T91A (p.Thr91Ala) variant of IL2RA (P01589)
T91A (p.Thr91Ala) in IL2RA (P01589) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.04 / 1. The record also includes population frequency data and structural context.
T91A (p.Thr91Ala) variant details
- p.Thr91Ala
- rs753853235
- NCI-TCGA Cosmic COSV9990
- cosmic curated COSV99906
- ExAC rs753853235
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.0373
- REVEL 0.01
- CADD 0.09
- PolyPhen-2 0.01
- SIFT 0.62
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the REMAINING population (allele frequency 3.3e-05)
- Structural context available