Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.218890149C>A | CA350586136 | WNT10A | c.542C>A (p.Ala181Glu) c.264-2625C>A c.491C>A (p.Ala164Glu) c.446C>A (p.Ala149Glu) c.377-2625C>A (n.377-2625C>A) | |
2 | g.218890149C>G | CA350586139 | WNT10A | c.542C>G (p.Ala181Gly) c.264-2625C>G c.491C>G (p.Ala164Gly) c.446C>G (p.Ala149Gly) c.377-2625C>G (n.377-2625C>G) | |
2 | g.218890149C>T | CA350586141 | WNT10A | c.542C>T (p.Ala181Val) c.264-2625C>T c.491C>T (p.Ala164Val) c.446C>T (p.Ala149Val) c.377-2625C>T (n.377-2625C>T) | ClinVar gnomAD v4 |
2 | g.218890150A>C | CA431416586 | WNT10A | c.543A>C (p.Ala181=) c.264-2624A>C c.492A>C (p.Ala164=) c.447A>C (p.Ala149=) c.377-2624A>C (n.377-2624A>C) | gnomAD v4 |
2 | g.218890150A>G | CA431416588 | WNT10A | c.543A>G (p.Ala181=) c.264-2624A>G c.492A>G (p.Ala164=) c.447A>G (p.Ala149=) c.377-2624A>G (n.377-2624A>G) | gnomAD v4 |
2 | g.218890150A>T | CA431416590 | WNT10A | c.543A>T (p.Ala181=) c.264-2624A>T c.492A>T (p.Ala164=) c.447A>T (p.Ala149=) c.377-2624A>T (n.377-2624A>T) | |
2 | g.218890151C>A | CA350586147 | WNT10A | c.544C>A (p.Leu182Met) c.264-2623C>A c.493C>A (p.Leu165Met) c.448C>A (p.Leu150Met) c.377-2623C>A (n.377-2623C>A) | |
2 | g.218890151C= | CA1328965070 | WNT10A | c.544C= (p.Leu182=) c.264-2623C= c.493C= (p.Leu165=) c.448C= (p.Leu150=) c.377-2623C= (n.377-2623C=) | |
2 | g.218890151C>G | CA350586151 | WNT10A | c.544C>G (p.Leu182Val) c.264-2623C>G c.493C>G (p.Leu165Val) c.448C>G (p.Leu150Val) c.377-2623C>G (n.377-2623C>G) | gnomAD v4 |
2 | g.218890151C>T | CA2113965 | WNT10A | c.544C>T (p.Leu182=) c.264-2623C>T c.493C>T (p.Leu165=) c.448C>T (p.Leu150=) c.377-2623C>T (n.377-2623C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.218890151_218890152insA | CA1328965071 | WNT10A | c.544_545insA (p.Leu182HisfsTer5) c.264-2623_264-2622insA c.493_494insA (p.Leu165HisfsTer5) c.448_449insA (p.Leu150HisfsTer5) c.377-2623_377-2622insA (n.377-2623_377-2622insA) | dbSNP |
2 | g.218890152T>A | CA350586159 | WNT10A | c.545T>A (p.Leu182Gln) c.264-2622T>A c.494T>A (p.Leu165Gln) c.449T>A (p.Leu150Gln) c.377-2622T>A (n.377-2622T>A) | |
2 | g.218890152T>C | CA350586157 | WNT10A | c.545T>C (p.Leu182Pro) c.264-2622T>C c.494T>C (p.Leu165Pro) c.449T>C (p.Leu150Pro) c.377-2622T>C (n.377-2622T>C) | gnomAD v4 |
2 | g.218890152T>G | CA350586156 | WNT10A | c.545T>G (p.Leu182Arg) c.264-2622T>G c.494T>G (p.Leu165Arg) c.449T>G (p.Leu150Arg) c.377-2622T>G (n.377-2622T>G) | dbSNP |
2 | g.218890152T= | CA1328965072 | WNT10A | c.545T= (p.Leu182=) c.264-2622T= c.494T= (p.Leu165=) c.449T= (p.Leu150=) c.377-2622T= (n.377-2622T=) | |
2 | g.218890153G>A | CA431416595 | WNT10A | c.546G>A (p.Leu182=) c.264-2621G>A c.495G>A (p.Leu165=) c.450G>A (p.Leu150=) c.377-2621G>A (n.377-2621G>A) | |
2 | g.218890153G>C | CA431416596 | WNT10A | c.546G>C (p.Leu182=) c.264-2621G>C c.495G>C (p.Leu165=) c.450G>C (p.Leu150=) c.377-2621G>C (n.377-2621G>C) | |
2 | g.218890153G= | CA1328965073 | WNT10A | c.546G= (p.Leu182=) c.264-2621G= c.495G= (p.Leu165=) c.450G= (p.Leu150=) c.377-2621G= (n.377-2621G=) | |
2 | g.218890153G>T | CA431416598 | WNT10A | c.546G>T (p.Leu182=) c.264-2621G>T c.495G>T (p.Leu165=) c.450G>T (p.Leu150=) c.377-2621G>T (n.377-2621G>T) | dbSNP |
2 | g.218890154C>A | CA350586162 | WNT10A | c.547C>A (p.Gln183Lys) c.264-2620C>A c.496C>A (p.Gln166Lys) c.451C>A (p.Gln151Lys) c.377-2620C>A (n.377-2620C>A) | |
2 | g.218890154C= | CA1328965074 | WNT10A | c.547C= (p.Gln183=) c.264-2620C= c.496C= (p.Gln166=) c.451C= (p.Gln151=) c.377-2620C= (n.377-2620C=) | |
2 | g.218890154C>G | CA350586164 | WNT10A | c.547C>G (p.Gln183Glu) c.264-2620C>G c.496C>G (p.Gln166Glu) c.451C>G (p.Gln151Glu) c.377-2620C>G (n.377-2620C>G) | dbSNP |
2 | g.218890154C>T | CA350586167 | WNT10A | c.547C>T (p.Gln183Ter) c.264-2620C>T c.496C>T (p.Gln166Ter) c.451C>T (p.Gln151Ter) c.377-2620C>T (n.377-2620C>T) | ClinVar gnomAD v4 |
2 | g.218890155A>C | CA350586173 | WNT10A | c.548A>C (p.Gln183Pro) c.264-2619A>C c.497A>C (p.Gln166Pro) c.452A>C (p.Gln151Pro) c.377-2619A>C (n.377-2619A>C) | |
2 | g.218890155A>G | CA350586175 | WNT10A | c.548A>G (p.Gln183Arg) c.264-2619A>G c.497A>G (p.Gln166Arg) c.452A>G (p.Gln151Arg) c.377-2619A>G (n.377-2619A>G) | |
2 | g.218890155A>T | CA350586181 | WNT10A | c.548A>T (p.Gln183Leu) c.264-2619A>T c.497A>T (p.Gln166Leu) c.452A>T (p.Gln151Leu) c.377-2619A>T (n.377-2619A>T) | |
2 | g.218890155_218890159delinsAGCGT | CA1328965075 | WNT10A | c.548_552delinsAGCGT (p.Gln183=) c.264-2619_264-2615delinsAGCGT c.497_501delinsAGCGT (p.Gln166=) c.452_456delinsAGCGT (p.Gln151=) c.377-2619_377-2615delinsAGCGT (n.377-2619_377-2615delinsAGCGT) | |
2 | g.218890156G>A | CA431416607 | WNT10A | c.549G>A (p.Gln183=) c.264-2618G>A c.498G>A (p.Gln166=) c.453G>A (p.Gln151=) c.377-2618G>A (n.377-2618G>A) | |
2 | g.218890156G>C | CA350586185 | WNT10A | c.549G>C (p.Gln183His) c.264-2618G>C c.498G>C (p.Gln166His) c.453G>C (p.Gln151His) c.377-2618G>C (n.377-2618G>C) | |
2 | g.218890156G>T | CA350586188 | WNT10A | c.549G>T (p.Gln183His) c.264-2618G>T c.498G>T (p.Gln166His) c.453G>T (p.Gln151His) c.377-2618G>T (n.377-2618G>T) | |
2 | g.218890157_218890160del | CA1328965076 | WNT10A | c.550_553del (p.Arg184ValfsTer4) c.264-2617_264-2614del c.499_502del (p.Arg167ValfsTer4) c.454_457del (p.Arg152ValfsTer4) c.377-2617_377-2614del (n.377-2617_377-2614del) | dbSNP |
2 | g.218890157C>A | CA350586200 | WNT10A | c.550C>A (p.Arg184Ser) c.264-2617C>A c.499C>A (p.Arg167Ser) c.454C>A (p.Arg152Ser) c.377-2617C>A (n.377-2617C>A) | gnomAD v4 |
2 | g.218890157C= | CA1328965077 | WNT10A | c.550C= (p.Arg184=) c.264-2617C= c.499C= (p.Arg167=) c.454C= (p.Arg152=) c.377-2617C= (n.377-2617C=) | |
2 | g.218890157C>G | CA350586204 | WNT10A | c.550C>G (p.Arg184Gly) c.264-2617C>G c.499C>G (p.Arg167Gly) c.454C>G (p.Arg152Gly) c.377-2617C>G (n.377-2617C>G) | |
2 | g.218890157C>T | CA2113966 | WNT10A | c.550C>T (p.Arg184Cys) c.264-2617C>T c.499C>T (p.Arg167Cys) c.454C>T (p.Arg152Cys) c.377-2617C>T (n.377-2617C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890158G>A | CA2113967 | WNT10A | c.551G>A (p.Arg184His) c.264-2616G>A c.500G>A (p.Arg167His) c.455G>A (p.Arg152His) c.377-2616G>A (n.377-2616G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890158G>C | CA65916723 | WNT10A | c.551G>C (p.Arg184Pro) c.264-2616G>C c.500G>C (p.Arg167Pro) c.455G>C (p.Arg152Pro) c.377-2616G>C (n.377-2616G>C) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890158G= | CA1328965078 | WNT10A | c.551G= (p.Arg184=) c.264-2616G= c.500G= (p.Arg167=) c.455G= (p.Arg152=) c.377-2616G= (n.377-2616G=) | |
2 | g.218890158G>T | CA350586241 | WNT10A | c.551G>T (p.Arg184Leu) c.264-2616G>T c.500G>T (p.Arg167Leu) c.455G>T (p.Arg152Leu) c.377-2616G>T (n.377-2616G>T) | |
2 | g.218890159T>A | CA431416612 | WNT10A | c.552T>A (p.Arg184=) c.264-2615T>A c.501T>A (p.Arg167=) c.456T>A (p.Arg152=) c.377-2615T>A (n.377-2615T>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890159T>C | CA431416613 | WNT10A | c.552T>C (p.Arg184=) c.264-2615T>C c.501T>C (p.Arg167=) c.456T>C (p.Arg152=) c.377-2615T>C (n.377-2615T>C) | |
2 | g.218890159T>G | CA431416614 | WNT10A | c.552T>G (p.Arg184=) c.264-2615T>G c.501T>G (p.Arg167=) c.456T>G (p.Arg152=) c.377-2615T>G (n.377-2615T>G) | |
2 | g.218890159T= | CA1328965079 | WNT10A | c.552T= (p.Arg184=) c.264-2615T= c.501T= (p.Arg167=) c.456T= (p.Arg152=) c.377-2615T= (n.377-2615T=) | |
2 | g.218890160G>A | CA350586246 | WNT10A | c.553G>A (p.Gly185Ser) c.264-2614G>A c.502G>A (p.Gly168Ser) c.457G>A (p.Gly153Ser) c.377-2614G>A (n.377-2614G>A) | gnomAD v4 |
2 | g.218890160G>C | CA350586251 | WNT10A | c.553G>C (p.Gly185Arg) c.264-2614G>C c.502G>C (p.Gly168Arg) c.457G>C (p.Gly153Arg) c.377-2614G>C (n.377-2614G>C) | |
