Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.218893174A= | CA1328965520 | WNT10A | c.1157A= (p.Gln386=) c.1106A= (p.Gln369=) c.1061A= (p.Gln354=) c.777A= (p.Pro259=) | |
2 | g.218893174A>C | CA350592074 | WNT10A | c.1157A>C (p.Gln386Pro) c.1106A>C (p.Gln369Pro) c.1061A>C (p.Gln354Pro) c.777A>C (p.Pro259=) | |
2 | g.218893174A>G | CA350592075 | WNT10A | c.1157A>G (p.Gln386Arg) c.1106A>G (p.Gln369Arg) c.1061A>G (p.Gln354Arg) c.777A>G (p.Pro259=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893174A>T | CA350592077 | WNT10A | c.1157A>T (p.Gln386Leu) c.1106A>T (p.Gln369Leu) c.1061A>T (p.Gln354Leu) c.777A>T (p.Pro259=) | |
2 | g.218893175G>A | CA431417564 | WNT10A | c.1158G>A (p.Gln386=) c.1107G>A (p.Gln369=) c.1062G>A (p.Gln354=) c.778G>A (p.Asp260Asn) | ClinVar dbSNP |
2 | g.218893175G>C | CA350592080 | WNT10A | c.1158G>C (p.Gln386His) c.1107G>C (p.Gln369His) c.1062G>C (p.Gln354His) c.778G>C (p.Asp260His) | |
2 | g.218893175G>T | CA350592084 | WNT10A | c.1158G>T (p.Gln386His) c.1107G>T (p.Gln369His) c.1062G>T (p.Gln354His) c.778G>T (p.Asp260Tyr) | |
2 | g.218893176A>C | CA350592095 | WNT10A | c.1159A>C (p.Thr387Pro) c.1108A>C (p.Thr370Pro) c.1063A>C (p.Thr355Pro) c.779A>C (p.Asp260Ala) | |
2 | g.218893176A>G | CA350592093 | WNT10A | c.1159A>G (p.Thr387Ala) c.1108A>G (p.Thr370Ala) c.1063A>G (p.Thr355Ala) c.779A>G (p.Asp260Gly) | |
2 | g.218893176A>T | CA350592089 | WNT10A | c.1159A>T (p.Thr387Ser) c.1108A>T (p.Thr370Ser) c.1063A>T (p.Thr355Ser) c.779A>T (p.Asp260Val) | |
2 | g.218893177C>A | CA2114121 | WNT10A | c.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 |
2 | g.218893177C= | CA1328965523 | WNT10A | c.1160C= (p.Thr387=) c.1109C= (p.Thr370=) c.1064C= (p.Thr355=) c.780C= (p.Asp260=) | |
2 | g.218893177C>G | CA350592099 | WNT10A | c.1160C>G (p.Thr387Arg) c.1109C>G (p.Thr370Arg) c.1064C>G (p.Thr355Arg) c.780C>G (p.Asp260Glu) | |
2 | g.218893177C>T | CA350592101 | WNT10A | c.1160C>T (p.Thr387Met) c.1109C>T (p.Thr370Met) c.1064C>T (p.Thr355Met) c.780C>T (p.Asp260=) | gnomAD v4 COSMIC |
2 | g.218893177_218893181del | CA2577276400 | WNT10A | c.1160_1164del (p.Thr387LysfsTer?) c.1109_1113del (p.Thr370LysfsTer?) c.1064_1068del (p.Thr355LysfsTer?) c.780_784del (p.Asp260GlufsTer?) | |
2 | g.218893178G>A | CA431417572 | WNT10A | c.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 |
2 | g.218893178G>C | CA431417574 | WNT10A | c.1161G>C (p.Thr387=) c.1110G>C (p.Thr370=) c.1065G>C (p.Thr355=) c.781G>C (p.Ala261Pro) | |
2 | g.218893178G= | CA1328965527 | WNT10A | c.1161G= (p.Thr387=) c.1110G= (p.Thr370=) c.1065G= (p.Thr355=) c.781G= (p.Ala261=) | |
2 | g.218893178G>T | CA431417577 | WNT10A | c.1161G>T (p.Thr387=) c.1110G>T (p.Thr370=) c.1065G>T (p.Thr355=) c.781G>T (p.Ala261Ser) | ClinVar dbSNP gnomAD v4 |
2 | g.218893179C>A | CA350592119 | WNT10A | c.1162C>A (p.Arg388Ser) c.1111C>A (p.Arg371Ser) c.1066C>A (p.Arg356Ser) c.782C>A (p.Ala261Glu) | dbSNP gnomAD v4 |
2 | g.218893179C= | CA1328965530 | WNT10A | c.1162C= (p.Arg388=) c.1111C= (p.Arg371=) c.1066C= (p.Arg356=) c.782C= (p.Ala261=) | |
2 | g.218893179C>G | CA350592122 | WNT10A | c.1162C>G (p.Arg388Gly) c.1111C>G (p.Arg371Gly) c.1066C>G (p.Arg356Gly) c.782C>G (p.Ala261Gly) | |
2 | g.218893179C>T | CA350592125 | WNT10A | c.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 |
2 | g.218893180G>A | CA350592141 | WNT10A | c.1163G>A (p.Arg388His) c.1112G>A (p.Arg371His) c.1067G>A (p.Arg356His) c.783G>A (p.Ala261=) | gnomAD v4 |
2 | g.218893180G>C | CA350592147 | WNT10A | c.1163G>C (p.Arg388Pro) c.1112G>C (p.Arg371Pro) c.1067G>C (p.Arg356Pro) c.783G>C (p.Ala261=) | |
2 | g.218893180G= | CA1328965533 | WNT10A | c.1163G= (p.Arg388=) c.1112G= (p.Arg371=) c.1067G= (p.Arg356=) c.783G= (p.Ala261=) | |
2 | g.218893180G>T | CA350592148 | WNT10A | c.1163G>T (p.Arg388Leu) c.1112G>T (p.Arg371Leu) c.1067G>T (p.Arg356Leu) c.783G>T (p.Ala261=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893181C>A | CA431417582 | WNT10A | c.1164C>A (p.Arg388=) c.1113C>A (p.Arg371=) c.1068C>A (p.Arg356=) c.784C>A (p.Gln262Lys) | |
2 | g.218893181C>G | CA431417583 | WNT10A | c.1164C>G (p.Arg388=) c.1113C>G (p.Arg371=) c.1068C>G (p.Arg356=) c.784C>G (p.Gln262Glu) | |
2 | g.218893181C>T | CA431417584 | WNT10A | c.1164C>T (p.Arg388=) c.1113C>T (p.Arg371=) c.1068C>T (p.Arg356=) c.784C>T (p.Gln262Ter) | ClinVar dbSNP |
2 | g.218893181_218893195delinsCAGCGAGCGCTGCCA | CA1328965537 | WNT10A | c.1164_1178delinsCAGCGAGCGCTGCCA (p.Arg388=) c.1113_1127delinsCAGCGAGCGCTGCCA (p.Arg371=) c.1068_1082delinsCAGCGAGCGCTGCCA (p.Arg356=) c.784_798delinsCAGCGAGCGCTGCCA (p.Gln262=) | |
2 | g.218893182A>C | CA350592151 | WNT10A | c.1165A>C (p.Ser389Arg) c.1114A>C (p.Ser372Arg) c.1069A>C (p.Ser357Arg) c.785A>C (p.Gln262Pro) | gnomAD v4 |
2 | g.218893182A>G | CA350592154 | WNT10A | c.1165A>G (p.Ser389Gly) c.1114A>G (p.Ser372Gly) c.1069A>G (p.Ser357Gly) c.785A>G (p.Gln262Arg) | gnomAD v4 |
2 | g.218893182A>T | CA350592155 | WNT10A | c.1165A>T (p.Ser389Cys) c.1114A>T (p.Ser372Cys) c.1069A>T (p.Ser357Cys) c.785A>T (p.Gln262Leu) | gnomAD v4 |
2 | g.218893182dup | CA2663174554 | WNT10A | c.1165dup (p.Ser389LysfsTer?) c.1114dup (p.Ser372LysfsTer?) c.1069dup (p.Ser357LysfsTer?) c.785dup (p.Arg263AlafsTer?) | gnomAD v4 |
2 | g.218893182_218893195delinsTTCCAGCACAACATC | CA1139657705 | WNT10A | c.1165_1178delinsTTCCAGCACAACATC (p.Ser389PhefsTer?) c.1114_1127delinsTTCCAGCACAACATC (p.Ser372PhefsTer?) c.1069_1082delinsTTCCAGCACAACATC (p.Ser357PhefsTer?) c.785_798delinsTTCCAGCACAACATC (p.Gln262LeufsTer?) | ClinVar dbSNP |
2 | g.218893183G>A | CA350592161 | WNT10A | c.1166G>A (p.Ser389Asn) c.1115G>A (p.Ser372Asn) c.1070G>A (p.Ser357Asn) c.786G>A (p.Gln262=) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218893183G>C | CA350592160 | WNT10A | c.1166G>C (p.Ser389Thr) c.1115G>C (p.Ser372Thr) c.1070G>C (p.Ser357Thr) c.786G>C (p.Gln262His) | |
2 | g.218893183G= | CA1328965541 | WNT10A | c.1166G= (p.Ser389=) c.1115G= (p.Ser372=) c.1070G= (p.Ser357=) c.786G= (p.Gln262=) | |
2 | g.218893183G>T | CA350592159 | WNT10A | c.1166G>T (p.Ser389Ile) c.1115G>T (p.Ser372Ile) c.1070G>T (p.Ser357Ile) c.786G>T (p.Gln262His) | |
2 | g.218893184C>A | CA350592164 | WNT10A | c.1167C>A (p.Ser389Arg) c.1116C>A (p.Ser372Arg) c.1071C>A (p.Ser357Arg) c.787C>A (p.Arg263=) | gnomAD v4 |
2 | g.218893184C= | CA1328965543 | WNT10A | c.1167C= (p.Ser389=) c.1116C= (p.Ser372=) c.1071C= (p.Ser357=) c.787C= (p.Arg263=) | |
2 | g.218893184C>G | CA2114122 | WNT10A | c.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 |
