A91D (p.Ala91Asp) variant of CD8B (P10966)
A91D (p.Ala91Asp) 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.
A91D (p.Ala91Asp) variant details
- p.Ala91Asp
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10051
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.09
- MetaSVM -1.01
- SIFT 0.02
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available