| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | APOBEC3F, LOC126863152 (R208C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | APOBEC3F, LOC126863152 (P230A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | APOBEC3F, LOC126863152 (S232F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | APOBEC3F, LOC126863152 (S232C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | APOBEC3F, LOC126863152 (W233R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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