| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94852738C>T | CA126961 | CYP2C19 | c.1297C>T (p.Arg433Trp) n.2208C>T c.2060C>T (n.2060C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.94852738C= | CA1929279868 | CYP2C19 | c.1297C= (p.Arg433=) n.2208C= c.2060C= (n.2060C=) | dbSNP |
| 10 | g.94852738C>A | CA470833087 | CYP2C19 | c.1297C>A (p.Arg433=) n.2208C>A c.2060C>A (n.2060C>A) | dbSNP gnomAD v4 |