"Gharavi Laboratory, Columbia University"[submitter] AND "STK11"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 237806	NM_000455.5(STK11):c.94A>G (p.Thr32Ala)	STK11 (T32A)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome +3 more	GUncertain significance
Select item 591825	NM_000455.5(STK11):c.359A>G (p.Glu120Gly)	STK11 (E120G)	Single nucleotide variant (missense variant)	Peutz-Jeghers syndrome	GUncertain significance
Select item 591694	NM_000455.5(STK11):c.389A>G (p.Glu130Gly)	STK11 (E130G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 141128	NM_000455.5(STK11):c.566C>T (p.Thr189Ile)	STK11 (T189I)	Single nucleotide variant (missense variant)	Carcinoma of pancreas +6 more	GConflicting classifications of pathogenicity
Select item 127705	NM_000455.5(STK11):c.842C>A (p.Pro281Gln)	STK11 (P281Q)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +3 more	GConflicting classifications of pathogenicity
Select item 591841	NM_000455.5(STK11):c.1260_1290del (p.Lys423fs)	STK11 (K423fs)	Deletion (frameshift variant)	not provided	GUncertain significance

ClinVar