G31V (p.Gly31Val) variant of NFE2L2 (Q16236)
G31V (p.Gly31Val) in NFE2L2 (Q16236) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in IMDDHH.
G31V (p.Gly31Val) variant details
- p.Gly31Val
- NCI-TCGA Cosmic COSV6795
- NCI-TCGA Cosmic COSV6796
- cosmic curated COSV67961
- Variant assessed as somatic; moderate impact.
- in IMDDHH
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in IMDDHH)