S143F (p.Ser143Phe) variant of C3 (Complement C3)
S143F (p.Ser143Phe) 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.
S143F (p.Ser143Phe) variant details
- p.Ser143Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available