2 | g.218893184C>T | CA431417591 | WNT10A | c.1167C>T (p.Ser389=) c.1116C>T (p.Ser372=) c.1071C>T (p.Ser357=) c.787C>T (p.Arg263Ter) | ClinVar gnomAD v4 |
2 | g.218893185G>A | CA350592168 | WNT10A | c.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 |
2 | g.218893185G>C | CA350592170 | WNT10A | c.1168G>C (p.Glu390Gln) c.1117G>C (p.Glu373Gln) c.1072G>C (p.Glu358Gln) c.788G>C (p.Arg263Pro) | |
2 | g.218893185G= | CA1328965550 | WNT10A | c.1168G= (p.Glu390=) c.1117G= (p.Glu373=) c.1072G= (p.Glu358=) c.788G= (p.Arg263=) | |
2 | g.218893185G>T | CA2114123 | WNT10A | c.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 |
2 | g.218893186A>C | CA350592173 | WNT10A | c.1169A>C (p.Glu390Ala) c.1118A>C (p.Glu373Ala) c.1073A>C (p.Glu358Ala) c.789A>C (p.Arg263=) | |
2 | g.218893186A>G | CA350592175 | WNT10A | c.1169A>G (p.Glu390Gly) c.1118A>G (p.Glu373Gly) c.1073A>G (p.Glu358Gly) c.789A>G (p.Arg263=) | |
2 | g.218893186A>T | CA350592182 | WNT10A | c.1169A>T (p.Glu390Val) c.1118A>T (p.Glu373Val) c.1073A>T (p.Glu358Val) c.789A>T (p.Arg263=) | |
2 | g.218893187G>A | CA431234828 | WNT10A | c.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 |
2 | g.218893187G>C | CA350592184 | WNT10A | c.1170G>C (p.Glu390Asp) c.1119G>C (p.Glu373Asp) c.1074G>C (p.Glu358Asp) c.790G>C (p.Ala264Pro) | |
2 | g.218893187G= | CA1328965553 | WNT10A | c.1170G= (p.Glu390=) c.1119G= (p.Glu373=) c.1074G= (p.Glu358=) c.790G= (p.Ala264=) | |
2 | g.218893187G>T | CA350592202 | WNT10A | c.1170G>T (p.Glu390Asp) c.1119G>T (p.Glu373Asp) c.1074G>T (p.Glu358Asp) c.790G>T (p.Ala264Ser) | dbSNP gnomAD v4 |
2 | g.218893188C>A | CA350592206 | WNT10A | c.1171C>A (p.Arg391Ser) c.1120C>A (p.Arg374Ser) c.1075C>A (p.Arg359Ser) c.791C>A (p.Ala264Glu) | gnomAD v4 |
2 | g.218893188C>G | CA350592207 | WNT10A | c.1171C>G (p.Arg391Gly) c.1120C>G (p.Arg374Gly) c.1075C>G (p.Arg359Gly) c.791C>G (p.Ala264Gly) | gnomAD v4 |
2 | g.218893188C>T | CA350592208 | WNT10A | c.1171C>T (p.Arg391Cys) c.1120C>T (p.Arg374Cys) c.1075C>T (p.Arg359Cys) c.791C>T (p.Ala264Val) | gnomAD v4 |
2 | g.218893189G>A | CA350592215 | WNT10A | c.1172G>A (p.Arg391His) c.1121G>A (p.Arg374His) c.1076G>A (p.Arg359His) c.792G>A (p.Ala264=) | gnomAD v4 |
2 | g.218893189G>C | CA350592209 | WNT10A | c.1172G>C (p.Arg391Pro) c.1121G>C (p.Arg374Pro) c.1076G>C (p.Arg359Pro) c.792G>C (p.Ala264=) | |
2 | g.218893189G>T | CA350592211 | WNT10A | c.1172G>T (p.Arg391Leu) c.1121G>T (p.Arg374Leu) c.1076G>T (p.Arg359Leu) c.792G>T (p.Ala264=) | |
2 | g.218893190C>A | CA431234829 | WNT10A | c.1173C>A (p.Arg391=) c.1122C>A (p.Arg374=) c.1077C>A (p.Arg359=) c.793C>A (p.Leu265Met) | |
2 | g.218893190C= | CA1328965561 | WNT10A | c.1173C= (p.Arg391=) c.1122C= (p.Arg374=) c.1077C= (p.Arg359=) c.793C= (p.Leu265=) | |
2 | g.218893190C>G | CA431234830 | WNT10A | c.1173C>G (p.Arg391=) c.1122C>G (p.Arg374=) c.1077C>G (p.Arg359=) c.793C>G (p.Leu265Val) | |
2 | g.218893190C>T | CA431234831 | WNT10A | c.1173C>T (p.Arg391=) c.1122C>T (p.Arg374=) c.1077C>T (p.Arg359=) c.793C>T (p.Leu265=) | ClinVar dbSNP |
2 | g.218893191T>A | CA350592223 | WNT10A | c.1174T>A (p.Cys392Ser) c.1123T>A (p.Cys375Ser) c.1078T>A (p.Cys360Ser) c.794T>A (p.Leu265Gln) | |
2 | g.218893191T>C | CA350592227 | WNT10A | c.1174T>C (p.Cys392Arg) c.1123T>C (p.Cys375Arg) c.1078T>C (p.Cys360Arg) c.794T>C (p.Leu265Pro) | dbSNP gnomAD v4 |
2 | g.218893191T>G | CA350592233 | WNT10A | c.1174T>G (p.Cys392Gly) c.1123T>G (p.Cys375Gly) c.1078T>G (p.Cys360Gly) c.794T>G (p.Leu265Arg) | |
2 | g.218893191T= | CA1328965565 | WNT10A | c.1174T= (p.Cys392=) c.1123T= (p.Cys375=) c.1078T= (p.Cys360=) c.794T= (p.Leu265=) | |
2 | g.218893192G>A | CA350592236 | WNT10A | c.1175G>A (p.Cys392Tyr) c.1124G>A (p.Cys375Tyr) c.1079G>A (p.Cys360Tyr) c.795G>A (p.Leu265=) | gnomAD v4 |
2 | g.218893192G>C | CA350592238 | WNT10A | c.1175G>C (p.Cys392Ser) c.1124G>C (p.Cys375Ser) c.1079G>C (p.Cys360Ser) c.795G>C (p.Leu265=) | |
2 | g.218893192G= | CA1328965569 | WNT10A | c.1175G= (p.Cys392=) c.1124G= (p.Cys375=) c.1079G= (p.Cys360=) c.795G= (p.Leu265=) | |
2 | g.218893192G>T | CA350592243 | WNT10A | c.1175G>T (p.Cys392Phe) c.1124G>T (p.Cys375Phe) c.1079G>T (p.Cys360Phe) c.795G>T (p.Leu265=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893193C>A | CA350592246 | WNT10A | c.1176C>A (p.Cys392Ter) c.1125C>A (p.Cys375Ter) c.1080C>A (p.Cys360Ter) c.796C>A (p.Pro266Thr) | ClinVar dbSNP gnomAD v4 |
2 | g.218893193C= | CA1328965574 | WNT10A | c.1176C= (p.Cys392=) c.1125C= (p.Cys375=) c.1080C= (p.Cys360=) c.796C= (p.Pro266=) | |
2 | g.218893193C>G | CA350592248 | WNT10A | c.1176C>G (p.Cys392Trp) c.1125C>G (p.Cys375Trp) c.1080C>G (p.Cys360Trp) c.796C>G (p.Pro266Ala) | |
2 | g.218893193C>T | CA431234832 | WNT10A | c.1176C>T (p.Cys392=) c.1125C>T (p.Cys375=) c.1080C>T (p.Cys360=) c.796C>T (p.Pro266Ser) | gnomAD v4 |
2 | g.218893199_218893210dup | CA2577276401 | WNT10A | c.1182_1193dup (p.His397_Trp398insCysArgPheHis) c.1131_1142dup (p.His380_Trp381insCysArgPheHis) c.1086_1097dup (p.His365_Trp366insCysArgPheHis) c.802_813dup (p.Leu271_Val272insProLeuProLeu) | |
2 | g.218893194C>A | CA350592251 | WNT10A | c.1177C>A (p.His393Asn) c.1126C>A (p.His376Asn) c.1081C>A (p.His361Asn) c.797C>A (p.Pro266Gln) | gnomAD v4 |
2 | g.218893194C>G | CA350592254 | WNT10A | c.1177C>G (p.His393Asp) c.1126C>G (p.His376Asp) c.1081C>G (p.His361Asp) c.797C>G (p.Pro266Arg) | |
2 | g.218893194C>T | CA350592257 | WNT10A | c.1177C>T (p.His393Tyr) c.1126C>T (p.His376Tyr) c.1081C>T (p.His361Tyr) c.797C>T (p.Pro266Leu) | gnomAD v4 |
2 | g.218893195A= | CA1328965581 | WNT10A | c.1178A= (p.His393=) c.1127A= (p.His376=) c.1082A= (p.His361=) c.798A= (p.Pro266=) | |
2 | g.218893195A>C | CA350592262 | WNT10A | c.1178A>C (p.His393Pro) c.1127A>C (p.His376Pro) c.1082A>C (p.His361Pro) c.798A>C (p.Pro266=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893195A>G | CA350592266 | WNT10A | c.1178A>G (p.His393Arg) c.1127A>G (p.His376Arg) c.1082A>G (p.His361Arg) c.798A>G (p.Pro266=) | gnomAD v4 |
2 | g.218893195A>T | CA350592261 | WNT10A | c.1178A>T (p.His393Leu) c.1127A>T (p.His376Leu) c.1082A>T (p.His361Leu) c.798A>T (p.Pro266=) | |
2 | g.218893196C>A | CA350592272 | WNT10A | c.1179C>A (p.His393Gln) c.1128C>A (p.His376Gln) c.1083C>A (p.His361Gln) c.799C>A (p.Leu267Met) | gnomAD v4 |
2 | g.218893196C>G | CA350592280 | WNT10A | c.1179C>G (p.His393Gln) c.1128C>G (p.His376Gln) c.1083C>G (p.His361Gln) c.799C>G (p.Leu267Val) | |
2 | g.218893196C>T | CA431234833 | WNT10A | c.1179C>T (p.His393=) c.1128C>T (p.His376=) c.1083C>T (p.His361=) c.799C>T (p.Leu267=) | ClinVar gnomAD v4 |
