Q26P (p.Gln26Pro) variant of NFE2L2 (Q16236)
Q26P (p.Gln26Pro) in NFE2L2 (Q16236) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact.
Q26P (p.Gln26Pro) variant details
- p.Gln26Pro
- NCI-TCGA Cosmic COSV1012
- NCI-TCGA Cosmic COSV6796
- cosmic curated COSV67961
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.