2 | g.218890160G>T | CA350586245 | WNT10A | c.553G>T (p.Gly185Cys) c.264-2614G>T c.502G>T (p.Gly168Cys) c.457G>T (p.Gly153Cys) c.377-2614G>T (n.377-2614G>T) | |
2 | g.218890161G>A | CA350586252 | WNT10A | c.554G>A (p.Gly185Asp) c.264-2613G>A c.503G>A (p.Gly168Asp) c.458G>A (p.Gly153Asp) c.377-2613G>A (n.377-2613G>A) | ClinVar dbSNP COSMIC |
2 | g.218890161G>C | CA350586253 | WNT10A | c.554G>C (p.Gly185Ala) c.264-2613G>C c.503G>C (p.Gly168Ala) c.458G>C (p.Gly153Ala) c.377-2613G>C (n.377-2613G>C) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218890161G= | CA1328965080 | WNT10A | c.554G= (p.Gly185=) c.264-2613G= c.503G= (p.Gly168=) c.458G= (p.Gly153=) c.377-2613G= (n.377-2613G=) | |
2 | g.218890161G>T | CA350586254 | WNT10A | c.554G>T (p.Gly185Val) c.264-2613G>T c.503G>T (p.Gly168Val) c.458G>T (p.Gly153Val) c.377-2613G>T (n.377-2613G>T) | |
2 | g.218890162T>A | CA431416618 | WNT10A | c.555T>A (p.Gly185=) c.264-2612T>A c.504T>A (p.Gly168=) c.459T>A (p.Gly153=) c.377-2612T>A (n.377-2612T>A) | |
2 | g.218890162T>C | CA431416617 | WNT10A | c.555T>C (p.Gly185=) c.264-2612T>C c.504T>C (p.Gly168=) c.459T>C (p.Gly153=) c.377-2612T>C (n.377-2612T>C) | ClinVar dbSNP |
2 | g.218890162T>G | CA431416616 | WNT10A | c.555T>G (p.Gly185=) c.264-2612T>G c.504T>G (p.Gly168=) c.459T>G (p.Gly153=) c.377-2612T>G (n.377-2612T>G) | |
2 | g.218890163A>C | CA350586255 | WNT10A | c.556A>C (p.Lys186Gln) c.264-2611A>C c.505A>C (p.Lys169Gln) c.460A>C (p.Lys154Gln) c.377-2611A>C (n.377-2611A>C) | |
2 | g.218890163A>G | CA350586256 | WNT10A | c.556A>G (p.Lys186Glu) c.264-2611A>G c.505A>G (p.Lys169Glu) c.460A>G (p.Lys154Glu) c.377-2611A>G (n.377-2611A>G) | |
2 | g.218890163A>T | CA350586257 | WNT10A | c.556A>T (p.Lys186Ter) c.264-2611A>T c.505A>T (p.Lys169Ter) c.460A>T (p.Lys154Ter) c.377-2611A>T (n.377-2611A>T) | |
2 | g.218890164A>C | CA350586259 | WNT10A | c.557A>C (p.Lys186Thr) c.264-2610A>C c.506A>C (p.Lys169Thr) c.461A>C (p.Lys154Thr) c.377-2610A>C (n.377-2610A>C) | |
2 | g.218890164A>G | CA350586262 | WNT10A | c.557A>G (p.Lys186Arg) c.264-2610A>G c.506A>G (p.Lys169Arg) c.461A>G (p.Lys154Arg) c.377-2610A>G (n.377-2610A>G) | |
2 | g.218890164A>T | CA350586264 | WNT10A | c.557A>T (p.Lys186Met) c.264-2610A>T c.506A>T (p.Lys169Met) c.461A>T (p.Lys154Met) c.377-2610A>T (n.377-2610A>T) | |
2 | g.218890165G>A | CA2113968 | WNT10A | c.558G>A (p.Lys186=) c.264-2609G>A c.507G>A (p.Lys169=) c.462G>A (p.Lys154=) c.377-2609G>A (n.377-2609G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890165G>C | CA350586266 | WNT10A | c.558G>C (p.Lys186Asn) c.264-2609G>C c.507G>C (p.Lys169Asn) c.462G>C (p.Lys154Asn) c.377-2609G>C (n.377-2609G>C) | |
2 | g.218890165G= | CA1328965081 | WNT10A | c.558G= (p.Lys186=) c.264-2609G= c.507G= (p.Lys169=) c.462G= (p.Lys154=) c.377-2609G= (n.377-2609G=) | |
2 | g.218890165G>T | CA350586267 | WNT10A | c.558G>T (p.Lys186Asn) c.264-2609G>T c.507G>T (p.Lys169Asn) c.462G>T (p.Lys154Asn) c.377-2609G>T (n.377-2609G>T) | |
2 | g.218890166G>A | CA350586273 | WNT10A | c.559G>A (p.Gly187Ser) c.264-2608G>A c.508G>A (p.Gly170Ser) c.463G>A (p.Gly155Ser) c.377-2608G>A (n.377-2608G>A) | |
2 | g.218890166G>C | CA350586272 | WNT10A | c.559G>C (p.Gly187Arg) c.264-2608G>C c.508G>C (p.Gly170Arg) c.463G>C (p.Gly155Arg) c.377-2608G>C (n.377-2608G>C) | |
2 | g.218890166G>T | CA350586270 | WNT10A | c.559G>T (p.Gly187Cys) c.264-2608G>T c.508G>T (p.Gly170Cys) c.463G>T (p.Gly155Cys) c.377-2608G>T (n.377-2608G>T) | |
2 | g.218890167G>A | CA350586276 | WNT10A | c.560G>A (p.Gly187Asp) c.264-2607G>A c.509G>A (p.Gly170Asp) c.464G>A (p.Gly155Asp) c.377-2607G>A (n.377-2607G>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218890167G>C | CA350586279 | WNT10A | c.560G>C (p.Gly187Ala) c.264-2607G>C c.509G>C (p.Gly170Ala) c.464G>C (p.Gly155Ala) c.377-2607G>C (n.377-2607G>C) | |
2 | g.218890167G= | CA1328965082 | WNT10A | c.560G= (p.Gly187=) c.264-2607G= c.509G= (p.Gly170=) c.464G= (p.Gly155=) c.377-2607G= (n.377-2607G=) | |
2 | g.218890167G>T | CA2113969 | WNT10A | c.560G>T (p.Gly187Val) c.264-2607G>T c.509G>T (p.Gly170Val) c.464G>T (p.Gly155Val) c.377-2607G>T (n.377-2607G>T) | dbSNP ExAC gnomAD v2 |
2 | g.218890168C>A | CA431416629 | WNT10A | c.561C>A (p.Gly187=) c.264-2606C>A c.510C>A (p.Gly170=) c.465C>A (p.Gly155=) c.377-2606C>A (n.377-2606C>A) | |
2 | g.218890168C= | CA1328965083 | WNT10A | c.561C= (p.Gly187=) c.264-2606C= c.510C= (p.Gly170=) c.465C= (p.Gly155=) c.377-2606C= (n.377-2606C=) | |
2 | g.218890168C>G | CA431416630 | WNT10A | c.561C>G (p.Gly187=) c.264-2606C>G c.510C>G (p.Gly170=) c.465C>G (p.Gly155=) c.377-2606C>G (n.377-2606C>G) | |
2 | g.218890168C>T | CA2113970 | WNT10A | c.561C>T (p.Gly187=) c.264-2606C>T c.510C>T (p.Gly170=) c.465C>T (p.Gly155=) c.377-2606C>T (n.377-2606C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890169C>A | CA350586299 | WNT10A | c.562C>A (p.Leu188Met) c.264-2605C>A c.511C>A (p.Leu171Met) c.466C>A (p.Leu156Met) c.377-2605C>A (n.377-2605C>A) | |
2 | g.218890169C>G | CA350586302 | WNT10A | c.562C>G (p.Leu188Val) c.264-2605C>G c.511C>G (p.Leu171Val) c.466C>G (p.Leu156Val) c.377-2605C>G (n.377-2605C>G) | |
2 | g.218890169C>T | CA431416632 | WNT10A | c.562C>T (p.Leu188=) c.264-2605C>T c.511C>T (p.Leu171=) c.466C>T (p.Leu156=) c.377-2605C>T (n.377-2605C>T) | |
2 | g.218890170T>A | CA350586304 | WNT10A | c.563T>A (p.Leu188Gln) c.264-2604T>A c.512T>A (p.Leu171Gln) c.467T>A (p.Leu156Gln) c.377-2604T>A (n.377-2604T>A) | |
2 | g.218890170T>C | CA350586308 | WNT10A | c.563T>C (p.Leu188Pro) c.264-2604T>C c.512T>C (p.Leu171Pro) c.467T>C (p.Leu156Pro) c.377-2604T>C (n.377-2604T>C) | |
2 | g.218890170T>G | CA350586314 | WNT10A | c.563T>G (p.Leu188Arg) c.264-2604T>G c.512T>G (p.Leu171Arg) c.467T>G (p.Leu156Arg) c.377-2604T>G (n.377-2604T>G) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218890170T= | CA1328965084 | WNT10A | c.563T= (p.Leu188=) c.264-2604T= c.512T= (p.Leu171=) c.467T= (p.Leu156=) c.377-2604T= (n.377-2604T=) | |
2 | g.218890171G>A | CA431416634 | WNT10A | c.564G>A (p.Leu188=) c.264-2603G>A c.513G>A (p.Leu171=) c.468G>A (p.Leu156=) c.377-2603G>A (n.377-2603G>A) | ClinVar |
2 | g.218890171G>C | CA431416635 | WNT10A | c.564G>C (p.Leu188=) c.264-2603G>C c.513G>C (p.Leu171=) c.468G>C (p.Leu156=) c.377-2603G>C (n.377-2603G>C) | |
2 | g.218890171G>T | CA431416636 | WNT10A | c.564G>T (p.Leu188=) c.264-2603G>T c.513G>T (p.Leu171=) c.468G>T (p.Leu156=) c.377-2603G>T (n.377-2603G>T) | |
2 | g.218890172A>C | CA350586315 | WNT10A | c.565A>C (p.Ser189Arg) c.264-2602A>C c.514A>C (p.Ser172Arg) c.469A>C (p.Ser157Arg) c.377-2602A>C (n.377-2602A>C) | |
2 | g.218890172A>G | CA350586316 | WNT10A | c.565A>G (p.Ser189Gly) c.264-2602A>G c.514A>G (p.Ser172Gly) c.469A>G (p.Ser157Gly) c.377-2602A>G (n.377-2602A>G) | |
2 | g.218890172A>T | CA350586320 | WNT10A | c.565A>T (p.Ser189Cys) c.264-2602A>T c.514A>T (p.Ser172Cys) c.469A>T (p.Ser157Cys) c.377-2602A>T (n.377-2602A>T) | |
2 | g.218890173G>A | CA350586326 | WNT10A | c.566G>A (p.Ser189Asn) c.264-2601G>A c.515G>A (p.Ser172Asn) c.470G>A (p.Ser157Asn) c.377-2601G>A (n.377-2601G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890173G>C | CA350586329 | WNT10A | c.566G>C (p.Ser189Thr) c.264-2601G>C c.515G>C (p.Ser172Thr) c.470G>C (p.Ser157Thr) c.377-2601G>C (n.377-2601G>C) | |
2 | g.218890173G= | CA1328965085 | WNT10A | c.566G= (p.Ser189=) c.264-2601G= c.515G= (p.Ser172=) c.470G= (p.Ser157=) c.377-2601G= (n.377-2601G=) | |
2 | g.218890173G>T | CA350586327 | WNT10A | c.566G>T (p.Ser189Ile) c.264-2601G>T c.515G>T (p.Ser172Ile) c.470G>T (p.Ser157Ile) c.377-2601G>T (n.377-2601G>T) | |
