R5G (p.Arg5Gly) variant of RAD51D (O75771)
R5G (p.Arg5Gly) 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 published literature and structural context.
R5G (p.Arg5Gly) variant details
- p.Arg5Gly
- rs876660779
- ClinGen CA399092577
- ClinVar RCV003380063
- TOPMed rs876660779
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available
- Cited in: A practice guideline from the American College of Medical Genetics and Genomics and the National Society of Genetic… (PMID 25394175)