Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32434843A>C | CA379964798 | WT1 | c.518T>G (p.Phe173Cys) c.503T>G (p.Phe168Cys) n.697T>G | |
11 | g.32434843A>G | CA379964800 | WT1 | c.518T>C (p.Phe173Ser) c.503T>C (p.Phe168Ser) n.697T>C | |
11 | g.32434843A>T | CA379964802 | WT1 | c.518T>A (p.Phe173Tyr) c.503T>A (p.Phe168Tyr) n.697T>A | |
11 | g.32434843_32434844insC | CA2612989399 | WT1 | c.517_518insG (p.Phe173CysfsTer?) c.502_503insG (p.Phe168CysfsTer?) n.696_697insG | gnomAD v4 |
11 | g.32434844A>C | CA379964803 | WT1 | c.517T>G (p.Phe173Val) c.502T>G (p.Phe168Val) n.696T>G | |
11 | g.32434844A>G | CA379964804 | WT1 | c.517T>C (p.Phe173Leu) c.502T>C (p.Phe168Leu) n.696T>C | |
11 | g.32434844A>T | CA379964805 | WT1 | c.517T>A (p.Phe173Ile) c.502T>A (p.Phe168Ile) n.696T>A | |
11 | g.32434844_32434845insGG | CA2612989400 | WT1 | c.516_517insCC (p.Phe173ProfsTer?) c.501_502insCC (p.Phe168ProfsTer?) n.695_696insCC | gnomAD v4 |
11 | g.32434845C>A | CA379964806 | WT1 | c.516G>T (p.Gln172His) c.501G>T (p.Gln167His) n.695G>T | |
11 | g.32434845C>G | CA379964807 | WT1 | c.516G>C (p.Gln172His) c.501G>C (p.Gln167His) n.695G>C | gnomAD v4 |
11 | g.32434845C>T | CA473571559 | WT1 | c.516G>A (p.Gln172=) c.501G>A (p.Gln167=) n.695G>A | |
11 | g.32434846T>A | CA379964809 | WT1 | c.515A>T (p.Gln172Leu) c.500A>T (p.Gln167Leu) n.694A>T | |
11 | g.32434846T>C | CA379964812 | WT1 | c.515A>G (p.Gln172Arg) c.500A>G (p.Gln167Arg) n.694A>G | |
11 | g.32434846T>G | CA379964810 | WT1 | c.515A>C (p.Gln172Pro) c.500A>C (p.Gln167Pro) n.694A>C | |
11 | g.32434846_32434847insCC | CA2612989401 | WT1 | c.514_515insGG (p.Gln172ArgfsTer?) c.499_500insGG (p.Gln167ArgfsTer?) n.693_694insGG | gnomAD v4 |
11 | g.32434847G>A | CA379964814 | WT1 | c.514C>T (p.Gln172Ter) c.499C>T (p.Gln167Ter) n.693C>T | ClinVar |
11 | g.32434847G>C | CA379964815 | WT1 | c.514C>G (p.Gln172Glu) c.499C>G (p.Gln167Glu) n.693C>G | |
11 | g.32434847G>T | CA379964816 | WT1 | c.514C>A (p.Gln172Lys) c.499C>A (p.Gln167Lys) n.693C>A | |
11 | g.32434848del | CA2580084154 | WT1 | c.514del (p.Gln172SerfsTer?) c.499del (p.Gln167SerfsTer?) n.693del | ClinVar dbSNP |
11 | g.32434848G>A | CA473571566 | WT1 | c.513C>T (p.Gly171=) c.498C>T (p.Gly166=) n.692C>T | ClinVar dbSNP |
11 | g.32434848G>C | CA473571568 | WT1 | c.513C>G (p.Gly171=) c.498C>G (p.Gly166=) n.692C>G | |
11 | g.32434848G= | CA1962327167 | WT1 | c.513C= (p.Gly171=) c.498C= (p.Gly166=) n.692C= | |
11 | g.32434848G>T | CA065010 | WT1 | c.513C>A (p.Gly171=) c.498C>A (p.Gly166=) n.692C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434849C>A | CA379964820 | WT1 | c.512G>T (p.Gly171Val) c.497G>T (p.Gly166Val) n.691G>T | ClinVar dbSNP |
11 | g.32434849C= | CA1962327168 | WT1 | c.512G= (p.Gly171=) c.497G= (p.Gly166=) n.691G= | |
11 | g.32434849C>G | CA379964821 | WT1 | c.512G>C (p.Gly171Ala) c.497G>C (p.Gly166Ala) n.691G>C | |
11 | g.32434849C>T | CA379964822 | WT1 | c.512G>A (p.Gly171Asp) c.497G>A (p.Gly166Asp) n.691G>A | gnomAD v4 |
11 | g.32434850C>A | CA379964824 | WT1 | c.511G>T (p.Gly171Cys) c.496G>T (p.Gly166Cys) n.690G>T | |
11 | g.32434850C>G | CA379964828 | WT1 | c.511G>C (p.Gly171Arg) c.496G>C (p.Gly166Arg) n.690G>C | ClinVar dbSNP |
11 | g.32434850C>T | CA379964826 | WT1 | c.511G>A (p.Gly171Ser) c.496G>A (p.Gly166Ser) n.690G>A | dbSNP |
11 | g.32434850_32434854delinsACAGTG | CA2580084156 | WT1 | c.507_511delinsCACTGT (p.Ser170ThrfsTer?) c.492_496delinsCACTGT (p.Ser165ThrfsTer?) n.686_690delinsCACTGT | ClinVar |
11 | g.32434851G>A | CA065003 | WT1 | c.510C>T (p.Ser170=) c.495C>T (p.Ser165=) n.689C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
11 | g.32434851G>C | CA473571577 | WT1 | c.510C>G (p.Ser170=) c.495C>G (p.Ser165=) n.689C>G | ClinVar dbSNP |
11 | g.32434851G= | CA1962327169 | WT1 | c.510C= (p.Ser170=) c.495C= (p.Ser165=) n.689C= | |
11 | g.32434851G>T | CA473571578 | WT1 | c.510C>A (p.Ser170=) c.495C>A (p.Ser165=) n.689C>A | gnomAD v4 |
11 | g.32434852G>A | CA379964830 | WT1 | c.509C>T (p.Ser170Phe) c.494C>T (p.Ser165Phe) n.688C>T | COSMIC COSMIC |
11 | g.32434852G>C | CA379964831 | WT1 | c.509C>G (p.Ser170Cys) c.494C>G (p.Ser165Cys) n.688C>G | |
11 | g.32434852G>T | CA379964832 | WT1 | c.509C>A (p.Ser170Tyr) c.494C>A (p.Ser165Tyr) n.688C>A | |
11 | g.32434853A>C | CA379964837 | WT1 | c.508T>G (p.Ser170Ala) c.493T>G (p.Ser165Ala) n.687T>G | |
11 | g.32434853A>G | CA379964834 | WT1 | c.508T>C (p.Ser170Pro) c.493T>C (p.Ser165Pro) n.687T>C | |
11 | g.32434853A>T | CA379964835 | WT1 | c.508T>A (p.Ser170Thr) c.493T>A (p.Ser165Thr) n.687T>A | |
11 | g.32434854A>C | CA379964839 | WT1 | c.507T>G (p.Phe169Leu) c.492T>G (p.Phe164Leu) n.686T>G | |
11 | g.32434854A>G | CA473571585 | WT1 | c.507T>C (p.Phe169=) c.492T>C (p.Phe164=) n.686T>C | |
11 | g.32434854A>T | CA379964841 | WT1 | c.507T>A (p.Phe169Leu) c.492T>A (p.Phe164Leu) n.686T>A | |
11 | g.32434855A>C | CA379964842 | WT1 | c.506T>G (p.Phe169Cys) c.491T>G (p.Phe164Cys) n.685T>G | |
11 | g.32434855A>G | CA379964844 | WT1 | c.506T>C (p.Phe169Ser) c.491T>C (p.Phe164Ser) n.685T>C | ClinVar |
11 | g.32434855A>T | CA379964845 | WT1 | c.506T>A (p.Phe169Tyr) c.491T>A (p.Phe164Tyr) n.685T>A | |
