I138M (p.Ile138Met) variant of C3 (Complement C3)
I138M (p.Ile138Met) in C3 (Complement C3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
I138M (p.Ile138Met) variant details
- p.Ile138Met
- NCI-TCGA Cosmic COSV5557
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available