ClinVar Miner

List of variants in gene STK11 reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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Gene type:
ClinVar version:
Total variants: 58
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HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.920+5G>A rs587780013 0.00008
NM_000455.5(STK11):c.1127A>C (p.Glu376Ala) rs373888280 0.00007
NM_000455.5(STK11):c.1254C>G (p.Cys418Trp) rs587780715 0.00005
NM_000455.5(STK11):c.298C>G (p.Gln100Glu) rs757841535 0.00004
NM_000455.5(STK11):c.316C>T (p.Arg106Trp) rs587782115 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.1193C>T (p.Ala398Val) rs768058962 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.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.1135C>A (p.His379Asn) rs762124698 0.00001
NM_000455.5(STK11):c.1142G>C (p.Gly381Ala) rs765419233 0.00001
NM_000455.5(STK11):c.1147C>T (p.Arg383Cys) rs535449626 0.00001
NM_000455.5(STK11):c.1148G>A (p.Arg383His) rs730881990 0.00001
NM_000455.5(STK11):c.1151G>A (p.Arg384Gln) rs371102112 0.00001
NM_000455.5(STK11):c.1163A>G (p.Lys388Arg) rs756877141 0.00001
NM_000455.5(STK11):c.116G>T (p.Arg39Leu) rs786203250 0.00001
NM_000455.5(STK11):c.1175T>C (p.Met392Thr) rs876661013 0.00001
NM_000455.5(STK11):c.1189G>T (p.Ala397Ser) rs587780008 0.00001
NM_000455.5(STK11):c.1217C>T (p.Ala406Val) rs748202003 0.00001
NM_000455.5(STK11):c.1248G>C (p.Lys416Asn) rs1459406168 0.00001
NM_000455.5(STK11):c.1276C>T (p.Arg426Trp) rs587782687 0.00001
NM_000455.5(STK11):c.299A>G (p.Gln100Arg) rs1060499957 0.00001
NM_000455.5(STK11):c.301C>G (p.Leu101Val) rs587780716 0.00001
NM_000455.5(STK11):c.358G>A (p.Glu120Lys) rs775595174 0.00001
NM_000455.5(STK11):c.427G>A (p.Val143Met) rs779987540 0.00001
NM_000455.5(STK11):c.434A>G (p.Glu145Gly) rs369764220 0.00001
NM_000455.5(STK11):c.449T>C (p.Val150Ala) rs587781802 0.00001
NM_000455.5(STK11):c.464+8del rs878853989 0.00001
NM_000455.5(STK11):c.817G>A (p.Ala273Thr) rs587782199 0.00001
NM_000455.5(STK11):c.839C>T (p.Pro280Leu) rs1356762205 0.00001
NM_000455.5(STK11):c.921-9C>T rs761688641 0.00001
NM_000455.5(STK11):c.947C>G (p.Ala316Gly) rs751709130 0.00001
NM_000455.5(STK11):c.94A>G (p.Thr32Ala) rs755210880 0.00001
NM_000455.5(STK11):c.103A>G (p.Ile35Val) rs587781437
NM_000455.5(STK11):c.113C>G (p.Pro38Arg) rs1568690036
NM_000455.5(STK11):c.1180G>A (p.Gly394Ser) rs768780695
NM_000455.5(STK11):c.1205C>G (p.Thr402Ser) rs750055790
NM_000455.5(STK11):c.1243C>T (p.Arg415Cys) rs864622448
NM_000455.5(STK11):c.1282T>A (p.Ser428Thr) rs1064793938
NM_000455.5(STK11):c.1283C>G (p.Ser428Trp) rs587781537
NM_000455.5(STK11):c.374+6del rs2080759180
NM_000455.5(STK11):c.397G>A (p.Val133Met) rs567769257
NM_000455.5(STK11):c.407T>C (p.Met136Thr) rs1060499958
NM_000455.5(STK11):c.425G>A (p.Ser142Asn) rs1568705518
NM_000455.5(STK11):c.463G>A (p.Gly155Arg) rs763353991
NM_000455.5(STK11):c.465-5C>A rs567202367
NM_000455.5(STK11):c.621C>A (p.Asp207Glu)
NM_000455.5(STK11):c.634A>G (p.Thr212Ala) rs1300171938
NM_000455.5(STK11):c.735-3A>G rs864622128
NM_000455.5(STK11):c.767A>T (p.Glu256Val) rs2145426849
NM_000455.5(STK11):c.863-5_863-3del rs764739106
NM_000455.5(STK11):c.920+7G>A rs2075607
NM_000455.5(STK11):c.946G>T (p.Ala316Ser) rs864622303

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