F37S (p.Phe37Ser) variant of NFE2L2 (Q16236)
F37S (p.Phe37Ser) 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.
F37S (p.Phe37Ser) variant details
- p.Phe37Ser
- NCI-TCGA Cosmic COSV6796
- cosmic curated COSV67962
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available