Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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.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 |
11 | g.32435078C>A | CA379966007 | WT1 | c.283G>T (p.Gly95Cys) c.268G>T (p.Gly90Cys) n.462G>T | gnomAD v4 |
11 | g.32435078C>G | CA379966008 | WT1 | c.283G>C (p.Gly95Arg) c.268G>C (p.Gly90Arg) n.462G>C | dbSNP gnomAD v4 |
11 | g.32435078C>T | CA379966009 | WT1 | c.283G>A (p.Gly95Ser) c.268G>A (p.Gly90Ser) n.462G>A | dbSNP gnomAD v4 |
11 | g.32435079G>A | CA473773952 | WT1 | c.282C>T (p.Gly94=) c.267C>T (p.Gly89=) n.461C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435079G>C | CA473773953 | WT1 | c.282C>G (p.Gly94=) c.267C>G (p.Gly89=) n.461C>G | dbSNP |
11 | g.32435079G= | CA1962327321 | WT1 | c.282C= (p.Gly94=) c.267C= (p.Gly89=) n.461C= | |
11 | g.32435079G>T | CA473773954 | WT1 | c.282C>A (p.Gly94=) c.267C>A (p.Gly89=) n.461C>A | gnomAD v4 |
11 | g.32435080C>A | CA379966012 | WT1 | c.281G>T (p.Gly94Val) c.266G>T (p.Gly89Val) n.460G>T | gnomAD v4 |
11 | g.32435080C= | CA1962327322 | WT1 | c.281G= (p.Gly94=) c.266G= (p.Gly89=) n.460G= | |
11 | g.32435080C>G | CA379966011 | WT1 | c.281G>C (p.Gly94Ala) c.266G>C (p.Gly89Ala) n.460G>C | |
11 | g.32435080C>T | CA379966010 | WT1 | c.281G>A (p.Gly94Asp) c.266G>A (p.Gly89Asp) n.460G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435081C>A | CA379966014 | WT1 | c.280G>T (p.Gly94Cys) c.265G>T (p.Gly89Cys) n.459G>T | gnomAD v4 |
11 | g.32435081C= | CA1962327323 | WT1 | c.280G= (p.Gly94=) c.265G= (p.Gly89=) n.459G= | |
11 | g.32435081C>G | CA379966013 | WT1 | c.280G>C (p.Gly94Arg) c.265G>C (p.Gly89Arg) n.459G>C | gnomAD v4 |
11 | g.32435081C>T | CA064798 | WT1 | c.280G>A (p.Gly94Ser) c.265G>A (p.Gly89Ser) n.459G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435082G>A | CA473773960 | WT1 | c.279C>T (p.Gly93=) c.264C>T (p.Gly88=) n.458C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435082G>C | CA473773962 | WT1 | c.279C>G (p.Gly93=) c.264C>G (p.Gly88=) n.458C>G | dbSNP |
11 | g.32435082G= | CA1962327324 | WT1 | c.279C= (p.Gly93=) c.264C= (p.Gly88=) n.458C= | |
11 | g.32435082G>T | CA473773961 | WT1 | c.279C>A (p.Gly93=) c.264C>A (p.Gly88=) n.458C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435084_32435112del | CA2695213680 | WT1 | c.251_279del (p.Leu84ArgfsTer?) c.236_264del (p.Leu79ArgfsTer?) n.430_458del | |
11 | g.32435083C>A | CA379966015 | WT1 | c.278G>T (p.Gly93Val) c.263G>T (p.Gly88Val) n.457G>T | gnomAD v4 |
11 | g.32435083C= | CA1962327325 | WT1 | c.278G= (p.Gly93=) c.263G= (p.Gly88=) n.457G= | |
11 | g.32435083C>G | CA379966016 | WT1 | c.278G>C (p.Gly93Ala) c.263G>C (p.Gly88Ala) n.457G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435083C>T | CA379966017 | WT1 | c.278G>A (p.Gly93Asp) c.263G>A (p.Gly88Asp) n.457G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435085_32435087del | CA2612989581 | WT1 | c.276_278del (p.Gly93del) c.261_263del (p.Gly88del) n.455_457del | gnomAD v4 |
