D38V (p.Asp38Val) variant of NFE2L2 (Q16236)
D38V (p.Asp38Val) in NFE2L2 (Q16236) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D38V (p.Asp38Val) variant details
- p.Asp38Val
- NCI-TCGA TCGA novel
- Ensembl rs2105459314
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available