Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.40846048G>C | CA9452878 | CYP2A6 | c.881C>G (p.Thr294Ser) n.732C>G c.*693C>G (n.*693C>G) c.119+44633G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.40846048G>A | CA405963177 | CYP2A6 | c.881C>T (p.Thr294Ile) n.732C>T c.*693C>T (n.*693C>T) c.119+44633G>A | dbSNP gnomAD v4 |