G116S (p.Gly116Ser) variant of TNFRSF9 (Q07011)
G116S (p.Gly116Ser) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
G116S (p.Gly116Ser) variant details
- p.Gly116Ser
- cosmic curated COSV66349
- Missense
- Variant Prioritization Score for Impact Estimate 0.431
- REVEL 0.14
- CADD 32.00
- PolyPhen-2 0.66
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 9.2e-07)
- Structural context available