G116C (p.Gly116Cys) variant of TNFRSF9 (Q07011)
G116C (p.Gly116Cys) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.48 / 1. The record also includes population frequency data and structural context.
G116C (p.Gly116Cys) variant details
- p.Gly116Cys
- TOPMed rs1639850356
- Missense
- Variant Prioritization Score for Impact Estimate 0.477
- REVEL 0.21
- CADD 33.00
- PolyPhen-2 0.74
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available