A56P (p.Ala56Pro) variant of TNFRSF13C (Q96RJ3)
A56P (p.Ala56Pro) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.32 / 1. The record also includes population frequency data.
A56P (p.Ala56Pro) variant details
- p.Ala56Pro
- TOPMed rs1453310836
- gnomAD rs1453310836
- Missense
- Variant Prioritization Score for Impact Estimate 0.317
- REVEL 0.15
- CADD 22.80
- PolyPhen-2 0.78
- SIFT 0.01
- Most common in the REMAINING population (allele frequency 0.00048)