Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 |
11 | g.32434982G>A | CA379965813 | WT1 | c.379C>T (p.Pro127Ser) c.364C>T (p.Pro122Ser) n.558C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434982G>C | CA379965814 | WT1 | c.379C>G (p.Pro127Ala) c.364C>G (p.Pro122Ala) n.558C>G | |
11 | g.32434982G= | CA1962327254 | WT1 | c.379C= (p.Pro127=) c.364C= (p.Pro122=) n.558C= | |
11 | g.32434982G>T | CA379965815 | WT1 | c.379C>A (p.Pro127Thr) c.364C>A (p.Pro122Thr) n.558C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434983G>A | CA473773732 | WT1 | c.378C>T (p.Gly126=) c.363C>T (p.Gly121=) n.557C>T | gnomAD v4 |
11 | g.32434983G>C | CA473773734 | WT1 | c.378C>G (p.Gly126=) c.363C>G (p.Gly121=) n.557C>G | |
11 | g.32434983G>T | CA473773736 | WT1 | c.378C>A (p.Gly126=) c.363C>A (p.Gly121=) n.557C>A | |
11 | g.32434984C>A | CA379965816 | WT1 | c.377G>T (p.Gly126Val) c.362G>T (p.Gly121Val) n.556G>T | gnomAD v4 |
11 | g.32434984C>G | CA379965818 | WT1 | c.377G>C (p.Gly126Ala) c.362G>C (p.Gly121Ala) n.556G>C | ClinVar dbSNP |
11 | g.32434984C>T | CA379965817 | WT1 | c.377G>A (p.Gly126Asp) c.362G>A (p.Gly121Asp) n.556G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434985C>A | CA379965819 | WT1 | c.376G>T (p.Gly126Cys) c.361G>T (p.Gly121Cys) n.555G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434985C= | CA1962327255 | WT1 | c.376G= (p.Gly126=) c.361G= (p.Gly121=) n.555G= | |
11 | g.32434985C>G | CA379965820 | WT1 | c.376G>C (p.Gly126Arg) c.361G>C (p.Gly121Arg) n.555G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32434985C>T | CA379965821 | WT1 | c.376G>A (p.Gly126Ser) c.361G>A (p.Gly121Ser) n.555G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434986G>A | CA064860 | WT1 | c.375C>T (p.Gly125=) c.360C>T (p.Gly120=) n.554C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434986G>C | CA473773743 | WT1 | c.375C>G (p.Gly125=) c.360C>G (p.Gly120=) n.554C>G | dbSNP |
11 | g.32434986G= | CA1962327256 | WT1 | c.375C= (p.Gly125=) c.360C= (p.Gly120=) n.554C= | |
11 | g.32434986G>T | CA473773745 | WT1 | c.375C>A (p.Gly125=) c.360C>A (p.Gly120=) n.554C>A | dbSNP gnomAD v4 |
11 | g.32434987C>A | CA379965824 | WT1 | c.374G>T (p.Gly125Val) c.359G>T (p.Gly120Val) n.553G>T | |
11 | g.32434987C= | CA1962327257 | WT1 | c.374G= (p.Gly125=) c.359G= (p.Gly120=) n.553G= | |
11 | g.32434987C>G | CA379965822 | WT1 | c.374G>C (p.Gly125Ala) c.359G>C (p.Gly120Ala) n.553G>C | dbSNP |
11 | g.32434987C>T | CA379965823 | WT1 | c.374G>A (p.Gly125Asp) c.359G>A (p.Gly120Asp) n.553G>A | dbSNP gnomAD v4 COSMIC |
11 | g.32434989del | CA2612989553 | WT1 | c.374del (p.Gly125AlafsTer?) c.359del (p.Gly120AlafsTer?) n.553del | gnomAD v4 |
11 | g.32434988C>A | CA379965825 | WT1 | c.373G>T (p.Gly125Cys) c.358G>T (p.Gly120Cys) n.552G>T | |
