| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.83278973A>C | CA16044186 | COQ2 | c.545T>G (p.Met182Arg) c.395T>G (p.Met132Arg) c.86T>G (p.Met29Arg) n.307T>G c.191T>G (p.Met64Arg) n.704T>G n.720T>G n.426T>G | ClinVar dbSNP |
| 4 | g.83278973A= | CA1472713037 | COQ2 | c.545T= (p.Met182=) c.395T= (p.Met132=) c.86T= (p.Met29=) n.307T= c.191T= (p.Met64=) n.704T= n.720T= n.426T= | dbSNP |