M36T (p.Met36Thr) variant of CD8B (P10966)
M36T (p.Met36Thr) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
M36T (p.Met36Thr) variant details
- p.Met36Thr
- TOPMed rs953935080
- gnomAD rs953935080
- Missense
- Variant Prioritization Score for Impact Estimate 0.0825
- REVEL 0.04
- MetaLR 0.10
- MetaSVM -1.03
- CADD 0.00
- PolyPhen-2 0.01
- SIFT 1.00
- Most common in the East Asian population (allele frequency 0.00019)
- Structural context available