P11T (p.Pro11Thr) variant of IL2RB (P14784)
P11T (p.Pro11Thr) in IL2RB (P14784) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not specified; not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data.
P11T (p.Pro11Thr) variant details
- p.Pro11Thr
- rs796822195
- ClinGen CA324056640
- ClinVar RCV002035831
- ClinVar RCV004046161
- Uncertain significance
- not specified; not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.254
- REVEL 0.38
- CADD 2.79
- PolyPhen-2 0.09
- SIFT 0.24
- ClinVar: Uncertain significance (not specified; not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Latino/Admixed American population (allele frequency 0.0002)