G54R (p.Gly54Arg) variant of NFKB1 (P19838)
G54R (p.Gly54Arg) in NFKB1 (P19838) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Inborn genetic diseases. The record also includes structural context.
G54R (p.Gly54Arg) variant details
- p.Gly54Arg
- NCI-TCGA TCGA novel
- Uncertain significance
- Inborn genetic diseases
- Missense
- ClinVar: Uncertain significance (Inborn genetic diseases)
- UniProt: Uncertain significance
- Structural context available