| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number loss | not specified | |
| | H3C13, LOC129931372 (K80N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Copy number gain | Chromosome 1q21.1 duplication syndrome | |
| | H3C13, LOC129931372 (T23A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication | Parathyroid carcinoma +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | Chromosome 1q21.1 duplication syndrome | |
| | | Copy number gain | Breast ductal adenocarcinoma | |
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