E35D (p.Glu35Asp) variant of NFE2L2 (Q16236)
E35D (p.Glu35Asp) 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.
E35D (p.Glu35Asp) variant details
- p.Glu35Asp
- Ensembl rs2105459368
- NCI-TCGA Cosmic COSV6796
- cosmic curated COSV67961
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available