F37L (p.Phe37Leu) variant of NFE2L2 (Q16236)
F37L (p.Phe37Leu) in NFE2L2 (Q16236) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
F37L (p.Phe37Leu) variant details
- p.Phe37Leu
- Ensembl rs2105459336
- Missense
- Variant Prioritization Score for Impact Estimate 0.0847
- CADD 0.61
- Most common in the South Asian population (allele frequency 3.3e-05)
- Structural context available