G92S (p.Gly92Ser) variant of SLC2A4 (P14672)
G92S (p.Gly92Ser) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.79 / 1. The record also includes population frequency data and structural context.
G92S (p.Gly92Ser) variant details
- p.Gly92Ser
- cosmic curated COSV50300
- TOPMed rs1268203327
- gnomAD rs1268203327
- Missense
- Variant Prioritization Score for Impact Estimate 0.791
- REVEL 0.78
- CADD 28.50
- PolyPhen-2 1.00
- SIFT 0.00
- Most common in the South Asian population (allele frequency 3.5e-05)
- Structural context available