Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32434964_32434978dup | CA1962327232 | WT1 | c.393_407dup (p.Pro136_Pro137insAlaProProProPro) c.378_392dup (p.Pro131_Pro132insAlaProProProPro) n.572_586dup | ClinVar dbSNP gnomAD v4 |
11 | g.32434964_32434978del | CA2499220923 | WT1 | c.393_407del (p.Ala132_Pro136del) c.378_392del (p.Ala127_Pro131del) n.572_586del | ClinVar dbSNP gnomAD v4 |
11 | g.32434974_32434981del | CA645584488 | WT1 | c.382_389del (p.Ala128ThrfsTer?) c.367_374del (p.Ala123ThrfsTer?) n.561_568del | COSMIC COSMIC |
11 | g.32434978_32434987del | CA2695213677 | WT1 | c.376_385del (p.Gly126ArgfsTer?) c.361_370del (p.Gly121ArgfsTer?) n.555_564del | |
11 | g.32434977C>A | CA473773720 | WT1 | c.384G>T (p.Ala128=) c.369G>T (p.Ala123=) n.563G>T | |
11 | g.32434977C>G | CA473773716 | WT1 | c.384G>C (p.Ala128=) c.369G>C (p.Ala123=) n.563G>C | dbSNP gnomAD v4 |
11 | g.32434977C>T | CA473773718 | WT1 | c.384G>A (p.Ala128=) c.369G>A (p.Ala123=) n.563G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434978G>A | CA379965804 | WT1 | c.383C>T (p.Ala128Val) c.368C>T (p.Ala123Val) n.562C>T | |
11 | g.32434978G>C | CA379965805 | WT1 | c.383C>G (p.Ala128Gly) c.368C>G (p.Ala123Gly) n.562C>G | |
11 | g.32434978G= | CA1962327250 | WT1 | c.383C= (p.Ala128=) c.368C= (p.Ala123=) n.562C= | |
11 | g.32434978G>T | CA379965806 | WT1 | c.383C>A (p.Ala128Glu) c.368C>A (p.Ala123Glu) n.562C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434979C>A | CA379965807 | WT1 | c.382G>T (p.Ala128Ser) c.367G>T (p.Ala123Ser) n.561G>T | |
11 | g.32434979C= | CA1962327251 | WT1 | c.382G= (p.Ala128=) c.367G= (p.Ala123=) n.561G= | |
11 | g.32434979C>G | CA379965809 | WT1 | c.382G>C (p.Ala128Pro) c.367G>C (p.Ala123Pro) n.561G>C | dbSNP |
11 | g.32434979C>T | CA379965808 | WT1 | c.382G>A (p.Ala128Thr) c.367G>A (p.Ala123Thr) n.561G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434980G>A | CA473773723 | WT1 | c.381C>T (p.Pro127=) c.366C>T (p.Pro122=) n.560C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434980G>C | CA064867 | WT1 | c.381C>G (p.Pro127=) c.366C>G (p.Pro122=) n.560C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434980G= | CA1962327252 | WT1 | c.381C= (p.Pro127=) c.366C= (p.Pro122=) n.560C= | |
11 | g.32434980G>T | CA473773725 | WT1 | c.381C>A (p.Pro127=) c.366C>A (p.Pro122=) n.560C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434983del | CA2695201112 | WT1 | c.381del (p.Ala128ArgfsTer?) c.366del (p.Ala123ArgfsTer?) n.560del | ClinVar |
11 | g.32434981G>A | CA379965810 | WT1 | c.380C>T (p.Pro127Leu) c.365C>T (p.Pro122Leu) n.559C>T | ClinVar gnomAD v4 |
11 | g.32434981G>C | CA379965811 | WT1 | c.380C>G (p.Pro127Arg) c.365C>G (p.Pro122Arg) n.559C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434981G= | CA1962327253 | WT1 | c.380C= (p.Pro127=) c.365C= (p.Pro122=) n.559C= | |
11 | g.32434981G>T | CA379965812 | WT1 | c.380C>A (p.Pro127His) c.365C>A (p.Pro122His) n.559C>A | gnomAD v4 |
11 | g.32434982G>A | CA379965813 | WT1 | c.379C>T (p.Pro127Ser) c.364C>T (p.Pro122Ser) n.558C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434982G>C | CA379965814 | WT1 | c.379C>G (p.Pro127Ala) c.364C>G (p.Pro122Ala) n.558C>G | |
11 | g.32434982G= | CA1962327254 | WT1 | c.379C= (p.Pro127=) c.364C= (p.Pro122=) n.558C= | |
11 | g.32434982G>T | CA379965815 | WT1 | c.379C>A (p.Pro127Thr) c.364C>A (p.Pro122Thr) n.558C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434983G>A | CA473773732 | WT1 | c.378C>T (p.Gly126=) c.363C>T (p.Gly121=) n.557C>T | gnomAD v4 |
11 | g.32434983G>C | CA473773734 | WT1 | c.378C>G (p.Gly126=) c.363C>G (p.Gly121=) n.557C>G | |
11 | g.32434983G>T | CA473773736 | WT1 | c.378C>A (p.Gly126=) c.363C>A (p.Gly121=) n.557C>A | |
11 | g.32434984C>A | CA379965816 | WT1 | c.377G>T (p.Gly126Val) c.362G>T (p.Gly121Val) n.556G>T | gnomAD v4 |
11 | g.32434984C>G | CA379965818 | WT1 | c.377G>C (p.Gly126Ala) c.362G>C (p.Gly121Ala) n.556G>C | ClinVar dbSNP |
11 | g.32434984C>T | CA379965817 | WT1 | c.377G>A (p.Gly126Asp) c.362G>A (p.Gly121Asp) n.556G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434985C>A | CA379965819 | WT1 | c.376G>T (p.Gly126Cys) c.361G>T (p.Gly121Cys) n.555G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434985C= | CA1962327255 | WT1 | c.376G= (p.Gly126=) c.361G= (p.Gly121=) n.555G= | |
11 | g.32434985C>G | CA379965820 | WT1 | c.376G>C (p.Gly126Arg) c.361G>C (p.Gly121Arg) n.555G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32434985C>T | CA379965821 | WT1 | c.376G>A (p.Gly126Ser) c.361G>A (p.Gly121Ser) n.555G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434986G>A | CA064860 | WT1 | c.375C>T (p.Gly125=) c.360C>T (p.Gly120=) n.554C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434986G>C | CA473773743 | WT1 | c.375C>G (p.Gly125=) c.360C>G (p.Gly120=) n.554C>G | dbSNP |
11 | g.32434986G= | CA1962327256 | WT1 | c.375C= (p.Gly125=) c.360C= (p.Gly120=) n.554C= | |
11 | g.32434986G>T | CA473773745 | WT1 | c.375C>A (p.Gly125=) c.360C>A (p.Gly120=) n.554C>A | dbSNP gnomAD v4 |
11 | g.32434987C>A | CA379965824 | WT1 | c.374G>T (p.Gly125Val) c.359G>T (p.Gly120Val) n.553G>T | |
11 | g.32434987C= | CA1962327257 | WT1 | c.374G= (p.Gly125=) c.359G= (p.Gly120=) n.553G= | |
11 | g.32434987C>G | CA379965822 | WT1 | c.374G>C (p.Gly125Ala) c.359G>C (p.Gly120Ala) n.553G>C | dbSNP |
11 | g.32434987C>T | CA379965823 | WT1 | c.374G>A (p.Gly125Asp) c.359G>A (p.Gly120Asp) n.553G>A | dbSNP gnomAD v4 COSMIC |
11 | g.32434989del | CA2612989553 | WT1 | c.374del (p.Gly125AlafsTer?) c.359del (p.Gly120AlafsTer?) n.553del | gnomAD v4 |
