List of variants in gene STK11 reported as not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.1127A>C (p.Glu376Ala)	rs373888280	0.00007
NM_000455.5(STK11):c.316C>T (p.Arg106Trp)	rs587782115	0.00004
NM_000455.5(STK11):c.1226G>A (p.Arg409Gln)	rs587782364	0.00003
NM_000455.5(STK11):c.841C>A (p.Pro281Thr)	rs377208033	0.00001
NM_000455.5(STK11):c.971C>T (p.Pro324Leu)	rs367807476	0.00001
NM_000455.5(STK11):c.1225C>G (p.Arg409Gly)	rs368466538
NM_000455.5(STK11):c.1250C>G (p.Ala417Gly)	rs1166243253
NM_000455.5(STK11):c.1294C>T (p.Gln432Ter)	rs1057523149
NM_000455.5(STK11):c.291-1G>T	rs112675807
NM_000455.5(STK11):c.619G>A (p.Asp207Asn)	rs587778694
NM_000455.5(STK11):c.735-1G>T	rs1057517830
NM_000455.5(STK11):c.863-2A>T	rs1131690944

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