H96Y (p.His96Tyr) variant of PTPN2 (P17706)
H96Y (p.His96Tyr) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.23 / 1. The record also includes population frequency data, published literature, and structural context.
H96Y (p.His96Tyr) variant details
- p.His96Tyr
- gnomAD 18-12793567-G-A
- Missense
- Variant Prioritization Score for Impact Estimate 0.232
- CADD 10.50
- Most common in the Non-Finnish European population (allele frequency 1.3e-06)
- Structural context available
- Literature evidence available