F14I (p.Phe14Ile) variant of SLC37A4 (O43826)
F14I (p.Phe14Ile) in SLC37A4 (O43826) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.65 / 1. The record also includes population frequency data and structural context.
F14I (p.Phe14Ile) variant details
- p.Phe14Ile
- TOPMed rs1478775690
- gnomAD rs1478775690
- Missense
- Variant Prioritization Score for Impact Estimate 0.651
- CADD 28.40
- Most common in the Ashkenazi Jewish population (allele frequency 0.00029)
- Structural context available