| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 2 | g.218893162_218893164del | CA1328965489 | WNT10A | c.1145_1147del (p.Asn382del) c.1094_1096del (p.Asn365del) c.1049_1051del (p.Asn350del) c.765_767del (p.Gln255del) | dbSNP gnomAD v4 |
| 2 | g.218893164A>C | CA350591966 | WNT10A | c.1147A>C (p.Ile383Leu) c.1096A>C (p.Ile366Leu) c.1051A>C (p.Ile351Leu) c.767A>C (p.His256Pro) | |
| 2 | g.218893164A>G | CA350591973 | WNT10A | c.1147A>G (p.Ile383Val) c.1096A>G (p.Ile366Val) c.1051A>G (p.Ile351Val) c.767A>G (p.His256Arg) | |
| 2 | g.218893164A>T | CA350591976 | WNT10A | c.1147A>T (p.Ile383Phe) c.1096A>T (p.Ile366Phe) c.1051A>T (p.Ile351Phe) c.767A>T (p.His256Leu) | |
| 2 | g.218893165T>A | CA350591982 | WNT10A | c.1148T>A (p.Ile383Asn) c.1097T>A (p.Ile366Asn) c.1052T>A (p.Ile351Asn) c.768T>A (p.His256Gln) | |
| 2 | g.218893165T>C | CA350591991 | WNT10A | c.1148T>C (p.Ile383Thr) c.1097T>C (p.Ile366Thr) c.1052T>C (p.Ile351Thr) c.768T>C (p.His256=) | |
| 2 | g.218893165T>G | CA350591999 | WNT10A | c.1148T>G (p.Ile383Ser) c.1097T>G (p.Ile366Ser) c.1052T>G (p.Ile351Ser) c.768T>G (p.His256Gln) | dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.218893165T= | CA1328965505 | WNT10A | c.1148T= (p.Ile383=) c.1097T= (p.Ile366=) c.1052T= (p.Ile351=) c.768T= (p.His256=) | |
| 2 | g.218893166C>A | CA431417533 | WNT10A | c.1149C>A (p.Ile383=) c.1098C>A (p.Ile366=) c.1053C>A (p.Ile351=) c.769C>A (p.Pro257Thr) | |
| 2 | g.218893166C>G | CA350592001 | WNT10A | c.1149C>G (p.Ile383Met) c.1098C>G (p.Ile366Met) c.1053C>G (p.Ile351Met) c.769C>G (p.Pro257Ala) | |
| 2 | g.218893166C>T | CA431417536 | WNT10A | c.1149C>T (p.Ile383=) c.1098C>T (p.Ile366=) c.1053C>T (p.Ile351=) c.769C>T (p.Pro257Ser) | ClinVar dbSNP gnomAD v4 |
| 2 | g.218893167C>A | CA350592011 | WNT10A | c.1150C>A (p.Leu384Met) c.1099C>A (p.Leu367Met) c.1054C>A (p.Leu352Met) c.770C>A (p.Pro257His) | |
| 2 | g.218893167C>G | CA350592016 | WNT10A | c.1150C>G (p.Leu384Val) c.1099C>G (p.Leu367Val) c.1054C>G (p.Leu352Val) c.770C>G (p.Pro257Arg) | |
| 2 | g.218893167C>T | CA431417539 | WNT10A | c.1150C>T (p.Leu384=) c.1099C>T (p.Leu367=) c.1054C>T (p.Leu352=) c.770C>T (p.Pro257Leu) | gnomAD v4 |
| 2 | g.218893168T>A | CA350592029 | WNT10A | c.1151T>A (p.Leu384Gln) c.1100T>A (p.Leu367Gln) c.1055T>A (p.Leu352Gln) c.771T>A (p.Pro257=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 2 | g.218893168T>C | CA350592046 | WNT10A | c.1151T>C (p.Leu384Pro) c.1100T>C (p.Leu367Pro) c.1055T>C (p.Leu352Pro) c.771T>C (p.Pro257=) | |
| 2 | g.218893168T>G | CA350592047 | WNT10A | c.1151T>G (p.Leu384Arg) c.1100T>G (p.Leu367Arg) c.1055T>G (p.Leu352Arg) c.771T>G (p.Pro257=) | |
| 2 | g.218893168T= | CA1328965508 | WNT10A | c.1151T= (p.Leu384=) c.1100T= (p.Leu367=) c.1055T= (p.Leu352=) c.771T= (p.Pro257=) | |
| 2 | g.218893169G>A | CA431417544 | WNT10A | c.1152G>A (p.Leu384=) c.1101G>A (p.Leu367=) c.1056G>A (p.Leu352=) c.772G>A (p.Ala258Thr) | gnomAD v4 |
| 2 | g.218893169G>C | CA431417545 | WNT10A | c.1152G>C (p.Leu384=) c.1101G>C (p.Leu367=) c.1056G>C (p.Leu352=) c.772G>C (p.Ala258Pro) | |
| 2 | g.218893169G>T | CA431417549 | WNT10A | c.1152G>T (p.Leu384=) c.1101G>T (p.Leu367=) c.1056G>T (p.Leu352=) c.772G>T (p.Ala258Ser) | |
| 2 | g.218893170C>A | CA350592055 | WNT10A | c.1153C>A (p.Arg385Ser) c.1102C>A (p.Arg368Ser) c.1057C>A (p.Arg353Ser) c.773C>A (p.Ala258Glu) | |
| 2 | g.218893170C>G | CA350592051 | WNT10A | c.1153C>G (p.Arg385Gly) c.1102C>G (p.Arg368Gly) c.1057C>G (p.Arg353Gly) c.773C>G (p.Ala258Gly) | |
| 2 | g.218893170C>T | CA350592049 | WNT10A | c.1153C>T (p.Arg385Cys) c.1102C>T (p.Arg368Cys) c.1057C>T (p.Arg353Cys) c.773C>T (p.Ala258Val) | |
| 2 | g.218893171G>A | CA2114119 | WNT10A | c.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 |
| 2 | g.218893171G>C | CA350592059 | WNT10A | c.1154G>C (p.Arg385Pro) c.1103G>C (p.Arg368Pro) c.1058G>C (p.Arg353Pro) c.774G>C (p.Ala258=) | |
| 2 | g.218893171G= | CA1328965512 | WNT10A | c.1154G= (p.Arg385=) c.1103G= (p.Arg368=) c.1058G= (p.Arg353=) c.774G= (p.Ala258=) | |
| 2 | g.218893171G>T | CA350592064 | WNT10A | c.1154G>T (p.Arg385Leu) c.1103G>T (p.Arg368Leu) c.1058G>T (p.Arg353Leu) c.774G>T (p.Ala258=) | |
| 2 | g.218893172C>A | CA431417552 | WNT10A | c.1155C>A (p.Arg385=) c.1104C>A (p.Arg368=) c.1059C>A (p.Arg353=) c.775C>A (p.Pro259Thr) | gnomAD v4 |
| 2 | g.218893172C= | CA1328965514 | WNT10A | c.1155C= (p.Arg385=) c.1104C= (p.Arg368=) c.1059C= (p.Arg353=) c.775C= (p.Pro259=) | |
| 2 | g.218893172C>G | CA431417555 | WNT10A | c.1155C>G (p.Arg385=) c.1104C>G (p.Arg368=) c.1059C>G (p.Arg353=) c.775C>G (p.Pro259Ala) | dbSNP |
| 2 | g.218893172C>T | CA431417558 | WNT10A | c.1155C>T (p.Arg385=) c.1104C>T (p.Arg368=) c.1059C>T (p.Arg353=) c.775C>T (p.Pro259Ser) | ClinVar |
| 2 | g.218893173C>A | CA350592067 | WNT10A | c.1156C>A (p.Gln386Lys) c.1105C>A (p.Gln369Lys) c.1060C>A (p.Gln354Lys) c.776C>A (p.Pro259Gln) | |
| 2 | g.218893173C= | CA1328965516 | WNT10A | c.1156C= (p.Gln386=) c.1105C= (p.Gln369=) c.1060C= (p.Gln354=) c.776C= (p.Pro259=) | |
| 2 | g.218893173C>G | CA350592069 | WNT10A | c.1156C>G (p.Gln386Glu) c.1105C>G (p.Gln369Glu) c.1060C>G (p.Gln354Glu) c.776C>G (p.Pro259Arg) | |
| 2 | g.218893173C>T | CA2114120 | WNT10A | c.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 |
| 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 |