G24S (p.Gly24Ser) variant of TNFRSF13B (O14836)
G24S (p.Gly24Ser) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.44 / 1. The record also includes population frequency data and structural context.
G24S (p.Gly24Ser) variant details
- p.Gly24Ser
- ExAC rs774505373
- TOPMed rs774505373
- gnomAD rs774505373
- Missense
- Variant Prioritization Score for Impact Estimate 0.442
- REVEL 0.49
- CADD 22.30
- PolyPhen-2 0.49
- SIFT 0.08
- Most common in the 1KG:CLM population (allele frequency 0.0053)
- Structural context available