R18P (p.Arg18Pro) variant of BRCA2 (P51587)
R18P (p.Arg18Pro) in BRCA2 (P51587) is a missense change. Clinical records from EBI and UniProt describe it as benign.
R18P (p.Arg18Pro) variant details
- p.Arg18Pro
- 1000Genomes rs80358762
- ExAC rs80358762
- TOPMed rs80358762
- gnomAD rs80358762
- Benign
- Missense
- EBI: Benign
- UniProt: Benign