11 | g.32434856A>C | CA379964847 | WT1 | c.505T>G (p.Phe169Val) c.490T>G (p.Phe164Val) n.684T>G | |
11 | g.32434856A>G | CA379964848 | WT1 | c.505T>C (p.Phe169Leu) c.490T>C (p.Phe164Leu) n.684T>C | ClinVar dbSNP |
11 | g.32434856A>T | CA379964850 | WT1 | c.505T>A (p.Phe169Ile) c.490T>A (p.Phe164Ile) n.684T>A | |
11 | g.32434857G>A | CA473571593 | WT1 | c.504C>T (p.His168=) c.489C>T (p.His163=) n.683C>T | |
11 | g.32434857G>C | CA379964851 | WT1 | c.504C>G (p.His168Gln) c.489C>G (p.His163Gln) n.683C>G | |
11 | g.32434857G>T | CA379964853 | WT1 | c.504C>A (p.His168Gln) c.489C>A (p.His163Gln) n.683C>A | |
11 | g.32434858T>A | CA379964855 | WT1 | c.503A>T (p.His168Leu) c.488A>T (p.His163Leu) n.682A>T | dbSNP |
11 | g.32434858T>C | CA064994 | WT1 | c.503A>G (p.His168Arg) c.488A>G (p.His163Arg) n.682A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434858T>G | CA379964857 | WT1 | c.503A>C (p.His168Pro) c.488A>C (p.His163Pro) n.682A>C | |
11 | g.32434858T= | CA1962327170 | WT1 | c.503A= (p.His168=) c.488A= (p.His163=) n.682A= | |
11 | g.32434859G>A | CA379964862 | WT1 | c.502C>T (p.His168Tyr) c.487C>T (p.His163Tyr) n.681C>T | gnomAD v4 |
11 | g.32434859G>C | CA379964859 | WT1 | c.502C>G (p.His168Asp) c.487C>G (p.His163Asp) n.681C>G | |
11 | g.32434859G>T | CA379964860 | WT1 | c.502C>A (p.His168Asn) c.487C>A (p.His163Asn) n.681C>A | |
11 | g.32434860G>A | CA473571604 | WT1 | c.501C>T (p.Val167=) c.486C>T (p.Val162=) n.680C>T | |
11 | g.32434860G>C | CA473571607 | WT1 | c.501C>G (p.Val167=) c.486C>G (p.Val162=) n.680C>G | dbSNP |
11 | g.32434860G>T | CA473571605 | WT1 | c.501C>A (p.Val167=) c.486C>A (p.Val162=) n.680C>A | |
11 | g.32434861A= | CA1962327171 | WT1 | c.500T= (p.Val167=) c.485T= (p.Val162=) n.679T= | |
11 | g.32434861A>C | CA379964864 | WT1 | c.500T>G (p.Val167Gly) c.485T>G (p.Val162Gly) n.679T>G | |
11 | g.32434861A>G | CA379964865 | WT1 | c.500T>C (p.Val167Ala) c.485T>C (p.Val162Ala) n.679T>C | ClinVar |
11 | g.32434861A>T | CA379964866 | WT1 | c.500T>A (p.Val167Asp) c.485T>A (p.Val162Asp) n.679T>A | ClinVar dbSNP |
11 | g.32434862_32434863del | CA2695213674 | WT1 | c.499_500del (p.Val167ProfsTer?) c.484_485del (p.Val162ProfsTer?) n.678_679del | |
11 | g.32434862C>A | CA379964868 | WT1 | c.499G>T (p.Val167Phe) c.484G>T (p.Val162Phe) n.678G>T | |
11 | g.32434862C= | CA1962327172 | WT1 | c.499G= (p.Val167=) c.484G= (p.Val162=) n.678G= | |
11 | g.32434862C>G | CA379964870 | WT1 | c.499G>C (p.Val167Leu) c.484G>C (p.Val162Leu) n.678G>C | dbSNP |
11 | g.32434862C>T | CA379964871 | WT1 | c.499G>A (p.Val167Ile) c.484G>A (p.Val162Ile) n.678G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434863A= | CA1962327173 | WT1 | c.498T= (p.Thr166=) c.483T= (p.Thr161=) n.677T= | |
11 | g.32434863A>C | CA473571616 | WT1 | c.498T>G (p.Thr166=) c.483T>G (p.Thr161=) n.677T>G | |
11 | g.32434863A>G | CA473571619 | WT1 | c.498T>C (p.Thr166=) c.483T>C (p.Thr161=) n.677T>C | ClinVar dbSNP |
11 | g.32434863A>T | CA473571623 | WT1 | c.498T>A (p.Thr166=) c.483T>A (p.Thr161=) n.677T>A | |
11 | g.32434864G>A | CA379964875 | WT1 | c.497C>T (p.Thr166Ile) c.482C>T (p.Thr161Ile) n.676C>T | dbSNP |
11 | g.32434864G>C | CA379964872 | WT1 | c.497C>G (p.Thr166Ser) c.482C>G (p.Thr161Ser) n.676C>G | ClinVar |
11 | g.32434864G>T | CA379964873 | WT1 | c.497C>A (p.Thr166Asn) c.482C>A (p.Thr161Asn) n.676C>A | |
11 | g.32434865T>A | CA379964878 | WT1 | c.496A>T (p.Thr166Ser) c.481A>T (p.Thr161Ser) n.675A>T | |
11 | g.32434865T>C | CA379964879 | WT1 | c.496A>G (p.Thr166Ala) c.481A>G (p.Thr161Ala) n.675A>G | ClinVar dbSNP |
11 | g.32434865T>G | CA379964880 | WT1 | c.496A>C (p.Thr166Pro) c.481A>C (p.Thr161Pro) n.675A>C | |
11 | g.32434865T= | CA1962327174 | WT1 | c.496A= (p.Thr166=) c.481A= (p.Thr161=) n.675A= | |
11 | g.32434866G>A | CA473571631 | WT1 | c.495C>T (p.Phe165=) c.480C>T (p.Phe160=) n.674C>T | |
11 | g.32434866G>C | CA379964882 | WT1 | c.495C>G (p.Phe165Leu) c.480C>G (p.Phe160Leu) n.674C>G | |
11 | g.32434866G>T | CA379964883 | WT1 | c.495C>A (p.Phe165Leu) c.480C>A (p.Phe160Leu) n.674C>A | |
11 | g.32434867A>C | CA379964885 | WT1 | c.494T>G (p.Phe165Cys) c.479T>G (p.Phe160Cys) n.673T>G | |
11 | g.32434867A>G | CA379964888 | WT1 | c.494T>C (p.Phe165Ser) c.479T>C (p.Phe160Ser) n.673T>C | dbSNP |
11 | g.32434867A>T | CA379964886 | WT1 | c.494T>A (p.Phe165Tyr) c.479T>A (p.Phe160Tyr) n.673T>A | |
11 | g.32434868A>C | CA379964890 | WT1 | c.493T>G (p.Phe165Val) c.478T>G (p.Phe160Val) n.672T>G | |
11 | g.32434868A>G | CA379964892 | WT1 | c.493T>C (p.Phe165Leu) c.478T>C (p.Phe160Leu) n.672T>C | gnomAD v4 |
11 | g.32434868A>T | CA379964893 | WT1 | c.493T>A (p.Phe165Ile) c.478T>A (p.Phe160Ile) n.672T>A | |
11 | g.32434869G>A | CA473571639 | WT1 | c.492C>T (p.Ala164=) c.477C>T (p.Ala159=) n.671C>T | |
11 | g.32434869G>C | CA473571645 | WT1 | c.492C>G (p.Ala164=) c.477C>G (p.Ala159=) n.671C>G | dbSNP |
11 | g.32434869G>T | CA473571647 | WT1 | c.492C>A (p.Ala164=) c.477C>A (p.Ala159=) n.671C>A | |
11 | g.32434870G>A | CA379964895 | WT1 | c.491C>T (p.Ala164Val) c.476C>T (p.Ala159Val) n.670C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434870G>C | CA379964896 | WT1 | c.491C>G (p.Ala164Gly) c.476C>G (p.Ala159Gly) n.670C>G | |
11 | g.32434870G= | CA1962327175 | WT1 | c.491C= (p.Ala164=) c.476C= (p.Ala159=) n.670C= | |
