| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CUL4A, LOC130010176 (G16D) | Single nucleotide variant (5 prime UTR variant +2 more) | Inborn genetic diseases | |
| | CUL4A, LOC130010176 (G35R) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CUL4A, LOC130010176 (G38D) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | CUL4A, LOC130010176 (R49Q) | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | LOC130010177, CUL4A (T59R) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene