Y38F (p.Tyr38Phe) variant of IL7R (P16871)
Y38F (p.Tyr38Phe) in IL7R (P16871) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
Y38F (p.Tyr38Phe) variant details
- p.Tyr38Phe
- ExAC rs751358220
- gnomAD rs751358220
- Missense
- Variant Prioritization Score for Impact Estimate 0.139
- REVEL 0.04
- CADD 13.80
- PolyPhen-2 0.04
- SIFT 0.44
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available