| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94988878C>A | CA5617392 | CYP2C9 | c.1323C>A (p.Ala441=) c.*332C>A (n.*332C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.94988878C>T | CA5617391 | CYP2C9 | c.1323C>T (p.Ala441=) c.*332C>T (n.*332C>T) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94988878C= | CA1929349550 | CYP2C9 | c.1323C= (p.Ala441=) c.*332C= (n.*332C=) | dbSNP |