2 | g.218893197T>A | CA350592284 | WNT10A | c.1180T>A (p.Cys394Ser) c.1129T>A (p.Cys377Ser) c.1084T>A (p.Cys362Ser) c.800T>A (p.Leu267Gln) | |
2 | g.218893197T>C | CA350592290 | WNT10A | c.1180T>C (p.Cys394Arg) c.1129T>C (p.Cys377Arg) c.1084T>C (p.Cys362Arg) c.800T>C (p.Leu267Pro) | dbSNP gnomAD v4 |
2 | g.218893197T>G | CA350592292 | WNT10A | c.1180T>G (p.Cys394Gly) c.1129T>G (p.Cys377Gly) c.1084T>G (p.Cys362Gly) c.800T>G (p.Leu267Arg) | |
2 | g.218893197T= | CA1328965583 | WNT10A | c.1180T= (p.Cys394=) c.1129T= (p.Cys377=) c.1084T= (p.Cys362=) c.800T= (p.Leu267=) | |
2 | g.218893198G>A | CA350592314 | WNT10A | c.1181G>A (p.Cys394Tyr) c.1130G>A (p.Cys377Tyr) c.1085G>A (p.Cys362Tyr) c.801G>A (p.Leu267=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893198G>C | CA350592295 | WNT10A | c.1181G>C (p.Cys394Ser) c.1130G>C (p.Cys377Ser) c.1085G>C (p.Cys362Ser) c.801G>C (p.Leu267=) | |
2 | g.218893198G= | CA1328965584 | WNT10A | c.1181G= (p.Cys394=) c.1130G= (p.Cys377=) c.1085G= (p.Cys362=) c.801G= (p.Leu267=) | |
2 | g.218893198G>T | CA350592312 | WNT10A | c.1181G>T (p.Cys394Phe) c.1130G>T (p.Cys377Phe) c.1085G>T (p.Cys362Phe) c.801G>T (p.Leu267=) | gnomAD v4 |
2 | g.218893199C>A | CA350592316 | WNT10A | c.1182C>A (p.Cys394Ter) c.1131C>A (p.Cys377Ter) c.1086C>A (p.Cys362Ter) c.802C>A (p.Pro268Thr) | gnomAD v4 |
2 | g.218893199C>G | CA350592318 | WNT10A | c.1182C>G (p.Cys394Trp) c.1131C>G (p.Cys377Trp) c.1086C>G (p.Cys362Trp) c.802C>G (p.Pro268Ala) | |
2 | g.218893199C>T | CA431234834 | WNT10A | c.1182C>T (p.Cys394=) c.1131C>T (p.Cys377=) c.1086C>T (p.Cys362=) c.802C>T (p.Pro268Ser) | gnomAD v4 |
2 | g.218893200del | CA2663174555 | WNT10A | c.1183del (p.Arg395AlafsTer?) c.1132del (p.Arg378AlafsTer?) c.1087del (p.Arg363AlafsTer?) c.803del (p.Pro268ArgfsTer24) | gnomAD v4 |
2 | g.218893201_218893206del | CA2663174556 | WNT10A | c.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 |
2 | g.218893200C>A | CA350592319 | WNT10A | c.1183C>A (p.Arg395Ser) c.1132C>A (p.Arg378Ser) c.1087C>A (p.Arg363Ser) c.803C>A (p.Pro268Gln) | gnomAD v4 |
2 | g.218893200C= | CA1328965587 | WNT10A | c.1183C= (p.Arg395=) c.1132C= (p.Arg378=) c.1087C= (p.Arg363=) c.803C= (p.Pro268=) | |
2 | g.218893200C>G | CA350592322 | WNT10A | c.1183C>G (p.Arg395Gly) c.1132C>G (p.Arg378Gly) c.1087C>G (p.Arg363Gly) c.803C>G (p.Pro268Arg) | |
2 | g.218893200C>T | CA2114124 | WNT10A | c.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 |
2 | g.218893201G>A | CA2114125 | WNT10A | c.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 |
2 | g.218893201G>C | CA350592331 | WNT10A | c.1184G>C (p.Arg395Pro) c.1133G>C (p.Arg378Pro) c.1088G>C (p.Arg363Pro) c.804G>C (p.Pro268=) | |
2 | g.218893201G= | CA1328965593 | WNT10A | c.1184G= (p.Arg395=) c.1133G= (p.Arg378=) c.1088G= (p.Arg363=) c.804G= (p.Pro268=) | |
2 | g.218893201G>T | CA65919428 | WNT10A | c.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 |
2 | g.218893202C>A | CA431234835 | WNT10A | c.1185C>A (p.Arg395=) c.1134C>A (p.Arg378=) c.1089C>A (p.Arg363=) c.805C>A (p.Leu269Ile) | gnomAD v4 |
2 | g.218893202C= | CA1328965595 | WNT10A | c.1185C= (p.Arg395=) c.1134C= (p.Arg378=) c.1089C= (p.Arg363=) c.805C= (p.Leu269=) | |
2 | g.218893202C>G | CA431234836 | WNT10A | c.1185C>G (p.Arg395=) c.1134C>G (p.Arg378=) c.1089C>G (p.Arg363=) c.805C>G (p.Leu269Val) | gnomAD v4 |
2 | g.218893202C>T | CA2114126 | WNT10A | c.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 |
2 | g.218893203T>A | CA350592339 | WNT10A | c.1186T>A (p.Phe396Ile) c.1135T>A (p.Phe379Ile) c.1090T>A (p.Phe364Ile) c.806T>A (p.Leu269His) | |
2 | g.218893203T>C | CA350592346 | WNT10A | c.1186T>C (p.Phe396Leu) c.1135T>C (p.Phe379Leu) c.1090T>C (p.Phe364Leu) c.806T>C (p.Leu269Pro) | gnomAD v4 |
2 | g.218893203T>G | CA350592359 | WNT10A | c.1186T>G (p.Phe396Val) c.1135T>G (p.Phe379Val) c.1090T>G (p.Phe364Val) c.806T>G (p.Leu269Arg) | gnomAD v4 |
2 | g.218893204T>A | CA350592381 | WNT10A | c.1187T>A (p.Phe396Tyr) c.1136T>A (p.Phe379Tyr) c.1091T>A (p.Phe364Tyr) c.807T>A (p.Leu269=) | |
2 | g.218893204T>C | CA350592382 | WNT10A | c.1187T>C (p.Phe396Ser) c.1136T>C (p.Phe379Ser) c.1091T>C (p.Phe364Ser) c.807T>C (p.Leu269=) | |
2 | g.218893204T>G | CA350592383 | WNT10A | c.1187T>G (p.Phe396Cys) c.1136T>G (p.Phe379Cys) c.1091T>G (p.Phe364Cys) c.807T>G (p.Leu269=) | |
2 | g.218893205C>A | CA350592384 | WNT10A | c.1188C>A (p.Phe396Leu) c.1137C>A (p.Phe379Leu) c.1092C>A (p.Phe364Leu) c.808C>A (p.Pro270Thr) | gnomAD v4 |
2 | g.218893205C= | CA1328965598 | WNT10A | c.1188C= (p.Phe396=) c.1137C= (p.Phe379=) c.1092C= (p.Phe364=) c.808C= (p.Pro270=) | |
2 | g.218893205C>G | CA350592386 | WNT10A | c.1188C>G (p.Phe396Leu) c.1137C>G (p.Phe379Leu) c.1092C>G (p.Phe364Leu) c.808C>G (p.Pro270Ala) | dbSNP gnomAD v4 |
2 | g.218893205C>T | CA431234837 | WNT10A | c.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 |
2 | g.218893206C>A | CA350592389 | WNT10A | c.1189C>A (p.His397Asn) c.1138C>A (p.His380Asn) c.1093C>A (p.His365Asn) c.809C>A (p.Pro270Gln) | gnomAD v4 |
2 | g.218893206C>G | CA350592393 | WNT10A | c.1189C>G (p.His397Asp) c.1138C>G (p.His380Asp) c.1093C>G (p.His365Asp) c.809C>G (p.Pro270Arg) | |
2 | g.218893206C>T | CA350592394 | WNT10A | c.1189C>T (p.His397Tyr) c.1138C>T (p.His380Tyr) c.1093C>T (p.His365Tyr) c.809C>T (p.Pro270Leu) | |
2 | g.218893206_218893207insGAA | CA2754311150 | WNT10A | c.1189_1190insGAA (p.His397delinsArgAsn) c.1138_1139insGAA (p.His380delinsArgAsn) c.1093_1094insGAA (p.His365delinsArgAsn) c.809_810insGAA (p.Pro270_Leu271insLys) | |
2 | g.218893207A>C | CA350592396 | WNT10A | c.1190A>C (p.His397Pro) c.1139A>C (p.His380Pro) c.1094A>C (p.His365Pro) c.810A>C (p.Pro270=) | |
2 | g.218893207A>G | CA350592398 | WNT10A | c.1190A>G (p.His397Arg) c.1139A>G (p.His380Arg) c.1094A>G (p.His365Arg) c.810A>G (p.Pro270=) | |
2 | g.218893207A>T | CA350592395 | WNT10A | c.1190A>T (p.His397Leu) c.1139A>T (p.His380Leu) c.1094A>T (p.His365Leu) c.810A>T (p.Pro270=) | |
2 | g.218893208C>A | CA350592415 | WNT10A | c.1191C>A (p.His397Gln) c.1140C>A (p.His380Gln) c.1095C>A (p.His365Gln) c.811C>A (p.Leu271Met) | gnomAD v4 |
2 | g.218893208C= | CA1328965600 | WNT10A | c.1191C= (p.His397=) c.1140C= (p.His380=) c.1095C= (p.His365=) c.811C= (p.Leu271=) | |
2 | g.218893208C>G | CA350592405 | WNT10A | c.1191C>G (p.His397Gln) c.1140C>G (p.His380Gln) c.1095C>G (p.His365Gln) c.811C>G (p.Leu271Val) | |
2 | g.218893208C>T | CA431234838 | WNT10A | c.1191C>T (p.His397=) c.1140C>T (p.His380=) c.1095C>T (p.His365=) c.811C>T (p.Leu271=) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893209T>A | CA350592446 | WNT10A | c.1192T>A (p.Trp398Arg) c.1141T>A (p.Trp381Arg) c.1096T>A (p.Trp366Arg) c.812T>A (p.Leu271Gln) | gnomAD v4 |
