20G>C
c.1172G>C (p.Arg391Pro)
c.1127G>C (p.Arg376Pro)
c.843G>C (p.Pro281=)
 gnomAD v4
2g.218893240G=CA1328965646WNT10Ac.1223G= (p.Arg408=)
n.20G=
c.1172G= (p.Arg391=)
c.1127G= (p.Arg376=)
c.843G= (p.Pro281=)
2g.218893240G>TCA350592730WNT10Ac.1223G>T (p.Arg408Leu)
n.20G>T
c.1172G>T (p.Arg391Leu)
c.1127G>T (p.Arg376Leu)
c.843G>T (p.Pro281=)
 gnomAD v4
2g.218893241C>ACA431234852WNT10Ac.1224C>A (p.Arg408=)
n.21C>A
c.1173C>A (p.Arg391=)
c.1128C>A (p.Arg376=)
c.844C>A (p.His282Asn)
 gnomAD v4
2g.218893241C>GCA431234853WNT10Ac.1224C>G (p.Arg408=)
n.21C>G
c.1173C>G (p.Arg391=)
c.1128C>G (p.Arg376=)
c.844C>G (p.His282Asp)
2g.218893241C>TCA431234854WNT10Ac.1224C>T (p.Arg408=)
n.21C>T
c.1173C>T (p.Arg391=)
c.1128C>T (p.Arg376=)
c.844C>T (p.His282Tyr)
2g.218893242A>CCA350592731WNT10Ac.1225A>C (p.Ile409Leu)
n.22A>C
c.1174A>C (p.Ile392Leu)
c.1129A>C (p.Ile377Leu)
c.845A>C (p.His282Pro)
2g.218893242A>GCA350592732WNT10Ac.1225A>G (p.Ile409Val)
n.22A>G
c.1174A>G (p.Ile392Val)
c.1129A>G (p.Ile377Val)
c.845A>G (p.His282Arg)
2g.218893242A>TCA350592734WNT10Ac.1225A>T (p.Ile409Phe)
n.22A>T
c.1174A>T (p.Ile392Phe)
c.1129A>T (p.Ile377Phe)
c.845A>T (p.His282Leu)
 gnomAD v4
2g.218893242_218893247delinsATCACCCA1328965648WNT10Ac.1225_1230delinsATCACC (p.Ile409=)
n.22_27delinsATCACC
c.1174_1179delinsATCACC (p.Ile392=)
c.1129_1134delinsATCACC (p.Ile377=)
c.845_850delinsATCACC (p.His282=)
2g.218893243T>ACA350592736WNT10Ac.1226T>A (p.Ile409Asn)
n.23T>A
c.1175T>A (p.Ile392Asn)
c.1130T>A (p.Ile377Asn)
c.846T>A (p.His282Gln)
 gnomAD v4
2g.218893243T>CCA350592742WNT10Ac.1226T>C (p.Ile409Thr)
n.23T>C
c.1175T>C (p.Ile392Thr)
c.1130T>C (p.Ile377Thr)
c.846T>C (p.His282=)
 gnomAD v4
2g.218893243T>GCA350592744WNT10Ac.1226T>G (p.Ile409Ser)
n.23T>G
c.1175T>G (p.Ile392Ser)
c.1130T>G (p.Ile377Ser)
c.846T>G (p.His282Gln)
2g.218893243_218893247delCA1328965650WNT10Ac.1226_1230del (p.Ile409ArgfsTer17)
n.23_27del
c.1175_1179del (p.Ile392ArgfsTer17)
c.1130_1134del (p.Ile377ArgfsTer17)
c.846_850del (p.His282GlnfsTer28)
 dbSNP gnomAD v4
2g.218893244delCA2663174557WNT10Ac.1227del (p.Thr410ProfsTer28)
n.24del
c.1176del (p.Thr393ProfsTer28)
c.1131del (p.Thr378ProfsTer28)
c.847del (p.His283ThrfsTer9)
 gnomAD v4
2g.218893244C>ACA431234855WNT10Ac.1227C>A (p.Ile409=)
n.24C>A
c.1176C>A (p.Ile392=)
c.1131C>A (p.Ile377=)
c.847C>A (p.His283Asn)
 gnomAD v4
2g.218893244C>GCA350592747WNT10Ac.1227C>G (p.Ile409Met)
n.24C>G
c.1176C>G (p.Ile392Met)
c.1131C>G (p.Ile377Met)
c.847C>G (p.His283Asp)
