S24T (p.Ser24Thr) variant of FH (P07954)
S24T (p.Ser24Thr) in FH (P07954) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome; not provided. The record also includes published literature and structural context.
S24T (p.Ser24Thr) variant details
- p.Ser24Thr
- rs2527345375
- ClinGen CA345442836
- ClinVar RCV002715741
- ClinVar RCV004067679
- Uncertain significance
- Hereditary cancer-predisposing syndrome; not provided
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome; not provided)
- 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)