C19W (p.Cys19Trp) variant of BRCA2 (P51587)
C19W (p.Cys19Trp) in BRCA2 (P51587) is a missense change. Clinical records from EBI and UniProt describe it as likely benign.
C19W (p.Cys19Trp) variant details
- p.Cys19Trp
- Ensembl rs878853592
- Likely benign
- Missense
- EBI: Likely benign
- UniProt: Likely benign