L20W (p.Leu20Trp) variant of NFKB2 (Q00653)
L20W (p.Leu20Trp) in NFKB2 (Q00653) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.52 / 1. The record also includes population frequency data and structural context.
L20W (p.Leu20Trp) variant details
- p.Leu20Trp
- TOPMed rs1424290307
- gnomAD rs1424290307
- Missense
- Variant Prioritization Score for Impact Estimate 0.52
- CADD 23.70
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available