| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130062072, THOC1 (F17V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130062072, THOC1 (A13V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130062072, THOC1 (P11S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
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