Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32434978_32434987delCA2695213677WT1c.376_385del (p.Gly126ArgfsTer?)
c.361_370del (p.Gly121ArgfsTer?)
n.555_564del
11g.32434986G>ACA064860WT1c.375C>T (p.Gly125=)
c.360C>T (p.Gly120=)
n.554C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434986G>CCA473773743WT1c.375C>G (p.Gly125=)
c.360C>G (p.Gly120=)
n.554C>G
 dbSNP
11g.32434986G=CA1962327256WT1c.375C= (p.Gly125=)
c.360C= (p.Gly120=)
n.554C=
11g.32434986G>TCA473773745WT1c.375C>A (p.Gly125=)
c.360C>A (p.Gly120=)
n.554C>A
 dbSNP gnomAD v4
11g.32434987C>ACA379965824WT1c.374G>T (p.Gly125Val)
c.359G>T (p.Gly120Val)
n.553G>T
11g.32434987C=CA1962327257WT1c.374G= (p.Gly125=)
c.359G= (p.Gly120=)
n.553G=
11g.32434987C>GCA379965822WT1c.374G>C (p.Gly125Ala)
c.359G>C (p.Gly120Ala)
n.553G>C
 dbSNP
11g.32434987C>TCA379965823WT1c.374G>A (p.Gly125Asp)
c.359G>A (p.Gly120Asp)
n.553G>A
 dbSNP gnomAD v4 COSMIC
11g.32434989delCA2612989553WT1c.374del (p.Gly125AlafsTer?)
c.359del (p.Gly120AlafsTer?)
n.553del
 gnomAD v4
11g.32434988C>ACA379965825WT1c.373G>T (p.Gly125Cys)
c.358G>T (p.Gly120Cys)
n.552G>T
11g.32434988C=CA1962327258WT1c.373G= (p.Gly125=)
c.358G= (p.Gly120=)
n.552G=
11g.32434988C>GCA379965826WT1c.373G>C (p.Gly125Arg)
c.358G>C (p.Gly120Arg)
n.552G>C
 dbSNP
11g.32434988C>TCA379965827WT1c.373G>A (p.Gly125Ser)
c.358G>A (p.Gly120Ser)
n.552G>A
 dbSNP gnomAD v2 gnomAD v4
11g.32434989C>ACA379965828WT1c.372G>T (p.Leu124Phe)
c.357G>T (p.Leu119Phe)
n.551G>T
 ClinVar
11g.32434989C>GCA379965829WT1c.372G>C (p.Leu124Phe)
c.357G>C (p.Leu119Phe)
n.551G>C
11g.32434989C>TCA473773753WT1c.372G>A (p.Leu124=)
c.357G>A (p.Leu119=)
n.551G>A
 gnomAD v4
11g.32434990A>CCA379965830WT1c.371T>G (p.Leu124Trp)
c.356T>G (p.Leu119Trp)
n.550T>G
 dbSNP
11g.32434990A>GCA379965831WT1c.371T>C (p.Leu124Ser)
c.356T>C (p.Leu119Ser)
n.550T>C
11g.32434990A>TCA379965832WT1c.371T>A (p.Leu124Ter)
c.356T>A (p.Leu119Ter)
n.550T>A
11g.32434991A>CCA379965833WT1c.370T>G (p.Leu124Val)
c.355T>G (p.Leu119Val)
n.549T>G
 dbSNP
11g.32434991A>GCA473773757WT1c.370T>C (p.Leu124=)
c.355T>C (p.Leu119=)
n.549T>C
 ClinVar gnomAD v4
11g.32434991A>TCA379965834WT1c.370T>A (p.Leu124Met)
c.355T>A (p.Leu119Met)
n.549T>A
11g.32434992C>ACA473773759WT1c.369G>T (p.Ser123=)
c.354G>T (p.Ser118=)
n.548G>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32434992C=CA1962327259WT1c.369G= (p.Ser123=)
c.354G= (p.Ser118=)
n.548G=
11g.32434992C>GCA473773761WT1c.369G>C (p.Ser123=)
