Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32435084_32435112del | CA2695213680 | WT1 | c.251_279del (p.Leu84ArgfsTer?) c.236_264del (p.Leu79ArgfsTer?) n.430_458del | |
11 | g.32435110A>C | CA379966066 | WT1 | c.251T>G (p.Leu84Arg) c.236T>G (p.Leu79Arg) n.430T>G | gnomAD v4 |
11 | g.32435110A>G | CA379966067 | WT1 | c.251T>C (p.Leu84Pro) c.236T>C (p.Leu79Pro) n.430T>C | gnomAD v4 |
11 | g.32435110A>T | CA379966068 | WT1 | c.251T>A (p.Leu84Gln) c.236T>A (p.Leu79Gln) n.430T>A | |
11 | g.32435111G>A | CA064783 | WT1 | c.250C>T (p.Leu84=) c.235C>T (p.Leu79=) n.429C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435111G>C | CA379966069 | WT1 | c.250C>G (p.Leu84Val) c.235C>G (p.Leu79Val) n.429C>G | |
11 | g.32435111G= | CA1962327340 | WT1 | c.250C= (p.Leu84=) c.235C= (p.Leu79=) n.429C= | |
11 | g.32435111G>T | CA379966070 | WT1 | c.250C>A (p.Leu84Met) c.235C>A (p.Leu79Met) n.429C>A | gnomAD v4 |
11 | g.32435112C>A | CA473774039 | WT1 | c.249G>T (p.Ala83=) c.234G>T (p.Ala78=) n.428G>T | ClinVar gnomAD v4 |
11 | g.32435112C= | CA1962327341 | WT1 | c.249G= (p.Ala83=) c.234G= (p.Ala78=) n.428G= | |
11 | g.32435112C>G | CA473774040 | WT1 | c.249G>C (p.Ala83=) c.234G>C (p.Ala78=) n.428G>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435112C>T | CA473774041 | WT1 | c.249G>A (p.Ala83=) c.234G>A (p.Ala78=) n.428G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435113G>A | CA379966071 | WT1 | c.248C>T (p.Ala83Val) c.233C>T (p.Ala78Val) n.427C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
11 | g.32435113G>C | CA379966073 | WT1 | c.248C>G (p.Ala83Gly) c.233C>G (p.Ala78Gly) n.427C>G | |
11 | g.32435113G= | CA1962327342 | WT1 | c.248C= (p.Ala83=) c.233C= (p.Ala78=) n.427C= | |
11 | g.32435113G>T | CA379966072 | WT1 | c.248C>A (p.Ala83Glu) c.233C>A (p.Ala78Glu) n.427C>A | gnomAD v4 |
11 | g.32435113_32435114delinsAG | CA2740093681 | WT1 | c.247_248delinsCT (p.Ala83Leu) c.232_233delinsCT (p.Ala78Leu) n.426_427delinsCT | ClinVar |
11 | g.32435114C>A | CA10634698 | WT1 | c.247G>T (p.Ala83Ser) c.232G>T (p.Ala78Ser) n.426G>T | ClinVar dbSNP gnomAD v4 |
11 | g.32435114C= | CA1962327343 | WT1 | c.247G= (p.Ala83=) c.232G= (p.Ala78=) n.426G= | |
11 | g.32435114C>G | CA379966074 | WT1 | c.247G>C (p.Ala83Pro) c.232G>C (p.Ala78Pro) n.426G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435114C>T | CA379966075 | WT1 | c.247G>A (p.Ala83Thr) c.232G>A (p.Ala78Thr) n.426G>A | ClinVar gnomAD v4 |
11 | g.32435115G>A | CA473774047 | WT1 | c.246C>T (p.Asn82=) c.231C>T (p.Asn77=) n.425C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435115G>C | CA379966076 | WT1 | c.246C>G (p.Asn82Lys) c.231C>G (p.Asn77Lys) n.425C>G | ClinVar |
11 | g.32435115G= | CA1962327344 | WT1 | c.246C= (p.Asn82=) c.231C= (p.Asn77=) n.425C= | |
