| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant +1 more) | ASPN-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | ASPN-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | ASPN-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | ASPN-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | ASPN-related disorder | |
| | | Microsatellite (inframe_insertion +1 more) | CENPP-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Microsatellite (no sequence alteration +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | not provided | |
| | | Microsatellite (inframe_insertion +1 more) | CENPP-related disorder +1 more | |
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