A67G (p.Ala67Gly) variant of TNFRSF13C (Q96RJ3)
A67G (p.Ala67Gly) in TNFRSF13C (Q96RJ3) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.20 / 1. The record also includes population frequency data and published literature.
A67G (p.Ala67Gly) variant details
- p.Ala67Gly
- gnomAD 22-41926268-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.203
- REVEL 0.03
- MetaLR 0.04
- MetaSVM -1.02
- CADD 7.96
- PolyPhen-2 0.00
- SIFT 0.20
- Population evidence available
- Literature evidence available