| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | LOC126805616, PEX14 (V173F) | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | LOC126805616, PEX14 (A193T) | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K +1 more | |
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