A79S (p.Ala79Ser) variant of C3 (Complement C3)
A79S (p.Ala79Ser) 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.
A79S (p.Ala79Ser) variant details
- p.Ala79Ser
- NCI-TCGA Cosmic COSV9983
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available