R74G (p.Arg74Gly) variant of NFKB2 (Q00653)
R74G (p.Arg74Gly) in NFKB2 (Q00653) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
R74G (p.Arg74Gly) variant details
- p.Arg74Gly
- NCI-TCGA Cosmic COSV9950
- cosmic curated COSV99502
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.467
- CADD 25.40
- PolyPhen-2 0.52
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available