E111G (p.Glu111Gly) variant of TNFRSF9 (Q07011)
E111G (p.Glu111Gly) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.30 / 1. The record also includes population frequency data and structural context.
E111G (p.Glu111Gly) variant details
- p.Glu111Gly
- ExAC rs780116617
- TOPMed rs780116617
- gnomAD rs780116617
- Missense
- Variant Prioritization Score for Impact Estimate 0.302
- REVEL 0.33
- CADD 17.60
- PolyPhen-2 0.42
- SIFT 0.06
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available