| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | EIF3F, LOC126861132 (I263V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | EIF3F, LOC126861132 (R278C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | EIF3F, LOC126861132 (T285I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | EIF3F, LOC126861132 (D292E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene