G78E (p.Gly78Glu) variant of CD8B (P10966)
G78E (p.Gly78Glu) in CD8B (P10966) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G78E (p.Gly78Glu) variant details
- p.Gly78Glu
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10051
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available