| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DDX10, LOC106865368 (T99I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC106865368, DDX10 (P149R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC106865368, DDX10 (V160F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DDX10, LOC106865368 (L201R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC106865368, DDX10 (G231R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DDX10, LOC106865368 (K246E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene