| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.99770202T>C | CA4369795 | CYP3A4 | c.352A>G (p.Ile118Val) c.58-1695A>G (n.58-1695A>G) c.205A>G (p.Ile69Val) c.72-1700A>G (n.72-1700A>G) c.391A>G (p.Ile131Val) n.249A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.99770202T>A | CA163153897 | CYP3A4 | c.352A>T (p.Ile118Phe) c.58-1695A>T (n.58-1695A>T) c.205A>T (p.Ile69Phe) c.72-1700A>T (n.72-1700A>T) c.391A>T (p.Ile131Phe) n.249A>T | dbSNP |
| 7 | g.99770202T= | CA1729182585 | CYP3A4 | c.352A= (p.Ile118=) c.58-1695A= (n.58-1695A=) c.205A= (p.Ile69=) c.72-1700A= (n.72-1700A=) c.391A= (p.Ile131=) n.249A= | dbSNP |