| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder | |
| | | Indel (frameshift variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (synonymous variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Duplication (nonsense) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Indel (frameshift variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | TRIP12-related disorder | |
| | | Insertion (intron variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Duplication (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Deletion (frameshift variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (frameshift variant) | Clark-Baraitser syndrome | |
| | | Indel (frameshift variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Indel (frameshift variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Deletion (frameshift variant) | See cases | |
| | | Single nucleotide variant (intron variant) | TRIP12-related disorder | |
| | | Deletion (frameshift variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (splice acceptor variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TRIP12-related disorder | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (nonsense) | not provided | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Clark-Baraitser syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | Clark-Baraitser syndrome | |
| | | Duplication (intron variant) | not provided | |
| | | Deletion (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (splice donor variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | See cases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | TRIP12 (L1205del +11 more) | Microsatellite (inframe_deletion) | Clark-Baraitser syndrome | |