R18S (p.Arg18Ser) variant of BRCA2 (P51587)
R18S (p.Arg18Ser) in BRCA2 (P51587) is a missense change. Clinical records from EBI and UniProt describe it as likely benign. The record also includes variant effect predictions.
R18S (p.Arg18Ser) variant details
- p.Arg18Ser
- TOPMed rs786201560
- Likely benign
- Missense
- SIFT 0.00
- EBI: Likely benign
- UniProt: Likely benign