G45A (p.Gly45Ala) variant of TNFRSF13B (O14836)
G45A (p.Gly45Ala) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.17 / 1. The record also includes population frequency data.
G45A (p.Gly45Ala) variant details
- p.Gly45Ala
- ExAC rs777041889
- gnomAD rs777041889
- Missense
- Variant Prioritization Score for Impact Estimate 0.17
- REVEL 0.24
- CADD 1.64
- PolyPhen-2 0.01
- SIFT 0.55
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00019)