2 | g.218893209T>C | CA350592428 | WNT10A | c.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 |
2 | g.218893209T>G | CA350592443 | WNT10A | c.1192T>G (p.Trp398Gly) c.1141T>G (p.Trp381Gly) c.1096T>G (p.Trp366Gly) c.812T>G (p.Leu271Arg) | gnomAD v4 |
2 | g.218893209T= | CA1328965604 | WNT10A | c.1192T= (p.Trp398=) c.1141T= (p.Trp381=) c.1096T= (p.Trp366=) c.812T= (p.Leu271=) | |
2 | g.218893210G>A | CA350592453 | WNT10A | c.1193G>A (p.Trp398Ter) c.1142G>A (p.Trp381Ter) c.1097G>A (p.Trp366Ter) c.813G>A (p.Leu271=) | gnomAD v4 |
2 | g.218893210G>C | CA350592459 | WNT10A | c.1193G>C (p.Trp398Ser) c.1142G>C (p.Trp381Ser) c.1097G>C (p.Trp366Ser) c.813G>C (p.Leu271=) | |
2 | g.218893210G>T | CA350592462 | WNT10A | c.1193G>T (p.Trp398Leu) c.1142G>T (p.Trp381Leu) c.1097G>T (p.Trp366Leu) c.813G>T (p.Leu271=) | gnomAD v4 |
2 | g.218893211G>A | CA350592463 | WNT10A | c.1194G>A (p.Trp398Ter) c.1143G>A (p.Trp381Ter) c.1098G>A (p.Trp366Ter) c.814G>A (p.Val272Met) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893211G>C | CA350592464 | WNT10A | c.1194G>C (p.Trp398Cys) c.1143G>C (p.Trp381Cys) c.1098G>C (p.Trp366Cys) c.814G>C (p.Val272Leu) | |
2 | g.218893211G= | CA1328965609 | WNT10A | c.1194G= (p.Trp398=) c.1143G= (p.Trp381=) c.1098G= (p.Trp366=) c.814G= (p.Val272=) | |
2 | g.218893211G>T | CA350592466 | WNT10A | c.1194G>T (p.Trp398Cys) c.1143G>T (p.Trp381Cys) c.1098G>T (p.Trp366Cys) c.814G>T (p.Val272Leu) | gnomAD v4 |
2 | g.218893212T>A | CA350592468 | WNT10A | c.1195T>A (p.Cys399Ser) c.1144T>A (p.Cys382Ser) c.1099T>A (p.Cys367Ser) c.815T>A (p.Val272Glu) | |
2 | g.218893212T>C | CA350592476 | WNT10A | c.1195T>C (p.Cys399Arg) c.1144T>C (p.Cys382Arg) c.1099T>C (p.Cys367Arg) c.815T>C (p.Val272Ala) | |
2 | g.218893212T>G | CA350592479 | WNT10A | c.1195T>G (p.Cys399Gly) c.1144T>G (p.Cys382Gly) c.1099T>G (p.Cys367Gly) c.815T>G (p.Val272Gly) | |
2 | g.218893213G>A | CA350592486 | WNT10A | c.1196G>A (p.Cys399Tyr) c.1145G>A (p.Cys382Tyr) c.1100G>A (p.Cys367Tyr) c.816G>A (p.Val272=) | |
2 | g.218893213G>C | CA350592488 | WNT10A | c.1196G>C (p.Cys399Ser) c.1145G>C (p.Cys382Ser) c.1100G>C (p.Cys367Ser) c.816G>C (p.Val272=) | |
2 | g.218893213G>T | CA350592493 | WNT10A | c.1196G>T (p.Cys399Phe) c.1145G>T (p.Cys382Phe) c.1100G>T (p.Cys367Phe) c.816G>T (p.Val272=) | gnomAD v4 |
2 | g.218893214C>A | CA350592495 | WNT10A | c.1197C>A (p.Cys399Ter) c.1146C>A (p.Cys382Ter) c.1101C>A (p.Cys367Ter) c.817C>A (p.Leu273Met) | gnomAD v4 |
2 | g.218893214C>G | CA350592498 | WNT10A | c.1197C>G (p.Cys399Trp) c.1146C>G (p.Cys382Trp) c.1101C>G (p.Cys367Trp) c.817C>G (p.Leu273Val) | |
2 | g.218893214C>T | CA431234839 | WNT10A | c.1197C>T (p.Cys399=) c.1146C>T (p.Cys382=) c.1101C>T (p.Cys367=) c.817C>T (p.Leu273=) | ClinVar gnomAD v4 |
2 | g.218893215T>A | CA350592503 | WNT10A | c.1198T>A (p.Cys400Ser) c.1147T>A (p.Cys383Ser) c.1102T>A (p.Cys368Ser) c.818T>A (p.Leu273Gln) | |
2 | g.218893215T>C | CA350592507 | WNT10A | c.1198T>C (p.Cys400Arg) c.1147T>C (p.Cys383Arg) c.1102T>C (p.Cys368Arg) c.818T>C (p.Leu273Pro) | |
2 | g.218893215T>G | CA350592509 | WNT10A | c.1198T>G (p.Cys400Gly) c.1147T>G (p.Cys383Gly) c.1102T>G (p.Cys368Gly) c.818T>G (p.Leu273Arg) | |
2 | g.218893216G>A | CA350592511 | WNT10A | c.1199G>A (p.Cys400Tyr) c.1148G>A (p.Cys383Tyr) c.1103G>A (p.Cys368Tyr) c.819G>A (p.Leu273=) | ClinVar dbSNP gnomAD v4 |
2 | g.218893216G>C | CA350592514 | WNT10A | c.1199G>C (p.Cys400Ser) c.1148G>C (p.Cys383Ser) c.1103G>C (p.Cys368Ser) c.819G>C (p.Leu273=) | ClinVar dbSNP gnomAD v4 |
2 | g.218893216G= | CA1328965615 | WNT10A | c.1199G= (p.Cys400=) c.1148G= (p.Cys383=) c.1103G= (p.Cys368=) c.819G= (p.Leu273=) | |
2 | g.218893216G>T | CA350592515 | WNT10A | c.1199G>T (p.Cys400Phe) c.1148G>T (p.Cys383Phe) c.1103G>T (p.Cys368Phe) c.819G>T (p.Leu273=) | gnomAD v4 |
2 | g.218893217T>A | CA350592519 | WNT10A | c.1200T>A (p.Cys400Ter) c.1149T>A (p.Cys383Ter) c.1104T>A (p.Cys368Ter) c.820T>A (p.Phe274Ile) | |
2 | g.218893217T>C | CA431234840 | WNT10A | c.1200T>C (p.Cys400=) c.1149T>C (p.Cys383=) c.1104T>C (p.Cys368=) c.820T>C (p.Phe274Leu) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893217T>G | CA350592523 | WNT10A | c.1200T>G (p.Cys400Trp) c.1149T>G (p.Cys383Trp) c.1104T>G (p.Cys368Trp) c.820T>G (p.Phe274Val) | |
2 | g.218893217T= | CA1328965621 | WNT10A | c.1200T= (p.Cys400=) c.1149T= (p.Cys383=) c.1104T= (p.Cys368=) c.820T= (p.Phe274=) | |
2 | g.218893218T>A | CA350592528 | WNT10A | c.1201T>A (p.Phe401Ile) c.1150T>A (p.Phe384Ile) c.1105T>A (p.Phe369Ile) c.821T>A (p.Phe274Tyr) | gnomAD v4 |
2 | g.218893218T>C | CA350592529 | WNT10A | c.1201T>C (p.Phe401Leu) c.1150T>C (p.Phe384Leu) c.1105T>C (p.Phe369Leu) c.821T>C (p.Phe274Ser) | gnomAD v4 |
2 | g.218893218T>G | CA350592530 | WNT10A | c.1201T>G (p.Phe401Val) c.1150T>G (p.Phe384Val) c.1105T>G (p.Phe369Val) c.821T>G (p.Phe274Cys) | |
2 | g.218893219T>A | CA350592535 | WNT10A | c.1202T>A (p.Phe401Tyr) c.1151T>A (p.Phe384Tyr) c.1106T>A (p.Phe369Tyr) c.822T>A (p.Phe274Leu) | |
2 | g.218893219T>C | CA350592533 | WNT10A | c.1202T>C (p.Phe401Ser) c.1151T>C (p.Phe384Ser) c.1106T>C (p.Phe369Ser) c.822T>C (p.Phe274=) | gnomAD v4 |
2 | g.218893219T>G | CA350592531 | WNT10A | c.1202T>G (p.Phe401Cys) c.1151T>G (p.Phe384Cys) c.1106T>G (p.Phe369Cys) c.822T>G (p.Phe274Leu) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218893219T= | CA1328965624 | WNT10A | c.1202T= (p.Phe401=) c.1151T= (p.Phe384=) c.1106T= (p.Phe369=) c.822T= (p.Phe274=) | |
2 | g.218893220C>A | CA350592537 | WNT10A | c.1203C>A (p.Phe401Leu) c.1152C>A (p.Phe384Leu) c.1107C>A (p.Phe369Leu) c.823C>A (p.Arg275Ser) | gnomAD v4 |
2 | g.218893220C= | CA1328965626 | WNT10A | c.1203C= (p.Phe401=) c.1152C= (p.Phe384=) c.1107C= (p.Phe369=) c.823C= (p.Arg275=) | |
2 | g.218893220C>G | CA350592539 | WNT10A | c.1203C>G (p.Phe401Leu) c.1152C>G (p.Phe384Leu) c.1107C>G (p.Phe369Leu) c.823C>G (p.Arg275Gly) | gnomAD v4 |
2 | g.218893220C>T | CA431234841 | WNT10A | c.1203C>T (p.Phe401=) c.1152C>T (p.Phe384=) c.1107C>T (p.Phe369=) c.823C>T (p.Arg275Cys) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893221G>A | CA350592543 | WNT10A | c.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 |
2 | g.218893221G>C | CA350592545 | WNT10A | c.1204G>C (p.Val402Leu) n.1G>C c.1153G>C (p.Val385Leu) c.1108G>C (p.Val370Leu) c.824G>C (p.Arg275Pro) | |
2 | g.218893221G>T | CA350592548 | WNT10A | c.1204G>T (p.Val402Leu) n.1G>T c.1153G>T (p.Val385Leu) c.1108G>T (p.Val370Leu) c.824G>T (p.Arg275Leu) | |
