S112L (p.Ser112Leu) variant of C5 (Complement C5)
S112L (p.Ser112Leu) 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.
S112L (p.Ser112Leu) variant details
- p.Ser112Leu
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available