G39G (p.Gly39Gly) variant of SLC2A4 (P14672)
G39G (p.Gly39Gly) in SLC2A4 (P14672) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.29 / 1. The record also includes population frequency data, published literature, and structural context.
G39G (p.Gly39Gly) variant details
- p.Gly39Gly
- rs1448302639
- gnomAD 17-7283328-G-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.29
- CADD 9.73
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available
- Literature evidence available