ClinVar Miner

List of variants in gene STK11 reported by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
Download table as spreadsheet
HGVS dbSNP
NM_000455.4(STK11):c.*121A>C rs886054219
NM_000455.4(STK11):c.*16+10G>A rs587781180
NM_000455.4(STK11):c.*201G>A rs528679025
NM_000455.4(STK11):c.*202C>G rs886054220
NM_000455.4(STK11):c.*237C>A rs886054221
NM_000455.4(STK11):c.*317C>G rs550127419
NM_000455.4(STK11):c.*365C>G rs535975204
NM_000455.4(STK11):c.*372C>T rs886054222
NM_000455.4(STK11):c.*388A>G rs886054223
NM_000455.4(STK11):c.*413C>A rs533940465
NM_000455.4(STK11):c.*483_*484delCT rs545375742
NM_000455.4(STK11):c.*494T>A rs577030468
NM_000455.4(STK11):c.*616T>C rs10415095
NM_000455.4(STK11):c.*678G>A rs532639857
NM_000455.4(STK11):c.*685C>A rs111773256
NM_000455.4(STK11):c.*8C>T rs587782259
NM_000455.4(STK11):c.-1024C>T rs147615524
NM_000455.4(STK11):c.-1055C>T rs886054202
NM_000455.4(STK11):c.-106C>T rs886054213
NM_000455.4(STK11):c.-107dupT rs927999961
NM_000455.4(STK11):c.-1098G>A rs886054201
NM_000455.4(STK11):c.-127T>C rs532196225
NM_000455.4(STK11):c.-137C>T rs527710714
NM_000455.4(STK11):c.-193C>G rs561818770
NM_000455.4(STK11):c.-216A>C rs886054211
NM_000455.4(STK11):c.-229C>G rs886054210
NM_000455.4(STK11):c.-274C>T rs372994361
NM_000455.4(STK11):c.-2G>T rs774072752
NM_000455.4(STK11):c.-311C>T rs149756065
NM_000455.4(STK11):c.-387C>T rs886054209
NM_000455.4(STK11):c.-430C>T rs115594813
NM_000455.4(STK11):c.-447C>T rs867231569
NM_000455.4(STK11):c.-461G>A rs552610464
NM_000455.4(STK11):c.-520C>T rs886054208
NM_000455.4(STK11):c.-546G>A rs886054207
NM_000455.4(STK11):c.-55C>T rs886054215
NM_000455.4(STK11):c.-562G>C rs187649480
NM_000455.4(STK11):c.-577C>T rs560480063
NM_000455.4(STK11):c.-587G>C rs886054206
NM_000455.4(STK11):c.-635delC rs886054205
NM_000455.4(STK11):c.-723G>T rs886054204
NM_000455.4(STK11):c.-81A>G rs886054214
NM_000455.4(STK11):c.-925C>T rs886054203
NM_000455.4(STK11):c.1062C>G (p.Phe354Leu) rs59912467
NM_000455.4(STK11):c.1211C>T (p.Ser404Phe) rs200078204
NM_000455.4(STK11):c.1249G>T (p.Ala417Ser) rs587782876
NM_000455.4(STK11):c.264C>A (p.Ile88=) rs56354945
NM_000455.4(STK11):c.357C>T (p.Asn119=) rs372511774
NM_000455.4(STK11):c.369G>A (p.Gln123=) rs140112347
NM_000455.4(STK11):c.374+11C>T rs368923696
NM_000455.4(STK11):c.464+9G>A rs376313955
NM_000455.4(STK11):c.597+14delA rs536282050
NM_000455.4(STK11):c.597+21dupG rs534445875
NM_000455.4(STK11):c.666C>T (p.Pro222=) rs542189325
NM_000455.4(STK11):c.723T>C (p.Ala241=) rs533550278
NM_000455.4(STK11):c.746C>T (p.Thr249Ile) rs886054218
NM_000455.4(STK11):c.816C>T (p.Tyr272=) rs9282859
NM_000455.4(STK11):c.825G>A (p.Pro275=) rs202011521
NM_000455.4(STK11):c.8T>G (p.Val3Gly) rs886054216
NM_000455.4(STK11):c.920+7G>C rs2075607

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.