V6A (p.Val6Ala) variant of RAD51D (O75771)
V6A (p.Val6Ala) in RAD51D (O75771) is a missense change. Clinical records from ClinVar and UniProt describe it as likely benign in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
V6A (p.Val6Ala) variant details
- p.Val6Ala
- Ensembl rs2142480900
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (Hereditary cancer-predisposing syndrome)
- UniProt: Likely benign
- Structural context available