11 | g.32434988C>A | CA379965825 | WT1 | c.373G>T (p.Gly125Cys) c.358G>T (p.Gly120Cys) n.552G>T | |
11 | g.32434988C= | CA1962327258 | WT1 | c.373G= (p.Gly125=) c.358G= (p.Gly120=) n.552G= | |
11 | g.32434988C>G | CA379965826 | WT1 | c.373G>C (p.Gly125Arg) c.358G>C (p.Gly120Arg) n.552G>C | dbSNP |
11 | g.32434988C>T | CA379965827 | WT1 | c.373G>A (p.Gly125Ser) c.358G>A (p.Gly120Ser) n.552G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434989C>A | CA379965828 | WT1 | c.372G>T (p.Leu124Phe) c.357G>T (p.Leu119Phe) n.551G>T | ClinVar |
11 | g.32434989C>G | CA379965829 | WT1 | c.372G>C (p.Leu124Phe) c.357G>C (p.Leu119Phe) n.551G>C | |
11 | g.32434989C>T | CA473773753 | WT1 | c.372G>A (p.Leu124=) c.357G>A (p.Leu119=) n.551G>A | gnomAD v4 |
11 | g.32434990A>C | CA379965830 | WT1 | c.371T>G (p.Leu124Trp) c.356T>G (p.Leu119Trp) n.550T>G | dbSNP |
11 | g.32434990A>G | CA379965831 | WT1 | c.371T>C (p.Leu124Ser) c.356T>C (p.Leu119Ser) n.550T>C | |
11 | g.32434990A>T | CA379965832 | WT1 | c.371T>A (p.Leu124Ter) c.356T>A (p.Leu119Ter) n.550T>A | |
11 | g.32434991A>C | CA379965833 | WT1 | c.370T>G (p.Leu124Val) c.355T>G (p.Leu119Val) n.549T>G | dbSNP |
11 | g.32434991A>G | CA473773757 | WT1 | c.370T>C (p.Leu124=) c.355T>C (p.Leu119=) n.549T>C | ClinVar gnomAD v4 |
11 | g.32434991A>T | CA379965834 | WT1 | c.370T>A (p.Leu124Met) c.355T>A (p.Leu119Met) n.549T>A | |
11 | g.32434992C>A | CA473773759 | WT1 | c.369G>T (p.Ser123=) c.354G>T (p.Ser118=) n.548G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434992C= | CA1962327259 | WT1 | c.369G= (p.Ser123=) c.354G= (p.Ser118=) n.548G= | |
11 | g.32434992C>G | CA473773761 | WT1 | c.369G>C (p.Ser123=) c.354G>C (p.Ser118=) n.548G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434992C>T | CA473773762 | WT1 | c.369G>A (p.Ser123=) c.354G>A (p.Ser118=) n.548G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434993G>A | CA379965835 | WT1 | c.368C>T (p.Ser123Leu) c.353C>T (p.Ser118Leu) n.547C>T | ClinVar dbSNP |
11 | g.32434993G>C | CA379965836 | WT1 | c.368C>G (p.Ser123Trp) c.353C>G (p.Ser118Trp) n.547C>G | dbSNP |
11 | g.32434993G>T | CA379965837 | WT1 | c.368C>A (p.Ser123Ter) c.353C>A (p.Ser118Ter) n.547C>A | ClinVar gnomAD v4 |
11 | g.32434994A>C | CA379965838 | WT1 | c.367T>G (p.Ser123Ala) c.352T>G (p.Ser118Ala) n.546T>G | ClinVar dbSNP COSMIC COSMIC |
11 | g.32434994A>G | CA379965840 | WT1 | c.367T>C (p.Ser123Pro) c.352T>C (p.Ser118Pro) n.546T>C | dbSNP |
11 | g.32434994A>T | CA379965839 | WT1 | c.367T>A (p.Ser123Thr) c.352T>A (p.Ser118Thr) n.546T>A | |
11 | g.32434995C>A | CA473773767 | WT1 | c.366G>T (p.Gly122=) c.351G>T (p.Gly117=) n.545G>T | ClinVar gnomAD v4 |
11 | g.32434995C= | CA1962327260 | WT1 | c.366G= (p.Gly122=) c.351G= (p.Gly117=) n.545G= | |
11 | g.32434995C>G | CA473773770 | WT1 | c.366G>C (p.Gly122=) c.351G>C (p.Gly117=) n.545G>C | dbSNP |
11 | g.32434995C>T | CA473773768 | WT1 | c.366G>A (p.Gly122=) c.351G>A (p.Gly117=) n.545G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434996C>A | CA379965841 | WT1 | c.365G>T (p.Gly122Val) c.350G>T (p.Gly117Val) n.544G>T | gnomAD v4 |
11 | g.32434996C>G | CA379965842 | WT1 | c.365G>C (p.Gly122Ala) c.350G>C (p.Gly117Ala) n.544G>C | |
11 | g.32434996C>T | CA379965843 | WT1 | c.365G>A (p.Gly122Glu) c.350G>A (p.Gly117Glu) n.544G>A | gnomAD v4 |
11 | g.32434997C>A | CA379965844 | WT1 | c.364G>T (p.Gly122Trp) c.349G>T (p.Gly117Trp) n.543G>T | gnomAD v4 |
11 | g.32434997C>G | CA379965845 | WT1 | c.364G>C (p.Gly122Arg) c.349G>C (p.Gly117Arg) n.543G>C | gnomAD v4 |
11 | g.32434997C>T | CA379965846 | WT1 | c.364G>A (p.Gly122Arg) c.349G>A (p.Gly117Arg) n.543G>A | gnomAD v4 |
11 | g.32434998G>A | CA219511101 | WT1 | c.363C>T (p.Tyr121=) c.348C>T (p.Tyr116=) n.542C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434998G>C | CA379965847 | WT1 | c.363C>G (p.Tyr121Ter) c.348C>G (p.Tyr116Ter) n.542C>G | dbSNP gnomAD v4 COSMIC |
11 | g.32434998G= | CA1962327261 | WT1 | c.363C= (p.Tyr121=) c.348C= (p.Tyr116=) n.542C= | |
11 | g.32434998G>T | CA379965848 | WT1 | c.363C>A (p.Tyr121Ter) c.348C>A (p.Tyr116Ter) n.542C>A | ClinVar gnomAD v4 COSMIC |
11 | g.32434999T>A | CA379965849 | WT1 | c.362A>T (p.Tyr121Phe) c.347A>T (p.Tyr116Phe) n.541A>T | |
11 | g.32434999T>C | CA379965850 | WT1 | c.362A>G (p.Tyr121Cys) c.347A>G (p.Tyr116Cys) n.541A>G | dbSNP |
11 | g.32434999T>G | CA379965851 | WT1 | c.362A>C (p.Tyr121Ser) c.347A>C (p.Tyr116Ser) n.541A>C | dbSNP |
11 | g.32434999T= | CA1962327262 | WT1 | c.362A= (p.Tyr121=) c.347A= (p.Tyr116=) n.541A= | |
11 | g.32435000A= | CA1962327263 | WT1 | c.361T= (p.Tyr121=) c.346T= (p.Tyr116=) n.540T= | |
11 | g.32435000A>C | CA219511102 | WT1 | c.361T>G (p.Tyr121Asp) c.346T>G (p.Tyr116Asp) n.540T>G | dbSNP |
11 | g.32435000A>G | CA379965853 | WT1 | c.361T>C (p.Tyr121His) c.346T>C (p.Tyr116His) n.540T>C | gnomAD v4 |
11 | g.32435000A>T | CA379965852 | WT1 | c.361T>A (p.Tyr121Asn) c.346T>A (p.Tyr116Asn) n.540T>A | |
11 | g.32435001A>C | CA473773778 | WT1 | c.360T>G (p.Ala120=) c.345T>G (p.Ala115=) n.539T>G | |
11 | g.32435001A>G | CA473773779 | WT1 | c.360T>C (p.Ala120=) c.345T>C (p.Ala115=) n.539T>C | |
11 | g.32435001A>T | CA473773780 | WT1 | c.360T>A (p.Ala120=) c.345T>A (p.Ala115=) n.539T>A | |
11 | g.32435002G>A | CA379965854 | WT1 | c.359C>T (p.Ala120Val) c.344C>T (p.Ala115Val) n.538C>T | gnomAD v4 |
11 | g.32435002G>C | CA379965855 | WT1 | c.359C>G (p.Ala120Gly) c.344C>G (p.Ala115Gly) n.538C>G | dbSNP |
11 | g.32435002G>T | CA379965856 | WT1 | c.359C>A (p.Ala120Asp) c.344C>A (p.Ala115Asp) n.538C>A | gnomAD v4 |
11 | g.32435003C>A | CA379965857 | WT1 | c.358G>T (p.Ala120Ser) c.343G>T (p.Ala115Ser) n.537G>T | |
