F97I (p.Phe97Ile) variant of PTPN2 (P17706)
F97I (p.Phe97Ile) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data, published literature, and structural context.
F97I (p.Phe97Ile) variant details
- p.Phe97Ile
- rs1188209060
- gnomAD 18-12793573-A-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.396
- CADD 15.70
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available
- Literature evidence available