M36V (p.Met36Val) variant of CD8B (P10966)
M36V (p.Met36Val) in CD8B (P10966) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
M36V (p.Met36Val) variant details
- p.Met36Val
- ExAC rs763949278
- gnomAD rs763949278
- Missense
- Variant Prioritization Score for Impact Estimate 0.0929
- REVEL 0.06
- MetaLR 0.18
- MetaSVM -0.97
- CADD 0.05
- PolyPhen-2 0.02
- SIFT 0.31
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available