Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32434878_32434911del | CA645584483 | WT1 | c.453_486del (p.Trp151Ter) c.438_471del (p.Trp146Ter) n.632_665del | COSMIC |
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 | |
11 | g.32434944C>A | CA473773613 | WT1 | c.417G>T (p.Pro139=) c.402G>T (p.Pro134=) n.596G>T | ClinVar dbSNP |
11 | g.32434944C= | CA1962327223 | WT1 | c.417G= (p.Pro139=) c.402G= (p.Pro134=) n.596G= | |
11 | g.32434944C>G | CA473773615 | WT1 | c.417G>C (p.Pro139=) c.402G>C (p.Pro134=) n.596G>C | dbSNP |
11 | g.32434944C>T | CA064912 | WT1 | c.417G>A (p.Pro139=) c.402G>A (p.Pro134=) n.596G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434945G>A | CA379965721 | WT1 | c.416C>T (p.Pro139Leu) c.401C>T (p.Pro134Leu) n.595C>T | gnomAD v4 |
11 | g.32434945G>C | CA10582913 | WT1 | c.416C>G (p.Pro139Arg) c.401C>G (p.Pro134Arg) n.595C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434945G= | CA1962327224 | WT1 | c.416C= (p.Pro139=) c.401C= (p.Pro134=) n.595C= | |
11 | g.32434945G>T | CA379965724 | WT1 | c.416C>A (p.Pro139Gln) c.401C>A (p.Pro134Gln) n.595C>A | ClinVar gnomAD v4 |
11 | g.32434953_32434964dup | CA675622615 | WT1 | c.405_416dup (p.Pro139_Pro140insProProProPro) c.390_401dup (p.Pro134_Pro135insProProProPro) n.584_595dup | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434946G>A | CA379965726 | WT1 | c.415C>T (p.Pro139Ser) c.400C>T (p.Pro134Ser) n.594C>T | |
11 | g.32434946G>C | CA379965728 | WT1 | c.415C>G (p.Pro139Ala) c.400C>G (p.Pro134Ala) n.594C>G | |
11 | g.32434946G>T | CA379965729 | WT1 | c.415C>A (p.Pro139Thr) c.400C>A (p.Pro134Thr) n.594C>A | gnomAD v4 |
11 | g.32434947C>A | CA473773622 | WT1 | c.414G>T (p.Pro138=) c.399G>T (p.Pro133=) n.593G>T | |
11 | g.32434947C>G | CA473773623 | WT1 | c.414G>C (p.Pro138=) c.399G>C (p.Pro133=) n.593G>C | dbSNP |
11 | g.32434947C>T | CA473773624 | WT1 | c.414G>A (p.Pro138=) c.399G>A (p.Pro133=) n.593G>A | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.32434948G>A | CA379965733 | WT1 | c.413C>T (p.Pro138Leu) c.398C>T (p.Pro133Leu) n.592C>T | ClinVar gnomAD v4 |
11 | g.32434948G>C | CA379965734 | WT1 | c.413C>G (p.Pro138Arg) c.398C>G (p.Pro133Arg) n.592C>G | ClinVar dbSNP |
11 | g.32434948G= | CA1962327225 | WT1 | c.413C= (p.Pro138=) c.398C= (p.Pro133=) n.592C= | |
11 | g.32434948G>T | CA379965731 | WT1 | c.413C>A (p.Pro138Gln) c.398C>A (p.Pro133Gln) n.592C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434953_32434961dup | CA2740093679 | WT1 | c.405_413dup (p.Pro138_Pro139insProProPro) c.390_398dup (p.Pro133_Pro134insProProPro) n.584_592dup | ClinVar |