11 | g.32435003C= | CA1962327264 | WT1 | c.358G= (p.Ala120=) c.343G= (p.Ala115=) n.537G= | |
11 | g.32435003C>G | CA379965858 | WT1 | c.358G>C (p.Ala120Pro) c.343G>C (p.Ala115Pro) n.537G>C | dbSNP |
11 | g.32435003C>T | CA379965859 | WT1 | c.358G>A (p.Ala120Thr) c.343G>A (p.Ala115Thr) n.537G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435004C>A | CA473773786 | WT1 | c.357G>T (p.Ser119=) c.342G>T (p.Ser114=) n.536G>T | ClinVar gnomAD v4 |
11 | g.32435004C= | CA1962327265 | WT1 | c.357G= (p.Ser119=) c.342G= (p.Ser114=) n.536G= | |
11 | g.32435004C>G | CA473773787 | WT1 | c.357G>C (p.Ser119=) c.342G>C (p.Ser114=) n.536G>C | dbSNP gnomAD v4 |
11 | g.32435004C>T | CA473773788 | WT1 | c.357G>A (p.Ser119=) c.342G>A (p.Ser114=) n.536G>A | gnomAD v4 |
11 | g.32435005G>A | CA379965860 | WT1 | c.356C>T (p.Ser119Leu) c.341C>T (p.Ser114Leu) n.535C>T | ClinVar gnomAD v4 |
11 | g.32435005G>C | CA379965861 | WT1 | c.356C>G (p.Ser119Trp) c.341C>G (p.Ser114Trp) n.535C>G | ClinVar dbSNP |
11 | g.32435005G= | CA1962327266 | WT1 | c.356C= (p.Ser119=) c.341C= (p.Ser114=) n.535C= | |
11 | g.32435005G>T | CA379965862 | WT1 | c.356C>A (p.Ser119Ter) c.341C>A (p.Ser114Ter) n.535C>A | COSMIC |
11 | g.32435006A= | CA1962327267 | WT1 | c.355T= (p.Ser119=) c.340T= (p.Ser114=) n.534T= | |
11 | g.32435006A>C | CA379965863 | WT1 | c.355T>G (p.Ser119Ala) c.340T>G (p.Ser114Ala) n.534T>G | |
11 | g.32435006A>G | CA379965864 | WT1 | c.355T>C (p.Ser119Pro) c.340T>C (p.Ser114Pro) n.534T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435006A>T | CA379965865 | WT1 | c.355T>A (p.Ser119Thr) c.340T>A (p.Ser114Thr) n.534T>A | gnomAD v4 |
11 | g.32435007A>C | CA473773795 | WT1 | c.354T>G (p.Ala118=) c.339T>G (p.Ala113=) n.533T>G | dbSNP |
11 | g.32435007A>G | CA473773794 | WT1 | c.354T>C (p.Ala118=) c.339T>C (p.Ala113=) n.533T>C | dbSNP gnomAD v4 |
11 | g.32435007A>T | CA473773793 | WT1 | c.354T>A (p.Ala118=) c.339T>A (p.Ala113=) n.533T>A | dbSNP |
11 | g.32435008G>A | CA064850 | WT1 | c.353C>T (p.Ala118Val) c.338C>T (p.Ala113Val) n.532C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435008G>C | CA379965867 | WT1 | c.353C>G (p.Ala118Gly) c.338C>G (p.Ala113Gly) n.532C>G | |
11 | g.32435008G= | CA1962327268 | WT1 | c.353C= (p.Ala118=) c.338C= (p.Ala113=) n.532C= | |
11 | g.32435008G>T | CA379965866 | WT1 | c.353C>A (p.Ala118Asp) c.338C>A (p.Ala113Asp) n.532C>A | gnomAD v4 |
11 | g.32435009C>A | CA379965868 | WT1 | c.352G>T (p.Ala118Ser) c.337G>T (p.Ala113Ser) n.531G>T | gnomAD v4 |
11 | g.32435009C= | CA1962327269 | WT1 | c.352G= (p.Ala118=) c.337G= (p.Ala113=) n.531G= | |
11 | g.32435009C>G | CA379965870 | WT1 | c.352G>C (p.Ala118Pro) c.337G>C (p.Ala113Pro) n.531G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435009C>T | CA379965869 | WT1 | c.352G>A (p.Ala118Thr) c.337G>A (p.Ala113Thr) n.531G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435010G>A | CA473773799 | WT1 | c.351C>T (p.Gly117=) c.336C>T (p.Gly112=) n.530C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435010G>C | CA473773798 | WT1 | c.351C>G (p.Gly117=) c.336C>G (p.Gly112=) n.530C>G | |
11 | g.32435010G= | CA1962327270 | WT1 | c.351C= (p.Gly117=) c.336C= (p.Gly112=) n.530C= | |
11 | g.32435010G>T | CA473773797 | WT1 | c.351C>A (p.Gly117=) c.336C>A (p.Gly112=) n.530C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435011C>A | CA379965871 | WT1 | c.350G>T (p.Gly117Val) c.335G>T (p.Gly112Val) n.529G>T | |
11 | g.32435011C= | CA1962327271 | WT1 | c.350G= (p.Gly117=) c.335G= (p.Gly112=) n.529G= | |
11 | g.32435011C>G | CA379965872 | WT1 | c.350G>C (p.Gly117Ala) c.335G>C (p.Gly112Ala) n.529G>C | dbSNP |
11 | g.32435011C>T | CA219511109 | WT1 | c.350G>A (p.Gly117Asp) c.335G>A (p.Gly112Asp) n.529G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435012C>A | CA379965873 | WT1 | c.349G>T (p.Gly117Cys) c.334G>T (p.Gly112Cys) n.528G>T | gnomAD v4 |
11 | g.32435012C= | CA1962327272 | WT1 | c.349G= (p.Gly117=) c.334G= (p.Gly112=) n.528G= | |
11 | g.32435012C>G | CA379965875 | WT1 | c.349G>C (p.Gly117Arg) c.334G>C (p.Gly112Arg) n.528G>C | dbSNP |
11 | g.32435012C>T | CA379965874 | WT1 | c.349G>A (p.Gly117Ser) c.334G>A (p.Gly112Ser) n.528G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435013C>A | CA473773802 | WT1 | c.348G>T (p.Pro116=) c.333G>T (p.Pro111=) n.527G>T | gnomAD v4 |
11 | g.32435013C= | CA1962327273 | WT1 | c.348G= (p.Pro116=) c.333G= (p.Pro111=) n.527G= | |
11 | g.32435013C>G | CA473773804 | WT1 | c.348G>C (p.Pro116=) c.333G>C (p.Pro111=) n.527G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435013C>T | CA473773803 | WT1 | c.348G>A (p.Pro116=) c.333G>A (p.Pro111=) n.527G>A | gnomAD v4 |
11 | g.32435014G>A | CA10638965 | WT1 | c.347C>T (p.Pro116Leu) c.332C>T (p.Pro111Leu) n.526C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435014G>C | CA379965877 | WT1 | c.347C>G (p.Pro116Arg) c.332C>G (p.Pro111Arg) n.526C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32435014G= | CA1962327274 | WT1 | c.347C= (p.Pro116=) c.332C= (p.Pro111=) n.526C= | |
11 | g.32435014G>T | CA379965876 | WT1 | c.347C>A (p.Pro116Gln) c.332C>A (p.Pro111Gln) n.526C>A | gnomAD v4 |
11 | g.32435018dup | CA2612989557 | WT1 | c.347dup (p.Ala118ArgfsTer?) c.332dup (p.Ala113ArgfsTer?) n.526dup | gnomAD v4 |
11 | g.32435018del | CA2612989558 | WT1 | c.347del (p.Pro116ArgfsTer?) c.332del (p.Pro111ArgfsTer?) n.526del | gnomAD v4 |
11 | g.32435015G>A | CA379965878 | WT1 | c.346C>T (p.Pro116Ser) c.331C>T (p.Pro111Ser) n.525C>T | |
11 | g.32435015G>C | CA379965879 | WT1 | c.346C>G (p.Pro116Ala) c.331C>G (p.Pro111Ala) n.525C>G | |
11 | g.32435015G= | CA1962327275 | WT1 | c.346C= (p.Pro116=) c.331C= (p.Pro111=) n.525C= | |
11 | g.32435015G>T | CA379965880 | WT1 | c.346C>A (p.Pro116Thr) c.331C>A (p.Pro111Thr) n.525C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435015_32435016insA | CA2723467872 | WT1 | c.345_346insT (p.Pro116SerfsTer?) c.330_331insT (p.Pro111SerfsTer?) n.524_525insT | dbSNP |
11 | g.32435016G>A | CA017474 | WT1 | c.345C>T (p.Pro115=) c.330C>T (p.Pro110=) n.524C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435016G>C | CA473773808 | WT1 | c.345C>G (p.Pro115=) c.330C>G (p.Pro110=) n.524C>G | dbSNP |
11 | g.32435016G= | CA1962327276 | WT1 | c.345C= (p.Pro115=) c.330C= (p.Pro110=) n.524C= | |
11 | g.32435016G>T | CA473773809 | WT1 | c.345C>A (p.Pro115=) c.330C>A (p.Pro110=) n.524C>A | gnomAD v4 |
11 | g.32435017G>A | CA379965881 | WT1 | c.344C>T (p.Pro115Leu) c.329C>T (p.Pro110Leu) n.523C>T | gnomAD v4 |
11 | g.32435017G>C | CA379965882 | WT1 | c.344C>G (p.Pro115Arg) c.329C>G (p.Pro110Arg) n.523C>G | |
11 | g.32435017G= | CA1962327277 | WT1 | c.344C= (p.Pro115=) c.329C= (p.Pro110=) n.523C= | |
11 | g.32435017G>T | CA379965883 | WT1 | c.344C>A (p.Pro115His) c.329C>A (p.Pro110His) n.523C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435018G>A | CA16613338 | WT1 | c.343C>T (p.Pro115Ser) c.328C>T (p.Pro110Ser) n.522C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435018G>C | CA379965884 | WT1 | c.343C>G (p.Pro115Ala) c.328C>G (p.Pro110Ala) n.522C>G | |
11 | g.32435018G= | CA1962327278 | WT1 | c.343C= (p.Pro115=) c.328C= (p.Pro110=) n.522C= | |
11 | g.32435018G>T | CA379965885 | WT1 | c.343C>A (p.Pro115Thr) c.328C>A (p.Pro110Thr) n.522C>A | ClinVar dbSNP |
11 | g.32435019C>A | CA473773813 | WT1 | c.342G>T (p.Ala114=) c.327G>T (p.Ala109=) n.521G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435019C= | CA1962327279 | WT1 | c.342G= (p.Ala114=) c.327G= (p.Ala109=) n.521G= | |
11 | g.32435019C>G | CA473773814 | WT1 | c.342G>C (p.Ala114=) c.327G>C (p.Ala109=) n.521G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435019C>T | CA473773815 | WT1 | c.342G>A (p.Ala114=) c.327G>A (p.Ala109=) n.521G>A | gnomAD v4 |
11 | g.32435020G>A | CA379965888 | WT1 | c.341C>T (p.Ala114Val) c.326C>T (p.Ala109Val) n.520C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435020G>C | CA379965887 | WT1 | c.341C>G (p.Ala114Gly) c.326C>G (p.Ala109Gly) n.520C>G | gnomAD v4 |
11 | g.32435020G= | CA1962327280 | WT1 | c.341C= (p.Ala114=) c.326C= (p.Ala109=) n.520C= | |
11 | g.32435020G>T | CA379965886 | WT1 | c.341C>A (p.Ala114Glu) c.326C>A (p.Ala109Glu) n.520C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435021C>A | CA379965889 | WT1 | c.340G>T (p.Ala114Ser) c.325G>T (p.Ala109Ser) n.519G>T | gnomAD v4 |
11 | g.32435021C= | CA1962327281 | WT1 | c.340G= (p.Ala114=) c.325G= (p.Ala109=) n.519G= | |
11 | g.32435021C>G | CA379965890 | WT1 | c.340G>C (p.Ala114Pro) c.325G>C (p.Ala109Pro) n.519G>C | |
11 | g.32435021C>T | CA379965891 | WT1 | c.340G>A (p.Ala114Thr) c.325G>A (p.Ala109Thr) n.519G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435022A>C | CA379965892 | WT1 | c.339T>G (p.Phe113Leu) c.324T>G (p.Phe108Leu) n.518T>G | gnomAD v4 |
11 | g.32435022A>G | CA473773817 | WT1 | c.339T>C (p.Phe113=) c.324T>C (p.Phe108=) n.518T>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435022A>T | CA379965893 | WT1 | c.339T>A (p.Phe113Leu) c.324T>A (p.Phe108Leu) n.518T>A | |
11 | g.32435022_32435023insGGCAA | CA645584490 | WT1 | c.339_340insTGCCT (p.Ala114CysfsTer?) c.324_325insTGCCT (p.Ala109CysfsTer?) n.518_519insTGCCT | COSMIC COSMIC |
11 | g.32435024dup | CA645584489 | WT1 | c.339dup (p.Ala114CysfsTer?) c.324dup (p.Ala109CysfsTer?) n.518dup | COSMIC |
11 | g.32435024del | CA2695213678 | WT1 | c.339del (p.Phe113LeufsTer?) c.324del (p.Phe108LeufsTer?) n.518del | |
11 | g.32435022_32435023insT | CA473773819 | WT1 | c.338_339insA (p.Phe113LeufsTer?) c.323_324insA (p.Phe108LeufsTer?) n.517_518insA | |
11 | g.32435023A>C | CA379965894 | WT1 | c.338T>G (p.Phe113Cys) c.323T>G (p.Phe108Cys) n.517T>G | |
11 | g.32435023A>G | CA379965895 | WT1 | c.338T>C (p.Phe113Ser) c.323T>C (p.Phe108Ser) n.517T>C | ClinVar gnomAD v4 |
11 | g.32435023A>T | CA379965896 | WT1 | c.338T>A (p.Phe113Tyr) c.323T>A (p.Phe108Tyr) n.517T>A | ClinVar |
11 | g.32435024A= | CA1962327282 | WT1 | c.337T= (p.Phe113=) c.322T= (p.Phe108=) n.516T= | |
11 | g.32435024A>C | CA379965897 | WT1 | c.337T>G (p.Phe113Val) c.322T>G (p.Phe108Val) n.516T>G | |
11 | g.32435024A>G | CA379965898 | WT1 | c.337T>C (p.Phe113Leu) c.322T>C (p.Phe108Leu) n.516T>C | dbSNP |
11 | g.32435024A>T | CA379965899 | WT1 | c.337T>A (p.Phe113Ile) c.322T>A (p.Phe108Ile) n.516T>A | |
11 | g.32435025G>A | CA473773824 | WT1 | c.336C>T (p.Asp112=) c.321C>T (p.Asp107=) n.515C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435025G>C | CA379965901 | WT1 | c.336C>G (p.Asp112Glu) c.321C>G (p.Asp107Glu) n.515C>G | dbSNP |
11 | g.32435025G>T | CA379965900 | WT1 | c.336C>A (p.Asp112Glu) c.321C>A (p.Asp107Glu) n.515C>A | gnomAD v4 |
11 | g.32435026T>A | CA379965902 | WT1 | c.335A>T (p.Asp112Val) c.320A>T (p.Asp107Val) n.514A>T | dbSNP |
11 | g.32435026T>C | CA379965903 | WT1 | c.335A>G (p.Asp112Gly) c.320A>G (p.Asp107Gly) n.514A>G | dbSNP |
11 | g.32435026T>G | CA379965904 | WT1 | c.335A>C (p.Asp112Ala) c.320A>C (p.Asp107Ala) n.514A>C | dbSNP |
11 | g.32435026_32435027delinsTC | CA1962327283 | WT1 | c.334_335delinsGA (p.Asp112=) c.319_320delinsGA (p.Asp107=) n.513_514delinsGA | |
11 | g.32435027C>A | CA379965905 | WT1 | c.334G>T (p.Asp112Tyr) c.319G>T (p.Asp107Tyr) n.513G>T | gnomAD v4 |
