S29T (p.Ser29Thr) variant of RAD51C (O43502)
S29T (p.Ser29Thr) in RAD51C (O43502) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
S29T (p.Ser29Thr) variant details
- p.Ser29Thr
- Ensembl rs2143677521
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available