T27R (p.Thr27Arg) variant of RAD51D (O75771)
T27R (p.Thr27Arg) in RAD51D (O75771) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The record also includes population frequency data and structural context.
T27R (p.Thr27Arg) variant details
- p.Thr27Arg
- 1000Genomes rs139642328
- TOPMed rs139642328
- gnomAD rs139642328
- Uncertain significance
- Missense
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Population evidence available
- Structural context available