2 | g.218890174C>A | CA350586330 | WNT10A | c.567C>A (p.Ser189Arg) c.264-2600C>A c.516C>A (p.Ser172Arg) c.471C>A (p.Ser157Arg) c.377-2600C>A (n.377-2600C>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890174C= | CA1328965086 | WNT10A | c.567C= (p.Ser189=) c.264-2600C= c.516C= (p.Ser172=) c.471C= (p.Ser157=) c.377-2600C= (n.377-2600C=) | |
2 | g.218890174C>G | CA350586331 | WNT10A | c.567C>G (p.Ser189Arg) c.264-2600C>G c.516C>G (p.Ser172Arg) c.471C>G (p.Ser157Arg) c.377-2600C>G (n.377-2600C>G) | |
2 | g.218890174C>T | CA431416638 | WNT10A | c.567C>T (p.Ser189=) c.264-2600C>T c.516C>T (p.Ser172=) c.471C>T (p.Ser157=) c.377-2600C>T (n.377-2600C>T) | ClinVar dbSNP gnomAD v4 |
2 | g.218890175C>A | CA350586334 | WNT10A | c.568C>A (p.His190Asn) c.264-2599C>A c.517C>A (p.His173Asn) c.472C>A (p.His158Asn) c.377-2599C>A (n.377-2599C>A) | |
2 | g.218890175C>G | CA350586335 | WNT10A | c.568C>G (p.His190Asp) c.264-2599C>G c.517C>G (p.His173Asp) c.472C>G (p.His158Asp) c.377-2599C>G (n.377-2599C>G) | |
2 | g.218890175C>T | CA350586344 | WNT10A | c.568C>T (p.His190Tyr) c.264-2599C>T c.517C>T (p.His173Tyr) c.472C>T (p.His158Tyr) c.377-2599C>T (n.377-2599C>T) | gnomAD v4 |
2 | g.218890176A= | CA1328965087 | WNT10A | c.569A= (p.His190=) c.264-2598A= c.518A= (p.His173=) c.473A= (p.His158=) c.377-2598A= (n.377-2598A=) | |
2 | g.218890176A>C | CA350586348 | WNT10A | c.569A>C (p.His190Pro) c.264-2598A>C c.518A>C (p.His173Pro) c.473A>C (p.His158Pro) c.377-2598A>C (n.377-2598A>C) | |
2 | g.218890176A>G | CA2113971 | WNT10A | c.569A>G (p.His190Arg) c.264-2598A>G c.518A>G (p.His173Arg) c.473A>G (p.His158Arg) c.377-2598A>G (n.377-2598A>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890176A>T | CA350586355 | WNT10A | c.569A>T (p.His190Leu) c.264-2598A>T c.518A>T (p.His173Leu) c.473A>T (p.His158Leu) c.377-2598A>T (n.377-2598A>T) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890177T>A | CA350586360 | WNT10A | c.570T>A (p.His190Gln) c.264-2597T>A c.519T>A (p.His173Gln) c.474T>A (p.His158Gln) c.377-2597T>A (n.377-2597T>A) | gnomAD v4 |
2 | g.218890177T>C | CA431416643 | WNT10A | c.570T>C (p.His190=) c.264-2597T>C c.519T>C (p.His173=) c.474T>C (p.His158=) c.377-2597T>C (n.377-2597T>C) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.218890177T>G | CA350586367 | WNT10A | c.570T>G (p.His190Gln) c.264-2597T>G c.519T>G (p.His173Gln) c.474T>G (p.His158Gln) c.377-2597T>G (n.377-2597T>G) | |
2 | g.218890177T= | CA1328965088 | WNT10A | c.570T= (p.His190=) c.264-2597T= c.519T= (p.His173=) c.474T= (p.His158=) c.377-2597T= (n.377-2597T=) | |
2 | g.218890178G>A | CA350586371 | WNT10A | c.571G>A (p.Gly191Arg) c.264-2596G>A c.520G>A (p.Gly174Arg) c.475G>A (p.Gly159Arg) c.377-2596G>A (n.377-2596G>A) | dbSNP gnomAD v4 |
2 | g.218890178G>C | CA350586373 | WNT10A | c.571G>C (p.Gly191Arg) c.264-2596G>C c.520G>C (p.Gly174Arg) c.475G>C (p.Gly159Arg) c.377-2596G>C (n.377-2596G>C) | |
2 | g.218890178G= | CA1328965089 | WNT10A | c.571G= (p.Gly191=) c.264-2596G= c.520G= (p.Gly174=) c.475G= (p.Gly159=) c.377-2596G= (n.377-2596G=) | |
2 | g.218890178G>T | CA350586379 | WNT10A | c.571G>T (p.Gly191Trp) c.264-2596G>T c.520G>T (p.Gly174Trp) c.475G>T (p.Gly159Trp) c.377-2596G>T (n.377-2596G>T) | |
2 | g.218890181del | CA2580065714 | WNT10A | c.574del (p.Val192SerfsTer?) c.264-2593del c.523del (p.Val175SerfsTer?) c.478del (p.Val160SerfsTer?) c.377-2593del (n.377-2593del) | ClinVar |
2 | g.218890179G>A | CA350586384 | WNT10A | c.572G>A (p.Gly191Glu) c.264-2595G>A c.521G>A (p.Gly174Glu) c.476G>A (p.Gly159Glu) c.377-2595G>A (n.377-2595G>A) | gnomAD v4 |
2 | g.218890179G>C | CA2113972 | WNT10A | c.572G>C (p.Gly191Ala) c.264-2595G>C c.521G>C (p.Gly174Ala) c.476G>C (p.Gly159Ala) c.377-2595G>C (n.377-2595G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.218890179G= | CA1328965090 | WNT10A | c.572G= (p.Gly191=) c.264-2595G= c.521G= (p.Gly174=) c.476G= (p.Gly159=) c.377-2595G= (n.377-2595G=) | |
2 | g.218890179G>T | CA350586383 | WNT10A | c.572G>T (p.Gly191Val) c.264-2595G>T c.521G>T (p.Gly174Val) c.476G>T (p.Gly159Val) c.377-2595G>T (n.377-2595G>T) | |
2 | g.218890180G>A | CA65916760 | WNT10A | c.573G>A (p.Gly191=) c.264-2594G>A c.522G>A (p.Gly174=) c.477G>A (p.Gly159=) c.377-2594G>A (n.377-2594G>A) | dbSNP |
2 | g.218890180G>C | CA431416648 | WNT10A | c.573G>C (p.Gly191=) c.264-2594G>C c.522G>C (p.Gly174=) c.477G>C (p.Gly159=) c.377-2594G>C (n.377-2594G>C) | |
2 | g.218890180G= | CA1328965091 | WNT10A | c.573G= (p.Gly191=) c.264-2594G= c.522G= (p.Gly174=) c.477G= (p.Gly159=) c.377-2594G= (n.377-2594G=) | |
2 | g.218890180G>T | CA431416650 | WNT10A | c.573G>T (p.Gly191=) c.264-2594G>T c.522G>T (p.Gly174=) c.477G>T (p.Gly159=) c.377-2594G>T (n.377-2594G>T) | gnomAD v4 |
2 | g.218890181G>A | CA350586385 | WNT10A | c.574G>A (p.Val192Ile) c.264-2593G>A c.523G>A (p.Val175Ile) c.478G>A (p.Val160Ile) c.377-2593G>A (n.377-2593G>A) | gnomAD v4 |
2 | g.218890181G>C | CA350586386 | WNT10A | c.574G>C (p.Val192Leu) c.264-2593G>C c.523G>C (p.Val175Leu) c.478G>C (p.Val160Leu) c.377-2593G>C (n.377-2593G>C) | |
2 | g.218890181G>T | CA350586389 | WNT10A | c.574G>T (p.Val192Phe) c.264-2593G>T c.523G>T (p.Val175Phe) c.478G>T (p.Val160Phe) c.377-2593G>T (n.377-2593G>T) | |
2 | g.218890182T>A | CA350586392 | WNT10A | c.575T>A (p.Val192Asp) c.264-2592T>A c.524T>A (p.Val175Asp) c.479T>A (p.Val160Asp) c.377-2592T>A (n.377-2592T>A) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218890182T>C | CA350586396 | WNT10A | c.575T>C (p.Val192Ala) c.264-2592T>C c.524T>C (p.Val175Ala) c.479T>C (p.Val160Ala) c.377-2592T>C (n.377-2592T>C) | |
2 | g.218890182T>G | CA350586400 | WNT10A | c.575T>G (p.Val192Gly) c.264-2592T>G c.524T>G (p.Val175Gly) c.479T>G (p.Val160Gly) c.377-2592T>G (n.377-2592T>G) | |
2 | g.218890182T= | CA1328965092 | WNT10A | c.575T= (p.Val192=) c.264-2592T= c.524T= (p.Val175=) c.479T= (p.Val160=) c.377-2592T= (n.377-2592T=) | |
2 | g.218890183C>A | CA431416656 | WNT10A | c.576C>A (p.Val192=) c.264-2591C>A c.525C>A (p.Val175=) c.480C>A (p.Val160=) c.377-2591C>A (n.377-2591C>A) | |
2 | g.218890183C= | CA1328965093 | WNT10A | c.576C= (p.Val192=) c.264-2591C= c.525C= (p.Val175=) c.480C= (p.Val160=) c.377-2591C= (n.377-2591C=) | |
2 | g.218890183C>G | CA431416658 | WNT10A | c.576C>G (p.Val192=) c.264-2591C>G c.525C>G (p.Val175=) c.480C>G (p.Val160=) c.377-2591C>G (n.377-2591C>G) | ClinVar |
2 | g.218890183C>T | CA2113973 | WNT10A | c.576C>T (p.Val192=) c.264-2591C>T c.525C>T (p.Val175=) c.480C>T (p.Val160=) c.377-2591C>T (n.377-2591C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890183_218890186del | CA2550516589 | WNT10A | c.576_579del (p.Pro193AsnfsTer?) c.264-2591_264-2588del c.525_528del (p.Pro176AsnfsTer?) c.480_483del (p.Pro161AsnfsTer?) c.377-2591_377-2588del (n.377-2591_377-2588del) | |
2 | g.218890186_218890199del | CA2586971347 | WNT10A | c.579_592del (p.Glu194AlafsTer28) c.264-2588_264-2575del c.528_541del (p.Glu177AlafsTer28) c.483_496del (p.Glu162AlafsTer28) c.377-2588_377-2575del (n.377-2588_377-2575del) | |
2 | g.218890184C>A | CA350586411 | WNT10A | c.577C>A (p.Pro193Thr) c.264-2590C>A c.526C>A (p.Pro176Thr) c.481C>A (p.Pro161Thr) c.377-2590C>A (n.377-2590C>A) | gnomAD v4 |
2 | g.218890184C>G | CA350586413 | WNT10A | c.577C>G (p.Pro193Ala) c.264-2590C>G c.526C>G (p.Pro176Ala) c.481C>G (p.Pro161Ala) c.377-2590C>G (n.377-2590C>G) | gnomAD v4 |
2 | g.218890184C>T | CA350586418 | WNT10A | c.577C>T (p.Pro193Ser) c.264-2590C>T c.526C>T (p.Pro176Ser) c.481C>T (p.Pro161Ser) c.377-2590C>T (n.377-2590C>T) | |
2 | g.218890185C>A | CA350586424 | WNT10A | c.578C>A (p.Pro193Gln) c.264-2589C>A c.527C>A (p.Pro176Gln) c.482C>A (p.Pro161Gln) c.377-2589C>A (n.377-2589C>A) | |
2 | g.218890185C= | CA1328965094 | WNT10A | c.578C= (p.Pro193=) c.264-2589C= c.527C= (p.Pro176=) c.482C= (p.Pro161=) c.377-2589C= (n.377-2589C=) | |
