H96Y (p.His96Tyr) variant of TNFRSF13B (O14836)
H96Y (p.His96Tyr) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.75 / 1. The record also includes population frequency data.
H96Y (p.His96Tyr) variant details
- p.His96Tyr
- TOPMed rs1306985017
- gnomAD rs1306985017
- Missense
- Variant Prioritization Score for Impact Estimate 0.747
- REVEL 0.73
- CADD 24.70
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the HGDP:FRENCH population (allele frequency 0.019)