| | | Single nucleotide variant (intron variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant | not provided +1 more | |
| | | Single nucleotide variant | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (intron variant) | Familial melanoma +1 more | |
| | | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Deletion (splice donor variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 3 +2 more | |
| | | Single nucleotide variant (intron variant) | Familial melanoma +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Familial melanoma +2 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | Familial melanoma +4 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Familial melanoma +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (5 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (synonymous variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 3 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 3 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 | |
| | | Single nucleotide variant (3 prime UTR variant) | Melanoma, cutaneous malignant, susceptibility to, 3 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | CDK4, LOC130008148 (G48del) | Microsatellite (inframe_deletion) | Familial melanoma +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Familial melanoma +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Familial melanoma +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +4 more | |
| | | Single nucleotide variant (missense variant +1 more) | Familial melanoma +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 3 +4 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | | Single nucleotide variant (missense variant +1 more) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Familial melanoma +1 more | |
| | | Single nucleotide variant (missense variant) | Familial melanoma +3 more | |