N19S (p.Asn19Ser) variant of CD8B (P10966)
N19S (p.Asn19Ser) 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.
N19S (p.Asn19Ser) variant details
- p.Asn19Ser
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10051
- Variant assessed as somatic; moderate impact.
- Missense
- MetaLR 0.02
- MetaSVM -0.98
- SIFT 1.00
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available