11 | g.32434949G>A | CA064909 | WT1 | c.412C>T (p.Pro138Ser) c.397C>T (p.Pro133Ser) n.591C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434949G>C | CA379965736 | WT1 | c.412C>G (p.Pro138Ala) c.397C>G (p.Pro133Ala) n.591C>G | |
11 | g.32434949G= | CA1962327226 | WT1 | c.412C= (p.Pro138=) c.397C= (p.Pro133=) n.591C= | |
11 | g.32434949G>T | CA379965738 | WT1 | c.412C>A (p.Pro138Thr) c.397C>A (p.Pro133Thr) n.591C>A | ClinVar |
11 | g.32434950del | CA2612989498 | WT1 | c.411del (p.Pro138ArgfsTer25) c.396del (p.Pro133ArgfsTer25) n.590del | gnomAD v4 |
11 | g.32434950C>A | CA473773631 | WT1 | c.411G>T (p.Pro137=) c.396G>T (p.Pro132=) n.590G>T | |
11 | g.32434950C= | CA1962327227 | WT1 | c.411G= (p.Pro137=) c.396G= (p.Pro132=) n.590G= | |
11 | g.32434950C>G | CA473773633 | WT1 | c.411G>C (p.Pro137=) c.396G>C (p.Pro132=) n.590G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32434950C>T | CA473773634 | WT1 | c.411G>A (p.Pro137=) c.396G>A (p.Pro132=) n.590G>A | dbSNP gnomAD v4 |
11 | g.32434951G>A | CA379965739 | WT1 | c.410C>T (p.Pro137Leu) c.395C>T (p.Pro132Leu) n.589C>T | |
11 | g.32434951G>C | CA379965741 | WT1 | c.410C>G (p.Pro137Arg) c.395C>G (p.Pro132Arg) n.589C>G | |
11 | g.32434951G= | CA1962327228 | WT1 | c.410C= (p.Pro137=) c.395C= (p.Pro132=) n.589C= | |
11 | g.32434951G>T | CA379965743 | WT1 | c.410C>A (p.Pro137Gln) c.395C>A (p.Pro132Gln) n.589C>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434951_32434952delinsTT | CA645584487 | WT1 | c.409_410delinsAA (p.Pro137Lys) c.394_395delinsAA (p.Pro132Lys) n.588_589delinsAA | COSMIC COSMIC |
11 | g.32434952_32434953insTGG | CA2574790567 | WT1 | c.410_411insACC (p.Pro137_Pro138insPro) c.395_396insACC (p.Pro132_Pro133insPro) n.589_590insACC | |
11 | g.32434955dup | CA2573320816 | WT1 | c.410dup (p.Pro138AlafsTer?) c.395dup (p.Pro133AlafsTer?) n.589dup | |
11 | g.32434955del | CA2573334573 | WT1 | c.410del (p.Pro137ArgfsTer26) c.395del (p.Pro132ArgfsTer26) n.589del | ClinVar gnomAD v4 |
11 | g.32434952G>A | CA379965749 | WT1 | c.409C>T (p.Pro137Ser) c.394C>T (p.Pro132Ser) n.588C>T | gnomAD v4 |
11 | g.32434952G>C | CA379965745 | WT1 | c.409C>G (p.Pro137Ala) c.394C>G (p.Pro132Ala) n.588C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434952G= | CA1962327229 | WT1 | c.409C= (p.Pro137=) c.394C= (p.Pro132=) n.588C= | |
11 | g.32434952G>T | CA379965747 | WT1 | c.409C>A (p.Pro137Thr) c.394C>A (p.Pro132Thr) n.588C>A | |
11 | g.32434953G>A | CA473773639 | WT1 | c.408C>T (p.Pro136=) c.393C>T (p.Pro131=) n.587C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434953G>C | CA473773640 | WT1 | c.408C>G (p.Pro136=) c.393C>G (p.Pro131=) n.587C>G | gnomAD v4 |
11 | g.32434953G= | CA1962327230 | WT1 | c.408C= (p.Pro136=) c.393C= (p.Pro131=) n.587C= | |
