F18S (p.Phe18Ser) variant of TNFRSF9 (Q07011)
F18S (p.Phe18Ser) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.18 / 1. The record also includes population frequency data and structural context.
F18S (p.Phe18Ser) variant details
- p.Phe18Ser
- TOPMed rs1639877131
- Missense
- Variant Prioritization Score for Impact Estimate 0.176
- REVEL 0.11
- CADD 13.70
- PolyPhen-2 0.03
- SIFT 0.26
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available