11 | g.32434870G>T | CA379964898 | WT1 | c.491C>A (p.Ala164Asp) c.476C>A (p.Ala159Asp) n.670C>A | |
11 | g.32434871C>A | CA219510930 | WT1 | c.490G>T (p.Ala164Ser) c.475G>T (p.Ala159Ser) n.669G>T | dbSNP gnomAD v4 |
11 | g.32434871C= | CA1962327176 | WT1 | c.490G= (p.Ala164=) c.475G= (p.Ala159=) n.669G= | |
11 | g.32434871C>G | CA379964899 | WT1 | c.490G>C (p.Ala164Pro) c.475G>C (p.Ala159Pro) n.669G>C | ClinVar dbSNP |
11 | g.32434871C>T | CA379964900 | WT1 | c.490G>A (p.Ala164Thr) c.475G>A (p.Ala159Thr) n.669G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434872G>A | CA219510935 | WT1 | c.489C>T (p.Ser163=) c.474C>T (p.Ser158=) n.668C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434872G>C | CA379964901 | WT1 | c.489C>G (p.Ser163Arg) c.474C>G (p.Ser158Arg) n.668C>G | ClinVar |
11 | g.32434872G= | CA1962327177 | WT1 | c.489C= (p.Ser163=) c.474C= (p.Ser158=) n.668C= | |
11 | g.32434872G>T | CA379964903 | WT1 | c.489C>A (p.Ser163Arg) c.474C>A (p.Ser158Arg) n.668C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434873C>A | CA379964905 | WT1 | c.488G>T (p.Ser163Ile) c.473G>T (p.Ser158Ile) n.667G>T | |
11 | g.32434873C= | CA1962327178 | WT1 | c.488G= (p.Ser163=) c.473G= (p.Ser158=) n.667G= | |
11 | g.32434873C>G | CA379964907 | WT1 | c.488G>C (p.Ser163Thr) c.473G>C (p.Ser158Thr) n.667G>C | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434873C>T | CA379964906 | WT1 | c.488G>A (p.Ser163Asn) c.473G>A (p.Ser158Asn) n.667G>A | ClinVar dbSNP |
11 | g.32434874T>A | CA379964909 | WT1 | c.487A>T (p.Ser163Cys) c.472A>T (p.Ser158Cys) n.666A>T | |
11 | g.32434874T>C | CA379964911 | WT1 | c.487A>G (p.Ser163Gly) c.472A>G (p.Ser158Gly) n.666A>G | dbSNP |
11 | g.32434874T>G | CA379964913 | WT1 | c.487A>C (p.Ser163Arg) c.472A>C (p.Ser158Arg) n.666A>C | |
11 | g.32434875C>A | CA473571666 | WT1 | c.486G>T (p.Leu162=) c.471G>T (p.Leu157=) n.665G>T | dbSNP |
11 | g.32434875C= | CA1962327179 | WT1 | c.486G= (p.Leu162=) c.471G= (p.Leu157=) n.665G= | |
11 | g.32434875C>G | CA473571667 | WT1 | c.486G>C (p.Leu162=) c.471G>C (p.Leu157=) n.665G>C | |
11 | g.32434875C>T | CA473571668 | WT1 | c.486G>A (p.Leu162=) c.471G>A (p.Leu157=) n.665G>A | |
11 | g.32434878_32434911del | CA645584483 | WT1 | c.453_486del (p.Trp151Ter) c.438_471del (p.Trp146Ter) n.632_665del | COSMIC |
11 | g.32434876A>C | CA379964914 | WT1 | c.485T>G (p.Leu162Arg) c.470T>G (p.Leu157Arg) n.664T>G | gnomAD v4 |
11 | g.32434876A>G | CA379964915 | WT1 | c.485T>C (p.Leu162Pro) c.470T>C (p.Leu157Pro) n.664T>C | gnomAD v4 |
11 | g.32434876A>T | CA379964917 | WT1 | c.485T>A (p.Leu162Gln) c.470T>A (p.Leu157Gln) n.664T>A | |
11 | g.32434877G>A | CA064984 | WT1 | c.484C>T (p.Leu162=) c.469C>T (p.Leu157=) n.663C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434877G>C | CA379964920 | WT1 | c.484C>G (p.Leu162Val) c.469C>G (p.Leu157Val) n.663C>G | dbSNP gnomAD v4 |
11 | g.32434877G= | CA1962327180 | WT1 | c.484C= (p.Leu162=) c.469C= (p.Leu157=) n.663C= | |
11 | g.32434877G>T | CA379964919 | WT1 | c.484C>A (p.Leu162Met) c.469C>A (p.Leu157Met) n.663C>A | |
11 | g.32434878G>A | CA064979 | WT1 | c.483C>T (p.Cys161=) c.468C>T (p.Cys156=) n.662C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434878G>C | CA379964922 | WT1 | c.483C>G (p.Cys161Trp) c.468C>G (p.Cys156Trp) n.662C>G | |
11 | g.32434878G= | CA1962327181 | WT1 | c.483C= (p.Cys161=) c.468C= (p.Cys156=) n.662C= | |
11 | g.32434878G>T | CA379964924 | WT1 | c.483C>A (p.Cys161Ter) c.468C>A (p.Cys156Ter) n.662C>A | |
11 | g.32434879C>A | CA379964926 | WT1 | c.482G>T (p.Cys161Phe) c.467G>T (p.Cys156Phe) n.661G>T | ClinVar dbSNP |
11 | g.32434879C= | CA1962327182 | WT1 | c.482G= (p.Cys161=) c.467G= (p.Cys156=) n.661G= | |
11 | g.32434879C>G | CA379964928 | WT1 | c.482G>C (p.Cys161Ser) c.467G>C (p.Cys156Ser) n.661G>C | |
11 | g.32434879C>T | CA379964929 | WT1 | c.482G>A (p.Cys161Tyr) c.467G>A (p.Cys156Tyr) n.661G>A | dbSNP gnomAD v4 |
11 | g.32434880A>C | CA379964931 | WT1 | c.481T>G (p.Cys161Gly) c.466T>G (p.Cys156Gly) n.660T>G | ClinVar |
11 | g.32434880A>G | CA379964934 | WT1 | c.481T>C (p.Cys161Arg) c.466T>C (p.Cys156Arg) n.660T>C | |
11 | g.32434880A>T | CA379964932 | WT1 | c.481T>A (p.Cys161Ser) c.466T>A (p.Cys156Ser) n.660T>A | dbSNP |
11 | g.32434881C>A | CA379964936 | WT1 | c.480G>T (p.Gln160His) c.465G>T (p.Gln155His) n.659G>T | |
11 | g.32434881C= | CA1962327183 | WT1 | c.480G= (p.Gln160=) c.465G= (p.Gln155=) n.659G= | |
11 | g.32434881C>G | CA379964937 | WT1 | c.480G>C (p.Gln160His) c.465G>C (p.Gln155His) n.659G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32434881C>T | CA064974 | WT1 | c.480G>A (p.Gln160=) c.465G>A (p.Gln155=) n.659G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434882T>A | CA379964940 | WT1 | c.479A>T (p.Gln160Leu) c.464A>T (p.Gln155Leu) n.658A>T | |
11 | g.32434882T>C | CA379964941 | WT1 | c.479A>G (p.Gln160Arg) c.464A>G (p.Gln155Arg) n.658A>G | |
11 | g.32434882T>G | CA379964943 | WT1 | c.479A>C (p.Gln160Pro) c.464A>C (p.Gln155Pro) n.658A>C | |
11 | g.32434883del | CA473571694 | WT1 | c.478del (p.Gln160SerfsTer3) c.463del (p.Gln155SerfsTer3) n.657del | COSMIC |
