S133R (p.Ser133Arg) variant of CD8B (P10966)
S133R (p.Ser133Arg) in CD8B (P10966) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data and structural context.
S133R (p.Ser133Arg) variant details
- p.Ser133Arg
- NCI-TCGA Cosmic COSV5892
- cosmic curated COSV58925
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.226
- REVEL 0.10
- MetaLR 0.20
- MetaSVM -0.89
- CADD 19.80
- PolyPhen-2 0.08
- SIFT 0.25
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available