2 | g.218890185C>G | CA2113975 | WNT10A | c.578C>G (p.Pro193Arg) c.264-2589C>G c.527C>G (p.Pro176Arg) c.482C>G (p.Pro161Arg) c.377-2589C>G (n.377-2589C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.218890185C>T | CA2113974 | WNT10A | c.578C>T (p.Pro193Leu) c.264-2589C>T c.527C>T (p.Pro176Leu) c.482C>T (p.Pro161Leu) c.377-2589C>T (n.377-2589C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890186G>A | CA2113976 | WNT10A | c.579G>A (p.Pro193=) c.264-2588G>A c.528G>A (p.Pro176=) c.483G>A (p.Pro161=) c.377-2588G>A (n.377-2588G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890186G>C | CA431416666 | WNT10A | c.579G>C (p.Pro193=) c.264-2588G>C c.528G>C (p.Pro176=) c.483G>C (p.Pro161=) c.377-2588G>C (n.377-2588G>C) | |
2 | g.218890186G= | CA1328965095 | WNT10A | c.579G= (p.Pro193=) c.264-2588G= c.528G= (p.Pro176=) c.483G= (p.Pro161=) c.377-2588G= (n.377-2588G=) | |
2 | g.218890186G>T | CA431416667 | WNT10A | c.579G>T (p.Pro193=) c.264-2588G>T c.528G>T (p.Pro176=) c.483G>T (p.Pro161=) c.377-2588G>T (n.377-2588G>T) | |
2 | g.218890187del | CA2573135230 | WNT10A | c.580del (p.Glu194AsnfsTer?) c.264-2587del c.529del (p.Glu177AsnfsTer?) c.484del (p.Glu162AsnfsTer?) c.377-2587del (n.377-2587del) | ClinVar dbSNP |
2 | g.218890187G>A | CA350586436 | WNT10A | c.580G>A (p.Glu194Lys) c.264-2587G>A c.529G>A (p.Glu177Lys) c.484G>A (p.Glu162Lys) c.377-2587G>A (n.377-2587G>A) | |
2 | g.218890187G>C | CA350586434 | WNT10A | c.580G>C (p.Glu194Gln) c.264-2587G>C c.529G>C (p.Glu177Gln) c.484G>C (p.Glu162Gln) c.377-2587G>C (n.377-2587G>C) | |
2 | g.218890187G>T | CA350586435 | WNT10A | c.580G>T (p.Glu194Ter) c.264-2587G>T c.529G>T (p.Glu177Ter) c.484G>T (p.Glu162Ter) c.377-2587G>T (n.377-2587G>T) | |
2 | g.218890188A>C | CA350586439 | WNT10A | c.581A>C (p.Glu194Ala) c.264-2586A>C c.530A>C (p.Glu177Ala) c.485A>C (p.Glu162Ala) c.377-2586A>C (n.377-2586A>C) | |
2 | g.218890188A>G | CA350586440 | WNT10A | c.581A>G (p.Glu194Gly) c.264-2586A>G c.530A>G (p.Glu177Gly) c.485A>G (p.Glu162Gly) c.377-2586A>G (n.377-2586A>G) | |
2 | g.218890188A>T | CA350586444 | WNT10A | c.581A>T (p.Glu194Val) c.264-2586A>T c.530A>T (p.Glu177Val) c.485A>T (p.Glu162Val) c.377-2586A>T (n.377-2586A>T) | |
2 | g.218890189A>C | CA350586446 | WNT10A | c.582A>C (p.Glu194Asp) c.264-2585A>C c.531A>C (p.Glu177Asp) c.486A>C (p.Glu162Asp) c.377-2585A>C (n.377-2585A>C) | |
2 | g.218890189A>G | CA431416673 | WNT10A | c.582A>G (p.Glu194=) c.264-2585A>G c.531A>G (p.Glu177=) c.486A>G (p.Glu162=) c.377-2585A>G (n.377-2585A>G) | |
2 | g.218890189A>T | CA350586448 | WNT10A | c.582A>T (p.Glu194Asp) c.264-2585A>T c.531A>T (p.Glu177Asp) c.486A>T (p.Glu162Asp) c.377-2585A>T (n.377-2585A>T) | |
2 | g.218890190C>A | CA350586450 | WNT10A | c.583C>A (p.His195Asn) c.264-2584C>A c.532C>A (p.His178Asn) c.487C>A (p.His163Asn) c.377-2584C>A (n.377-2584C>A) | |
2 | g.218890190C>G | CA350586452 | WNT10A | c.583C>G (p.His195Asp) c.264-2584C>G c.532C>G (p.His178Asp) c.487C>G (p.His163Asp) c.377-2584C>G (n.377-2584C>G) | |
2 | g.218890190C>T | CA350586454 | WNT10A | c.583C>T (p.His195Tyr) c.264-2584C>T c.532C>T (p.His178Tyr) c.487C>T (p.His163Tyr) c.377-2584C>T (n.377-2584C>T) | |
2 | g.218890191A= | CA1328965096 | WNT10A | c.584A= (p.His195=) c.264-2583A= c.533A= (p.His178=) c.488A= (p.His163=) c.377-2583A= (n.377-2583A=) | |
2 | g.218890191A>C | CA350586458 | WNT10A | c.584A>C (p.His195Pro) c.264-2583A>C c.533A>C (p.His178Pro) c.488A>C (p.His163Pro) c.377-2583A>C (n.377-2583A>C) | dbSNP gnomAD v4 |
2 | g.218890191A>G | CA350586462 | WNT10A | c.584A>G (p.His195Arg) c.264-2583A>G c.533A>G (p.His178Arg) c.488A>G (p.His163Arg) c.377-2583A>G (n.377-2583A>G) | |
2 | g.218890191A>T | CA350586465 | WNT10A | c.584A>T (p.His195Leu) c.264-2583A>T c.533A>T (p.His178Leu) c.488A>T (p.His163Leu) c.377-2583A>T (n.377-2583A>T) | |
2 | g.218890192C>A | CA350586474 | WNT10A | c.585C>A (p.His195Gln) c.264-2582C>A c.534C>A (p.His178Gln) c.489C>A (p.His163Gln) c.377-2582C>A (n.377-2582C>A) | gnomAD v4 |
2 | g.218890192C= | CA1328965097 | WNT10A | c.585C= (p.His195=) c.264-2582C= c.534C= (p.His178=) c.489C= (p.His163=) c.377-2582C= (n.377-2582C=) | |
2 | g.218890192C>G | CA350586470 | WNT10A | c.585C>G (p.His195Gln) c.264-2582C>G c.534C>G (p.His178Gln) c.489C>G (p.His163Gln) c.377-2582C>G (n.377-2582C>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890192C>T | CA431416677 | WNT10A | c.585C>T (p.His195=) c.264-2582C>T c.534C>T (p.His178=) c.489C>T (p.His163=) c.377-2582C>T (n.377-2582C>T) | ClinVar dbSNP |
2 | g.218890193C>A | CA350586476 | WNT10A | c.586C>A (p.Pro196Thr) c.264-2581C>A c.535C>A (p.Pro179Thr) c.490C>A (p.Pro164Thr) c.377-2581C>A (n.377-2581C>A) | |
2 | g.218890193C= | CA1328965098 | WNT10A | c.586C= (p.Pro196=) c.264-2581C= c.535C= (p.Pro179=) c.490C= (p.Pro164=) c.377-2581C= (n.377-2581C=) | |
2 | g.218890193C>G | CA350586478 | WNT10A | c.586C>G (p.Pro196Ala) c.264-2581C>G c.535C>G (p.Pro179Ala) c.490C>G (p.Pro164Ala) c.377-2581C>G (n.377-2581C>G) | |
2 | g.218890193C>T | CA65916783 | WNT10A | c.586C>T (p.Pro196Ser) c.264-2581C>T c.535C>T (p.Pro179Ser) c.490C>T (p.Pro164Ser) c.377-2581C>T (n.377-2581C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890194C>A | CA350586483 | WNT10A | c.587C>A (p.Pro196Gln) c.264-2580C>A c.536C>A (p.Pro179Gln) c.491C>A (p.Pro164Gln) c.377-2580C>A (n.377-2580C>A) | dbSNP gnomAD v2 |
2 | g.218890194C= | CA1328965099 | WNT10A | c.587C= (p.Pro196=) c.264-2580C= c.536C= (p.Pro179=) c.491C= (p.Pro164=) c.377-2580C= (n.377-2580C=) | |
2 | g.218890194C>G | CA350586486 | WNT10A | c.587C>G (p.Pro196Arg) c.264-2580C>G c.536C>G (p.Pro179Arg) c.491C>G (p.Pro164Arg) c.377-2580C>G (n.377-2580C>G) | |
2 | g.218890194C>T | CA350586491 | WNT10A | c.587C>T (p.Pro196Leu) c.264-2580C>T c.536C>T (p.Pro179Leu) c.491C>T (p.Pro164Leu) c.377-2580C>T (n.377-2580C>T) | |
2 | g.218890195A>C | CA431416681 | WNT10A | c.588A>C (p.Pro196=) c.264-2579A>C c.537A>C (p.Pro179=) c.492A>C (p.Pro164=) c.377-2579A>C (n.377-2579A>C) | |
2 | g.218890195A>G | CA431416682 | WNT10A | c.588A>G (p.Pro196=) c.264-2579A>G c.537A>G (p.Pro179=) c.492A>G (p.Pro164=) c.377-2579A>G (n.377-2579A>G) | |
2 | g.218890195A>T | CA431416683 | WNT10A | c.588A>T (p.Pro196=) c.264-2579A>T c.537A>T (p.Pro179=) c.492A>T (p.Pro164=) c.377-2579A>T (n.377-2579A>T) | |
2 | g.218890196G>A | CA350586494 | WNT10A | c.589G>A (p.Ala197Thr) c.264-2578G>A c.538G>A (p.Ala180Thr) c.493G>A (p.Ala165Thr) c.377-2578G>A (n.377-2578G>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890196G>C | CA2113977 | WNT10A | c.589G>C (p.Ala197Pro) c.264-2578G>C c.538G>C (p.Ala180Pro) c.493G>C (p.Ala165Pro) c.377-2578G>C (n.377-2578G>C) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890196G= | CA1328965100 | WNT10A | c.589G= (p.Ala197=) c.264-2578G= c.538G= (p.Ala180=) c.493G= (p.Ala165=) c.377-2578G= (n.377-2578G=) | |
2 | g.218890196G>T | CA350586495 | WNT10A | c.589G>T (p.Ala197Ser) c.264-2578G>T c.538G>T (p.Ala180Ser) c.493G>T (p.Ala165Ser) c.377-2578G>T (n.377-2578G>T) | COSMIC |
2 | g.218890196dup | CA2663174290 | WNT10A | c.589dup (p.Ala197GlyfsTer30) c.264-2578dup c.538dup (p.Ala180GlyfsTer30) c.493dup (p.Ala165GlyfsTer30) c.377-2578dup (n.377-2578dup) | gnomAD v4 |
2 | g.218890197C>A | CA350586501 | WNT10A | c.590C>A (p.Ala197Asp) c.264-2577C>A c.539C>A (p.Ala180Asp) c.494C>A (p.Ala165Asp) c.377-2577C>A (n.377-2577C>A) | dbSNP |
2 | g.218890197C= | CA1328965101 | WNT10A | c.590C= (p.Ala197=) c.264-2577C= c.539C= (p.Ala180=) c.494C= (p.Ala165=) c.377-2577C= (n.377-2577C=) | |
2 | g.218890197C>G | CA350586502 | WNT10A | c.590C>G (p.Ala197Gly) c.264-2577C>G c.539C>G (p.Ala180Gly) c.494C>G (p.Ala165Gly) c.377-2577C>G (n.377-2577C>G) | |
2 | g.218890197C>T | CA350586505 | WNT10A | c.590C>T (p.Ala197Val) c.264-2577C>T c.539C>T (p.Ala180Val) c.494C>T (p.Ala165Val) c.377-2577C>T (n.377-2577C>T) | |
2 | g.218890198C>A | CA431416687 | WNT10A | c.591C>A (p.Ala197=) c.264-2576C>A c.540C>A (p.Ala180=) c.495C>A (p.Ala165=) c.377-2576C>A (n.377-2576C>A) | |
2 | g.218890198C= | CA1328965102 | WNT10A | c.591C= (p.Ala197=) c.264-2576C= c.540C= (p.Ala180=) c.495C= (p.Ala165=) c.377-2576C= (n.377-2576C=) | |
2 | g.218890198C>G | CA431416688 | WNT10A | c.591C>G (p.Ala197=) c.264-2576C>G c.540C>G (p.Ala180=) c.495C>G (p.Ala165=) c.377-2576C>G (n.377-2576C>G) | |
2 | g.218890198C>T | CA2113978 | WNT10A | c.591C>T (p.Ala197=) c.264-2576C>T c.540C>T (p.Ala180=) c.495C>T (p.Ala165=) c.377-2576C>T (n.377-2576C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890199C>A | CA350586515 | WNT10A | c.592C>A (p.Leu198Met) c.264-2575C>A c.541C>A (p.Leu181Met) c.496C>A (p.Leu166Met) c.377-2575C>A (n.377-2575C>A) | |
2 | g.218890199C= | CA1328965103 | WNT10A | c.592C= (p.Leu198=) c.264-2575C= c.541C= (p.Leu181=) c.496C= (p.Leu166=) c.377-2575C= (n.377-2575C=) | |
2 | g.218890199C>G | CA350586511 | WNT10A | c.592C>G (p.Leu198Val) c.264-2575C>G c.541C>G (p.Leu181Val) c.496C>G (p.Leu166Val) c.377-2575C>G (n.377-2575C>G) | gnomAD v4 |
2 | g.218890199C>T | CA431416690 | WNT10A | c.592C>T (p.Leu198=) c.264-2575C>T c.541C>T (p.Leu181=) c.496C>T (p.Leu166=) c.377-2575C>T (n.377-2575C>T) | dbSNP |
2 | g.218890200T>A | CA350586525 | WNT10A | c.593T>A (p.Leu198Gln) c.264-2574T>A c.542T>A (p.Leu181Gln) c.497T>A (p.Leu166Gln) c.377-2574T>A (n.377-2574T>A) | |
2 | g.218890200T>C | CA350586532 | WNT10A | c.593T>C (p.Leu198Pro) c.264-2574T>C c.542T>C (p.Leu181Pro) c.497T>C (p.Leu166Pro) c.377-2574T>C (n.377-2574T>C) | |
2 | g.218890200T>G | CA350586530 | WNT10A | c.593T>G (p.Leu198Arg) c.264-2574T>G c.542T>G (p.Leu181Arg) c.497T>G (p.Leu166Arg) c.377-2574T>G (n.377-2574T>G) | |
2 | g.218890201G>A | CA2113979 | WNT10A | c.594G>A (p.Leu198=) c.264-2573G>A c.543G>A (p.Leu181=) c.498G>A (p.Leu166=) c.377-2573G>A (n.377-2573G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890201G>C | CA431416693 | WNT10A | c.594G>C (p.Leu198=) c.264-2573G>C c.543G>C (p.Leu181=) c.498G>C (p.Leu166=) c.377-2573G>C (n.377-2573G>C) | gnomAD v4 |
2 | g.218890201G= | CA1328965104 | WNT10A | c.594G= (p.Leu198=) c.264-2573G= c.543G= (p.Leu181=) c.498G= (p.Leu166=) c.377-2573G= (n.377-2573G=) | |
2 | g.218890201G>T | CA431416692 | WNT10A | c.594G>T (p.Leu198=) c.264-2573G>T c.543G>T (p.Leu181=) c.498G>T (p.Leu166=) c.377-2573G>T (n.377-2573G>T) | |
2 | g.218890202C>A | CA350586541 | WNT10A | c.595C>A (p.Pro199Thr) c.264-2572C>A c.544C>A (p.Pro182Thr) c.499C>A (p.Pro167Thr) c.377-2572C>A (n.377-2572C>A) | |
2 | g.218890202C>G | CA350586537 | WNT10A | c.595C>G (p.Pro199Ala) c.264-2572C>G c.544C>G (p.Pro182Ala) c.499C>G (p.Pro167Ala) c.377-2572C>G (n.377-2572C>G) | gnomAD v4 |
2 | g.218890202C>T | CA350586539 | WNT10A | c.595C>T (p.Pro199Ser) c.264-2572C>T c.544C>T (p.Pro182Ser) c.499C>T (p.Pro167Ser) c.377-2572C>T (n.377-2572C>T) | gnomAD v4 COSMIC |
2 | g.218890203C>A | CA350586547 | WNT10A | c.596C>A (p.Pro199His) c.264-2571C>A c.545C>A (p.Pro182His) c.500C>A (p.Pro167His) c.377-2571C>A (n.377-2571C>A) | |
2 | g.218890203C= | CA1328965105 | WNT10A | c.596C= (p.Pro199=) c.264-2571C= c.545C= (p.Pro182=) c.500C= (p.Pro167=) c.377-2571C= (n.377-2571C=) | |
2 | g.218890203C>G | CA350586551 | WNT10A | c.596C>G (p.Pro199Arg) c.264-2571C>G c.545C>G (p.Pro182Arg) c.500C>G (p.Pro167Arg) c.377-2571C>G (n.377-2571C>G) | |
2 | g.218890203C>T | CA350586552 | WNT10A | c.596C>T (p.Pro199Leu) c.264-2571C>T c.545C>T (p.Pro182Leu) c.500C>T (p.Pro167Leu) c.377-2571C>T (n.377-2571C>T) | dbSNP gnomAD v4 |
2 | g.218890204C>A | CA431416697 | WNT10A | c.597C>A (p.Pro199=) c.264-2570C>A c.546C>A (p.Pro182=) c.501C>A (p.Pro167=) c.377-2570C>A (n.377-2570C>A) | |
2 | g.218890204C>G | CA431416698 | WNT10A | c.597C>G (p.Pro199=) c.264-2570C>G c.546C>G (p.Pro182=) c.501C>G (p.Pro167=) c.377-2570C>G (n.377-2570C>G) | |
2 | g.218890204C>T | CA431416699 | WNT10A | c.597C>T (p.Pro199=) c.264-2570C>T c.546C>T (p.Pro182=) c.501C>T (p.Pro167=) c.377-2570C>T (n.377-2570C>T) | gnomAD v4 |
2 | g.218890205A>C | CA350586557 | WNT10A | c.598A>C (p.Thr200Pro) c.264-2569A>C c.547A>C (p.Thr183Pro) c.502A>C (p.Thr168Pro) c.377-2569A>C (n.377-2569A>C) | |
2 | g.218890205A>G | CA350586558 | WNT10A | c.598A>G (p.Thr200Ala) c.264-2569A>G c.547A>G (p.Thr183Ala) c.502A>G (p.Thr168Ala) c.377-2569A>G (n.377-2569A>G) | |
2 | g.218890205A>T | CA350586559 | WNT10A | c.598A>T (p.Thr200Ser) c.264-2569A>T c.547A>T (p.Thr183Ser) c.502A>T (p.Thr168Ser) c.377-2569A>T (n.377-2569A>T) | |
2 | g.218890206C>A | CA350586560 | WNT10A | c.599C>A (p.Thr200Lys) c.264-2568C>A c.548C>A (p.Thr183Lys) c.503C>A (p.Thr168Lys) c.377-2568C>A (n.377-2568C>A) | |
2 | g.218890206C= | CA1328965106 | WNT10A | c.599C= (p.Thr200=) c.264-2568C= c.548C= (p.Thr183=) c.503C= (p.Thr168=) c.377-2568C= (n.377-2568C=) | |
2 | g.218890206C>G | CA350586563 | WNT10A | c.599C>G (p.Thr200Arg) c.264-2568C>G c.548C>G (p.Thr183Arg) c.503C>G (p.Thr168Arg) c.377-2568C>G (n.377-2568C>G) | dbSNP gnomAD v4 |
2 | g.218890206C>T | CA350586568 | WNT10A | c.599C>T (p.Thr200Ile) c.264-2568C>T c.548C>T (p.Thr183Ile) c.503C>T (p.Thr168Ile) c.377-2568C>T (n.377-2568C>T) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890207A>C | CA431416701 | WNT10A | c.600A>C (p.Thr200=) c.264-2567A>C c.549A>C (p.Thr183=) c.504A>C (p.Thr168=) c.377-2567A>C (n.377-2567A>C) | |
2 | g.218890207A>G | CA431416702 | WNT10A | c.600A>G (p.Thr200=) c.264-2567A>G c.549A>G (p.Thr183=) c.504A>G (p.Thr168=) c.377-2567A>G (n.377-2567A>G) | |
2 | g.218890207A>T | CA431416704 | WNT10A | c.600A>T (p.Thr200=) c.264-2567A>T c.549A>T (p.Thr183=) c.504A>T (p.Thr168=) c.377-2567A>T (n.377-2567A>T) | |
2 | g.218890208G>A | CA350586580 | WNT10A | c.601G>A (p.Ala201Thr) c.264-2566G>A c.550G>A (p.Ala184Thr) c.505G>A (p.Ala169Thr) c.377-2566G>A (n.377-2566G>A) | |
2 | g.218890208G>C | CA350586571 | WNT10A | c.601G>C (p.Ala201Pro) c.264-2566G>C c.550G>C (p.Ala184Pro) c.505G>C (p.Ala169Pro) c.377-2566G>C (n.377-2566G>C) | |
2 | g.218890208G>T | CA350586577 | WNT10A | c.601G>T (p.Ala201Ser) c.264-2566G>T c.550G>T (p.Ala184Ser) c.505G>T (p.Ala169Ser) c.377-2566G>T (n.377-2566G>T) | |
2 | g.218890209C>A | CA350586583 | WNT10A | c.602C>A (p.Ala201Asp) c.264-2565C>A c.551C>A (p.Ala184Asp) c.506C>A (p.Ala169Asp) c.377-2565C>A (n.377-2565C>A) | |
2 | g.218890209C>G | CA350586584 | WNT10A | c.602C>G (p.Ala201Gly) c.264-2565C>G c.551C>G (p.Ala184Gly) c.506C>G (p.Ala169Gly) c.377-2565C>G (n.377-2565C>G) | |
2 | g.218890209C>T | CA350586585 | WNT10A | c.602C>T (p.Ala201Val) c.264-2565C>T c.551C>T (p.Ala184Val) c.506C>T (p.Ala169Val) c.377-2565C>T (n.377-2565C>T) | |
2 | g.218890210C>A | CA431416707 | WNT10A | c.603C>A (p.Ala201=) c.264-2564C>A c.552C>A (p.Ala184=) c.507C>A (p.Ala169=) c.377-2564C>A (n.377-2564C>A) | |
2 | g.218890210C>G | CA431416709 | WNT10A | c.603C>G (p.Ala201=) c.264-2564C>G c.552C>G (p.Ala184=) c.507C>G (p.Ala169=) c.377-2564C>G (n.377-2564C>G) | |
2 | g.218890210C>T | CA431416711 | WNT10A | c.603C>T (p.Ala201=) c.264-2564C>T c.552C>T (p.Ala184=) c.507C>T (p.Ala169=) c.377-2564C>T (n.377-2564C>T) | |
2 | g.218890211del | CA2754310510 | WNT10A | c.604del (p.Ser202AlafsTer?) c.264-2563del c.553del (p.Ser185AlafsTer?) c.508del (p.Ser170AlafsTer?) c.377-2563del (n.377-2563del) | |
2 | g.218890211A>C | CA350586586 | WNT10A | c.604A>C (p.Ser202Arg) c.264-2563A>C c.553A>C (p.Ser185Arg) c.508A>C (p.Ser170Arg) c.377-2563A>C (n.377-2563A>C) | |
2 | g.218890211A>G | CA350586587 | WNT10A | c.604A>G (p.Ser202Gly) c.264-2563A>G c.553A>G (p.Ser185Gly) c.508A>G (p.Ser170Gly) c.377-2563A>G (n.377-2563A>G) | |
