Q17R (p.Gln17Arg) variant of SLC2A4 (P14672)
Q17R (p.Gln17Arg) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.14 / 1. The record also includes population frequency data and structural context.
Q17R (p.Gln17Arg) variant details
- p.Gln17Arg
- ExAC rs778865343
- TOPMed rs778865343
- gnomAD rs778865343
- Missense
- Variant Prioritization Score for Impact Estimate 0.136
- REVEL 0.10
- MetaLR 0.21
- MetaSVM -0.95
- CADD 6.43
- PolyPhen-2 0.00
- SIFT 0.91
- Most common in the Latino/Admixed American population (allele frequency 2.2e-05)
- Structural context available