| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94974582G>T | CA211724774 | CYP2C9 | c.961+2337G>T (n.961+2337G>T) c.820-6601G>T (n.820-6601G>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94974582G>A | CA1929335111 | CYP2C9 | c.961+2337G>A (n.961+2337G>A) c.820-6601G>A (n.820-6601G>A) | dbSNP |