11 | g.32435027C= | CA1962327284 | WT1 | c.334G= (p.Asp112=) c.319G= (p.Asp107=) n.513G= | |
11 | g.32435027C>G | CA379965906 | WT1 | c.334G>C (p.Asp112His) c.319G>C (p.Asp107His) n.513G>C | |
11 | g.32435027C>T | CA379965907 | WT1 | c.334G>A (p.Asp112Asn) c.319G>A (p.Asp107Asn) n.513G>A | dbSNP |
11 | g.32435028del | CA658658040 | WT1 | c.334del (p.Asp112ThrfsTer?) c.319del (p.Asp107ThrfsTer?) n.513del | ClinVar dbSNP gnomAD v4 |
11 | g.32435028C>A | CA473773832 | WT1 | c.333G>T (p.Leu111=) c.318G>T (p.Leu106=) n.512G>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435028C= | CA1962327285 | WT1 | c.333G= (p.Leu111=) c.318G= (p.Leu106=) n.512G= | |
11 | g.32435028C>G | CA473773833 | WT1 | c.333G>C (p.Leu111=) c.318G>C (p.Leu106=) n.512G>C | |
11 | g.32435028C>T | CA473773834 | WT1 | c.333G>A (p.Leu111=) c.318G>A (p.Leu106=) n.512G>A | gnomAD v4 |
11 | g.32435029del | CA2695202566 | WT1 | c.332del (p.Leu111ArgfsTer?) c.317del (p.Leu106ArgfsTer?) n.511del | |
11 | g.32435029A>C | CA379965910 | WT1 | c.332T>G (p.Leu111Arg) c.317T>G (p.Leu106Arg) n.511T>G | dbSNP |
11 | g.32435029A>G | CA379965908 | WT1 | c.332T>C (p.Leu111Pro) c.317T>C (p.Leu106Pro) n.511T>C | ClinVar gnomAD v4 |
11 | g.32435029A>T | CA379965909 | WT1 | c.332T>A (p.Leu111Gln) c.317T>A (p.Leu106Gln) n.511T>A | |
11 | g.32435030G>A | CA473773836 | WT1 | c.331C>T (p.Leu111=) c.316C>T (p.Leu106=) n.510C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435030G>C | CA379965911 | WT1 | c.331C>G (p.Leu111Val) c.316C>G (p.Leu106Val) n.510C>G | dbSNP |
11 | g.32435030G>T | CA379965912 | WT1 | c.331C>A (p.Leu111Met) c.316C>A (p.Leu106Met) n.510C>A | gnomAD v4 |
11 | g.32435031C>A | CA473773838 | WT1 | c.330G>T (p.Val110=) c.315G>T (p.Val105=) n.509G>T | gnomAD v4 |
11 | g.32435031C>G | CA473773839 | WT1 | c.330G>C (p.Val110=) c.315G>C (p.Val105=) n.509G>C | |
11 | g.32435031C>T | CA473773840 | WT1 | c.330G>A (p.Val110=) c.315G>A (p.Val105=) n.509G>A | ClinVar |
11 | g.32435032A= | CA1962327286 | WT1 | c.329T= (p.Val110=) c.314T= (p.Val105=) n.508T= | |
11 | g.32435032A>C | CA379965913 | WT1 | c.329T>G (p.Val110Gly) c.314T>G (p.Val105Gly) n.508T>G | dbSNP |
11 | g.32435032A>G | CA379965914 | WT1 | c.329T>C (p.Val110Ala) c.314T>C (p.Val105Ala) n.508T>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435032A>T | CA379965915 | WT1 | c.329T>A (p.Val110Glu) c.314T>A (p.Val105Glu) n.508T>A | gnomAD v4 |
11 | g.32435033C>A | CA379965916 | WT1 | c.328G>T (p.Val110Leu) c.313G>T (p.Val105Leu) n.507G>T | ClinVar gnomAD v4 |
11 | g.32435033C>G | CA379965918 | WT1 | c.328G>C (p.Val110Leu) c.313G>C (p.Val105Leu) n.507G>C | |
11 | g.32435033C>T | CA379965917 | WT1 | c.328G>A (p.Val110Met) c.313G>A (p.Val105Met) n.507G>A | gnomAD v4 |
11 | g.32435034C>A | CA473773843 | WT1 | c.327G>T (p.Pro109=) c.312G>T (p.Pro104=) n.506G>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435034C= | CA1962327287 | WT1 | c.327G= (p.Pro109=) c.312G= (p.Pro104=) n.506G= | |
11 | g.32435034C>G | CA064841 | WT1 | c.327G>C (p.Pro109=) c.312G>C (p.Pro104=) n.506G>C | ClinVar dbSNP ExAC gnomAD v3 gnomAD v4 |
11 | g.32435034C>T | CA473773842 | WT1 | c.327G>A (p.Pro109=) c.312G>A (p.Pro104=) n.506G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435035G>A | CA379965919 | WT1 | c.326C>T (p.Pro109Leu) c.311C>T (p.Pro104Leu) n.505C>T | gnomAD v4 |
11 | g.32435035G>C | CA379965920 | WT1 | c.326C>G (p.Pro109Arg) c.311C>G (p.Pro104Arg) n.505C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435035G= | CA1962327288 | WT1 | c.326C= (p.Pro109=) c.311C= (p.Pro104=) n.505C= | |
11 | g.32435035G>T | CA379965921 | WT1 | c.326C>A (p.Pro109Gln) c.311C>A (p.Pro104Gln) n.505C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435036G>A | CA379965922 | WT1 | c.325C>T (p.Pro109Ser) c.310C>T (p.Pro104Ser) n.504C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435036G>C | CA379965923 | WT1 | c.325C>G (p.Pro109Ala) c.310C>G (p.Pro104Ala) n.504C>G | ClinVar dbSNP |
11 | g.32435036G>T | CA379965924 | WT1 | c.325C>A (p.Pro109Thr) c.310C>A (p.Pro104Thr) n.504C>A | gnomAD v4 |
11 | g.32435037C>A | CA473773846 | WT1 | c.324G>T (p.Ala108=) c.309G>T (p.Ala103=) n.503G>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435037C= | CA1962327289 | WT1 | c.324G= (p.Ala108=) c.309G= (p.Ala103=) n.503G= | |
11 | g.32435037C>G | CA473773847 | WT1 | c.324G>C (p.Ala108=) c.309G>C (p.Ala103=) n.503G>C | |
11 | g.32435037C>T | CA473773849 | WT1 | c.324G>A (p.Ala108=) c.309G>A (p.Ala103=) n.503G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435038G>A | CA379965925 | WT1 | c.323C>T (p.Ala108Val) c.308C>T (p.Ala103Val) n.502C>T | dbSNP gnomAD v4 |
11 | g.32435038G>C | CA379965926 | WT1 | c.323C>G (p.Ala108Gly) c.308C>G (p.Ala103Gly) n.502C>G | dbSNP gnomAD v4 |
11 | g.32435038G>T | CA379965927 | WT1 | c.323C>A (p.Ala108Glu) c.308C>A (p.Ala103Glu) n.502C>A | gnomAD v4 |
11 | g.32435039C>A | CA379965930 | WT1 | c.322G>T (p.Ala108Ser) c.307G>T (p.Ala103Ser) n.501G>T | gnomAD v4 |
11 | g.32435039C= | CA1962327290 | WT1 | c.322G= (p.Ala108=) c.307G= (p.Ala103=) n.501G= | |
11 | g.32435039C>G | CA379965929 | WT1 | c.322G>C (p.Ala108Pro) c.307G>C (p.Ala103Pro) n.501G>C | |
11 | g.32435039C>T | CA379965928 | WT1 | c.322G>A (p.Ala108Thr) c.307G>A (p.Ala103Thr) n.501G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435040C>A | CA379965931 | WT1 | c.321G>T (p.Trp107Cys) c.306G>T (p.Trp102Cys) n.500G>T | |
11 | g.32435040C>G | CA379965933 | WT1 | c.321G>C (p.Trp107Cys) c.306G>C (p.Trp102Cys) n.500G>C | |
11 | g.32435040C>T | CA379965932 | WT1 | c.321G>A (p.Trp107Ter) c.306G>A (p.Trp102Ter) n.500G>A | gnomAD v3 gnomAD v4 |
