| | | Single nucleotide variant | Alkaptonuria | |
| | | Single nucleotide variant (3 prime UTR variant) | Alkaptonuria | |
| | | Single nucleotide variant (3 prime UTR variant) | Alkaptonuria | |
| | | Single nucleotide variant (3 prime UTR variant) | Alkaptonuria | |
| | | Single nucleotide variant (3 prime UTR variant) | Alkaptonuria | |
| | | Single nucleotide variant (stop lost) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Deletion (frameshift variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Deletion (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (nonsense) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (nonsense) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Deletion (splice acceptor variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Deletion (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria +1 more | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Alkaptonuria | |
| | | Single nucleotide variant (intron variant) | Alkaptonuria | |
| | | Single nucleotide variant (intron variant) | Alkaptonuria | |
| | | Single nucleotide variant (intron variant) | Alkaptonuria | |
| | | Deletion (splice acceptor variant +1 more) | Alkaptonuria | |
| | | Deletion | Alkaptonuria | |
| | | Single nucleotide variant (intron variant) | Alkaptonuria | |
| | | Single nucleotide variant (intron variant) | Alkaptonuria | |
| | | Single nucleotide variant (intron variant) | Alkaptonuria | |
| | | Single nucleotide variant (splice donor variant) | Alkaptonuria | |
| | | Single nucleotide variant (splice donor variant) | Alkaptonuria | |
| | | Single nucleotide variant (splice donor variant) | Alkaptonuria | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Deletion (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | HGD-related disorder | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Deletion (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (nonsense) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Deletion (inframe_indel) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Duplication (frameshift variant) | Alkaptonuria | |
| | | Duplication (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Deletion (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria +2 more | |
| | | Duplication (inframe_insertion) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (synonymous variant) | Alkaptonuria | |
| | | Duplication (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (nonsense) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | not specified | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (nonsense) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Deletion (frameshift variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Single nucleotide variant (missense variant) | Alkaptonuria | |
| | | Indel (frameshift variant) | HGD-related disorder +1 more | |