T59K (p.Thr59Lys) variant of SLC2A4 (P14672)
T59K (p.Thr59Lys) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
T59K (p.Thr59Lys) variant details
- p.Thr59Lys
- ExAC rs754117775
- gnomAD rs754117775
- Missense
- Variant Prioritization Score for Impact Estimate 0.626
- REVEL 0.52
- CADD 24.70
- PolyPhen-2 0.81
- SIFT 0.01
- Most common in the Finnish in Finland (FIN) population (allele frequency 1.9e-05)
- Structural context available