2 | g.218893222T>A | CA350592553 | WNT10A | c.1205T>A (p.Val402Glu) n.2T>A c.1154T>A (p.Val385Glu) c.1109T>A (p.Val370Glu) c.825T>A (p.Arg275=) | |
2 | g.218893222T>C | CA350592551 | WNT10A | c.1205T>C (p.Val402Ala) n.2T>C c.1154T>C (p.Val385Ala) c.1109T>C (p.Val370Ala) c.825T>C (p.Arg275=) | gnomAD v4 |
2 | g.218893222T>G | CA350592550 | WNT10A | c.1205T>G (p.Val402Gly) n.2T>G c.1154T>G (p.Val385Gly) c.1109T>G (p.Val370Gly) c.825T>G (p.Arg275=) | |
2 | g.218893223G>A | CA431234842 | WNT10A | c.1206G>A (p.Val402=) n.3G>A c.1155G>A (p.Val385=) c.1110G>A (p.Val370=) c.826G>A (p.Gly276Ser) | gnomAD v4 |
2 | g.218893223G>C | CA431234843 | WNT10A | c.1206G>C (p.Val402=) n.3G>C c.1155G>C (p.Val385=) c.1110G>C (p.Val370=) c.826G>C (p.Gly276Arg) | ClinVar |
2 | g.218893223G>T | CA431234844 | WNT10A | c.1206G>T (p.Val402=) n.3G>T c.1155G>T (p.Val385=) c.1110G>T (p.Val370=) c.826G>T (p.Gly276Cys) | gnomAD v4 |
2 | g.218893224G>A | CA350592556 | WNT10A | c.1207G>A (p.Val403Ile) n.4G>A c.1156G>A (p.Val386Ile) c.1111G>A (p.Val371Ile) c.827G>A (p.Gly276Asp) | |
2 | g.218893224G>C | CA350592560 | WNT10A | c.1207G>C (p.Val403Leu) n.4G>C c.1156G>C (p.Val386Leu) c.1111G>C (p.Val371Leu) c.827G>C (p.Gly276Ala) | |
2 | g.218893224G>T | CA350592563 | WNT10A | c.1207G>T (p.Val403Phe) n.4G>T c.1156G>T (p.Val386Phe) c.1111G>T (p.Val371Phe) c.827G>T (p.Gly276Val) | gnomAD v4 |
2 | g.218893225T>A | CA350592571 | WNT10A | c.1208T>A (p.Val403Asp) n.5T>A c.1157T>A (p.Val386Asp) c.1112T>A (p.Val371Asp) c.828T>A (p.Gly276=) | |
2 | g.218893225T>C | CA350592574 | WNT10A | c.1208T>C (p.Val403Ala) n.5T>C c.1157T>C (p.Val386Ala) c.1112T>C (p.Val371Ala) c.828T>C (p.Gly276=) | |
2 | g.218893225T>G | CA350592580 | WNT10A | c.1208T>G (p.Val403Gly) n.5T>G c.1157T>G (p.Val386Gly) c.1112T>G (p.Val371Gly) c.828T>G (p.Gly276=) | |
2 | g.218893226C>A | CA431234845 | WNT10A | c.1209C>A (p.Val403=) n.6C>A c.1158C>A (p.Val386=) c.1113C>A (p.Val371=) c.829C>A (p.Leu277Met) | gnomAD v4 |
2 | g.218893226C>G | CA431234846 | WNT10A | c.1209C>G (p.Val403=) n.6C>G c.1158C>G (p.Val386=) c.1113C>G (p.Val371=) c.829C>G (p.Leu277Val) | |
2 | g.218893226C>T | CA431234847 | WNT10A | c.1209C>T (p.Val403=) n.6C>T c.1158C>T (p.Val386=) c.1113C>T (p.Val371=) c.829C>T (p.Leu277=) | gnomAD v4 |
2 | g.218893227T>A | CA2114127 | WNT10A | c.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 |
2 | g.218893227T>C | CA350592601 | WNT10A | c.1210T>C (p.Cys404Arg) n.7T>C c.1159T>C (p.Cys387Arg) c.1114T>C (p.Cys372Arg) c.830T>C (p.Leu277Pro) | |
2 | g.218893227T>G | CA350592599 | WNT10A | c.1210T>G (p.Cys404Gly) n.7T>G c.1159T>G (p.Cys387Gly) c.1114T>G (p.Cys372Gly) c.830T>G (p.Leu277Arg) | |
2 | g.218893227T= | CA1328965630 | WNT10A | c.1210T= (p.Cys404=) n.7T= c.1159T= (p.Cys387=) c.1114T= (p.Cys372=) c.830T= (p.Leu277=) | |
2 | g.218893228G>A | CA350592606 | WNT10A | c.1211G>A (p.Cys404Tyr) n.8G>A c.1160G>A (p.Cys387Tyr) c.1115G>A (p.Cys372Tyr) c.831G>A (p.Leu277=) | gnomAD v4 |
2 | g.218893228G>C | CA350592610 | WNT10A | c.1211G>C (p.Cys404Ser) n.8G>C c.1160G>C (p.Cys387Ser) c.1115G>C (p.Cys372Ser) c.831G>C (p.Leu277=) | |
2 | g.218893228G>T | CA350592618 | WNT10A | c.1211G>T (p.Cys404Phe) n.8G>T c.1160G>T (p.Cys387Phe) c.1115G>T (p.Cys372Phe) c.831G>T (p.Leu277=) | gnomAD v4 |
2 | g.218893229C>A | CA350592621 | WNT10A | c.1212C>A (p.Cys404Ter) n.9C>A c.1161C>A (p.Cys387Ter) c.1116C>A (p.Cys372Ter) c.832C>A (p.Arg278=) | gnomAD v4 |
2 | g.218893229C= | CA1328965633 | WNT10A | c.1212C= (p.Cys404=) n.9C= c.1161C= (p.Cys387=) c.1116C= (p.Cys372=) c.832C= (p.Arg278=) | |
2 | g.218893229C>G | CA350592627 | WNT10A | c.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 |
2 | g.218893229C>T | CA431234848 | WNT10A | c.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 |
2 | g.218893230G>A | CA350592631 | WNT10A | c.1213G>A (p.Glu405Lys) n.10G>A c.1162G>A (p.Glu388Lys) c.1117G>A (p.Glu373Lys) c.833G>A (p.Arg278Gln) | gnomAD v4 |
2 | g.218893230G>C | CA350592633 | WNT10A | c.1213G>C (p.Glu405Gln) n.10G>C c.1162G>C (p.Glu388Gln) c.1117G>C (p.Glu373Gln) c.833G>C (p.Arg278Pro) | |
2 | g.218893230G>T | CA350592635 | WNT10A | c.1213G>T (p.Glu405Ter) n.10G>T c.1162G>T (p.Glu388Ter) c.1117G>T (p.Glu373Ter) c.833G>T (p.Arg278Leu) | gnomAD v4 |
2 | g.218893231A>C | CA350592638 | WNT10A | c.1214A>C (p.Glu405Ala) n.11A>C c.1163A>C (p.Glu388Ala) c.1118A>C (p.Glu373Ala) c.834A>C (p.Arg278=) | |
2 | g.218893231A>G | CA350592639 | WNT10A | c.1214A>G (p.Glu405Gly) n.11A>G c.1163A>G (p.Glu388Gly) c.1118A>G (p.Glu373Gly) c.834A>G (p.Arg278=) | gnomAD v4 |
2 | g.218893231A>T | CA350592646 | WNT10A | c.1214A>T (p.Glu405Val) n.11A>T c.1163A>T (p.Glu388Val) c.1118A>T (p.Glu373Val) c.834A>T (p.Arg278=) | |
2 | g.218893232A>C | CA350592657 | WNT10A | c.1215A>C (p.Glu405Asp) n.12A>C c.1164A>C (p.Glu388Asp) c.1119A>C (p.Glu373Asp) c.835A>C (p.Arg279=) | |
2 | g.218893232A>G | CA431234849 | WNT10A | c.1215A>G (p.Glu405=) n.12A>G c.1164A>G (p.Glu388=) c.1119A>G (p.Glu373=) c.835A>G (p.Arg279Gly) | gnomAD v4 |
2 | g.218893232A>T | CA350592650 | WNT10A | c.1215A>T (p.Glu405Asp) n.12A>T c.1164A>T (p.Glu388Asp) c.1119A>T (p.Glu373Asp) c.835A>T (p.Arg279Ter) | |
2 | g.218893233G>A | CA350592660 | WNT10A | c.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 |
2 | g.218893233G>C | CA350592663 | WNT10A | c.1216G>C (p.Glu406Gln) n.13G>C c.1165G>C (p.Glu389Gln) c.1120G>C (p.Glu374Gln) c.836G>C (p.Arg279Thr) | |
2 | g.218893233G= | CA1328965638 | WNT10A | c.1216G= (p.Glu406=) n.13G= c.1165G= (p.Glu389=) c.1120G= (p.Glu374=) c.836G= (p.Arg279=) | |
2 | g.218893233G>T | CA350592662 | WNT10A | c.1216G>T (p.Glu406Ter) n.13G>T c.1165G>T (p.Glu389Ter) c.1120G>T (p.Glu374Ter) c.836G>T (p.Arg279Ile) | gnomAD v4 |
2 | g.218893234A>C | CA350592666 | WNT10A | c.1217A>C (p.Glu406Ala) n.14A>C c.1166A>C (p.Glu389Ala) c.1121A>C (p.Glu374Ala) c.837A>C (p.Arg279Ser) | |
2 | g.218893234A>G | CA350592670 | WNT10A | c.1217A>G (p.Glu406Gly) n.14A>G c.1166A>G (p.Glu389Gly) c.1121A>G (p.Glu374Gly) c.837A>G (p.Arg279=) | |
2 | g.218893234A>T | CA350592672 | WNT10A | c.1217A>T (p.Glu406Val) n.14A>T c.1166A>T (p.Glu389Val) c.1121A>T (p.Glu374Val) c.837A>T (p.Arg279Ser) | |
2 | g.218893235G>A | CA431234850 | WNT10A | c.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 |
2 | g.218893235G>C | CA350592674 | WNT10A | c.1218G>C (p.Glu406Asp) n.15G>C c.1167G>C (p.Glu389Asp) c.1122G>C (p.Glu374Asp) c.838G>C (p.Val280Leu) | gnomAD v4 |
2 | g.218893235G= | CA1328965640 | WNT10A | c.1218G= (p.Glu406=) n.15G= c.1167G= (p.Glu389=) c.1122G= (p.Glu374=) c.838G= (p.Val280=) | |
