| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.41004158G>T | CA230626 | CYP2B6 | c.329G>T (p.Gly110Val) c.231G>T c.101G>T (p.Gly34Val) n.231G>T c.209G>T (p.Gly70Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.41004158G>C | CA405973212 | CYP2B6 | c.329G>C (p.Gly110Ala) c.231G>C c.101G>C (p.Gly34Ala) n.231G>C c.209G>C (p.Gly70Ala) | dbSNP gnomAD v2 gnomAD v4 |