D38H (p.Asp38His) variant of NFE2L2 (Q16236)
D38H (p.Asp38His) 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.
D38H (p.Asp38His) variant details
- p.Asp38His
- NCI-TCGA Cosmic COSV6796
- cosmic curated COSV67960
- Ensembl rs2105459323
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available