| | | Duplication | See cases | |
| | | Duplication (3 prime UTR variant) | Spastic Paraplegia, Recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary spastic paraplegia 11 | |
| | | Duplication (3 prime UTR variant) | Spastic Paraplegia, Recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Spastic Paraplegia, Recessive | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (3 prime UTR variant) | SPG11-related disorder | |
| | | Deletion (frameshift variant) | Hereditary spastic paraplegia 11 | |
| | | Deletion (frameshift variant) | Amyotrophic lateral sclerosis type 5 +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Duplication (frameshift variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Duplication (nonsense +1 more) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Charcot-Marie-Tooth disease axonal type 2X +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (frameshift variant) | Hereditary spastic paraplegia 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Amyotrophic lateral sclerosis +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Indel (frameshift variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (nonsense) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Duplication (nonsense +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | See cases | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Deletion (inframe_deletion) | Hereditary spastic paraplegia 11 | |
| | | Duplication (nonsense) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Hereditary spastic paraplegia 11 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Duplication (frameshift variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Amyotrophic lateral sclerosis type 5 +3 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Duplication (frameshift variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Microsatellite (inframe_deletion) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Duplication (frameshift variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Insertion (frameshift variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | Hereditary spastic paraplegia 11 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (splice acceptor variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (splice acceptor variant) | Hereditary spastic paraplegia 11 +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 11 | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 11 | |
| | | Insertion (intron variant) | Hereditary spastic paraplegia | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 11 | |
| | | Duplication (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 11 | |
| | | Duplication (intron variant) | Hereditary spastic paraplegia 11 | |
| | | Deletion (intron variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 11 | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Hereditary spastic paraplegia 11 | |