Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94965778A>C | CA10576168 | CYP2C9 | c.820-6326A>C (n.820-6326A>C) c.820-15405A>C (n.820-15405A>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94965778A>T | CA670172524 | CYP2C9 | c.820-6326A>T (n.820-6326A>T) c.820-15405A>T (n.820-15405A>T) | dbSNP |