H56Y (p.His56Tyr) variant of TNFRSF13B (O14836)
H56Y (p.His56Tyr) in TNFRSF13B (O14836) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data.
H56Y (p.His56Tyr) variant details
- p.His56Tyr
- gnomAD rs2087595725
- Missense
- Variant Prioritization Score for Impact Estimate 0.242
- REVEL 0.23
- CADD 3.41
- Most common in the Non-Finnish European population (allele frequency 8.8e-05)