F97I (p.Phe97Ile) variant of SLC2A4 (P14672)
F97I (p.Phe97Ile) in SLC2A4 (P14672) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.56 / 1. The record also includes population frequency data and structural context.
F97I (p.Phe97Ile) variant details
- p.Phe97Ile
- gnomAD rs1292711972
- Missense
- Variant Prioritization Score for Impact Estimate 0.556
- REVEL 0.51
- CADD 24.60
- SIFT 0.00
- Most common in the South Asian population (allele frequency 0.00021)
- Structural context available