G38R (p.Gly38Arg) variant of GNAT1 (P11488)
G38R (p.Gly38Arg) in GNAT1 (P11488) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact in the context of in CSNBAD3. The record also includes structural context.
G38R (p.Gly38Arg) variant details
- p.Gly38Arg
- NCI-TCGA TCGA novel
- Variant assessed as somatic; moderate impact.
- in CSNBAD3
- Missense
- UniProt: Variant assessed as somatic; moderate impact. (in CSNBAD3)
- Structural context available