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.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 |