G56S (p.Gly56Ser) variant of TG (Thyroglobulin)
G56S (p.Gly56Ser) in TG (Thyroglobulin) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The available variant effect predictions contribute to a CATVariant prioritization score of 0.87 / 1. The record also includes population frequency data and structural context.
G56S (p.Gly56Ser) variant details
- p.Gly56Ser
- NCI-TCGA Cosmic COSV9960
- Variant assessed as somatic; moderate impact.
- Missense
- Variant Prioritization Score for Impact Estimate 0.871
- REVEL 0.90
- MetaLR 0.94
- MetaSVM 1.09
- CADD 26.70
- PolyPhen-2 1.00
- SIFT 0.00
- UniProt: Variant assessed as somatic; moderate impact.
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available