Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.218890162T>ACA431416618WNT10Ac.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)
2g.218890162T>CCA431416617WNT10Ac.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
2g.218890162T>GCA431416616WNT10Ac.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)
2g.218890163A>CCA350586255WNT10Ac.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)
2g.218890163A>GCA350586256WNT10Ac.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)
2g.218890163A>TCA350586257WNT10Ac.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)
2g.218890164A>CCA350586259WNT10Ac.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)
2g.218890164A>GCA350586262WNT10Ac.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)
2g.218890164A>TCA350586264WNT10Ac.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)
2g.218890165G>ACA2113968WNT10Ac.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
2g.218890165G>CCA350586266WNT10Ac.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)
2g.218890165G=CA1328965081WNT10Ac.558G= (p.Lys186=)
c.264-2609G=
c.507G= (p.Lys169=)
c.462G= (p.Lys154=)
c.377-2609G= (n.377-2609G=)
2g.218890165G>TCA350586267WNT10Ac.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)
2g.218890166G>ACA350586273WNT10Ac.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)
2g.218890166G>CCA350586272WNT10Ac.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)
2g.218890166G>TCA350586270WNT10Ac.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)
2g.218890167G>ACA350586276WNT10Ac.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
2g.218890167G>CCA350586279WNT10Ac.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)
2g.218890167G=CA1328965082WNT10Ac.560G= (p.Gly187=)
c.264-2607G=
c.509G= (p.Gly170=)
c.464G= (p.Gly155=)
c.377-2607G= (n.377-2607G=)
2g.218890167G>TCA2113969WNT10Ac.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
2g.218890168C>ACA431416629WNT10Ac.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)
2g.218890168C=CA1328965083WNT10Ac.561C= (p.Gly187=)
c.264-2606C=
c.510C= (p.Gly170=)
c.465C= (p.Gly155=)
c.377-2606C= (n.377-2606C=)
2g.218890168C>GCA431416630WNT10Ac.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)
2g.218890168C>TCA2113970WNT10Ac.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
2g.218890169C>ACA350586299WNT10Ac.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)
2g.218890169C>GCA350586302WNT10Ac.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)
2g.218890169C>TCA431416632WNT10Ac.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)
2g.218890170T>ACA350586304WNT10Ac.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)
2g.218890170T>CCA350586308WNT10Ac.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)
2g.218890170T>GCA350586314WNT10Ac.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
2g.218890170T=CA1328965084WNT10Ac.563T= (p.Leu188=)
c.264-2604T=
c.512T= (p.Leu171=)
c.467T= (p.Leu156=)
c.377-2604T= (n.377-2604T=)
2g.218890171G>ACA431416634WNT10Ac.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
2g.218890171G>CCA431416635WNT10Ac.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)
2g.218890171G>TCA431416636WNT10Ac.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)
2g.218890172A>CCA350586315WNT10Ac.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)
2g.218890172A>GCA350586316WNT10Ac.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)
2g.218890172A>TCA350586320WNT10Ac.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)
2g.218890173G>ACA350586326WNT10Ac.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
2g.218890173G>CCA350586329WNT10Ac.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)
2g.218890173G=CA1328965085WNT10Ac.566G= (p.Ser189=)
c.264-2601G=
c.515G= (p.Ser172=)
c.470G= (p.Ser157=)
c.377-2601G= (n.377-2601G=)
2g.218890173G>TCA350586327WNT10Ac.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)
2g.218890174C>ACA350586330WNT10Ac.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
2g.218890174C=CA1328965086WNT10Ac.567C= (p.Ser189=)
c.264-2600C=
c.516C= (p.Ser172=)
c.471C= (p.Ser157=)
c.377-2600C= (n.377-2600C=)
2g.218890174C>GCA350586331WNT10Ac.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)
2g.218890174C>TCA431416638WNT10Ac.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
2g.218890175C>ACA350586334WNT10Ac.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)
2g.218890175C>GCA350586335WNT10Ac.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)
2g.218890175C>TCA350586344WNT10Ac.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
2g.218890176A=CA1328965087WNT10Ac.569A= (p.His190=)
c.264-2598A=
c.518A= (p.His173=)
c.473A= (p.His158=)
c.377-2598A= (n.377-2598A=)
2g.218890176A>CCA350586348WNT10Ac.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)
2g.218890176A>GCA2113971WNT10Ac.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
2g.218890176A>TCA350586355WNT10Ac.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
2g.218890177T>ACA350586360WNT10Ac.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
2g.218890177T>CCA431416643WNT10Ac.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
2g.218890177T>GCA350586367WNT10Ac.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)
2g.218890177T=CA1328965088WNT10Ac.570T= (p.His190=)
c.264-2597T=
c.519T= (p.His173=)
c.474T= (p.His158=)
c.377-2597T= (n.377-2597T=)
2g.218890178G>ACA350586371WNT10Ac.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
2g.218890178G>CCA350586373WNT10Ac.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)
2g.218890178G=CA1328965089WNT10Ac.571G= (p.Gly191=)
c.264-2596G=
c.520G= (p.Gly174=)
c.475G= (p.Gly159=)
c.377-2596G= (n.377-2596G=)
2g.218890178G>TCA350586379WNT10Ac.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)
2g.218890181delCA2580065714WNT10Ac.574del (p.Val192SerfsTer?)
