L26I (p.Leu26Ile) variant of SLC2A4 (P14672)
L26I (p.Leu26Ile) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.46 / 1. The record also includes population frequency data and structural context.
L26I (p.Leu26Ile) variant details
- p.Leu26Ile
- TOPMed rs2072418111
- gnomAD rs2072418111
- Missense
- Variant Prioritization Score for Impact Estimate 0.46
- REVEL 0.27
- CADD 21.00
- PolyPhen-2 0.30
- SIFT 0.04
- Most common in the Latino/Admixed American population (allele frequency 0.00013)
- Structural context available