2g.218893244C>TCA431234856WNT10Ac.1227C>T (p.Ile409=)
n.24C>T
c.1176C>T (p.Ile392=)
c.1131C>T (p.Ile377=)
c.847C>T (p.His283Tyr)
 gnomAD v4
2g.218893245A>CCA350592751WNT10Ac.1228A>C (p.Thr410Pro)
n.25A>C
c.1177A>C (p.Thr393Pro)
c.1132A>C (p.Thr378Pro)
c.848A>C (p.His283Pro)
2g.218893245A>GCA350592753WNT10Ac.1228A>G (p.Thr410Ala)
n.25A>G
c.1177A>G (p.Thr393Ala)
c.1132A>G (p.Thr378Ala)
c.848A>G (p.His283Arg)
 gnomAD v4
2g.218893245A>TCA350592749WNT10Ac.1228A>T (p.Thr410Ser)
n.25A>T
c.1177A>T (p.Thr393Ser)
c.1132A>T (p.Thr378Ser)
c.848A>T (p.His283Leu)
2g.218893246C>ACA2114128WNT10Ac.1229C>A (p.Thr410Asn)
n.26C>A
c.1178C>A (p.Thr393Asn)
c.1133C>A (p.Thr378Asn)
c.849C>A (p.His283Gln)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893246C=CA1328965652WNT10Ac.1229C= (p.Thr410=)
n.26C=
c.1178C= (p.Thr393=)
c.1133C= (p.Thr378=)
c.849C= (p.His283=)
2g.218893246C>GCA350592756WNT10Ac.1229C>G (p.Thr410Ser)
n.26C>G
c.1178C>G (p.Thr393Ser)
c.1133C>G (p.Thr378Ser)
c.849C>G (p.His283Gln)
2g.218893246C>TCA350592759WNT10Ac.1229C>T (p.Thr410Ile)
n.26C>T
c.1178C>T (p.Thr393Ile)
c.1133C>T (p.Thr378Ile)
c.849C>T (p.His283=)
 dbSNP gnomAD v2 gnomAD v4
2g.218893247C>ACA431234857WNT10Ac.1230C>A (p.Thr410=)
n.27C>A
c.1179C>A (p.Thr393=)
c.1134C>A (p.Thr378=)
c.850C>A (p.Arg284=)
 gnomAD v4
2g.218893247C>GCA431234858WNT10Ac.1230C>G (p.Thr410=)
n.27C>G
c.1179C>G (p.Thr393=)
c.1134C>G (p.Thr378=)
c.850C>G (p.Arg284Gly)
2g.218893247C>TCA431234859WNT10Ac.1230C>T (p.Thr410=)
n.27C>T
c.1179C>T (p.Thr393=)
c.1134C>T (p.Thr378=)
c.850C>T (p.Arg284Ter)
 gnomAD v4
2g.218893248G>ACA350592763WNT10Ac.1231G>A (p.Glu411Lys)
n.28G>A
c.1180G>A (p.Glu394Lys)
c.1135G>A (p.Glu379Lys)
c.851G>A (p.Arg284Gln)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893248G>CCA350592764WNT10Ac.1231G>C (p.Glu411Gln)
n.28G>C
c.1180G>C (p.Glu394Gln)
c.1135G>C (p.Glu379Gln)
c.851G>C (p.Arg284Pro)
 gnomAD v4
2g.218893248G=CA1328965654WNT10Ac.1231G= (p.Glu411=)
n.28G=
c.1180G= (p.Glu394=)
c.1135G= (p.Glu379=)
c.851G= (p.Arg284=)
2g.218893248G>TCA350592766WNT10Ac.1231G>T (p.Glu411Ter)
n.28G>T
c.1180G>T (p.Glu394Ter)
c.1135G>T (p.Glu379Ter)
c.851G>T (p.Arg284Leu)
 gnomAD v4
2g.218893249A>CCA350592773WNT10Ac.1232A>C (p.Glu411Ala)
n.29A>C
c.1181A>C (p.Glu394Ala)
c.1136A>C (p.Glu379Ala)
c.852A>C (p.Arg284=)
2g.218893249A>GCA350592768WNT10Ac.1232A>G (p.Glu411Gly)
n.29A>G
c.1181A>G (p.Glu394Gly)
c.1136A>G (p.Glu379Gly)
c.852A>G (p.Arg284=)
2g.218893249A>TCA350592771WNT10Ac.1232A>T (p.Glu411Val)
