G9A (p.Gly9Ala) variant of SLC2A4 (P14672)
G9A (p.Gly9Ala) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.38 / 1. The record also includes population frequency data and structural context.
G9A (p.Gly9Ala) variant details
- p.Gly9Ala
- ExAC rs777053264
- gnomAD rs777053264
- Missense
- Variant Prioritization Score for Impact Estimate 0.383
- REVEL 0.22
- MetaLR 0.34
- MetaSVM -0.94
- CADD 23.60
- PolyPhen-2 0.00
- SIFT 0.06
- Most common in the Ashkenazi Jewish population (allele frequency 4.5e-05)
- Structural context available