E26K (p.Glu26Lys) variant of XRCC2 (DNA repair protein XRCC2)
E26K (p.Glu26Lys) 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.
E26K (p.Glu26Lys) variant details
- p.Glu26Lys
- Ensembl rs2116999619
- 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