N40S (p.Asn40Ser) variant of TNFRSF9 (Q07011)
N40S (p.Asn40Ser) 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.
N40S (p.Asn40Ser) variant details
- p.Asn40Ser
- ESP rs149613995
- TOPMed rs149613995
- gnomAD rs149613995
- Missense
- Variant Prioritization Score for Impact Estimate 0.127
- REVEL 0.17
- CADD 0.01
- PolyPhen-2 0.01
- SIFT 0.49
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available