ClinVar Miner

List of variants studied for Hereditary diffuse gastric adenocarcinoma by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 110
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004360.4(CDH1):c.*2047A>G rs8045438 0.98944
NM_004360.5(CDH1):c.48+6C>T rs3743674 0.80384
NM_004360.5(CDH1):c.2076T>C (p.Ala692=) rs1801552 0.70379
NM_004360.5(CDH1):c.*1120T>C rs13689 0.18034
NM_004360.5(CDH1):c.*54C>T rs1801026 0.17023
NM_004360.5(CDH1):c.1937-13T>C rs2276330 0.09635
NM_004360.5(CDH1):c.*589C>T rs8049282 0.07789
NM_004360.5(CDH1):c.531+10G>C rs33963999 0.03907
NM_004360.5(CDH1):c.2253C>T (p.Asn751=) rs33964119 0.03869
NM_004360.5(CDH1):c.48+5C>G rs77312180 0.03370
NM_004360.5(CDH1):c.1896C>T (p.His632=) rs33969373 0.02054
NM_004360.5(CDH1):c.*621C>T rs33956791 0.02011
NM_004360.5(CDH1):c.*410A>T rs33956133 0.01714
NM_004360.5(CDH1):c.2634C>T (p.Gly878=) rs2229044 0.01638
NM_004360.5(CDH1):c.*1873G>A rs35779350 0.01533
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr) rs33935154 0.01412
NM_004360.5(CDH1):c.933C>G (p.Leu311=) rs35539711 0.00974
NM_004360.5(CDH1):c.-71C>G rs34033771 0.00927
NM_004360.4(CDH1):c.*2050T>A rs181705992 0.00746
NM_004360.5(CDH1):c.*1835T>C rs13339481 0.00738
NM_004360.5(CDH1):c.*1662G>C rs33967108 0.00618
NM_004360.5(CDH1):c.*988G>A rs9282653 0.00604
NM_004360.5(CDH1):c.1774G>A (p.Ala592Thr) rs35187787 0.00311
NM_004360.5(CDH1):c.1680G>C (p.Thr560=) rs35741240 0.00261
NM_004360.5(CDH1):c.345G>A (p.Thr115=) rs1801023 0.00236
NM_004360.5(CDH1):c.-54G>C rs5030874 0.00208
NM_004360.5(CDH1):c.2292C>T (p.Asp764=) rs61747636 0.00159
NM_004360.5(CDH1):c.2440-6C>G rs139757930 0.00145
NM_004360.5(CDH1):c.88C>A (p.Pro30Thr) rs139866691 0.00129
NM_004360.5(CDH1):c.*1693G>T rs138279201 0.00069
NM_004360.5(CDH1):c.*746C>A rs140240766 0.00069
NM_004360.5(CDH1):c.*424T>A rs867174076 0.00056
NM_004360.5(CDH1):c.*346A>T rs754600872 0.00045
NM_004360.5(CDH1):c.1744C>T (p.Leu582=) rs1801025 0.00045
NM_004360.5(CDH1):c.808T>G (p.Ser270Ala) rs587776399 0.00038
NM_004360.5(CDH1):c.*623A>G rs142125691 0.00034
NM_004360.5(CDH1):c.892G>A (p.Ala298Thr) rs142822590 0.00028
NM_004360.5(CDH1):c.2413G>A (p.Asp805Asn) rs200894246 0.00026
NM_004360.5(CDH1):c.*1872C>T rs545034372 0.00022
NM_004360.5(CDH1):c.1018A>G (p.Thr340Ala) rs116093741 0.00022
NM_004360.5(CDH1):c.2589C>T (p.Asn863=) rs115817750 0.00022
NM_004360.5(CDH1):c.33G>C (p.Leu11=) rs730881654 0.00022
NM_004360.5(CDH1):c.*196T>G rs576484193 0.00021
NM_004360.5(CDH1):c.*1545T>C rs186584057 0.00011
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly) rs121964872 0.00011
NM_004360.5(CDH1):c.2451G>A (p.Ala817=) rs149450874 0.00010
NM_004360.5(CDH1):c.1359C>T (p.His453=) rs114861467 0.00009
NM_004360.5(CDH1):c.1888C>G (p.Leu630Val) rs2276331 0.00009
NM_004360.5(CDH1):c.894C>T (p.Ala298=) rs139110184 0.00009
NM_004360.5(CDH1):c.1020G>A (p.Thr340=) rs61747632 0.00008
NM_004360.5(CDH1):c.1298A>G (p.Asp433Gly) rs376097289 0.00007
NM_004360.5(CDH1):c.*1076T>C rs541517386 0.00006
NM_004360.5(CDH1):c.*1691G>T rs373181046 0.00006
