| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94762755T>A | CA211666331 | CYP2C19 | c.50T>A (p.Leu17His) c.932-12303T>A (n.932-12303T>A) | dbSNP |
| 10 | g.94762755T>C | CA211666343 | CYP2C19 | c.50T>C (p.Leu17Pro) c.932-12303T>C (n.932-12303T>C) | dbSNP gnomAD v4 |