P89R (p.Pro89Arg) variant of C5 (Complement C5)
P89R (p.Pro89Arg) 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 variant effect predictions and structural context.
P89R (p.Pro89Arg) variant details
- p.Pro89Arg
- NCI-TCGA Cosmic COSV5633
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.17
- MetaSVM -0.85
- SIFT 0.01
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available