V118L (p.Val118Leu) variant of IL2RB (P14784)
V118L (p.Val118Leu) in IL2RB (P14784) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data.
V118L (p.Val118Leu) variant details
- p.Val118Leu
- ExAC rs767844744
- gnomAD rs767844744
- Missense
- Variant Prioritization Score for Impact Estimate 0.195
- REVEL 0.29
- CADD 0.00
- PolyPhen-2 0.00
- SIFT 0.72
- Most common in the Non-Finnish European population (allele frequency 9e-07)