| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.99762206G>T | CA4369563 | CYP3A4 | c.1088C>A (p.Thr363Lys) n.523C>A c.629C>A (p.Thr210Lys) c.941C>A (p.Thr314Lys) c.638C>A (p.Thr213Lys) c.1085C>A (p.Thr362Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.99762206G>A | CA4369562 | CYP3A4 | c.1088C>T (p.Thr363Met) n.523C>T c.629C>T (p.Thr210Met) c.941C>T (p.Thr314Met) c.638C>T (p.Thr213Met) c.1085C>T (p.Thr362Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |