| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.32434307G>C | CA1962326852 | WT1 | c.661+393C>G (n.661+393C>G) c.646+393C>G (n.646+393C>G) n.840+393C>G | dbSNP |
| 11 | g.32434307G>T | CA13458874 | WT1 | c.661+393C>A (n.661+393C>A) c.646+393C>A (n.646+393C>A) n.840+393C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |