M38V (p.Met38Val) variant of CD8B (P10966)
M38V (p.Met38Val) 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.
M38V (p.Met38Val) variant details
- p.Met38Val
- cosmic curated COSV58926
- Missense
- Variant Prioritization Score for Impact Estimate 0.076
- REVEL 0.03
- MetaLR 0.11
- MetaSVM -1.02
- CADD 0.04
- PolyPhen-2 0.01
- SIFT 0.34
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available