Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32435125del | CA2612989627 | WT1 | c.238del (p.Asp80ThrfsTer2) c.223del (p.Asp75ThrfsTer2) n.417del | gnomAD v4 |
11 | g.32435125C>A | CA379966096 | WT1 | c.236G>T (p.Arg79Leu) c.221G>T (p.Arg74Leu) n.415G>T | gnomAD v4 |
11 | g.32435125C= | CA1962327347 | WT1 | c.236G= (p.Arg79=) c.221G= (p.Arg74=) n.415G= | |
11 | g.32435125C>G | CA379966097 | WT1 | c.236G>C (p.Arg79Pro) c.221G>C (p.Arg74Pro) n.415G>C | gnomAD v4 |
11 | g.32435125C>T | CA379966098 | WT1 | c.236G>A (p.Arg79Gln) c.221G>A (p.Arg74Gln) n.415G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435126G>A | CA379966099 | WT1 | c.235C>T (p.Arg79Trp) c.220C>T (p.Arg74Trp) n.414C>T | dbSNP gnomAD v4 |
11 | g.32435126G>C | CA379966100 | WT1 | c.235C>G (p.Arg79Gly) c.220C>G (p.Arg74Gly) n.414C>G | |
11 | g.32435126G= | CA1962327348 | WT1 | c.235C= (p.Arg79=) c.220C= (p.Arg74=) n.414C= | |
11 | g.32435126G>T | CA473774078 | WT1 | c.235C>A (p.Arg79=) c.220C>A (p.Arg74=) n.414C>A | gnomAD v4 |
11 | g.32435127C>A | CA473774079 | WT1 | c.234G>T (p.Val78=) c.219G>T (p.Val73=) n.413G>T | gnomAD v4 |
11 | g.32435127C>G | CA473774082 | WT1 | c.234G>C (p.Val78=) c.219G>C (p.Val73=) n.413G>C | |
11 | g.32435127C>T | CA473774084 | WT1 | c.234G>A (p.Val78=) c.219G>A (p.Val73=) n.413G>A | gnomAD v4 |
11 | g.32435128A>C | CA379966101 | WT1 | c.233T>G (p.Val78Gly) c.218T>G (p.Val73Gly) n.412T>G | |
11 | g.32435128A>G | CA379966103 | WT1 | c.233T>C (p.Val78Ala) c.218T>C (p.Val73Ala) n.412T>C | gnomAD v4 |
11 | g.32435128A>T | CA379966102 | WT1 | c.233T>A (p.Val78Glu) c.218T>A (p.Val73Glu) n.412T>A | |
11 | g.32435129C>A | CA379966104 | WT1 | c.232G>T (p.Val78Leu) c.217G>T (p.Val73Leu) n.411G>T | ClinVar gnomAD v4 |
11 | g.32435129C= | CA1962327349 | WT1 | c.232G= (p.Val78=) c.217G= (p.Val73=) n.411G= | |
11 | g.32435129C>G | CA379966105 | WT1 | c.232G>C (p.Val78Leu) c.217G>C (p.Val73Leu) n.411G>C | gnomAD v4 |
11 | g.32435129C>T | CA379966106 | WT1 | c.232G>A (p.Val78Met) c.217G>A (p.Val73Met) n.411G>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435130G>A | CA473774085 | WT1 | c.231C>T (p.Asp77=) c.216C>T (p.Asp72=) n.410C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435130G>C | CA379966107 | WT1 | c.231C>G (p.Asp77Glu) c.216C>G (p.Asp72Glu) n.410C>G | |
11 | g.32435130G= | CA1962327350 | WT1 | c.231C= (p.Asp77=) c.216C= (p.Asp72=) n.410C= | |
11 | g.32435130G>T | CA379966108 | WT1 | c.231C>A (p.Asp77Glu) c.216C>A (p.Asp72Glu) n.410C>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.32435131T>A | CA379966111 | WT1 | c.230A>T (p.Asp77Val) c.215A>T (p.Asp72Val) n.409A>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435131T>C | CA379966110 | WT1 | c.230A>G (p.Asp77Gly) c.215A>G (p.Asp72Gly) n.409A>G | gnomAD v4 |