2 | g.218893235G>T | CA350592676 | WNT10A | c.1218G>T (p.Glu406Asp) n.15G>T c.1167G>T (p.Glu389Asp) c.1122G>T (p.Glu374Asp) c.838G>T (p.Val280Leu) | gnomAD v4 |
2 | g.218893236T>A | CA350592680 | WNT10A | c.1219T>A (p.Cys407Ser) n.16T>A c.1168T>A (p.Cys390Ser) c.1123T>A (p.Cys375Ser) c.839T>A (p.Val280Glu) | |
2 | g.218893236T>C | CA350592694 | WNT10A | c.1219T>C (p.Cys407Arg) n.16T>C c.1168T>C (p.Cys390Arg) c.1123T>C (p.Cys375Arg) c.839T>C (p.Val280Ala) | |
2 | g.218893236T>G | CA350592696 | WNT10A | c.1219T>G (p.Cys407Gly) n.16T>G c.1168T>G (p.Cys390Gly) c.1123T>G (p.Cys375Gly) c.839T>G (p.Val280Gly) | |
2 | g.218893237G>A | CA350592699 | WNT10A | c.1220G>A (p.Cys407Tyr) n.17G>A c.1169G>A (p.Cys390Tyr) c.1124G>A (p.Cys375Tyr) c.840G>A (p.Val280=) | gnomAD v4 |
2 | g.218893237G>C | CA350592707 | WNT10A | c.1220G>C (p.Cys407Ser) n.17G>C c.1169G>C (p.Cys390Ser) c.1124G>C (p.Cys375Ser) c.840G>C (p.Val280=) | |
2 | g.218893237G>T | CA350592708 | WNT10A | c.1220G>T (p.Cys407Phe) n.17G>T c.1169G>T (p.Cys390Phe) c.1124G>T (p.Cys375Phe) c.840G>T (p.Val280=) | gnomAD v4 |
2 | g.218893238C>A | CA350592711 | WNT10A | c.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 |
2 | g.218893238C= | CA1328965642 | WNT10A | c.1221C= (p.Cys407=) n.18C= c.1170C= (p.Cys390=) c.1125C= (p.Cys375=) c.841C= (p.Pro281=) | |
2 | g.218893238C>G | CA350592715 | WNT10A | c.1221C>G (p.Cys407Trp) n.18C>G c.1170C>G (p.Cys390Trp) c.1125C>G (p.Cys375Trp) c.841C>G (p.Pro281Ala) | |
2 | g.218893238C>T | CA431234851 | WNT10A | c.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 |
2 | g.218893239C>A | CA350592718 | WNT10A | c.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 |
2 | g.218893239C= | CA1328965644 | WNT10A | c.1222C= (p.Arg408=) n.19C= c.1171C= (p.Arg391=) c.1126C= (p.Arg376=) c.842C= (p.Pro281=) | |
2 | g.218893239C>G | CA350592723 | WNT10A | c.1222C>G (p.Arg408Gly) n.19C>G c.1171C>G (p.Arg391Gly) c.1126C>G (p.Arg376Gly) c.842C>G (p.Pro281Arg) | |
2 | g.218893239C>T | CA350592721 | WNT10A | c.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 |
2 | g.218893240G>A | CA65919439 | WNT10A | c.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 |
2 | g.218893240G>C | CA350592728 | WNT10A | c.1223G>C (p.Arg408Pro) n.20G>C c.1172G>C (p.Arg391Pro) c.1127G>C (p.Arg376Pro) c.843G>C (p.Pro281=) | gnomAD v4 |
2 | g.218893240G= | CA1328965646 | WNT10A | c.1223G= (p.Arg408=) n.20G= c.1172G= (p.Arg391=) c.1127G= (p.Arg376=) c.843G= (p.Pro281=) | |
2 | g.218893240G>T | CA350592730 | WNT10A | c.1223G>T (p.Arg408Leu) n.20G>T c.1172G>T (p.Arg391Leu) c.1127G>T (p.Arg376Leu) c.843G>T (p.Pro281=) | gnomAD v4 |
2 | g.218893241C>A | CA431234852 | WNT10A | c.1224C>A (p.Arg408=) n.21C>A c.1173C>A (p.Arg391=) c.1128C>A (p.Arg376=) c.844C>A (p.His282Asn) | gnomAD v4 |
2 | g.218893241C>G | CA431234853 | WNT10A | c.1224C>G (p.Arg408=) n.21C>G c.1173C>G (p.Arg391=) c.1128C>G (p.Arg376=) c.844C>G (p.His282Asp) | |
2 | g.218893241C>T | CA431234854 | WNT10A | c.1224C>T (p.Arg408=) n.21C>T c.1173C>T (p.Arg391=) c.1128C>T (p.Arg376=) c.844C>T (p.His282Tyr) | |
2 | g.218893242A>C | CA350592731 | WNT10A | c.1225A>C (p.Ile409Leu) n.22A>C c.1174A>C (p.Ile392Leu) c.1129A>C (p.Ile377Leu) c.845A>C (p.His282Pro) | |
2 | g.218893242A>G | CA350592732 | WNT10A | c.1225A>G (p.Ile409Val) n.22A>G c.1174A>G (p.Ile392Val) c.1129A>G (p.Ile377Val) c.845A>G (p.His282Arg) | |
2 | g.218893242A>T | CA350592734 | WNT10A | c.1225A>T (p.Ile409Phe) n.22A>T c.1174A>T (p.Ile392Phe) c.1129A>T (p.Ile377Phe) c.845A>T (p.His282Leu) | gnomAD v4 |
2 | g.218893242_218893247delinsATCACC | CA1328965648 | WNT10A | c.1225_1230delinsATCACC (p.Ile409=) n.22_27delinsATCACC c.1174_1179delinsATCACC (p.Ile392=) c.1129_1134delinsATCACC (p.Ile377=) c.845_850delinsATCACC (p.His282=) | |
2 | g.218893243T>A | CA350592736 | WNT10A | c.1226T>A (p.Ile409Asn) n.23T>A c.1175T>A (p.Ile392Asn) c.1130T>A (p.Ile377Asn) c.846T>A (p.His282Gln) | gnomAD v4 |
2 | g.218893243T>C | CA350592742 | WNT10A | c.1226T>C (p.Ile409Thr) n.23T>C c.1175T>C (p.Ile392Thr) c.1130T>C (p.Ile377Thr) c.846T>C (p.His282=) | gnomAD v4 |
2 | g.218893243T>G | CA350592744 | WNT10A | c.1226T>G (p.Ile409Ser) n.23T>G c.1175T>G (p.Ile392Ser) c.1130T>G (p.Ile377Ser) c.846T>G (p.His282Gln) | |
2 | g.218893243_218893247del | CA1328965650 | WNT10A | c.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 |
2 | g.218893244del | CA2663174557 | WNT10A | c.1227del (p.Thr410ProfsTer28) n.24del c.1176del (p.Thr393ProfsTer28) c.1131del (p.Thr378ProfsTer28) c.847del (p.His283ThrfsTer9) | gnomAD v4 |
2 | g.218893244C>A | CA431234855 | WNT10A | c.1227C>A (p.Ile409=) n.24C>A c.1176C>A (p.Ile392=) c.1131C>A (p.Ile377=) c.847C>A (p.His283Asn) | gnomAD v4 |
2 | g.218893244C>G | CA350592747 | WNT10A | c.1227C>G (p.Ile409Met) n.24C>G c.1176C>G (p.Ile392Met) c.1131C>G (p.Ile377Met) c.847C>G (p.His283Asp) | |
2 | g.218893244C>T | CA431234856 | WNT10A | c.1227C>T (p.Ile409=) n.24C>T c.1176C>T (p.Ile392=) c.1131C>T (p.Ile377=) c.847C>T (p.His283Tyr) | gnomAD v4 |
2 | g.218893245A>C | CA350592751 | WNT10A | c.1228A>C (p.Thr410Pro) n.25A>C c.1177A>C (p.Thr393Pro) c.1132A>C (p.Thr378Pro) c.848A>C (p.His283Pro) | |
2 | g.218893245A>G | CA350592753 | WNT10A | c.1228A>G (p.Thr410Ala) n.25A>G c.1177A>G (p.Thr393Ala) c.1132A>G (p.Thr378Ala) c.848A>G (p.His283Arg) | gnomAD v4 |
2 | g.218893245A>T | CA350592749 | WNT10A | c.1228A>T (p.Thr410Ser) n.25A>T c.1177A>T (p.Thr393Ser) c.1132A>T (p.Thr378Ser) c.848A>T (p.His283Leu) | |
2 | g.218893246C>A | CA2114128 | WNT10A | c.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 |
2 | g.218893246C= | CA1328965652 | WNT10A | c.1229C= (p.Thr410=) n.26C= c.1178C= (p.Thr393=) c.1133C= (p.Thr378=) c.849C= (p.His283=) | |
2 | g.218893246C>G | CA350592756 | WNT10A | c.1229C>G (p.Thr410Ser) n.26C>G c.1178C>G (p.Thr393Ser) c.1133C>G (p.Thr378Ser) c.849C>G (p.His283Gln) | |
2 | g.218893246C>T | CA350592759 | WNT10A | c.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 |
2 | g.218893247C>A | CA431234857 | WNT10A | c.1230C>A (p.Thr410=) n.27C>A c.1179C>A (p.Thr393=) c.1134C>A (p.Thr378=) c.850C>A (p.Arg284=) | gnomAD v4 |
2 | g.218893247C>G | CA431234858 | WNT10A | c.1230C>G (p.Thr410=) n.27C>G c.1179C>G (p.Thr393=) c.1134C>G (p.Thr378=) c.850C>G (p.Arg284Gly) | |
2 | g.218893247C>T | CA431234859 | WNT10A | c.1230C>T (p.Thr410=) n.27C>T c.1179C>T (p.Thr393=) c.1134C>T (p.Thr378=) c.850C>T (p.Arg284Ter) | gnomAD v4 |
2 | g.218893248G>A | CA350592763 | WNT10A | c.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 |
