| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130067635, TTLL12 (S16N) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130067635, TTLL12 (R10G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130067635, TTLL12 (R5Q) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130067635, TTLL12 (E4Q) | Single nucleotide variant (missense variant) | not specified | |
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