T79P (p.Thr79Pro) variant of CD8B (P10966)
T79P (p.Thr79Pro) 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 0.07 / 1. The record also includes population frequency data and structural context.
T79P (p.Thr79Pro) variant details
- p.Thr79Pro
- NCI-TCGA Cosmic COSV5892
- cosmic curated COSV58925
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0749
- REVEL 0.03
- MetaLR 0.15
- MetaSVM -0.96
- CADD 0.13
- PolyPhen-2 0.01
- SIFT 0.17
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available