c.264-2593del
c.523del (p.Val175SerfsTer?)
c.478del (p.Val160SerfsTer?)
c.377-2593del (n.377-2593del)
 ClinVar
2g.218890179G>ACA350586384WNT10Ac.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
2g.218890179G>CCA2113972WNT10Ac.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
2g.218890179G=CA1328965090WNT10Ac.572G= (p.Gly191=)
c.264-2595G=
c.521G= (p.Gly174=)
c.476G= (p.Gly159=)
c.377-2595G= (n.377-2595G=)
2g.218890179G>TCA350586383WNT10Ac.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)
2g.218890180G>ACA65916760WNT10Ac.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
2g.218890180G>CCA431416648WNT10Ac.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)
2g.218890180G=CA1328965091WNT10Ac.573G= (p.Gly191=)
c.264-2594G=
c.522G= (p.Gly174=)
c.477G= (p.Gly159=)
c.377-2594G= (n.377-2594G=)
2g.218890180G>TCA431416650WNT10Ac.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
2g.218890181G>ACA350586385WNT10Ac.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
2g.218890181G>CCA350586386WNT10Ac.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)
2g.218890181G>TCA350586389WNT10Ac.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)
2g.218890182T>ACA350586392WNT10Ac.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
2g.218890182T>CCA350586396WNT10Ac.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)
2g.218890182T>GCA350586400WNT10Ac.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)
2g.218890182T=CA1328965092WNT10Ac.575T= (p.Val192=)
c.264-2592T=
c.524T= (p.Val175=)
c.479T= (p.Val160=)
c.377-2592T= (n.377-2592T=)
2g.218890183C>ACA431416656WNT10Ac.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)
2g.218890183C=CA1328965093WNT10Ac.576C= (p.Val192=)
c.264-2591C=
c.525C= (p.Val175=)
c.480C= (p.Val160=)
c.377-2591C= (n.377-2591C=)
2g.218890183C>GCA431416658WNT10Ac.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
2g.218890183C>TCA2113973WNT10Ac.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
2g.218890183_218890186delCA2550516589WNT10Ac.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)
2g.218890186_218890199delCA2586971347WNT10Ac.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)
2g.218890184C>ACA350586411WNT10Ac.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
2g.218890184C>GCA350586413WNT10Ac.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
2g.218890184C>TCA350586418WNT10Ac.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)
2g.218890185C>ACA350586424WNT10Ac.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)
2g.218890185C=CA1328965094WNT10Ac.578C= (p.Pro193=)
c.264-2589C=
c.527C= (p.Pro176=)
c.482C= (p.Pro161=)
c.377-2589C= (n.377-2589C=)
2g.218890185C>GCA2113975WNT10Ac.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
2g.218890185C>TCA2113974WNT10Ac.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
2g.218890186G>ACA2113976WNT10Ac.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
2g.218890186G>CCA431416666WNT10Ac.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)
2g.218890186G=CA1328965095WNT10Ac.579G= (p.Pro193=)
c.264-2588G=
c.528G= (p.Pro176=)
c.483G= (p.Pro161=)
c.377-2588G= (n.377-2588G=)
2g.218890186G>TCA431416667WNT10Ac.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)
2g.218890187delCA2573135230WNT10Ac.580del (p.Glu194AsnfsTer?)
c.264-2587del
c.529del (p.Glu177AsnfsTer?)
c.484del (p.Glu162AsnfsTer?)
