G2R (p.Gly2Arg) variant of RAD51D (O75771)
G2R (p.Gly2Arg) in RAD51D (O75771) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes structural context.
G2R (p.Gly2Arg) variant details
- p.Gly2Arg
- ESP rs372082751
- ExAC rs372082751
- TOPMed rs372082751
- gnomAD rs372082751
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available