11 | g.32434883G>A | CA379964944 | WT1 | c.478C>T (p.Gln160Ter) c.463C>T (p.Gln155Ter) n.657C>T | ClinVar dbSNP |
11 | g.32434883G>C | CA379964946 | WT1 | c.478C>G (p.Gln160Glu) c.463C>G (p.Gln155Glu) n.657C>G | ClinVar dbSNP |
11 | g.32434883G= | CA1962327184 | WT1 | c.478C= (p.Gln160=) c.463C= (p.Gln155=) n.657C= | |
11 | g.32434883G>T | CA379964948 | WT1 | c.478C>A (p.Gln160Lys) c.463C>A (p.Gln155Lys) n.657C>A | |
11 | g.32434884C>A | CA379964949 | WT1 | c.477G>T (p.Glu159Asp) c.462G>T (p.Glu154Asp) n.656G>T | |
11 | g.32434884C>G | CA379964951 | WT1 | c.477G>C (p.Glu159Asp) c.462G>C (p.Glu154Asp) n.656G>C | ClinVar dbSNP |
11 | g.32434884C>T | CA473571698 | WT1 | c.477G>A (p.Glu159=) c.462G>A (p.Glu154=) n.656G>A | ClinVar dbSNP |
11 | g.32434885T>A | CA379964952 | WT1 | c.476A>T (p.Glu159Val) c.461A>T (p.Glu154Val) n.655A>T | |
11 | g.32434885T>C | CA379964956 | WT1 | c.476A>G (p.Glu159Gly) c.461A>G (p.Glu154Gly) n.655A>G | ClinVar dbSNP |
11 | g.32434885T>G | CA379964954 | WT1 | c.476A>C (p.Glu159Ala) c.461A>C (p.Glu154Ala) n.655A>C | |
11 | g.32434885T= | CA1962327185 | WT1 | c.476A= (p.Glu159=) c.461A= (p.Glu154=) n.655A= | |
11 | g.32434886C>A | CA379964958 | WT1 | c.475G>T (p.Glu159Ter) c.460G>T (p.Glu154Ter) n.654G>T | |
11 | g.32434886C= | CA1962327186 | WT1 | c.475G= (p.Glu159=) c.460G= (p.Glu154=) n.654G= | |
11 | g.32434886C>G | CA379964959 | WT1 | c.475G>C (p.Glu159Gln) c.460G>C (p.Glu154Gln) n.654G>C | |
11 | g.32434886C>T | CA064967 | WT1 | c.475G>A (p.Glu159Lys) c.460G>A (p.Glu154Lys) n.654G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434887del | CA2695213675 | WT1 | c.475del (p.Glu159SerfsTer4) c.460del (p.Glu154SerfsTer4) n.654del | |
11 | g.32434888_32434909del | CA645584484 | WT1 | c.454_475del (p.Gly152SerfsTer4) c.439_460del (p.Gly147SerfsTer4) n.633_654del | COSMIC COSMIC |
11 | g.32434887C>A | CA379964962 | WT1 | c.474G>T (p.Glu158Asp) c.459G>T (p.Glu153Asp) n.653G>T | |
11 | g.32434887C= | CA1962327187 | WT1 | c.474G= (p.Glu158=) c.459G= (p.Glu153=) n.653G= | |
11 | g.32434887C>G | CA379964963 | WT1 | c.474G>C (p.Glu158Asp) c.459G>C (p.Glu153Asp) n.653G>C | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434887C>T | CA219510972 | WT1 | c.474G>A (p.Glu158=) c.459G>A (p.Glu153=) n.653G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434888T>A | CA379964965 | WT1 | c.473A>T (p.Glu158Val) c.458A>T (p.Glu153Val) n.652A>T | |
11 | g.32434888T>C | CA379964966 | WT1 | c.473A>G (p.Glu158Gly) c.458A>G (p.Glu153Gly) n.652A>G | |
11 | g.32434888T>G | CA379964968 | WT1 | c.473A>C (p.Glu158Ala) c.458A>C (p.Glu153Ala) n.652A>C | |
11 | g.32434889C>A | CA379964969 | WT1 | c.472G>T (p.Glu158Ter) c.457G>T (p.Glu153Ter) n.651G>T | ClinVar dbSNP |
11 | g.32434889C= | CA1962327188 | WT1 | c.472G= (p.Glu158=) c.457G= (p.Glu153=) n.651G= | |
11 | g.32434889C>G | CA379964971 | WT1 | c.472G>C (p.Glu158Gln) c.457G>C (p.Glu153Gln) n.651G>C | ClinVar dbSNP |
11 | g.32434889C>T | CA379964973 | WT1 | c.472G>A (p.Glu158Lys) c.457G>A (p.Glu153Lys) n.651G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434890G>A | CA064961 | WT1 | c.471C>T (p.His157=) c.456C>T (p.His152=) n.650C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
11 | g.32434890G>C | CA379964975 | WT1 | c.471C>G (p.His157Gln) c.456C>G (p.His152Gln) n.650C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434890G= | CA1962327189 | WT1 | c.471C= (p.His157=) c.456C= (p.His152=) n.650C= | |
11 | g.32434890G>T | CA379964974 | WT1 | c.471C>A (p.His157Gln) c.456C>A (p.His152Gln) n.650C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434891T>A | CA379964976 | WT1 | c.470A>T (p.His157Leu) c.455A>T (p.His152Leu) n.649A>T | dbSNP |
11 | g.32434891T>C | CA379964977 | WT1 | c.470A>G (p.His157Arg) c.455A>G (p.His152Arg) n.649A>G | dbSNP |
11 | g.32434891T>G | CA379964979 | WT1 | c.470A>C (p.His157Pro) c.455A>C (p.His152Pro) n.649A>C | dbSNP |
11 | g.32434892G>A | CA379964981 | WT1 | c.469C>T (p.His157Tyr) c.454C>T (p.His152Tyr) n.648C>T | |
11 | g.32434892G>C | CA379964983 | WT1 | c.469C>G (p.His157Asp) c.454C>G (p.His152Asp) n.648C>G | |
11 | g.32434892G>T | CA379964986 | WT1 | c.469C>A (p.His157Asn) c.454C>A (p.His152Asn) n.648C>A | gnomAD v4 |
11 | g.32434893C>A | CA16613331 | WT1 | c.468G>T (p.Pro156=) c.453G>T (p.Pro151=) n.647G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434893C= | CA1962327190 | WT1 | c.468G= (p.Pro156=) c.453G= (p.Pro151=) n.647G= | |
11 | g.32434893C>G | CA473571721 | WT1 | c.468G>C (p.Pro156=) c.453G>C (p.Pro151=) n.647G>C | gnomAD v4 |
11 | g.32434893C>T | CA473571723 | WT1 | c.468G>A (p.Pro156=) c.453G>A (p.Pro151=) n.647G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434894G>A | CA379964988 | WT1 | c.467C>T (p.Pro156Leu) c.452C>T (p.Pro151Leu) n.646C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434894G>C | CA379964989 | WT1 | c.467C>G (p.Pro156Arg) c.452C>G (p.Pro151Arg) n.646C>G | |
11 | g.32434894G= | CA1962327191 | WT1 | c.467C= (p.Pro156=) c.452C= (p.Pro151=) n.646C= | |
11 | g.32434894G>T | CA379964991 | WT1 | c.467C>A (p.Pro156Gln) c.452C>A (p.Pro151Gln) n.646C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434895G>A | CA379964993 | WT1 | c.466C>T (p.Pro156Ser) c.451C>T (p.Pro151Ser) n.645C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434895G>C | CA379964995 | WT1 | c.466C>G (p.Pro156Ala) c.451C>G (p.Pro151Ala) n.645C>G | |
