P15L (p.Pro15Leu) variant of CTNNA1 (Catenin alpha-1)
P15L (p.Pro15Leu) 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; not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.61 / 1. The record also includes published literature and structural context.
P15L (p.Pro15Leu) variant details
- p.Pro15Leu
- rs988942117
- ClinGen CA361477117
- cosmic curated COSV10884
- ClinVar RCV001303666
- Uncertain significance
- Hereditary cancer-predisposing syndrome; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.613
- AlphaMissense 0.94
- MetaLR 0.61
- MetaSVM 0.25
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 0.58
- 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)