| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 7 | g.99762047G>C | CA4369534 | CYP3A4 | c.1247C>G (p.Pro416Arg) n.682C>G c.788C>G (p.Pro263Arg) c.1100C>G (p.Pro367Arg) c.797C>G (p.Pro266Arg) c.1244C>G (p.Pro415Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 7 | g.99762047G>A | CA4369535 | CYP3A4 | c.1247C>T (p.Pro416Leu) n.682C>T c.788C>T (p.Pro263Leu) c.1100C>T (p.Pro367Leu) c.797C>T (p.Pro266Leu) c.1244C>T (p.Pro415Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 7 | g.99762047G= | CA1729177289 | CYP3A4 | c.1247C= (p.Pro416=) n.682C= c.788C= (p.Pro263=) c.1100C= (p.Pro367=) c.797C= (p.Pro266=) c.1244C= (p.Pro415=) | dbSNP |