C94G (p.Cys94Gly) variant of TNFRSF9 (Q07011)
C94G (p.Cys94Gly) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
C94G (p.Cys94Gly) variant details
- p.Cys94Gly
- TOPMed rs1639851859
- Missense
- Variant Prioritization Score for Impact Estimate 0.458
- REVEL 0.33
- CADD 24.60
- PolyPhen-2 0.96
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available