ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 26
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HGVS dbSNP
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.1211C>T (p.Ser404Phe) rs200078204
NM_000455.4(STK11):c.1284G>A (p.Ser428=) rs369097329
NM_000455.4(STK11):c.312G>A (p.Arg104=) rs780749732
NM_000455.4(STK11):c.375-7G>A rs587781176
NM_000455.4(STK11):c.426C>T (p.Ser142=) rs758448869
NM_000455.4(STK11):c.464+10C>T rs587782445
NM_000455.4(STK11):c.464+9G>A rs376313955
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.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.615G>A (p.Ala205=) rs532889728
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.787T>C (p.Leu263=) rs372378119
NM_000455.4(STK11):c.825G>A (p.Pro275=) rs202011521
NM_000455.4(STK11):c.921-10G>A rs183406870
NM_000455.4(STK11):c.942T>C (p.Pro314=) rs1256260277
NM_000455.4(STK11):c.970C>G (p.Pro324Ala) rs549474196

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