D85G (p.Asp85Gly) variant of TNFRSF13B (O14836)
D85G (p.Asp85Gly) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data.
D85G (p.Asp85Gly) variant details
- p.Asp85Gly
- TOPMed rs1170456533
- gnomAD rs1170456533
- Missense
- Variant Prioritization Score for Impact Estimate 0.228
- REVEL 0.23
- CADD 11.50
- Most common in the REMAINING population (allele frequency 0.00048)