Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94982060A>C | CA670183439 | CYP2C9 | c.1149+690A>C (n.1149+690A>C) c.*158+690A>C (n.*158+690A>C) | dbSNP |
10 | g.94982060A>G | CA211730505 | CYP2C9 | c.1149+690A>G (n.1149+690A>G) c.*158+690A>G (n.*158+690A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |