D18G (p.Asp18Gly) variant of NFKB1 (P19838)
D18G (p.Asp18Gly) in NFKB1 (P19838) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
D18G (p.Asp18Gly) variant details
- p.Asp18Gly
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available