A24T (p.Ala24Thr) variant of CTNNA1 (Catenin alpha-1)
A24T (p.Ala24Thr) 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.
A24T (p.Ala24Thr) variant details
- p.Ala24Thr
- gnomAD rs1472535447
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- UniProt: Uncertain significance
- Structural context available