| | | Single nucleotide variant (synonymous variant) | AP4M1-related disorder | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 50 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 50 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | AP4M1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Microsatellite (intron variant) | Hereditary spastic paraplegia 50 +1 more | |
| | | Single nucleotide variant (synonymous variant) | AP4M1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | AP4M1-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | AP4M1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | AP4M1-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | AP4M1-related disorder | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 50 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | AP4M1-related disorder | |
| | | Single nucleotide variant (splice donor variant) | AP4M1-related disorder +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 50 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 50 +4 more | GConflicting classifications of pathogenicity |