Q27R (p.Gln27Arg) variant of SDHA (P31040)
Q27R (p.Gln27Arg) in SDHA (P31040) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely benign in the context of Hereditary cancer-predisposing syndrome. The record also includes published literature and structural context.
Q27R (p.Gln27Arg) variant details
- p.Gln27Arg
- rs2477280077
- ClinGen CA359008095
- ClinVar RCV004516522
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (Hereditary cancer-predisposing syndrome)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- 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)