11 | g.32435084C>A | CA379966020 | WT1 | c.277G>T (p.Gly93Cys) c.262G>T (p.Gly88Cys) n.456G>T | gnomAD v4 |
11 | g.32435084C>G | CA379966019 | WT1 | c.277G>C (p.Gly93Arg) c.262G>C (p.Gly88Arg) n.456G>C | |
11 | g.32435084C>T | CA379966018 | WT1 | c.277G>A (p.Gly93Ser) c.262G>A (p.Gly88Ser) n.456G>A | gnomAD v4 |
11 | g.32435085del | CA2573146230 | WT1 | c.276del (p.Gly93AlafsTer9) c.261del (p.Gly88AlafsTer9) n.455del | ClinVar dbSNP |
11 | g.32435085A>C | CA473773968 | WT1 | c.276T>G (p.Gly92=) c.261T>G (p.Gly87=) n.455T>G | dbSNP |
11 | g.32435085A>G | CA473773970 | WT1 | c.276T>C (p.Gly92=) c.261T>C (p.Gly87=) n.455T>C | gnomAD v4 |
11 | g.32435085A>T | CA473773972 | WT1 | c.276T>A (p.Gly92=) c.261T>A (p.Gly87=) n.455T>A | |
11 | g.32435086C>A | CA379966021 | WT1 | c.275G>T (p.Gly92Val) c.260G>T (p.Gly87Val) n.454G>T | gnomAD v4 |
11 | g.32435086C>G | CA379966022 | WT1 | c.275G>C (p.Gly92Ala) c.260G>C (p.Gly87Ala) n.454G>C | |
11 | g.32435086C>T | CA379966023 | WT1 | c.275G>A (p.Gly92Asp) c.260G>A (p.Gly87Asp) n.454G>A | ClinVar |
11 | g.32435088dup | CA2740093680 | WT1 | c.275dup (p.Gly93TrpfsTer?) c.260dup (p.Gly88TrpfsTer?) n.454dup | ClinVar |
11 | g.32435088del | CA2612989583 | WT1 | c.275del (p.Gly92ValfsTer10) c.260del (p.Gly87ValfsTer10) n.454del | gnomAD v4 |
11 | g.32435087C>A | CA379966024 | WT1 | c.274G>T (p.Gly92Cys) c.259G>T (p.Gly87Cys) n.453G>T | gnomAD v4 |
11 | g.32435087C>G | CA379966025 | WT1 | c.274G>C (p.Gly92Arg) c.259G>C (p.Gly87Arg) n.453G>C | |
11 | g.32435087C>T | CA379966026 | WT1 | c.274G>A (p.Gly92Ser) c.259G>A (p.Gly87Ser) n.453G>A | gnomAD v4 |
11 | g.32435088C>A | CA473773977 | WT1 | c.273G>T (p.Leu91=) c.258G>T (p.Leu86=) n.452G>T | dbSNP gnomAD v4 |
11 | g.32435088C= | CA1962327326 | WT1 | c.273G= (p.Leu91=) c.258G= (p.Leu86=) n.452G= | |
11 | g.32435088C>G | CA473773978 | WT1 | c.273G>C (p.Leu91=) c.258G>C (p.Leu86=) n.452G>C | |
11 | g.32435088C>T | CA473773980 | WT1 | c.273G>A (p.Leu91=) c.258G>A (p.Leu86=) n.452G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435089A>C | CA379966027 | WT1 | c.272T>G (p.Leu91Arg) c.257T>G (p.Leu86Arg) n.451T>G | |
11 | g.32435089A>G | CA379966029 | WT1 | c.272T>C (p.Leu91Pro) c.257T>C (p.Leu86Pro) n.451T>C | gnomAD v4 |
11 | g.32435089A>T | CA379966028 | WT1 | c.272T>A (p.Leu91Gln) c.257T>A (p.Leu86Gln) n.451T>A | gnomAD v4 |
11 | g.32435090G>A | CA473773984 | WT1 | c.271C>T (p.Leu91=) c.256C>T (p.Leu86=) n.450C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435090G>C | CA379966030 | WT1 | c.271C>G (p.Leu91Val) c.256C>G (p.Leu86Val) n.450C>G | dbSNP |
11 | g.32435090G= | CA1962327327 | WT1 | c.271C= (p.Leu91=) c.256C= (p.Leu86=) n.450C= | |
11 | g.32435090G>T | CA379966031 | WT1 | c.271C>A (p.Leu91Met) c.256C>A (p.Leu86Met) n.450C>A | gnomAD v4 |
