L14F (p.Leu14Phe) variant of RAD51C (O43502)
L14F (p.Leu14Phe) in RAD51C (O43502) 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.
L14F (p.Leu14Phe) variant details
- p.Leu14Phe
- Ensembl rs1598448777
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available