11 | g.32434953G>T | CA473773642 | WT1 | c.408C>A (p.Pro136=) c.393C>A (p.Pro131=) n.587C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434954G>A | CA379965751 | WT1 | c.407C>T (p.Pro136Leu) c.392C>T (p.Pro131Leu) n.586C>T | |
11 | g.32434954G>C | CA379965753 | WT1 | c.407C>G (p.Pro136Arg) c.392C>G (p.Pro131Arg) n.586C>G | |
11 | g.32434954G>T | CA379965755 | WT1 | c.407C>A (p.Pro136His) c.392C>A (p.Pro131His) n.586C>A | |
11 | g.32434955_32434956insCGG | CA2580582997 | WT1 | c.407_408insGCC (p.Pro136_Pro137insPro) c.392_393insGCC (p.Pro131_Pro132insPro) n.586_587insGCC | |
11 | g.32434956_32434958dup | CA1962327231 | WT1 | c.405_407dup (p.Pro136_Pro137insPro) c.390_392dup (p.Pro131_Pro132insPro) n.584_586dup | dbSNP |
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.32434955G>A | CA379965757 | WT1 | c.406C>T (p.Pro136Ser) c.391C>T (p.Pro131Ser) n.585C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434955G>C | CA379965759 | WT1 | c.406C>G (p.Pro136Ala) c.391C>G (p.Pro131Ala) n.585C>G | gnomAD v4 |
11 | g.32434955G= | CA1962327233 | WT1 | c.406C= (p.Pro136=) c.391C= (p.Pro131=) n.585C= | |
11 | g.32434955G>T | CA064905 | WT1 | c.406C>A (p.Pro136Thr) c.391C>A (p.Pro131Thr) n.585C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434956T>A | CA473773646 | WT1 | c.405A>T (p.Pro135=) c.390A>T (p.Pro130=) n.584A>T | dbSNP |
11 | g.32434956T>C | CA473773647 | WT1 | c.405A>G (p.Pro135=) c.390A>G (p.Pro130=) n.584A>G | gnomAD v4 |
11 | g.32434956T>G | CA219511062 | WT1 | c.405A>C (p.Pro135=) c.390A>C (p.Pro130=) n.584A>C | dbSNP gnomAD v4 |
11 | g.32434956T= | CA1962327234 | WT1 | c.405A= (p.Pro135=) c.390A= (p.Pro130=) n.584A= | |
11 | g.32434957G>A | CA064898 | WT1 | c.404C>T (p.Pro135Leu) c.389C>T (p.Pro130Leu) n.583C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434957G>C | CA379965765 | WT1 | c.404C>G (p.Pro135Arg) c.389C>G (p.Pro130Arg) n.583C>G | |
11 | g.32434957G= | CA1962327235 | WT1 | c.404C= (p.Pro135=) c.389C= (p.Pro130=) n.583C= | |
11 | g.32434957G>T | CA379965763 | WT1 | c.404C>A (p.Pro135Gln) c.389C>A (p.Pro130Gln) n.583C>A | gnomAD v4 |
11 | g.32434958G>A | CA379965767 | WT1 | c.403C>T (p.Pro135Ser) c.388C>T (p.Pro130Ser) n.582C>T | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434958G>C | CA379965769 | WT1 | c.403C>G (p.Pro135Ala) c.388C>G (p.Pro130Ala) n.582C>G | |
11 | g.32434958G= | CA1962327236 | WT1 | c.403C= (p.Pro135=) c.388C= (p.Pro130=) n.582C= | |
11 | g.32434958G>T | CA379965771 | WT1 | c.403C>A (p.Pro135Thr) c.388C>A (p.Pro130Thr) n.582C>A | gnomAD v4 |
11 | g.32434959C>A | CA473773653 | WT1 | c.402G>T (p.Pro134=) c.387G>T (p.Pro129=) n.581G>T | ClinVar gnomAD v4 |
