I47N (p.Ile47Asn) variant of HLA-B (P01889)
I47N (p.Ile47Asn) in HLA-B (P01889) 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.
I47N (p.Ile47Asn) variant details
- p.Ile47Asn
- Ensembl rs281864588
- Missense
- Variant Prioritization Score for Impact Estimate 0.268
- REVEL 0.12
- CADD 23.80
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available