11 | g.32434895G= | CA1962327192 | WT1 | c.466C= (p.Pro156=) c.451C= (p.Pro151=) n.645C= | |
11 | g.32434895G>T | CA379964996 | WT1 | c.466C>A (p.Pro156Thr) c.451C>A (p.Pro151Thr) n.645C>A | gnomAD v4 |
11 | g.32434896C>A | CA379965000 | WT1 | c.465G>T (p.Glu155Asp) c.450G>T (p.Glu150Asp) n.644G>T | |
11 | g.32434896C= | CA1962327193 | WT1 | c.465G= (p.Glu155=) c.450G= (p.Glu150=) n.644G= | |
11 | g.32434896C>G | CA379964998 | WT1 | c.465G>C (p.Glu155Asp) c.450G>C (p.Glu150Asp) n.644G>C | |
11 | g.32434896C>T | CA473571731 | WT1 | c.465G>A (p.Glu155=) c.450G>A (p.Glu150=) n.644G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434897T>A | CA379965001 | WT1 | c.464A>T (p.Glu155Val) c.449A>T (p.Glu150Val) n.643A>T | |
11 | g.32434897T>C | CA379965004 | WT1 | c.464A>G (p.Glu155Gly) c.449A>G (p.Glu150Gly) n.643A>G | dbSNP |
11 | g.32434897T>G | CA379965003 | WT1 | c.464A>C (p.Glu155Ala) c.449A>C (p.Glu150Ala) n.643A>C | |
11 | g.32434898C>A | CA379965006 | WT1 | c.463G>T (p.Glu155Ter) c.448G>T (p.Glu150Ter) n.642G>T | |
11 | g.32434898C= | CA1962327194 | WT1 | c.463G= (p.Glu155=) c.448G= (p.Glu150=) n.642G= | |
11 | g.32434898C>G | CA379965011 | WT1 | c.463G>C (p.Glu155Gln) c.448G>C (p.Glu150Gln) n.642G>C | |
11 | g.32434898C>T | CA379965008 | WT1 | c.463G>A (p.Glu155Lys) c.448G>A (p.Glu150Lys) n.642G>A | ClinVar dbSNP |
11 | g.32434899C>A | CA473571737 | WT1 | c.462G>T (p.Ala154=) c.447G>T (p.Ala149=) n.641G>T | |
11 | g.32434899C>G | CA473571738 | WT1 | c.462G>C (p.Ala154=) c.447G>C (p.Ala149=) n.641G>C | |
11 | g.32434899C>T | CA473571739 | WT1 | c.462G>A (p.Ala154=) c.447G>A (p.Ala149=) n.641G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434902_32434903del | CA2723464976 | WT1 | c.461_462del (p.Ala154GlyfsTer?) c.446_447del (p.Ala149GlyfsTer?) n.640_641del | dbSNP |
11 | g.32434900G>A | CA379965013 | WT1 | c.461C>T (p.Ala154Val) c.446C>T (p.Ala149Val) n.640C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434900G>C | CA379965015 | WT1 | c.461C>G (p.Ala154Gly) c.446C>G (p.Ala149Gly) n.640C>G | dbSNP |
11 | g.32434900G>T | CA379965014 | WT1 | c.461C>A (p.Ala154Glu) c.446C>A (p.Ala149Glu) n.640C>A | |
11 | g.32434901C>A | CA379965018 | WT1 | c.460G>T (p.Ala154Ser) c.445G>T (p.Ala149Ser) n.639G>T | gnomAD v4 |
11 | g.32434901C>G | CA379965019 | WT1 | c.460G>C (p.Ala154Pro) c.445G>C (p.Ala149Pro) n.639G>C | |
11 | g.32434901C>T | CA379965021 | WT1 | c.460G>A (p.Ala154Thr) c.445G>A (p.Ala149Thr) n.639G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434902G>A | CA473571744 | WT1 | c.459C>T (p.Gly153=) c.444C>T (p.Gly148=) n.638C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434902G>C | CA473571747 | WT1 | c.459C>G (p.Gly153=) c.444C>G (p.Gly148=) n.638C>G | |
11 | g.32434902G= | CA1962327195 | WT1 | c.459C= (p.Gly153=) c.444C= (p.Gly148=) n.638C= | |
11 | g.32434902G>T | CA473571745 | WT1 | c.459C>A (p.Gly153=) c.444C>A (p.Gly148=) n.638C>A | |
11 | g.32434903C>A | CA379965022 | WT1 | c.458G>T (p.Gly153Val) c.443G>T (p.Gly148Val) n.637G>T | |
11 | g.32434903C>G | CA379965024 | WT1 | c.458G>C (p.Gly153Ala) c.443G>C (p.Gly148Ala) n.637G>C | |
11 | g.32434903C>T | CA379965025 | WT1 | c.458G>A (p.Gly153Asp) c.443G>A (p.Gly148Asp) n.637G>A | |
11 | g.32434904C>A | CA379965027 | WT1 | c.457G>T (p.Gly153Cys) c.442G>T (p.Gly148Cys) n.636G>T | gnomAD v4 |
11 | g.32434904C>G | CA379965029 | WT1 | c.457G>C (p.Gly153Arg) c.442G>C (p.Gly148Arg) n.636G>C | |
11 | g.32434904C>T | CA379965030 | WT1 | c.457G>A (p.Gly153Ser) c.442G>A (p.Gly148Ser) n.636G>A | gnomAD v4 |
11 | g.32434905G>A | CA473571755 | WT1 | c.456C>T (p.Gly152=) c.441C>T (p.Gly147=) n.635C>T | ClinVar dbSNP COSMIC COSMIC |
11 | g.32434905G>C | CA473571756 | WT1 | c.456C>G (p.Gly152=) c.441C>G (p.Gly147=) n.635C>G | |
11 | g.32434905G>T | CA473571758 | WT1 | c.456C>A (p.Gly152=) c.441C>A (p.Gly147=) n.635C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434906C>A | CA379965032 | WT1 | c.455G>T (p.Gly152Val) c.440G>T (p.Gly147Val) n.634G>T | |
11 | g.32434906C= | CA1962327196 | WT1 | c.455G= (p.Gly152=) c.440G= (p.Gly147=) n.634G= | |
11 | g.32434906C>G | CA379965034 | WT1 | c.455G>C (p.Gly152Ala) c.440G>C (p.Gly147Ala) n.634G>C | |
11 | g.32434906C>T | CA379965035 | WT1 | c.455G>A (p.Gly152Asp) c.440G>A (p.Gly147Asp) n.634G>A | ClinVar dbSNP |
11 | g.32434909del | CA2499220922 | WT1 | c.455del (p.Gly152AlafsTer11) c.440del (p.Gly147AlafsTer11) n.634del | ClinVar dbSNP |
11 | g.32434907C>A | CA379965037 | WT1 | c.454G>T (p.Gly152Cys) c.439G>T (p.Gly147Cys) n.633G>T | dbSNP |
11 | g.32434907C= | CA1962327197 | WT1 | c.454G= (p.Gly152=) c.439G= (p.Gly147=) n.633G= | |
11 | g.32434907C>G | CA379965040 | WT1 | c.454G>C (p.Gly152Arg) c.439G>C (p.Gly147Arg) n.633G>C | |
11 | g.32434907C>T | CA379965038 | WT1 | c.454G>A (p.Gly152Ser) c.439G>A (p.Gly147Ser) n.633G>A | gnomAD v4 |
11 | g.32434908C>A | CA379965042 | WT1 | c.453G>T (p.Trp151Cys) c.438G>T (p.Trp146Cys) n.632G>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434908C= | CA1962327198 | WT1 | c.453G= (p.Trp151=) c.438G= (p.Trp146=) n.632G= | |
