D66G (p.Asp66Gly) variant of TG (Thyroglobulin)
D66G (p.Asp66Gly) in TG (Thyroglobulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data and structural context.
D66G (p.Asp66Gly) variant details
- p.Asp66Gly
- TOPMed rs1186537684
- gnomAD rs1186537684
- Missense
- Variant Prioritization Score for Impact Estimate 0.153
- REVEL 0.09
- MetaLR 0.10
- MetaSVM -1.03
- CADD 9.82
- PolyPhen-2 0.01
- SIFT 0.57
- Most common in the Non-Finnish European population (allele frequency 1.5e-05)
- Structural context available