S33Y (p.Ser33Tyr) variant of MET (P08581)
S33Y (p.Ser33Tyr) in MET (P08581) 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.
S33Y (p.Ser33Tyr) variant details
- p.Ser33Tyr
- rs2485505223
- ClinGen CA368968335
- ClinVar RCV002387448
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (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)