11 | g.32434959C= | CA1962327237 | WT1 | c.402G= (p.Pro134=) c.387G= (p.Pro129=) n.581G= | |
11 | g.32434959C>G | CA473773654 | WT1 | c.402G>C (p.Pro134=) c.387G>C (p.Pro129=) n.581G>C | dbSNP |
11 | g.32434959C>T | CA064893 | WT1 | c.402G>A (p.Pro134=) c.387G>A (p.Pro129=) n.581G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434964_32434965insGGGTGTCGGCGG | CA2790963047 | WT1 | c.402_403insACACCCCCGCCG (p.Pro134_Pro135insThrProProPro) c.387_388insACACCCCCGCCG (p.Pro129_Pro130insThrProProPro) n.581_582insACACCCCCGCCG | |
11 | g.32434960G>A | CA379965775 | WT1 | c.401C>T (p.Pro134Leu) c.386C>T (p.Pro129Leu) n.580C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434960G>C | CA379965776 | WT1 | c.401C>G (p.Pro134Arg) c.386C>G (p.Pro129Arg) n.580C>G | ClinVar dbSNP |
11 | g.32434960G= | CA1962327238 | WT1 | c.401C= (p.Pro134=) c.386C= (p.Pro129=) n.580C= | |
11 | g.32434960G>T | CA064889 | WT1 | c.401C>A (p.Pro134Gln) c.386C>A (p.Pro129Gln) n.580C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434965_32434976dup | CA2573146228 | WT1 | c.390_401dup (p.Pro134_Pro135insProAlaProPro) c.375_386dup (p.Pro129_Pro130insProAlaProPro) n.569_580dup | ClinVar dbSNP |
11 | g.32434961G>A | CA379965777 | WT1 | c.400C>T (p.Pro134Ser) c.385C>T (p.Pro129Ser) n.579C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434961G>C | CA379965778 | WT1 | c.400C>G (p.Pro134Ala) c.385C>G (p.Pro129Ala) n.579C>G | |
11 | g.32434961G>T | CA379965779 | WT1 | c.400C>A (p.Pro134Thr) c.385C>A (p.Pro129Thr) n.579C>A | gnomAD v4 |
11 | g.32434962C>A | CA473773661 | WT1 | c.399G>T (p.Pro133=) c.384G>T (p.Pro128=) n.578G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434962C>G | CA473773662 | WT1 | c.399G>C (p.Pro133=) c.384G>C (p.Pro128=) n.578G>C | dbSNP gnomAD v4 |
11 | g.32434962C>T | CA473773663 | WT1 | c.399G>A (p.Pro133=) c.384G>A (p.Pro128=) n.578G>A | gnomAD v4 |
11 | g.32434963G>A | CA064884 | WT1 | c.398C>T (p.Pro133Leu) c.383C>T (p.Pro128Leu) n.577C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434963G>C | CA379965780 | WT1 | c.398C>G (p.Pro133Arg) c.383C>G (p.Pro128Arg) n.577C>G | |
11 | g.32434963G= | CA1962327239 | WT1 | c.398C= (p.Pro133=) c.383C= (p.Pro128=) n.577C= | |
11 | g.32434963G>T | CA379965781 | WT1 | c.398C>A (p.Pro133Gln) c.383C>A (p.Pro128Gln) n.577C>A | ClinVar |
11 | g.32434964G>A | CA379965782 | WT1 | c.397C>T (p.Pro133Ser) c.382C>T (p.Pro128Ser) n.576C>T | ClinVar dbSNP |
11 | g.32434964G>C | CA379965784 | WT1 | c.397C>G (p.Pro133Ala) c.382C>G (p.Pro128Ala) n.576C>G | |
11 | g.32434964G= | CA1962327240 | WT1 | c.397C= (p.Pro133=) c.382C= (p.Pro128=) n.576C= | |
