Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32434752G>A | CA065105 | WT1 | c.609C>T (p.Asn203=) c.594C>T (p.Asn198=) n.788C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32434752G>C | CA16613601 | WT1 | c.609C>G (p.Asn203Lys) c.594C>G (p.Asn198Lys) n.788C>G | ClinVar dbSNP gnomAD v4 |
11 | g.32434752G>T | CA379964538 | WT1 | c.609C>A (p.Asn203Lys) c.594C>A (p.Asn198Lys) n.788C>A | ClinVar dbSNP gnomAD v4 |
11 | g.32434752G= | CA1962327112 | WT1 | c.609C= (p.Asn203=) c.594C= (p.Asn198=) n.788C= | dbSNP |