V33A (p.Val33Ala) variant of CTNNA1 (Catenin alpha-1)
V33A (p.Val33Ala) in CTNNA1 (Catenin alpha-1) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Hereditary cancer-predisposing syndrome. The record also includes structural context.
V33A (p.Val33Ala) variant details
- p.Val33Ala
- NCI-TCGA Cosmic COSV1002
- cosmic curated COSV10024
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available