I99L (p.Ile99Leu) variant of SLC2A4 (P14672)
I99L (p.Ile99Leu) in SLC2A4 (P14672) 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.
I99L (p.Ile99Leu) variant details
- p.Ile99Leu
- ExAC rs754025923
- gnomAD rs754025923
- Missense
- Variant Prioritization Score for Impact Estimate 0.148
- REVEL 0.12
- CADD 16.80
- PolyPhen-2 0.01
- SIFT 0.13
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available