11 | g.32434988C= | CA1962327258 | WT1 | c.373G= (p.Gly125=) c.358G= (p.Gly120=) n.552G= | |
11 | g.32434988C>G | CA379965826 | WT1 | c.373G>C (p.Gly125Arg) c.358G>C (p.Gly120Arg) n.552G>C | dbSNP |
11 | g.32434988C>T | CA379965827 | WT1 | c.373G>A (p.Gly125Ser) c.358G>A (p.Gly120Ser) n.552G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434989C>A | CA379965828 | WT1 | c.372G>T (p.Leu124Phe) c.357G>T (p.Leu119Phe) n.551G>T | ClinVar |
11 | g.32434989C>G | CA379965829 | WT1 | c.372G>C (p.Leu124Phe) c.357G>C (p.Leu119Phe) n.551G>C | |
11 | g.32434989C>T | CA473773753 | WT1 | c.372G>A (p.Leu124=) c.357G>A (p.Leu119=) n.551G>A | gnomAD v4 |
11 | g.32434990A>C | CA379965830 | WT1 | c.371T>G (p.Leu124Trp) c.356T>G (p.Leu119Trp) n.550T>G | dbSNP |
11 | g.32434990A>G | CA379965831 | WT1 | c.371T>C (p.Leu124Ser) c.356T>C (p.Leu119Ser) n.550T>C | |
11 | g.32434990A>T | CA379965832 | WT1 | c.371T>A (p.Leu124Ter) c.356T>A (p.Leu119Ter) n.550T>A | |
11 | g.32434991A>C | CA379965833 | WT1 | c.370T>G (p.Leu124Val) c.355T>G (p.Leu119Val) n.549T>G | dbSNP |
11 | g.32434991A>G | CA473773757 | WT1 | c.370T>C (p.Leu124=) c.355T>C (p.Leu119=) n.549T>C | ClinVar gnomAD v4 |
11 | g.32434991A>T | CA379965834 | WT1 | c.370T>A (p.Leu124Met) c.355T>A (p.Leu119Met) n.549T>A | |
11 | g.32434992C>A | CA473773759 | WT1 | c.369G>T (p.Ser123=) c.354G>T (p.Ser118=) n.548G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32434992C= | CA1962327259 | WT1 | c.369G= (p.Ser123=) c.354G= (p.Ser118=) n.548G= | |
11 | g.32434992C>G | CA473773761 | WT1 | c.369G>C (p.Ser123=) c.354G>C (p.Ser118=) n.548G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434992C>T | CA473773762 | WT1 | c.369G>A (p.Ser123=) c.354G>A (p.Ser118=) n.548G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434993G>A | CA379965835 | WT1 | c.368C>T (p.Ser123Leu) c.353C>T (p.Ser118Leu) n.547C>T | ClinVar dbSNP |
11 | g.32434993G>C | CA379965836 | WT1 | c.368C>G (p.Ser123Trp) c.353C>G (p.Ser118Trp) n.547C>G | dbSNP |
11 | g.32434993G>T | CA379965837 | WT1 | c.368C>A (p.Ser123Ter) c.353C>A (p.Ser118Ter) n.547C>A | ClinVar gnomAD v4 |
11 | g.32434994A>C | CA379965838 | WT1 | c.367T>G (p.Ser123Ala) c.352T>G (p.Ser118Ala) n.546T>G | ClinVar dbSNP COSMIC COSMIC |
11 | g.32434994A>G | CA379965840 | WT1 | c.367T>C (p.Ser123Pro) c.352T>C (p.Ser118Pro) n.546T>C | dbSNP |
11 | g.32434994A>T | CA379965839 | WT1 | c.367T>A (p.Ser123Thr) c.352T>A (p.Ser118Thr) n.546T>A | |
11 | g.32434995C>A | CA473773767 | WT1 | c.366G>T (p.Gly122=) c.351G>T (p.Gly117=) n.545G>T | ClinVar gnomAD v4 |
11 | g.32434995C= | CA1962327260 | WT1 | c.366G= (p.Gly122=) c.351G= (p.Gly117=) n.545G= | |
11 | g.32434995C>G | CA473773770 | WT1 | c.366G>C (p.Gly122=) c.351G>C (p.Gly117=) n.545G>C | dbSNP |
