ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 120
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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.-311C>T rs149756065 0.01265
NM_000455.5(STK11):c.374+272G>A rs74697381 0.00955
NM_000455.5(STK11):c.369G>A (p.Gln123=) rs140112347 0.00636
NM_000455.5(STK11):c.374+254C>T rs116773689 0.00617
NM_000455.5(STK11):c.*17-162C>T rs567972989 0.00406
NM_000455.5(STK11):c.-127T>C rs532196225 0.00374
NM_000455.5(STK11):c.598-8C>T rs373610101 0.00123
NM_000455.5(STK11):c.735-87G>A rs537831482 0.00110
NM_000455.5(STK11):c.894C>A (p.Phe298Leu) rs199681533 0.00100
NM_000455.5(STK11):c.*16+10G>A rs587781180 0.00077
NM_000455.5(STK11):c.597+14del rs536282050 0.00067
NM_000455.5(STK11):c.945G>A (p.Pro315=) rs376329042 0.00060
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.1108+531G>C rs925652247 0.00029
NM_000455.5(STK11):c.*8C>T rs587782259 0.00027
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.825G>A (p.Pro275=) rs202011521 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.1257C>T (p.Ser419=) rs375328708 0.00006
NM_000455.5(STK11):c.842C>T (p.Pro281Leu) rs121913322 0.00006
NM_000455.5(STK11):c.921-10G>A rs183406870 0.00006
NM_000455.5(STK11):c.237C>T (p.Ile79=) rs751859508 0.00005
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.465-18G>T rs587781177 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.678C>T (p.Asn226=) rs748832988 0.00005
NM_000455.5(STK11):c.920+6C>T rs730881964 0.00005
NM_000455.5(STK11):c.970C>G (p.Pro324Ala) rs549474196 0.00005
NM_000455.5(STK11):c.*17-10C>T rs926599353 0.00004
NM_000455.5(STK11):c.1109-3C>T rs864622219 0.00004
NM_000455.5(STK11):c.1200G>A (p.Leu400=) rs368661707 0.00004
NM_000455.5(STK11):c.374+11C>T rs368923696 0.00004
NM_000455.5(STK11):c.432G>A (p.Pro144=) rs376788924 0.00004
NM_000455.5(STK11):c.723T>C (p.Ala241=) rs533550278 0.00004
NM_000455.5(STK11):c.734+11C>T rs773604294 0.00004
NM_000455.5(STK11):c.795G>A (p.Glu265=) rs730881963 0.00004
NM_000455.5(STK11):c.374+9T>A rs762297795 0.00003
NM_000455.5(STK11):c.615G>A (p.Ala205=) rs532889728 0.00003
NM_000455.5(STK11):c.735-9G>C rs201899557 0.00003
NM_000455.5(STK11):c.876C>T (p.Tyr292=) rs148928808 0.00003
NM_000455.5(STK11):c.1109-13G>A rs568152768 0.00002
NM_000455.5(STK11):c.1229C>T (p.Ala410Val) rs372329880 0.00002
NM_000455.5(STK11):c.735C>G (p.Leu245=) rs773147894 0.00002
NM_000455.5(STK11):c.771G>A (p.Gly257=) rs777998890 0.00002
NM_000455.5(STK11):c.828C>T (p.Gly276=) rs200824447 0.00002
NM_000455.5(STK11):c.921-24G>A rs760399075 0.00002
NM_000455.5(STK11):c.*16+13G>A rs1170510440 0.00001
NM_000455.5(STK11):c.*16+19C>G rs1040395243 0.00001
NM_000455.5(STK11):c.-1C>T rs759284466 0.00001
NM_000455.5(STK11):c.1108+521C>T rs572562074 0.00001
NM_000455.5(STK11):c.1109-4C>T rs1407794756 0.00001
NM_000455.5(STK11):c.1128G>A (p.Glu376=) rs747018506 0.00001
NM_000455.5(STK11):c.1173T>C (p.Cys391=) rs1229258407 0.00001
