P11S (p.Pro11Ser) variant of IL2RB (P14784)
P11S (p.Pro11Ser) in IL2RB (P14784) is a missense change. Clinical records from EBI and UniProt describe it as uncertain significance. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data.
P11S (p.Pro11Ser) variant details
- p.Pro11Ser
- TOPMed rs796822195
- gnomAD rs796822195
- Uncertain significance
- Missense
- Variant Prioritization Score for Impact Estimate 0.25
- REVEL 0.38
- CADD 0.52
- PolyPhen-2 0.00
- SIFT 0.91
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the African/African-American population (allele frequency 3.2e-05)