A76S (p.Ala76Ser) variant of CD8B (P10966)
A76S (p.Ala76Ser) in CD8B (P10966) 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.
A76S (p.Ala76Ser) variant details
- p.Ala76Ser
- NCI-TCGA Cosmic COSV5892
- cosmic curated COSV58926
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.08
- MetaSVM -1.02
- SIFT 0.44
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available