T59M (p.Thr59Met) variant of SLC2A4 (P14672)
T59M (p.Thr59Met) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data and structural context.
T59M (p.Thr59Met) variant details
- p.Thr59Met
- ExAC rs754117775
- gnomAD rs754117775
- Missense
- Variant Prioritization Score for Impact Estimate 0.616
- REVEL 0.52
- CADD 23.40
- PolyPhen-2 0.39
- SIFT 0.00
- Most common in the South Asian population (allele frequency 2.3e-05)
- Structural context available