ClinVar Miner

List of variants in gene STK11 reported as uncertain significance for not specified

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Gene type:
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Total variants: 64
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HGVS dbSNP
NM_000455.4(STK11):c.*16+20G>A rs1044825795
NM_000455.4(STK11):c.*16+5G>A rs876661268
NM_000455.4(STK11):c.*17-10C>T rs926599353
NM_000455.4(STK11):c.*35G>T rs1016942739
NM_000455.4(STK11):c.*8C>T rs587782259
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.1036G>A (p.Gly346Ser) rs375431906
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.1044C>T (p.Asp348=) rs778274196
NM_000455.4(STK11):c.1062C>G (p.Phe354Leu) rs59912467
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.116G>T (p.Arg39Leu) rs786203250
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.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.1248G>C (p.Lys416Asn) rs1459406168
NM_000455.4(STK11):c.1258G>A (p.Ala420Thr) rs762482152
NM_000455.4(STK11):c.125G>T (p.Arg42Leu) rs148830698
NM_000455.4(STK11):c.1262_1263del (p.Ser421fs) rs876661216
NM_000455.4(STK11):c.1283C>G (p.Ser428Trp) rs587781537
NM_000455.4(STK11):c.1286C>T (p.Ala429Val) rs757369900
NM_000455.4(STK11):c.143A>G (p.Lys48Arg) rs766776431
NM_000455.4(STK11):c.159_170del (p.Asp53_Gly56del) rs1131690953
NM_000455.4(STK11):c.189G>A (p.Val63=) rs1342321548
NM_000455.4(STK11):c.298C>G (p.Gln100Glu) rs757841535
NM_000455.4(STK11):c.318G>T (p.Arg106=) rs777784520
NM_000455.4(STK11):c.348G>T (p.Val116=) rs774482643
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.434A>G (p.Glu145Gly) rs369764220
NM_000455.4(STK11):c.441T>C (p.Arg147=) rs786201456
NM_000455.4(STK11):c.449T>C (p.Val150Ala) rs587781802
NM_000455.4(STK11):c.464+5G>A rs587781681
NM_000455.4(STK11):c.464+8C>T rs863224669
NM_000455.4(STK11):c.465-5C>A rs567202367
NM_000455.4(STK11):c.465-8G>A rs878853990
NM_000455.4(STK11):c.527A>C (p.Asp176Ala) rs1064794805
NM_000455.4(STK11):c.566C>T (p.Thr189Ile) rs587781515
NM_000455.4(STK11):c.613G>A (p.Ala205Thr) rs730881981
NM_000455.4(STK11):c.618G>A (p.Ala206=) rs370976710
NM_000455.4(STK11):c.710A>G (p.Asp237Gly) rs1555738459
NM_000455.4(STK11):c.734+20G>A rs375315233
NM_000455.4(STK11):c.735-16_735-15delTC rs775965325
NM_000455.4(STK11):c.838_839delinsGT (p.Pro280Val) rs786205863
NM_000455.4(STK11):c.841_842delCC (p.Pro281Alafs) rs121913321
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.876C>T (p.Tyr292=) rs148928808
NM_000455.4(STK11):c.894C>A (p.Phe298Leu) rs199681533
NM_000455.4(STK11):c.90C>T (p.Asp30=) rs771765869
NM_000455.4(STK11):c.920+5G>A rs587780013
NM_000455.4(STK11):c.921-9C>T rs761688641
NM_000455.4(STK11):c.970C>G (p.Pro324Ala) rs549474196
NM_000455.4(STK11):c.976C>A (p.Pro326Thr) rs771632414

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