A18V (p.Ala18Val) variant of HLA-A (P04439)
A18V (p.Ala18Val) in HLA-A (P04439) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.27 / 1. The record also includes population frequency data and structural context.
A18V (p.Ala18Val) variant details
- p.Ala18Val
- TOPMed rs1279237267
- gnomAD rs1279237267
- Missense
- Variant Prioritization Score for Impact Estimate 0.268
- REVEL 0.14
- CADD 8.26
- PolyPhen-2 0.01
- SIFT 0.29
- Most common in the Finnish in Finland (FIN) population (allele frequency 2.7e-05)
- Structural context available