11 | g.32435131T>G | CA379966109 | WT1 | c.230A>C (p.Asp77Ala) c.215A>C (p.Asp72Ala) n.409A>C | |
11 | g.32435132C>A | CA379966112 | WT1 | c.229G>T (p.Asp77Tyr) c.214G>T (p.Asp72Tyr) n.408G>T | gnomAD v4 |
11 | g.32435132C>G | CA379966113 | WT1 | c.229G>C (p.Asp77His) c.214G>C (p.Asp72His) n.408G>C | gnomAD v4 |
11 | g.32435132C>T | CA379966114 | WT1 | c.229G>A (p.Asp77Asn) c.214G>A (p.Asp72Asn) n.408G>A | dbSNP gnomAD v4 |
11 | g.32435133G>A | CA473774094 | WT1 | c.228C>T (p.Ser76=) c.213C>T (p.Ser71=) n.407C>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435133G>C | CA473774098 | WT1 | c.228C>G (p.Ser76=) c.213C>G (p.Ser71=) n.407C>G | gnomAD v4 |
11 | g.32435133G>T | CA473774100 | WT1 | c.228C>A (p.Ser76=) c.213C>A (p.Ser71=) n.407C>A | gnomAD v4 |
11 | g.32435134G>A | CA379966115 | WT1 | c.227C>T (p.Ser76Phe) c.212C>T (p.Ser71Phe) n.406C>T | gnomAD v4 |
11 | g.32435134G>C | CA379966116 | WT1 | c.227C>G (p.Ser76Cys) c.212C>G (p.Ser71Cys) n.406C>G | |
11 | g.32435134G>T | CA379966117 | WT1 | c.227C>A (p.Ser76Tyr) c.212C>A (p.Ser71Tyr) n.406C>A | gnomAD v4 |
11 | g.32435135A>C | CA379966120 | WT1 | c.226T>G (p.Ser76Ala) c.211T>G (p.Ser71Ala) n.405T>G | |
11 | g.32435135A>G | CA379966118 | WT1 | c.226T>C (p.Ser76Pro) c.211T>C (p.Ser71Pro) n.405T>C | dbSNP |
11 | g.32435135A>T | CA379966119 | WT1 | c.226T>A (p.Ser76Thr) c.211T>A (p.Ser71Thr) n.405T>A | dbSNP gnomAD v4 |
11 | g.32435136del | CA2740093682 | WT1 | c.225del (p.Ser76ProfsTer6) c.210del (p.Ser71ProfsTer6) n.404del | ClinVar |
11 | g.32435136G>A | CA473774105 | WT1 | c.225C>T (p.Gly75=) c.210C>T (p.Gly70=) n.404C>T | ClinVar dbSNP |
11 | g.32435136G>C | CA473774106 | WT1 | c.225C>G (p.Gly75=) c.210C>G (p.Gly70=) n.404C>G | ClinVar dbSNP |
11 | g.32435136G= | CA1962327351 | WT1 | c.225C= (p.Gly75=) c.210C= (p.Gly70=) n.404C= | |
11 | g.32435136G>T | CA473774108 | WT1 | c.225C>A (p.Gly75=) c.210C>A (p.Gly70=) n.404C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435137C>A | CA379966121 | WT1 | c.224G>T (p.Gly75Val) c.209G>T (p.Gly70Val) n.403G>T | |
11 | g.32435137C= | CA1962327352 | WT1 | c.224G= (p.Gly75=) c.209G= (p.Gly70=) n.403G= | |
11 | g.32435137C>G | CA379966122 | WT1 | c.224G>C (p.Gly75Ala) c.209G>C (p.Gly70Ala) n.403G>C | COSMIC COSMIC |
11 | g.32435137C>T | CA379966123 | WT1 | c.224G>A (p.Gly75Asp) c.209G>A (p.Gly70Asp) n.403G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435138C>A | CA379966124 | WT1 | c.223G>T (p.Gly75Cys) c.208G>T (p.Gly70Cys) n.402G>T | dbSNP gnomAD v4 |
11 | g.32435138C= | CA1962327353 | WT1 | c.223G= (p.Gly75=) c.208G= (p.Gly70=) n.402G= | |
11 | g.32435138C>G | CA379966125 | WT1 | c.223G>C (p.Gly75Arg) c.208G>C (p.Gly70Arg) n.402G>C |