| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | CDKN2A-related condition +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma-pancreatic cancer syndrome +6 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Familial melanoma +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +2 more) | not specified +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma | |
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