Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.32434964_32434978dupCA1962327232WT1c.393_407dup (p.Pro136_Pro137insAlaProProProPro)
c.378_392dup (p.Pro131_Pro132insAlaProProProPro)
n.572_586dup
ClinVar dbSNP gnomAD v4
11g.32434964_32434978delCA2499220923WT1c.393_407del (p.Ala132_Pro136del)
c.378_392del (p.Ala127_Pro131del)
n.572_586del
ClinVar dbSNP gnomAD v4
11g.32434974_32434981delCA645584488WT1c.382_389del (p.Ala128ThrfsTer?)
c.367_374del (p.Ala123ThrfsTer?)
n.561_568del
COSMIC COSMIC
11g.32434978_32434987delCA2695213677WT1c.376_385del (p.Gly126ArgfsTer?)
c.361_370del (p.Gly121ArgfsTer?)
n.555_564del
11g.32434977C>ACA473773720WT1c.384G>T (p.Ala128=)
c.369G>T (p.Ala123=)
n.563G>T
11g.32434977C>GCA473773716WT1c.384G>C (p.Ala128=)
c.369G>C (p.Ala123=)
n.563G>C
dbSNP gnomAD v4
11g.32434977C>TCA473773718WT1c.384G>A (p.Ala128=)
c.369G>A (p.Ala123=)
n.563G>A
ClinVar dbSNP gnomAD v4
11g.32434978G>ACA379965804WT1c.383C>T (p.Ala128Val)
c.368C>T (p.Ala123Val)
n.562C>T
11g.32434978G>CCA379965805WT1c.383C>G (p.Ala128Gly)
c.368C>G (p.Ala123Gly)
n.562C>G
11g.32434978G=CA1962327250WT1c.383C= (p.Ala128=)
c.368C= (p.Ala123=)
n.562C=
11g.32434978G>TCA379965806WT1c.383C>A (p.Ala128Glu)
c.368C>A (p.Ala123Glu)
n.562C>A
ClinVar dbSNP gnomAD v4
11g.32434979C>ACA379965807WT1c.382G>T (p.Ala128Ser)
c.367G>T (p.Ala123Ser)
n.561G>T
11g.32434979C=CA1962327251WT1c.382G= (p.Ala128=)
c.367G= (p.Ala123=)
n.561G=
11g.32434979C>GCA379965809WT1c.382G>C (p.Ala128Pro)
c.367G>C (p.Ala123Pro)
n.561G>C
dbSNP
11g.32434979C>TCA379965808WT1c.382G>A (p.Ala128Thr)
c.367G>A (p.Ala123Thr)
n.561G>A
ClinVar dbSNP gnomAD v4 COSMIC COSMIC
11g.32434980G>ACA473773723WT1c.381C>T (p.Pro127=)
c.366C>T (p.Pro122=)
n.560C>T
ClinVar dbSNP gnomAD v4
11g.32434980G>CCA064867WT1c.381C>G (p.Pro127=)
c.366C>G (p.Pro122=)
n.560C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32434980G=CA1962327252WT1c.381C= (p.Pro127=)
c.366C= (p.Pro122=)
n.560C=
11g.32434980G>TCA473773725WT1c.381C>A (p.Pro127=)
c.366C>A (p.Pro122=)
n.560C>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32434983delCA2695201112WT1c.381del (p.Ala128ArgfsTer?)
c.366del (p.Ala123ArgfsTer?)
n.560del
ClinVar
11g.32434981G>ACA379965810WT1c.380C>T (p.Pro127Leu)
c.365C>T (p.Pro122Leu)
n.559C>T
ClinVar gnomAD v4
11g.32434981G>CCA379965811WT1c.380C>G (p.Pro127Arg)
c.365C>G (p.Pro122Arg)
n.559C>G
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32434981G=CA1962327253WT1c.380C= (p.Pro127=)
c.365C= (p.Pro122=)
n.559C=
11g.32434981G>TCA379965812WT1c.380C>A (p.Pro127His)
c.365C>A (p.Pro122His)
n.559C>A
gnomAD v4
11g.32434982G>ACA379965813WT1c.379C>T (p.Pro127Ser)
c.364C>T (p.Pro122Ser)
n.558C>T
ClinVar dbSNP gnomAD v4
11g.32434982G>CCA379965814WT1c.379C>G (p.Pro127Ala)
c.364C>G (p.Pro122Ala)
n.558C>G
11g.32434982G=CA1962327254WT1c.379C= (p.Pro127=)
c.364C= (p.Pro122=)
n.558C=
11g.32434982G>TCA379965815WT1c.379C>A (p.Pro127Thr)
c.364C>A (p.Pro122Thr)
n.558C>A
ClinVar dbSNP gnomAD v4
11g.32434983G>ACA473773732WT1c.378C>T (p.Gly126=)
c.363C>T (p.Gly121=)
n.557C>T
gnomAD v4
11g.32434983G>CCA473773734WT1c.378C>G (p.Gly126=)
c.363C>G (p.Gly121=)
n.557C>G
11g.32434983G>TCA473773736WT1c.378C>A (p.Gly126=)
c.363C>A (p.Gly121=)
n.557C>A
11g.32434984C>ACA379965816WT1c.377G>T (p.Gly126Val)
c.362G>T (p.Gly121Val)
n.556G>T
gnomAD v4
11g.32434984C>GCA379965818WT1c.377G>C (p.Gly126Ala)
c.362G>C (p.Gly121Ala)
n.556G>C
ClinVar dbSNP
11g.32434984C>TCA379965817WT1c.377G>A (p.Gly126Asp)
c.362G>A (p.Gly121Asp)
n.556G>A
ClinVar dbSNP gnomAD v4
11g.32434985C>ACA379965819WT1c.376G>T (p.Gly126Cys)
c.361G>T (p.Gly121Cys)
n.555G>T
ClinVar dbSNP gnomAD v4
11g.32434985C=CA1962327255WT1c.376G= (p.Gly126=)
c.361G= (p.Gly121=)
n.555G=
11g.32434985C>GCA379965820WT1c.376G>C (p.Gly126Arg)
c.361G>C (p.Gly121Arg)
n.555G>C
ClinVar dbSNP gnomAD v4
11g.32434985C>TCA379965821WT1c.376G>A (p.Gly126Ser)
c.361G>A (p.Gly121Ser)
n.555G>A
ClinVar dbSNP gnomAD v4
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
11g.32434999T=CA1962327262WT1c.362A= (p.Tyr121=)
c.347A= (p.Tyr116=)
n.541A=
11g.32435000A=CA1962327263WT1c.361T= (p.Tyr121=)
c.346T= (p.Tyr116=)
n.540T=
11g.32435000A>CCA219511102WT1c.361T>G (p.Tyr121Asp)
c.346T>G (p.Tyr116Asp)
n.540T>G
dbSNP
11g.32435000A>GCA379965853WT1c.361T>C (p.Tyr121His)
c.346T>C (p.Tyr116His)
n.540T>C
gnomAD v4
11g.32435000A>TCA379965852WT1c.361T>A (p.Tyr121Asn)
c.346T>A (p.Tyr116Asn)
n.540T>A
11g.32435001A>CCA473773778WT1c.360T>G (p.Ala120=)
c.345T>G (p.Ala115=)
n.539T>G
11g.32435001A>GCA473773779WT1c.360T>C (p.Ala120=)
c.345T>C (p.Ala115=)
n.539T>C
11g.32435001A>TCA473773780WT1c.360T>A (p.Ala120=)
c.345T>A (p.Ala115=)
n.539T>A
11g.32435002G>ACA379965854WT1c.359C>T (p.Ala120Val)
c.344C>T (p.Ala115Val)
n.538C>T
gnomAD v4
