A46V (p.Ala46Val) variant of GALT (P07902)
A46V (p.Ala46Val) 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.
A46V (p.Ala46Val) variant details
- p.Ala46Val
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available