R18R (p.Arg18Arg) variant of BRCA2 (P51587)
R18R (p.Arg18Arg) in BRCA2 (P51587) is a synonymous change. The record also includes variant effect predictions, population frequency data, and published literature.
R18R (p.Arg18Arg) variant details
- p.Arg18Arg
- rs879915769
- gnomAD 13-32316514-C-G
- Synonymous
- CADD 8.32
- Most common in the Non-Finnish European population (allele frequency 9.3e-07)
- Literature evidence available