ClinVar Miner

List of variants in gene STK11 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 59
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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.920+32G>A rs374147918 0.00080
NM_000455.5(STK11):c.597+14del rs536282050 0.00067
NM_000455.5(STK11):c.426C>T (p.Ser142=) rs758448869 0.00053
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.1194G>A (p.Ala398=) rs184271025 0.00023
NM_000455.5(STK11):c.597+8C>T rs565387911 0.00017
NM_000455.5(STK11):c.787T>C (p.Leu263=) rs372378119 0.00010
NM_000455.5(STK11):c.598-7G>A rs377502057 0.00008
NM_000455.5(STK11):c.-2G>T rs774072752 0.00007
NM_000455.5(STK11):c.734+20G>A rs375315233 0.00007
NM_000455.5(STK11):c.1257C>T (p.Ser419=) rs375328708 0.00006
NM_000455.5(STK11):c.921-10G>A rs183406870 0.00006
NM_000455.5(STK11):c.375-7G>A rs587781176 0.00005
NM_000455.5(STK11):c.465-18G>T rs587781177 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.1109-5C>T rs587782020 0.00004
NM_000455.5(STK11):c.1200G>A (p.Leu400=) rs368661707 0.00004
NM_000455.5(STK11):c.374+11C>T rs368923696 0.00004
NM_000455.5(STK11):c.432G>A (p.Pro144=) rs376788924 0.00004
NM_000455.5(STK11):c.795G>A (p.Glu265=) rs730881963 0.00004
NM_000455.5(STK11):c.374+9T>A rs762297795 0.00003
NM_000455.5(STK11):c.464+10C>T rs587782445 0.00003
NM_000455.5(STK11):c.552C>T (p.Leu184=) rs587780719 0.00003
NM_000455.5(STK11):c.57G>C (p.Ser19=) rs748698151 0.00003
NM_000455.5(STK11):c.828C>T (p.Gly276=) rs200824447 0.00002
NM_000455.5(STK11):c.921-24G>A rs760399075 0.00002
NM_000455.5(STK11):c.1109-4C>T rs1407794756 0.00001
NM_000455.5(STK11):c.1137C>T (p.His379=) rs786201505 0.00001
NM_000455.5(STK11):c.1251C>T (p.Ala417=) rs1060503786 0.00001
NM_000455.5(STK11):c.312G>A (p.Arg104=) rs780749732 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.579C>T (p.Ser193=) rs730881961 0.00001
NM_000455.5(STK11):c.594C>T (p.Ala198=) rs772940660 0.00001
NM_000455.5(STK11):c.621C>T (p.Asp207=) rs569380138 0.00001
NM_000455.5(STK11):c.734+19C>T rs372338167 0.00001
NM_000455.5(STK11):c.765C>T (p.Phe255=) rs769912677 0.00001
NM_000455.5(STK11):c.843G>A (p.Pro281=) rs756095270 0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=) rs777872290 0.00001
NM_000455.5(STK11):c.863-6C>T rs757276643 0.00001
NM_000455.5(STK11):c.882G>A (p.Pro294=) rs587781178 0.00001
NM_000455.5(STK11):c.921-9C>T rs761688641 0.00001
NM_000455.5(STK11):c.*9G>A rs1057522868
NM_000455.5(STK11):c.1230C>T (p.Ala410=) rs864622171
NM_000455.5(STK11):c.129C>G (p.Ala43=) rs1555734970
NM_000455.5(STK11):c.240C>T (p.Leu80=) rs2145405739
NM_000455.5(STK11):c.351A>G (p.Leu117=) rs2080758837
NM_000455.5(STK11):c.464+10C>G
NM_000455.5(STK11):c.464+32CGGGGGC[3] rs58579265
NM_000455.5(STK11):c.609G>C (p.Pro203=) rs786201228
NM_000455.5(STK11):c.726G>T (p.Gly242=) rs776823114
NM_000455.5(STK11):c.734+14C>T rs763346212
NM_000455.5(STK11):c.777C>T (p.Asn259=) rs786201105
NM_000455.5(STK11):c.920+7G>A rs2075607
NM_000455.5(STK11):c.921-29_921-28del rs1568711791

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