N41T (p.Asn41Thr) variant of CTNNA1 (Catenin alpha-1)
N41T (p.Asn41Thr) in CTNNA1 (Catenin alpha-1) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
N41T (p.Asn41Thr) variant details
- p.Asn41Thr
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available