ClinVar Miner

Variants in gene STK11 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 138
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.894C>A (p.Phe298Leu) rs199681533 0.00100
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.1284G>A (p.Ser428=) rs369097329 0.00035
NM_000455.5(STK11):c.*8C>T rs587782259 0.00027
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.-461G>A rs552610464 0.00016
NM_000455.5(STK11):c.825G>A (p.Pro275=) rs202011521 0.00011
NM_000455.5(STK11):c.920+5G>A rs587780013 0.00008
NM_000455.5(STK11):c.-2G>T rs774072752 0.00007
NM_000455.5(STK11):c.1127A>C (p.Glu376Ala) rs373888280 0.00007
NM_000455.5(STK11):c.357C>T (p.Asn119=) rs372511774 0.00007
NM_000455.5(STK11):c.734+20G>A rs375315233 0.00007
NM_000455.5(STK11):c.125G>T (p.Arg42Leu) rs148830698 0.00006
NM_000455.5(STK11):c.842C>T (p.Pro281Leu) rs121913322 0.00006
NM_000455.5(STK11):c.1254C>G (p.Cys418Trp) rs587780715 0.00005
NM_000455.5(STK11):c.1286C>G (p.Ala429Gly) rs757369900 0.00005
NM_000455.5(STK11):c.375-7G>A rs587781176 0.00005
NM_000455.5(STK11):c.465-5C>T rs567202367 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.1109-3C>T rs864622219 0.00004
NM_000455.5(STK11):c.1109-5C>T rs587782020 0.00004
NM_000455.5(STK11):c.298C>G (p.Gln100Glu) rs757841535 0.00004
NM_000455.5(STK11):c.355A>G (p.Asn119Asp) rs545015076 0.00004
NM_000455.5(STK11):c.374+11C>T rs368923696 0.00004
NM_000455.5(STK11):c.613G>A (p.Ala205Thr) rs730881981 0.00004
NM_000455.5(STK11):c.631C>T (p.Arg211Trp) rs185087320 0.00004
NM_000455.5(STK11):c.827G>T (p.Gly276Val) rs749927908 0.00004
NM_000455.5(STK11):c.1118C>T (p.Pro373Leu) rs876661153 0.00003
NM_000455.5(STK11):c.1130C>T (p.Ala377Val) rs199973552 0.00003
NM_000455.5(STK11):c.1168G>C (p.Val390Leu) rs374078532 0.00003
NM_000455.5(STK11):c.1193C>T (p.Ala398Val) rs768058962 0.00003
NM_000455.5(STK11):c.1226G>A (p.Arg409Gln) rs587782364 0.00003
NM_000455.5(STK11):c.1258G>T (p.Ala420Ser) rs762482152 0.00003
NM_000455.5(STK11):c.374+9T>A rs762297795 0.00003
NM_000455.5(STK11):c.566C>T (p.Thr189Ile) rs587781515 0.00003
NM_000455.5(STK11):c.-9G>A rs770466669 0.00002
NM_000455.5(STK11):c.1168G>A (p.Val390Met) rs374078532 0.00002
NM_000455.5(STK11):c.1229C>T (p.Ala410Val) rs372329880 0.00002
NM_000455.5(STK11):c.439C>T (p.Arg147Cys) rs748464757 0.00002
NM_000455.5(STK11):c.464+5G>A rs587781681 0.00002
NM_000455.5(STK11):c.608C>T (p.Pro203Leu) rs587782379 0.00002
NM_000455.5(STK11):c.735C>G (p.Leu245=) rs773147894 0.00002
NM_000455.5(STK11):c.828C>T (p.Gly276=) rs200824447 0.00002
NM_000455.5(STK11):c.944C>T (p.Pro315Leu) rs766958608 0.00002
NM_000455.5(STK11):c.-1C>T rs759284466 0.00001
NM_000455.5(STK11):c.1109-4C>T rs1407794756 0.00001
NM_000455.5(STK11):c.1139A>G (p.Asn380Ser) rs1247102370 0.00001
NM_000455.5(STK11):c.1145A>G (p.Gln382Arg) rs985937027 0.00001
NM_000455.5(STK11):c.1147C>T (p.Arg383Cys) rs535449626 0.00001
NM_000455.5(STK11):c.1150C>T (p.Arg384Trp) rs752015385 0.00001
NM_000455.5(STK11):c.1153G>A (p.Gly385Ser) rs763586612 0.00001
NM_000455.5(STK11):c.1167C>G (p.Ala389=) rs547919101 0.00001
NM_000455.5(STK11):c.1174A>G (p.Met392Val) rs565993396 0.00001
NM_000455.5(STK11):c.1182C>T (p.Gly394=) rs376679847 0.00001
NM_000455.5(STK11):c.1189G>T (p.Ala397Ser) rs587780008 0.00001
NM_000455.5(STK11):c.1190C>T (p.Ala397Val) rs558040549 0.00001
NM_000455.5(STK11):c.1217C>T (p.Ala406Val) rs748202003 0.00001
NM_000455.5(STK11):c.1222G>A (p.Gly408Ser) rs749463771 0.00001
NM_000455.5(STK11):c.1231C>G (p.Pro411Ala) rs772527201 0.00001
NM_000455.5(STK11):c.1245C>T (p.Arg415=) rs878853985 0.00001
NM_000455.5(STK11):c.1247A>G (p.Lys416Arg) rs1446554442 0.00001
NM_000455.5(STK11):c.1251C>T (p.Ala417=) rs1060503786 0.00001
NM_000455.5(STK11):c.1252T>A (p.Cys418Ser) rs730881991 0.00001
NM_000455.5(STK11):c.1259C>T (p.Ala420Val) rs369033659 0.00001
NM_000455.5(STK11):c.291-13C>T rs1332978515 0.00001
NM_000455.5(STK11):c.317G>A (p.Arg106Gln) rs375622587 0.00001
NM_000455.5(STK11):c.434A>G (p.Glu145Gly) rs369764220 0.00001
NM_000455.5(STK11):c.447A>G (p.Pro149=) rs587780718 0.00001
NM_000455.5(STK11):c.449T>C (p.Val150Ala) rs587781802 0.00001
NM_000455.5(STK11):c.45C>T (p.Gly15=) rs786201234 0.00001
NM_000455.5(STK11):c.464+4C>T rs373167735 0.00001
NM_000455.5(STK11):c.464+8C>T rs863224669 0.00001
NM_000455.5(STK11):c.465-10C>G rs1060503780 0.00001
NM_000455.5(STK11):c.465-8G>A rs878853990 0.00001
NM_000455.5(STK11):c.559G>A (p.Gly187Ser) rs587782032 0.00001
NM_000455.5(STK11):c.579C>T (p.Ser193=) rs730881961 0.00001
NM_000455.5(STK11):c.632G>A (p.Arg211Gln) rs730881982 0.00001
NM_000455.5(STK11):c.71C>T (p.Thr24Met) rs770503805 0.00001
NM_000455.5(STK11):c.720G>A (p.Ser240=) rs759743897 0.00001
NM_000455.5(STK11):c.750G>A (p.Thr250=) rs748112446 0.00001
NM_000455.5(STK11):c.841C>A (p.Pro281Thr) rs377208033 0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=) rs777872290 0.00001
NM_000455.5(STK11):c.877G>A (p.Glu293Lys) rs398123405 0.00001
NM_000455.5(STK11):c.902G>A (p.Arg301Gln) rs370222210 0.00001
NM_000455.5(STK11):c.921-8G>A rs863224362 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.976C>A (p.Pro326Thr) rs771632414 0.00001
NM_000455.5(STK11):c.1109-4C>A rs1407794756
NM_000455.5(STK11):c.1129G>C (p.Ala377Pro) rs768870802
NM_000455.5(STK11):c.120C>T (p.Arg40=) rs878853984
NM_000455.5(STK11):c.1225C>G (p.Arg409Gly) rs368466538
NM_000455.5(STK11):c.1225C>T (p.Arg409Trp) rs368466538
NM_000455.5(STK11):c.1230C>T (p.Ala410=) rs864622171
NM_000455.5(STK11):c.1236C>T (p.Asn412=) rs1158714606
NM_000455.5(STK11):c.1244G>A (p.Arg415His) rs775978755
NM_000455.5(STK11):c.1261_1262inv (p.Ser421Leu)
NM_000455.5(STK11):c.1276C>G (p.Arg426Gly) rs587782687
NM_000455.5(STK11):c.1283C>G (p.Ser428Trp) rs587781537
NM_000455.5(STK11):c.163C>T (p.Leu55=) rs1057520869
NM_000455.5(STK11):c.189G>A (p.Val63=) rs1342321548
NM_000455.5(STK11):c.248A>G (p.Lys83Arg) rs374006397
NM_000455.5(STK11):c.318G>T (p.Arg106=) rs777784520
NM_000455.5(STK11):c.345T>C (p.Asp115=) rs2145420737
NM_000455.5(STK11):c.375-5C>T rs1057517626
NM_000455.5(STK11):c.397G>A (p.Val133Met) rs567769257
NM_000455.5(STK11):c.399G>A (p.Val133=) rs757021648
NM_000455.5(STK11):c.440G>A (p.Arg147His) rs587780717
NM_000455.5(STK11):c.464+14G>A rs587782421
NM_000455.5(STK11):c.464+15C>T rs1057521355
NM_000455.5(STK11):c.464+3G>A rs1060499956
NM_000455.5(STK11):c.464G>A (p.Gly155Glu) rs1555737830
NM_000455.5(STK11):c.465-4G>A rs587780009
NM_000455.5(STK11):c.489C>T (p.Gly163=) rs1060499959
NM_000455.5(STK11):c.564C>T (p.Gly188=) rs786201344
NM_000455.5(STK11):c.579C>A (p.Ser193=) rs730881961
NM_000455.5(STK11):c.598-11C>T rs587782431
NM_000455.5(STK11):c.617C>T (p.Ala206Val) rs764244639
NM_000455.5(STK11):c.618G>C (p.Ala206=) rs370976710
NM_000455.5(STK11):c.693C>T (p.Phe231=) rs1568708275
NM_000455.5(STK11):c.69C>T (p.Asp23=) rs1599914867
NM_000455.5(STK11):c.735-16_735-15del rs775965325
NM_000455.5(STK11):c.735-6_735-2del rs759090799
NM_000455.5(STK11):c.840C>T (p.Pro280=) rs1471868090
NM_000455.5(STK11):c.842C>A (p.Pro281Gln) rs121913322
NM_000455.5(STK11):c.863-14C>G rs756001994
NM_000455.5(STK11):c.863-3C>T rs1599928254
NM_000455.5(STK11):c.863-5C>T rs1599928248
NM_000455.5(STK11):c.863-5_863-3del rs764739106
NM_000455.5(STK11):c.864G>A (p.Gly288=) rs2080787350
NM_000455.5(STK11):c.894C>G (p.Phe298Leu) rs199681533
NM_000455.5(STK11):c.920+7G>A rs2075607
NM_000455.5(STK11):c.920+7_920+8delinsCA rs1057517545
NM_000455.5(STK11):c.940C>T (p.Pro314Ser) rs758416485
NM_000455.5(STK11):c.942T>C (p.Pro314=) rs1256260277

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