G13D (p.Gly13Asp) variant of PTPN11 (Q06124)
G13D (p.Gly13Asp) in PTPN11 (Q06124) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G13D (p.Gly13Asp) variant details
- p.Gly13Asp
- NCI-TCGA Cosmic COSV6101
- cosmic curated COSV61011
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available