c.354G>C (p.Ser118=)
n.548G>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434992C>TCA473773762WT1c.369G>A (p.Ser123=)
c.354G>A (p.Ser118=)
n.548G>A
 ClinVar dbSNP gnomAD v4
11g.32434993G>ACA379965835WT1c.368C>T (p.Ser123Leu)
c.353C>T (p.Ser118Leu)
n.547C>T
 ClinVar dbSNP
11g.32434993G>CCA379965836WT1c.368C>G (p.Ser123Trp)
c.353C>G (p.Ser118Trp)
n.547C>G
 dbSNP
11g.32434993G>TCA379965837WT1c.368C>A (p.Ser123Ter)
c.353C>A (p.Ser118Ter)
n.547C>A
 ClinVar gnomAD v4
11g.32434994A>CCA379965838WT1c.367T>G (p.Ser123Ala)
c.352T>G (p.Ser118Ala)
n.546T>G
 ClinVar dbSNP COSMIC COSMIC
11g.32434994A>GCA379965840WT1c.367T>C (p.Ser123Pro)
c.352T>C (p.Ser118Pro)
n.546T>C
 dbSNP
11g.32434994A>TCA379965839WT1c.367T>A (p.Ser123Thr)
c.352T>A (p.Ser118Thr)
n.546T>A
11g.32434995C>ACA473773767WT1c.366G>T (p.Gly122=)
c.351G>T (p.Gly117=)
n.545G>T
 ClinVar gnomAD v4
11g.32434995C=CA1962327260WT1c.366G= (p.Gly122=)
c.351G= (p.Gly117=)
n.545G=
11g.32434995C>GCA473773770WT1c.366G>C (p.Gly122=)
c.351G>C (p.Gly117=)
n.545G>C
 dbSNP
11g.32434995C>TCA473773768WT1c.366G>A (p.Gly122=)
c.351G>A (p.Gly117=)
n.545G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434996C>ACA379965841WT1c.365G>T (p.Gly122Val)
c.350G>T (p.Gly117Val)
n.544G>T
 gnomAD v4
11g.32434996C>GCA379965842WT1c.365G>C (p.Gly122Ala)
c.350G>C (p.Gly117Ala)
n.544G>C
11g.32434996C>TCA379965843WT1c.365G>A (p.Gly122Glu)
c.350G>A (p.Gly117Glu)
n.544G>A
 gnomAD v4
11g.32434997C>ACA379965844WT1c.364G>T (p.Gly122Trp)
c.349G>T (p.Gly117Trp)
n.543G>T
 gnomAD v4
11g.32434997C>GCA379965845WT1c.364G>C (p.Gly122Arg)
c.349G>C (p.Gly117Arg)
n.543G>C
 gnomAD v4
11g.32434997C>TCA379965846WT1c.364G>A (p.Gly122Arg)
c.349G>A (p.Gly117Arg)
n.543G>A
 gnomAD v4
11g.32434998G>ACA219511101WT1c.363C>T (p.Tyr121=)
c.348C>T (p.Tyr116=)
n.542C>T
 ClinVar dbSNP gnomAD v4
11g.32434998G>CCA379965847WT1c.363C>G (p.Tyr121Ter)
c.348C>G (p.Tyr116Ter)
n.542C>G
 dbSNP gnomAD v4 COSMIC
11g.32434998G=CA1962327261WT1c.363C= (p.Tyr121=)
c.348C= (p.Tyr116=)
n.542C=
11g.32434998G>TCA379965848WT1c.363C>A (p.Tyr121Ter)
c.348C>A (p.Tyr116Ter)
n.542C>A
 ClinVar gnomAD v4 COSMIC
11g.32434999T>ACA379965849WT1c.362A>T (p.Tyr121Phe)
c.347A>T (p.Tyr116Phe)
n.541A>T
11g.32434999T>CCA379965850WT1c.362A>G (p.Tyr121Cys)
c.347A>G (p.Tyr116Cys)
n.541A>G
 dbSNP
11g.32434999T>GCA379965851WT1c.362A>C (p.Tyr121Ser)
c.347A>C (p.Tyr116Ser)
n.541A>C
 dbSNP

Number of alleles fetched