E78D (p.Glu78Asp) variant of PTPN2 (P17706)
E78D (p.Glu78Asp) in PTPN2 (P17706) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E78D (p.Glu78Asp) variant details
- p.Glu78Asp
- NCI-TCGA Cosmic COSV1005
- cosmic curated COSV10051
- ExAC rs764654245
- TOPMed rs764654245
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available