| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | PEX14-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant) | PEX14-related disorder | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Indel (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K +1 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (splice donor variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K +1 more | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder 13A (Zellweger) +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Deletion (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K +1 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K +2 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (nonsense) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K +1 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Peroxisome biogenesis disorder, complementation group K +1 more | |
| | | Single nucleotide variant (synonymous variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | PEX14-related disorder | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Duplication (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | Peroxisome biogenesis disorder, complementation group K | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |