| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94943463G>C | CA1929293007 | CYP2C9 | c.481+1122G>C (n.481+1122G>C) n.634+1122G>C n.252+1122G>C | dbSNP |
| 10 | g.94943463G>A | CA15675153 | CYP2C9 | c.481+1122G>A (n.481+1122G>A) n.634+1122G>A n.252+1122G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |