R18G (p.Arg18Gly) variant of BRCA2 (P51587)
R18G (p.Arg18Gly) in BRCA2 (P51587) is a missense change. Clinical records from EBI and UniProt describe it as likely benign.
R18G (p.Arg18Gly) variant details
- p.Arg18Gly
- TOPMed rs786201560
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign