G116V (p.Gly116Val) variant of TNFRSF9 (Q07011)
G116V (p.Gly116Val) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
G116V (p.Gly116Val) variant details
- p.Gly116Val
- gnomAD 1-7937756-C-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.15
- CADD 33.00
- PolyPhen-2 0.74
- SIFT 0.04
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available
- Literature evidence available