G55D (p.Gly55Asp) variant of GALT (P07902)
G55D (p.Gly55Asp) in GALT (P07902) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in GALAC1. The record also includes structural context.
G55D (p.Gly55Asp) variant details
- p.Gly55Asp
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- in GALAC1
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in GALAC1)
- Structural context available