11 | g.32434964G>T | CA379965783 | WT1 | c.397C>A (p.Pro133Thr) c.382C>A (p.Pro128Thr) n.576C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434965A= | CA1962327241 | WT1 | c.396T= (p.Ala132=) c.381T= (p.Ala127=) n.575T= | |
11 | g.32434965A>C | CA473773668 | WT1 | c.396T>G (p.Ala132=) c.381T>G (p.Ala127=) n.575T>G | |
11 | g.32434965A>G | CA473773666 | WT1 | c.396T>C (p.Ala132=) c.381T>C (p.Ala127=) n.575T>C | dbSNP gnomAD v4 |
11 | g.32434965A>T | CA473773667 | WT1 | c.396T>A (p.Ala132=) c.381T>A (p.Ala127=) n.575T>A | |
11 | g.32434966G>A | CA379965785 | WT1 | c.395C>T (p.Ala132Val) c.380C>T (p.Ala127Val) n.574C>T | |
11 | g.32434966G>C | CA379965786 | WT1 | c.395C>G (p.Ala132Gly) c.380C>G (p.Ala127Gly) n.574C>G | ClinVar |
11 | g.32434966G>T | CA379965787 | WT1 | c.395C>A (p.Ala132Asp) c.380C>A (p.Ala127Asp) n.574C>A | |
11 | g.32434967C>A | CA379965788 | WT1 | c.394G>T (p.Ala132Ser) c.379G>T (p.Ala127Ser) n.573G>T | ClinVar gnomAD v4 |
11 | g.32434967C= | CA1962327242 | WT1 | c.394G= (p.Ala132=) c.379G= (p.Ala127=) n.573G= | |
11 | g.32434967C>G | CA379965789 | WT1 | c.394G>C (p.Ala132Pro) c.379G>C (p.Ala127Pro) n.573G>C | dbSNP |
11 | g.32434967C>T | CA064879 | WT1 | c.394G>A (p.Ala132Thr) c.379G>A (p.Ala127Thr) n.573G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32434968C>A | CA473773678 | WT1 | c.393G>T (p.Pro131=) c.378G>T (p.Pro126=) n.572G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434968C= | CA1962327243 | WT1 | c.393G= (p.Pro131=) c.378G= (p.Pro126=) n.572G= | |
11 | g.32434968C>G | CA473773681 | WT1 | c.393G>C (p.Pro131=) c.378G>C (p.Pro126=) n.572G>C | ClinVar dbSNP |
11 | g.32434968C>T | CA473773683 | WT1 | c.393G>A (p.Pro131=) c.378G>A (p.Pro126=) n.572G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434969G>A | CA379965790 | WT1 | c.392C>T (p.Pro131Leu) c.377C>T (p.Pro126Leu) n.571C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434969G>C | CA379965791 | WT1 | c.392C>G (p.Pro131Arg) c.377C>G (p.Pro126Arg) n.571C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434969G= | CA1962327244 | WT1 | c.392C= (p.Pro131=) c.377C= (p.Pro126=) n.571C= | |
11 | g.32434969G>T | CA379965792 | WT1 | c.392C>A (p.Pro131Gln) c.377C>A (p.Pro126Gln) n.571C>A | dbSNP gnomAD v4 |
11 | g.32434970del | CA473773685 | WT1 | c.392del (p.Pro131ArgfsTer?) c.377del (p.Pro126ArgfsTer?) n.571del | COSMIC |
11 | g.32434970G>A | CA219511084 | WT1 | c.391C>T (p.Pro131Ser) c.376C>T (p.Pro126Ser) n.570C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434970G>C | CA379965793 | WT1 | c.391C>G (p.Pro131Ala) c.376C>G (p.Pro126Ala) n.570C>G | |
11 | g.32434970G= | CA1962327245 | WT1 | c.391C= (p.Pro131=) c.376C= (p.Pro126=) n.570C= | |