c.377-2587del (n.377-2587del)
 ClinVar dbSNP
2g.218890187G>ACA350586436WNT10Ac.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)
2g.218890187G>CCA350586434WNT10Ac.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)
2g.218890187G>TCA350586435WNT10Ac.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)
2g.218890188A>CCA350586439WNT10Ac.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)
2g.218890188A>GCA350586440WNT10Ac.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)
2g.218890188A>TCA350586444WNT10Ac.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)
2g.218890189A>CCA350586446WNT10Ac.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)
2g.218890189A>GCA431416673WNT10Ac.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)
2g.218890189A>TCA350586448WNT10Ac.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)
2g.218890190C>ACA350586450WNT10Ac.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)
2g.218890190C>GCA350586452WNT10Ac.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)
2g.218890190C>TCA350586454WNT10Ac.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)
2g.218890191A=CA1328965096WNT10Ac.584A= (p.His195=)
c.264-2583A=
c.533A= (p.His178=)
c.488A= (p.His163=)
c.377-2583A= (n.377-2583A=)
2g.218890191A>CCA350586458WNT10Ac.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
2g.218890191A>GCA350586462WNT10Ac.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)
2g.218890191A>TCA350586465WNT10Ac.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)
2g.218890192C>ACA350586474WNT10Ac.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
2g.218890192C=CA1328965097WNT10Ac.585C= (p.His195=)
c.264-2582C=
c.534C= (p.His178=)
c.489C= (p.His163=)
c.377-2582C= (n.377-2582C=)
2g.218890192C>GCA350586470WNT10Ac.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
2g.218890192C>TCA431416677WNT10Ac.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
2g.218890193C>ACA350586476WNT10Ac.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)
2g.218890193C=CA1328965098WNT10Ac.586C= (p.Pro196=)
c.264-2581C=
c.535C= (p.Pro179=)
c.490C= (p.Pro164=)
c.377-2581C= (n.377-2581C=)
2g.218890193C>GCA350586478WNT10Ac.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)
2g.218890193C>TCA65916783WNT10Ac.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
2g.218890194C>ACA350586483WNT10Ac.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
2g.218890194C=CA1328965099WNT10Ac.587C= (p.Pro196=)
c.264-2580C=
c.536C= (p.Pro179=)
c.491C= (p.Pro164=)
c.377-2580C= (n.377-2580C=)
2g.218890194C>GCA350586486WNT10Ac.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)
2g.218890194C>TCA350586491WNT10Ac.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)
2g.218890195A>CCA431416681WNT10Ac.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)
2g.218890195A>GCA431416682WNT10Ac.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)
2g.218890195A>TCA431416683WNT10Ac.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)
2g.218890196G>ACA350586494WNT10Ac.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
2g.218890196G>CCA2113977WNT10Ac.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
2g.218890196G=CA1328965100WNT10Ac.589G= (p.Ala197=)
c.264-2578G=
c.538G= (p.Ala180=)
c.493G= (p.Ala165=)
c.377-2578G= (n.377-2578G=)
2g.218890196G>TCA350586495WNT10Ac.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
2g.218890196dupCA2663174290WNT10Ac.589dup (p.Ala197GlyfsTer30)
c.264-2578dup
c.538dup (p.Ala180GlyfsTer30)
c.493dup (p.Ala165GlyfsTer30)
c.377-2578dup (n.377-2578dup)
 gnomAD v4
2g.218890197C>ACA350586501WNT10Ac.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
2g.218890197C=CA1328965101WNT10Ac.590C= (p.Ala197=)
c.264-2577C=
c.539C= (p.Ala180=)
c.494C= (p.Ala165=)
c.377-2577C= (n.377-2577C=)
2g.218890197C>GCA350586502WNT10Ac.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)
2g.218890197C>TCA350586505WNT10Ac.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)
2g.218890198C>ACA431416687WNT10Ac.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)
2g.218890198C=CA1328965102WNT10Ac.591C= (p.Ala197=)
c.264-2576C=
c.540C= (p.Ala180=)
c.495C= (p.Ala165=)
c.377-2576C= (n.377-2576C=)
2g.218890198C>GCA431416688WNT10Ac.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)
2g.218890198C>TCA2113978WNT10Ac.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
2g.218890199C>ACA350586515WNT10Ac.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)
2g.218890199C=CA1328965103WNT10Ac.592C= (p.Leu198=)
c.264-2575C=
c.541C= (p.Leu181=)
c.496C= (p.Leu166=)
c.377-2575C= (n.377-2575C=)
2g.218890199C>GCA350586511WNT10Ac.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
2g.218890199C>TCA431416690WNT10Ac.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
2g.218890200T>ACA350586525WNT10Ac.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)
2g.218890200T>CCA350586532WNT10Ac.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)
2g.218890200T>GCA350586530WNT10Ac.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)
2g.218890201G>ACA2113979WNT10Ac.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
2g.218890201G>CCA431416693WNT10Ac.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
2g.218890201G=CA1328965104WNT10Ac.594G= (p.Leu198=)
c.264-2573G=
c.543G= (p.Leu181=)
c.498G= (p.Leu166=)
c.377-2573G= (n.377-2573G=)
2g.218890201G>TCA431416692WNT10Ac.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)
2g.218890202C>ACA350586541WNT10Ac.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)
2g.218890202C>GCA350586537WNT10Ac.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
2g.218890202C>TCA350586539WNT10Ac.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
2g.218890203C>ACA350586547WNT10Ac.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)
2g.218890203C=CA1328965105WNT10Ac.596C= (p.Pro199=)
c.264-2571C=
c.545C= (p.Pro182=)
c.500C= (p.Pro167=)
c.377-2571C= (n.377-2571C=)
2g.218890203C>GCA350586551WNT10Ac.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)
2g.218890203C>TCA350586552WNT10Ac.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
2g.218890204C>ACA431416697WNT10Ac.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)
2g.218890204C>GCA431416698WNT10Ac.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)
2g.218890204C>TCA431416699WNT10Ac.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
2g.218890205A>CCA350586557WNT10Ac.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)
2g.218890205A>GCA350586558WNT10Ac.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)
2g.218890205A>TCA350586559WNT10Ac.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)
2g.218890206C>ACA350586560WNT10Ac.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)
2g.218890206C=CA1328965106WNT10Ac.599C= (p.Thr200=)
c.264-2568C=
c.548C= (p.Thr183=)
c.503C= (p.Thr168=)
c.377-2568C= (n.377-2568C=)
2g.218890206C>GCA350586563WNT10Ac.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
2g.218890206C>TCA350586568WNT10Ac.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
2g.218890207A>CCA431416701WNT10Ac.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)
2g.218890207A>GCA431416702WNT10Ac.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)
2g.218890207A>TCA431416704WNT10Ac.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)
2g.218890208G>ACA350586580WNT10Ac.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)
2g.218890208G>CCA350586571WNT10Ac.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)
2g.218890208G>TCA350586577WNT10Ac.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)
2g.218890209C>ACA350586583WNT10Ac.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)
2g.218890209C>GCA350586584WNT10Ac.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)
2g.218890209C>TCA350586585WNT10Ac.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)
2g.218890210C>ACA431416707WNT10Ac.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)
2g.218890210C>GCA431416709WNT10Ac.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)
2g.218890210C>TCA431416711WNT10Ac.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)
2g.218890211delCA2754310510WNT10Ac.604del (p.Ser202AlafsTer?)
