R49I (p.Arg49Ile) variant of PTPN2 (P17706)
R49I (p.Arg49Ile) 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.
R49I (p.Arg49Ile) variant details
- p.Arg49Ile
- NCI-TCGA Cosmic COSV5899
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available