11 | g.32434995C>T | CA473773768 | WT1 | c.366G>A (p.Gly122=) c.351G>A (p.Gly117=) n.545G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32434996C>A | CA379965841 | WT1 | c.365G>T (p.Gly122Val) c.350G>T (p.Gly117Val) n.544G>T | gnomAD v4 |
11 | g.32434996C>G | CA379965842 | WT1 | c.365G>C (p.Gly122Ala) c.350G>C (p.Gly117Ala) n.544G>C | |
11 | g.32434996C>T | CA379965843 | WT1 | c.365G>A (p.Gly122Glu) c.350G>A (p.Gly117Glu) n.544G>A | gnomAD v4 |
11 | g.32434997C>A | CA379965844 | WT1 | c.364G>T (p.Gly122Trp) c.349G>T (p.Gly117Trp) n.543G>T | gnomAD v4 |
11 | g.32434997C>G | CA379965845 | WT1 | c.364G>C (p.Gly122Arg) c.349G>C (p.Gly117Arg) n.543G>C | gnomAD v4 |
11 | g.32434997C>T | CA379965846 | WT1 | c.364G>A (p.Gly122Arg) c.349G>A (p.Gly117Arg) n.543G>A | gnomAD v4 |
11 | g.32434998G>A | CA219511101 | WT1 | c.363C>T (p.Tyr121=) c.348C>T (p.Tyr116=) n.542C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32434998G>C | CA379965847 | WT1 | c.363C>G (p.Tyr121Ter) c.348C>G (p.Tyr116Ter) n.542C>G | dbSNP gnomAD v4 COSMIC |
11 | g.32434998G= | CA1962327261 | WT1 | c.363C= (p.Tyr121=) c.348C= (p.Tyr116=) n.542C= | |
11 | g.32434998G>T | CA379965848 | WT1 | c.363C>A (p.Tyr121Ter) c.348C>A (p.Tyr116Ter) n.542C>A | ClinVar gnomAD v4 COSMIC |
11 | g.32434999T>A | CA379965849 | WT1 | c.362A>T (p.Tyr121Phe) c.347A>T (p.Tyr116Phe) n.541A>T | |
11 | g.32434999T>C | CA379965850 | WT1 | c.362A>G (p.Tyr121Cys) c.347A>G (p.Tyr116Cys) n.541A>G | dbSNP |
11 | g.32434999T>G | CA379965851 | WT1 | c.362A>C (p.Tyr121Ser) c.347A>C (p.Tyr116Ser) n.541A>C | dbSNP |
11 | g.32434999T= | CA1962327262 | WT1 | c.362A= (p.Tyr121=) c.347A= (p.Tyr116=) n.541A= | |
11 | g.32435000A= | CA1962327263 | WT1 | c.361T= (p.Tyr121=) c.346T= (p.Tyr116=) n.540T= | |
11 | g.32435000A>C | CA219511102 | WT1 | c.361T>G (p.Tyr121Asp) c.346T>G (p.Tyr116Asp) n.540T>G | dbSNP |
11 | g.32435000A>G | CA379965853 | WT1 | c.361T>C (p.Tyr121His) c.346T>C (p.Tyr116His) n.540T>C | gnomAD v4 |
11 | g.32435000A>T | CA379965852 | WT1 | c.361T>A (p.Tyr121Asn) c.346T>A (p.Tyr116Asn) n.540T>A | |
11 | g.32435001A>C | CA473773778 | WT1 | c.360T>G (p.Ala120=) c.345T>G (p.Ala115=) n.539T>G | |
11 | g.32435001A>G | CA473773779 | WT1 | c.360T>C (p.Ala120=) c.345T>C (p.Ala115=) n.539T>C | |
11 | g.32435001A>T | CA473773780 | WT1 | c.360T>A (p.Ala120=) c.345T>A (p.Ala115=) n.539T>A | |
11 | g.32435002G>A | CA379965854 | WT1 | c.359C>T (p.Ala120Val) c.344C>T (p.Ala115Val) n.538C>T | gnomAD v4 |
11 | g.32435002G>C | CA379965855 | WT1 | c.359C>G (p.Ala120Gly) c.344C>G (p.Ala115Gly) n.538C>G | dbSNP |
11 | g.32435002G>T | CA379965856 | WT1 | c.359C>A (p.Ala120Asp) c.344C>A (p.Ala115Asp) n.538C>A | gnomAD v4 |
11 | g.32435003C>A | CA379965857 | WT1 | c.358G>T (p.Ala120Ser) c.343G>T (p.Ala115Ser) n.537G>T | |
11 | g.32435003C= | CA1962327264 | WT1 | c.358G= (p.Ala120=) c.343G= (p.Ala115=) n.537G= | |