c.264-2563del
c.553del (p.Ser185AlafsTer?)
c.508del (p.Ser170AlafsTer?)
c.377-2563del (n.377-2563del)
2g.218890211A>CCA350586586WNT10Ac.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)
2g.218890211A>GCA350586587WNT10Ac.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)
2g.218890211A>TCA350586590WNT10Ac.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)
2g.218890212G>ACA2113980WNT10Ac.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
2g.218890212G>CCA350586598WNT10Ac.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)
2g.218890212G=CA1328965107WNT10Ac.605G= (p.Ser202=)
c.264-2562G=
c.554G= (p.Ser185=)
c.509G= (p.Ser170=)
c.377-2562G= (n.377-2562G=)
2g.218890212G>TCA350586601WNT10Ac.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)
2g.218890213C>ACA350586602WNT10Ac.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)
2g.218890213C=CA1328965108WNT10Ac.606C= (p.Ser202=)
c.264-2561C=
c.555C= (p.Ser185=)
c.510C= (p.Ser170=)
c.377-2561C= (n.377-2561C=)
2g.218890213C>GCA350586603WNT10Ac.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
2g.218890213C>TCA431416716WNT10Ac.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
2g.218890214C>ACA350586607WNT10Ac.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)
2g.218890214C>GCA350586609WNT10Ac.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)
2g.218890214C>TCA350586604WNT10Ac.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)
2g.218890215C>ACA350586611WNT10Ac.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)
2g.218890215C>GCA350586612WNT10Ac.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
2g.218890215C>TCA350586614WNT10Ac.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)
2g.218890216A=CA1328965109WNT10Ac.609A= (p.Pro203=)
c.264-2558A=
c.558A= (p.Pro186=)
c.513A= (p.Pro171=)
c.377-2558A= (n.377-2558A=)
2g.218890216A>CCA431416720WNT10Ac.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)
2g.218890216A>GCA2113981WNT10Ac.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
2g.218890216A>TCA431416721WNT10Ac.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)
2g.218890216_218890218delCA2754310511WNT10Ac.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)
2g.218890217G>ACA350586617WNT10Ac.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
2g.218890217G>CCA350586625WNT10Ac.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)
2g.218890217G>TCA350586628WNT10Ac.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)
2g.218890218G>ACA350586631WNT10Ac.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)
2g.218890218G>CCA350586636WNT10Ac.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)
2g.218890218G>TCA350586638WNT10Ac.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)
2g.218890219C>ACA431416725WNT10Ac.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
2g.218890219C>GCA431416726WNT10Ac.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)
2g.218890219C>TCA431416727WNT10Ac.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)
2g.218890220C>ACA350586642WNT10Ac.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)
2g.218890220C>GCA350586646WNT10Ac.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)
2g.218890220C>TCA431416728WNT10Ac.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
2g.218890220_218890226delCA2754310512WNT10Ac.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)
2g.218890221T>ACA350586655WNT10Ac.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)
2g.218890221T>CCA350586658WNT10Ac.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)
2g.218890221T>GCA350586650WNT10Ac.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)
2g.218890222G>ACA431416732WNT10Ac.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
2g.218890222G>CCA431416731WNT10Ac.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)
2g.218890222G>TCA431416730WNT10Ac.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)
2g.218890223C>ACA350586665WNT10Ac.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
2g.218890223C=CA1328965110WNT10Ac.616C= (p.Gln206=)
c.264-2551C=
c.565C= (p.Gln189=)
c.520C= (p.Gln174=)
c.377-2551C= (n.377-2551C=)
2g.218890223C>GCA350586666WNT10Ac.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)
