S98P (p.Ser98Pro) variant of SLC2A2 (P11168)
S98P (p.Ser98Pro) in SLC2A2 (P11168) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.76 / 1. The record also includes population frequency data and structural context.
S98P (p.Ser98Pro) variant details
- p.Ser98Pro
- TOPMed rs1716038093
- Missense
- Variant Prioritization Score for Impact Estimate 0.762
- REVEL 0.92
- CADD 27.60
- PolyPhen-2 0.91
- SIFT 0.00
- Most common in the South Asian population (allele frequency 1.2e-05)
- Structural context available