R37M (p.Arg37Met) variant of CPS1 (P31327)
R37M (p.Arg37Met) 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.
R37M (p.Arg37Met) variant details
- p.Arg37Met
- NCI-TCGA Cosmic COSV5180
- cosmic curated COSV51808
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available