List of variants in gene STK11 reported as uncertain significance for cancer

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: 35

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.375-49G>A	rs34928889	0.45190
NM_000455.5(STK11):c.465-51T>C	rs2075606	0.29935
NM_000455.5(STK11):c.374+24G>T	rs2075604	0.18985
NM_000455.5(STK11):c.894C>A (p.Phe298Leu)	rs199681533	0.00100
NM_000455.5(STK11):c.125G>T (p.Arg42Leu)	rs148830698	0.00006
NM_000455.5(STK11):c.465-5C>T	rs567202367	0.00005
NM_000455.5(STK11):c.355A>G (p.Asn119Asp)	rs545015076	0.00004
NM_000455.5(STK11):c.1193C>T (p.Ala398Val)	rs768058962	0.00003
NM_000455.5(STK11):c.566C>T (p.Thr189Ile)	rs587781515	0.00003
NM_000455.5(STK11):c.464+5G>A	rs587781681	0.00002
NM_000455.5(STK11):c.1145A>G (p.Gln382Arg)	rs985937027	0.00001
NM_000455.5(STK11):c.1148G>A (p.Arg383His)	rs730881990	0.00001
NM_000455.5(STK11):c.1150C>T (p.Arg384Trp)	rs752015385	0.00001
NM_000455.5(STK11):c.1183A>G (p.Thr395Ala)	rs587782138	0.00001
NM_000455.5(STK11):c.1195C>A (p.Gln399Lys)	rs1060499968	0.00001
NM_000455.5(STK11):c.1208A>G (p.Lys403Arg)	rs587781633	0.00001
NM_000455.5(STK11):c.358G>A (p.Glu120Lys)	rs775595174	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.632G>A (p.Arg211Gln)	rs730881982	0.00001
NM_000455.5(STK11):c.976C>A (p.Pro326Thr)	rs771632414	0.00001
NM_000455.5(STK11):c.1180G>A (p.Gly394Ser)	rs768780695
NM_000455.5(STK11):c.1225C>T (p.Arg409Trp)	rs368466538
NM_000455.5(STK11):c.1243C>G (p.Arg415Gly)	rs864622448
NM_000455.5(STK11):c.25C>G (p.Leu9Val)	rs876661079
NM_000455.5(STK11):c.31A>T (p.Met11Leu)	rs753834428
NM_000455.5(STK11):c.375-19del	rs2080764943
NM_000455.5(STK11):c.397G>A (p.Val133Met)	rs567769257
NM_000455.5(STK11):c.464+44dup	rs544282452
NM_000455.5(STK11):c.464+95T>C	rs2080767432
NM_000455.5(STK11):c.465-4G>A	rs587780009
NM_000455.5(STK11):c.598-32C>T	rs2080775539
NM_000455.5(STK11):c.842C>A (p.Pro281Gln)	rs121913322
t(17;19)(q25.1;p13.3)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.