G69C (p.Gly69Cys) variant of C5 (Complement C5)
G69C (p.Gly69Cys) in C5 (Complement C5) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G69C (p.Gly69Cys) variant details
- p.Gly69Cys
- NCI-TCGA Cosmic COSV5632
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available