G13A (p.Gly13Ala) variant of SLC2A4 (P14672)
G13A (p.Gly13Ala) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.34 / 1. The record also includes population frequency data and structural context.
G13A (p.Gly13Ala) variant details
- p.Gly13Ala
- ExAC rs755868694
- TOPMed rs755868694
- gnomAD rs755868694
- Missense
- Variant Prioritization Score for Impact Estimate 0.34
- REVEL 0.11
- MetaLR 0.26
- MetaSVM -0.90
- CADD 17.40
- PolyPhen-2 0.00
- SIFT 0.21
- Most common in the Non-Finnish European population (allele frequency 2.9e-05)
- Structural context available