2g.218890223C>TCA16616901WNT10Ac.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
2g.218890224A>CCA350586667WNT10Ac.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)
2g.218890224A>GCA350586668WNT10Ac.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)
2g.218890224A>TCA350586669WNT10Ac.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
2g.218890225G>ACA431416735WNT10Ac.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
2g.218890225G>CCA350586670WNT10Ac.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)
2g.218890225G=CA1328965111WNT10Ac.618G= (p.Gln206=)
c.264-2549G=
c.567G= (p.Gln189=)
c.522G= (p.Gln174=)
c.377-2549G= (n.377-2549G=)
2g.218890225G>TCA350586671WNT10Ac.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)
2g.218890226G>ACA350586673WNT10Ac.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)
2g.218890226G>CCA350586674WNT10Ac.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
2g.218890226G=CA1328965112WNT10Ac.619G= (p.Asp207=)
c.264-2548G=
c.568G= (p.Asp190=)
c.523G= (p.Asp175=)
c.377-2548G= (n.377-2548G=)
2g.218890226G>TCA350586676WNT10Ac.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
2g.218890227A>CCA350586678WNT10Ac.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)
2g.218890227A>GCA350586679WNT10Ac.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
2g.218890227A>TCA350586680WNT10Ac.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)
2g.218890227_218890229delCA2577276381WNT10Ac.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)
2g.218890228C>ACA350586684WNT10Ac.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
2g.218890228C>GCA350586681WNT10Ac.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)
2g.218890228C>TCA431416740WNT10Ac.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
2g.218890229T>ACA350586689WNT10Ac.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)
2g.218890229T>CCA350586696WNT10Ac.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
2g.218890229T>GCA350586691WNT10Ac.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)
2g.218890229T=CA1328965113WNT10Ac.622T= (p.Ser208=)
c.264-2545T=
c.571T= (p.Ser191=)
c.526T= (p.Ser176=)
c.377-2545T= (n.377-2545T=)
2g.218890230C>ACA350586702WNT10Ac.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)
2g.218890230C=CA1328965114WNT10Ac.623C= (p.Ser208=)
c.264-2544C=
c.572C= (p.Ser191=)
c.527C= (p.Ser176=)
c.377-2544C= (n.377-2544C=)
2g.218890230C>GCA350586703WNT10Ac.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)
2g.218890230C>TCA2113982WNT10Ac.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
2g.218890231C>ACA431416743WNT10Ac.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)
2g.218890231C>GCA431416745WNT10Ac.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)
2g.218890231C>TCA431416746WNT10Ac.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)
2g.218890232T>ACA350586717WNT10Ac.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)
2g.218890232T>CCA350586721WNT10Ac.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)
2g.218890232T>GCA350586726WNT10Ac.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)
2g.218890233G>ACA350586729WNT10Ac.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)
2g.218890233G>CCA350586730WNT10Ac.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)
2g.218890233G>TCA350586731WNT10Ac.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)
2g.218890234G>ACA350586738WNT10Ac.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
2g.218890234G>CCA350586740WNT10Ac.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)
2g.218890234G=CA1328965115WNT10Ac.627G= (p.Trp209=)
c.264-2540G=
c.576G= (p.Trp192=)
c.531G= (p.Trp177=)
c.377-2540G= (n.377-2540G=)
2g.218890234G>TCA350586742WNT10Ac.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)
2g.218890235G>ACA350586752WNT10Ac.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)
2g.218890235G>CCA350586750WNT10Ac.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)
2g.218890235G>TCA350586751WNT10Ac.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)
2g.218890236A=CA1328965116WNT10Ac.629A= (p.Glu210=)
c.264-2538A=
c.578A= (p.Glu193=)
c.533A= (p.Glu178=)
