| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | ZC3HC1, UBE2H-DT (T434M +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (A381T +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (R383H +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (A360P +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (R402Q +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (R377Q +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (D335E +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (R310Q +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (R353W +2 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ZC3HC1, UBE2H-DT (R271C +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (G264R +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | UBE2H-DT, ZC3HC1 (R228L +1 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
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