11g.32435002G>CCA379965855WT1c.359C>G (p.Ala120Gly)
c.344C>G (p.Ala115Gly)
n.538C>G
dbSNP
11g.32435002G>TCA379965856WT1c.359C>A (p.Ala120Asp)
c.344C>A (p.Ala115Asp)
n.538C>A
gnomAD v4
11g.32435003C>ACA379965857WT1c.358G>T (p.Ala120Ser)
c.343G>T (p.Ala115Ser)
n.537G>T
11g.32435003C=CA1962327264WT1c.358G= (p.Ala120=)
c.343G= (p.Ala115=)
n.537G=
11g.32435003C>GCA379965858WT1c.358G>C (p.Ala120Pro)
c.343G>C (p.Ala115Pro)
n.537G>C
dbSNP
11g.32435003C>TCA379965859WT1c.358G>A (p.Ala120Thr)
c.343G>A (p.Ala115Thr)
n.537G>A
ClinVar dbSNP gnomAD v4
11g.32435004C>ACA473773786WT1c.357G>T (p.Ser119=)
c.342G>T (p.Ser114=)
n.536G>T
ClinVar gnomAD v4
11g.32435004C=CA1962327265WT1c.357G= (p.Ser119=)
c.342G= (p.Ser114=)
n.536G=
11g.32435004C>GCA473773787WT1c.357G>C (p.Ser119=)
c.342G>C (p.Ser114=)
n.536G>C
dbSNP gnomAD v4
11g.32435004C>TCA473773788WT1c.357G>A (p.Ser119=)
c.342G>A (p.Ser114=)
n.536G>A
gnomAD v4
11g.32435005G>ACA379965860WT1c.356C>T (p.Ser119Leu)
c.341C>T (p.Ser114Leu)
n.535C>T
ClinVar gnomAD v4
11g.32435005G>CCA379965861WT1c.356C>G (p.Ser119Trp)
c.341C>G (p.Ser114Trp)
n.535C>G
ClinVar dbSNP
11g.32435005G=CA1962327266WT1c.356C= (p.Ser119=)
c.341C= (p.Ser114=)
n.535C=
11g.32435005G>TCA379965862WT1c.356C>A (p.Ser119Ter)
c.341C>A (p.Ser114Ter)
n.535C>A
COSMIC
11g.32435006A=CA1962327267WT1c.355T= (p.Ser119=)
c.340T= (p.Ser114=)
n.534T=
11g.32435006A>CCA379965863WT1c.355T>G (p.Ser119Ala)
c.340T>G (p.Ser114Ala)
n.534T>G
11g.32435006A>GCA379965864WT1c.355T>C (p.Ser119Pro)
c.340T>C (p.Ser114Pro)
n.534T>C
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435006A>TCA379965865WT1c.355T>A (p.Ser119Thr)
c.340T>A (p.Ser114Thr)
n.534T>A
gnomAD v4
11g.32435007A>CCA473773795WT1c.354T>G (p.Ala118=)
c.339T>G (p.Ala113=)
n.533T>G
dbSNP
11g.32435007A>GCA473773794WT1c.354T>C (p.Ala118=)
c.339T>C (p.Ala113=)
n.533T>C
dbSNP gnomAD v4
11g.32435007A>TCA473773793WT1c.354T>A (p.Ala118=)
c.339T>A (p.Ala113=)
n.533T>A
dbSNP
11g.32435008G>ACA064850WT1c.353C>T (p.Ala118Val)
c.338C>T (p.Ala113Val)
n.532C>T
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435008G>CCA379965867WT1c.353C>G (p.Ala118Gly)
c.338C>G (p.Ala113Gly)
n.532C>G
11g.32435008G=CA1962327268WT1c.353C= (p.Ala118=)
c.338C= (p.Ala113=)
n.532C=
11g.32435008G>TCA379965866WT1c.353C>A (p.Ala118Asp)
c.338C>A (p.Ala113Asp)
n.532C>A
gnomAD v4
11g.32435009C>ACA379965868WT1c.352G>T (p.Ala118Ser)
c.337G>T (p.Ala113Ser)
n.531G>T
gnomAD v4
11g.32435009C=CA1962327269WT1c.352G= (p.Ala118=)
c.337G= (p.Ala113=)
n.531G=
11g.32435009C>GCA379965870WT1c.352G>C (p.Ala118Pro)
c.337G>C (p.Ala113Pro)
n.531G>C
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435009C>TCA379965869WT1c.352G>A (p.Ala118Thr)
c.337G>A (p.Ala113Thr)
n.531G>A
ClinVar dbSNP gnomAD v4
11g.32435010G>ACA473773799WT1c.351C>T (p.Gly117=)
c.336C>T (p.Gly112=)
n.530C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435010G>CCA473773798WT1c.351C>G (p.Gly117=)
c.336C>G (p.Gly112=)
n.530C>G
11g.32435010G=CA1962327270WT1c.351C= (p.Gly117=)
c.336C= (p.Gly112=)
n.530C=
11g.32435010G>TCA473773797WT1c.351C>A (p.Gly117=)
c.336C>A (p.Gly112=)
n.530C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435011C>ACA379965871WT1c.350G>T (p.Gly117Val)
c.335G>T (p.Gly112Val)
n.529G>T
11g.32435011C=CA1962327271WT1c.350G= (p.Gly117=)
c.335G= (p.Gly112=)
n.529G=
11g.32435011C>GCA379965872WT1c.350G>C (p.Gly117Ala)
c.335G>C (p.Gly112Ala)
n.529G>C
dbSNP
11g.32435011C>TCA219511109WT1c.350G>A (p.Gly117Asp)
c.335G>A (p.Gly112Asp)
n.529G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435012C>ACA379965873WT1c.349G>T (p.Gly117Cys)
c.334G>T (p.Gly112Cys)
n.528G>T
gnomAD v4
11g.32435012C=CA1962327272WT1c.349G= (p.Gly117=)
c.334G= (p.Gly112=)
n.528G=
11g.32435012C>GCA379965875WT1c.349G>C (p.Gly117Arg)
c.334G>C (p.Gly112Arg)
n.528G>C
dbSNP
11g.32435012C>TCA379965874WT1c.349G>A (p.Gly117Ser)
c.334G>A (p.Gly112Ser)
n.528G>A
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435013C>ACA473773802WT1c.348G>T (p.Pro116=)
c.333G>T (p.Pro111=)
n.527G>T
gnomAD v4
11g.32435013C=CA1962327273WT1c.348G= (p.Pro116=)
c.333G= (p.Pro111=)
n.527G=
11g.32435013C>GCA473773804WT1c.348G>C (p.Pro116=)
c.333G>C (p.Pro111=)
n.527G>C
ClinVar dbSNP gnomAD v4
11g.32435013C>TCA473773803WT1c.348G>A (p.Pro116=)
c.333G>A (p.Pro111=)
n.527G>A
gnomAD v4
11g.32435014G>ACA10638965WT1c.347C>T (p.Pro116Leu)
c.332C>T (p.Pro111Leu)
n.526C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435014G>CCA379965877WT1c.347C>G (p.Pro116Arg)
c.332C>G (p.Pro111Arg)
n.526C>G
ClinVar dbSNP gnomAD v4
11g.32435014G=CA1962327274WT1c.347C= (p.Pro116=)
c.332C= (p.Pro111=)
n.526C=
11g.32435014G>TCA379965876WT1c.347C>A (p.Pro116Gln)
c.332C>A (p.Pro111Gln)
n.526C>A
gnomAD v4
11g.32435018dupCA2612989557WT1c.347dup (p.Ala118ArgfsTer?)
