S13F (p.Ser13Phe) variant of TG (Thyroglobulin)
S13F (p.Ser13Phe) in TG (Thyroglobulin) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.24 / 1. The record also includes population frequency data and structural context.
S13F (p.Ser13Phe) variant details
- p.Ser13Phe
- ExAC rs753032118
- gnomAD rs753032118
- Missense
- Variant Prioritization Score for Impact Estimate 0.243
- REVEL 0.26
- MetaLR 0.15
- MetaSVM -0.95
- CADD 2.64
- PolyPhen-2 0.25
- SIFT 0.78
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available