G116D (p.Gly116Asp) variant of TNFRSF9 (Q07011)
G116D (p.Gly116Asp) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.41 / 1. The record also includes population frequency data and structural context.
G116D (p.Gly116Asp) variant details
- p.Gly116Asp
- ExAC rs752004630
- gnomAD rs752004630
- Missense
- Variant Prioritization Score for Impact Estimate 0.41
- REVEL 0.17
- CADD 33.00
- PolyPhen-2 0.98
- SIFT 0.00
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available