ClinVar Miner

List of variants in gene STK11 reported by Mendelics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 50
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000455.5(STK11):c.894C>A (p.Phe298Leu) rs199681533 0.00100
NM_000455.5(STK11):c.945G>A (p.Pro315=) rs376329042 0.00060
NM_000455.5(STK11):c.426C>T (p.Ser142=) rs758448869 0.00053
NM_000455.5(STK11):c.1211C>T (p.Ser404Phe) rs200078204 0.00051
NM_000455.5(STK11):c.1185A>G (p.Thr395=) rs370207155 0.00047
NM_000455.5(STK11):c.*8C>T rs587782259 0.00027
NM_000455.5(STK11):c.-137C>T rs527710714 0.00027
NM_000455.5(STK11):c.-461G>A rs552610464 0.00016
NM_000455.5(STK11):c.920+12C>T rs186518799 0.00014
NM_000455.5(STK11):c.825G>A (p.Pro275=) rs202011521 0.00011
NM_000455.5(STK11):c.920+5G>A rs587780013 0.00008
NM_000455.5(STK11):c.842C>T (p.Pro281Leu) rs121913322 0.00006
NM_000455.5(STK11):c.375-7G>A rs587781176 0.00005
NM_000455.5(STK11):c.-167C>T rs1273032629 0.00004
NM_000455.5(STK11):c.613G>A (p.Ala205Thr) rs730881981 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.911G>A (p.Arg304Gln) rs376280361 0.00003
NM_000455.5(STK11):c.-4C>T rs1181075160 0.00001
NM_000455.5(STK11):c.1148G>A (p.Arg383His) rs730881990 0.00001
NM_000455.5(STK11):c.1163A>G (p.Lys388Arg) rs756877141 0.00001
NM_000455.5(STK11):c.375-33C>T rs1246317136 0.00001
NM_000455.5(STK11):c.465-3C>T rs587781619 0.00001
NM_000455.5(STK11):c.559G>A (p.Gly187Ser) rs587782032 0.00001
NM_000455.5(STK11):c.877G>A (p.Glu293Lys) rs398123405 0.00001
NM_000455.5(STK11):c.921-9C>T rs761688641 0.00001
NM_000455.5(STK11):c.*16+6G>A rs2145436787
NM_000455.5(STK11):c.*16+8_*16+17dup rs1453954065
NM_000455.5(STK11):c.*17-6C>G rs866505758
NM_000455.5(STK11):c.-107dup rs927999961
NM_000455.5(STK11):c.-280C>A rs893914050
NM_000455.5(STK11):c.-551C>T rs1316450313
NM_000455.5(STK11):c.-95G>T rs1323638467
NM_000455.5(STK11):c.-99C>T rs1407068597
NM_000455.5(STK11):c.1128G>T (p.Glu376Asp) rs747018506
NM_000455.5(STK11):c.1178A>G (p.Asn393Ser) rs1060499965
NM_000455.5(STK11):c.1180G>A (p.Gly394Ser) rs768780695
NM_000455.5(STK11):c.1225C>T (p.Arg409Trp) rs368466538
NM_000455.5(STK11):c.188T>C (p.Val63Ala) rs1568690276
NM_000455.5(STK11):c.217T>C (p.Cys73Arg) rs1568690354
NM_000455.5(STK11):c.375-13C>T rs1568705244
NM_000455.5(STK11):c.458C>A (p.Ala153Asp) rs1555737824
NM_000455.5(STK11):c.465-4G>A rs587780009
NM_000455.5(STK11):c.617C>T (p.Ala206Val) rs764244639
NM_000455.5(STK11):c.784A>T (p.Lys262Ter) rs2145426930
NM_000455.5(STK11):c.82dup (p.Arg28fs) rs1568689930
NM_000455.5(STK11):c.843dup (p.Leu282fs) rs1131690949
NM_000455.5(STK11):c.863-5C>T rs1599928248
NM_000455.5(STK11):c.920+1G>A rs1131690920
NM_000455.5(STK11):c.970C>T (p.Pro324Ser) rs549474196

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.