Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.94762706A>G | CA250055 | CYP2C19 | c.1A>G (p.Met1Val) c.932-12352A>G (n.932-12352A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.94762706A>T | CA5616274 | CYP2C19 | c.1A>T (p.Met1Leu) c.932-12352A>T (n.932-12352A>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |