| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | Congenital heart defects and skeletal malformations syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | Congenital heart defects and skeletal malformations syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Chronic myelogenous leukemia, BCR-ABL1 positive +2 more | |
| | | Single nucleotide variant (missense variant) | ABL1-related disorder +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
Click to view in NCBI Gene