| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.32435148C>A | CA064733 | WT1 | c.213G>T (p.Pro71=) c.198G>T (p.Pro66=) n.392G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.32435148C>T | CA473774133 | WT1 | c.213G>A (p.Pro71=) c.198G>A (p.Pro66=) n.392G>A | dbSNP gnomAD v4 |
| 11 | g.32435148C= | CA1962327356 | WT1 | c.213G= (p.Pro71=) c.198G= (p.Pro66=) n.392G= | dbSNP |