A38T (p.Ala38Thr) variant of IL2RA (P01589)
A38T (p.Ala38Thr) in IL2RA (P01589) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
A38T (p.Ala38Thr) variant details
- p.Ala38Thr
- gnomAD rs1191996028
- Missense
- Variant Prioritization Score for Impact Estimate 0.207
- REVEL 0.08
- CADD 16.60
- PolyPhen-2 0.86
- SIFT 0.14
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available