G94R (p.Gly94Arg) variant of TNFRSF13B (O14836)
G94R (p.Gly94Arg) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.53 / 1. The record also includes population frequency data.
G94R (p.Gly94Arg) variant details
- p.Gly94Arg
- 1000Genomes rs200612226
- TOPMed rs200612226
- gnomAD rs200612226
- Missense
- Variant Prioritization Score for Impact Estimate 0.527
- REVEL 0.51
- CADD 25.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the 1KG:MSL population (allele frequency 0.013)