ClinVar Miner

List of variants reported as uncertain significance for adenocarcinoma by Mendelics

Included ClinVar conditions (112):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 82
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000245.4(MET):c.406G>A (p.Val136Ile) rs199701987 0.00058
NM_002529.4(NTRK1):c.940C>T (p.Arg314Cys) rs137994522 0.00027
NM_000245.4(MET):c.1771C>T (p.Arg591Trp) rs45602940 0.00015
NM_002529.4(NTRK1):c.1661G>A (p.Arg554Gln) rs764417252 0.00013
NM_002529.4(NTRK1):c.570C>G (p.Ser190Arg) rs138608619 0.00013
NM_002529.4(NTRK1):c.1808C>G (p.Ser603Cys) rs188270548 0.00011
NM_002529.4(NTRK1):c.1187C>T (p.Ser396Leu) rs199646180 0.00009
NM_004360.5(CDH1):c.1996A>C (p.Asn666His) rs150427791 0.00009
NM_000245.4(MET):c.803C>T (p.Thr268Ile) rs757427533 0.00007
NM_004360.5(CDH1):c.854C>T (p.Thr285Ile) rs587781634 0.00007
NM_004360.5(CDH1):c.214G>A (p.Asp72Asn) rs35606263 0.00006
NM_000245.4(MET):c.1988C>T (p.Ser663Leu) rs376459715 0.00005
NM_000245.4(MET):c.4007G>A (p.Arg1336Gln) rs369312680 0.00005
NM_000245.4(MET):c.2825C>T (p.Ser942Leu) rs375576430 0.00004
NM_000245.4(MET):c.428G>A (p.Arg143Gln) rs35469582 0.00004
NM_002529.4(NTRK1):c.355C>T (p.Arg119Cys) rs757031354 0.00004
NM_004360.5(CDH1):c.2387G>A (p.Arg796Gln) rs587782549 0.00004
NM_000245.4(MET):c.3356G>C (p.Gly1119Ala) rs201037977 0.00003
NM_000245.4(MET):c.4100C>G (p.Ser1367Cys) rs747239403 0.00003
NM_001007792.1(NTRK1):c.119C>A (p.Ala40Glu) rs779943666 0.00003
NM_004360.5(CDH1):c.1417G>A (p.Val473Ile) rs36087757 0.00003
NM_004360.5(CDH1):c.2074G>A (p.Ala692Thr) rs376854556 0.00003
NM_002529.4(NTRK1):c.1463G>A (p.Gly488Asp) rs760222071 0.00002
NM_004360.5(CDH1):c.1004G>A (p.Arg335Gln) rs373364873 0.00002
NM_004360.5(CDH1):c.2359G>A (p.Val787Ile) rs766270336 0.00002
NM_004360.5(CDH1):c.371G>A (p.Arg124His) rs115418995 0.00002
NM_000245.4(MET):c.1171G>A (p.Gly391Arg) rs587778443 0.00001
NM_000245.4(MET):c.1238G>A (p.Arg413His) rs375391602 0.00001
NM_000245.4(MET):c.1444G>A (p.Asp482Asn) rs863224694 0.00001
NM_000245.4(MET):c.1451A>G (p.His484Arg) rs781545528 0.00001
NM_000245.4(MET):c.1904A>G (p.Asn635Ser) rs773826297 0.00001
NM_000245.4(MET):c.215T>C (p.Val72Ala) rs973796037 0.00001
NM_000245.4(MET):c.2192G>A (p.Arg731Gln) rs45446492 0.00001
NM_000245.4(MET):c.2716G>A (p.Glu906Lys) rs778115147 0.00001
NM_000245.4(MET):c.362T>C (p.Val121Ala) rs879254339 0.00001
NM_000245.4(MET):c.3878C>G (p.Thr1293Ser) rs779121848 0.00001
NM_001007792.1(NTRK1):c.10-562dup rs761392074 0.00001