11 | g.32434908C>G | CA379965044 | WT1 | c.453G>C (p.Trp151Cys) c.438G>C (p.Trp146Cys) n.632G>C | |
11 | g.32434908C>T | CA379965045 | WT1 | c.453G>A (p.Trp151Ter) c.438G>A (p.Trp146Ter) n.632G>A | ClinVar |
11 | g.32434909C>A | CA379965047 | WT1 | c.452G>T (p.Trp151Leu) c.437G>T (p.Trp146Leu) n.631G>T | gnomAD v4 |
11 | g.32434909C>G | CA379965048 | WT1 | c.452G>C (p.Trp151Ser) c.437G>C (p.Trp146Ser) n.631G>C | |
11 | g.32434909C>T | CA379965050 | WT1 | c.452G>A (p.Trp151Ter) c.437G>A (p.Trp146Ter) n.631G>A | |
11 | g.32434909_32434913delinsCAGCT | CA1962327199 | WT1 | c.448_452delinsAGCTG (p.Ser150=) c.433_437delinsAGCTG (p.Ser145=) n.627_631delinsAGCTG | |
11 | g.32434910A= | CA1962327200 | WT1 | c.451T= (p.Trp151=) c.436T= (p.Trp146=) n.630T= | |
11 | g.32434910A>C | CA379965052 | WT1 | c.451T>G (p.Trp151Gly) c.436T>G (p.Trp146Gly) n.630T>G | ClinVar |
11 | g.32434910A>G | CA379965053 | WT1 | c.451T>C (p.Trp151Arg) c.436T>C (p.Trp146Arg) n.630T>C | |
11 | g.32434910A>T | CA379965055 | WT1 | c.451T>A (p.Trp151Arg) c.436T>A (p.Trp146Arg) n.630T>A | ClinVar dbSNP |
11 | g.32434910_32434913del | CA598513625 | WT1 | c.448_451del (p.Ser150GlyfsTer12) c.433_436del (p.Ser145GlyfsTer12) n.627_630del | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434911G>A | CA473571771 | WT1 | c.450C>T (p.Ser150=) c.435C>T (p.Ser145=) n.629C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434911G>C | CA379965057 | WT1 | c.450C>G (p.Ser150Arg) c.435C>G (p.Ser145Arg) n.629C>G | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434911G= | CA1962327201 | WT1 | c.450C= (p.Ser150=) c.435C= (p.Ser145=) n.629C= | |
11 | g.32434911G>T | CA379965058 | WT1 | c.450C>A (p.Ser150Arg) c.435C>A (p.Ser145Arg) n.629C>A | ClinVar dbSNP |
11 | g.32434912C>A | CA379965060 | WT1 | c.449G>T (p.Ser150Ile) c.434G>T (p.Ser145Ile) n.628G>T | ClinVar |
11 | g.32434912C= | CA1962327202 | WT1 | c.449G= (p.Ser150=) c.434G= (p.Ser145=) n.628G= | |
11 | g.32434912C>G | CA379965061 | WT1 | c.449G>C (p.Ser150Thr) c.434G>C (p.Ser145Thr) n.628G>C | |
11 | g.32434912C>T | CA379965063 | WT1 | c.449G>A (p.Ser150Asn) c.434G>A (p.Ser145Asn) n.628G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434913T>A | CA379965065 | WT1 | c.448A>T (p.Ser150Cys) c.433A>T (p.Ser145Cys) n.627A>T | dbSNP |
11 | g.32434913T>C | CA379965066 | WT1 | c.448A>G (p.Ser150Gly) c.433A>G (p.Ser145Gly) n.627A>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434913T>G | CA379965068 | WT1 | c.448A>C (p.Ser150Arg) c.433A>C (p.Ser145Arg) n.627A>C | |
11 | g.32434913T= | CA1962327203 | WT1 | c.448A= (p.Ser150=) c.433A= (p.Ser145=) n.627A= | |
11 | g.32434914C>A | CA219510988 | WT1 | c.447G>T (p.Pro149=) c.432G>T (p.Pro144=) n.626G>T | dbSNP gnomAD v4 |
11 | g.32434914C= | CA1962327204 | WT1 | c.447G= (p.Pro149=) c.432G= (p.Pro144=) n.626G= | |
11 | g.32434914C>G | CA473571783 | WT1 | c.447G>C (p.Pro149=) c.432G>C (p.Pro144=) n.626G>C | |
11 | g.32434914C>T | CA473571785 | WT1 | c.447G>A (p.Pro149=) c.432G>A (p.Pro144=) n.626G>A | ClinVar |
11 | g.32434915G>A | CA379965070 | WT1 | c.446C>T (p.Pro149Leu) c.431C>T (p.Pro144Leu) n.625C>T | |
11 | g.32434915G>C | CA379965071 | WT1 | c.446C>G (p.Pro149Arg) c.431C>G (p.Pro144Arg) n.625C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434915G= | CA1962327205 | WT1 | c.446C= (p.Pro149=) c.431C= (p.Pro144=) n.625C= | |
11 | g.32434915G>T | CA379965073 | WT1 | c.446C>A (p.Pro149Gln) c.431C>A (p.Pro144Gln) n.625C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434916G>A | CA379965074 | WT1 | c.445C>T (p.Pro149Ser) c.430C>T (p.Pro144Ser) n.624C>T | ClinVar dbSNP |
11 | g.32434916G>C | CA379965076 | WT1 | c.445C>G (p.Pro149Ala) c.430C>G (p.Pro144Ala) n.624C>G | |
11 | g.32434916G= | CA1962327206 | WT1 | c.445C= (p.Pro149=) c.430C= (p.Pro144=) n.624C= | |
11 | g.32434916G>T | CA379965078 | WT1 | c.445C>A (p.Pro149Thr) c.430C>A (p.Pro144Thr) n.624C>A | gnomAD v4 |
11 | g.32434917C>A | CA379965082 | WT1 | c.444G>T (p.Glu148Asp) c.429G>T (p.Glu143Asp) n.623G>T | gnomAD v4 |
11 | g.32434917C= | CA1962327207 | WT1 | c.444G= (p.Glu148=) c.429G= (p.Glu143=) n.623G= | |
11 | g.32434917C>G | CA379965080 | WT1 | c.444G>C (p.Glu148Asp) c.429G>C (p.Glu143Asp) n.623G>C | |
11 | g.32434917C>T | CA064949 | WT1 | c.444G>A (p.Glu148=) c.429G>A (p.Glu143=) n.623G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434918T>A | CA379965084 | WT1 | c.443A>T (p.Glu148Val) c.428A>T (p.Glu143Val) n.622A>T | |
11 | g.32434918T>C | CA379965086 | WT1 | c.443A>G (p.Glu148Gly) c.428A>G (p.Glu143Gly) n.622A>G | |
11 | g.32434918T>G | CA379965087 | WT1 | c.443A>C (p.Glu148Ala) c.428A>C (p.Glu143Ala) n.622A>C | |
11 | g.32434919C>A | CA379965088 | WT1 | c.442G>T (p.Glu148Ter) c.427G>T (p.Glu143Ter) n.621G>T | COSMIC COSMIC |
11 | g.32434919C>G | CA379965090 | WT1 | c.442G>C (p.Glu148Gln) c.427G>C (p.Glu143Gln) n.621G>C | |
11 | g.32434919C>T | CA379965092 | WT1 | c.442G>A (p.Glu148Lys) c.427G>A (p.Glu143Lys) n.621G>A | |
11 | g.32434920C>A | CA379965093 | WT1 | c.441G>T (p.Gln147His) c.426G>T (p.Gln142His) n.620G>T | |
11 | g.32434920C>G | CA379965094 | WT1 | c.441G>C (p.Gln147His) c.426G>C (p.Gln142His) n.620G>C | dbSNP |
11 | g.32434920C>T | CA473571803 | WT1 | c.441G>A (p.Gln147=) c.426G>A (p.Gln142=) n.620G>A | ClinVar |
