F97S (p.Phe97Ser) variant of SLC2A4 (P14672)
F97S (p.Phe97Ser) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.63 / 1. The record also includes population frequency data and structural context.
F97S (p.Phe97Ser) variant details
- p.Phe97Ser
- TOPMed rs1428213073
- gnomAD rs1428213073
- Missense
- Variant Prioritization Score for Impact Estimate 0.628
- REVEL 0.64
- CADD 24.90
- PolyPhen-2 0.17
- SIFT 0.02
- Most common in the REMAINING population (allele frequency 1.7e-05)
- Structural context available