| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 19 | g.40847202T>C | CA14689507 | CYP2A6 | c.655-151A>G (n.655-151A>G) n.506-151A>G c.*467-151A>G (n.*467-151A>G) c.120-44789T>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 19 | g.40847202T= | CA2336178276 | CYP2A6 | c.655-151A= (n.655-151A=) n.506-151A= c.*467-151A= (n.*467-151A=) c.120-44789T= | dbSNP |