List of variants in gene STK11 reported as uncertain significance for Malignant tumor of breast

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.125G>T (p.Arg42Leu)	rs148830698	0.00006
NM_000455.5(STK11):c.355A>G (p.Asn119Asp)	rs545015076	0.00002
NM_000455.5(STK11):c.464+5G>A	rs587781681	0.00002
NM_000455.5(STK11):c.1150C>T (p.Arg384Trp)	rs752015385	0.00001
NM_000455.5(STK11):c.462C>T (p.His154=)	rs786201418	0.00001
NM_000455.5(STK11):c.465-10C>G	rs1060503780	0.00001
NM_000455.5(STK11):c.559G>A (p.Gly187Ser)	rs587782032	0.00001
NM_000455.5(STK11):c.976C>A (p.Pro326Thr)	rs771632414	0.00001

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