n.29A>T
c.1181A>T (p.Glu394Val)
c.1136A>T (p.Glu379Val)
c.852A>T (p.Arg284=)
 gnomAD v4
2g.218893250G>ACA431234860WNT10Ac.1233G>A (p.Glu411=)
n.30G>A
c.1182G>A (p.Glu394=)
c.1137G>A (p.Glu379=)
c.853G>A (p.Val285Met)
 dbSNP gnomAD v4
2g.218893250G>CCA350592774WNT10Ac.1233G>C (p.Glu411Asp)
n.30G>C
c.1182G>C (p.Glu394Asp)
c.1137G>C (p.Glu379Asp)
c.853G>C (p.Val285Leu)
 gnomAD v4
2g.218893250G>TCA350592775WNT10Ac.1233G>T (p.Glu411Asp)
n.30G>T
c.1182G>T (p.Glu394Asp)
c.1137G>T (p.Glu379Asp)
c.853G>T (p.Val285Leu)
 gnomAD v4
2g.218893251T>ACA350592776WNT10Ac.1234T>A (p.Trp412Arg)
n.31T>A
c.1183T>A (p.Trp395Arg)
c.1138T>A (p.Trp380Arg)
c.854T>A (p.Val285Glu)
2g.218893251T>CCA350592778WNT10Ac.1234T>C (p.Trp412Arg)
n.31T>C
c.1183T>C (p.Trp395Arg)
c.1138T>C (p.Trp380Arg)
c.854T>C (p.Val285Ala)
2g.218893251T>GCA350592780WNT10Ac.1234T>G (p.Trp412Gly)
n.31T>G
c.1183T>G (p.Trp395Gly)
c.1138T>G (p.Trp380Gly)
c.854T>G (p.Val285Gly)
2g.218893252G>ACA350592784WNT10Ac.1235G>A (p.Trp412Ter)
n.32G>A
c.1184G>A (p.Trp395Ter)
c.1139G>A (p.Trp380Ter)
c.855G>A (p.Val285=)
 gnomAD v4
2g.218893252G>CCA350592790WNT10Ac.1235G>C (p.Trp412Ser)
n.32G>C
c.1184G>C (p.Trp395Ser)
c.1139G>C (p.Trp380Ser)
c.855G>C (p.Val285=)
2g.218893252G>TCA350592785WNT10Ac.1235G>T (p.Trp412Leu)
n.32G>T
c.1184G>T (p.Trp395Leu)
c.1139G>T (p.Trp380Leu)
c.855G>T (p.Val285=)
 gnomAD v4
2g.218893253G>ACA350592793WNT10Ac.1236G>A (p.Trp412Ter)
n.33G>A
c.1185G>A (p.Trp395Ter)
c.1140G>A (p.Trp380Ter)
c.856G>A (p.Gly286Ser)
 gnomAD v4
2g.218893253G>CCA350592795WNT10Ac.1236G>C (p.Trp412Cys)
n.33G>C
c.1185G>C (p.Trp395Cys)
c.1140G>C (p.Trp380Cys)
c.856G>C (p.Gly286Arg)
 dbSNP
2g.218893253G=CA1328965656WNT10Ac.1236G= (p.Trp412=)
n.33G=
c.1185G= (p.Trp395=)
c.1140G= (p.Trp380=)
c.856G= (p.Gly286=)
2g.218893253G>TCA350592796WNT10Ac.1236G>T (p.Trp412Cys)
n.33G>T
c.1185G>T (p.Trp395Cys)
c.1140G>T (p.Trp380Cys)
c.856G>T (p.Gly286Cys)
 gnomAD v4
2g.218893254G>ACA2114129WNT10Ac.1237G>A (p.Val413Ile)
n.34G>A
c.1186G>A (p.Val396Ile)
c.1141G>A (p.Val381Ile)
c.857G>A (p.Gly286Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218893254G>CCA350592802WNT10Ac.1237G>C (p.Val413Leu)
n.34G>C
c.1186G>C (p.Val396Leu)
c.1141G>C (p.Val381Leu)
c.857G>C (p.Gly286Ala)
2g.218893254G=CA1328965658WNT10Ac.1237G= (p.Val413=)
n.34G=
c.1186G= (p.Val396=)
c.1141G= (p.Val381=)
c.857G= (p.Gly286=)
2g.218893254G>TCA350592803WNT10Ac.1237G>T (p.Val413Phe)
n.34G>T
c.1186G>T (p.Val396Phe)
c.1141G>T (p.Val381Phe)
