G3D (p.Gly3Asp) variant of TNFRSF13B (O14836)
G3D (p.Gly3Asp) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data.
G3D (p.Gly3Asp) variant details
- p.Gly3Asp
- 1000Genomes rs201599964
- ExAC rs201599964
- TOPMed rs201599964
- gnomAD rs201599964
- Missense
- Variant Prioritization Score for Impact Estimate 0.332
- REVEL 0.24
- CADD 16.80
- PolyPhen-2 0.02
- SIFT 0.28
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)