| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.94989020C>T | CA5617424 | CYP2C9 | c.1465C>T (p.Pro489Ser) c.*474C>T (n.*474C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.94989020C= | CA1929349835 | CYP2C9 | c.1465C= (p.Pro489=) c.*474C= (n.*474C=) | dbSNP |
| 10 | g.94989020C>G | CA377677202 | CYP2C9 | c.1465C>G (p.Pro489Ala) c.*474C>G (n.*474C>G) | dbSNP gnomAD v4 |