C19C (p.Cys19Cys) variant of BRCA2 (P51587)
C19C (p.Cys19Cys) in BRCA2 (P51587) is a synonymous change. The record also includes variant effect predictions, population frequency data, and published literature.
C19C (p.Cys19Cys) variant details
- p.Cys19Cys
- rs878853592
- gnomAD 13-32316517-C-T
- Synonymous
- CADD 15.80
- Most common in the Non-Finnish European population (allele frequency 9.9e-07)
- Literature evidence available