| | | 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 (missense variant +1 more) | Melanoma and neural system tumor syndrome +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma-pancreatic cancer syndrome +5 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial melanoma +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma-pancreatic cancer syndrome +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma and neural system tumor syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Microsatellite (inframe_insertion +2 more) | Melanoma-pancreatic cancer syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Melanoma-pancreatic cancer syndrome +6 more | |
| | | Single nucleotide variant (genic upstream transcript variant +1 more) | Melanoma and neural system tumor syndrome +7 more | |
| | | Single nucleotide variant (missense variant +2 more) | Melanoma and neural system tumor syndrome +5 more | |