"Pathway Genomics"[submitter] AND "STK11"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 156514	NM_000455.5(STK11):c.149T>G (p.Leu50Arg)	STK11 (L50R)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 127703	NM_000455.5(STK11):c.465-4G>A	STK11	Single nucleotide variant (intron variant)	Breast and/or ovarian cancer +5 more	GConflicting classifications of pathogenicity
Select item 192227	NM_000455.5(STK11):c.842del (p.Pro281fs)	STK11 (P281fs)	Deletion (frameshift variant)	Hereditary cancer-predisposing syndrome +1 more	GPathogenic
Select item 192225	NM_000455.5(STK11):c.838_839delinsGT (p.Pro280Val)	STK11 (P280V)	Indel	not specified +2 more	GUncertain significance
Select item 192226	NM_000455.5(STK11):c.844dup (p.Leu282fs)	STK11 (L282fs)	Duplication (frameshift variant)	Peutz-Jeghers syndrome	GPathogenic
Select item 7461	NM_000455.5(STK11):c.1062C>G (p.Phe354Leu)	LOC130062899, STK11 (F354L)	Single nucleotide variant (missense variant)	Melanoma, cutaneous malignant, susceptibility to, 1 +7 more	GBenign/Likely benign

ClinVar