Q41L (p.Gln41Leu) variant of NFE2L2 (Q16236)
Q41L (p.Gln41Leu) in NFE2L2 (Q16236) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of not provided. The record also includes structural context.
Q41L (p.Gln41Leu) variant details
- p.Gln41Leu
- Ensembl rs2105459268
- Uncertain significance
- not provided
- Missense
- ClinVar: Uncertain significance (not provided)
- UniProt: Uncertain significance
- Structural context available