11 | g.32435094_32435098del | CA645584492 | WT1 | c.267_271del (p.Ser90GlyfsTer?) c.252_256del (p.Ser85GlyfsTer?) n.446_450del | COSMIC COSMIC |
11 | g.32435091G>A | CA473773986 | WT1 | c.270C>T (p.Ser90=) c.255C>T (p.Ser85=) n.449C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435091G>C | CA064793 | WT1 | c.270C>G (p.Ser90=) c.255C>G (p.Ser85=) n.449C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435091G= | CA1962327328 | WT1 | c.270C= (p.Ser90=) c.255C= (p.Ser85=) n.449C= | |
11 | g.32435091G>T | CA473773987 | WT1 | c.270C>A (p.Ser90=) c.255C>A (p.Ser85=) n.449C>A | gnomAD v4 |
11 | g.32435092G>A | CA379966032 | WT1 | c.269C>T (p.Ser90Phe) c.254C>T (p.Ser85Phe) n.448C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435092G>C | CA379966033 | WT1 | c.269C>G (p.Ser90Cys) c.254C>G (p.Ser85Cys) n.448C>G | |
11 | g.32435092G= | CA1962327329 | WT1 | c.269C= (p.Ser90=) c.254C= (p.Ser85=) n.448C= | |
11 | g.32435092G>T | CA379966034 | WT1 | c.269C>A (p.Ser90Tyr) c.254C>A (p.Ser85Tyr) n.448C>A | gnomAD v4 |
11 | g.32435093A= | CA1962327330 | WT1 | c.268T= (p.Ser90=) c.253T= (p.Ser85=) n.447T= | |
11 | g.32435093A>C | CA379966035 | WT1 | c.268T>G (p.Ser90Ala) c.253T>G (p.Ser85Ala) n.447T>G | |
11 | g.32435093A>G | CA379966036 | WT1 | c.268T>C (p.Ser90Pro) c.253T>C (p.Ser85Pro) n.447T>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435093A>T | CA379966037 | WT1 | c.268T>A (p.Ser90Thr) c.253T>A (p.Ser85Thr) n.447T>A | |
11 | g.32435094G>A | CA473773990 | WT1 | c.267C>T (p.Pro89=) c.252C>T (p.Pro84=) n.446C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435094G>C | CA473773995 | WT1 | c.267C>G (p.Pro89=) c.252C>G (p.Pro84=) n.446C>G | gnomAD v4 |
11 | g.32435094G= | CA1962327331 | WT1 | c.267C= (p.Pro89=) c.252C= (p.Pro84=) n.446C= | |
11 | g.32435094G>T | CA473773996 | WT1 | c.267C>A (p.Pro89=) c.252C>A (p.Pro84=) n.446C>A | gnomAD v4 |
11 | g.32435095G>A | CA379966038 | WT1 | c.266C>T (p.Pro89Leu) c.251C>T (p.Pro84Leu) n.445C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435095G>C | CA379966039 | WT1 | c.266C>G (p.Pro89Arg) c.251C>G (p.Pro84Arg) n.445C>G | ClinVar |
11 | g.32435095G= | CA1962327332 | WT1 | c.266C= (p.Pro89=) c.251C= (p.Pro84=) n.445C= | |
11 | g.32435095G>T | CA379966040 | WT1 | c.266C>A (p.Pro89His) c.251C>A (p.Pro84His) n.445C>A | gnomAD v4 |
11 | g.32435096G>A | CA379966042 | WT1 | c.265C>T (p.Pro89Ser) c.250C>T (p.Pro84Ser) n.444C>T | gnomAD v4 |
11 | g.32435096G>C | CA379966043 | WT1 | c.265C>G (p.Pro89Ala) c.250C>G (p.Pro84Ala) n.444C>G | dbSNP |
11 | g.32435096G>T | CA379966041 | WT1 | c.265C>A (p.Pro89Thr) c.250C>A (p.Pro84Thr) n.444C>A | ClinVar gnomAD v4 COSMIC COSMIC |
11 | g.32435096_32435098del | CA2574790568 | WT1 | c.263_265del (p.Val88_Pro89delinsAla) c.248_250del (p.Val83_Pro84delinsAla) n.442_444del | |
