Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.35577445T>A | CA119068 | PEX12 | c.273A>T (p.Arg91Ser) | ClinVar dbSNP |
17 | g.35577445T= | CA2257561983 | PEX12 | c.273A= (p.Arg91=) | dbSNP |
17 | g.35577445T>C | CA499903576 | PEX12 | c.273A>G (p.Arg91=) | ClinVar dbSNP |