E69D (p.Glu69Asp) variant of TNFRSF13C (Q96RJ3)
E69D (p.Glu69Asp) 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.
E69D (p.Glu69Asp) variant details
- p.Glu69Asp
- gnomAD 22-41926261-C-G
- Missense
- Variant Prioritization Score for Impact Estimate 0.261
- REVEL 0.02
- MetaLR 0.04
- MetaSVM -1.03
- CADD 9.41
- PolyPhen-2 0.00
- SIFT 0.35
- Most common in the 1KG:MSL population (allele frequency 0.013)
- Literature evidence available