NM_000455.5(STK11):c.1190C>T (p.Ala397Val) rs558040549 0.00001
NM_000455.5(STK11):c.147C>T (p.Tyr49=) rs751949296 0.00001
NM_000455.5(STK11):c.180C>T (p.Tyr60=) rs778376925 0.00001
NM_000455.5(STK11):c.186G>A (p.Lys62=) rs1215771465 0.00001
NM_000455.5(STK11):c.279C>G (p.Ala93=) rs786201852 0.00001
NM_000455.5(STK11):c.312G>A (p.Arg104=) rs780749732 0.00001
NM_000455.5(STK11):c.321C>T (p.His107=) rs878853987 0.00001
NM_000455.5(STK11):c.348G>T (p.Val116=) rs774482643 0.00001
NM_000455.5(STK11):c.48G>A (p.Glu16=) rs969419908 0.00001
NM_000455.5(STK11):c.576C>T (p.Ile192=) rs878853991 0.00001
NM_000455.5(STK11):c.621C>T (p.Asp207=) rs569380138 0.00001
NM_000455.5(STK11):c.648C>T (p.Ser216=) rs376083300 0.00001
NM_000455.5(STK11):c.720G>A (p.Ser240=) rs759743897 0.00001
NM_000455.5(STK11):c.801C>T (p.Ile267=) rs539772540 0.00001
NM_000455.5(STK11):c.843G>A (p.Pro281=) rs756095270 0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=) rs777872290 0.00001
NM_000455.5(STK11):c.863-4T>C rs778853572 0.00001
NM_000455.5(STK11):c.902G>A (p.Arg301Gln) rs370222210 0.00001
NM_000455.5(STK11):c.921-9C>T rs761688641 0.00001
NM_000455.5(STK11):c.957A>G (p.Pro319=) rs755126393 0.00001
NM_000455.5(STK11):c.972G>A (p.Pro324=) rs553474397 0.00001
NC_000019.10:g.1201926G>A rs185744805
NM_000455.5(STK11):c.*16+20G>A rs1044825795
NM_000455.5(STK11):c.*16+234G>C rs55694801
NM_000455.5(STK11):c.*475C>T rs2080840327
NM_000455.5(STK11):c.*9G>A rs1057522868
NM_000455.5(STK11):c.-430C>T rs115594813
NM_000455.5(STK11):c.1108+460C>T
NM_000455.5(STK11):c.1108+527C>T
NM_000455.5(STK11):c.1191G>A (p.Ala397=) rs774759899
NM_000455.5(STK11):c.1191G>C (p.Ala397=) rs774759899
NM_000455.5(STK11):c.1212C>T (p.Ser404=) rs754945004
NM_000455.5(STK11):c.1225C>T (p.Arg409Trp) rs368466538
NM_000455.5(STK11):c.1279C>T (p.Leu427=) rs1222940657
NM_000455.5(STK11):c.129C>G (p.Ala43=) rs1555734970
NM_000455.5(STK11):c.163C>T (p.Leu55=) rs1057520869
NM_000455.5(STK11):c.216G>T (p.Leu72=) rs1057524353
NM_000455.5(STK11):c.246G>A (p.Lys82=) rs759751510
NM_000455.5(STK11):c.464+44dup rs544282452
NM_000455.5(STK11):c.465-4G>A rs587780009
NM_000455.5(STK11):c.537G>A (p.Pro179=) rs528535500
NM_000455.5(STK11):c.544C>T (p.Leu182=) rs1057522875
NM_000455.5(STK11):c.597+21dup rs534445875
NM_000455.5(STK11):c.618G>T (p.Ala206=) rs370976710
NM_000455.5(STK11):c.666C>G (p.Pro222=) rs542189325
NM_000455.5(STK11):c.672T>A (p.Ile224=) rs1230000936
NM_000455.5(STK11):c.735-6_735-2del rs759090799
NM_000455.5(STK11):c.738C>T (p.Tyr246=) rs137853083
NM_000455.5(STK11):c.777C>T (p.Asn259=) rs786201105
NM_000455.5(STK11):c.840C>T (p.Pro280=) rs1471868090
NM_000455.5(STK11):c.862+199C>A rs117741423
NM_000455.5(STK11):c.862+6A>G rs2145427322
NM_000455.5(STK11):c.920+195C>T rs143726471
NM_000455.5(STK11):c.920+7G>A rs2075607
NM_000455.5(STK11):c.921-29_921-28del rs1568711791
NM_000455.5(STK11):c.96C>G (p.Thr32=) rs79175212

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