G3V (p.Gly3Val) variant of TNFRSF13B (O14836)
G3V (p.Gly3Val) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data.
G3V (p.Gly3Val) variant details
- p.Gly3Val
- 1000Genomes rs201599964
- ExAC rs201599964
- TOPMed rs201599964
- gnomAD rs201599964
- Missense
- Variant Prioritization Score for Impact Estimate 0.356
- REVEL 0.25
- CADD 21.80
- Most common in the 1KG:CLM population (allele frequency 0.0053)