11 | g.32435115G>T | CA379966077 | WT1 | c.246C>A (p.Asn82Lys) c.231C>A (p.Asn77Lys) n.425C>A | ClinVar gnomAD v4 |
11 | g.32435116T>A | CA379966078 | WT1 | c.245A>T (p.Asn82Ile) c.230A>T (p.Asn77Ile) n.424A>T | |
11 | g.32435116T>C | CA379966079 | WT1 | c.245A>G (p.Asn82Ser) c.230A>G (p.Asn77Ser) n.424A>G | |
11 | g.32435116T>G | CA379966080 | WT1 | c.245A>C (p.Asn82Thr) c.230A>C (p.Asn77Thr) n.424A>C | dbSNP |
11 | g.32435117T>A | CA379966081 | WT1 | c.244A>T (p.Asn82Tyr) c.229A>T (p.Asn77Tyr) n.423A>T | |
11 | g.32435117T>C | CA379966082 | WT1 | c.244A>G (p.Asn82Asp) c.229A>G (p.Asn77Asp) n.423A>G | ClinVar gnomAD v4 |
11 | g.32435117T>G | CA379966083 | WT1 | c.244A>C (p.Asn82His) c.229A>C (p.Asn77His) n.423A>C | |
11 | g.32435118C>A | CA473774054 | WT1 | c.243G>T (p.Leu81=) c.228G>T (p.Leu76=) n.422G>T | gnomAD v4 |
11 | g.32435118C>G | CA473774055 | WT1 | c.243G>C (p.Leu81=) c.228G>C (p.Leu76=) n.422G>C | |
11 | g.32435118C>T | CA473774056 | WT1 | c.243G>A (p.Leu81=) c.228G>A (p.Leu76=) n.422G>A | gnomAD v4 |
11 | g.32435119A>C | CA379966086 | WT1 | c.242T>G (p.Leu81Arg) c.227T>G (p.Leu76Arg) n.421T>G | ClinVar dbSNP |
11 | g.32435119A>G | CA379966085 | WT1 | c.242T>C (p.Leu81Pro) c.227T>C (p.Leu76Pro) n.421T>C | dbSNP gnomAD v4 |
11 | g.32435119A>T | CA379966084 | WT1 | c.242T>A (p.Leu81Gln) c.227T>A (p.Leu76Gln) n.421T>A | gnomAD v4 |
11 | g.32435120G>A | CA473774057 | WT1 | c.241C>T (p.Leu81=) c.226C>T (p.Leu76=) n.420C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.32435120G>C | CA064777 | WT1 | c.241C>G (p.Leu81Val) c.226C>G (p.Leu76Val) n.420C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.32435120G= | CA1962327345 | WT1 | c.241C= (p.Leu81=) c.226C= (p.Leu76=) n.420C= | |
11 | g.32435120G>T | CA379966087 | WT1 | c.241C>A (p.Leu81Met) c.226C>A (p.Leu76Met) n.420C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32435121G>A | CA473774063 | WT1 | c.240C>T (p.Asp80=) c.225C>T (p.Asp75=) n.419C>T | gnomAD v4 |
11 | g.32435121G>C | CA379966088 | WT1 | c.240C>G (p.Asp80Glu) c.225C>G (p.Asp75Glu) n.419C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32435121G>T | CA379966089 | WT1 | c.240C>A (p.Asp80Glu) c.225C>A (p.Asp75Glu) n.419C>A | gnomAD v4 |
11 | g.32435122T>A | CA379966090 | WT1 | c.239A>T (p.Asp80Val) c.224A>T (p.Asp75Val) n.418A>T | |
11 | g.32435122T>C | CA379966091 | WT1 | c.239A>G (p.Asp80Gly) c.224A>G (p.Asp75Gly) n.418A>G | gnomAD v4 |
11 | g.32435122T>G | CA379966092 | WT1 | c.239A>C (p.Asp80Ala) c.224A>C (p.Asp75Ala) n.418A>C | |
11 | g.32435123C>A | CA379966093 | WT1 | c.238G>T (p.Asp80Tyr) c.223G>T (p.Asp75Tyr) n.417G>T | gnomAD v4 |
11 | g.32435123C>G | CA379966094 | WT1 | c.238G>C (p.Asp80His) c.223G>C (p.Asp75His) n.417G>C | ClinVar |
11 | g.32435123C>T | CA379966095 | WT1 | c.238G>A (p.Asp80Asn) c.223G>A (p.Asp75Asn) n.417G>A |