ClinVar Miner

List of variants in gene STK11 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 86
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.*616T>C rs10415095 0.57700
NM_000455.5(STK11):c.920+263A>G rs60977562 0.57699
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.290+36G>T rs3764640 0.25746
NM_000455.5(STK11):c.862+206C>T rs741765 0.22991
NM_000455.5(STK11):c.*16+110C>T rs2277746 0.22884
NM_000455.5(STK11):c.*16+239G>T rs72618592 0.20825
NM_000455.5(STK11):c.374+24G>T rs2075604 0.18985
NM_000455.5(STK11):c.920+7G>C rs2075607 0.16357
NM_000455.5(STK11):c.290+78C>T rs3764641 0.10382
NM_000455.5(STK11):c.*685C>A rs111773256 0.05323
NM_000455.5(STK11):c.*17-97A>C rs62128833 0.05046
NM_000455.5(STK11):c.735-51C>T rs9282860 0.05036
NM_000455.5(STK11):c.291-32C>T rs57281474 0.04127
NM_000455.5(STK11):c.*17-87C>T rs7259447 0.03600
NM_000455.5(STK11):c.1108+199C>T rs60269795 0.02627
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.734+41T>C rs115624397 0.02258
NM_000455.5(STK11):c.465-195C>T rs73918390 0.02104
NM_000455.5(STK11):c.*16+217A>C rs112601969 0.02100
NM_000455.5(STK11):c.374+270G>T rs114556379 0.01971
NM_000455.5(STK11):c.375-99G>T rs78995829 0.00968
NM_000455.5(STK11):c.369G>A (p.Gln123=) rs140112347 0.00636
NM_000455.5(STK11):c.*365C>G rs535975204 0.00633
NM_000455.5(STK11):c.-127T>C rs532196225 0.00374
NM_000455.5(STK11):c.-577C>T rs560480063 0.00210
NM_000455.5(STK11):c.464+9G>A rs376313955 0.00208
NM_000455.5(STK11):c.598-8C>T rs373610101 0.00123
NM_000455.5(STK11):c.426C>T (p.Ser142=) rs758448869 0.00053
NM_000455.5(STK11):c.1211C>T (p.Ser404Phe) rs200078204 0.00051
NM_000455.5(STK11):c.1185A>G (p.Thr395=) rs370207155 0.00047
NM_000455.5(STK11):c.1194G>A (p.Ala398=) rs184271025 0.00023
NM_000455.5(STK11):c.1296G>A (p.Gln432=) rs587781179 0.00020
NM_000455.5(STK11):c.618G>A (p.Ala206=) rs370976710 0.00018
NM_000455.5(STK11):c.597+8C>T rs565387911 0.00017
NM_000455.5(STK11):c.900C>T (p.Ile300=) rs546089394 0.00011
NM_000455.5(STK11):c.787T>C (p.Leu263=) rs372378119 0.00010
NM_000455.5(STK11):c.735-9G>A rs201899557 0.00009
NM_000455.5(STK11):c.598-7G>A rs377502057 0.00008
NM_000455.5(STK11):c.-2G>T rs774072752 0.00007
NM_000455.5(STK11):c.357C>T (p.Asn119=) rs372511774 0.00007
NM_000455.5(STK11):c.863-16G>A rs373096204 0.00007
NM_000455.5(STK11):c.1257C>T (p.Ser419=) rs375328708 0.00006
NM_000455.5(STK11):c.842C>T (p.Pro281Leu) rs121913322 0.00006
NM_000455.5(STK11):c.366G>A (p.Lys122=) rs376969448 0.00005
NM_000455.5(STK11):c.375-7G>A rs587781176 0.00005
NM_000455.5(STK11):c.465-5C>T rs567202367 0.00005
NM_000455.5(STK11):c.920+6C>T rs730881964 0.00005
NM_000455.5(STK11):c.-48C>T rs1044460918 0.00004
NM_000455.5(STK11):c.1109-5C>T rs587782020 0.00004
NM_000455.5(STK11):c.1200G>A (p.Leu400=) rs368661707 0.00004
NM_000455.5(STK11):c.42G>A (p.Glu14=) rs758769888 0.00004
NM_000455.5(STK11):c.598-14C>T rs769378511 0.00004
NM_000455.5(STK11):c.612C>T (p.Phe204=) rs774100153 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.464+10C>T rs587782445 0.00003
NM_000455.5(STK11):c.552C>T (p.Leu184=) rs587780719 0.00003
NM_000455.5(STK11):c.57G>C (p.Ser19=) rs748698151 0.00003
NM_000455.5(STK11):c.828C>T (p.Gly276=) rs200824447 0.00002
NM_000455.5(STK11):c.*16+9C>T rs868216201 0.00001
NM_000455.5(STK11):c.*17-11C>A rs982112837 0.00001
NM_000455.5(STK11):c.*494T>A rs577030468 0.00001
NM_000455.5(STK11):c.1128G>A (p.Glu376=) rs747018506 0.00001
NM_000455.5(STK11):c.327T>C (p.Asn109=) rs749251218 0.00001
NM_000455.5(STK11):c.464+8C>T rs863224669 0.00001
NM_000455.5(STK11):c.465-17G>A rs761361803 0.00001
NM_000455.5(STK11):c.594C>T (p.Ala198=) rs772940660 0.00001
NM_000455.5(STK11):c.765C>T (p.Phe255=) rs769912677 0.00001
NM_000455.5(STK11):c.897C>T (p.Ser299=) rs769013935 0.00001
NM_000455.5(STK11):c.921-8G>A rs863224362 0.00001
NM_000455.5(STK11):c.*16+6del rs1248239568
NM_000455.5(STK11):c.*34C>A rs727503761
NM_000455.5(STK11):c.1167C>T (p.Ala389=) rs547919101
NM_000455.5(STK11):c.375-194G>A rs35113943
NM_000455.5(STK11):c.375-194_375-193del rs2145421730
NM_000455.5(STK11):c.464+32CGGGGGC[3] rs58579265
NM_000455.5(STK11):c.465-17GT[2] rs749644491
NM_000455.5(STK11):c.558C>T (p.Thr186=) rs749563734
NM_000455.5(STK11):c.597+21dup rs534445875
NM_000455.5(STK11):c.735-10C>T rs553975112
NM_000455.5(STK11):c.747C>T (p.Thr249=) rs759546076
NM_000455.5(STK11):c.862+145C>T rs741764
NM_000455.5(STK11):c.863-295G>A rs112215794

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