ClinVar Miner

List of variants in gene STK11 reported as pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 54
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HGVS dbSNP
NM_000455.4(STK11):c.106delT (p.Tyr36Thrfs) rs1131690924
NM_000455.4(STK11):c.108C>G (p.Tyr36Ter) rs137853079
NM_000455.4(STK11):c.109C>T (p.Gln37Ter) rs121913324
NM_000455.4(STK11):c.134_145delTCATCGGCAAGT (p.Leu45_Tyr49delinsHis) rs730881958
NM_000455.4(STK11):c.156_157delGG (p.Asp53Profs) rs1131690917
NM_000455.4(STK11):c.169dupG (p.Glu57Glyfs) rs121913319
NM_000455.4(STK11):c.180C>A (p.Tyr60Ter) rs778376925
NM_000455.4(STK11):c.180C>G (p.Tyr60Ter) rs778376925
NM_000455.4(STK11):c.195_198delGGTG (p.Glu65Aspfs) rs1131690936
NM_000455.4(STK11):c.209dup (p.Thr71Aspfs) rs1131690929
NM_000455.4(STK11):c.218_230delGCAGGAGGGCCGT (p.Cys73Serfs) rs730881959
NM_000455.4(STK11):c.250A>T (p.Lys84Ter) rs137853076
NM_000455.4(STK11):c.290+1G>A rs1131690950
NM_000455.4(STK11):c.291-2A>G rs876658584
NM_000455.4(STK11):c.357delC (p.Asn119Lysfs) rs1555737444
NM_000455.4(STK11):c.358G>T (p.Glu120Ter) rs775595174
NM_000455.4(STK11):c.363_367dup (p.Gln123Argfs) rs1131690933
NM_000455.4(STK11):c.367C>T (p.Gln123Ter) rs1131690925
NM_000455.4(STK11):c.373dup (p.Met125Asnfs) rs1131690952
NM_000455.4(STK11):c.374+1A>G rs1131690951
NM_000455.4(STK11):c.396C>A (p.Cys132Ter) rs730881969
NM_000455.4(STK11):c.402_403delTG (p.Cys134Trpfs) rs587782424
NM_000455.4(STK11):c.409C>T (p.Gln137Ter) rs730881970
NM_000455.4(STK11):c.418delC (p.Leu140Trpfs) rs397518440
NM_000455.4(STK11):c.446delC (p.Pro149Glnfs) rs1131690926
NM_000455.4(STK11):c.487delGins19 (p.?)
NM_000455.4(STK11):c.488G>A (p.Gly163Asp) rs137853078
NM_000455.4(STK11):c.497_500dup (p.His168Profs) rs1131690922
NM_000455.4(STK11):c.540dup (p.Asn181Glufs) rs1131690939
NM_000455.4(STK11):c.542A>G (p.Asn181Ser) rs886037859
NM_000455.4(STK11):c.543C>G (p.Asn181Lys) rs730881973
NM_000455.4(STK11):c.574delA (p.Ile192Serfs) rs587781856
NM_000455.4(STK11):c.598-2A>G rs1131690934
NM_000455.4(STK11):c.608dup (p.Phe204Valfs) rs1131690946
NM_000455.4(STK11):c.640C>T (p.Gln214Ter) rs1131690923
NM_000455.4(STK11):c.658C>T (p.Gln220Ter) rs1131690940
NM_000455.4(STK11):c.67delG (p.Asp23Thrfs) rs1555734904
NM_000455.4(STK11):c.734+1G>C rs587782018
NM_000455.4(STK11):c.734+1G>T rs587782018
NM_000455.4(STK11):c.735-1G>A rs1057517830
NM_000455.4(STK11):c.752delG (p.Gly251Valfs) rs1131690948
NM_000455.4(STK11):c.790_793delTTTG (p.Phe264Argfs) rs121913320
NM_000455.4(STK11):c.816C>G (p.Tyr272Ter) rs9282859
NM_000455.4(STK11):c.842dupC (p.Leu282Alafs) rs121913321
NM_000455.4(STK11):c.843dup (p.Leu282Alafs) rs1131690949
NM_000455.4(STK11):c.862+1G>T rs1131690921
NM_000455.4(STK11):c.876delC (p.Tyr292Terfs) rs1131690947
NM_000455.4(STK11):c.899delT (p.Ile300Thrfs) rs786203624
NM_000455.4(STK11):c.911G>C (p.Arg304Pro) rs376280361
NM_000455.4(STK11):c.913C>T (p.Gln305Ter) rs1131690945
NM_000455.4(STK11):c.920+1G>A rs1131690920
NM_000455.4(STK11):c.921-1G>C rs398123406
NM_000455.4(STK11):c.923G>A (p.Trp308Ter) rs864622488
NM_000455.4(STK11):c.93dup (p.Thr32Hisfs) rs1131690930

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