K51E (p.Lys51Glu) variant of CTNNA1 (Catenin alpha-1)
K51E (p.Lys51Glu) in CTNNA1 (Catenin alpha-1) 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.
K51E (p.Lys51Glu) variant details
- p.Lys51Glu
- rs2532178172
- ClinGen CA361477357
- ClinVar RCV002392387
- 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)