| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Hypotonia +2 more | |
| | | Deletion (frameshift variant) | Hypotonia +3 more | |
| | | Microsatellite (frameshift variant) | Hypotonia +4 more | |
| | | Deletion (inframe_indel) | Global developmental delay +4 more | |
| | | Single nucleotide variant (missense variant) | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome | |
| | | Microsatellite (frameshift variant) | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Global developmental delay +3 more | |
| | | Single nucleotide variant (nonsense) | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome +5 more | |
| | | Single nucleotide variant (missense variant) | PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | Global developmental delay +4 more | |
| | | Deletion (inframe_deletion) | not provided +1 more | |
Click to view in NCBI Gene