11 | g.32435041C>A | CA219511154 | WT1 | c.320G>T (p.Trp107Leu) c.305G>T (p.Trp102Leu) n.499G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435041C= | CA1962327291 | WT1 | c.320G= (p.Trp107=) c.305G= (p.Trp102=) n.499G= | |
11 | g.32435041C>G | CA379965934 | WT1 | c.320G>C (p.Trp107Ser) c.305G>C (p.Trp102Ser) n.499G>C | |
11 | g.32435041C>T | CA379965935 | WT1 | c.320G>A (p.Trp107Ter) c.305G>A (p.Trp102Ter) n.499G>A | gnomAD v4 |
11 | g.32435042A= | CA1962327292 | WT1 | c.319T= (p.Trp107=) c.304T= (p.Trp102=) n.498T= | |
11 | g.32435042A>C | CA379965936 | WT1 | c.319T>G (p.Trp107Gly) c.304T>G (p.Trp102Gly) n.498T>G | ClinVar dbSNP |
11 | g.32435042A>G | CA379965937 | WT1 | c.319T>C (p.Trp107Arg) c.304T>C (p.Trp102Arg) n.498T>C | |
11 | g.32435042A>T | CA379965938 | WT1 | c.319T>A (p.Trp107Arg) c.304T>A (p.Trp102Arg) n.498T>A | |
11 | g.32435043C>A | CA379965939 | WT1 | c.318G>T (p.Gln106His) c.303G>T (p.Gln101His) n.497G>T | gnomAD v4 |
11 | g.32435043C>G | CA379965940 | WT1 | c.318G>C (p.Gln106His) c.303G>C (p.Gln101His) n.497G>C | |
11 | g.32435043C>T | CA473773857 | WT1 | c.318G>A (p.Gln106=) c.303G>A (p.Gln101=) n.497G>A | ClinVar gnomAD v4 |
11 | g.32435044_32435048dup | CA2573146229 | WT1 | c.314_318dup (p.Trp107ArgfsTer?) c.299_303dup (p.Trp102ArgfsTer?) n.493_497dup | ClinVar dbSNP |
11 | g.32435044T>A | CA379965941 | WT1 | c.317A>T (p.Gln106Leu) c.302A>T (p.Gln101Leu) n.496A>T | dbSNP |
11 | g.32435044T>C | CA379965942 | WT1 | c.317A>G (p.Gln106Arg) c.302A>G (p.Gln101Arg) n.496A>G | dbSNP gnomAD v4 |
11 | g.32435044T>G | CA379965943 | WT1 | c.317A>C (p.Gln106Pro) c.302A>C (p.Gln101Pro) n.496A>C | |
11 | g.32435044T= | CA1962327293 | WT1 | c.317A= (p.Gln106=) c.302A= (p.Gln101=) n.496A= | |
11 | g.32435045G>A | CA379965945 | WT1 | c.316C>T (p.Gln106Ter) c.301C>T (p.Gln101Ter) n.495C>T | gnomAD v4 COSMIC COSMIC |
11 | g.32435045G>C | CA379965944 | WT1 | c.316C>G (p.Gln106Glu) c.301C>G (p.Gln101Glu) n.495C>G | |
11 | g.32435045G= | CA1962327294 | WT1 | c.316C= (p.Gln106=) c.301C= (p.Gln101=) n.495C= | |
11 | g.32435045G>T | CA064832 | WT1 | c.316C>A (p.Gln106Lys) c.301C>A (p.Gln101Lys) n.495C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435046C>A | CA473773863 | WT1 | c.315G>T (p.Ala105=) c.300G>T (p.Ala100=) n.494G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435046C= | CA1962327295 | WT1 | c.315G= (p.Ala105=) c.300G= (p.Ala100=) n.494G= | |
11 | g.32435046C>G | CA473773866 | WT1 | c.315G>C (p.Ala105=) c.300G>C (p.Ala100=) n.494G>C | |
11 | g.32435046C>T | CA473773865 | WT1 | c.315G>A (p.Ala105=) c.300G>A (p.Ala100=) n.494G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435047G>A | CA379965946 | WT1 | c.314C>T (p.Ala105Val) c.299C>T (p.Ala100Val) n.493C>T | dbSNP gnomAD v4 |
11 | g.32435047G>C | CA219511175 | WT1 | c.314C>G (p.Ala105Gly) c.299C>G (p.Ala100Gly) n.493C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435047G= | CA1962327296 | WT1 | c.314C= (p.Ala105=) c.299C= (p.Ala100=) n.493C= | |
11 | g.32435047G>T | CA379965947 | WT1 | c.314C>A (p.Ala105Glu) c.299C>A (p.Ala100Glu) n.493C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435048C>A | CA379965948 | WT1 | c.313G>T (p.Ala105Ser) c.298G>T (p.Ala100Ser) n.492G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435048C= | CA1962327297 | WT1 | c.313G= (p.Ala105=) c.298G= (p.Ala100=) n.492G= | |
11 | g.32435048C>G | CA379965949 | WT1 | c.313G>C (p.Ala105Pro) c.298G>C (p.Ala100Pro) n.492G>C | |
11 | g.32435048C>T | CA379965950 | WT1 | c.313G>A (p.Ala105Thr) c.298G>A (p.Ala100Thr) n.492G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435049C>A | CA473773876 | WT1 | c.312G>T (p.Ala104=) c.297G>T (p.Ala99=) n.491G>T | ClinVar gnomAD v4 |
11 | g.32435049C= | CA1962327298 | WT1 | c.312G= (p.Ala104=) c.297G= (p.Ala99=) n.491G= | |
11 | g.32435049C>G | CA473773878 | WT1 | c.312G>C (p.Ala104=) c.297G>C (p.Ala99=) n.491G>C | |
11 | g.32435049C>T | CA473773879 | WT1 | c.312G>A (p.Ala104=) c.297G>A (p.Ala99=) n.491G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435050G>A | CA379965951 | WT1 | c.311C>T (p.Ala104Val) c.296C>T (p.Ala99Val) n.490C>T | ClinVar gnomAD v4 COSMIC |
11 | g.32435050G>C | CA219511188 | WT1 | c.311C>G (p.Ala104Gly) c.296C>G (p.Ala99Gly) n.490C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435050G= | CA1962327299 | WT1 | c.311C= (p.Ala104=) c.296C= (p.Ala99=) n.490C= | |
11 | g.32435050G>T | CA379965952 | WT1 | c.311C>A (p.Ala104Glu) c.296C>A (p.Ala99Glu) n.490C>A | gnomAD v4 |
11 | g.32435051C>A | CA379965953 | WT1 | c.310G>T (p.Ala104Ser) c.295G>T (p.Ala99Ser) n.489G>T | gnomAD v4 |
11 | g.32435051C= | CA1962327300 | WT1 | c.310G= (p.Ala104=) c.295G= (p.Ala99=) n.489G= | |
11 | g.32435051C>G | CA379965954 | WT1 | c.310G>C (p.Ala104Pro) c.295G>C (p.Ala99Pro) n.489G>C | dbSNP |
11 | g.32435051C>T | CA379965955 | WT1 | c.310G>A (p.Ala104Thr) c.295G>A (p.Ala99Thr) n.489G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435051dup | CA2723468786 | WT1 | c.310dup (p.Ala104GlyfsTer?) c.295dup (p.Ala99GlyfsTer?) n.489dup | dbSNP |
11 | g.32435052G>A | CA473773888 | WT1 | c.309C>T (p.Gly103=) c.294C>T (p.Gly98=) n.488C>T | dbSNP gnomAD v4 |
11 | g.32435052G>C | CA473773889 | WT1 | c.309C>G (p.Gly103=) c.294C>G (p.Gly98=) n.488C>G | dbSNP |
11 | g.32435052G= | CA1962327301 | WT1 | c.309C= (p.Gly103=) c.294C= (p.Gly98=) n.488C= | |
11 | g.32435052G>T | CA064811 | WT1 | c.309C>A (p.Gly103=) c.294C>A (p.Gly98=) n.488C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435053C>A | CA379965958 | WT1 | c.308G>T (p.Gly103Val) c.293G>T (p.Gly98Val) n.487G>T | gnomAD v4 |
