| | LOC130062899, STK11 (P339A) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +4 more | |
| | LOC130062899, STK11 (P339R) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +2 more | |
| | LOC130062899, STK11 (P339L) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +4 more | |
| | LOC130062899, STK11 (D343Y) | Single nucleotide variant (missense variant +1 more) | Melanoma, cutaneous malignant, susceptibility to, 1 | |
| | | Deletion (inframe_deletion) | Peutz-Jeghers syndrome +3 more | |
| | LOC130062899, STK11 (E351K) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +3 more | |
| | LOC130062899, STK11 (I356T) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +1 more | |
| | LOC130062899, STK11 (D359N) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +1 more | |
| | LOC130062899, STK11 (I360F) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +1 more | |
| | LOC130062899, STK11 (T363N) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +1 more | |
| | LOC130062899, STK11 (P369S) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +2 more | |
| | LOC130062899, STK11 (G370R) | Single nucleotide variant (missense variant) | Melanoma, cutaneous malignant, susceptibility to, 1 +2 more | |