NM_004360.5(CDH1):c.*192C>T rs576309125 0.00006
NM_004360.5(CDH1):c.*575A>C rs886052242 0.00006
NM_004360.5(CDH1):c.*615G>A rs148655354 0.00006
NM_004360.5(CDH1):c.*959C>A rs886052243 0.00006
NM_004360.5(CDH1):c.393C>T (p.Ser131=) rs145430811 0.00006
NM_004360.5(CDH1):c.*1049A>C rs886052244 0.00004
NM_004360.5(CDH1):c.*1285T>C rs369689471 0.00004
NM_004360.5(CDH1):c.*193G>C rs886052238 0.00004
NM_004360.5(CDH1):c.-41C>A rs730881658 0.00004
NM_004360.5(CDH1):c.-63C>A rs572272864 0.00004
NM_004360.5(CDH1):c.1023T>C (p.Tyr341=) rs587776398 0.00004
NM_004360.5(CDH1):c.2165-15C>A rs552874184 0.00004
NM_004360.5(CDH1):c.2280C>T (p.Gly760=) rs768547540 0.00004
NM_004360.5(CDH1):c.*209C>T rs35942505 0.00003
NM_004360.5(CDH1):c.*409T>A rs778711236 0.00003
NM_004360.5(CDH1):c.1689C>T (p.Ala563=) rs587780786 0.00003
NM_004360.5(CDH1):c.184G>A (p.Gly62Ser) rs587781898 0.00003
NM_004360.5(CDH1):c.2331C>T (p.Asp777=) rs114265540 0.00003
NM_004360.5(CDH1):c.304G>A (p.Ala102Thr) rs368492235 0.00003
NM_004360.5(CDH1):c.671G>A (p.Arg224His) rs201511530 0.00003
NM_004360.5(CDH1):c.*1435A>T rs886052245 0.00002
NM_004360.5(CDH1):c.*582C>A rs920956371 0.00002
NM_004360.5(CDH1):c.2079C>T (p.Gly693=) rs771993728 0.00002
NM_004360.5(CDH1):c.*172A>C rs886052237 0.00001
NM_004360.5(CDH1):c.*1765A>G rs1343770513 0.00001
NM_004360.5(CDH1):c.*774A>G rs549231645 0.00001
NM_004360.5(CDH1):c.1315G>A (p.Ala439Thr) rs758764445 0.00001
NM_004360.5(CDH1):c.150C>A (p.Arg50=) rs786201262 0.00001
NM_004360.5(CDH1):c.1843A>G (p.Ile615Val) rs1003012321 0.00001
NM_004360.5(CDH1):c.1936A>G (p.Thr646Ala) rs771064558 0.00001
NM_004360.5(CDH1):c.2219C>A (p.Pro740His) rs730881669 0.00001
NM_004360.5(CDH1):c.2505T>C (p.Tyr835=) rs786202613 0.00001
NM_004360.5(CDH1):c.370C>T (p.Arg124Cys) rs748086082 0.00001
NM_004360.5(CDH1):c.462A>G (p.Arg154=) rs1057520261 0.00001
NM_004360.5(CDH1):c.604G>A (p.Val202Ile) rs546716073 0.00001
NM_004360.5(CDH1):c.794A>T (p.Glu265Val) rs587782728 0.00001
NM_004360.5(CDH1):c.867G>A (p.Ala289=) rs754143182 0.00001
NM_004360.5(CDH1):c.*1176T>G rs9282654
NM_004360.5(CDH1):c.*1591T>C rs886052246
NM_004360.5(CDH1):c.*1974_*1978del rs557163298
NM_004360.5(CDH1):c.*221del rs145920869
NM_004360.5(CDH1):c.*221dup rs145920869
NM_004360.5(CDH1):c.*236C>T rs1961559604
NM_004360.5(CDH1):c.*309C>T rs562205897
NM_004360.5(CDH1):c.*474_*475dup rs113202135
NM_004360.5(CDH1):c.*475del rs113202135
NM_004360.5(CDH1):c.*627T>G rs1567518268
NM_004360.5(CDH1):c.1018A>T (p.Thr340Ser) rs116093741
NM_004360.5(CDH1):c.1137+9A>T rs780705655
NM_004360.5(CDH1):c.1170C>T (p.Asn390=) rs766505270
NM_004360.5(CDH1):c.1308G>A (p.Leu436=) rs557551011
NM_004360.5(CDH1):c.1360G>C (p.Val454Leu) rs587780112
NM_004360.5(CDH1):c.1366G>T (p.Val456Leu) rs974965262
NM_004360.5(CDH1):c.1716T>C (p.Ser572=) rs876660176
NM_004360.5(CDH1):c.1887A>G (p.Glu629=) rs886052236
NM_004360.5(CDH1):c.2164+17dup rs34939176
NM_004360.5(CDH1):c.597A>G (p.Thr199=) rs1960738532

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.