E58D (p.Glu58Asp) variant of GALT (P07902)
E58D (p.Glu58Asp) in GALT (P07902) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
E58D (p.Glu58Asp) variant details
- p.Glu58Asp
- NCI-TCGA Cosmic COSV6659
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available