R19Q (p.Arg19Gln) variant of SLC2A4 (P14672)
R19Q (p.Arg19Gln) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.11 / 1. The record also includes population frequency data and structural context.
R19Q (p.Arg19Gln) variant details
- p.Arg19Gln
- TOPMed rs1368055195
- gnomAD rs1368055195
- Missense
- Variant Prioritization Score for Impact Estimate 0.109
- REVEL 0.04
- CADD 16.10
- PolyPhen-2 0.00
- SIFT 1.00
- Most common in the African/African-American population (allele frequency 2.4e-05)
- Structural context available