V110F (p.Val110Phe) variant of PTPN2 (P17706)
V110F (p.Val110Phe) 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.
V110F (p.Val110Phe) variant details
- p.Val110Phe
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available