F39I (p.Phe39Ile) variant of NFE2L2 (Q16236)
F39I (p.Phe39Ile) in NFE2L2 (Q16236) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.25 / 1. The record also includes population frequency data and structural context.
F39I (p.Phe39Ile) variant details
- p.Phe39Ile
- Ensembl rs2105459306
- Missense
- Variant Prioritization Score for Impact Estimate 0.249
- REVEL 0.09
- CADD 22.20
- PolyPhen-2 0.10
- SIFT 0.10
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available