P26P (p.Pro26Pro) variant of BRCA2 (P51587)
P26P (p.Pro26Pro) in BRCA2 (P51587) is a synonymous change. The record also includes variant effect predictions, population frequency data, and published literature.
P26P (p.Pro26Pro) variant details
- p.Pro26Pro
- rs772146565
- gnomAD 13-32319087-A-G
- Synonymous
- CADD 7.42
- Most common in the Ashkenazi Jewish population (allele frequency 7.7e-05)
- Literature evidence available