| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (synonymous variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (missense variant +2 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (nonsense +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (nonsense +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (intron variant) | TP53I3-related disorder | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (synonymous variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | TP53I3-related disorder | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | TP53I3-related disorder | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +2 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | FAM228B, TP53I3 (Q311E +1 more) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number loss | See cases | |
| | | Copy number gain | Mosaic trisomy 2 | |
| | | Copy number loss | 2p24.1p23.3 microdeletion syndrome | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | | Copy number loss | not provided | |
| | | Copy number gain | See cases | |
| | TRY-GTA2-1, UBXN2A +321 more | Copy number loss | See cases | |
| | ATAD2B, ATP6V1C2 +653 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |
| | LOC126806252, LOC126806253 +2457 more | Copy number gain | See cases | |
| | LOC129933312, LOC129933313 +736 more | Copy number gain | See cases | |
| | | Copy number loss | See cases | |
| | C2orf48, C2orf50 +893 more | Copy number gain | See cases | |
| | | Copy number gain | See cases | |