11 | g.32434921T>A | CA379965096 | WT1 | c.440A>T (p.Gln147Leu) c.425A>T (p.Gln142Leu) n.619A>T | |
11 | g.32434921T>C | CA064944 | WT1 | c.440A>G (p.Gln147Arg) c.425A>G (p.Gln142Arg) n.619A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434921T>G | CA379965099 | WT1 | c.440A>C (p.Gln147Pro) c.425A>C (p.Gln142Pro) n.619A>C | ClinVar |
11 | g.32434921T= | CA1962327208 | WT1 | c.440A= (p.Gln147=) c.425A= (p.Gln142=) n.619A= | |
11 | g.32434922G>A | CA379965624 | WT1 | c.439C>T (p.Gln147Ter) c.424C>T (p.Gln142Ter) n.618C>T | |
11 | g.32434922G>C | CA16613373 | WT1 | c.439C>G (p.Gln147Glu) c.424C>G (p.Gln142Glu) n.618C>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434922G= | CA1962327209 | WT1 | c.439C= (p.Gln147=) c.424C= (p.Gln142=) n.618C= | |
11 | g.32434922G>T | CA379965622 | WT1 | c.439C>A (p.Gln147Lys) c.424C>A (p.Gln142Lys) n.618C>A | gnomAD v4 |
11 | g.32434923T>A | CA379965627 | WT1 | c.438A>T (p.Lys146Asn) c.423A>T (p.Lys141Asn) n.617A>T | |
11 | g.32434923T>C | CA473773520 | WT1 | c.438A>G (p.Lys146=) c.423A>G (p.Lys141=) n.617A>G | |
11 | g.32434923T>G | CA379965626 | WT1 | c.438A>C (p.Lys146Asn) c.423A>C (p.Lys141Asn) n.617A>C | |
11 | g.32434924T>A | CA379965630 | WT1 | c.437A>T (p.Lys146Ile) c.422A>T (p.Lys141Ile) n.616A>T | |
11 | g.32434924T>C | CA379965631 | WT1 | c.437A>G (p.Lys146Arg) c.422A>G (p.Lys141Arg) n.616A>G | |
11 | g.32434924T>G | CA379965633 | WT1 | c.437A>C (p.Lys146Thr) c.422A>C (p.Lys141Thr) n.616A>C | |
11 | g.32434925T>A | CA379965634 | WT1 | c.436A>T (p.Lys146Ter) c.421A>T (p.Lys141Ter) n.615A>T | |
11 | g.32434925T>C | CA379965635 | WT1 | c.436A>G (p.Lys146Glu) c.421A>G (p.Lys141Glu) n.615A>G | |
11 | g.32434925T>G | CA379965638 | WT1 | c.436A>C (p.Lys146Gln) c.421A>C (p.Lys141Gln) n.615A>C | ClinVar |
11 | g.32434926G>A | CA473773531 | WT1 | c.435C>T (p.Ile145=) c.420C>T (p.Ile140=) n.614C>T | dbSNP |
11 | g.32434926G>C | CA379965639 | WT1 | c.435C>G (p.Ile145Met) c.420C>G (p.Ile140Met) n.614C>G | |
11 | g.32434926G>T | CA473773530 | WT1 | c.435C>A (p.Ile145=) c.420C>A (p.Ile140=) n.614C>A | gnomAD v4 |
11 | g.32434927A>C | CA379965641 | WT1 | c.434T>G (p.Ile145Ser) c.419T>G (p.Ile140Ser) n.613T>G | |
11 | g.32434927A>G | CA379965643 | WT1 | c.434T>C (p.Ile145Thr) c.419T>C (p.Ile140Thr) n.613T>C | |
11 | g.32434927A>T | CA379965645 | WT1 | c.434T>A (p.Ile145Asn) c.419T>A (p.Ile140Asn) n.613T>A | |
11 | g.32434928T>A | CA379965647 | WT1 | c.433A>T (p.Ile145Phe) c.418A>T (p.Ile140Phe) n.612A>T | |
11 | g.32434928T>C | CA379965649 | WT1 | c.433A>G (p.Ile145Val) c.418A>G (p.Ile140Val) n.612A>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434928T>G | CA379965651 | WT1 | c.433A>C (p.Ile145Leu) c.418A>C (p.Ile140Leu) n.612A>C | |
11 | g.32434928_32434931delinsTGAA | CA1962327210 | WT1 | c.430_433delinsTTCA (p.Phe144=) c.415_418delinsTTCA (p.Phe139=) n.609_612delinsTTCA | |
11 | g.32434929G>A | CA064939 | WT1 | c.432C>T (p.Phe144=) c.417C>T (p.Phe139=) n.611C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434929G>C | CA379965656 | WT1 | c.432C>G (p.Phe144Leu) c.417C>G (p.Phe139Leu) n.611C>G | |
11 | g.32434929G= | CA1962327211 | WT1 | c.432C= (p.Phe144=) c.417C= (p.Phe139=) n.611C= | |
11 | g.32434929G>T | CA379965654 | WT1 | c.432C>A (p.Phe144Leu) c.417C>A (p.Phe139Leu) n.611C>A | |
11 | g.32434930_32434932del | CA598508257 | WT1 | c.430_432del (p.Phe144del) c.415_417del (p.Phe139del) n.609_611del | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434930A>C | CA379965657 | WT1 | c.431T>G (p.Phe144Cys) c.416T>G (p.Phe139Cys) n.610T>G | |
11 | g.32434930A>G | CA379965658 | WT1 | c.431T>C (p.Phe144Ser) c.416T>C (p.Phe139Ser) n.610T>C | |
11 | g.32434930A>T | CA379965662 | WT1 | c.431T>A (p.Phe144Tyr) c.416T>A (p.Phe139Tyr) n.610T>A | |
11 | g.32434931A>C | CA379965664 | WT1 | c.430T>G (p.Phe144Val) c.415T>G (p.Phe139Val) n.609T>G | |
11 | g.32434931A>G | CA379965666 | WT1 | c.430T>C (p.Phe144Leu) c.415T>C (p.Phe139Leu) n.609T>C | |
11 | g.32434931A>T | CA379965668 | WT1 | c.430T>A (p.Phe144Ile) c.415T>A (p.Phe139Ile) n.609T>A | |
11 | g.32434932G>A | CA473773556 | WT1 | c.429C>T (p.Ser143=) c.414C>T (p.Ser138=) n.608C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434932G>C | CA064936 | WT1 | c.429C>G (p.Ser143=) c.414C>G (p.Ser138=) n.608C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434932G= | CA1962327212 | WT1 | c.429C= (p.Ser143=) c.414C= (p.Ser138=) n.608C= | |
11 | g.32434932G>T | CA473773561 | WT1 | c.429C>A (p.Ser143=) c.414C>A (p.Ser138=) n.608C>A | gnomAD v4 |
11 | g.32434934_32434946dup | CA2695213676 | WT1 | c.417_429dup (p.Phe144AlafsTer?) c.402_414dup (p.Phe139AlafsTer?) n.596_608dup | |
11 | g.32434933G>A | CA379965672 | WT1 | c.428C>T (p.Ser143Phe) c.413C>T (p.Ser138Phe) n.607C>T | |
11 | g.32434933G>C | CA379965673 | WT1 | c.428C>G (p.Ser143Cys) c.413C>G (p.Ser138Cys) n.607C>G | ClinVar dbSNP |
11 | g.32434933G= | CA1962327213 | WT1 | c.428C= (p.Ser143=) c.413C= (p.Ser138=) n.607C= | |
11 | g.32434933G>T | CA379965675 | WT1 | c.428C>A (p.Ser143Tyr) c.413C>A (p.Ser138Tyr) n.607C>A | |
11 | g.32434936_32434939del | CA645584485 | WT1 | c.425_428del (p.His142ProfsTer20) c.410_413del (p.His137ProfsTer20) n.604_607del | COSMIC |
