| | | Deletion (inframe_deletion +1 more) | Melanoma, cutaneous malignant, susceptibility to, 2 | |
| | | Single nucleotide variant (missense variant +2 more) | not specified +5 more | |
| | | Single nucleotide variant (missense variant +2 more) | Familial melanoma +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +6 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +2 more) | Melanoma, cutaneous malignant, susceptibility to, 2 +4 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | Familial melanoma +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma-pancreatic cancer syndrome +5 more | |
| | | Single nucleotide variant (intron variant) | not provided +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma and neural system tumor syndrome +4 more | |
| | | Single nucleotide variant (intron variant +1 more) | Familial melanoma +1 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Single nucleotide variant (missense variant +2 more) | Hereditary cancer-predisposing syndrome +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 2 +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (genic upstream transcript variant +1 more) | Hereditary cancer-predisposing syndrome +7 more | |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary cancer-predisposing syndrome +6 more | |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma and neural system tumor syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Microsatellite (inframe_insertion +2 more) | not provided +5 more | GPathogenic/Likely pathogenic |
| | | 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) | Hereditary cancer-predisposing syndrome | |
| | | Single nucleotide variant (missense variant +2 more) | Familial melanoma +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GPathogenic/Likely pathogenic |
| | | Indel (missense variant +1 more) | Familial melanoma +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma and neural system tumor syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +5 more | |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma and neural system tumor syndrome +5 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma and neural system tumor syndrome +3 more | |
| | | Microsatellite (inframe_insertion +1 more) | Melanoma, cutaneous malignant, susceptibility to, 2 | |
| | | Single nucleotide variant (missense variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 2 +6 more | |
| | | Deletion | Melanoma, cutaneous malignant, susceptibility to, 2 | |
| | | Deletion (frameshift variant +1 more) | Melanoma-pancreatic cancer syndrome +1 more | |
| | | Single nucleotide variant (nonsense +2 more) | not provided +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +1 more | |