| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder with language delay and seizures | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (intron variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Duplication (intron variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (intron variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (intron variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Microsatellite (intron variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (intron variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | TIAM1-related disorder | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Duplication (frameshift variant) | TIAM1-related disorder | |
| | | Duplication (frameshift variant) | TIAM1-related disorder | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |