G9R (p.Gly9Arg) variant of SLC2A4 (P14672)
G9R (p.Gly9Arg) 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, published literature, and structural context.
G9R (p.Gly9Arg) variant details
- p.Gly9Arg
- gnomAD 17-7281959-G-C
- Missense
- Variant Prioritization Score for Impact Estimate 0.398
- REVEL 0.29
- MetaLR 0.29
- MetaSVM -0.75
- CADD 24.80
- PolyPhen-2 0.10
- SIFT 0.11
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available