| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Deletion (splice donor variant) | MYH3-related disorder | |
| | | Deletion (frameshift variant) | MYH3-related disorder | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | MYH3-related disorder | |
| | | Deletion (frameshift variant) | MYH3-related disorder | |
| | | Deletion (inframe_deletion) | MYH3-related disorder | |
| | | Deletion (nonsense) | MYH3-related disorder | |
| | | Single nucleotide variant (missense variant) | MYH3-related disorder | |
| | | Single nucleotide variant (splice donor variant) | MYH3-related disorder | |
| | | Single nucleotide variant (missense variant) | MYH3-related disorder | |
Click to view in NCBI Gene