F11L (p.Phe11Leu) variant of CTNNA1 (Catenin alpha-1)
F11L (p.Phe11Leu) 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 record also includes structural context.
F11L (p.Phe11Leu) variant details
- p.Phe11Leu
- rs2532170351
- ClinGen CA361477089
- ClinVar RCV003541898
- 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