c.857G>T (p.Gly286Val)
 gnomAD v4
2g.218893255T>ACA350592804WNT10Ac.1238T>A (p.Val413Asp)
n.35T>A
c.1187T>A (p.Val396Asp)
c.1142T>A (p.Val381Asp)
c.858T>A (p.Gly286=)
 gnomAD v4
2g.218893255T>CCA350592807WNT10Ac.1238T>C (p.Val413Ala)
n.35T>C
c.1187T>C (p.Val396Ala)
c.1142T>C (p.Val381Ala)
c.858T>C (p.Gly286=)
 gnomAD v4
2g.218893255T>GCA350592810WNT10Ac.1238T>G (p.Val413Gly)
n.35T>G
c.1187T>G (p.Val396Gly)
c.1142T>G (p.Val381Gly)
c.858T>G (p.Gly286=)
 gnomAD v4
2g.218893256C>ACA431234861WNT10Ac.1239C>A (p.Val413=)
n.36C>A
c.1188C>A (p.Val396=)
c.1143C>A (p.Val381=)
c.859C>A (p.Gln287Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893256C=CA1328965662WNT10Ac.1239C= (p.Val413=)
n.36C=
c.1188C= (p.Val396=)
c.1143C= (p.Val381=)
c.859C= (p.Gln287=)
2g.218893256C>GCA431234862WNT10Ac.1239C>G (p.Val413=)
n.36C>G
c.1188C>G (p.Val396=)
c.1143C>G (p.Val381=)
c.859C>G (p.Gln287Glu)
2g.218893256C>TCA431234863WNT10Ac.1239C>T (p.Val413=)
n.36C>T
c.1188C>T (p.Val396=)
c.1143C>T (p.Val381=)
c.859C>T (p.Gln287Ter)
 gnomAD v4
2g.218893257A>CCA350592811WNT10Ac.1240A>C (p.Ser414Arg)
n.37A>C
c.1189A>C (p.Ser397Arg)
c.1144A>C (p.Ser382Arg)
c.860A>C (p.Gln287Pro)
2g.218893257A>GCA350592813WNT10Ac.1240A>G (p.Ser414Gly)
n.37A>G
c.1189A>G (p.Ser397Gly)
c.1144A>G (p.Ser382Gly)
c.860A>G (p.Gln287Arg)
 gnomAD v4
2g.218893257A>TCA350592816WNT10Ac.1240A>T (p.Ser414Cys)
n.37A>T
c.1189A>T (p.Ser397Cys)
c.1144A>T (p.Ser382Cys)
c.860A>T (p.Gln287Leu)
2g.218893258G>ACA350592826WNT10Ac.1241G>A (p.Ser414Asn)
n.38G>A
c.1190G>A (p.Ser397Asn)
c.1145G>A (p.Ser382Asn)
c.861G>A (p.Gln287=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893258G>CCA350592823WNT10Ac.1241G>C (p.Ser414Thr)
n.38G>C
c.1190G>C (p.Ser397Thr)
c.1145G>C (p.Ser382Thr)
c.861G>C (p.Gln287His)
2g.218893258G=CA1328965665WNT10Ac.1241G= (p.Ser414=)
n.38G=
c.1190G= (p.Ser397=)
c.1145G= (p.Ser382=)
c.861G= (p.Gln287=)
2g.218893258G>TCA350592821WNT10Ac.1241G>T (p.Ser414Ile)
n.38G>T
c.1190G>T (p.Ser397Ile)
c.1145G>T (p.Ser382Ile)
c.861G>T (p.Gln287His)
 gnomAD v4
2g.218893259C>ACA350592831WNT10Ac.1242C>A (p.Ser414Arg)
n.39C>A
c.1191C>A (p.Ser397Arg)
c.1146C>A (p.Ser382Arg)
c.862C>A (p.Arg288Ser)
 gnomAD v4
2g.218893259C>GCA350592839WNT10Ac.1242C>G (p.Ser414Arg)
n.39C>G
c.1191C>G (p.Ser397Arg)
c.1146C>G (p.Ser382Arg)
c.862C>G (p.Arg288Gly)
2g.218893259C>TCA431234864WNT10Ac.1242C>T (p.Ser414=)
n.39C>T
c.1191C>T (p.Ser397=)
c.1146C>T (p.Ser382=)
c.862C>T (p.Arg288Cys)
 ClinVar gnomAD v4
2g.218893260G>ACA350592840WNT10Ac.1243G>A (p.Val415Ile)
n.40G>A
c.1192G>A (p.Val398Ile)
c.1147G>A (p.Val383Ile)
c.863G>A (p.Arg288His)
 dbSNP gnomAD v4
2g.218893260G>CCA350592849WNT10Ac.1243G>C (p.Val415Leu)
n.40G>C
c.1192G>C (p.Val398Leu)
c.1147G>C (p.Val383Leu)
c.863G>C (p.Arg288Pro)
2g.218893260G=CA1328965667WNT10Ac.1243G= (p.Val415=)
n.40G=
c.1192G= (p.Val398=)
c.1147G= (p.Val383=)
c.863G= (p.Arg288=)
2g.218893260G>TCA350592846WNT10Ac.1243G>T (p.Val415Phe)
n.40G>T
c.1192G>T (p.Val398Phe)
c.1147G>T (p.Val383Phe)
c.863G>T (p.Arg288Leu)
 gnomAD v4
2g.218893261T>ACA350592852WNT10Ac.1244T>A (p.Val415Asp)
n.41T>A
c.1193T>A (p.Val398Asp)
c.1148T>A (p.Val383Asp)
c.864T>A (p.Arg288=)
 gnomAD v4
2g.218893261T>CCA350592856WNT10Ac.1244T>C (p.Val415Ala)
n.41T>C
c.1193T>C (p.Val398Ala)
c.1148T>C (p.Val383Ala)
c.864T>C (p.Arg288=)
2g.218893261T>GCA350592854WNT10Ac.1244T>G (p.Val415Gly)
n.41T>G
c.1193T>G (p.Val398Gly)
c.1148T>G (p.Val383Gly)
c.864T>G (p.Arg288=)
2g.218893262C>ACA431234865WNT10Ac.1245C>A (p.Val415=)
n.42C>A
c.1194C>A (p.Val398=)
c.1149C>A (p.Val383=)
c.865C>A (p.Leu289Met)
 gnomAD v4
2g.218893262C>GCA431234866WNT10Ac.1245C>G (p.Val415=)
n.42C>G
c.1194C>G (p.Val398=)
c.1149C>G (p.Val383=)
c.865C>G (p.Leu289Val)
2g.218893262C>TCA431234867WNT10Ac.1245C>T (p.Val415=)
n.42C>T
c.1194C>T (p.Val398=)
c.1149C>T (p.Val383=)
c.865C>T (p.Leu289=)
2g.218893263T>ACA350592859WNT10Ac.1246T>A (p.Cys416Ser)
n.43T>A
c.1195T>A (p.Cys399Ser)
c.1150T>A (p.Cys384Ser)
c.866T>A (p.Leu289Gln)
2g.218893263T>CCA350592866WNT10Ac.1246T>C (p.Cys416Arg)
n.43T>C
c.1195T>C (p.Cys399Arg)
c.1150T>C (p.Cys384Arg)
c.866T>C (p.Leu289Pro)
 gnomAD v4
2g.218893263T>GCA350592869WNT10Ac.1246T>G (p.Cys416Gly)
n.43T>G
c.1195T>G (p.Cys399Gly)
c.1150T>G (p.Cys384Gly)
c.866T>G (p.Leu289Arg)
2g.218893264G>ACA350592882WNT10Ac.1247G>A (p.Cys416Tyr)
n.44G>A
c.1196G>A (p.Cys399Tyr)
c.1151G>A (p.Cys384Tyr)
c.867G>A (p.Leu289=)
 ClinVar dbSNP gnomAD v4
2g.218893264G>CCA350592886WNT10Ac.1247G>C (p.Cys416Ser)
n.44G>C
c.1196G>C (p.Cys399Ser)
c.1151G>C (p.Cys384Ser)
c.867G>C (p.Leu289=)
 ClinVar gnomAD v4
2g.218893264G=CA1328965674WNT10Ac.1247G= (p.Cys416=)
n.44G=
c.1196G= (p.Cys399=)
c.1151G= (p.Cys384=)
c.867G= (p.Leu289=)
2g.218893264G>TCA350592888WNT10Ac.1247G>T (p.Cys416Phe)
n.44G>T
c.1196G>T (p.Cys399Phe)
c.1151G>T (p.Cys384Phe)
c.867G>T (p.Leu289=)
 gnomAD v4
2g.218893265C>ACA350592891WNT10Ac.1248C>A (p.Cys416Ter)
n.45C>A
c.1197C>A (p.Cys399Ter)
c.1152C>A (p.Cys384Ter)
c.868C>A (p.Gln290Lys)