11 | g.32435097G>A | CA473774000 | WT1 | c.264C>T (p.Val88=) c.249C>T (p.Val83=) n.443C>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435097G>C | CA473774001 | WT1 | c.264C>G (p.Val88=) c.249C>G (p.Val83=) n.443C>G | gnomAD v4 |
11 | g.32435097G= | CA1962327333 | WT1 | c.264C= (p.Val88=) c.249C= (p.Val83=) n.443C= | |
11 | g.32435097G>T | CA473774003 | WT1 | c.264C>A (p.Val88=) c.249C>A (p.Val83=) n.443C>A | gnomAD v4 |
11 | g.32435098A>C | CA379966044 | WT1 | c.263T>G (p.Val88Gly) c.248T>G (p.Val83Gly) n.442T>G | |
11 | g.32435098A>G | CA379966045 | WT1 | c.263T>C (p.Val88Ala) c.248T>C (p.Val83Ala) n.442T>C | dbSNP gnomAD v4 |
11 | g.32435098A>T | CA379966046 | WT1 | c.263T>A (p.Val88Asp) c.248T>A (p.Val83Asp) n.442T>A | ClinVar gnomAD v4 |
11 | g.32435099C>A | CA379966047 | WT1 | c.262G>T (p.Val88Phe) c.247G>T (p.Val83Phe) n.441G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435099C= | CA1962327334 | WT1 | c.262G= (p.Val88=) c.247G= (p.Val83=) n.441G= | |
11 | g.32435099C>G | CA379966048 | WT1 | c.262G>C (p.Val88Leu) c.247G>C (p.Val83Leu) n.441G>C | gnomAD v4 |
11 | g.32435099C>T | CA379966049 | WT1 | c.262G>A (p.Val88Ile) c.247G>A (p.Val83Ile) n.441G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435099_32435100delinsAA | CA2580084189 | WT1 | c.261_262delinsTT (p.Val88Phe) c.246_247delinsTT (p.Val83Phe) n.440_441delinsTT | ClinVar |
11 | g.32435100G>A | CA473774006 | WT1 | c.261C>T (p.Ala87=) c.246C>T (p.Ala82=) n.440C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435100G>C | CA473774007 | WT1 | c.261C>G (p.Ala87=) c.246C>G (p.Ala82=) n.440C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435100G= | CA1962327335 | WT1 | c.261C= (p.Ala87=) c.246C= (p.Ala82=) n.440C= | |
11 | g.32435100G>T | CA473774009 | WT1 | c.261C>A (p.Ala87=) c.246C>A (p.Ala82=) n.440C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435101G>A | CA379966052 | WT1 | c.260C>T (p.Ala87Val) c.245C>T (p.Ala82Val) n.439C>T | dbSNP gnomAD v4 |
11 | g.32435101G>C | CA379966051 | WT1 | c.260C>G (p.Ala87Gly) c.245C>G (p.Ala82Gly) n.439C>G | |
11 | g.32435101G>T | CA379966050 | WT1 | c.260C>A (p.Ala87Asp) c.245C>A (p.Ala82Asp) n.439C>A | |
11 | g.32435102C>A | CA379966053 | WT1 | c.259G>T (p.Ala87Ser) c.244G>T (p.Ala82Ser) n.438G>T | gnomAD v4 |
11 | g.32435102C= | CA1962327336 | WT1 | c.259G= (p.Ala87=) c.244G= (p.Ala82=) n.438G= | |
11 | g.32435102C>G | CA379966054 | WT1 | c.259G>C (p.Ala87Pro) c.244G>C (p.Ala82Pro) n.438G>C | dbSNP gnomAD v4 |
11 | g.32435102C>T | CA064789 | WT1 | c.259G>A (p.Ala87Thr) c.244G>A (p.Ala82Thr) n.438G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435103G>A | CA473774014 | WT1 | c.258C>T (p.Pro86=) c.243C>T (p.Pro81=) n.437C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435103G>C | CA473774015 | WT1 | c.258C>G (p.Pro86=) c.243C>G (p.Pro81=) n.437C>G | |
11 | g.32435103G= | CA1962327337 | WT1 | c.258C= (p.Pro86=) c.243C= (p.Pro81=) n.437C= | |
11 | g.32435103G>T | CA473774012 | WT1 | c.258C>A (p.Pro86=) c.243C>A (p.Pro81=) n.437C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435105_32435106insGCCCGGGCGCCTGGG | CA2790963048 | WT1 | c.258_259insAGGCGCCCGGGCCCC (p.Pro86_Ala87insArgArgProGlyPro) c.243_244insAGGCGCCCGGGCCCC (p.Pro81_Ala82insArgArgProGlyPro) n.437_438insAGGCGCCCGGGCCCC | |
11 | g.32435104G>A | CA379966055 | WT1 | c.257C>T (p.Pro86Leu) c.242C>T (p.Pro81Leu) n.436C>T | ClinVar gnomAD v4 |
11 | g.32435104G>C | CA379966056 | WT1 | c.257C>G (p.Pro86Arg) c.242C>G (p.Pro81Arg) n.436C>G | |
11 | g.32435104G>T | CA379966057 | WT1 | c.257C>A (p.Pro86His) c.242C>A (p.Pro81His) n.436C>A | gnomAD v4 |
11 | g.32435105G>A | CA379966058 | WT1 | c.256C>T (p.Pro86Ser) c.241C>T (p.Pro81Ser) n.435C>T | dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32435105G>C | CA379966060 | WT1 | c.256C>G (p.Pro86Ala) c.241C>G (p.Pro81Ala) n.435C>G | |
11 | g.32435105G>T | CA379966059 | WT1 | c.256C>A (p.Pro86Thr) c.241C>A (p.Pro81Thr) n.435C>A | gnomAD v4 |
11 | g.32435106C>A | CA473774031 | WT1 | c.255G>T (p.Leu85=) c.240G>T (p.Leu80=) n.434G>T | gnomAD v4 |
11 | g.32435106C= | CA1962327338 | WT1 | c.255G= (p.Leu85=) c.240G= (p.Leu80=) n.434G= | |
11 | g.32435106C>G | CA473774024 | WT1 | c.255G>C (p.Leu85=) c.240G>C (p.Leu80=) n.434G>C | |
11 | g.32435106C>T | CA473774023 | WT1 | c.255G>A (p.Leu85=) c.240G>A (p.Leu80=) n.434G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435107A>C | CA379966061 | WT1 | c.254T>G (p.Leu85Arg) c.239T>G (p.Leu80Arg) n.433T>G | |
11 | g.32435107A>G | CA379966062 | WT1 | c.254T>C (p.Leu85Pro) c.239T>C (p.Leu80Pro) n.433T>C | ClinVar gnomAD v4 |
11 | g.32435107A>T | CA379966063 | WT1 | c.254T>A (p.Leu85Gln) c.239T>A (p.Leu80Gln) n.433T>A | gnomAD v4 |
11 | g.32435108G>A | CA473774032 | WT1 | c.253C>T (p.Leu85=) c.238C>T (p.Leu80=) n.432C>T | dbSNP gnomAD v4 |
11 | g.32435108G>C | CA379966064 | WT1 | c.253C>G (p.Leu85Val) c.238C>G (p.Leu80Val) n.432C>G | |
11 | g.32435108G>T | CA379966065 | WT1 | c.253C>A (p.Leu85Met) c.238C>A (p.Leu80Met) n.432C>A | gnomAD v4 |
11 | g.32435109C>A | CA473774035 | WT1 | c.252G>T (p.Leu84=) c.237G>T (p.Leu79=) n.431G>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435109C= | CA1962327339 | WT1 | c.252G= (p.Leu84=) c.237G= (p.Leu79=) n.431G= | |
11 | g.32435109C>G | CA473774038 | WT1 | c.252G>C (p.Leu84=) c.237G>C (p.Leu79=) n.431G>C | |
11 | g.32435109C>T | CA473774037 | WT1 | c.252G>A (p.Leu84=) c.237G>A (p.Leu79=) n.431G>A | dbSNP gnomAD v4 |
11 | g.32435110A>C | CA379966066 | WT1 | c.251T>G (p.Leu84Arg) c.236T>G (p.Leu79Arg) n.430T>G | gnomAD v4 |
11 | g.32435110A>G | CA379966067 | WT1 | c.251T>C (p.Leu84Pro) c.236T>C (p.Leu79Pro) n.430T>C | gnomAD v4 |
11 | g.32435110A>T | CA379966068 | WT1 | c.251T>A (p.Leu84Gln) c.236T>A (p.Leu79Gln) n.430T>A | |
11 | g.32435111G>A | CA064783 | WT1 | c.250C>T (p.Leu84=) c.235C>T (p.Leu79=) n.429C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435111G>C | CA379966069 | WT1 | c.250C>G (p.Leu84Val) c.235C>G (p.Leu79Val) n.429C>G | |
11 | g.32435111G= | CA1962327340 | WT1 | c.250C= (p.Leu84=) c.235C= (p.Leu79=) n.429C= | |
11 | g.32435111G>T | CA379966070 | WT1 | c.250C>A (p.Leu84Met) c.235C>A (p.Leu79Met) n.429C>A | gnomAD v4 |
11 | g.32435112C>A | CA473774039 | WT1 | c.249G>T (p.Ala83=) c.234G>T (p.Ala78=) n.428G>T | ClinVar gnomAD v4 |
11 | g.32435112C= | CA1962327341 | WT1 | c.249G= (p.Ala83=) c.234G= (p.Ala78=) n.428G= | |
11 | g.32435112C>G | CA473774040 | WT1 | c.249G>C (p.Ala83=) c.234G>C (p.Ala78=) n.428G>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435112C>T | CA473774041 | WT1 | c.249G>A (p.Ala83=) c.234G>A (p.Ala78=) n.428G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435113G>A | CA379966071 | WT1 | c.248C>T (p.Ala83Val) c.233C>T (p.Ala78Val) n.427C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
11 | g.32435113G>C | CA379966073 | WT1 | c.248C>G (p.Ala83Gly) c.233C>G (p.Ala78Gly) n.427C>G | |
11 | g.32435113G= | CA1962327342 | WT1 | c.248C= (p.Ala83=) c.233C= (p.Ala78=) n.427C= | |
11 | g.32435113G>T | CA379966072 | WT1 | c.248C>A (p.Ala83Glu) c.233C>A (p.Ala78Glu) n.427C>A | gnomAD v4 |
11 | g.32435113_32435114delinsAG | CA2740093681 | WT1 | c.247_248delinsCT (p.Ala83Leu) c.232_233delinsCT (p.Ala78Leu) n.426_427delinsCT | ClinVar |
11 | g.32435114C>A | CA10634698 | WT1 | c.247G>T (p.Ala83Ser) c.232G>T (p.Ala78Ser) n.426G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435114C= | CA1962327343 | WT1 | c.247G= (p.Ala83=) c.232G= (p.Ala78=) n.426G= | |
11 | g.32435114C>G | CA379966074 | WT1 | c.247G>C (p.Ala83Pro) c.232G>C (p.Ala78Pro) n.426G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435114C>T | CA379966075 | WT1 | c.247G>A (p.Ala83Thr) c.232G>A (p.Ala78Thr) n.426G>A | ClinVar gnomAD v4 |
11 | g.32435115G>A | CA473774047 | WT1 | c.246C>T (p.Asn82=) c.231C>T (p.Asn77=) n.425C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435115G>C | CA379966076 | WT1 | c.246C>G (p.Asn82Lys) c.231C>G (p.Asn77Lys) n.425C>G | ClinVar |
11 | g.32435115G= | CA1962327344 | WT1 | c.246C= (p.Asn82=) c.231C= (p.Asn77=) n.425C= | |
11 | g.32435115G>T | CA379966077 | WT1 | c.246C>A (p.Asn82Lys) c.231C>A (p.Asn77Lys) n.425C>A | ClinVar gnomAD v4 |
11 | g.32435116T>A | CA379966078 | WT1 | c.245A>T (p.Asn82Ile) c.230A>T (p.Asn77Ile) n.424A>T | |
11 | g.32435116T>C | CA379966079 | WT1 | c.245A>G (p.Asn82Ser) c.230A>G (p.Asn77Ser) n.424A>G | |
11 | g.32435116T>G | CA379966080 | WT1 | c.245A>C (p.Asn82Thr) c.230A>C (p.Asn77Thr) n.424A>C | dbSNP |
11 | g.32435117T>A | CA379966081 | WT1 | c.244A>T (p.Asn82Tyr) c.229A>T (p.Asn77Tyr) n.423A>T | |
11 | g.32435117T>C | CA379966082 | WT1 | c.244A>G (p.Asn82Asp) c.229A>G (p.Asn77Asp) n.423A>G | ClinVar gnomAD v4 |
11 | g.32435117T>G | CA379966083 | WT1 | c.244A>C (p.Asn82His) c.229A>C (p.Asn77His) n.423A>C |