c.332dup (p.Ala113ArgfsTer?)
n.526dup
gnomAD v4
11g.32435018delCA2612989558WT1c.347del (p.Pro116ArgfsTer?)
c.332del (p.Pro111ArgfsTer?)
n.526del
gnomAD v4
11g.32435015G>ACA379965878WT1c.346C>T (p.Pro116Ser)
c.331C>T (p.Pro111Ser)
n.525C>T
11g.32435015G>CCA379965879WT1c.346C>G (p.Pro116Ala)
c.331C>G (p.Pro111Ala)
n.525C>G
11g.32435015G=CA1962327275WT1c.346C= (p.Pro116=)
c.331C= (p.Pro111=)
n.525C=
11g.32435015G>TCA379965880WT1c.346C>A (p.Pro116Thr)
c.331C>A (p.Pro111Thr)
n.525C>A
ClinVar dbSNP gnomAD v4
11g.32435015_32435016insACA2723467872WT1c.345_346insT (p.Pro116SerfsTer?)
c.330_331insT (p.Pro111SerfsTer?)
n.524_525insT
dbSNP
11g.32435016G>ACA017474WT1c.345C>T (p.Pro115=)
c.330C>T (p.Pro110=)
n.524C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435016G>CCA473773808WT1c.345C>G (p.Pro115=)
c.330C>G (p.Pro110=)
n.524C>G
dbSNP
11g.32435016G=CA1962327276WT1c.345C= (p.Pro115=)
c.330C= (p.Pro110=)
n.524C=
11g.32435016G>TCA473773809WT1c.345C>A (p.Pro115=)
c.330C>A (p.Pro110=)
n.524C>A
gnomAD v4
11g.32435017G>ACA379965881WT1c.344C>T (p.Pro115Leu)
c.329C>T (p.Pro110Leu)
n.523C>T
gnomAD v4
11g.32435017G>CCA379965882WT1c.344C>G (p.Pro115Arg)
c.329C>G (p.Pro110Arg)
n.523C>G
11g.32435017G=CA1962327277WT1c.344C= (p.Pro115=)
c.329C= (p.Pro110=)
n.523C=
11g.32435017G>TCA379965883WT1c.344C>A (p.Pro115His)
c.329C>A (p.Pro110His)
n.523C>A
ClinVar dbSNP gnomAD v4
11g.32435018G>ACA16613338WT1c.343C>T (p.Pro115Ser)
c.328C>T (p.Pro110Ser)
n.522C>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435018G>CCA379965884WT1c.343C>G (p.Pro115Ala)
c.328C>G (p.Pro110Ala)
n.522C>G
11g.32435018G=CA1962327278WT1c.343C= (p.Pro115=)
c.328C= (p.Pro110=)
n.522C=
11g.32435018G>TCA379965885WT1c.343C>A (p.Pro115Thr)
c.328C>A (p.Pro110Thr)
n.522C>A
ClinVar dbSNP
11g.32435019C>ACA473773813WT1c.342G>T (p.Ala114=)
c.327G>T (p.Ala109=)
n.521G>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435019C=CA1962327279WT1c.342G= (p.Ala114=)
c.327G= (p.Ala109=)
n.521G=
11g.32435019C>GCA473773814WT1c.342G>C (p.Ala114=)
c.327G>C (p.Ala109=)
n.521G>C
ClinVar dbSNP gnomAD v4
11g.32435019C>TCA473773815WT1c.342G>A (p.Ala114=)
c.327G>A (p.Ala109=)
n.521G>A
gnomAD v4
11g.32435020G>ACA379965888WT1c.341C>T (p.Ala114Val)
c.326C>T (p.Ala109Val)
n.520C>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435020G>CCA379965887WT1c.341C>G (p.Ala114Gly)
c.326C>G (p.Ala109Gly)
n.520C>G
gnomAD v4
11g.32435020G=CA1962327280WT1c.341C= (p.Ala114=)
c.326C= (p.Ala109=)
n.520C=
11g.32435020G>TCA379965886WT1c.341C>A (p.Ala114Glu)
c.326C>A (p.Ala109Glu)
n.520C>A
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435021C>ACA379965889WT1c.340G>T (p.Ala114Ser)
c.325G>T (p.Ala109Ser)
n.519G>T
gnomAD v4
11g.32435021C=CA1962327281WT1c.340G= (p.Ala114=)
c.325G= (p.Ala109=)
n.519G=
11g.32435021C>GCA379965890WT1c.340G>C (p.Ala114Pro)
c.325G>C (p.Ala109Pro)
n.519G>C
11g.32435021C>TCA379965891WT1c.340G>A (p.Ala114Thr)
c.325G>A (p.Ala109Thr)
n.519G>A
ClinVar dbSNP gnomAD v4
11g.32435022A>CCA379965892WT1c.339T>G (p.Phe113Leu)
c.324T>G (p.Phe108Leu)
n.518T>G
gnomAD v4
11g.32435022A>GCA473773817WT1c.339T>C (p.Phe113=)
c.324T>C (p.Phe108=)
n.518T>C
ClinVar dbSNP gnomAD v4
11g.32435022A>TCA379965893WT1c.339T>A (p.Phe113Leu)
c.324T>A (p.Phe108Leu)
n.518T>A
11g.32435022_32435023insGGCAACA645584490WT1c.339_340insTGCCT (p.Ala114CysfsTer?)
c.324_325insTGCCT (p.Ala109CysfsTer?)
n.518_519insTGCCT
COSMIC COSMIC
11g.32435024dupCA645584489WT1c.339dup (p.Ala114CysfsTer?)
c.324dup (p.Ala109CysfsTer?)
