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