A46T (p.Ala46Thr) variant of CPS1 (P31327)
A46T (p.Ala46Thr) in CPS1 (P31327) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
A46T (p.Ala46Thr) variant details
- p.Ala46Thr
- NCI-TCGA Cosmic COSV5181
- cosmic curated COSV51813
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available