n.518dup
COSMIC
11g.32435024delCA2695213678WT1c.339del (p.Phe113LeufsTer?)
c.324del (p.Phe108LeufsTer?)
n.518del
11g.32435022_32435023insTCA473773819WT1c.338_339insA (p.Phe113LeufsTer?)
c.323_324insA (p.Phe108LeufsTer?)
n.517_518insA
11g.32435023A>CCA379965894WT1c.338T>G (p.Phe113Cys)
c.323T>G (p.Phe108Cys)
n.517T>G
11g.32435023A>GCA379965895WT1c.338T>C (p.Phe113Ser)
c.323T>C (p.Phe108Ser)
n.517T>C
ClinVar gnomAD v4
11g.32435023A>TCA379965896WT1c.338T>A (p.Phe113Tyr)
c.323T>A (p.Phe108Tyr)
n.517T>A
ClinVar
11g.32435024A=CA1962327282WT1c.337T= (p.Phe113=)
c.322T= (p.Phe108=)
n.516T=
11g.32435024A>CCA379965897WT1c.337T>G (p.Phe113Val)
c.322T>G (p.Phe108Val)
n.516T>G
11g.32435024A>GCA379965898WT1c.337T>C (p.Phe113Leu)
c.322T>C (p.Phe108Leu)
n.516T>C
dbSNP
11g.32435024A>TCA379965899WT1c.337T>A (p.Phe113Ile)
c.322T>A (p.Phe108Ile)
n.516T>A
11g.32435025G>ACA473773824WT1c.336C>T (p.Asp112=)
c.321C>T (p.Asp107=)
n.515C>T
ClinVar dbSNP gnomAD v4
11g.32435025G>CCA379965901WT1c.336C>G (p.Asp112Glu)
c.321C>G (p.Asp107Glu)
n.515C>G
dbSNP
11g.32435025G>TCA379965900WT1c.336C>A (p.Asp112Glu)
c.321C>A (p.Asp107Glu)
n.515C>A
gnomAD v4
11g.32435026T>ACA379965902WT1c.335A>T (p.Asp112Val)
c.320A>T (p.Asp107Val)
n.514A>T
dbSNP
11g.32435026T>CCA379965903WT1c.335A>G (p.Asp112Gly)
c.320A>G (p.Asp107Gly)
n.514A>G
dbSNP
11g.32435026T>GCA379965904WT1c.335A>C (p.Asp112Ala)
c.320A>C (p.Asp107Ala)
n.514A>C
dbSNP
11g.32435026_32435027delinsTCCA1962327283WT1c.334_335delinsGA (p.Asp112=)
c.319_320delinsGA (p.Asp107=)
n.513_514delinsGA
11g.32435027C>ACA379965905WT1c.334G>T (p.Asp112Tyr)
c.319G>T (p.Asp107Tyr)
n.513G>T
gnomAD v4
11g.32435027C=CA1962327284WT1c.334G= (p.Asp112=)
c.319G= (p.Asp107=)
n.513G=
11g.32435027C>GCA379965906WT1c.334G>C (p.Asp112His)
c.319G>C (p.Asp107His)
n.513G>C
11g.32435027C>TCA379965907WT1c.334G>A (p.Asp112Asn)
c.319G>A (p.Asp107Asn)
n.513G>A
dbSNP
11g.32435028delCA658658040WT1c.334del (p.Asp112ThrfsTer?)
c.319del (p.Asp107ThrfsTer?)
n.513del
ClinVar dbSNP gnomAD v4
11g.32435028C>ACA473773832WT1c.333G>T (p.Leu111=)
c.318G>T (p.Leu106=)
n.512G>T
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435028C=CA1962327285WT1c.333G= (p.Leu111=)
c.318G= (p.Leu106=)
n.512G=
11g.32435028C>GCA473773833WT1c.333G>C (p.Leu111=)
c.318G>C (p.Leu106=)
n.512G>C
11g.32435028C>TCA473773834WT1c.333G>A (p.Leu111=)
c.318G>A (p.Leu106=)
n.512G>A
gnomAD v4
11g.32435029delCA2695202566WT1c.332del (p.Leu111ArgfsTer?)
c.317del (p.Leu106ArgfsTer?)
n.511del
11g.32435029A>CCA379965910WT1c.332T>G (p.Leu111Arg)
c.317T>G (p.Leu106Arg)
n.511T>G
dbSNP
11g.32435029A>GCA379965908WT1c.332T>C (p.Leu111Pro)
c.317T>C (p.Leu106Pro)
n.511T>C
ClinVar gnomAD v4
11g.32435029A>TCA379965909WT1c.332T>A (p.Leu111Gln)
c.317T>A (p.Leu106Gln)
n.511T>A
11g.32435030G>ACA473773836WT1c.331C>T (p.Leu111=)
c.316C>T (p.Leu106=)
n.510C>T
ClinVar dbSNP gnomAD v4
11g.32435030G>CCA379965911WT1c.331C>G (p.Leu111Val)
c.316C>G (p.Leu106Val)
n.510C>G
dbSNP
11g.32435030G>TCA379965912WT1c.331C>A (p.Leu111Met)
c.316C>A (p.Leu106Met)
n.510C>A
gnomAD v4
11g.32435031C>ACA473773838WT1c.330G>T (p.Val110=)
c.315G>T (p.Val105=)
n.509G>T
gnomAD v4
11g.32435031C>GCA473773839WT1c.330G>C (p.Val110=)
c.315G>C (p.Val105=)
n.509G>C
11g.32435031C>TCA473773840WT1c.330G>A (p.Val110=)
c.315G>A (p.Val105=)
n.509G>A
ClinVar
11g.32435032A=CA1962327286WT1c.329T= (p.Val110=)
c.314T= (p.Val105=)
n.508T=
11g.32435032A>CCA379965913WT1c.329T>G (p.Val110Gly)
c.314T>G (p.Val105Gly)
n.508T>G
dbSNP
11g.32435032A>GCA379965914WT1c.329T>C (p.Val110Ala)
c.314T>C (p.Val105Ala)
n.508T>C
ClinVar dbSNP gnomAD v4
11g.32435032A>TCA379965915WT1c.329T>A (p.Val110Glu)
c.314T>A (p.Val105Glu)
n.508T>A
gnomAD v4
11g.32435033C>ACA379965916WT1c.328G>T (p.Val110Leu)
c.313G>T (p.Val105Leu)
