S112F (p.Ser112Phe) variant of C5 (Complement C5)
S112F (p.Ser112Phe) in C5 (Complement C5) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact. The record also includes structural context.
S112F (p.Ser112Phe) variant details
- p.Ser112Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.
- Structural context available