Y83H (p.Tyr83His) variant of PTPN2 (P17706)
Y83H (p.Tyr83His) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.77 / 1. The record also includes population frequency data and structural context.
Y83H (p.Tyr83His) variant details
- p.Tyr83His
- TOPMed rs943757284
- gnomAD rs943757284
- Missense
- Variant Prioritization Score for Impact Estimate 0.767
- REVEL 0.85
- CADD 28.40
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available