ClinVar Miner

List of variants in gene STK11 reported by Quest Diagnostics Nichols Institute San Juan Capistrano

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Gene type:
ClinVar version:
Total variants: 73
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HGVS dbSNP
NM_000455.4(STK11):c.-2G>T rs774072752
NM_000455.4(STK11):c.1012G>A (p.Val338Met) rs587782302
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.1041G>A (p.Ala347=) rs537906142
NM_000455.4(STK11):c.1063G>A (p.Asp355Asn) rs769403473
NM_000455.4(STK11):c.1108+3G>A rs755746417
NM_000455.4(STK11):c.1109-4C>T rs1407794756
NM_000455.4(STK11):c.1128G>A (p.Glu376=) rs747018506
NM_000455.4(STK11):c.117C>T (p.Arg39=) rs786203942
NM_000455.4(STK11):c.1185A>G (p.Thr395=) rs370207155
NM_000455.4(STK11):c.1190C>T (p.Ala397Val) rs558040549
NM_000455.4(STK11):c.1193C>T (p.Ala398Val) rs768058962
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.1226G>A (p.Arg409Gln) rs587782364
NM_000455.4(STK11):c.1243C>G (p.Arg415Gly) rs864622448
NM_000455.4(STK11):c.1258G>T (p.Ala420Ser) rs762482152
NM_000455.4(STK11):c.1259C>T (p.Ala420Val) rs369033659
NM_000455.4(STK11):c.1283C>G (p.Ser428Trp) rs587781537
NM_000455.4(STK11):c.1284G>A (p.Ser428=) rs369097329
NM_000455.4(STK11):c.1286C>G (p.Ala429Gly) rs757369900
NM_000455.4(STK11):c.1286C>T (p.Ala429Val) rs757369900
NM_000455.4(STK11):c.1296G>A (p.Gln432=) rs587781179
NM_000455.4(STK11):c.179dup (p.Tyr60Ter) rs876661012
NM_000455.4(STK11):c.189G>A (p.Val63=) rs1342321548
NM_000455.4(STK11):c.199del (p.Leu67fs) rs1555735014
NM_000455.4(STK11):c.250A>T (p.Lys84Ter) rs137853076
NM_000455.4(STK11):c.312G>A (p.Arg104=) rs780749732
NM_000455.4(STK11):c.312G>C (p.Arg104Ser) rs780749732
NM_000455.4(STK11):c.348G>T (p.Val116=) rs774482643
NM_000455.4(STK11):c.375-7G>A rs587781176
NM_000455.4(STK11):c.426C>T (p.Ser142=) rs758448869
NM_000455.4(STK11):c.42G>A (p.Glu14=) rs758769888
NM_000455.4(STK11):c.464+10C>T rs587782445
NM_000455.4(STK11):c.464+8C>T rs863224669
NM_000455.4(STK11):c.464+9G>A rs376313955
NM_000455.4(STK11):c.465-8G>A rs878853990
NM_000455.4(STK11):c.526G>A (p.Asp176Asn) rs730881979
NM_000455.4(STK11):c.537G>A (p.Pro179=) rs528535500
NM_000455.4(STK11):c.552C>T (p.Leu184=) rs587780719
NM_000455.4(STK11):c.566C>T (p.Thr189Ile) rs587781515
NM_000455.4(STK11):c.597+8C>T rs565387911
NM_000455.4(STK11):c.598-7G>A rs377502057
NM_000455.4(STK11):c.598-8C>T rs373610101
NM_000455.4(STK11):c.612C>T (p.Phe204=) rs774100153
NM_000455.4(STK11):c.613G>A (p.Ala205Thr) rs730881981
NM_000455.4(STK11):c.615G>A (p.Ala205=) rs532889728
NM_000455.4(STK11):c.618G>A (p.Ala206=) rs370976710
NM_000455.4(STK11):c.621C>T (p.Asp207=) rs569380138
NM_000455.4(STK11):c.648C>T (p.Ser216=) rs376083300
NM_000455.4(STK11):c.666C>G (p.Pro222=) rs542189325
NM_000455.4(STK11):c.693C>T (p.Phe231=) rs1568708275
NM_000455.4(STK11):c.725G>A (p.Gly242Glu) rs1568708382
NM_000455.4(STK11):c.781_788dup (p.Leu263fs) rs1568709203
NM_000455.4(STK11):c.787T>C (p.Leu263=) rs372378119
NM_000455.4(STK11):c.825G>A (p.Pro275=) rs202011521
NM_000455.4(STK11):c.840C>T (p.Pro280=) rs1471868090
NM_000455.4(STK11):c.842C>A (p.Pro281Gln) rs121913322
NM_000455.4(STK11):c.842C>T (p.Pro281Leu) rs121913322
NM_000455.4(STK11):c.854T>C (p.Leu285Pro) rs1555738724
NM_000455.4(STK11):c.894C>A (p.Phe298Leu) rs199681533
NM_000455.4(STK11):c.920+5G>A rs587780013
NM_000455.4(STK11):c.921-10G>A rs183406870
NM_000455.4(STK11):c.921-9C>T rs761688641
NM_000455.4(STK11):c.942T>C (p.Pro314=) rs1256260277
NM_000455.4(STK11):c.945G>A (p.Pro315=) rs376329042
NM_000455.4(STK11):c.94A>G (p.Thr32Ala) rs755210880
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.970C>T (p.Pro324Ser) rs549474196
NM_000455.4(STK11):c.976C>A (p.Pro326Thr) rs771632414

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