Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.32435016G>C | CA473773808 | WT1 | c.345C>G (p.Pro115=) c.330C>G (p.Pro110=) n.524C>G | dbSNP |
11 | g.32435016G>A | CA017474 | WT1 | c.345C>T (p.Pro115=) c.330C>T (p.Pro110=) n.524C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.32435016G= | CA1962327276 | WT1 | c.345C= (p.Pro115=) c.330C= (p.Pro110=) n.524C= | dbSNP |