| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (intron variant) | EXOSC9-related disorder +1 more | |
| | | Single nucleotide variant (missense variant) | EXOSC9-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Microsatellite (inframe_deletion) | EXOSC9-related disorder +2 more | |
| | CCNA2, EXOSC9 (S425T +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
Click to view in NCBI Gene