Q59H (p.Gln59His) variant of TG (Thyroglobulin)
Q59H (p.Gln59His) in TG (Thyroglobulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.47 / 1. The record also includes population frequency data and structural context.
Q59H (p.Gln59His) variant details
- p.Gln59His
- gnomAD rs1239281001
- Missense
- Variant Prioritization Score for Impact Estimate 0.471
- REVEL 0.27
- MetaLR 0.29
- MetaSVM -0.66
- CADD 32.00
- PolyPhen-2 0.88
- SIFT 0.01
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available