Y38N (p.Tyr38Asn) variant of IL7R (P16871)
Y38N (p.Tyr38Asn) in IL7R (P16871) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, published literature, and structural context.
Y38N (p.Tyr38Asn) variant details
- p.Tyr38Asn
- gnomAD 5-35860881-T-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.34
- CADD 22.90
- PolyPhen-2 0.80
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available