| | | Single nucleotide variant (3 prime UTR variant) | BAP1-related disorder +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | BAP1-related disorder | |
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | BAP1-related tumor predisposition syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related tumor predisposition syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | BAP1-related tumor predisposition syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | BAP1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +5 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | BAP1-related tumor predisposition syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related disorder +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | BAP1-related tumor predisposition syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | BAP1-related disorder +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related tumor predisposition syndrome +4 more | |
| | | Single nucleotide variant (intron variant) | BAP1-related disorder +2 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related disorder +3 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (missense variant) | BAP1-related tumor predisposition syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | BAP1-related disorder +3 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related tumor predisposition syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | BAP1-related disorder | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related tumor predisposition syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Deletion (frameshift variant +1 more) | BAP1-related disorder | |
| | | Single nucleotide variant (missense variant) | BAP1-related tumor predisposition syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related tumor predisposition syndrome +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | BAP1-related tumor predisposition syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | BAP1-related tumor predisposition syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | BAP1-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |