| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | ACIN1, LOC126861893 (G275R +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | ACIN1, LOC126861893 (G1013R +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | ACIN1, LOC126861893 (T1055M +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | ACIN1, LOC126861893 (V981M +5 more) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | See cases | |
| | LOC126861920, LOC126861921 +3280 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC130055392, LOC130055393 +780 more | Copy number gain | See cases | |
| | LOC130055370, LOC130055371 +840 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
Click to view in NCBI Gene