n.507G>T
ClinVar gnomAD v4
11g.32435033C>GCA379965918WT1c.328G>C (p.Val110Leu)
c.313G>C (p.Val105Leu)
n.507G>C
11g.32435033C>TCA379965917WT1c.328G>A (p.Val110Met)
c.313G>A (p.Val105Met)
n.507G>A
gnomAD v4
11g.32435034C>ACA473773843WT1c.327G>T (p.Pro109=)
c.312G>T (p.Pro104=)
n.506G>T
dbSNP gnomAD v2 gnomAD v4
11g.32435034C=CA1962327287WT1c.327G= (p.Pro109=)
c.312G= (p.Pro104=)
n.506G=
11g.32435034C>GCA064841WT1c.327G>C (p.Pro109=)
c.312G>C (p.Pro104=)
n.506G>C
ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
11g.32435034C>TCA473773842WT1c.327G>A (p.Pro109=)
c.312G>A (p.Pro104=)
n.506G>A
ClinVar dbSNP gnomAD v4
11g.32435035G>ACA379965919WT1c.326C>T (p.Pro109Leu)
c.311C>T (p.Pro104Leu)
n.505C>T
gnomAD v4
11g.32435035G>CCA379965920WT1c.326C>G (p.Pro109Arg)
c.311C>G (p.Pro104Arg)
n.505C>G
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435035G=CA1962327288WT1c.326C= (p.Pro109=)
c.311C= (p.Pro104=)
n.505C=
11g.32435035G>TCA379965921WT1c.326C>A (p.Pro109Gln)
c.311C>A (p.Pro104Gln)
n.505C>A
ClinVar dbSNP gnomAD v4
11g.32435036G>ACA379965922WT1c.325C>T (p.Pro109Ser)
c.310C>T (p.Pro104Ser)
n.504C>T
ClinVar dbSNP gnomAD v4
11g.32435036G>CCA379965923WT1c.325C>G (p.Pro109Ala)
c.310C>G (p.Pro104Ala)
n.504C>G
ClinVar dbSNP
11g.32435036G>TCA379965924WT1c.325C>A (p.Pro109Thr)
c.310C>A (p.Pro104Thr)
n.504C>A
gnomAD v4
11g.32435037C>ACA473773846WT1c.324G>T (p.Ala108=)
c.309G>T (p.Ala103=)
n.503G>T
dbSNP gnomAD v2 gnomAD v4
11g.32435037C=CA1962327289WT1c.324G= (p.Ala108=)
c.309G= (p.Ala103=)
n.503G=
11g.32435037C>GCA473773847WT1c.324G>C (p.Ala108=)
c.309G>C (p.Ala103=)
n.503G>C
11g.32435037C>TCA473773849WT1c.324G>A (p.Ala108=)
c.309G>A (p.Ala103=)
n.503G>A
ClinVar dbSNP gnomAD v4
11g.32435038G>ACA379965925WT1c.323C>T (p.Ala108Val)
c.308C>T (p.Ala103Val)
n.502C>T
dbSNP gnomAD v4
11g.32435038G>CCA379965926WT1c.323C>G (p.Ala108Gly)
c.308C>G (p.Ala103Gly)
n.502C>G
dbSNP gnomAD v4
11g.32435038G>TCA379965927WT1c.323C>A (p.Ala108Glu)
c.308C>A (p.Ala103Glu)
n.502C>A
gnomAD v4
11g.32435039C>ACA379965930WT1c.322G>T (p.Ala108Ser)
c.307G>T (p.Ala103Ser)
n.501G>T
gnomAD v4
11g.32435039C=CA1962327290WT1c.322G= (p.Ala108=)
c.307G= (p.Ala103=)
n.501G=
11g.32435039C>GCA379965929WT1c.322G>C (p.Ala108Pro)
c.307G>C (p.Ala103Pro)
n.501G>C
11g.32435039C>TCA379965928WT1c.322G>A (p.Ala108Thr)
c.307G>A (p.Ala103Thr)
n.501G>A
ClinVar dbSNP gnomAD v4
11g.32435040C>ACA379965931WT1c.321G>T (p.Trp107Cys)
c.306G>T (p.Trp102Cys)
n.500G>T
11g.32435040C>GCA379965933WT1c.321G>C (p.Trp107Cys)
c.306G>C (p.Trp102Cys)
n.500G>C
11g.32435040C>TCA379965932WT1c.321G>A (p.Trp107Ter)
c.306G>A (p.Trp102Ter)
n.500G>A
gnomAD v3 gnomAD v4
11g.32435041C>ACA219511154WT1c.320G>T (p.Trp107Leu)
c.305G>T (p.Trp102Leu)
n.499G>T
ClinVar dbSNP gnomAD v4
11g.32435041C=CA1962327291WT1c.320G= (p.Trp107=)
c.305G= (p.Trp102=)
n.499G=
11g.32435041C>GCA379965934WT1c.320G>C (p.Trp107Ser)
c.305G>C (p.Trp102Ser)
n.499G>C
11g.32435041C>TCA379965935WT1c.320G>A (p.Trp107Ter)
c.305G>A (p.Trp102Ter)
n.499G>A
gnomAD v4
11g.32435042A=CA1962327292WT1c.319T= (p.Trp107=)
c.304T= (p.Trp102=)
n.498T=
11g.32435042A>CCA379965936WT1c.319T>G (p.Trp107Gly)
c.304T>G (p.Trp102Gly)
n.498T>G
ClinVar dbSNP
11g.32435042A>GCA379965937WT1c.319T>C (p.Trp107Arg)
c.304T>C (p.Trp102Arg)
n.498T>C
11g.32435042A>TCA379965938WT1c.319T>A (p.Trp107Arg)
c.304T>A (p.Trp102Arg)
n.498T>A
11g.32435043C>ACA379965939WT1c.318G>T (p.Gln106His)
c.303G>T (p.Gln101His)
n.497G>T
gnomAD v4
11g.32435043C>GCA379965940WT1c.318G>C (p.Gln106His)
c.303G>C (p.Gln101His)
n.497G>C
11g.32435043C>TCA473773857WT1c.318G>A (p.Gln106=)
c.303G>A (p.Gln101=)
n.497G>A
ClinVar gnomAD v4
11g.32435044_32435048dupCA2573146229WT1c.314_318dup (p.Trp107ArgfsTer?)
c.299_303dup (p.Trp102ArgfsTer?)