11 | g.32434970G>T | CA219511089 | WT1 | c.391C>A (p.Pro131Thr) c.376C>A (p.Pro126Thr) n.570C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434971T>A | CA473773688 | WT1 | c.390A>T (p.Pro130=) c.375A>T (p.Pro125=) n.569A>T | dbSNP |
11 | g.32434971T>C | CA10630774 | WT1 | c.390A>G (p.Pro130=) c.375A>G (p.Pro125=) n.569A>G | ClinVar dbSNP |
11 | g.32434971T>G | CA473773690 | WT1 | c.390A>C (p.Pro130=) c.375A>C (p.Pro125=) n.569A>C | ClinVar dbSNP |
11 | g.32434971T= | CA1962327246 | WT1 | c.390A= (p.Pro130=) c.375A= (p.Pro125=) n.569A= | |
11 | g.32434972G>A | CA379965796 | WT1 | c.389C>T (p.Pro130Leu) c.374C>T (p.Pro125Leu) n.568C>T | ClinVar |
11 | g.32434972G>C | CA379965794 | WT1 | c.389C>G (p.Pro130Arg) c.374C>G (p.Pro125Arg) n.568C>G | dbSNP |
11 | g.32434972G>T | CA379965795 | WT1 | c.389C>A (p.Pro130Gln) c.374C>A (p.Pro125Gln) n.568C>A | 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.32434973G>A | CA379965797 | WT1 | c.388C>T (p.Pro130Ser) c.373C>T (p.Pro125Ser) n.567C>T | ClinVar dbSNP |
11 | g.32434973G>C | CA379965798 | WT1 | c.388C>G (p.Pro130Ala) c.373C>G (p.Pro125Ala) n.567C>G | |
11 | g.32434973G= | CA1962327247 | WT1 | c.388C= (p.Pro130=) c.373C= (p.Pro125=) n.567C= | |
11 | g.32434973G>T | CA379965799 | WT1 | c.388C>A (p.Pro130Thr) c.373C>A (p.Pro125Thr) n.567C>A | |
11 | g.32434974del | CA473773701 | WT1 | c.387del (p.Pro130HisfsTer?) c.372del (p.Pro125HisfsTer?) n.566del | COSMIC |
11 | g.32434974C>A | CA473773702 | WT1 | c.387G>T (p.Pro129=) c.372G>T (p.Pro124=) n.566G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434974C= | CA1962327248 | WT1 | c.387G= (p.Pro129=) c.372G= (p.Pro124=) n.566G= | |
11 | g.32434974C>G | CA473773704 | WT1 | c.387G>C (p.Pro129=) c.372G>C (p.Pro124=) n.566G>C | dbSNP |
11 | g.32434974C>T | CA473773700 | WT1 | c.387G>A (p.Pro129=) c.372G>A (p.Pro124=) n.566G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434975G>A | CA064875 | WT1 | c.386C>T (p.Pro129Leu) c.371C>T (p.Pro124Leu) n.565C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434975G>C | CA379965800 | WT1 | c.386C>G (p.Pro129Arg) c.371C>G (p.Pro124Arg) n.565C>G | |
11 | g.32434975G= | CA1962327249 | WT1 | c.386C= (p.Pro129=) c.371C= (p.Pro124=) n.565C= | |
11 | g.32434975G>T | CA219511099 | WT1 | c.386C>A (p.Pro129Gln) c.371C>A (p.Pro124Gln) n.565C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434976G>A | CA379965801 | WT1 | c.385C>T (p.Pro129Ser) c.370C>T (p.Pro124Ser) n.564C>T | dbSNP gnomAD v4 |
11 | g.32434976G>C | CA379965802 | WT1 | c.385C>G (p.Pro129Ala) c.370C>G (p.Pro124Ala) n.564C>G | |
11 | g.32434976G>T | CA379965803 | WT1 | c.385C>A (p.Pro129Thr) c.370C>A (p.Pro124Thr) n.564C>A | |
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 |