G9V (p.Gly9Val) variant of SLC2A4 (P14672)
G9V (p.Gly9Val) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.40 / 1. The record also includes population frequency data and structural context.
G9V (p.Gly9Val) variant details
- p.Gly9Val
- ExAC rs777053264
- gnomAD rs777053264
- Missense
- Variant Prioritization Score for Impact Estimate 0.403
- REVEL 0.26
- MetaLR 0.36
- MetaSVM -0.91
- CADD 24.10
- PolyPhen-2 0.01
- SIFT 0.02
- Most common in the Non-Finnish European population (allele frequency 4.8e-06)
- Structural context available