| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.32434815G>A | CA473571428 | WT1 | c.546C>T (p.Tyr182=) c.531C>T (p.Tyr177=) n.725C>T | ClinVar dbSNP gnomAD v4 |
| 11 | g.32434815G>T | CA016351 | WT1 | c.546C>A (p.Tyr182Ter) c.531C>A (p.Tyr177Ter) n.725C>A | ClinVar dbSNP |
| 11 | g.32434815G= | CA1962327154 | WT1 | c.546C= (p.Tyr182=) c.531C= (p.Tyr177=) n.725C= | dbSNP |
| 11 | g.32434815G>C | CA379964707 | WT1 | c.546C>G (p.Tyr182Ter) c.531C>G (p.Tyr177Ter) n.725C>G | dbSNP |