| | LOC129999451, TRIM24 (A15V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999451, TRIM24 (A19P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999452, TRIM24 (G45S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999452, TRIM24 (S65C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999452, TRIM24 (Q86L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999452, TRIM24 (G97A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999452, TRIM24 (A99G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129999452, TRIM24 (G114V) | 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 | |
| | | 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 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |