| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | DDX39B, ATP6V1G2-DDX39B (N288S) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | DDX39B, ATP6V1G2-DDX39B (V61F) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | ATP6V1G2-DDX39B, DDX39B (A31P) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
| | DDX39B, ATP6V1G2-DDX39B (A22G) | Single nucleotide variant (non-coding transcript variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene