G91R (p.Gly91Arg) variant of IL2RB (P14784)
G91R (p.Gly91Arg) in IL2RB (P14784) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of not provided. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data.
G91R (p.Gly91Arg) variant details
- p.Gly91Arg
- rs773733100
- ClinGen CA10216679
- ClinVar RCV003682248
- ExAC rs773733100
- Uncertain significance
- not provided
- Missense
- Variant Prioritization Score for Impact Estimate 0.444
- REVEL 0.33
- CADD 24.10
- PolyPhen-2 0.99
- SIFT 0.00
- ClinVar: Uncertain significance (not provided)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)