D55G (p.Asp55Gly) variant of PTPN2 (P17706)
D55G (p.Asp55Gly) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.83 / 1. The record also includes population frequency data and structural context.
D55G (p.Asp55Gly) variant details
- p.Asp55Gly
- Ensembl rs913379921
- Missense
- Variant Prioritization Score for Impact Estimate 0.828
- REVEL 0.95
- CADD 28.10
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the Non-Finnish European population (allele frequency 9.1e-07)
- Structural context available