| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.19962712C>T | CA10104478 | COMT | c.186C>T (p.His62=) c.36C>T (p.His12=) n.34C>T n.382C>T c.300C>T (p.His100=) c.597C>T (p.His199=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.19962712C= | CA1139772227 | COMT | c.186C= (p.His62=) c.36C= (p.His12=) n.34C= n.382C= c.300C= (p.His100=) c.597C= (p.His199=) | dbSNP |