T42A (p.Thr42Ala) variant of CTNNA1 (Catenin alpha-1)
T42A (p.Thr42Ala) 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.
T42A (p.Thr42Ala) variant details
- p.Thr42Ala
- Ensembl rs1755322861
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available