| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC129998143, NFE2L3 (D669E) | Single nucleotide variant (missense variant) | not specified | |
| | LOC129998142, NFE2L3 (A630S) | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC129998143, NFE2L3 (H684Y) | Single nucleotide variant (missense variant) | not specified | |
| | | Copy number gain | not provided | |
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