2 | g.218893248G>C | CA350592764 | WNT10A | c.1231G>C (p.Glu411Gln) n.28G>C c.1180G>C (p.Glu394Gln) c.1135G>C (p.Glu379Gln) c.851G>C (p.Arg284Pro) | gnomAD v4 |
2 | g.218893248G= | CA1328965654 | WNT10A | c.1231G= (p.Glu411=) n.28G= c.1180G= (p.Glu394=) c.1135G= (p.Glu379=) c.851G= (p.Arg284=) | |
2 | g.218893248G>T | CA350592766 | WNT10A | c.1231G>T (p.Glu411Ter) n.28G>T c.1180G>T (p.Glu394Ter) c.1135G>T (p.Glu379Ter) c.851G>T (p.Arg284Leu) | gnomAD v4 |
2 | g.218893249A>C | CA350592773 | WNT10A | c.1232A>C (p.Glu411Ala) n.29A>C c.1181A>C (p.Glu394Ala) c.1136A>C (p.Glu379Ala) c.852A>C (p.Arg284=) | |
2 | g.218893249A>G | CA350592768 | WNT10A | c.1232A>G (p.Glu411Gly) n.29A>G c.1181A>G (p.Glu394Gly) c.1136A>G (p.Glu379Gly) c.852A>G (p.Arg284=) | |
2 | g.218893249A>T | CA350592771 | WNT10A | c.1232A>T (p.Glu411Val) n.29A>T c.1181A>T (p.Glu394Val) c.1136A>T (p.Glu379Val) c.852A>T (p.Arg284=) | gnomAD v4 |
2 | g.218893250G>A | CA431234860 | WNT10A | c.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 |
2 | g.218893250G>C | CA350592774 | WNT10A | c.1233G>C (p.Glu411Asp) n.30G>C c.1182G>C (p.Glu394Asp) c.1137G>C (p.Glu379Asp) c.853G>C (p.Val285Leu) | gnomAD v4 |
2 | g.218893250G>T | CA350592775 | WNT10A | c.1233G>T (p.Glu411Asp) n.30G>T c.1182G>T (p.Glu394Asp) c.1137G>T (p.Glu379Asp) c.853G>T (p.Val285Leu) | gnomAD v4 |
2 | g.218893251T>A | CA350592776 | WNT10A | c.1234T>A (p.Trp412Arg) n.31T>A c.1183T>A (p.Trp395Arg) c.1138T>A (p.Trp380Arg) c.854T>A (p.Val285Glu) | |
2 | g.218893251T>C | CA350592778 | WNT10A | c.1234T>C (p.Trp412Arg) n.31T>C c.1183T>C (p.Trp395Arg) c.1138T>C (p.Trp380Arg) c.854T>C (p.Val285Ala) | |
2 | g.218893251T>G | CA350592780 | WNT10A | c.1234T>G (p.Trp412Gly) n.31T>G c.1183T>G (p.Trp395Gly) c.1138T>G (p.Trp380Gly) c.854T>G (p.Val285Gly) | |
2 | g.218893252G>A | CA350592784 | WNT10A | c.1235G>A (p.Trp412Ter) n.32G>A c.1184G>A (p.Trp395Ter) c.1139G>A (p.Trp380Ter) c.855G>A (p.Val285=) | gnomAD v4 |
2 | g.218893252G>C | CA350592790 | WNT10A | c.1235G>C (p.Trp412Ser) n.32G>C c.1184G>C (p.Trp395Ser) c.1139G>C (p.Trp380Ser) c.855G>C (p.Val285=) | |
2 | g.218893252G>T | CA350592785 | WNT10A | c.1235G>T (p.Trp412Leu) n.32G>T c.1184G>T (p.Trp395Leu) c.1139G>T (p.Trp380Leu) c.855G>T (p.Val285=) | gnomAD v4 |
2 | g.218893254del | CA2843142785 | WNT10A | c.1237del (p.Val413SerfsTer25) n.34del c.1186del (p.Val396SerfsTer25) c.1141del (p.Val381SerfsTer25) c.857del (p.Gly286ValfsTer6) | |
2 | g.218893253G>A | CA350592793 | WNT10A | c.1236G>A (p.Trp412Ter) n.33G>A c.1185G>A (p.Trp395Ter) c.1140G>A (p.Trp380Ter) c.856G>A (p.Gly286Ser) | gnomAD v4 |
2 | g.218893253G>C | CA350592795 | WNT10A | c.1236G>C (p.Trp412Cys) n.33G>C c.1185G>C (p.Trp395Cys) c.1140G>C (p.Trp380Cys) c.856G>C (p.Gly286Arg) | dbSNP |
2 | g.218893253G= | CA1328965656 | WNT10A | c.1236G= (p.Trp412=) n.33G= c.1185G= (p.Trp395=) c.1140G= (p.Trp380=) c.856G= (p.Gly286=) | |
2 | g.218893253G>T | CA350592796 | WNT10A | c.1236G>T (p.Trp412Cys) n.33G>T c.1185G>T (p.Trp395Cys) c.1140G>T (p.Trp380Cys) c.856G>T (p.Gly286Cys) | gnomAD v4 |
2 | g.218893254G>A | CA2114129 | WNT10A | c.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 |
2 | g.218893254G>C | CA350592802 | WNT10A | c.1237G>C (p.Val413Leu) n.34G>C c.1186G>C (p.Val396Leu) c.1141G>C (p.Val381Leu) c.857G>C (p.Gly286Ala) | |
2 | g.218893254G= | CA1328965658 | WNT10A | c.1237G= (p.Val413=) n.34G= c.1186G= (p.Val396=) c.1141G= (p.Val381=) c.857G= (p.Gly286=) | |
2 | g.218893254G>T | CA350592803 | WNT10A | c.1237G>T (p.Val413Phe) n.34G>T c.1186G>T (p.Val396Phe) c.1141G>T (p.Val381Phe) c.857G>T (p.Gly286Val) | gnomAD v4 |
2 | g.218893255T>A | CA350592804 | WNT10A | c.1238T>A (p.Val413Asp) n.35T>A c.1187T>A (p.Val396Asp) c.1142T>A (p.Val381Asp) c.858T>A (p.Gly286=) | gnomAD v4 |
2 | g.218893255T>C | CA350592807 | WNT10A | c.1238T>C (p.Val413Ala) n.35T>C c.1187T>C (p.Val396Ala) c.1142T>C (p.Val381Ala) c.858T>C (p.Gly286=) | gnomAD v4 |
2 | g.218893255T>G | CA350592810 | WNT10A | c.1238T>G (p.Val413Gly) n.35T>G c.1187T>G (p.Val396Gly) c.1142T>G (p.Val381Gly) c.858T>G (p.Gly286=) | gnomAD v4 |
2 | g.218893256C>A | CA431234861 | WNT10A | c.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 |
2 | g.218893256C= | CA1328965662 | WNT10A | c.1239C= (p.Val413=) n.36C= c.1188C= (p.Val396=) c.1143C= (p.Val381=) c.859C= (p.Gln287=) | |
2 | g.218893256C>G | CA431234862 | WNT10A | c.1239C>G (p.Val413=) n.36C>G c.1188C>G (p.Val396=) c.1143C>G (p.Val381=) c.859C>G (p.Gln287Glu) | |
2 | g.218893256C>T | CA431234863 | WNT10A | c.1239C>T (p.Val413=) n.36C>T c.1188C>T (p.Val396=) c.1143C>T (p.Val381=) c.859C>T (p.Gln287Ter) | gnomAD v4 |
2 | g.218893257A>C | CA350592811 | WNT10A | c.1240A>C (p.Ser414Arg) n.37A>C c.1189A>C (p.Ser397Arg) c.1144A>C (p.Ser382Arg) c.860A>C (p.Gln287Pro) | |
2 | g.218893257A>G | CA350592813 | WNT10A | c.1240A>G (p.Ser414Gly) n.37A>G c.1189A>G (p.Ser397Gly) c.1144A>G (p.Ser382Gly) c.860A>G (p.Gln287Arg) | gnomAD v4 |
2 | g.218893257A>T | CA350592816 | WNT10A | c.1240A>T (p.Ser414Cys) n.37A>T c.1189A>T (p.Ser397Cys) c.1144A>T (p.Ser382Cys) c.860A>T (p.Gln287Leu) | |
2 | g.218893258G>A | CA350592826 | WNT10A | c.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 |
2 | g.218893258G>C | CA350592823 | WNT10A | c.1241G>C (p.Ser414Thr) n.38G>C c.1190G>C (p.Ser397Thr) c.1145G>C (p.Ser382Thr) c.861G>C (p.Gln287His) | |
2 | g.218893258G= | CA1328965665 | WNT10A | c.1241G= (p.Ser414=) n.38G= c.1190G= (p.Ser397=) c.1145G= (p.Ser382=) c.861G= (p.Gln287=) | |
2 | g.218893258G>T | CA350592821 | WNT10A | c.1241G>T (p.Ser414Ile) n.38G>T c.1190G>T (p.Ser397Ile) c.1145G>T (p.Ser382Ile) c.861G>T (p.Gln287His) | gnomAD v4 |
2 | g.218893259C>A | CA350592831 | WNT10A | c.1242C>A (p.Ser414Arg) n.39C>A c.1191C>A (p.Ser397Arg) c.1146C>A (p.Ser382Arg) c.862C>A (p.Arg288Ser) | gnomAD v4 |
2 | g.218893259C>G | CA350592839 | WNT10A | c.1242C>G (p.Ser414Arg) n.39C>G c.1191C>G (p.Ser397Arg) c.1146C>G (p.Ser382Arg) c.862C>G (p.Arg288Gly) | |
2 | g.218893259C>T | CA431234864 | WNT10A | c.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 |
2 | g.218893260G>A | CA350592840 | WNT10A | c.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 |
2 | g.218893260G>C | CA350592849 | WNT10A | c.1243G>C (p.Val415Leu) n.40G>C c.1192G>C (p.Val398Leu) c.1147G>C (p.Val383Leu) c.863G>C (p.Arg288Pro) | |
2 | g.218893260G= | CA1328965667 | WNT10A | c.1243G= (p.Val415=) n.40G= c.1192G= (p.Val398=) c.1147G= (p.Val383=) c.863G= (p.Arg288=) | |
2 | g.218893260G>T | CA350592846 | WNT10A | c.1243G>T (p.Val415Phe) n.40G>T c.1192G>T (p.Val398Phe) c.1147G>T (p.Val383Phe) c.863G>T (p.Arg288Leu) | gnomAD v4 |
