| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Microsatellite (inframe_insertion) | not provided | |
| | LOC108663996, TBP (Q95del +1 more) | Deletion (inframe_deletion) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | LOC108663996, TBP (Q77fs +1 more) | Deletion (frameshift variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Copy number loss | See cases | |
Click to view in NCBI Gene