11 | g.32434934A= | CA1962327214 | WT1 | c.427T= (p.Ser143=) c.412T= (p.Ser138=) n.606T= | |
11 | g.32434934A>C | CA379965679 | WT1 | c.427T>G (p.Ser143Ala) c.412T>G (p.Ser138Ala) n.606T>G | |
11 | g.32434934A>G | CA379965677 | WT1 | c.427T>C (p.Ser143Pro) c.412T>C (p.Ser138Pro) n.606T>C | ClinVar dbSNP |
11 | g.32434934A>T | CA064931 | WT1 | c.427T>A (p.Ser143Thr) c.412T>A (p.Ser138Thr) n.606T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434935G>A | CA473773570 | WT1 | c.426C>T (p.His142=) c.411C>T (p.His137=) n.605C>T | dbSNP |
11 | g.32434935G>C | CA379965681 | WT1 | c.426C>G (p.His142Gln) c.411C>G (p.His137Gln) n.605C>G | ClinVar dbSNP |
11 | g.32434935G= | CA1962327215 | WT1 | c.426C= (p.His142=) c.411C= (p.His137=) n.605C= | |
11 | g.32434935G>T | CA379965683 | WT1 | c.426C>A (p.His142Gln) c.411C>A (p.His137Gln) n.605C>A | |
11 | g.32434936T>A | CA379965685 | WT1 | c.425A>T (p.His142Leu) c.410A>T (p.His137Leu) n.604A>T | ClinVar dbSNP |
11 | g.32434936T>C | CA379965686 | WT1 | c.425A>G (p.His142Arg) c.410A>G (p.His137Arg) n.604A>G | dbSNP |
11 | g.32434936T>G | CA379965687 | WT1 | c.425A>C (p.His142Pro) c.410A>C (p.His137Pro) n.604A>C | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434936T= | CA1962327216 | WT1 | c.425A= (p.His142=) c.410A= (p.His137=) n.604A= | |
11 | g.32434936_32434938delinsGG | CA645584486 | WT1 | c.423_425delinsCC (p.His142ProfsTer21) c.408_410delinsCC (p.His137ProfsTer21) n.602_604delinsCC | COSMIC |
11 | g.32434937G>A | CA379965690 | WT1 | c.424C>T (p.His142Tyr) c.409C>T (p.His137Tyr) n.603C>T | ClinVar |
11 | g.32434937G>C | CA379965692 | WT1 | c.424C>G (p.His142Asp) c.409C>G (p.His137Asp) n.603C>G | |
11 | g.32434937G>T | CA379965693 | WT1 | c.424C>A (p.His142Asn) c.409C>A (p.His137Asn) n.603C>A | |
11 | g.32434938A= | CA1962327217 | WT1 | c.423T= (p.Pro141=) c.408T= (p.Pro136=) n.602T= | |
11 | g.32434938A>C | CA473773578 | WT1 | c.423T>G (p.Pro141=) c.408T>G (p.Pro136=) n.602T>G | ClinVar |
11 | g.32434938A>G | CA473773579 | WT1 | c.423T>C (p.Pro141=) c.408T>C (p.Pro136=) n.602T>C | dbSNP gnomAD v4 |
11 | g.32434938A>T | CA473773586 | WT1 | c.423T>A (p.Pro141=) c.408T>A (p.Pro136=) n.602T>A | |
11 | g.32434938_32434941delinsAGGC | CA1962327218 | WT1 | c.420_423delinsGCCT (p.Pro140=) c.405_408delinsGCCT (p.Pro135=) n.599_602delinsGCCT | |
11 | g.32434939G>A | CA379965699 | WT1 | c.422C>T (p.Pro141Leu) c.407C>T (p.Pro136Leu) n.601C>T | ClinVar |
11 | g.32434939G>C | CA379965700 | WT1 | c.422C>G (p.Pro141Arg) c.407C>G (p.Pro136Arg) n.601C>G | gnomAD v4 |
11 | g.32434939G>T | CA379965702 | WT1 | c.422C>A (p.Pro141His) c.407C>A (p.Pro136His) n.601C>A | |
11 | g.32434950_32434952dup | CA5934336 | WT1 | c.420_422dup (p.Pro141_His142insPro) c.405_407dup (p.Pro136_His137insPro) n.599_601dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434950_32434952del | CA064917 | WT1 | c.420_422del (p.Pro141del) c.405_407del (p.Pro136del) n.599_601del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434947_32434964dup | CA916081630 | WT1 | c.405_422dup (p.Pro141_His142insProProProProProPro) c.390_407dup (p.Pro136_His137insProProProProProPro) n.584_601dup | ClinVar dbSNP gnomAD v4 |
11 | g.32434940G>A | CA064922 | WT1 | c.421C>T (p.Pro141Ser) c.406C>T (p.Pro136Ser) n.600C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434940G>C | CA379965705 | WT1 | c.421C>G (p.Pro141Ala) c.406C>G (p.Pro136Ala) n.600C>G | |
11 | g.32434940G= | CA1962327219 | WT1 | c.421C= (p.Pro141=) c.406C= (p.Pro136=) n.600C= | |
11 | g.32434940G>T | CA379965707 | WT1 | c.421C>A (p.Pro141Thr) c.406C>A (p.Pro136Thr) n.600C>A | |
11 | g.32434941C>A | CA473773603 | WT1 | c.420G>T (p.Pro140=) c.405G>T (p.Pro135=) n.599G>T | ClinVar gnomAD v4 |
11 | g.32434941C= | CA1962327220 | WT1 | c.420G= (p.Pro140=) c.405G= (p.Pro135=) n.599G= | |
11 | g.32434941C>G | CA473773606 | WT1 | c.420G>C (p.Pro140=) c.405G>C (p.Pro135=) n.599G>C | dbSNP |
11 | g.32434941C>T | CA219511039 | WT1 | c.420G>A (p.Pro140=) c.405G>A (p.Pro135=) n.599G>A | dbSNP |
11 | g.32434942G>A | CA379965710 | WT1 | c.419C>T (p.Pro140Leu) c.404C>T (p.Pro135Leu) n.598C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434942G>C | CA379965711 | WT1 | c.419C>G (p.Pro140Arg) c.404C>G (p.Pro135Arg) n.598C>G | |
11 | g.32434942G= | CA1962327221 | WT1 | c.419C= (p.Pro140=) c.404C= (p.Pro135=) n.598C= | |
11 | g.32434942G>T | CA379965712 | WT1 | c.419C>A (p.Pro140Gln) c.404C>A (p.Pro135Gln) n.598C>A | |
11 | g.32434944_32434955del | CA2612989444 | WT1 | c.408_419del (p.Pro137_Pro140del) c.393_404del (p.Pro132_Pro135del) n.587_598del | gnomAD v4 |
11 | g.32434950_32434964del | CA2573146227 | WT1 | c.405_419del (p.Pro136_Pro140del) c.390_404del (p.Pro131_Pro135del) n.584_598del | ClinVar dbSNP |
11 | g.32434943G>A | CA379965714 | WT1 | c.418C>T (p.Pro140Ser) c.403C>T (p.Pro135Ser) n.597C>T | dbSNP gnomAD v2 |
11 | g.32434943G>C | CA379965716 | WT1 | c.418C>G (p.Pro140Ala) c.403C>G (p.Pro135Ala) n.597C>G | |
11 | g.32434943G= | CA1962327222 | WT1 | c.418C= (p.Pro140=) c.403C= (p.Pro135=) n.597C= | |
11 | g.32434943G>T | CA379965718 | WT1 | c.418C>A (p.Pro140Thr) c.403C>A (p.Pro135Thr) n.597C>A |