NM_002529.4(NTRK1):c.1381G>A (p.Gly461Arg) rs761247634 0.00001
NM_002529.4(NTRK1):c.2105G>A (p.Arg702His) rs200022271 0.00001
NM_002529.4(NTRK1):c.422A>C (p.Gln141Pro) rs1306924167 0.00001
NM_002529.4(NTRK1):c.842A>G (p.Asn281Ser) rs547972574 0.00001
NM_004360.5(CDH1):c.1136C>T (p.Thr379Met) rs587782856 0.00001
NM_004360.5(CDH1):c.2351G>A (p.Arg784His) rs763203357 0.00001
NM_004360.5(CDH1):c.2638G>A (p.Glu880Lys) rs34507583 0.00001
NM_004360.5(CDH1):c.79C>T (p.Pro27Ser) rs878854696 0.00001
NM_000245.4(MET):c.1125C>G (p.Asn375Lys) rs776693512
NM_000245.4(MET):c.135C>G (p.Asn45Lys) rs1562883006
NM_000245.4(MET):c.1393-1G>T rs1584921909
NM_000245.4(MET):c.1496A>G (p.Asn499Ser) rs1253878709
NM_000245.4(MET):c.1508T>A (p.Leu503Gln) rs1562908826
NM_000245.4(MET):c.1866G>C (p.Leu622Phe) rs1562921668
NM_000245.4(MET):c.1933G>A (p.Gly645Arg) rs763849125
NM_000245.4(MET):c.236A>G (p.Gln79Arg) rs1562883214
NM_000245.4(MET):c.2568T>G (p.Asn856Lys) rs118057172
NM_000245.4(MET):c.2672C>G (p.Ala891Gly) rs1562929174
NM_000245.4(MET):c.2887+5A>T rs752292538
NM_000245.4(MET):c.2892G>A (p.Leu964=) rs1584955273
NM_000245.4(MET):c.2995G>C (p.Glu999Gln) rs1404824650
NM_000245.4(MET):c.3352A>G (p.Ile1118Val) rs755234697
NM_000245.4(MET):c.3991T>G (p.Ser1331Ala) rs1562941559
NM_000245.4(MET):c.4041G>T (p.Glu1347Asp) rs1562941622
NM_000245.4(MET):c.410A>G (p.Asn137Ser) rs1584876716
NM_000245.4(MET):c.4140C>A (p.Asp1380Glu) rs370368651
NM_000245.4(MET):c.569A>G (p.Asp190Gly) rs1028165414
NM_000245.4(MET):c.728A>G (p.Asp243Gly) rs1562883992
NM_000245.4(MET):c.925A>C (p.Thr309Pro) rs35601148
NM_001007792.1(NTRK1):c.37del (p.Val13fs) rs1451820799
NM_002529.4(NTRK1):c.1525G>C (p.Asp509His) rs1035934237
NM_004360.5(CDH1):c.1008+8G>T rs990193541
NM_004360.5(CDH1):c.1468G>A (p.Glu490Lys) rs1555516147
NM_004360.5(CDH1):c.1721T>G (p.Val574Gly) rs1567512117
NM_004360.5(CDH1):c.1784C>G (p.Pro595Arg) rs1555516843
NM_004360.5(CDH1):c.1937-4C>T rs1057523153
NM_004360.5(CDH1):c.2204C>A (p.Ala735Glu) rs587782464
NM_004360.5(CDH1):c.2467A>G (p.Thr823Ala) rs878854686
NM_004360.5(CDH1):c.29C>A (p.Ala10Glu) rs1375360857
NM_004360.5(CDH1):c.32T>G (p.Leu11Arg) rs1393903966
NM_004360.5(CDH1):c.417G>C (p.Leu139Phe) rs1057521858
NM_004360.5(CDH1):c.778C>T (p.Pro260Ser) rs1567505715
NM_004360.5(CDH1):c.949T>C (p.Phe317Leu) rs1555515643
NM_004360.5(CDH1):c.976A>G (p.Ile326Val) rs1567506764
NM_024529.5(CDC73):c.1450C>T (p.Arg484Cys) rs1225502334

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.