| | | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | LOC129936144, LOC129936145 +271 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | LOC112935932, LOC112935963 +331 more | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129936094, LOC129936095 +647 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | LOC129936377, LOC129936378 +1111 more | Copy number gain | See cases | |
| | LOC110120630, LOC111429626 +608 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | ARPC4, ARPC4-TTLL3 +307 more | Copy number gain | See cases | |
| | LOC129929025, LOC129929026 +190 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +146 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +68 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +81 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +40 more | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +48 more | Copy number loss | See cases | |
| | ARPC4, ARPC4-TTLL3 +118 more | Copy number loss | See cases | |
| | ARPC4, ARPC4-TTLL3 +47 more | Copy number loss | See cases | |
| | ARPC4, ARPC4-TTLL3 +63 more | Copy number loss | See cases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | OGG1-related condition | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +2 more) | OGG1-related condition +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant +3 more) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +3 more) | OGG1-related condition | |
| | | Single nucleotide variant (3 prime UTR variant +3 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +4 more) | OGG1-related condition | |
| | | Single nucleotide variant (3 prime UTR variant +4 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (3 prime UTR variant +4 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | CAMK1, OGG1 (E290K +3 more) | Single nucleotide variant (missense variant +1 more) | not provided | |
| | CAMK1, OGG1 (G348E +2 more) | Single nucleotide variant (missense variant +2 more) | Nonpapillary renal cell carcinoma | |
| | CAMK1, OGG1 (L292F +1 more) | Single nucleotide variant (synonymous variant +3 more) | OGG1-related condition | |
| | CAMK1, OGG1 (A333T +1 more) | Single nucleotide variant (3 prime UTR variant +2 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | ARPC4, ARPC4-TTLL3 +23 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Deletion | not provided | |
| | ARPC4, ARPC4-TTLL3 +29 more | Copy number loss | 3p- syndrome | |
| | | Copy number loss | not provided | |
| | | Copy number loss | not provided | |
| | ARPC4, ARPC4-TTLL3 +20 more | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not specified | |
| | ARPC4, ARPC4-TTLL3 +28 more | Copy number loss | not specified | |
| | FANCD2OS, THUMPD3 +148 more | Copy number gain | not specified | |
| | | Copy number gain | not specified | |
| | | Copy number loss | not specified | |
| | | Duplication | Long QT syndrome | |
| | ARPC4, ARPC4-TTLL3 +38 more | Duplication | Atrioventricular septal defect, susceptibility to, 2 | |
| | ARPC4, ARPC4-TTLL3 +16 more | Copy number gain | not provided | |
| | ARPC4, ARPC4-TTLL3 +13 more | Duplication | Atrioventricular septal defect, susceptibility to, 2 | |
| | | Copy number loss | not provided | |
| | ARPC4, ARPC4-TTLL3 +16 more | Copy number gain | not provided | |
| | | Duplication | Neurodevelopmental disorder | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | not provided | |
| | ARPC4, ARPC4-TTLL3 +14 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | | Copy number gain | See cases | |
| | ARPC4, ARPC4-TTLL3 +15 more | Copy number loss | See cases | |
| | ARPC4, ARPC4-TTLL3 +39 more | Copy number loss | See cases | |