| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (splice donor variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | LOC130064467, SPTBN4 (R2394P +1 more) | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | |
| | | Deletion (frameshift variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | LOC130064467, SPTBN4 (P2384fs) | Deletion (frameshift variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | LOC130064467, SPTBN4 (A2410P) | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness +1 more | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (synonymous variant) | SPTBN4-related disorder +1 more | |
| | | Single nucleotide variant (synonymous variant) | SPTBN4-related disorder +1 more | |
| | | Deletion (intron variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Deletion (frameshift variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Duplication (frameshift variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Deletion (frameshift variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (splice donor variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Deletion (frameshift variant) | Inborn genetic diseases | |
| | LOC130064467, SPTBN4 (R2435C) | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with hypotonia, neuropathy, and deafness | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | not specified | |