| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94974919T>C | CA16398893 | CYP2C9 | c.961+2674T>C (n.961+2674T>C) c.820-6264T>C (n.820-6264T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94974919T= | CA1929335398 | CYP2C9 | c.961+2674T= (n.961+2674T=) c.820-6264T= (n.820-6264T=) | dbSNP |