S29C (p.Ser29Cys) variant of RAD51C (O43502)
S29C (p.Ser29Cys) in RAD51C (O43502) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
S29C (p.Ser29Cys) variant details
- p.Ser29Cys
- gnomAD rs876659683
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available