E74D (p.Glu74Asp) variant of TNFRSF13B (O14836)
E74D (p.Glu74Asp) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data.
E74D (p.Glu74Asp) variant details
- p.Glu74Asp
- TOPMed rs1167588510
- gnomAD rs1167588510
- Missense
- Variant Prioritization Score for Impact Estimate 0.568
- REVEL 0.42
- CADD 18.80
- Most common in the HGDP:MAKRANI population (allele frequency 0.023)