| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Duplication (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (3 prime UTR variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (3 prime UTR variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (3 prime UTR variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum +1 more | |
| | | Deletion (inframe_deletion) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum +1 more | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Trichothiodystrophy 2, photosensitive +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (nonsense) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum | |
| | | Duplication (frameshift variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B | |
| | | Duplication (frameshift variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Xeroderma pigmentosum group B +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (frameshift variant) | Trichothiodystrophy 2, photosensitive +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B +2 more | |
| | | Single nucleotide variant (nonsense) | Trichothiodystrophy 2, photosensitive +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (nonsense) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum +1 more | |
| | | Duplication (frameshift variant) | Xeroderma pigmentosum group B +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Xeroderma pigmentosum group B +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Trichothiodystrophy 2, photosensitive +3 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (nonsense) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B | |
| | | Duplication (nonsense) | Trichothiodystrophy 2, photosensitive +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (synonymous variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Deletion (nonsense) | not provided | |
| | | Microsatellite (frameshift variant) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (nonsense) | Xeroderma pigmentosum group B | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum +2 more | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (intron variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum group B +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice donor variant) | Xeroderma pigmentosum +1 more | |
| | | Single nucleotide variant (missense variant) | Xeroderma pigmentosum | |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Xeroderma pigmentosum group B +1 more | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | Xeroderma pigmentosum +1 more | GConflicting classifications of pathogenicity |