2 | g.218890211A>T | CA350586590 | WNT10A | c.604A>T (p.Ser202Cys) c.264-2563A>T c.553A>T (p.Ser185Cys) c.508A>T (p.Ser170Cys) c.377-2563A>T (n.377-2563A>T) | |
2 | g.218890212G>A | CA2113980 | WNT10A | c.605G>A (p.Ser202Asn) c.264-2562G>A c.554G>A (p.Ser185Asn) c.509G>A (p.Ser170Asn) c.377-2562G>A (n.377-2562G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.218890212G>C | CA350586598 | WNT10A | c.605G>C (p.Ser202Thr) c.264-2562G>C c.554G>C (p.Ser185Thr) c.509G>C (p.Ser170Thr) c.377-2562G>C (n.377-2562G>C) | |
2 | g.218890212G= | CA1328965107 | WNT10A | c.605G= (p.Ser202=) c.264-2562G= c.554G= (p.Ser185=) c.509G= (p.Ser170=) c.377-2562G= (n.377-2562G=) | |
2 | g.218890212G>T | CA350586601 | WNT10A | c.605G>T (p.Ser202Ile) c.264-2562G>T c.554G>T (p.Ser185Ile) c.509G>T (p.Ser170Ile) c.377-2562G>T (n.377-2562G>T) | |
2 | g.218890213C>A | CA350586602 | WNT10A | c.606C>A (p.Ser202Arg) c.264-2561C>A c.555C>A (p.Ser185Arg) c.510C>A (p.Ser170Arg) c.377-2561C>A (n.377-2561C>A) | |
2 | g.218890213C= | CA1328965108 | WNT10A | c.606C= (p.Ser202=) c.264-2561C= c.555C= (p.Ser185=) c.510C= (p.Ser170=) c.377-2561C= (n.377-2561C=) | |
2 | g.218890213C>G | CA350586603 | WNT10A | c.606C>G (p.Ser202Arg) c.264-2561C>G c.555C>G (p.Ser185Arg) c.510C>G (p.Ser170Arg) c.377-2561C>G (n.377-2561C>G) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218890213C>T | CA431416716 | WNT10A | c.606C>T (p.Ser202=) c.264-2561C>T c.555C>T (p.Ser185=) c.510C>T (p.Ser170=) c.377-2561C>T (n.377-2561C>T) | ClinVar dbSNP gnomAD v4 |
2 | g.218890214C>A | CA350586607 | WNT10A | c.607C>A (p.Pro203Thr) c.264-2560C>A c.556C>A (p.Pro186Thr) c.511C>A (p.Pro171Thr) c.377-2560C>A (n.377-2560C>A) | |
2 | g.218890214C>G | CA350586609 | WNT10A | c.607C>G (p.Pro203Ala) c.264-2560C>G c.556C>G (p.Pro186Ala) c.511C>G (p.Pro171Ala) c.377-2560C>G (n.377-2560C>G) | |
2 | g.218890214C>T | CA350586604 | WNT10A | c.607C>T (p.Pro203Ser) c.264-2560C>T c.556C>T (p.Pro186Ser) c.511C>T (p.Pro171Ser) c.377-2560C>T (n.377-2560C>T) | |
2 | g.218890215C>A | CA350586611 | WNT10A | c.608C>A (p.Pro203Gln) c.264-2559C>A c.557C>A (p.Pro186Gln) c.512C>A (p.Pro171Gln) c.377-2559C>A (n.377-2559C>A) | |
2 | g.218890215C>G | CA350586612 | WNT10A | c.608C>G (p.Pro203Arg) c.264-2559C>G c.557C>G (p.Pro186Arg) c.512C>G (p.Pro171Arg) c.377-2559C>G (n.377-2559C>G) | gnomAD v4 |
2 | g.218890215C>T | CA350586614 | WNT10A | c.608C>T (p.Pro203Leu) c.264-2559C>T c.557C>T (p.Pro186Leu) c.512C>T (p.Pro171Leu) c.377-2559C>T (n.377-2559C>T) | |
2 | g.218890216A= | CA1328965109 | WNT10A | c.609A= (p.Pro203=) c.264-2558A= c.558A= (p.Pro186=) c.513A= (p.Pro171=) c.377-2558A= (n.377-2558A=) | |
2 | g.218890216A>C | CA431416720 | WNT10A | c.609A>C (p.Pro203=) c.264-2558A>C c.558A>C (p.Pro186=) c.513A>C (p.Pro171=) c.377-2558A>C (n.377-2558A>C) | |
2 | g.218890216A>G | CA2113981 | WNT10A | c.609A>G (p.Pro203=) c.264-2558A>G c.558A>G (p.Pro186=) c.513A>G (p.Pro171=) c.377-2558A>G (n.377-2558A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890216A>T | CA431416721 | WNT10A | c.609A>T (p.Pro203=) c.264-2558A>T c.558A>T (p.Pro186=) c.513A>T (p.Pro171=) c.377-2558A>T (n.377-2558A>T) | |
2 | g.218890216_218890218del | CA2754310511 | WNT10A | c.609_611del (p.Gly204del) c.264-2558_264-2556del c.558_560del (p.Gly187del) c.513_515del (p.Gly172del) c.377-2558_377-2556del (n.377-2558_377-2556del) | |
2 | g.218890217G>A | CA350586617 | WNT10A | c.610G>A (p.Gly204Ser) c.264-2557G>A c.559G>A (p.Gly187Ser) c.514G>A (p.Gly172Ser) c.377-2557G>A (n.377-2557G>A) | COSMIC |
2 | g.218890217G>C | CA350586625 | WNT10A | c.610G>C (p.Gly204Arg) c.264-2557G>C c.559G>C (p.Gly187Arg) c.514G>C (p.Gly172Arg) c.377-2557G>C (n.377-2557G>C) | |
2 | g.218890217G>T | CA350586628 | WNT10A | c.610G>T (p.Gly204Cys) c.264-2557G>T c.559G>T (p.Gly187Cys) c.514G>T (p.Gly172Cys) c.377-2557G>T (n.377-2557G>T) | |
2 | g.218890218G>A | CA350586631 | WNT10A | c.611G>A (p.Gly204Asp) c.264-2556G>A c.560G>A (p.Gly187Asp) c.515G>A (p.Gly172Asp) c.377-2556G>A (n.377-2556G>A) | |
2 | g.218890218G>C | CA350586636 | WNT10A | c.611G>C (p.Gly204Ala) c.264-2556G>C c.560G>C (p.Gly187Ala) c.515G>C (p.Gly172Ala) c.377-2556G>C (n.377-2556G>C) | |
2 | g.218890218G>T | CA350586638 | WNT10A | c.611G>T (p.Gly204Val) c.264-2556G>T c.560G>T (p.Gly187Val) c.515G>T (p.Gly172Val) c.377-2556G>T (n.377-2556G>T) | |
2 | g.218890219C>A | CA431416725 | WNT10A | c.612C>A (p.Gly204=) c.264-2555C>A c.561C>A (p.Gly187=) c.516C>A (p.Gly172=) c.377-2555C>A (n.377-2555C>A) | ClinVar |
2 | g.218890219C>G | CA431416726 | WNT10A | c.612C>G (p.Gly204=) c.264-2555C>G c.561C>G (p.Gly187=) c.516C>G (p.Gly172=) c.377-2555C>G (n.377-2555C>G) | |
2 | g.218890219C>T | CA431416727 | WNT10A | c.612C>T (p.Gly204=) c.264-2555C>T c.561C>T (p.Gly187=) c.516C>T (p.Gly172=) c.377-2555C>T (n.377-2555C>T) | |
2 | g.218890220C>A | CA350586642 | WNT10A | c.613C>A (p.Leu205Met) c.264-2554C>A c.562C>A (p.Leu188Met) c.517C>A (p.Leu173Met) c.377-2554C>A (n.377-2554C>A) | |
2 | g.218890220C>G | CA350586646 | WNT10A | c.613C>G (p.Leu205Val) c.264-2554C>G c.562C>G (p.Leu188Val) c.517C>G (p.Leu173Val) c.377-2554C>G (n.377-2554C>G) | |
2 | g.218890220C>T | CA431416728 | WNT10A | c.613C>T (p.Leu205=) c.264-2554C>T c.562C>T (p.Leu188=) c.517C>T (p.Leu173=) c.377-2554C>T (n.377-2554C>T) | ClinVar dbSNP |
2 | g.218890220_218890226del | CA2754310512 | WNT10A | c.613_619del (p.Leu205ThrfsTer?) c.264-2554_264-2548del c.562_568del (p.Leu188ThrfsTer?) c.517_523del (p.Leu173ThrfsTer?) c.377-2554_377-2548del (n.377-2554_377-2548del) | |
2 | g.218890221T>A | CA350586655 | WNT10A | c.614T>A (p.Leu205Gln) c.264-2553T>A c.563T>A (p.Leu188Gln) c.518T>A (p.Leu173Gln) c.377-2553T>A (n.377-2553T>A) | |
2 | g.218890221T>C | CA350586658 | WNT10A | c.614T>C (p.Leu205Pro) c.264-2553T>C c.563T>C (p.Leu188Pro) c.518T>C (p.Leu173Pro) c.377-2553T>C (n.377-2553T>C) | |
2 | g.218890221T>G | CA350586650 | WNT10A | c.614T>G (p.Leu205Arg) c.264-2553T>G c.563T>G (p.Leu188Arg) c.518T>G (p.Leu173Arg) c.377-2553T>G (n.377-2553T>G) | |
2 | g.218890222G>A | CA431416732 | WNT10A | c.615G>A (p.Leu205=) c.264-2552G>A c.564G>A (p.Leu188=) c.519G>A (p.Leu173=) c.377-2552G>A (n.377-2552G>A) | dbSNP |
2 | g.218890222G>C | CA431416731 | WNT10A | c.615G>C (p.Leu205=) c.264-2552G>C c.564G>C (p.Leu188=) c.519G>C (p.Leu173=) c.377-2552G>C (n.377-2552G>C) | |
2 | g.218890222G>T | CA431416730 | WNT10A | c.615G>T (p.Leu205=) c.264-2552G>T c.564G>T (p.Leu188=) c.519G>T (p.Leu173=) c.377-2552G>T (n.377-2552G>T) | |
2 | g.218890223C>A | CA350586665 | WNT10A | c.616C>A (p.Gln206Lys) c.264-2551C>A c.565C>A (p.Gln189Lys) c.520C>A (p.Gln174Lys) c.377-2551C>A (n.377-2551C>A) | gnomAD v4 |
2 | g.218890223C= | CA1328965110 | WNT10A | c.616C= (p.Gln206=) c.264-2551C= c.565C= (p.Gln189=) c.520C= (p.Gln174=) c.377-2551C= (n.377-2551C=) | |
2 | g.218890223C>G | CA350586666 | WNT10A | c.616C>G (p.Gln206Glu) c.264-2551C>G c.565C>G (p.Gln189Glu) c.520C>G (p.Gln174Glu) c.377-2551C>G (n.377-2551C>G) | |
2 | g.218890223C>T | CA16616901 | WNT10A | c.616C>T (p.Gln206Ter) c.264-2551C>T c.565C>T (p.Gln189Ter) c.520C>T (p.Gln174Ter) c.377-2551C>T (n.377-2551C>T) | ClinVar dbSNP |
2 | g.218890224A>C | CA350586667 | WNT10A | c.617A>C (p.Gln206Pro) c.264-2550A>C c.566A>C (p.Gln189Pro) c.521A>C (p.Gln174Pro) c.377-2550A>C (n.377-2550A>C) | |
2 | g.218890224A>G | CA350586668 | WNT10A | c.617A>G (p.Gln206Arg) c.264-2550A>G c.566A>G (p.Gln189Arg) c.521A>G (p.Gln174Arg) c.377-2550A>G (n.377-2550A>G) | |
2 | g.218890224A>T | CA350586669 | WNT10A | c.617A>T (p.Gln206Leu) c.264-2550A>T c.566A>T (p.Gln189Leu) c.521A>T (p.Gln174Leu) c.377-2550A>T (n.377-2550A>T) | COSMIC |
