| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126859624, TRIM38 (L198I) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859624, TRIM38 (N224K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859624, TRIM38 (L201P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859624, TRIM38 (R180W) | Single nucleotide variant (missense variant) | not specified | |
| | LOC126859624, TRIM38 (K236R) | Single nucleotide variant (missense variant) | not specified | |
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