D131N (p.Asp131Asn) variant of PTPN2 (P17706)
D131N (p.Asp131Asn) in PTPN2 (P17706) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.36 / 1. The record also includes population frequency data and structural context.
D131N (p.Asp131Asn) variant details
- p.Asp131Asn
- Ensembl rs2042435956
- Missense
- Variant Prioritization Score for Impact Estimate 0.36
- REVEL 0.28
- CADD 22.60
- PolyPhen-2 0.01
- SIFT 0.07
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available