A27T (p.Ala27Thr) variant of CD8B (P10966)
A27T (p.Ala27Thr) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
A27T (p.Ala27Thr) variant details
- p.Ala27Thr
- gnomAD rs1293097913
- Missense
- Variant Prioritization Score for Impact Estimate 0.119
- REVEL 0.11
- MetaLR 0.16
- MetaSVM -0.94
- CADD 0.21
- SIFT 0.52
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available