ClinVar Miner

List of variants in gene STK11 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 78
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.*629C>T rs368014506 0.00230
NM_000455.5(STK11):c.-893C>T rs867696290 0.00167
NM_000455.5(STK11):c.*16+10G>A rs587781180 0.00077
NM_000455.5(STK11):c.-590C>T rs1050439702 0.00048
NM_000455.5(STK11):c.1185A>G (p.Thr395=) rs370207155 0.00047
NM_000455.5(STK11):c.*631G>A rs565456677 0.00036
NM_000455.5(STK11):c.1284G>A (p.Ser428=) rs369097329 0.00035
NM_000455.5(STK11):c.*202C>G rs886054220 0.00034
NM_000455.5(STK11):c.*347G>A rs950829868 0.00034
NM_000455.5(STK11):c.-775G>A rs868538577 0.00032
NM_000455.5(STK11):c.*668C>A rs1045495924 0.00025
NM_000455.5(STK11):c.-806C>T rs1368940227 0.00021
NM_000455.5(STK11):c.1296G>A (p.Gln432=) rs587781179 0.00020
NM_000455.5(STK11):c.*678G>A rs532639857 0.00019
NM_000455.5(STK11):c.618G>A (p.Ala206=) rs370976710 0.00018
NM_000455.5(STK11):c.*332C>T rs1034644018 0.00016
NM_000455.5(STK11):c.-461G>A rs552610464 0.00016
NM_000455.5(STK11):c.-55C>T rs886054215 0.00015
NM_000455.5(STK11):c.825G>A (p.Pro275=) rs202011521 0.00011
NM_000455.5(STK11):c.*348C>G rs983491595 0.00007
NM_000455.5(STK11):c.357C>T (p.Asn119=) rs372511774 0.00007
NM_000455.5(STK11):c.*201G>A rs528679025 0.00006
NM_000455.5(STK11):c.-447C>T rs867231569 0.00006
NM_000455.5(STK11):c.*113T>G rs760703775 0.00005
NM_000455.5(STK11):c.*413C>A rs533940465 0.00005
NM_000455.5(STK11):c.*603T>G rs1220161134 0.00005
NM_000455.5(STK11):c.920+6C>T rs730881964 0.00005
NM_000455.5(STK11):c.-520C>T rs886054208 0.00004
NM_000455.5(STK11):c.316C>T (p.Arg106Trp) rs587782115 0.00004
NM_000455.5(STK11):c.374+11C>T rs368923696 0.00004
NM_000455.5(STK11):c.*237C>A rs886054221 0.00003
NM_000455.5(STK11):c.-136C>T rs777480684 0.00003
NM_000455.5(STK11):c.-229C>G rs886054210 0.00003
NM_000455.5(STK11):c.-546G>A rs886054207 0.00003
NM_000455.5(STK11):c.-81A>G rs886054214 0.00003
NM_000455.5(STK11):c.374+9T>A rs762297795 0.00003
NM_000455.5(STK11):c.*388A>G rs886054223 0.00002
NM_000455.5(STK11):c.-128G>T rs1340865672 0.00002
NM_000455.5(STK11):c.-835C>T rs1169622696 0.00002
NM_000455.5(STK11):c.*372C>T rs886054222 0.00001
NM_000455.5(STK11):c.-774C>T rs1388166210 0.00001
NM_000455.5(STK11):c.1249G>T (p.Ala417Ser) rs587782876 0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=) rs777872290 0.00001
NM_000455.5(STK11):c.*121A>C rs886054219
NM_000455.5(STK11):c.*142G>T rs2080836128
NM_000455.5(STK11):c.*411T>C rs1463819473
NM_000455.5(STK11):c.*565G>A rs1027644340
NM_000455.5(STK11):c.*634G>A rs903030190
NM_000455.5(STK11):c.*701C>A rs1015269208
NM_000455.5(STK11):c.-106C>T rs886054213
NM_000455.5(STK11):c.-107dup rs927999961
NM_000455.5(STK11):c.-1097G>T rs944606544
NM_000455.5(STK11):c.-1098G>A rs886054201
NM_000455.5(STK11):c.-150G>A rs1453851790
NM_000455.5(STK11):c.-193C>G rs561818770
NM_000455.5(STK11):c.-216A>C rs886054211
NM_000455.5(STK11):c.-302G>A rs935371253
NM_000455.5(STK11):c.-333G>T rs1208293548
NM_000455.5(STK11):c.-387C>T rs886054209
NM_000455.5(STK11):c.-388C>T rs2080666270
NM_000455.5(STK11):c.-474G>A rs866050909
NM_000455.5(STK11):c.-587G>C rs886054206
NM_000455.5(STK11):c.-635del rs886054205
NM_000455.5(STK11):c.-723G>T rs886054204
NM_000455.5(STK11):c.-783G>A rs2080662705
NM_000455.5(STK11):c.-925C>T rs886054203
NM_000455.5(STK11):c.312G>T (p.Arg104Ser) rs780749732
NM_000455.5(STK11):c.399G>C (p.Val133=) rs757021648
NM_000455.5(STK11):c.464+14G>A rs587782421
NM_000455.5(STK11):c.606C>G (p.His202Gln) rs2080775908
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.668A>G (p.Glu223Gly) rs2080776621
NM_000455.5(STK11):c.69C>T (p.Asp23=) rs1599914867
NM_000455.5(STK11):c.746C>T (p.Thr249Ile) rs886054218
NM_000455.5(STK11):c.791T>A (p.Phe264Tyr) rs876658978
NM_000455.5(STK11):c.8T>G (p.Val3Gly) rs886054216
NM_000455.5(STK11):c.942T>C (p.Pro314=) rs1256260277

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.