11 | g.32435053C>G | CA379965956 | WT1 | c.308G>C (p.Gly103Ala) c.293G>C (p.Gly98Ala) n.487G>C | |
11 | g.32435053C>T | CA379965957 | WT1 | c.308G>A (p.Gly103Asp) c.293G>A (p.Gly98Asp) n.487G>A | gnomAD v4 |
11 | g.32435054C>A | CA379965959 | WT1 | c.307G>T (p.Gly103Cys) c.292G>T (p.Gly98Cys) n.486G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435054C= | CA1962327302 | WT1 | c.307G= (p.Gly103=) c.292G= (p.Gly98=) n.486G= | |
11 | g.32435054C>G | CA379965960 | WT1 | c.307G>C (p.Gly103Arg) c.292G>C (p.Gly98Arg) n.486G>C | gnomAD v4 |
11 | g.32435054C>T | CA379965961 | WT1 | c.307G>A (p.Gly103Ser) c.292G>A (p.Gly98Ser) n.486G>A | gnomAD v4 |
11 | g.32435055G>A | CA473773896 | WT1 | c.306C>T (p.Ser102=) c.291C>T (p.Ser97=) n.485C>T | dbSNP gnomAD v4 |
11 | g.32435055G>C | CA379965962 | WT1 | c.306C>G (p.Ser102Arg) c.291C>G (p.Ser97Arg) n.485C>G | dbSNP |
11 | g.32435055G>T | CA379965963 | WT1 | c.306C>A (p.Ser102Arg) c.291C>A (p.Ser97Arg) n.485C>A | ClinVar gnomAD v4 |
11 | g.32435056C>A | CA379965964 | WT1 | c.305G>T (p.Ser102Ile) c.290G>T (p.Ser97Ile) n.484G>T | gnomAD v4 |
11 | g.32435056C= | CA1962327303 | WT1 | c.305G= (p.Ser102=) c.290G= (p.Ser97=) n.484G= | |
11 | g.32435056C>G | CA379965965 | WT1 | c.305G>C (p.Ser102Thr) c.290G>C (p.Ser97Thr) n.484G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435056C>T | CA379965966 | WT1 | c.305G>A (p.Ser102Asn) c.290G>A (p.Ser97Asn) n.484G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435058_32435059insCCCTC | CA2695213679 | WT1 | c.305_306insGGGAG (p.Ser102ArgfsTer?) c.290_291insGGGAG (p.Ser97ArgfsTer?) n.484_485insGGGAG | |
11 | g.32435057T>A | CA379965967 | WT1 | c.304A>T (p.Ser102Cys) c.289A>T (p.Ser97Cys) n.483A>T | dbSNP |
11 | g.32435057T>C | CA379965968 | WT1 | c.304A>G (p.Ser102Gly) c.289A>G (p.Ser97Gly) n.483A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435057T>G | CA379965969 | WT1 | c.304A>C (p.Ser102Arg) c.289A>C (p.Ser97Arg) n.483A>C | |
11 | g.32435057T= | CA1962327304 | WT1 | c.304A= (p.Ser102=) c.289A= (p.Ser97=) n.483A= | |
11 | g.32435058C>A | CA473773906 | WT1 | c.303G>T (p.Val101=) c.288G>T (p.Val96=) n.482G>T | gnomAD v4 |
11 | g.32435058C>G | CA473773907 | WT1 | c.303G>C (p.Val101=) c.288G>C (p.Val96=) n.482G>C | |
11 | g.32435058C>T | CA473773908 | WT1 | c.303G>A (p.Val101=) c.288G>A (p.Val96=) n.482G>A | ClinVar gnomAD v4 |
11 | g.32435059A>C | CA379965972 | WT1 | c.302T>G (p.Val101Gly) c.287T>G (p.Val96Gly) n.481T>G | |
11 | g.32435059A>G | CA379965970 | WT1 | c.302T>C (p.Val101Ala) c.287T>C (p.Val96Ala) n.481T>C | gnomAD v4 |
11 | g.32435059A>T | CA379965971 | WT1 | c.302T>A (p.Val101Glu) c.287T>A (p.Val96Glu) n.481T>A | gnomAD v4 |
11 | g.32435059_32435062del | CA645584491 | WT1 | c.299_302del (p.Pro100ArgfsTer?) c.284_287del (p.Pro95ArgfsTer?) n.478_481del | COSMIC |
11 | g.32435060C>A | CA379965973 | WT1 | c.301G>T (p.Val101Leu) c.286G>T (p.Val96Leu) n.480G>T | gnomAD v4 |
11 | g.32435060C= | CA1962327305 | WT1 | c.301G= (p.Val101=) c.286G= (p.Val96=) n.480G= | |
11 | g.32435060C>G | CA379965974 | WT1 | c.301G>C (p.Val101Leu) c.286G>C (p.Val96Leu) n.480G>C | ClinVar dbSNP |
11 | g.32435060C>T | CA379965975 | WT1 | c.301G>A (p.Val101Met) c.286G>A (p.Val96Met) n.480G>A | gnomAD v4 |
11 | g.32435061A= | CA1962327306 | WT1 | c.300T= (p.Pro100=) c.285T= (p.Pro95=) n.479T= | |
11 | g.32435061A>C | CA473773913 | WT1 | c.300T>G (p.Pro100=) c.285T>G (p.Pro95=) n.479T>G | dbSNP gnomAD v4 |
11 | g.32435061A>G | CA473773915 | WT1 | c.300T>C (p.Pro100=) c.285T>C (p.Pro95=) n.479T>C | gnomAD v4 |
11 | g.32435061A>T | CA473773916 | WT1 | c.300T>A (p.Pro100=) c.285T>A (p.Pro95=) n.479T>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435062G>A | CA379965976 | WT1 | c.299C>T (p.Pro100Leu) c.284C>T (p.Pro95Leu) n.478C>T | gnomAD v4 |
11 | g.32435062G>C | CA379965977 | WT1 | c.299C>G (p.Pro100Arg) c.284C>G (p.Pro95Arg) n.478C>G | ClinVar |
11 | g.32435062G>T | CA379965978 | WT1 | c.299C>A (p.Pro100His) c.284C>A (p.Pro95His) n.478C>A | gnomAD v4 |
11 | g.32435063G>A | CA219511235 | WT1 | c.298C>T (p.Pro100Ser) c.283C>T (p.Pro95Ser) n.477C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435063G>C | CA379965979 | WT1 | c.298C>G (p.Pro100Ala) c.283C>G (p.Pro95Ala) n.477C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32435063G= | CA1962327307 | WT1 | c.298C= (p.Pro100=) c.283C= (p.Pro95=) n.477C= | |
11 | g.32435063G>T | CA379965980 | WT1 | c.298C>A (p.Pro100Thr) c.283C>A (p.Pro95Thr) n.477C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435064C>A | CA473773924 | WT1 | c.297G>T (p.Leu99=) c.282G>T (p.Leu94=) n.476G>T | gnomAD v4 |
11 | g.32435064C= | CA1962327308 | WT1 | c.297G= (p.Leu99=) c.282G= (p.Leu94=) n.476G= | |
11 | g.32435064C>G | CA473773925 | WT1 | c.297G>C (p.Leu99=) c.282G>C (p.Leu94=) n.476G>C | gnomAD v4 |
11 | g.32435064C>T | CA473773926 | WT1 | c.297G>A (p.Leu99=) c.282G>A (p.Leu94=) n.476G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
11 | g.32435065A= | CA1962327309 | WT1 | c.296T= (p.Leu99=) c.281T= (p.Leu94=) n.475T= | |
11 | g.32435065A>C | CA379965981 | WT1 | c.296T>G (p.Leu99Arg) c.281T>G (p.Leu94Arg) n.475T>G | |
11 | g.32435065A>G | CA379965982 | WT1 | c.296T>C (p.Leu99Pro) c.281T>C (p.Leu94Pro) n.475T>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435065A>T | CA379965983 | WT1 | c.296T>A (p.Leu99Gln) c.281T>A (p.Leu94Gln) n.475T>A | ClinVar dbSNP |
11 | g.32435066G>A | CA473773931 | WT1 | c.295C>T (p.Leu99=) c.280C>T (p.Leu94=) n.474C>T | gnomAD v4 |
11 | g.32435066G>C | CA379965985 | WT1 | c.295C>G (p.Leu99Val) c.280C>G (p.Leu94Val) n.474C>G | ClinVar dbSNP |
