C86F (p.Cys86Phe) variant of IL2RB (P14784)
C86F (p.Cys86Phe) in IL2RB (P14784) 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 0.56 / 1. The record also includes population frequency data.
C86F (p.Cys86Phe) variant details
- p.Cys86Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.564
- REVEL 0.45
- CADD 22.30
- PolyPhen-2 0.17
- SIFT 0.04
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)