C78W (p.Cys78Trp) variant of TNFRSF9 (Q07011)
C78W (p.Cys78Trp) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
C78W (p.Cys78Trp) variant details
- p.Cys78Trp
- gnomAD rs1180566950
- Missense
- Variant Prioritization Score for Impact Estimate 0.567
- REVEL 0.70
- CADD 23.20
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 1.2e-05)
- Structural context available