R17G (p.Arg17Gly) variant of PTPN2 (P17706)
R17G (p.Arg17Gly) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data and structural context.
R17G (p.Arg17Gly) variant details
- p.Arg17Gly
- gnomAD rs1438599484
- Missense
- Variant Prioritization Score for Impact Estimate 0.207
- REVEL 0.08
- CADD 18.80
- PolyPhen-2 0.00
- SIFT 0.51
- Population evidence available
- Structural context available