G66A (p.Gly66Ala) variant of PYGM (P11217)
G66A (p.Gly66Ala) 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.
G66A (p.Gly66Ala) variant details
- p.Gly66Ala
- NCI-TCGA Cosmic COSV5122
- cosmic curated COSV51225
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available