S62T (p.Ser62Thr) variant of CD8B (P10966)
S62T (p.Ser62Thr) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and structural context.
S62T (p.Ser62Thr) variant details
- p.Ser62Thr
- TOPMed rs1377748160
- gnomAD rs1377748160
- Missense
- Variant Prioritization Score for Impact Estimate 0.201
- REVEL 0.10
- MetaLR 0.16
- MetaSVM -0.87
- CADD 11.70
- PolyPhen-2 0.30
- SIFT 0.15
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available