A56V (p.Ala56Val) variant of TNFRSF13C (Q96RJ3)
A56V (p.Ala56Val) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and published literature.
A56V (p.Ala56Val) variant details
- p.Ala56Val
- gnomAD 22-41926301-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.21
- REVEL 0.02
- MetaLR 0.04
- MetaSVM -1.06
- CADD 9.90
- PolyPhen-2 0.01
- SIFT 0.08
- Population evidence available
- Literature evidence available