c.377-2538A= (n.377-2538A=)
2g.218890236A>CCA350586757WNT10Ac.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)
2g.218890236A>GCA350586766WNT10Ac.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
2g.218890236A>TCA350586768WNT10Ac.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
2g.218890237G>ACA431416749WNT10Ac.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)
2g.218890237G>CCA2113983WNT10Ac.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
2g.218890237G=CA1328965117WNT10Ac.630G= (p.Glu210=)
c.264-2537G=
c.579G= (p.Glu193=)
c.534G= (p.Glu178=)
c.377-2537G= (n.377-2537G=)
2g.218890237G>TCA350586789WNT10Ac.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)
2g.218890238T>ACA350586793WNT10Ac.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)
2g.218890238T>CCA350586799WNT10Ac.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
2g.218890238T>GCA350586800WNT10Ac.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)
2g.218890239G>ACA350586801WNT10Ac.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
2g.218890239G>CCA350586802WNT10Ac.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)
2g.218890239G=CA1328965118WNT10Ac.632G= (p.Trp211=)
c.264-2535G=
c.581G= (p.Trp194=)
c.536G= (p.Trp179=)
c.377-2535G= (n.377-2535G=)
2g.218890239G>TCA350586803WNT10Ac.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)
2g.218890239_218890242delCA2754310513WNT10Ac.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)
2g.218890240G>ACA350586815WNT10Ac.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
2g.218890240G>CCA350586808WNT10Ac.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)
2g.218890240G=CA1328965119WNT10Ac.633G= (p.Trp211=)
c.264-2534G=
c.582G= (p.Trp194=)
c.537G= (p.Trp179=)
c.377-2534G= (n.377-2534G=)
2g.218890240G>TCA350586805WNT10Ac.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)
2g.218890241G>ACA350586822WNT10Ac.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
2g.218890241G>CCA350586818WNT10Ac.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)
2g.218890241G>TCA350586821WNT10Ac.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)
2g.218890242G>ACA350586823WNT10Ac.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
2g.218890242G>CCA350586824WNT10Ac.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)
2g.218890242G>TCA350586827WNT10Ac.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
2g.218890243C>ACA431416762WNT10Ac.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)
2g.218890243C=CA1328965120WNT10Ac.636C= (p.Gly212=)
c.264-2531C=
c.585C= (p.Gly195=)
c.540C= (p.Gly180=)
c.377-2531C= (n.377-2531C=)
2g.218890243C>GCA431416763WNT10Ac.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)
2g.218890243C>TCA2113984WNT10Ac.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
2g.218890244G>ACA211313WNT10Ac.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
2g.218890244G>CCA350586848WNT10Ac.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)
2g.218890244G=CA1328965121WNT10Ac.637G= (p.Gly213=)
c.264-2530G=
c.586G= (p.Gly196=)
c.541G= (p.Gly181=)
c.377-2530G= (n.377-2530G=)
2g.218890244G>TCA350586851WNT10Ac.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)
2g.218890244_218890245delCA2754310514WNT10Ac.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)
2g.218890245G>ACA2113985WNT10Ac.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
2g.218890245G>CCA350586856WNT10Ac.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)
2g.218890245G=CA1328965122WNT10Ac.638G= (p.Gly213=)
c.264-2529G=
c.587G= (p.Gly196=)
c.542G= (p.Gly181=)
c.377-2529G= (n.377-2529G=)
2g.218890245G>TCA350586860WNT10Ac.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)
2g.218890246C>ACA431416765WNT10Ac.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)
2g.218890246C>GCA431416766WNT10Ac.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
2g.218890246C>TCA431416767WNT10Ac.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)
2g.218890247T>ACA350586865WNT10Ac.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)
2g.218890247T>CCA350586864WNT10Ac.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
2g.218890247T>GCA350586863WNT10Ac.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)
