"Neuberg Centre For Genomic Medicine, NCGM"[submitter] AND "STK11"[gen - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2585205	NM_000455.5(STK11):c.26T>C (p.Leu9Pro)	STK11 (L9P)	Single nucleotide variant (missense variant +1 more)	Peutz-Jeghers syndrome +1 more	GUncertain significance
Select item 234791	NM_000455.5(STK11):c.463G>A (p.Gly155Arg)	STK11 (G155R)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 2585536	NM_000455.5(STK11):c.717del (p.Trp239fs)	STK11 (W239fs)	Deletion (frameshift variant +1 more)	Peutz-Jeghers syndrome	GLikely pathogenic

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