F122L (p.Phe122Leu) variant of TNFRSF9 (Q07011)
F122L (p.Phe122Leu) in TNFRSF9 (Q07011) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.09 / 1. The record also includes population frequency data and structural context.
F122L (p.Phe122Leu) variant details
- p.Phe122Leu
- TOPMed rs1639841494
- gnomAD rs1639841494
- Missense
- Variant Prioritization Score for Impact Estimate 0.0856
- REVEL 0.03
- CADD 12.20
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available