S100N (p.Ser100Asn) variant of TNFRSF9 (Q07011)
S100N (p.Ser100Asn) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
S100N (p.Ser100Asn) variant details
- p.Ser100Asn
- ExAC rs772618014
- gnomAD rs772618014
- Missense
- Variant Prioritization Score for Impact Estimate 0.134
- REVEL 0.19
- CADD 0.14
- PolyPhen-2 0.01
- SIFT 0.17
- Most common in the East Asian population (allele frequency 0.00018)
- Structural context available