F39L (p.Phe39Leu) variant of PTPN2 (P17706)
F39L (p.Phe39Leu) in PTPN2 (P17706) 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.
F39L (p.Phe39Leu) variant details
- p.Phe39Leu
- TOPMed rs1432117963
- gnomAD rs1432117963
- Missense
- Variant Prioritization Score for Impact Estimate 0.183
- REVEL 0.08
- CADD 16.00
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available