N78T (p.Asn78Thr) variant of IL2RA (P01589)
N78T (p.Asn78Thr) in IL2RA (P01589) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
N78T (p.Asn78Thr) variant details
- p.Asn78Thr
- TOPMed rs1191171742
- gnomAD rs1191171742
- Missense
- Variant Prioritization Score for Impact Estimate 0.159
- REVEL 0.09
- CADD 14.90
- PolyPhen-2 0.27
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available