S70G (p.Ser70Gly) variant of TNFRSF13B (O14836)
S70G (p.Ser70Gly) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.31 / 1. The record also includes population frequency data.
S70G (p.Ser70Gly) variant details
- p.Ser70Gly
- gnomAD rs1390711436
- Missense
- Variant Prioritization Score for Impact Estimate 0.312
- REVEL 0.29
- CADD 16.10
- PolyPhen-2 0.17
- SIFT 0.08
- Most common in the Finnish in Finland (FIN) population (allele frequency 0.00091)