2g.218890249_218890261delCA2663174291WNT10Ac.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
2g.218890248G>ACA350586866WNT10Ac.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)
2g.218890248G>CCA350586868WNT10Ac.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)
2g.218890248G>TCA350586869WNT10Ac.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)
2g.218890249C>ACA350586877WNT10Ac.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)
2g.218890249C=CA1328965123WNT10Ac.642C= (p.Cys214=)
c.264-2525C=
c.591C= (p.Cys197=)
c.546C= (p.Cys182=)
c.377-2525C= (n.377-2525C=)
2g.218890249C>GCA350586879WNT10Ac.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)
2g.218890249C>TCA431416772WNT10Ac.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
2g.218890250A=CA1328965124WNT10Ac.643A= (p.Ser215=)
c.264-2524A=
c.592A= (p.Ser198=)
c.547A= (p.Ser183=)
c.377-2524A= (n.377-2524A=)
2g.218890250A>CCA350586890WNT10Ac.643A>C (p.Ser215Arg)
c.264-2524A>C
c.592A>C (p.Ser198Arg)
c.547A>C (p.Ser183Arg)
c.377-2524A>C (n.377-2524A>C)
2g.218890250A>GCA350586895WNT10Ac.643A>G (p.Ser215Gly)
c.264-2524A>G
c.592A>G (p.Ser198Gly)
c.547A>G (p.Ser183Gly)
c.377-2524A>G (n.377-2524A>G)
 dbSNP gnomAD v2 gnomAD v4
2g.218890250A>TCA350586897WNT10Ac.643A>T (p.Ser215Cys)
c.264-2524A>T
c.592A>T (p.Ser198Cys)
c.547A>T (p.Ser183Cys)
c.377-2524A>T (n.377-2524A>T)
2g.218890251G>ACA350586899WNT10Ac.644G>A (p.Ser215Asn)
c.264-2523G>A
c.593G>A (p.Ser198Asn)
c.548G>A (p.Ser183Asn)
c.377-2523G>A (n.377-2523G>A)
2g.218890251G>CCA350586900WNT10Ac.644G>C (p.Ser215Thr)
c.264-2523G>C
c.593G>C (p.Ser198Thr)
c.548G>C (p.Ser183Thr)
c.377-2523G>C (n.377-2523G>C)
 gnomAD v4
2g.218890251G>TCA350586902WNT10Ac.644G>T (p.Ser215Ile)
c.264-2523G>T
c.593G>T (p.Ser198Ile)
c.548G>T (p.Ser183Ile)
c.377-2523G>T (n.377-2523G>T)
 gnomAD v4
2g.218890251_218890256delinsCCCCCCA2586971348WNT10Ac.644_649delinsCCCCC (p.Ser215ThrfsTer28)
c.264-2523_264-2518delinsCCCCC
c.593_598delinsCCCCC (p.Ser198ThrfsTer28)
c.548_553delinsCCCCC (p.Ser183ThrfsTer28)
c.377-2523_377-2518delinsCCCCC (n.377-2523_377-2518delinsCCCCC)
2g.218890252C>ACA350586905WNT10Ac.645C>A (p.Ser215Arg)
c.264-2522C>A
c.594C>A (p.Ser198Arg)
c.549C>A (p.Ser183Arg)
c.377-2522C>A (n.377-2522C>A)
2g.218890252C>GCA350586907WNT10Ac.645C>G (p.Ser215Arg)
c.264-2522C>G
c.594C>G (p.Ser198Arg)
c.549C>G (p.Ser183Arg)
c.377-2522C>G (n.377-2522C>G)
2g.218890252C>TCA431416777WNT10Ac.645C>T (p.Ser215=)
c.264-2522C>T
c.594C>T (p.Ser198=)
c.549C>T (p.Ser183=)
c.377-2522C>T (n.377-2522C>T)
 ClinVar dbSNP gnomAD v4
2g.218890255delCA2499215665WNT10Ac.648del (p.Asp217ThrfsTer26)
c.264-2519del
c.597del (p.Asp200ThrfsTer26)
c.552del (p.Asp185ThrfsTer26)
c.377-2519del (n.377-2519del)
 ClinVar dbSNP
2g.218890253C>ACA350586909WNT10Ac.646C>A (p.Pro216Thr)
c.264-2521C>A
c.595C>A (p.Pro199Thr)
c.550C>A (p.Pro184Thr)
c.377-2521C>A (n.377-2521C>A)
2g.218890253C=CA1328965125WNT10Ac.646C= (p.Pro216=)
c.264-2521C=
c.595C= (p.Pro199=)
c.550C= (p.Pro184=)
c.377-2521C= (n.377-2521C=)
2g.218890253C>GCA350586912WNT10Ac.646C>G (p.Pro216Ala)
c.264-2521C>G
c.595C>G (p.Pro199Ala)
c.550C>G (p.Pro184Ala)
c.377-2521C>G (n.377-2521C>G)
 dbSNP
2g.218890253C>TCA350586908WNT10Ac.646C>T (p.Pro216Ser)
c.264-2521C>T
c.595C>T (p.Pro199Ser)
c.550C>T (p.Pro184Ser)
c.377-2521C>T (n.377-2521C>T)
 gnomAD v4 COSMIC
2g.218890254C>ACA350586915WNT10Ac.647C>A (p.Pro216His)
c.264-2520C>A
c.596C>A (p.Pro199His)
c.551C>A (p.Pro184His)
c.377-2520C>A (n.377-2520C>A)
2g.218890254C>GCA350586931WNT10Ac.647C>G (p.Pro216Arg)
c.264-2520C>G
c.596C>G (p.Pro199Arg)
c.551C>G (p.Pro184Arg)
c.377-2520C>G (n.377-2520C>G)
2g.218890254C>TCA350586918WNT10Ac.647C>T (p.Pro216Leu)
c.264-2520C>T
c.596C>T (p.Pro199Leu)
c.551C>T (p.Pro184Leu)
c.377-2520C>T (n.377-2520C>T)
 COSMIC
2g.218890255C>ACA431416783WNT10Ac.648C>A (p.Pro216=)
c.264-2519C>A
c.597C>A (p.Pro199=)
c.552C>A (p.Pro184=)
c.377-2519C>A (n.377-2519C>A)
2g.218890255C=CA1328965126WNT10Ac.648C= (p.Pro216=)
c.264-2519C=
c.597C= (p.Pro199=)
c.552C= (p.Pro184=)
c.377-2519C= (n.377-2519C=)
2g.218890255C>GCA431416784WNT10Ac.648C>G (p.Pro216=)
c.264-2519C>G
c.597C>G (p.Pro199=)
c.552C>G (p.Pro184=)
