M1? variant of NFE2L2 (Q16236)
M1? in NFE2L2 (Q16236) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; high impact.
M1? variant details
- NCI-TCGA TCGA novel
- Variant assessed as somatic; high impact.
- Missense
- UniProt: Variant assessed as somatic; high impact.