2 | g.218890225G>A | CA431416735 | WNT10A | c.618G>A (p.Gln206=) c.264-2549G>A c.567G>A (p.Gln189=) c.522G>A (p.Gln174=) c.377-2549G>A (n.377-2549G>A) | dbSNP |
2 | g.218890225G>C | CA350586670 | WNT10A | c.618G>C (p.Gln206His) c.264-2549G>C c.567G>C (p.Gln189His) c.522G>C (p.Gln174His) c.377-2549G>C (n.377-2549G>C) | |
2 | g.218890225G= | CA1328965111 | WNT10A | c.618G= (p.Gln206=) c.264-2549G= c.567G= (p.Gln189=) c.522G= (p.Gln174=) c.377-2549G= (n.377-2549G=) | |
2 | g.218890225G>T | CA350586671 | WNT10A | c.618G>T (p.Gln206His) c.264-2549G>T c.567G>T (p.Gln189His) c.522G>T (p.Gln174His) c.377-2549G>T (n.377-2549G>T) | |
2 | g.218890226G>A | CA350586673 | WNT10A | c.619G>A (p.Asp207Asn) c.264-2548G>A c.568G>A (p.Asp190Asn) c.523G>A (p.Asp175Asn) c.377-2548G>A (n.377-2548G>A) | |
2 | g.218890226G>C | CA350586674 | WNT10A | c.619G>C (p.Asp207His) c.264-2548G>C c.568G>C (p.Asp190His) c.523G>C (p.Asp175His) c.377-2548G>C (n.377-2548G>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890226G= | CA1328965112 | WNT10A | c.619G= (p.Asp207=) c.264-2548G= c.568G= (p.Asp190=) c.523G= (p.Asp175=) c.377-2548G= (n.377-2548G=) | |
2 | g.218890226G>T | CA350586676 | WNT10A | c.619G>T (p.Asp207Tyr) c.264-2548G>T c.568G>T (p.Asp190Tyr) c.523G>T (p.Asp175Tyr) c.377-2548G>T (n.377-2548G>T) | dbSNP |
2 | g.218890227A>C | CA350586678 | WNT10A | c.620A>C (p.Asp207Ala) c.264-2547A>C c.569A>C (p.Asp190Ala) c.524A>C (p.Asp175Ala) c.377-2547A>C (n.377-2547A>C) | |
2 | g.218890227A>G | CA350586679 | WNT10A | c.620A>G (p.Asp207Gly) c.264-2547A>G c.569A>G (p.Asp190Gly) c.524A>G (p.Asp175Gly) c.377-2547A>G (n.377-2547A>G) | gnomAD v4 |
2 | g.218890227A>T | CA350586680 | WNT10A | c.620A>T (p.Asp207Val) c.264-2547A>T c.569A>T (p.Asp190Val) c.524A>T (p.Asp175Val) c.377-2547A>T (n.377-2547A>T) | |
2 | g.218890227_218890229del | CA2577276381 | WNT10A | c.620_622del (p.Asp207_Ser208delinsAla) c.264-2547_264-2545del c.569_571del (p.Asp190_Ser191delinsAla) c.524_526del (p.Asp175_Ser176delinsAla) c.377-2547_377-2545del (n.377-2547_377-2545del) | |
2 | g.218890228C>A | CA350586684 | WNT10A | c.621C>A (p.Asp207Glu) c.264-2546C>A c.570C>A (p.Asp190Glu) c.525C>A (p.Asp175Glu) c.377-2546C>A (n.377-2546C>A) | gnomAD v4 |
2 | g.218890228C>G | CA350586681 | WNT10A | c.621C>G (p.Asp207Glu) c.264-2546C>G c.570C>G (p.Asp190Glu) c.525C>G (p.Asp175Glu) c.377-2546C>G (n.377-2546C>G) | |
2 | g.218890228C>T | CA431416740 | WNT10A | c.621C>T (p.Asp207=) c.264-2546C>T c.570C>T (p.Asp190=) c.525C>T (p.Asp175=) c.377-2546C>T (n.377-2546C>T) | gnomAD v4 |
2 | g.218890229T>A | CA350586689 | WNT10A | c.622T>A (p.Ser208Thr) c.264-2545T>A c.571T>A (p.Ser191Thr) c.526T>A (p.Ser176Thr) c.377-2545T>A (n.377-2545T>A) | |
2 | g.218890229T>C | CA350586696 | WNT10A | c.622T>C (p.Ser208Pro) c.264-2545T>C c.571T>C (p.Ser191Pro) c.526T>C (p.Ser176Pro) c.377-2545T>C (n.377-2545T>C) | dbSNP gnomAD v2 gnomAD v4 |
2 | g.218890229T>G | CA350586691 | WNT10A | c.622T>G (p.Ser208Ala) c.264-2545T>G c.571T>G (p.Ser191Ala) c.526T>G (p.Ser176Ala) c.377-2545T>G (n.377-2545T>G) | |
2 | g.218890229T= | CA1328965113 | WNT10A | c.622T= (p.Ser208=) c.264-2545T= c.571T= (p.Ser191=) c.526T= (p.Ser176=) c.377-2545T= (n.377-2545T=) | |
2 | g.218890230C>A | CA350586702 | WNT10A | c.623C>A (p.Ser208Tyr) c.264-2544C>A c.572C>A (p.Ser191Tyr) c.527C>A (p.Ser176Tyr) c.377-2544C>A (n.377-2544C>A) | |
2 | g.218890230C= | CA1328965114 | WNT10A | c.623C= (p.Ser208=) c.264-2544C= c.572C= (p.Ser191=) c.527C= (p.Ser176=) c.377-2544C= (n.377-2544C=) | |
2 | g.218890230C>G | CA350586703 | WNT10A | c.623C>G (p.Ser208Cys) c.264-2544C>G c.572C>G (p.Ser191Cys) c.527C>G (p.Ser176Cys) c.377-2544C>G (n.377-2544C>G) | |
2 | g.218890230C>T | CA2113982 | WNT10A | c.623C>T (p.Ser208Phe) c.264-2544C>T c.572C>T (p.Ser191Phe) c.527C>T (p.Ser176Phe) c.377-2544C>T (n.377-2544C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.218890231C>A | CA431416743 | WNT10A | c.624C>A (p.Ser208=) c.264-2543C>A c.573C>A (p.Ser191=) c.528C>A (p.Ser176=) c.377-2543C>A (n.377-2543C>A) | |
2 | g.218890231C>G | CA431416745 | WNT10A | c.624C>G (p.Ser208=) c.264-2543C>G c.573C>G (p.Ser191=) c.528C>G (p.Ser176=) c.377-2543C>G (n.377-2543C>G) | |
2 | g.218890231C>T | CA431416746 | WNT10A | c.624C>T (p.Ser208=) c.264-2543C>T c.573C>T (p.Ser191=) c.528C>T (p.Ser176=) c.377-2543C>T (n.377-2543C>T) | |
2 | g.218890232T>A | CA350586717 | WNT10A | c.625T>A (p.Trp209Arg) c.264-2542T>A c.574T>A (p.Trp192Arg) c.529T>A (p.Trp177Arg) c.377-2542T>A (n.377-2542T>A) | |
2 | g.218890232T>C | CA350586721 | WNT10A | c.625T>C (p.Trp209Arg) c.264-2542T>C c.574T>C (p.Trp192Arg) c.529T>C (p.Trp177Arg) c.377-2542T>C (n.377-2542T>C) | |
2 | g.218890232T>G | CA350586726 | WNT10A | c.625T>G (p.Trp209Gly) c.264-2542T>G c.574T>G (p.Trp192Gly) c.529T>G (p.Trp177Gly) c.377-2542T>G (n.377-2542T>G) | |
2 | g.218890233G>A | CA350586729 | WNT10A | c.626G>A (p.Trp209Ter) c.264-2541G>A c.575G>A (p.Trp192Ter) c.530G>A (p.Trp177Ter) c.377-2541G>A (n.377-2541G>A) | |
2 | g.218890233G>C | CA350586730 | WNT10A | c.626G>C (p.Trp209Ser) c.264-2541G>C c.575G>C (p.Trp192Ser) c.530G>C (p.Trp177Ser) c.377-2541G>C (n.377-2541G>C) | |
2 | g.218890233G>T | CA350586731 | WNT10A | c.626G>T (p.Trp209Leu) c.264-2541G>T c.575G>T (p.Trp192Leu) c.530G>T (p.Trp177Leu) c.377-2541G>T (n.377-2541G>T) | |
2 | g.218890234G>A | CA350586738 | WNT10A | c.627G>A (p.Trp209Ter) c.264-2540G>A c.576G>A (p.Trp192Ter) c.531G>A (p.Trp177Ter) c.377-2540G>A (n.377-2540G>A) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890234G>C | CA350586740 | WNT10A | c.627G>C (p.Trp209Cys) c.264-2540G>C c.576G>C (p.Trp192Cys) c.531G>C (p.Trp177Cys) c.377-2540G>C (n.377-2540G>C) | |
2 | g.218890234G= | CA1328965115 | WNT10A | c.627G= (p.Trp209=) c.264-2540G= c.576G= (p.Trp192=) c.531G= (p.Trp177=) c.377-2540G= (n.377-2540G=) | |
2 | g.218890234G>T | CA350586742 | WNT10A | c.627G>T (p.Trp209Cys) c.264-2540G>T c.576G>T (p.Trp192Cys) c.531G>T (p.Trp177Cys) c.377-2540G>T (n.377-2540G>T) | |
2 | g.218890235G>A | CA350586752 | WNT10A | c.628G>A (p.Glu210Lys) c.264-2539G>A c.577G>A (p.Glu193Lys) c.532G>A (p.Glu178Lys) c.377-2539G>A (n.377-2539G>A) | |
2 | g.218890235G>C | CA350586750 | WNT10A | c.628G>C (p.Glu210Gln) c.264-2539G>C c.577G>C (p.Glu193Gln) c.532G>C (p.Glu178Gln) c.377-2539G>C (n.377-2539G>C) | |
2 | g.218890235G>T | CA350586751 | WNT10A | c.628G>T (p.Glu210Ter) c.264-2539G>T c.577G>T (p.Glu193Ter) c.532G>T (p.Glu178Ter) c.377-2539G>T (n.377-2539G>T) | |
2 | g.218890236A= | CA1328965116 | WNT10A | c.629A= (p.Glu210=) c.264-2538A= c.578A= (p.Glu193=) c.533A= (p.Glu178=) c.377-2538A= (n.377-2538A=) | |
2 | g.218890236A>C | CA350586757 | WNT10A | c.629A>C (p.Glu210Ala) c.264-2538A>C c.578A>C (p.Glu193Ala) c.533A>C (p.Glu178Ala) c.377-2538A>C (n.377-2538A>C) | |
2 | g.218890236A>G | CA350586766 | WNT10A | c.629A>G (p.Glu210Gly) c.264-2538A>G c.578A>G (p.Glu193Gly) c.533A>G (p.Glu178Gly) c.377-2538A>G (n.377-2538A>G) | gnomAD v4 |
2 | g.218890236A>T | CA350586768 | WNT10A | c.629A>T (p.Glu210Val) c.264-2538A>T c.578A>T (p.Glu193Val) c.533A>T (p.Glu178Val) c.377-2538A>T (n.377-2538A>T) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890237G>A | CA431416749 | WNT10A | c.630G>A (p.Glu210=) c.264-2537G>A c.579G>A (p.Glu193=) c.534G>A (p.Glu178=) c.377-2537G>A (n.377-2537G>A) | |
2 | g.218890237G>C | CA2113983 | WNT10A | c.630G>C (p.Glu210Asp) c.264-2537G>C c.579G>C (p.Glu193Asp) c.534G>C (p.Glu178Asp) c.377-2537G>C (n.377-2537G>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.218890237G= | CA1328965117 | WNT10A | c.630G= (p.Glu210=) c.264-2537G= c.579G= (p.Glu193=) c.534G= (p.Glu178=) c.377-2537G= (n.377-2537G=) | |
2 | g.218890237G>T | CA350586789 | WNT10A | c.630G>T (p.Glu210Asp) c.264-2537G>T c.579G>T (p.Glu193Asp) c.534G>T (p.Glu178Asp) c.377-2537G>T (n.377-2537G>T) | |