 gnomAD v4
2g.218893265C>GCA350592894WNT10Ac.1248C>G (p.Cys416Trp)
n.45C>G
c.1197C>G (p.Cys399Trp)
c.1152C>G (p.Cys384Trp)
c.868C>G (p.Gln290Glu)
2g.218893265C>TCA431234868WNT10Ac.1248C>T (p.Cys416=)
n.45C>T
c.1197C>T (p.Cys399=)
c.1152C>T (p.Cys384=)
c.868C>T (p.Gln290Ter)
 gnomAD v4
2g.218893266A=CA1328965678WNT10Ac.1249A= (p.Lys417=)
n.46A=
c.1198A= (p.Lys400=)
c.1153A= (p.Lys385=)
c.869A= (p.Gln290=)
2g.218893266A>CCA350592897WNT10Ac.1249A>C (p.Lys417Gln)
n.46A>C
c.1198A>C (p.Lys400Gln)
c.1153A>C (p.Lys385Gln)
c.869A>C (p.Gln290Pro)
2g.218893266A>GCA350592901WNT10Ac.1249A>G (p.Lys417Glu)
n.46A>G
c.1198A>G (p.Lys400Glu)
c.1153A>G (p.Lys385Glu)
c.869A>G (p.Gln290Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218893266A>TCA350592903WNT10Ac.1249A>T (p.Lys417Ter)
n.46A>T
c.1198A>T (p.Lys400Ter)
c.1153A>T (p.Lys385Ter)
c.869A>T (p.Gln290Leu)
2g.218893267delCA2663174558WNT10Ac.1250del (p.Lys417SerfsTer21)
n.47del
c.1199del (p.Lys400SerfsTer21)
c.1154del (p.Lys385SerfsTer21)
c.870del (p.Val291Ter)
 gnomAD v4
2g.218893267A>CCA350592907WNT10Ac.1250A>C (p.Lys417Thr)
n.47A>C
c.1199A>C (p.Lys400Thr)
c.1154A>C (p.Lys385Thr)
c.870A>C (p.Gln290His)
2g.218893267A>GCA350592905WNT10Ac.1250A>G (p.Lys417Arg)
n.47A>G
c.1199A>G (p.Lys400Arg)
c.1154A>G (p.Lys385Arg)
c.870A>G (p.Gln290=)
 gnomAD v4
2g.218893267A>TCA350592906WNT10Ac.1250A>T (p.Lys417Met)
n.47A>T
c.1199A>T (p.Lys400Met)
c.1154A>T (p.Lys385Met)
c.870A>T (p.Gln290His)
 gnomAD v4
2g.218893268G>ACA431234869WNT10Ac.1251G>A (p.Lys417=)
n.47+1G>A
c.1200G>A (p.Lys400=)
c.1155G>A (p.Lys385=)
c.871G>A (p.Val291Met)
 ClinVar dbSNP gnomAD v4
2g.218893268G>CCA350592910WNT10Ac.1251G>C (p.Lys417Asn)
n.47+1G>C
c.1200G>C (p.Lys400Asn)
c.1155G>C (p.Lys385Asn)
c.871G>C (p.Val291Leu)
2g.218893268G>TCA350592913WNT10Ac.1251G>T (p.Lys417Asn)
n.47+1G>T
c.1200G>T (p.Lys400Asn)
c.1155G>T (p.Lys385Asn)
c.871G>T (p.Val291Leu)
 gnomAD v4
2g.218893269T>ACA65919453WNT10Ac.1252T>A (p.Ter418Arg)
n.47+2T>A
c.1201T>A (p.Ter401Arg)
c.1156T>A (p.Ter386Arg)
c.872T>A (p.Val291Glu)
 dbSNP gnomAD v4
2g.218893269T>CCA350592914WNT10Ac.1252T>C (p.Ter418Arg)
n.47+2T>C
c.1201T>C (p.Ter401Arg)
c.1156T>C (p.Ter386Arg)
c.872T>C (p.Val291Ala)
2g.218893269T>GCA350592915WNT10Ac.1252T>G (p.Ter418Gly)
n.47+2T>G
c.1201T>G (p.Ter401Gly)
c.1156T>G (p.Ter386Gly)
c.872T>G (p.Val291Gly)
2g.218893269T=CA1328965680WNT10Ac.1252T= (p.Ter418=)
n.47+2T=
c.1201T= (p.Ter401=)
c.1156T= (p.Ter386=)
c.872T= (p.Val291=)

Number of alleles fetched