N17S (p.Asn17Ser) variant of TNFRSF9 (Q07011)
N17S (p.Asn17Ser) 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.
N17S (p.Asn17Ser) variant details
- p.Asn17Ser
- ExAC rs778222026
- gnomAD rs778222026
- Missense
- Variant Prioritization Score for Impact Estimate 0.0793
- REVEL 0.05
- CADD 6.99
- PolyPhen-2 0.01
- SIFT 0.27
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available