n.493_497dup
ClinVar dbSNP
11g.32435044T>ACA379965941WT1c.317A>T (p.Gln106Leu)
c.302A>T (p.Gln101Leu)
n.496A>T
dbSNP
11g.32435044T>CCA379965942WT1c.317A>G (p.Gln106Arg)
c.302A>G (p.Gln101Arg)
n.496A>G
dbSNP gnomAD v4
11g.32435044T>GCA379965943WT1c.317A>C (p.Gln106Pro)
c.302A>C (p.Gln101Pro)
n.496A>C
11g.32435044T=CA1962327293WT1c.317A= (p.Gln106=)
c.302A= (p.Gln101=)
n.496A=
11g.32435045G>ACA379965945WT1c.316C>T (p.Gln106Ter)
c.301C>T (p.Gln101Ter)
n.495C>T
gnomAD v4 COSMIC COSMIC
11g.32435045G>CCA379965944WT1c.316C>G (p.Gln106Glu)
c.301C>G (p.Gln101Glu)
n.495C>G
11g.32435045G=CA1962327294WT1c.316C= (p.Gln106=)
c.301C= (p.Gln101=)
n.495C=
11g.32435045G>TCA064832WT1c.316C>A (p.Gln106Lys)
c.301C>A (p.Gln101Lys)
n.495C>A
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435046C>ACA473773863WT1c.315G>T (p.Ala105=)
c.300G>T (p.Ala100=)
n.494G>T
ClinVar dbSNP gnomAD v4
11g.32435046C=CA1962327295WT1c.315G= (p.Ala105=)
c.300G= (p.Ala100=)
n.494G=
11g.32435046C>GCA473773866WT1c.315G>C (p.Ala105=)
c.300G>C (p.Ala100=)
n.494G>C
11g.32435046C>TCA473773865WT1c.315G>A (p.Ala105=)
c.300G>A (p.Ala100=)
n.494G>A
ClinVar dbSNP gnomAD v4
11g.32435047G>ACA379965946WT1c.314C>T (p.Ala105Val)
c.299C>T (p.Ala100Val)
n.493C>T
dbSNP gnomAD v4
11g.32435047G>CCA219511175WT1c.314C>G (p.Ala105Gly)
c.299C>G (p.Ala100Gly)
n.493C>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435047G=CA1962327296WT1c.314C= (p.Ala105=)
c.299C= (p.Ala100=)
n.493C=
11g.32435047G>TCA379965947WT1c.314C>A (p.Ala105Glu)
c.299C>A (p.Ala100Glu)
n.493C>A
ClinVar dbSNP gnomAD v4
11g.32435048C>ACA379965948WT1c.313G>T (p.Ala105Ser)
c.298G>T (p.Ala100Ser)
n.492G>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435048C=CA1962327297WT1c.313G= (p.Ala105=)
c.298G= (p.Ala100=)
n.492G=
11g.32435048C>GCA379965949WT1c.313G>C (p.Ala105Pro)
c.298G>C (p.Ala100Pro)
n.492G>C
11g.32435048C>TCA379965950WT1c.313G>A (p.Ala105Thr)
c.298G>A (p.Ala100Thr)
n.492G>A
ClinVar dbSNP gnomAD v4
11g.32435049C>ACA473773876WT1c.312G>T (p.Ala104=)
c.297G>T (p.Ala99=)
n.491G>T
ClinVar gnomAD v4
11g.32435049C=CA1962327298WT1c.312G= (p.Ala104=)
c.297G= (p.Ala99=)
n.491G=
11g.32435049C>GCA473773878WT1c.312G>C (p.Ala104=)
c.297G>C (p.Ala99=)
n.491G>C
11g.32435049C>TCA473773879WT1c.312G>A (p.Ala104=)
c.297G>A (p.Ala99=)
n.491G>A
ClinVar dbSNP gnomAD v4
11g.32435050G>ACA379965951WT1c.311C>T (p.Ala104Val)
c.296C>T (p.Ala99Val)
n.490C>T
ClinVar gnomAD v4 COSMIC
11g.32435050G>CCA219511188WT1c.311C>G (p.Ala104Gly)
c.296C>G (p.Ala99Gly)
n.490C>G
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435050G=CA1962327299WT1c.311C= (p.Ala104=)
c.296C= (p.Ala99=)
n.490C=
11g.32435050G>TCA379965952WT1c.311C>A (p.Ala104Glu)
c.296C>A (p.Ala99Glu)
n.490C>A
gnomAD v4
11g.32435051C>ACA379965953WT1c.310G>T (p.Ala104Ser)
c.295G>T (p.Ala99Ser)
n.489G>T
gnomAD v4
11g.32435051C=CA1962327300WT1c.310G= (p.Ala104=)
c.295G= (p.Ala99=)
n.489G=
11g.32435051C>GCA379965954WT1c.310G>C (p.Ala104Pro)
c.295G>C (p.Ala99Pro)
n.489G>C
dbSNP
11g.32435051C>TCA379965955WT1c.310G>A (p.Ala104Thr)
c.295G>A (p.Ala99Thr)
n.489G>A
ClinVar dbSNP gnomAD v4
11g.32435051dupCA2723468786WT1c.310dup (p.Ala104GlyfsTer?)
c.295dup (p.Ala99GlyfsTer?)
n.489dup
dbSNP
11g.32435052G>ACA473773888WT1c.309C>T (p.Gly103=)
c.294C>T (p.Gly98=)
n.488C>T
dbSNP gnomAD v4
11g.32435052G>CCA473773889WT1c.309C>G (p.Gly103=)
c.294C>G (p.Gly98=)
n.488C>G
dbSNP
11g.32435052G=CA1962327301WT1c.309C= (p.Gly103=)
c.294C= (p.Gly98=)
n.488C=
11g.32435052G>TCA064811WT1c.309C>A (p.Gly103=)
c.294C>A (p.Gly98=)
n.488C>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435053C>ACA379965958WT1c.308G>T (p.Gly103Val)
c.293G>T (p.Gly98Val)
n.487G>T
gnomAD v4
11g.32435053C>GCA379965956WT1c.308G>C (p.Gly103Ala)
c.293G>C (p.Gly98Ala)
n.487G>C
11g.32435053C>TCA379965957WT1c.308G>A (p.Gly103Asp)
c.293G>A (p.Gly98Asp)
n.487G>A
gnomAD v4
11g.32435054C>ACA379965959WT1c.307G>T (p.Gly103Cys)
c.292G>T (p.Gly98Cys)
n.486G>T
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435054C=CA1962327302WT1c.307G= (p.Gly103=)
c.292G= (p.Gly98=)
n.486G=
11g.32435054C>GCA379965960WT1c.307G>C (p.Gly103Arg)
c.292G>C (p.Gly98Arg)
n.486G>C
gnomAD v4
11g.32435054C>TCA379965961WT1c.307G>A (p.Gly103Ser)
c.292G>A (p.Gly98Ser)
n.486G>A
gnomAD v4
11g.32435055G>ACA473773896WT1c.306C>T (p.Ser102=)
c.291C>T (p.Ser97=)
n.485C>T
dbSNP gnomAD v4
11g.32435055G>CCA379965962WT1c.306C>G (p.Ser102Arg)
c.291C>G (p.Ser97Arg)
n.485C>G
dbSNP
11g.32435055G>TCA379965963WT1c.306C>A (p.Ser102Arg)
c.291C>A (p.Ser97Arg)
n.485C>A
ClinVar gnomAD v4
11g.32435056C>ACA379965964WT1c.305G>T (p.Ser102Ile)
c.290G>T (p.Ser97Ile)
n.484G>T
gnomAD v4
11g.32435056C=CA1962327303WT1c.305G= (p.Ser102=)
c.290G= (p.Ser97=)
n.484G=
11g.32435056C>GCA379965965WT1c.305G>C (p.Ser102Thr)
c.290G>C (p.Ser97Thr)
n.484G>C
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.32435056C>TCA379965966WT1c.305G>A (p.Ser102Asn)
c.290G>A (p.Ser97Asn)
n.484G>A
ClinVar dbSNP gnomAD v4
11g.32435058_32435059insCCCTCCA2695213679WT1c.305_306insGGGAG (p.Ser102ArgfsTer?)
