G9G (p.Gly9Gly) variant of SLC2A4 (P14672)
G9G (p.Gly9Gly) in SLC2A4 (P14672) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.62 / 1. The record also includes population frequency data, published literature, and structural context.
G9G (p.Gly9Gly) variant details
- p.Gly9Gly
- rs762128658
- gnomAD 17-7281961-C-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.623
- CADD 18.40
- Most common in the Non-Finnish European population (allele frequency 1.8e-06)
- Structural context available
- Literature evidence available