D110G (p.Asp110Gly) variant of CD8B (P10966)
D110G (p.Asp110Gly) 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.
D110G (p.Asp110Gly) variant details
- p.Asp110Gly
- NCI-TCGA Cosmic COSV5892
- cosmic curated COSV58926
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.81
- MetaSVM 0.79
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available