| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 22 | g.19963748G>A | CA127287 | COMT | c.472G>A (p.Val158Met) c.322G>A (p.Val108Met) n.255G>A n.272G>A n.320G>A n.282G>A c.50G>A n.210G>A c.586G>A (p.Val196Met) c.883G>A (p.Val295Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 22 | g.19963748G= | CA1139772229 | COMT | c.472G= (p.Val158=) c.322G= (p.Val108=) n.255G= n.272G= n.320G= n.282G= c.50G= n.210G= c.586G= (p.Val196=) c.883G= (p.Val295=) | dbSNP |