| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.43731789G>T | CA145916 | MAOA | c.492G>T (p.Arg164=) c.201G>T (p.Arg67=) n.1023G>T n.447G>T c.786G>T (p.Arg262=) c.891G>T (p.Arg297=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.43731789G= | CA2426669448 | MAOA | c.492G= (p.Arg164=) c.201G= (p.Arg67=) n.1023G= n.447G= c.786G= (p.Arg262=) c.891G= (p.Arg297=) | dbSNP |