ClinVar Miner

List of variants in gene STK11 studied for Breast and/or ovarian cancer

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Total variants: 47
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.816C>T (p.Tyr272=) rs9282859 0.02603
NM_000455.5(STK11):c.264C>A (p.Ile88=) rs56354945 0.02303
NM_000455.5(STK11):c.369G>A (p.Gln123=) rs140112347 0.00584
NM_000455.5(STK11):c.464+9G>A rs376313955 0.00208
NM_000455.5(STK11):c.597+14del rs536282050 0.00068
NM_000455.5(STK11):c.945G>A (p.Pro315=) rs376329042 0.00064
NM_000455.5(STK11):c.1211C>T (p.Ser404Phe) rs200078204 0.00050
NM_000455.5(STK11):c.1185A>G (p.Thr395=) rs370207155 0.00043
NM_000455.5(STK11):c.1284G>A (p.Ser428=) rs369097329 0.00035
NM_000455.5(STK11):c.*8C>T rs587782259 0.00027
NM_000455.5(STK11):c.1296G>A (p.Gln432=) rs587781179 0.00019
NM_000455.5(STK11):c.618G>A (p.Ala206=) rs370976710 0.00018
NM_000455.5(STK11):c.825G>A (p.Pro275=) rs202011521 0.00012
NM_000455.5(STK11):c.787T>C (p.Leu263=) rs372378119 0.00009
NM_000455.5(STK11):c.734+20G>A rs375315233 0.00008
NM_000455.5(STK11):c.1127A>C (p.Glu376Ala) rs373888280 0.00007
NM_000455.5(STK11):c.598-7G>A rs377502057 0.00007
NM_000455.5(STK11):c.921-10G>A rs183406870 0.00006
NM_000455.5(STK11):c.366G>A (p.Lys122=) rs376969448 0.00005
NM_000455.5(STK11):c.465-5C>T rs567202367 0.00005
NM_000455.5(STK11):c.666C>T (p.Pro222=) rs542189325 0.00005
NM_000455.5(STK11):c.464+10C>T rs587782445 0.00004
NM_000455.5(STK11):c.723T>C (p.Ala241=) rs533550278 0.00004
NM_000455.5(STK11):c.795G>A (p.Glu265=) rs730881963 0.00004
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.944C>T (p.Pro315Leu) rs766958608 0.00002
NM_000455.5(STK11):c.-1C>T rs759284466 0.00001
NM_000455.5(STK11):c.112C>G (p.Pro38Ala) rs1060499954 0.00001
NM_000455.5(STK11):c.1189G>T (p.Ala397Ser) rs587780008 0.00001
NM_000455.5(STK11):c.1190C>T (p.Ala397Val) rs558040549 0.00001
NM_000455.5(STK11):c.1249G>T (p.Ala417Ser) rs587782876 0.00001
NM_000455.5(STK11):c.1283C>T (p.Ser428Leu) rs587781537 0.00001
NM_000455.5(STK11):c.299A>G (p.Gln100Arg) rs1060499957 0.00001
NM_000455.5(STK11):c.440G>A (p.Arg147His) rs587780717 0.00001
NM_000455.5(STK11):c.464+4C>T rs373167735 0.00001
NM_000455.5(STK11):c.465-10C>G rs1060503780 0.00001
NM_000455.5(STK11):c.632G>A (p.Arg211Gln) rs730881982 0.00001
NM_000455.5(STK11):c.1253G>C (p.Cys418Ser) rs878853986
NM_000455.5(STK11):c.312G>C (p.Arg104Ser) rs780749732
NM_000455.5(STK11):c.318G>T (p.Arg106=) rs777784520
NM_000455.5(STK11):c.465-4G>A rs587780009
NM_000455.5(STK11):c.537G>T (p.Pro179=) rs528535500
NM_000455.5(STK11):c.543C>T (p.Asn181=) rs730881973
NM_000455.5(STK11):c.597+21dup rs534445875
NM_000455.5(STK11):c.721G>A (p.Ala241Thr) rs587780721
NM_000455.5(STK11):c.777C>T (p.Asn259=) rs786201105

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