c.290_291insGGGAG (p.Ser97ArgfsTer?)
n.484_485insGGGAG
11g.32435057T>ACA379965967WT1c.304A>T (p.Ser102Cys)
c.289A>T (p.Ser97Cys)
n.483A>T
dbSNP
11g.32435057T>CCA379965968WT1c.304A>G (p.Ser102Gly)
c.289A>G (p.Ser97Gly)
n.483A>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435057T>GCA379965969WT1c.304A>C (p.Ser102Arg)
c.289A>C (p.Ser97Arg)
n.483A>C
11g.32435057T=CA1962327304WT1c.304A= (p.Ser102=)
c.289A= (p.Ser97=)
n.483A=
11g.32435058C>ACA473773906WT1c.303G>T (p.Val101=)
c.288G>T (p.Val96=)
n.482G>T
gnomAD v4
11g.32435058C>GCA473773907WT1c.303G>C (p.Val101=)
c.288G>C (p.Val96=)
n.482G>C
11g.32435058C>TCA473773908WT1c.303G>A (p.Val101=)
c.288G>A (p.Val96=)
n.482G>A
ClinVar gnomAD v4
11g.32435059A>CCA379965972WT1c.302T>G (p.Val101Gly)
c.287T>G (p.Val96Gly)
n.481T>G
11g.32435059A>GCA379965970WT1c.302T>C (p.Val101Ala)
c.287T>C (p.Val96Ala)
n.481T>C
gnomAD v4
11g.32435059A>TCA379965971WT1c.302T>A (p.Val101Glu)
c.287T>A (p.Val96Glu)
n.481T>A
gnomAD v4
11g.32435059_32435062delCA645584491WT1c.299_302del (p.Pro100ArgfsTer?)
c.284_287del (p.Pro95ArgfsTer?)
n.478_481del
COSMIC
11g.32435060C>ACA379965973WT1c.301G>T (p.Val101Leu)
c.286G>T (p.Val96Leu)
n.480G>T
gnomAD v4
11g.32435060C=CA1962327305WT1c.301G= (p.Val101=)
c.286G= (p.Val96=)
n.480G=
11g.32435060C>GCA379965974WT1c.301G>C (p.Val101Leu)
c.286G>C (p.Val96Leu)
n.480G>C
ClinVar dbSNP
11g.32435060C>TCA379965975WT1c.301G>A (p.Val101Met)
c.286G>A (p.Val96Met)
n.480G>A
gnomAD v4
11g.32435061A=CA1962327306WT1c.300T= (p.Pro100=)
c.285T= (p.Pro95=)
n.479T=
11g.32435061A>CCA473773913WT1c.300T>G (p.Pro100=)
c.285T>G (p.Pro95=)
n.479T>G
dbSNP gnomAD v4
11g.32435061A>GCA473773915WT1c.300T>C (p.Pro100=)
c.285T>C (p.Pro95=)
n.479T>C
gnomAD v4
11g.32435061A>TCA473773916WT1c.300T>A (p.Pro100=)
c.285T>A (p.Pro95=)
n.479T>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435062G>ACA379965976WT1c.299C>T (p.Pro100Leu)
c.284C>T (p.Pro95Leu)
n.478C>T
gnomAD v4
11g.32435062G>CCA379965977WT1c.299C>G (p.Pro100Arg)
c.284C>G (p.Pro95Arg)
n.478C>G
ClinVar
11g.32435062G>TCA379965978WT1c.299C>A (p.Pro100His)
c.284C>A (p.Pro95His)
n.478C>A
gnomAD v4
11g.32435063G>ACA219511235WT1c.298C>T (p.Pro100Ser)
c.283C>T (p.Pro95Ser)
n.477C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.32435063G>CCA379965979WT1c.298C>G (p.Pro100Ala)
c.283C>G (p.Pro95Ala)
n.477C>G
ClinVar dbSNP gnomAD v4
11g.32435063G=CA1962327307WT1c.298C= (p.Pro100=)
c.283C= (p.Pro95=)
n.477C=
11g.32435063G>TCA379965980WT1c.298C>A (p.Pro100Thr)
c.283C>A (p.Pro95Thr)
n.477C>A
ClinVar dbSNP gnomAD v4
11g.32435064C>ACA473773924WT1c.297G>T (p.Leu99=)
c.282G>T (p.Leu94=)
n.476G>T
gnomAD v4
11g.32435064C=CA1962327308WT1c.297G= (p.Leu99=)
c.282G= (p.Leu94=)
n.476G=
11g.32435064C>GCA473773925WT1c.297G>C (p.Leu99=)
c.282G>C (p.Leu94=)
n.476G>C
gnomAD v4
11g.32435064C>TCA473773926WT1c.297G>A (p.Leu99=)
c.282G>A (p.Leu94=)
n.476G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
11g.32435065A=CA1962327309WT1c.296T= (p.Leu99=)
c.281T= (p.Leu94=)
n.475T=
11g.32435065A>CCA379965981WT1c.296T>G (p.Leu99Arg)
c.281T>G (p.Leu94Arg)
n.475T>G
11g.32435065A>GCA379965982WT1c.296T>C (p.Leu99Pro)
c.281T>C (p.Leu94Pro)
n.475T>C
ClinVar dbSNP gnomAD v4
11g.32435065A>TCA379965983WT1c.296T>A (p.Leu99Gln)
c.281T>A (p.Leu94Gln)
n.475T>A
ClinVar dbSNP
11g.32435066G>ACA473773931WT1c.295C>T (p.Leu99=)
c.280C>T (p.Leu94=)
n.474C>T
gnomAD v4
11g.32435066G>CCA379965985WT1c.295C>G (p.Leu99Val)
c.280C>G (p.Leu94Val)
n.474C>G
ClinVar dbSNP
11g.32435066G=CA1962327310WT1c.295C= (p.Leu99=)
c.280C= (p.Leu94=)
n.474C=
11g.32435066G>TCA379965984WT1c.295C>A (p.Leu99Met)
c.280C>A (p.Leu94Met)
n.474C>A
gnomAD v4
11g.32435067G>ACA219511241WT1c.294C>T (p.Ala98=)
c.279C>T (p.Ala93=)
n.473C>T
ClinVar dbSNP gnomAD v4
11g.32435067G>CCA473773933WT1c.294C>G (p.Ala98=)
c.279C>G (p.Ala93=)
n.473C>G
11g.32435067G=CA1962327311WT1c.294C= (p.Ala98=)
c.279C= (p.Ala93=)
n.473C=
11g.32435067G>TCA473773934WT1c.294C>A (p.Ala98=)
c.279C>A (p.Ala93=)
n.473C>A
11g.32435068G>ACA379965986WT1c.293C>T (p.Ala98Val)
c.278C>T (p.Ala93Val)
n.472C>T
ClinVar dbSNP gnomAD v4
11g.32435068G>CCA379965988WT1c.293C>G (p.Ala98Gly)
