R102A (p.Arg102Ala) variant of C3 (Complement C3)
R102A (p.Arg102Ala) in C3 (Complement C3) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact in the context of in allele C3F. The record also includes structural context.
R102A (p.Arg102Ala) variant details
- p.Arg102Ala
- NCI-TCGA Cosmic COSV9983
- Variant assessed as somatic; high impact.
- in allele C3F
- Missense
- UniProt: Variant assessed as somatic; high impact. (in allele C3F)
- Structural context available