E16Q (p.Glu16Gln) variant of GALT (P07902)
E16Q (p.Glu16Gln) 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.
E16Q (p.Glu16Gln) variant details
- p.Glu16Gln
- NCI-TCGA Cosmic COSV1011
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available