2 | g.218893261T>A | CA350592852 | WNT10A | c.1244T>A (p.Val415Asp) n.41T>A c.1193T>A (p.Val398Asp) c.1148T>A (p.Val383Asp) c.864T>A (p.Arg288=) | gnomAD v4 |
2 | g.218893261T>C | CA350592856 | WNT10A | c.1244T>C (p.Val415Ala) n.41T>C c.1193T>C (p.Val398Ala) c.1148T>C (p.Val383Ala) c.864T>C (p.Arg288=) | |
2 | g.218893261T>G | CA350592854 | WNT10A | c.1244T>G (p.Val415Gly) n.41T>G c.1193T>G (p.Val398Gly) c.1148T>G (p.Val383Gly) c.864T>G (p.Arg288=) | |
2 | g.218893262C>A | CA431234865 | WNT10A | c.1245C>A (p.Val415=) n.42C>A c.1194C>A (p.Val398=) c.1149C>A (p.Val383=) c.865C>A (p.Leu289Met) | gnomAD v4 |
2 | g.218893262C>G | CA431234866 | WNT10A | c.1245C>G (p.Val415=) n.42C>G c.1194C>G (p.Val398=) c.1149C>G (p.Val383=) c.865C>G (p.Leu289Val) | |
2 | g.218893262C>T | CA431234867 | WNT10A | c.1245C>T (p.Val415=) n.42C>T c.1194C>T (p.Val398=) c.1149C>T (p.Val383=) c.865C>T (p.Leu289=) | |
2 | g.218893263T>A | CA350592859 | WNT10A | c.1246T>A (p.Cys416Ser) n.43T>A c.1195T>A (p.Cys399Ser) c.1150T>A (p.Cys384Ser) c.866T>A (p.Leu289Gln) | |
2 | g.218893263T>C | CA350592866 | WNT10A | c.1246T>C (p.Cys416Arg) n.43T>C c.1195T>C (p.Cys399Arg) c.1150T>C (p.Cys384Arg) c.866T>C (p.Leu289Pro) | gnomAD v4 |
2 | g.218893263T>G | CA350592869 | WNT10A | c.1246T>G (p.Cys416Gly) n.43T>G c.1195T>G (p.Cys399Gly) c.1150T>G (p.Cys384Gly) c.866T>G (p.Leu289Arg) | |
2 | g.218893264G>A | CA350592882 | WNT10A | c.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 |
2 | g.218893264G>C | CA350592886 | WNT10A | c.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 |
2 | g.218893264G= | CA1328965674 | WNT10A | c.1247G= (p.Cys416=) n.44G= c.1196G= (p.Cys399=) c.1151G= (p.Cys384=) c.867G= (p.Leu289=) | |
2 | g.218893264G>T | CA350592888 | WNT10A | c.1247G>T (p.Cys416Phe) n.44G>T c.1196G>T (p.Cys399Phe) c.1151G>T (p.Cys384Phe) c.867G>T (p.Leu289=) | gnomAD v4 |
2 | g.218893265C>A | CA350592891 | WNT10A | c.1248C>A (p.Cys416Ter) n.45C>A c.1197C>A (p.Cys399Ter) c.1152C>A (p.Cys384Ter) c.868C>A (p.Gln290Lys) | gnomAD v4 |
2 | g.218893265C>G | CA350592894 | WNT10A | c.1248C>G (p.Cys416Trp) n.45C>G c.1197C>G (p.Cys399Trp) c.1152C>G (p.Cys384Trp) c.868C>G (p.Gln290Glu) | |
2 | g.218893265C>T | CA431234868 | WNT10A | c.1248C>T (p.Cys416=) n.45C>T c.1197C>T (p.Cys399=) c.1152C>T (p.Cys384=) c.868C>T (p.Gln290Ter) | gnomAD v4 |
2 | g.218893266A= | CA1328965678 | WNT10A | c.1249A= (p.Lys417=) n.46A= c.1198A= (p.Lys400=) c.1153A= (p.Lys385=) c.869A= (p.Gln290=) | |
2 | g.218893266A>C | CA350592897 | WNT10A | c.1249A>C (p.Lys417Gln) n.46A>C c.1198A>C (p.Lys400Gln) c.1153A>C (p.Lys385Gln) c.869A>C (p.Gln290Pro) | |
2 | g.218893266A>G | CA350592901 | WNT10A | c.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 |
2 | g.218893266A>T | CA350592903 | WNT10A | c.1249A>T (p.Lys417Ter) n.46A>T c.1198A>T (p.Lys400Ter) c.1153A>T (p.Lys385Ter) c.869A>T (p.Gln290Leu) | |
2 | g.218893267del | CA2663174558 | WNT10A | c.1250del (p.Lys417SerfsTer21) n.47del c.1199del (p.Lys400SerfsTer21) c.1154del (p.Lys385SerfsTer21) c.870del (p.Val291Ter) | gnomAD v4 |
2 | g.218893267A>C | CA350592907 | WNT10A | c.1250A>C (p.Lys417Thr) n.47A>C c.1199A>C (p.Lys400Thr) c.1154A>C (p.Lys385Thr) c.870A>C (p.Gln290His) | |
2 | g.218893267A>G | CA350592905 | WNT10A | c.1250A>G (p.Lys417Arg) n.47A>G c.1199A>G (p.Lys400Arg) c.1154A>G (p.Lys385Arg) c.870A>G (p.Gln290=) | gnomAD v4 |
2 | g.218893267A>T | CA350592906 | WNT10A | c.1250A>T (p.Lys417Met) n.47A>T c.1199A>T (p.Lys400Met) c.1154A>T (p.Lys385Met) c.870A>T (p.Gln290His) | gnomAD v4 |
2 | g.218893268G>A | CA431234869 | WNT10A | c.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 |
2 | g.218893268G>C | CA350592910 | WNT10A | c.1251G>C (p.Lys417Asn) n.47+1G>C c.1200G>C (p.Lys400Asn) c.1155G>C (p.Lys385Asn) c.871G>C (p.Val291Leu) | |
2 | g.218893268G>T | CA350592913 | WNT10A | c.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 |
2 | g.218893269T>A | CA65919453 | WNT10A | c.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 |
2 | g.218893269T>C | CA350592914 | WNT10A | c.1252T>C (p.Ter418Arg) n.47+2T>C c.1201T>C (p.Ter401Arg) c.1156T>C (p.Ter386Arg) c.872T>C (p.Val291Ala) | |
2 | g.218893269T>G | CA350592915 | WNT10A | c.1252T>G (p.Ter418Gly) n.47+2T>G c.1201T>G (p.Ter401Gly) c.1156T>G (p.Ter386Gly) c.872T>G (p.Val291Gly) | |
2 | g.218893269T= | CA1328965680 | WNT10A | c.1252T= (p.Ter418=) n.47+2T= c.1201T= (p.Ter401=) c.1156T= (p.Ter386=) c.872T= (p.Val291=) | |
2 | g.218893270G>A | CA431234870 | WNT10A | c.1253G>A (p.Ter418=) n.47+3G>A c.1202G>A (p.Ter401=) c.1157G>A (p.Ter386=) c.873G>A (p.Val291=) | gnomAD v4 |
2 | g.218893270G>C | CA350592920 | WNT10A | c.1253G>C (p.Ter418Ser) n.47+3G>C c.1202G>C (p.Ter401Ser) c.1157G>C (p.Ter386Ser) c.873G>C (p.Val291=) | |
2 | g.218893270G= | CA1328965683 | WNT10A | c.1253G= (p.Ter418=) n.47+3G= c.1202G= (p.Ter401=) c.1157G= (p.Ter386=) c.873G= (p.Val291=) | |
2 | g.218893270G>T | CA65919465 | WNT10A | c.1253G>T (p.Ter418Leu) n.47+3G>T c.1202G>T (p.Ter401Leu) c.1157G>T (p.Ter386Leu) c.873G>T (p.Val291=) | dbSNP gnomAD v4 |
2 | g.218893271A>C | CA350592931 | WNT10A | c.1254A>C (p.Ter418Cys) n.47+4A>C c.1203A>C (p.Ter401Cys) c.1158A>C (p.Ter386Cys) c.874A>C (p.Ser292Arg) | gnomAD v4 |
2 | g.218893271A>G | CA350592933 | WNT10A | c.1254A>G (p.Ter418Trp) n.47+4A>G c.1203A>G (p.Ter401Trp) c.1158A>G (p.Ter386Trp) c.874A>G (p.Ser292Gly) | |
2 | g.218893271A>T | CA350592936 | WNT10A | c.1254A>T (p.Ter418Cys) n.47+4A>T c.1203A>T (p.Ter401Cys) c.1158A>T (p.Ter386Cys) c.874A>T (p.Ser292Cys) | gnomAD v4 |
2 | g.218893272G>T | CA2663174559 | WNT10A | c.*1G>T (n.*1G>T) n.47+5G>T c.875G>T (p.Ser292Ile) | gnomAD v4 |
2 | g.218893273C>A | CA2663174560 | WNT10A | c.*2C>A (n.*2C>A) n.47+6C>A c.876C>A (p.Ser292Arg) | gnomAD v4 |
2 | g.218893273C= | CA1328965688 | WNT10A | c.*2C= (n.*2C=) n.47+6C= c.876C= (p.Ser292=) | |
2 | g.218893273C>G | CA539612128 | WNT10A | c.*2C>G (n.*2C>G) n.47+6C>G c.876C>G (p.Ser292Arg) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218893273C>T | CA1328965687 | WNT10A | c.*2C>T (n.*2C>T) n.47+6C>T c.876C>T (p.Ser292=) | dbSNP gnomAD v4 |
2 | g.218893274G>A | CA2577276402 | WNT10A | c.*3G>A (n.*3G>A) n.47+7G>A c.877G>A (p.Gly293Ser) | gnomAD v4 |
2 | g.218893274G>C | CA2663174561 | WNT10A | c.*3G>C (n.*3G>C) n.47+7G>C c.877G>C (p.Gly293Arg) | gnomAD v4 |
2 | g.218893274G= | CA1328965690 | WNT10A | c.*3G= (n.*3G=) n.47+7G= c.877G= (p.Gly293=) | |
2 | g.218893274G>T | CA2114130 | WNT10A | c.*3G>T (n.*3G>T) n.47+7G>T c.877G>T (p.Gly293Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |