S99G (p.Ser99Gly) variant of NFKB2 (Q00653)
S99G (p.Ser99Gly) in NFKB2 (Q00653) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and published literature.
S99G (p.Ser99Gly) variant details
- p.Ser99Gly
- gnomAD 10-102396955-A-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.515
- MetaLR 0.13
- MetaSVM -1.01
- CADD 24.40
- PolyPhen-2 0.81
- SIFT 0.51
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Literature evidence available