Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.43731695G>T | CA163205 | MAOA | c.398G>T (p.Cys133Phe) c.107G>T (p.Cys36Phe) n.929G>T n.353G>T c.692G>T (p.Cys231Phe) c.797G>T (p.Cys266Phe) | ClinVar dbSNP |
X | g.43731695G= | CA2426670049 | MAOA | c.398G= (p.Cys133=) c.107G= (p.Cys36=) n.929G= n.353G= c.692G= (p.Cys231=) c.797G= (p.Cys266=) | dbSNP |