| | | Copy number gain | See cases | |
| | LOC129995913, LOC129995914 +1340 more | Copy number gain | See cases | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | 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 (missense variant) | SOX4-related condition | |
| | | Single nucleotide variant (missense variant) | SOX4-related condition +1 more | |
| | | Indel (missense variant) | Coffin-Siris syndrome 10 | |
| | | Indel (nonsense) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Neurodevelopmental disorder | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not provided | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, mild | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | not provided | |
| | | Insertion (frameshift variant) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 | |
| | | Deletion (frameshift variant) | not provided | |
| | | Deletion (inframe_deletion) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | See cases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | SOX4-related condition | |
| | | Single nucleotide variant (missense variant) | SOX4-related condition | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | SOX4-related neurodevelopmental disorder | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Deletion (inframe_deletion) | not provided +1 more | |
| | | Insertion (inframe_insertion) | Coffin-Siris syndrome 10 | |
| | | Insertion (frameshift variant) | SOX4-related condition | |
| | | Insertion (frameshift variant) | SOX4-related condition | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Microsatellite (inframe_insertion) | SOX4-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | SOX4-related condition | |
| | | Single nucleotide variant (synonymous variant) | SOX4-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | SOX4-related condition +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Deletion (inframe_deletion) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Microsatellite (inframe_insertion) | SOX4-related condition +1 more | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (inframe_deletion) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (inframe_deletion) | Intellectual disability | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (frameshift variant) | not provided | |
| | | Deletion (nonsense) | SOX4-related condition | |
| | LOC129995965, SOX4 (K261T) | Single nucleotide variant (missense variant) | not provided | |
| | LOC129995965, SOX4 (S266G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Duplication (inframe_insertion) | See cases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC129995965, SOX4 (A274V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995965, SOX4 (A275V) | Single nucleotide variant (missense variant) | Disorder of sexual differentiation | |
| | LOC129995965, SOX4 (P284R) | Single nucleotide variant (missense variant) | not provided | |
| | LOC129995965, SOX4 (P284L) | Single nucleotide variant (missense variant) | SOX4-related condition | |
| | LOC129995965, SOX4 (A289V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Duplication (inframe_insertion) | not provided | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995966, SOX4 (G315R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC129995966, SOX4 (A316V) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Indel (inframe_indel) | Coffin-Siris syndrome 10 | |
| | LOC129995966, SOX4 (G323S) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (nonsense) | Coffin-Siris syndrome 10 | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |