N41K (p.Asn41Lys) variant of CTNNA1 (Catenin alpha-1)
N41K (p.Asn41Lys) 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. The record also includes structural context.
N41K (p.Asn41Lys) variant details
- p.Asn41Lys
- gnomAD rs1369656663
- Uncertain significance
- Hereditary cancer-predisposing syndrome
- Missense
- ClinVar: Uncertain significance (Hereditary cancer-predisposing syndrome)
- EBI: Likely benign
- UniProt: Likely benign
- Structural context available