11 | g.32435066G= | CA1962327310 | WT1 | c.295C= (p.Leu99=) c.280C= (p.Leu94=) n.474C= | |
11 | g.32435066G>T | CA379965984 | WT1 | c.295C>A (p.Leu99Met) c.280C>A (p.Leu94Met) n.474C>A | gnomAD v4 |
11 | g.32435067G>A | CA219511241 | WT1 | c.294C>T (p.Ala98=) c.279C>T (p.Ala93=) n.473C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435067G>C | CA473773933 | WT1 | c.294C>G (p.Ala98=) c.279C>G (p.Ala93=) n.473C>G | |
11 | g.32435067G= | CA1962327311 | WT1 | c.294C= (p.Ala98=) c.279C= (p.Ala93=) n.473C= | |
11 | g.32435067G>T | CA473773934 | WT1 | c.294C>A (p.Ala98=) c.279C>A (p.Ala93=) n.473C>A | |
11 | g.32435068G>A | CA379965986 | WT1 | c.293C>T (p.Ala98Val) c.278C>T (p.Ala93Val) n.472C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435068G>C | CA379965988 | WT1 | c.293C>G (p.Ala98Gly) c.278C>G (p.Ala93Gly) n.472C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32435068G= | CA1962327312 | WT1 | c.293C= (p.Ala98=) c.278C= (p.Ala93=) n.472C= | |
11 | g.32435068G>T | CA379965987 | WT1 | c.293C>A (p.Ala98Asp) c.278C>A (p.Ala93Asp) n.472C>A | gnomAD v4 |
11 | g.32435069C>A | CA379965989 | WT1 | c.292G>T (p.Ala98Ser) c.277G>T (p.Ala93Ser) n.471G>T | dbSNP gnomAD v4 |
11 | g.32435069C>G | CA379965990 | WT1 | c.292G>C (p.Ala98Pro) c.277G>C (p.Ala93Pro) n.471G>C | |
11 | g.32435069C>T | CA379965991 | WT1 | c.292G>A (p.Ala98Thr) c.277G>A (p.Ala93Thr) n.471G>A | gnomAD v4 |
11 | g.32435070A= | CA1962327313 | WT1 | c.291T= (p.Cys97=) c.276T= (p.Cys92=) n.470T= | |
11 | g.32435070A>C | CA064806 | WT1 | c.291T>G (p.Cys97Trp) c.276T>G (p.Cys92Trp) n.470T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435070A>G | CA473773939 | WT1 | c.291T>C (p.Cys97=) c.276T>C (p.Cys92=) n.470T>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435070A>T | CA379965992 | WT1 | c.291T>A (p.Cys97Ter) c.276T>A (p.Cys92Ter) n.470T>A | |
11 | g.32435071C>A | CA379965993 | WT1 | c.290G>T (p.Cys97Phe) c.275G>T (p.Cys92Phe) n.469G>T | gnomAD v4 |
11 | g.32435071C= | CA1962327314 | WT1 | c.290G= (p.Cys97=) c.275G= (p.Cys92=) n.469G= | |
11 | g.32435071C>G | CA379965994 | WT1 | c.290G>C (p.Cys97Ser) c.275G>C (p.Cys92Ser) n.469G>C | ClinVar dbSNP |
11 | g.32435071C>T | CA379965995 | WT1 | c.290G>A (p.Cys97Tyr) c.275G>A (p.Cys92Tyr) n.469G>A | gnomAD v4 |
11 | g.32435072A= | CA1962327315 | WT1 | c.289T= (p.Cys97=) c.274T= (p.Cys92=) n.468T= | |
11 | g.32435072A>C | CA379965996 | WT1 | c.289T>G (p.Cys97Gly) c.274T>G (p.Cys92Gly) n.468T>G | dbSNP |
11 | g.32435072A>G | CA379965997 | WT1 | c.289T>C (p.Cys97Arg) c.274T>C (p.Cys92Arg) n.468T>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435072A>T | CA379965998 | WT1 | c.289T>A (p.Cys97Ser) c.274T>A (p.Cys92Ser) n.468T>A | |
11 | g.32435072_32435075delinsAGCC | CA1962327316 | WT1 | c.286_289delinsGGCT (p.Gly96=) c.271_274delinsGGCT (p.Gly91=) n.465_468delinsGGCT | |
11 | g.32435072_32435073insTCC | CA2580084184 | WT1 | c.288_289insGGA (p.Gly96_Cys97insGly) c.273_274insGGA (p.Gly91_Cys92insGly) n.467_468insGGA | ClinVar |
11 | g.32435073G>A | CA473773942 | WT1 | c.288C>T (p.Gly96=) c.273C>T (p.Gly91=) n.467C>T | dbSNP gnomAD v4 |
11 | g.32435073G>C | CA473773943 | WT1 | c.288C>G (p.Gly96=) c.273C>G (p.Gly91=) n.467C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32435073G= | CA1962327317 | WT1 | c.288C= (p.Gly96=) c.273C= (p.Gly91=) n.467C= | |
11 | g.32435073G>T | CA473773944 | WT1 | c.288C>A (p.Gly96=) c.273C>A (p.Gly91=) n.467C>A | gnomAD v4 |
11 | g.32435082_32435084dup | CA2580615657 | WT1 | c.286_288dup (p.Gly96_Cys97insGly) c.271_273dup (p.Gly91_Cys92insGly) n.465_467dup | ClinVar dbSNP gnomAD v4 |
11 | g.32435082_32435084del | CA064802 | WT1 | c.286_288del (p.Gly96del) c.271_273del (p.Gly91del) n.465_467del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435073_32435074insTCC | CA2825001877 | WT1 | c.287_288insGGA (p.Gly96_Cys97insAsp) c.272_273insGGA (p.Gly91_Cys92insAsp) n.466_467insGGA | ClinVar |
11 | g.32435074C>A | CA379966001 | WT1 | c.287G>T (p.Gly96Val) c.272G>T (p.Gly91Val) n.466G>T | gnomAD v4 |
11 | g.32435074C>G | CA379965999 | WT1 | c.287G>C (p.Gly96Ala) c.272G>C (p.Gly91Ala) n.466G>C | |
11 | g.32435074C>T | CA379966000 | WT1 | c.287G>A (p.Gly96Asp) c.272G>A (p.Gly91Asp) n.466G>A | dbSNP gnomAD v4 |
11 | g.32435075C>A | CA379966002 | WT1 | c.286G>T (p.Gly96Cys) c.271G>T (p.Gly91Cys) n.465G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435075C= | CA1962327318 | WT1 | c.286G= (p.Gly96=) c.271G= (p.Gly91=) n.465G= | |
11 | g.32435075C>G | CA379966003 | WT1 | c.286G>C (p.Gly96Arg) c.271G>C (p.Gly91Arg) n.465G>C | |
11 | g.32435075C>T | CA16613605 | WT1 | c.286G>A (p.Gly96Ser) c.271G>A (p.Gly91Ser) n.465G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435076G>A | CA10638966 | WT1 | c.285C>T (p.Gly95=) c.270C>T (p.Gly90=) n.464C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435076G>C | CA473773947 | WT1 | c.285C>G (p.Gly95=) c.270C>G (p.Gly90=) n.464C>G | dbSNP |
11 | g.32435076G= | CA1962327319 | WT1 | c.285C= (p.Gly95=) c.270C= (p.Gly90=) n.464C= | |
11 | g.32435076G>T | CA473773948 | WT1 | c.285C>A (p.Gly95=) c.270C>A (p.Gly90=) n.464C>A | gnomAD v4 |
11 | g.32435077C>A | CA379966004 | WT1 | c.284G>T (p.Gly95Val) c.269G>T (p.Gly90Val) n.463G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435077C= | CA1962327320 | WT1 | c.284G= (p.Gly95=) c.269G= (p.Gly90=) n.463G= | |
11 | g.32435077C>G | CA379966005 | WT1 | c.284G>C (p.Gly95Ala) c.269G>C (p.Gly90Ala) n.463G>C | dbSNP |
11 | g.32435077C>T | CA379966006 | WT1 | c.284G>A (p.Gly95Asp) c.269G>A (p.Gly90Asp) n.463G>A | ClinVar dbSNP gnomAD v4 |