G29S (p.Gly29Ser) variant of FH (P07954)
G29S (p.Gly29Ser) in FH (P07954) 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.
G29S (p.Gly29Ser) variant details
- p.Gly29Ser
- rs2527345089
- ClinGen CA345442760
- ClinVar RCV004520615
- Likely benign
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Likely benign (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)