C138G (p.Cys138Gly) variant of GYS2 (P54840)
C138G (p.Cys138Gly) in GYS2 (P54840) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
C138G (p.Cys138Gly) variant details
- p.Cys138Gly
- NCI-TCGA Cosmic COSV5392
- NCI-TCGA Cosmic COSV9967
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available