| | | Copy number gain | See cases | |
| | LOC126861081, LOC126861082 +1036 more | Copy number gain | See cases | |
| | ABLIM1, ABRAXAS2 +1097 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Deletion | Desmoplastic/nodular medulloblastoma | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | not provided | |
| | | Single nucleotide variant (genic upstream transcript variant) | Medulloblastoma | |
| | | Single nucleotide variant (genic upstream transcript variant) | Medulloblastoma | |
| | | Single nucleotide variant (5 prime UTR variant) | Medulloblastoma | |
| | | Single nucleotide variant (5 prime UTR variant) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Medulloblastoma | |
| | | Single nucleotide variant (5 prime UTR variant) | Medulloblastoma | |
| | | Single nucleotide variant (5 prime UTR variant) | Medulloblastoma | |
| | | Single nucleotide variant (5 prime UTR variant) | Medulloblastoma | |
| | | Single nucleotide variant (5 prime UTR variant) | not specified +1 more | |
| | LOC124416895, LOC130004614 +3 more | Deletion | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +2 more | |
| | | Single nucleotide variant (missense variant) | Medulloblastoma +2 more | |
| | | Deletion (frameshift variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +4 more | |
| | | Single nucleotide variant (missense variant) | Familial meningioma +3 more | |
| | | Single nucleotide variant (synonymous variant) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Medulloblastoma +2 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +2 more | |
| | LOC130004614, SUFU (G19fs) | Duplication (frameshift variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Medulloblastoma +1 more | |
| | LOC130004614, SUFU (T13fs) | Deletion (frameshift variant) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant) | Gorlin syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | Gorlin syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Deletion (inframe_deletion) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +2 more | |
| | | Deletion (inframe_deletion) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Joubert syndrome 32 +4 more | |
| | | Single nucleotide variant (missense variant) | Medulloblastoma | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +2 more | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +2 more | |
| | | Single nucleotide variant (missense variant) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Gorlin syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +2 more | |
| | LOC130004614, SUFU (P18fs) | Deletion (frameshift variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | LOC130004614, SUFU (P18fs) | Deletion (frameshift variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Duplication (inframe_insertion) | Medulloblastoma +1 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (synonymous variant) | Medulloblastoma +2 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Familial meningioma | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Gorlin syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Familial meningioma | |