Q15H (p.Gln15His) variant of PTPN2 (P17706)
Q15H (p.Gln15His) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.12 / 1. The record also includes population frequency data and structural context.
Q15H (p.Gln15His) variant details
- p.Gln15His
- TOPMed rs1466257016
- gnomAD rs1466257016
- Missense
- Variant Prioritization Score for Impact Estimate 0.121
- REVEL 0.04
- CADD 15.60
- PolyPhen-2 0.00
- SIFT 0.11
- Most common in the East Asian population (allele frequency 2.7e-05)
- Structural context available