| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (inframe_deletion) | Pontocerebellar hypoplasia type 10 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Pontocerebellar hypoplasia type 10 | |
| | | Single nucleotide variant (nonsense +1 more) | Pontocerebellar hypoplasia type 10 | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
Click to view in NCBI Gene