ClinVar Miner

List of variants in gene STK11 reported as benign

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Gene type:
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Total variants: 72
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HGVS dbSNP
NM_000455.4(STK11):c.*16+10G>A rs587781180
NM_000455.4(STK11):c.*16+12C>T rs730881966
NM_000455.4(STK11):c.*17-8C>T rs554370182
NM_000455.4(STK11):c.*22_*23insG rs730881967
NM_000455.4(STK11):c.*29A>G rs730881968
NM_000455.4(STK11):c.*34C>T rs727503761
NM_000455.4(STK11):c.*616T>C rs10415095
NM_000455.4(STK11):c.*8C>T rs587782259
NM_000455.4(STK11):c.-2G>T rs774072752
NM_000455.4(STK11):c.-49A>C rs549974432
NM_000455.4(STK11):c.1041G>A (p.Ala347=) rs537906142
NM_000455.4(STK11):c.1062C>G (p.Phe354Leu) rs59912467
NM_000455.4(STK11):c.1109-14C>T rs780434041
NM_000455.4(STK11):c.1109-5C>T rs587782020
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.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.17-87C>T
NM_000455.4(STK11):c.17-97A>C
NM_000455.4(STK11):c.264C>A (p.Ile88=) rs56354945
NM_000455.4(STK11):c.290+36G>T rs3764640
NM_000455.4(STK11):c.357C>T (p.Asn119=) rs372511774
NM_000455.4(STK11):c.369G>A (p.Gln123=) rs140112347
NM_000455.4(STK11):c.374+11C>T rs368923696
NM_000455.4(STK11):c.374+24G>T rs2075604
NM_000455.4(STK11):c.375-49G>A rs34928889
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+17G>A rs587782429
NM_000455.4(STK11):c.464+20delG rs730881960
NM_000455.4(STK11):c.464+9G>A rs376313955
NM_000455.4(STK11):c.465-18G>T rs587781177
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.579C>T (p.Ser193=) rs730881961
NM_000455.4(STK11):c.597+14delA rs536282050
NM_000455.4(STK11):c.597+8C>T rs565387911
NM_000455.4(STK11):c.598-8C>T rs373610101
NM_000455.4(STK11):c.612C>T (p.Phe204=) rs774100153
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.651G>A (p.Pro217=) rs368348370
NM_000455.4(STK11):c.666C>T (p.Pro222=) rs542189325
NM_000455.4(STK11):c.696C>T (p.Ser232=) rs566823619
NM_000455.4(STK11):c.723T>C (p.Ala241=) rs533550278
NM_000455.4(STK11):c.734+17C>G rs751929304
NM_000455.4(STK11):c.734+20G>A rs375315233
NM_000455.4(STK11):c.734+41T>C rs115624397
NM_000455.4(STK11):c.787T>C (p.Leu263=) rs372378119
NM_000455.4(STK11):c.795G>A (p.Glu265=) rs730881963
NM_000455.4(STK11):c.816C>T (p.Tyr272=) rs9282859
NM_000455.4(STK11):c.825G>A (p.Pro275=) rs202011521
NM_000455.4(STK11):c.837C>T (p.Gly279=) rs373021819
NM_000455.4(STK11):c.842C>T (p.Pro281Leu) rs121913322
NM_000455.4(STK11):c.84C>T (p.Arg28=) rs778468876
NM_000455.4(STK11):c.863-6C>T rs757276643
NM_000455.4(STK11):c.876C>T (p.Tyr292=) rs148928808
NM_000455.4(STK11):c.882G>A (p.Pro294=) rs587781178
NM_000455.4(STK11):c.900C>T (p.Ile300=) rs546089394
NM_000455.4(STK11):c.920+6C>T rs730881964
NM_000455.4(STK11):c.920+7G>C rs2075607
NM_000455.4(STK11):c.921-10G>A rs183406870
NM_000455.4(STK11):c.921-58A>G
NM_000455.4(STK11):c.945G>A (p.Pro315=) rs376329042
NM_000455.4(STK11):c.96C>G (p.Thr32=) rs79175212
NM_000455.4(STK11):c.972G>A (p.Pro324=) rs553474397
NM_000455.4(STK11):c.984C>G (p.Thr328=) rs730881965

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