c.278C>G (p.Ala93Gly)
n.472C>G
ClinVar dbSNP gnomAD v4
11g.32435068G=CA1962327312WT1c.293C= (p.Ala98=)
c.278C= (p.Ala93=)
n.472C=
11g.32435068G>TCA379965987WT1c.293C>A (p.Ala98Asp)
c.278C>A (p.Ala93Asp)
n.472C>A
gnomAD v4
11g.32435069C>ACA379965989WT1c.292G>T (p.Ala98Ser)
c.277G>T (p.Ala93Ser)
n.471G>T
dbSNP gnomAD v4
11g.32435069C>GCA379965990WT1c.292G>C (p.Ala98Pro)
c.277G>C (p.Ala93Pro)
n.471G>C
11g.32435069C>TCA379965991WT1c.292G>A (p.Ala98Thr)
c.277G>A (p.Ala93Thr)
n.471G>A
gnomAD v4
11g.32435070A=CA1962327313WT1c.291T= (p.Cys97=)
c.276T= (p.Cys92=)
n.470T=
11g.32435070A>CCA064806WT1c.291T>G (p.Cys97Trp)
c.276T>G (p.Cys92Trp)
n.470T>G
dbSNP ExAC gnomAD v2 gnomAD v4
11g.32435070A>GCA473773939WT1c.291T>C (p.Cys97=)
c.276T>C (p.Cys92=)
n.470T>C
ClinVar dbSNP gnomAD v4
11g.32435070A>TCA379965992WT1c.291T>A (p.Cys97Ter)
c.276T>A (p.Cys92Ter)
n.470T>A
11g.32435071C>ACA379965993WT1c.290G>T (p.Cys97Phe)
c.275G>T (p.Cys92Phe)
n.469G>T
gnomAD v4
11g.32435071C=CA1962327314WT1c.290G= (p.Cys97=)
c.275G= (p.Cys92=)
n.469G=
11g.32435071C>GCA379965994WT1c.290G>C (p.Cys97Ser)
c.275G>C (p.Cys92Ser)
n.469G>C
ClinVar dbSNP
11g.32435071C>TCA379965995WT1c.290G>A (p.Cys97Tyr)
c.275G>A (p.Cys92Tyr)
n.469G>A
gnomAD v4
11g.32435072A=CA1962327315WT1c.289T= (p.Cys97=)
c.274T= (p.Cys92=)
n.468T=
11g.32435072A>CCA379965996WT1c.289T>G (p.Cys97Gly)
c.274T>G (p.Cys92Gly)
n.468T>G
dbSNP
11g.32435072A>GCA379965997WT1c.289T>C (p.Cys97Arg)
c.274T>C (p.Cys92Arg)
n.468T>C
ClinVar dbSNP gnomAD v4
11g.32435072A>TCA379965998WT1c.289T>A (p.Cys97Ser)
c.274T>A (p.Cys92Ser)
n.468T>A
11g.32435072_32435075delinsAGCCCA1962327316WT1c.286_289delinsGGCT (p.Gly96=)
c.271_274delinsGGCT (p.Gly91=)
n.465_468delinsGGCT
11g.32435072_32435073insTCCCA2580084184WT1c.288_289insGGA (p.Gly96_Cys97insGly)
c.273_274insGGA (p.Gly91_Cys92insGly)
n.467_468insGGA
ClinVar
11g.32435073G>ACA473773942WT1c.288C>T (p.Gly96=)
c.273C>T (p.Gly91=)
n.467C>T
dbSNP gnomAD v4
11g.32435073G>CCA473773943WT1c.288C>G (p.Gly96=)
c.273C>G (p.Gly91=)
n.467C>G
ClinVar dbSNP gnomAD v4
11g.32435073G=CA1962327317WT1c.288C= (p.Gly96=)
c.273C= (p.Gly91=)
n.467C=
11g.32435073G>TCA473773944WT1c.288C>A (p.Gly96=)
c.273C>A (p.Gly91=)
n.467C>A
gnomAD v4
11g.32435082_32435084dupCA2580615657WT1c.286_288dup (p.Gly96_Cys97insGly)
c.271_273dup (p.Gly91_Cys92insGly)
n.465_467dup
ClinVar dbSNP gnomAD v4
11g.32435082_32435084delCA064802WT1c.286_288del (p.Gly96del)
c.271_273del (p.Gly91del)
n.465_467del
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.32435073_32435074insTCCCA2825001877WT1c.287_288insGGA (p.Gly96_Cys97insAsp)
c.272_273insGGA (p.Gly91_Cys92insAsp)
n.466_467insGGA
ClinVar
11g.32435074C>ACA379966001WT1c.287G>T (p.Gly96Val)
c.272G>T (p.Gly91Val)
n.466G>T
gnomAD v4
11g.32435074C>GCA379965999WT1c.287G>C (p.Gly96Ala)
c.272G>C (p.Gly91Ala)
n.466G>C
11g.32435074C>TCA379966000WT1c.287G>A (p.Gly96Asp)
c.272G>A (p.Gly91Asp)
n.466G>A
dbSNP gnomAD v4
11g.32435075C>ACA379966002WT1c.286G>T (p.Gly96Cys)
c.271G>T (p.Gly91Cys)
n.465G>T
ClinVar dbSNP gnomAD v4
11g.32435075C=CA1962327318WT1c.286G= (p.Gly96=)
c.271G= (p.Gly91=)
n.465G=
11g.32435075C>GCA379966003WT1c.286G>C (p.Gly96Arg)
c.271G>C (p.Gly91Arg)
n.465G>C
11g.32435075C>TCA16613605WT1c.286G>A (p.Gly96Ser)
c.271G>A (p.Gly91Ser)
n.465G>A
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435076G>ACA10638966WT1c.285C>T (p.Gly95=)
c.270C>T (p.Gly90=)
n.464C>T
ClinVar dbSNP gnomAD v4
11g.32435076G>CCA473773947WT1c.285C>G (p.Gly95=)
c.270C>G (p.Gly90=)
n.464C>G
dbSNP
11g.32435076G=CA1962327319WT1c.285C= (p.Gly95=)
c.270C= (p.Gly90=)
n.464C=
11g.32435076G>TCA473773948WT1c.285C>A (p.Gly95=)
c.270C>A (p.Gly90=)
n.464C>A
gnomAD v4
11g.32435077C>ACA379966004WT1c.284G>T (p.Gly95Val)
c.269G>T (p.Gly90Val)
n.463G>T
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.32435077C=CA1962327320WT1c.284G= (p.Gly95=)
c.269G= (p.Gly90=)
n.463G=
11g.32435077C>GCA379966005WT1c.284G>C (p.Gly95Ala)
c.269G>C (p.Gly90Ala)
n.463G>C
dbSNP
11g.32435077C>TCA379966006WT1c.284G>A (p.Gly95Asp)
c.269G>A (p.Gly90Asp)
n.463G>A
ClinVar dbSNP gnomAD v4

Number of alleles fetched