R26G (p.Arg26Gly) variant of CYP2D6 (Cytochrome P450 2D6)
R26G (p.Arg26Gly) in CYP2D6 (Cytochrome P450 2D6) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance in the context of in allele CYP2D6*21 and allele CYP2D6*46. The record also includes structural context.
R26G (p.Arg26Gly) variant details
- p.Arg26Gly
- ESP rs145868402
- ExAC rs145868402
- TOPMed rs145868402
- gnomAD rs145868402
- Uncertain significance
- in allele CYP2D6*21 and allele CYP2D6*46
- Missense
- EBI: Variant of uncertain significance (in allele CYP2D6*21 and allele CYP2D6*46)
- UniProt: Uncertain significance (in allele CYP2D6*21 and allele CYP2D6*46)
- Structural context available