A156T (p.Ala156Thr) variant of IL2RG (P31785)
A156T (p.Ala156Thr) in IL2RG (P31785) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes population frequency data, published literature, and structural context.
A156T (p.Ala156Thr) variant details
- p.Ala156Thr
- gnomAD X-71110284-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.678
- REVEL 0.81
- CADD 24.50
- PolyPhen-2 0.99
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 1.2e-06)
- Structural context available
- Literature evidence available