R39G (p.Arg39Gly) variant of SLC30A8 (Q8IWU4)
R39G (p.Arg39Gly) in SLC30A8 (Q8IWU4) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.13 / 1. The record also includes population frequency data and structural context.
R39G (p.Arg39Gly) variant details
- p.Arg39Gly
- TOPMed rs1448460756
- gnomAD rs1448460756
- Missense
- Variant Prioritization Score for Impact Estimate 0.131
- REVEL 0.06
- CADD 5.80
- PolyPhen-2 0.00
- SIFT 0.88
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available