N49D (p.Asn49Asp) variant of CD8A (P01732)
N49D (p.Asn49Asp) in CD8A (P01732) 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.
N49D (p.Asn49Asp) variant details
- p.Asn49Asp
- NCI-TCGA Cosmic COSV5215
- cosmic curated COSV52157
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.22
- MetaSVM -0.86
- SIFT 0.31
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available