A79G (p.Ala79Gly) variant of PTPN2 (P17706)
A79G (p.Ala79Gly) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.57 / 1. The record also includes population frequency data and structural context.
A79G (p.Ala79Gly) variant details
- p.Ala79Gly
- TOPMed rs953123344
- Missense
- Variant Prioritization Score for Impact Estimate 0.566
- REVEL 0.54
- CADD 25.80
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available