| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | DST, DST-AS1 (A65V +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DST, DST-AS1 (M150V +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | DST, DST-AS1 (N5S +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene