E41G (p.Glu41Gly) variant of PTPN2 (P17706)
E41G (p.Glu41Gly) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
E41G (p.Glu41Gly) variant details
- p.Glu41Gly
- Ensembl rs2043702565
- Missense
- Variant Prioritization Score for Impact Estimate 0.376
- REVEL 0.17
- CADD 27.90
- PolyPhen-2 0.59
- SIFT 0.01
- Most common in the Non-Finnish European population (allele frequency 2.7e-06)
- Structural context available