A56G (p.Ala56Gly) variant of TNFRSF13C (Q96RJ3)
A56G (p.Ala56Gly) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.26 / 1. The record also includes population frequency data and published literature.
A56G (p.Ala56Gly) variant details
- p.Ala56Gly
- gnomAD 22-41926301-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.255
- REVEL 0.06
- MetaLR 0.07
- MetaSVM -1.06
- CADD 16.40
- PolyPhen-2 0.65
- SIFT 0.12
- Population evidence available
- Literature evidence available