T86I (p.Thr86Ile) variant of SLC2A2 (P11168)
T86I (p.Thr86Ile) in SLC2A2 (P11168) 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.
T86I (p.Thr86Ile) variant details
- p.Thr86Ile
- ExAC rs766762468
- TOPMed rs766762468
- gnomAD rs766762468
- Missense
- Variant Prioritization Score for Impact Estimate 0.153
- REVEL 0.20
- CADD 3.35
- PolyPhen-2 0.04
- SIFT 0.26
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available