c.377-2519C>G (n.377-2519C>G)
2g.218890255C>TCA2113986WNT10Ac.648C>T (p.Pro216=)
c.264-2519C>T
c.597C>T (p.Pro199=)
c.552C>T (p.Pro184=)
c.377-2519C>T (n.377-2519C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890256G>ACA211283WNT10Ac.649G>A (p.Asp217Asn)
c.264-2518G>A
c.598G>A (p.Asp200Asn)
c.553G>A (p.Asp185Asn)
c.377-2518G>A (n.377-2518G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890256G>CCA350586936WNT10Ac.649G>C (p.Asp217His)
c.264-2518G>C
c.598G>C (p.Asp200His)
c.553G>C (p.Asp185His)
c.377-2518G>C (n.377-2518G>C)
2g.218890256G=CA1328965127WNT10Ac.649G= (p.Asp217=)
c.264-2518G=
c.598G= (p.Asp200=)
c.553G= (p.Asp185=)
c.377-2518G= (n.377-2518G=)
2g.218890256G>TCA350586937WNT10Ac.649G>T (p.Asp217Tyr)
c.264-2518G>T
c.598G>T (p.Asp200Tyr)
c.553G>T (p.Asp185Tyr)
c.377-2518G>T (n.377-2518G>T)
2g.218890257A=CA1328965128WNT10Ac.650A= (p.Asp217=)
c.264-2517A=
c.599A= (p.Asp200=)
c.554A= (p.Asp185=)
c.377-2517A= (n.377-2517A=)
2g.218890257A>CCA350586944WNT10Ac.650A>C (p.Asp217Ala)
c.264-2517A>C
c.599A>C (p.Asp200Ala)
c.554A>C (p.Asp185Ala)
c.377-2517A>C (n.377-2517A>C)
2g.218890257A>GCA16604387WNT10Ac.650A>G (p.Asp217Gly)
c.264-2517A>G
c.599A>G (p.Asp200Gly)
c.554A>G (p.Asp185Gly)
c.377-2517A>G (n.377-2517A>G)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.218890257A>TCA350586961WNT10Ac.650A>T (p.Asp217Val)
c.264-2517A>T
c.599A>T (p.Asp200Val)
c.554A>T (p.Asp185Val)
c.377-2517A>T (n.377-2517A>T)
2g.218890258C>ACA350586966WNT10Ac.651C>A (p.Asp217Glu)
c.264-2516C>A
c.600C>A (p.Asp200Glu)
c.555C>A (p.Asp185Glu)
c.377-2516C>A (n.377-2516C>A)
2g.218890258C>GCA350586967WNT10Ac.651C>G (p.Asp217Glu)
c.264-2516C>G
c.600C>G (p.Asp200Glu)
c.555C>G (p.Asp185Glu)
c.377-2516C>G (n.377-2516C>G)
2g.218890258C>TCA431416789WNT10Ac.651C>T (p.Asp217=)
c.264-2516C>T
c.600C>T (p.Asp200=)
c.555C>T (p.Asp185=)
c.377-2516C>T (n.377-2516C>T)
 gnomAD v4
2g.218890259A=CA1328965129WNT10Ac.652A= (p.Met218=)
c.264-2515A=
c.601A= (p.Met201=)
c.556A= (p.Met186=)
c.377-2515A= (n.377-2515A=)
2g.218890259A>CCA65916870WNT10Ac.652A>C (p.Met218Leu)
c.264-2515A>C
c.601A>C (p.Met201Leu)
c.556A>C (p.Met186Leu)
c.377-2515A>C (n.377-2515A>C)
 dbSNP gnomAD v2 gnomAD v4
2g.218890259A>GCA2113987WNT10Ac.652A>G (p.Met218Val)
c.264-2515A>G
c.601A>G (p.Met201Val)
c.556A>G (p.Met186Val)
c.377-2515A>G (n.377-2515A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890259A>TCA350586978WNT10Ac.652A>T (p.Met218Leu)
c.264-2515A>T
c.601A>T (p.Met201Leu)
c.556A>T (p.Met186Leu)
c.377-2515A>T (n.377-2515A>T)
2g.218890260T>ACA350586981WNT10Ac.653T>A (p.Met218Lys)
c.264-2514T>A
c.602T>A (p.Met201Lys)
c.557T>A (p.Met186Lys)
c.377-2514T>A (n.377-2514T>A)
2g.218890260T>CCA2113988WNT10Ac.653T>C (p.Met218Thr)
c.264-2514T>C
c.602T>C (p.Met201Thr)
c.557T>C (p.Met186Thr)
c.377-2514T>C (n.377-2514T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.218890260T>GCA350586982WNT10Ac.653T>G (p.Met218Arg)
c.264-2514T>G
c.602T>G (p.Met201Arg)
c.557T>G (p.Met186Arg)
c.377-2514T>G (n.377-2514T>G)
 ClinVar dbSNP
2g.218890260T=CA1328965139WNT10Ac.653T= (p.Met218=)
c.264-2514T=
c.602T= (p.Met201=)
c.557T= (p.Met186=)
c.377-2514T= (n.377-2514T=)
2g.218890261G>ACA65916878WNT10Ac.654G>A (p.Met218Ile)
c.264-2513G>A
c.603G>A (p.Met201Ile)
c.558G>A (p.Met186Ile)
c.377-2513G>A (n.377-2513G>A)
 dbSNP
2g.218890261G>CCA350586983WNT10Ac.654G>C (p.Met218Ile)
c.264-2513G>C
c.603G>C (p.Met201Ile)
c.558G>C (p.Met186Ile)
c.377-2513G>C (n.377-2513G>C)
2g.218890261G=CA1328965144WNT10Ac.654G= (p.Met218=)
c.264-2513G=
c.603G= (p.Met201=)
c.558G= (p.Met186=)
c.377-2513G= (n.377-2513G=)
2g.218890261G>TCA350586985WNT10Ac.654G>T (p.Met218Ile)
c.264-2513G>T
c.603G>T (p.Met201Ile)
c.558G>T (p.Met186Ile)
c.377-2513G>T (n.377-2513G>T)
2g.218890262G>ACA350586994WNT10Ac.655G>A (p.Gly219Ser)
c.264-2512G>A
c.604G>A (p.Gly202Ser)
c.559G>A (p.Gly187Ser)
c.377-2512G>A (n.377-2512G>A)
2g.218890262G>CCA350586997WNT10Ac.655G>C (p.Gly219Arg)
c.264-2512G>C
c.604G>C (p.Gly202Arg)
c.559G>C (p.Gly187Arg)
c.377-2512G>C (n.377-2512G>C)
2g.218890262G>TCA350587004WNT10Ac.655G>T (p.Gly219Cys)
c.264-2512G>T
c.604G>T (p.Gly202Cys)
c.559G>T (p.Gly187Cys)
c.377-2512G>T (n.377-2512G>T)

Number of alleles fetched