N7S (p.Asn7Ser) variant of TNFRSF9 (Q07011)
N7S (p.Asn7Ser) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.06 / 1. The record also includes population frequency data and structural context.
N7S (p.Asn7Ser) variant details
- p.Asn7Ser
- ExAC rs764389515
- TOPMed rs764389515
- gnomAD rs764389515
- Missense
- Variant Prioritization Score for Impact Estimate 0.0612
- REVEL 0.06
- CADD 0.83
- PolyPhen-2 0.02
- SIFT 0.32
- Most common in the Ashkenazi Jewish population (allele frequency 0.00029)
- Structural context available