A33S (p.Ala33Ser) variant of XRCC2 (DNA repair protein XRCC2)
A33S (p.Ala33Ser) in XRCC2 (DNA repair protein XRCC2) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
A33S (p.Ala33Ser) variant details
- p.Ala33Ser
- ExAC rs774296079
- TOPMed rs774296079
- gnomAD rs774296079
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available