11 | g.32435003C>G | CA379965858 | WT1 | c.358G>C (p.Ala120Pro) c.343G>C (p.Ala115Pro) n.537G>C | dbSNP |
11 | g.32435003C>T | CA379965859 | WT1 | c.358G>A (p.Ala120Thr) c.343G>A (p.Ala115Thr) n.537G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435004C>A | CA473773786 | WT1 | c.357G>T (p.Ser119=) c.342G>T (p.Ser114=) n.536G>T | ClinVar gnomAD v4 |
11 | g.32435004C= | CA1962327265 | WT1 | c.357G= (p.Ser119=) c.342G= (p.Ser114=) n.536G= | |
11 | g.32435004C>G | CA473773787 | WT1 | c.357G>C (p.Ser119=) c.342G>C (p.Ser114=) n.536G>C | dbSNP gnomAD v4 |
11 | g.32435004C>T | CA473773788 | WT1 | c.357G>A (p.Ser119=) c.342G>A (p.Ser114=) n.536G>A | gnomAD v4 |
11 | g.32435005G>A | CA379965860 | WT1 | c.356C>T (p.Ser119Leu) c.341C>T (p.Ser114Leu) n.535C>T | ClinVar gnomAD v4 |
11 | g.32435005G>C | CA379965861 | WT1 | c.356C>G (p.Ser119Trp) c.341C>G (p.Ser114Trp) n.535C>G | ClinVar dbSNP |
11 | g.32435005G= | CA1962327266 | WT1 | c.356C= (p.Ser119=) c.341C= (p.Ser114=) n.535C= | |
11 | g.32435005G>T | CA379965862 | WT1 | c.356C>A (p.Ser119Ter) c.341C>A (p.Ser114Ter) n.535C>A | COSMIC |
11 | g.32435006A= | CA1962327267 | WT1 | c.355T= (p.Ser119=) c.340T= (p.Ser114=) n.534T= | |
11 | g.32435006A>C | CA379965863 | WT1 | c.355T>G (p.Ser119Ala) c.340T>G (p.Ser114Ala) n.534T>G | |
11 | g.32435006A>G | CA379965864 | WT1 | c.355T>C (p.Ser119Pro) c.340T>C (p.Ser114Pro) n.534T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435006A>T | CA379965865 | WT1 | c.355T>A (p.Ser119Thr) c.340T>A (p.Ser114Thr) n.534T>A | gnomAD v4 |
11 | g.32435007A>C | CA473773795 | WT1 | c.354T>G (p.Ala118=) c.339T>G (p.Ala113=) n.533T>G | dbSNP |
11 | g.32435007A>G | CA473773794 | WT1 | c.354T>C (p.Ala118=) c.339T>C (p.Ala113=) n.533T>C | dbSNP gnomAD v4 |
11 | g.32435007A>T | CA473773793 | WT1 | c.354T>A (p.Ala118=) c.339T>A (p.Ala113=) n.533T>A | dbSNP |
11 | g.32435008G>A | CA064850 | WT1 | c.353C>T (p.Ala118Val) c.338C>T (p.Ala113Val) n.532C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435008G>C | CA379965867 | WT1 | c.353C>G (p.Ala118Gly) c.338C>G (p.Ala113Gly) n.532C>G | |
11 | g.32435008G= | CA1962327268 | WT1 | c.353C= (p.Ala118=) c.338C= (p.Ala113=) n.532C= | |
11 | g.32435008G>T | CA379965866 | WT1 | c.353C>A (p.Ala118Asp) c.338C>A (p.Ala113Asp) n.532C>A | gnomAD v4 |
11 | g.32435009C>A | CA379965868 | WT1 | c.352G>T (p.Ala118Ser) c.337G>T (p.Ala113Ser) n.531G>T | gnomAD v4 |
11 | g.32435009C= | CA1962327269 | WT1 | c.352G= (p.Ala118=) c.337G= (p.Ala113=) n.531G= | |
11 | g.32435009C>G | CA379965870 | WT1 | c.352G>C (p.Ala118Pro) c.337G>C (p.Ala113Pro) n.531G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435009C>T | CA379965869 | WT1 | c.352G>A (p.Ala118Thr) c.337G>A (p.Ala113Thr) n.531G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435010G>A | CA473773799 | WT1 | c.351C>T (p.Gly117=) c.336C>T (p.Gly112=) n.530C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435010G>C | CA473773798 | WT1 | c.351C>G (p.Gly117=) c.336C>G (p.Gly112=) n.530C>G | |
