G21T (p.Gly21Thr) variant of PYGM (P11217)
G21T (p.Gly21Thr) in PYGM (P11217) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
G21T (p.Gly21Thr) variant details
- p.Gly21Thr
- NCI-TCGA Cosmic COSV5121
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available