V44G (p.Val44Gly) variant of GALT (P07902)
V44G (p.Val44Gly) 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.
V44G (p.Val44Gly) variant details
- p.Val44Gly
- NCI-TCGA Cosmic COSV1011
- Ensembl rs1587237018
- Variant assessed as somatic; moderate impact.
- in GALAC1
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in GALAC1)
- Structural context available