ClinVar Miner

List of variants in gene STK11 reported by Integrated Genetics/Laboratory Corporation of America

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Gene type:
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Total variants: 70
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HGVS dbSNP
NM_000455.4(STK11):c.-1C>T rs759284466
NM_000455.4(STK11):c.-2G>T rs774072752
NM_000455.4(STK11):c.1015C>G (p.Pro339Ala) rs769644352
NM_000455.4(STK11):c.1027G>A (p.Asp343Asn) rs368547224
NM_000455.4(STK11):c.1038C>T (p.Gly346=) rs767565606
NM_000455.4(STK11):c.1039G>A (p.Ala347Thr) rs369744528
NM_000455.4(STK11):c.1041G>A (p.Ala347=) rs537906142
NM_000455.4(STK11):c.1044C>T (p.Asp348=) rs778274196
NM_000455.4(STK11):c.1045G>A (p.Glu349Lys) rs553752236
NM_000455.4(STK11):c.1063G>A (p.Asp355Asn) rs769403473
NM_000455.4(STK11):c.1069G>A (p.Glu357Lys) rs759473833
NM_000455.4(STK11):c.1108+3G>A rs755746417
NM_000455.4(STK11):c.1109-4C>T rs1407794756
NM_000455.4(STK11):c.1109-5C>T rs587782020
NM_000455.4(STK11):c.1127A>C (p.Glu376Ala) rs373888280
NM_000455.4(STK11):c.1142G>C (p.Gly381Ala) rs765419233
NM_000455.4(STK11):c.1163A>G (p.Lys388Arg) rs756877141
NM_000455.4(STK11):c.116G>T (p.Arg39Leu) rs786203250
NM_000455.4(STK11):c.1185A>G (p.Thr395=) rs370207155
NM_000455.4(STK11):c.1194G>A (p.Ala398=) rs184271025
NM_000455.4(STK11):c.1211C>T (p.Ser404Phe) rs200078204
NM_000455.4(STK11):c.1225C>T (p.Arg409Trp) rs368466538
NM_000455.4(STK11):c.1248G>C (p.Lys416Asn) rs1459406168
NM_000455.4(STK11):c.1254C>G (p.Cys418Trp) rs587780715
NM_000455.4(STK11):c.1257C>T (p.Ser419=) rs375328708
NM_000455.4(STK11):c.1284G>A (p.Ser428=) rs369097329
NM_000455.4(STK11):c.1296G>A (p.Gln432=) rs587781179
NM_000455.4(STK11):c.15C>T (p.Asp5=) rs786201498
NM_000455.4(STK11):c.298C>G (p.Gln100Glu) rs757841535
NM_000455.4(STK11):c.301C>G (p.Leu101Val) rs587780716
NM_000455.4(STK11):c.318G>T (p.Arg106=) rs777784520
NM_000455.4(STK11):c.357C>T (p.Asn119=) rs372511774
NM_000455.4(STK11):c.375-7G>A rs587781176
NM_000455.4(STK11):c.396C>T (p.Cys132=) rs730881969
NM_000455.4(STK11):c.397G>A (p.Val133Met) rs567769257
NM_000455.4(STK11):c.425G>A (p.Ser142Asn) rs1568705518
NM_000455.4(STK11):c.426C>T (p.Ser142=) rs758448869
NM_000455.4(STK11):c.434A>G (p.Glu145Gly) rs369764220
NM_000455.4(STK11):c.435G>A (p.Glu145=) rs1555737810
NM_000455.4(STK11):c.441T>C (p.Arg147=) rs786201456
NM_000455.4(STK11):c.464+10C>T rs587782445
NM_000455.4(STK11):c.464+9G>A rs376313955
NM_000455.4(STK11):c.465-5C>A rs567202367
NM_000455.4(STK11):c.552C>T (p.Leu184=) rs587780719
NM_000455.4(STK11):c.558C>T (p.Thr186=) rs749563734
NM_000455.4(STK11):c.559G>A (p.Gly187Ser) rs587782032
NM_000455.4(STK11):c.566C>T (p.Thr189Ile) rs587781515
NM_000455.4(STK11):c.598-8C>T rs373610101
NM_000455.4(STK11):c.632G>A (p.Arg211Gln) rs730881982
NM_000455.4(STK11):c.651G>A (p.Pro217=) rs368348370
NM_000455.4(STK11):c.658C>T (p.Gln220Ter) rs1131690940
NM_000455.4(STK11):c.666C>T (p.Pro222=) rs542189325
NM_000455.4(STK11):c.723T>C (p.Ala241=) rs533550278
NM_000455.4(STK11):c.725G>A (p.Gly242Glu) rs1568708382
NM_000455.4(STK11):c.817G>A (p.Ala273Thr) rs587782199
NM_000455.4(STK11):c.842C>T (p.Pro281Leu) rs121913322
NM_000455.4(STK11):c.851del (p.Asp284fs) rs1555738723
NM_000455.4(STK11):c.876C>T (p.Tyr292=) rs148928808
NM_000455.4(STK11):c.894C>A (p.Phe298Leu) rs199681533
NM_000455.4(STK11):c.900C>T (p.Ile300=) rs546089394
NM_000455.4(STK11):c.90C>T (p.Asp30=) rs771765869
NM_000455.4(STK11):c.910C>T (p.Arg304Trp) rs786201090
NM_000455.4(STK11):c.920+5G>A rs587780013
NM_000455.4(STK11):c.920+6C>T rs730881964
NM_000455.4(STK11):c.920+7G>A rs2075607
NM_000455.4(STK11):c.920+7G>T rs2075607
NM_000455.4(STK11):c.921-10G>A rs183406870
NM_000455.4(STK11):c.96C>G (p.Thr32=) rs79175212
NM_000455.4(STK11):c.970C>G (p.Pro324Ala) rs549474196
NM_000455.4(STK11):c.972G>A (p.Pro324=) rs553474397

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