2 | g.218890238T>A | CA350586793 | WNT10A | c.631T>A (p.Trp211Arg) c.264-2536T>A c.580T>A (p.Trp194Arg) c.535T>A (p.Trp179Arg) c.377-2536T>A (n.377-2536T>A) | |
2 | g.218890238T>C | CA350586799 | WNT10A | c.631T>C (p.Trp211Arg) c.264-2536T>C c.580T>C (p.Trp194Arg) c.535T>C (p.Trp179Arg) c.377-2536T>C (n.377-2536T>C) | COSMIC |
2 | g.218890238T>G | CA350586800 | WNT10A | c.631T>G (p.Trp211Gly) c.264-2536T>G c.580T>G (p.Trp194Gly) c.535T>G (p.Trp179Gly) c.377-2536T>G (n.377-2536T>G) | |
2 | g.218890239G>A | CA350586801 | WNT10A | c.632G>A (p.Trp211Ter) c.264-2535G>A c.581G>A (p.Trp194Ter) c.536G>A (p.Trp179Ter) c.377-2535G>A (n.377-2535G>A) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.218890239G>C | CA350586802 | WNT10A | c.632G>C (p.Trp211Ser) c.264-2535G>C c.581G>C (p.Trp194Ser) c.536G>C (p.Trp179Ser) c.377-2535G>C (n.377-2535G>C) | |
2 | g.218890239G= | CA1328965118 | WNT10A | c.632G= (p.Trp211=) c.264-2535G= c.581G= (p.Trp194=) c.536G= (p.Trp179=) c.377-2535G= (n.377-2535G=) | |
2 | g.218890239G>T | CA350586803 | WNT10A | c.632G>T (p.Trp211Leu) c.264-2535G>T c.581G>T (p.Trp194Leu) c.536G>T (p.Trp179Leu) c.377-2535G>T (n.377-2535G>T) | |
2 | g.218890239_218890242del | CA2754310513 | WNT10A | c.632_635del (p.Trp211SerfsTer?) c.264-2535_264-2532del c.581_584del (p.Trp194SerfsTer?) c.536_539del (p.Trp179SerfsTer?) c.377-2535_377-2532del (n.377-2535_377-2532del) | |
2 | g.218890240G>A | CA350586815 | WNT10A | c.633G>A (p.Trp211Ter) c.264-2534G>A c.582G>A (p.Trp194Ter) c.537G>A (p.Trp179Ter) c.377-2534G>A (n.377-2534G>A) | dbSNP gnomAD v2 |
2 | g.218890240G>C | CA350586808 | WNT10A | c.633G>C (p.Trp211Cys) c.264-2534G>C c.582G>C (p.Trp194Cys) c.537G>C (p.Trp179Cys) c.377-2534G>C (n.377-2534G>C) | |
2 | g.218890240G= | CA1328965119 | WNT10A | c.633G= (p.Trp211=) c.264-2534G= c.582G= (p.Trp194=) c.537G= (p.Trp179=) c.377-2534G= (n.377-2534G=) | |
2 | g.218890240G>T | CA350586805 | WNT10A | c.633G>T (p.Trp211Cys) c.264-2534G>T c.582G>T (p.Trp194Cys) c.537G>T (p.Trp179Cys) c.377-2534G>T (n.377-2534G>T) | |
2 | g.218890241G>A | CA350586822 | WNT10A | c.634G>A (p.Gly212Ser) c.264-2533G>A c.583G>A (p.Gly195Ser) c.538G>A (p.Gly180Ser) c.377-2533G>A (n.377-2533G>A) | gnomAD v4 |
2 | g.218890241G>C | CA350586818 | WNT10A | c.634G>C (p.Gly212Arg) c.264-2533G>C c.583G>C (p.Gly195Arg) c.538G>C (p.Gly180Arg) c.377-2533G>C (n.377-2533G>C) | |
2 | g.218890241G>T | CA350586821 | WNT10A | c.634G>T (p.Gly212Cys) c.264-2533G>T c.583G>T (p.Gly195Cys) c.538G>T (p.Gly180Cys) c.377-2533G>T (n.377-2533G>T) | |
2 | g.218890242G>A | CA350586823 | WNT10A | c.635G>A (p.Gly212Asp) c.264-2532G>A c.584G>A (p.Gly195Asp) c.539G>A (p.Gly180Asp) c.377-2532G>A (n.377-2532G>A) | COSMIC |
2 | g.218890242G>C | CA350586824 | WNT10A | c.635G>C (p.Gly212Ala) c.264-2532G>C c.584G>C (p.Gly195Ala) c.539G>C (p.Gly180Ala) c.377-2532G>C (n.377-2532G>C) | |
2 | g.218890242G>T | CA350586827 | WNT10A | c.635G>T (p.Gly212Val) c.264-2532G>T c.584G>T (p.Gly195Val) c.539G>T (p.Gly180Val) c.377-2532G>T (n.377-2532G>T) | gnomAD v4 |
2 | g.218890243C>A | CA431416762 | WNT10A | c.636C>A (p.Gly212=) c.264-2531C>A c.585C>A (p.Gly195=) c.540C>A (p.Gly180=) c.377-2531C>A (n.377-2531C>A) | |
2 | g.218890243C= | CA1328965120 | WNT10A | c.636C= (p.Gly212=) c.264-2531C= c.585C= (p.Gly195=) c.540C= (p.Gly180=) c.377-2531C= (n.377-2531C=) | |
2 | g.218890243C>G | CA431416763 | WNT10A | c.636C>G (p.Gly212=) c.264-2531C>G c.585C>G (p.Gly195=) c.540C>G (p.Gly180=) c.377-2531C>G (n.377-2531C>G) | |
2 | g.218890243C>T | CA2113984 | WNT10A | c.636C>T (p.Gly212=) c.264-2531C>T c.585C>T (p.Gly195=) c.540C>T (p.Gly180=) c.377-2531C>T (n.377-2531C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.218890244G>A | CA211313 | WNT10A | c.637G>A (p.Gly213Ser) c.264-2530G>A c.586G>A (p.Gly196Ser) c.541G>A (p.Gly181Ser) c.377-2530G>A (n.377-2530G>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.218890244G>C | CA350586848 | WNT10A | c.637G>C (p.Gly213Arg) c.264-2530G>C c.586G>C (p.Gly196Arg) c.541G>C (p.Gly181Arg) c.377-2530G>C (n.377-2530G>C) | |
2 | g.218890244G= | CA1328965121 | WNT10A | c.637G= (p.Gly213=) c.264-2530G= c.586G= (p.Gly196=) c.541G= (p.Gly181=) c.377-2530G= (n.377-2530G=) | |
2 | g.218890244G>T | CA350586851 | WNT10A | c.637G>T (p.Gly213Cys) c.264-2530G>T c.586G>T (p.Gly196Cys) c.541G>T (p.Gly181Cys) c.377-2530G>T (n.377-2530G>T) | |
2 | g.218890244_218890245del | CA2754310514 | WNT10A | c.637_638del (p.Gly213LeufsTer13) c.264-2530_264-2529del c.586_587del (p.Gly196LeufsTer13) c.541_542del (p.Gly181LeufsTer13) c.377-2530_377-2529del (n.377-2530_377-2529del) | |
2 | g.218890245G>A | CA2113985 | WNT10A | c.638G>A (p.Gly213Asp) c.264-2529G>A c.587G>A (p.Gly196Asp) c.542G>A (p.Gly181Asp) c.377-2529G>A (n.377-2529G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.218890245G>C | CA350586856 | WNT10A | c.638G>C (p.Gly213Ala) c.264-2529G>C c.587G>C (p.Gly196Ala) c.542G>C (p.Gly181Ala) c.377-2529G>C (n.377-2529G>C) | |
2 | g.218890245G= | CA1328965122 | WNT10A | c.638G= (p.Gly213=) c.264-2529G= c.587G= (p.Gly196=) c.542G= (p.Gly181=) c.377-2529G= (n.377-2529G=) | |
2 | g.218890245G>T | CA350586860 | WNT10A | c.638G>T (p.Gly213Val) c.264-2529G>T c.587G>T (p.Gly196Val) c.542G>T (p.Gly181Val) c.377-2529G>T (n.377-2529G>T) | |
2 | g.218890246C>A | CA431416765 | WNT10A | c.639C>A (p.Gly213=) c.264-2528C>A c.588C>A (p.Gly196=) c.543C>A (p.Gly181=) c.377-2528C>A (n.377-2528C>A) | |
2 | g.218890246C>G | CA431416766 | WNT10A | c.639C>G (p.Gly213=) c.264-2528C>G c.588C>G (p.Gly196=) c.543C>G (p.Gly181=) c.377-2528C>G (n.377-2528C>G) | dbSNP |
2 | g.218890246C>T | CA431416767 | WNT10A | c.639C>T (p.Gly213=) c.264-2528C>T c.588C>T (p.Gly196=) c.543C>T (p.Gly181=) c.377-2528C>T (n.377-2528C>T) | |
2 | g.218890247T>A | CA350586865 | WNT10A | c.640T>A (p.Cys214Ser) c.264-2527T>A c.589T>A (p.Cys197Ser) c.544T>A (p.Cys182Ser) c.377-2527T>A (n.377-2527T>A) | |
2 | g.218890247T>C | CA350586864 | WNT10A | c.640T>C (p.Cys214Arg) c.264-2527T>C c.589T>C (p.Cys197Arg) c.544T>C (p.Cys182Arg) c.377-2527T>C (n.377-2527T>C) | ClinVar gnomAD v4 |
2 | g.218890247T>G | CA350586863 | WNT10A | c.640T>G (p.Cys214Gly) c.264-2527T>G c.589T>G (p.Cys197Gly) c.544T>G (p.Cys182Gly) c.377-2527T>G (n.377-2527T>G) | |
2 | g.218890249_218890261del | CA2663174291 | WNT10A | c.642_654del (p.Cys214TrpfsTer25) c.264-2525_264-2513del c.591_603del (p.Cys197TrpfsTer25) c.546_558del (p.Cys182TrpfsTer25) c.377-2525_377-2513del (n.377-2525_377-2513del) | gnomAD v4 |
2 | g.218890248G>A | CA350586866 | WNT10A | c.641G>A (p.Cys214Tyr) c.264-2526G>A c.590G>A (p.Cys197Tyr) c.545G>A (p.Cys182Tyr) c.377-2526G>A (n.377-2526G>A) | |
2 | g.218890248G>C | CA350586868 | WNT10A | c.641G>C (p.Cys214Ser) c.264-2526G>C c.590G>C (p.Cys197Ser) c.545G>C (p.Cys182Ser) c.377-2526G>C (n.377-2526G>C) | |
2 | g.218890248G>T | CA350586869 | WNT10A | c.641G>T (p.Cys214Phe) c.264-2526G>T c.590G>T (p.Cys197Phe) c.545G>T (p.Cys182Phe) c.377-2526G>T (n.377-2526G>T) | |
2 | g.218890249C>A | CA350586877 | WNT10A | c.642C>A (p.Cys214Ter) c.264-2525C>A c.591C>A (p.Cys197Ter) c.546C>A (p.Cys182Ter) c.377-2525C>A (n.377-2525C>A) | |
2 | g.218890249C= | CA1328965123 | WNT10A | c.642C= (p.Cys214=) c.264-2525C= c.591C= (p.Cys197=) c.546C= (p.Cys182=) c.377-2525C= (n.377-2525C=) | |
2 | g.218890249C>G | CA350586879 | WNT10A | c.642C>G (p.Cys214Trp) c.264-2525C>G c.591C>G (p.Cys197Trp) c.546C>G (p.Cys182Trp) c.377-2525C>G (n.377-2525C>G) | |
2 | g.218890249C>T | CA431416772 | WNT10A | c.642C>T (p.Cys214=) c.264-2525C>T c.591C>T (p.Cys197=) c.546C>T (p.Cys182=) c.377-2525C>T (n.377-2525C>T) | ClinVar dbSNP gnomAD v2 gnomAD v4 |