| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided | |
| | LOC130068748, MAP7D3 (P14S) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130068748, MAP7D3 (S13C) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | LOC130068748, MAP7D3 (G12V) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | MAP7D3, LOC130068748 (G11fs) | Deletion (frameshift variant +1 more) | not provided | |
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