P92Q (p.Pro92Gln) variant of NFKB1 (P19838)
P92Q (p.Pro92Gln) in NFKB1 (P19838) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.28 / 1. The record also includes population frequency data, published literature, and structural context.
P92Q (p.Pro92Gln) variant details
- p.Pro92Gln
- gnomAD 4-102567006-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.275
- REVEL 0.14
- CADD 22.20
- PolyPhen-2 0.06
- SIFT 0.30
- Most common in the African/African-American population (allele frequency 3e-05)
- Structural context available
- Literature evidence available