Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.41009358A>G | CA230624 | CYP2B6 | c.785A>G (p.Lys262Arg) c.809A>G c.257-2940A>G (n.257-2940A>G) c.485-2940A>G (n.485-2940A>G) c.194A>G (p.Lys65Arg) c.365-2940A>G (n.365-2940A>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.41009358A>T | CA405980728 | CYP2B6 | c.785A>T (p.Lys262Met) c.809A>T c.257-2940A>T (n.257-2940A>T) c.485-2940A>T (n.485-2940A>T) c.194A>T (p.Lys65Met) c.365-2940A>T (n.365-2940A>T) | dbSNP gnomAD v4 |