11 | g.32435010G= | CA1962327270 | WT1 | c.351C= (p.Gly117=) c.336C= (p.Gly112=) n.530C= | |
11 | g.32435010G>T | CA473773797 | WT1 | c.351C>A (p.Gly117=) c.336C>A (p.Gly112=) n.530C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435011C>A | CA379965871 | WT1 | c.350G>T (p.Gly117Val) c.335G>T (p.Gly112Val) n.529G>T | |
11 | g.32435011C= | CA1962327271 | WT1 | c.350G= (p.Gly117=) c.335G= (p.Gly112=) n.529G= | |
11 | g.32435011C>G | CA379965872 | WT1 | c.350G>C (p.Gly117Ala) c.335G>C (p.Gly112Ala) n.529G>C | dbSNP |
11 | g.32435011C>T | CA219511109 | WT1 | c.350G>A (p.Gly117Asp) c.335G>A (p.Gly112Asp) n.529G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435012C>A | CA379965873 | WT1 | c.349G>T (p.Gly117Cys) c.334G>T (p.Gly112Cys) n.528G>T | gnomAD v4 |
11 | g.32435012C= | CA1962327272 | WT1 | c.349G= (p.Gly117=) c.334G= (p.Gly112=) n.528G= | |
11 | g.32435012C>G | CA379965875 | WT1 | c.349G>C (p.Gly117Arg) c.334G>C (p.Gly112Arg) n.528G>C | dbSNP |
11 | g.32435012C>T | CA379965874 | WT1 | c.349G>A (p.Gly117Ser) c.334G>A (p.Gly112Ser) n.528G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435013C>A | CA473773802 | WT1 | c.348G>T (p.Pro116=) c.333G>T (p.Pro111=) n.527G>T | gnomAD v4 |
11 | g.32435013C= | CA1962327273 | WT1 | c.348G= (p.Pro116=) c.333G= (p.Pro111=) n.527G= | |
11 | g.32435013C>G | CA473773804 | WT1 | c.348G>C (p.Pro116=) c.333G>C (p.Pro111=) n.527G>C | ClinVar dbSNP gnomAD v4 |
11 | g.32435013C>T | CA473773803 | WT1 | c.348G>A (p.Pro116=) c.333G>A (p.Pro111=) n.527G>A | gnomAD v4 |
11 | g.32435014G>A | CA10638965 | WT1 | c.347C>T (p.Pro116Leu) c.332C>T (p.Pro111Leu) n.526C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435014G>C | CA379965877 | WT1 | c.347C>G (p.Pro116Arg) c.332C>G (p.Pro111Arg) n.526C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32435014G= | CA1962327274 | WT1 | c.347C= (p.Pro116=) c.332C= (p.Pro111=) n.526C= | |
11 | g.32435014G>T | CA379965876 | WT1 | c.347C>A (p.Pro116Gln) c.332C>A (p.Pro111Gln) n.526C>A | gnomAD v4 |
11 | g.32435018dup | CA2612989557 | WT1 | c.347dup (p.Ala118ArgfsTer?) c.332dup (p.Ala113ArgfsTer?) n.526dup | gnomAD v4 |
11 | g.32435018del | CA2612989558 | WT1 | c.347del (p.Pro116ArgfsTer?) c.332del (p.Pro111ArgfsTer?) n.526del | gnomAD v4 |
11 | g.32435015G>A | CA379965878 | WT1 | c.346C>T (p.Pro116Ser) c.331C>T (p.Pro111Ser) n.525C>T | |
11 | g.32435015G>C | CA379965879 | WT1 | c.346C>G (p.Pro116Ala) c.331C>G (p.Pro111Ala) n.525C>G | |
11 | g.32435015G= | CA1962327275 | WT1 | c.346C= (p.Pro116=) c.331C= (p.Pro111=) n.525C= | |
11 | g.32435015G>T | CA379965880 | WT1 | c.346C>A (p.Pro116Thr) c.331C>A (p.Pro111Thr) n.525C>A | ClinVar dbSNP gnomAD v4 |