T27A (p.Thr27Ala) variant of RAD51D (O75771)
T27A (p.Thr27Ala) in RAD51D (O75771) 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.
T27A (p.Thr27Ala) variant details
- p.Thr27Ala
- Ensembl rs2142480115
- 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