H47Q (p.His47Gln) variant of CPS1 (P31327)
H47Q (p.His47Gln) 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.
H47Q (p.His47Gln) variant details
- p.His47Gln
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available