| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.99760901A>G | CA4369498 | CYP3A4 | c.1427T>C (p.Met476Thr) n.769T>C c.1334T>C (p.Met445Thr) c.875T>C (p.Met292Thr) c.1187T>C (p.Met396Thr) c.884T>C (p.Met295Thr) c.1331T>C (p.Met444Thr) c.1424T>C (p.Met475Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.99760901A= | CA1729176769 | CYP3A4 | c.1427T= (p.Met476=) n.769T= c.1334T= (p.Met445=) c.875T= (p.Met292=) c.1187T= (p.Met396=) c.884T= (p.Met295=) c.1331T= (p.Met444=) c.1424T= (p.Met475=) | dbSNP |
| 7 | g.99760901A>C | CA368368596 | CYP3A4 | c.1427T>G (p.Met476Arg) n.769T>G c.1334T>G (p.Met445Arg) c.875T>G (p.Met292Arg) c.1187T>G (p.Met396Arg) c.884T>G (p.Met295Arg) c.1331T>G (p.Met444Arg) c.1424T>G (p.Met475Arg) | dbSNP gnomAD v3 gnomAD v4 |