Q37H (p.Gln37His) variant of TG (Thyroglobulin)
Q37H (p.Gln37His) in TG (Thyroglobulin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes structural context.
Q37H (p.Gln37His) variant details
- p.Gln37His
- NCI-TCGA Cosmic COSV5507
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available