C5S (p.Cys5Ser) variant of TNFRSF9 (Q07011)
C5S (p.Cys5Ser) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.08 / 1. The record also includes population frequency data and structural context.
C5S (p.Cys5Ser) variant details
- p.Cys5Ser
- TOPMed rs1364641614
- Missense
- Variant Prioritization Score for Impact Estimate 0.0807
- REVEL 0.10
- CADD 0.04
- PolyPhen-2 0.03
- SIFT 0.39
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available