ClinVar Miner

List of variants studied for hereditary gastric cancer by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (13):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 220
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000038.6(APC):c.4479G>A (p.Thr1493=) rs41115 0.59177
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr) rs33935154 0.01412
NM_004360.5(CDH1):c.-71C>G rs34033771 0.00927
NM_000038.6(APC):c.4326T>A (p.Pro1442=) rs67622085 0.00705
NM_004360.5(CDH1):c.1774G>A (p.Ala592Thr) rs35187787 0.00311
NM_004360.5(CDH1):c.88C>A (p.Pro30Thr) rs139866691 0.00129
NM_000038.6(APC):c.6821C>T (p.Ala2274Val) rs34919187 0.00088
NM_000038.6(APC):c.4336G>A (p.Ala1446Thr) rs146572883 0.00056
NM_000038.6(APC):c.2476T>G (p.Leu826Val) rs145245264 0.00054
NM_000038.6(APC):c.3511C>T (p.Arg1171Cys) rs201830995 0.00028
NM_004360.5(CDH1):c.303C>T (p.Tyr101=) rs150789339 0.00027
NM_004360.5(CDH1):c.670C>T (p.Arg224Cys) rs200310662 0.00021
NM_000038.6(APC):c.5801C>T (p.Pro1934Leu) rs587780600 0.00012
NM_004360.5(CDH1):c.1143G>C (p.Lys381Asn) rs143727462 0.00012
NM_004360.5(CDH1):c.1409C>T (p.Thr470Ile) rs370864592 0.00012
NM_004360.5(CDH1):c.2512A>G (p.Ser838Gly) rs121964872 0.00011
NM_000038.6(APC):c.4918C>T (p.Arg1640Trp) rs373440614 0.00010
NM_004360.5(CDH1):c.2644G>A (p.Asp882Asn) rs200104963 0.00009
NM_000038.6(APC):c.573T>C (p.Tyr191=) rs185154886 0.00008
NM_000038.6(APC):c.1193A>G (p.Lys398Arg) rs145912662 0.00006
NM_000038.6(APC):c.5216A>G (p.Lys1739Arg) rs769558291 0.00006
NM_004360.5(CDH1):c.48+15_48+16del rs730881655 0.00006
NM_000038.6(APC):c.1242C>T (p.Arg414=) rs751423790 0.00004
NM_000038.6(APC):c.3245C>G (p.Thr1082Ser) rs730881244 0.00004
NM_000038.6(APC):c.5528C>T (p.Pro1843Leu) rs368080169 0.00004
NM_000038.6(APC):c.5756A>G (p.Asn1919Ser) rs147740612 0.00004
NM_000038.6(APC):c.5839A>G (p.Thr1947Ala) rs746346292 0.00004
NM_000038.6(APC):c.5894A>C (p.His1965Pro) rs773776516 0.00004
NM_000038.6(APC):c.6020A>G (p.Tyr2007Cys) rs752604668 0.00004
NM_000038.6(APC):c.6117G>T (p.Leu2039Phe) rs372418435 0.00004
NM_000038.6(APC):c.7531C>T (p.Leu2511Phe) rs72541815 0.00004
NM_000038.6(APC):c.776G>A (p.Arg259Gln) rs767457050 0.00004
NM_001127511.3(APC):c.-167G>A rs1278244063 0.00004
NM_004360.5(CDH1):c.1501G>A (p.Val501Met) rs368690400 0.00004
NM_004360.5(CDH1):c.2336G>A (p.Arg779Gln) rs587781311 0.00004
NM_004360.5(CDH1):c.2474C>T (p.Pro825Leu) rs587781312 0.00004
NM_004360.5(CDH1):c.377C>T (p.Pro126Leu) rs746703615 0.00004
NM_004360.5(CDH1):c.84C>T (p.Cys28=) rs587780789 0.00004
NM_000038.6(APC):c.1241G>A (p.Arg414His) rs730881233 0.00003
NM_000038.6(APC):c.1495C>G (p.Arg499Gly) rs137854580 0.00003
NM_000038.6(APC):c.2966A>G (p.Asp989Gly) rs770976457 0.00003
NM_000038.6(APC):c.7174C>A (p.Pro2392Thr) rs730881257 0.00003
NM_000038.6(APC):c.7808A>G (p.Glu2603Gly) rs587779807 0.00003
NM_000038.6(APC):c.854A>G (p.Asp285Gly) rs201093383 0.00003
NM_001127511.3(APC):c.-32C>T rs1015952631 0.00003
NM_001127511.3(APC):c.-88T>G rs531931776 0.00003
NM_001127511.3(APC):c.71C>T (p.Ser24Phe) rs770241997 0.00003
NM_004360.5(CDH1):c.1225T>C (p.Trp409Arg) rs587778176 0.00003
NM_004360.5(CDH1):c.499G>A (p.Glu167Lys) rs769076258 0.00003
NM_000038.6(APC):c.1264G>A (p.Glu422Lys) rs755069015 0.00002
NM_000038.6(APC):c.1538T>C (p.Val513Ala) rs876658167 0.00002
NM_000038.6(APC):c.3425A>C (p.Asn1142Thr) rs138410865 0.00002
NM_000038.6(APC):c.3661C>T (p.Pro1221Ser) rs760999992 0.00002
NM_000038.6(APC):c.4399C>T (p.Pro1467Ser) rs749142480 0.00002
NM_000038.6(APC):c.5147A>G (p.Asn1716Ser) rs141298709 0.00002
NM_000038.6(APC):c.6497G>A (p.Arg2166Gln) rs752091655 0.00002
NM_000038.6(APC):c.6670A>G (p.Ile2224Val) rs374597207 0.00002
NM_000038.6(APC):c.7105C>T (p.Pro2369Ser) rs377308875 0.00002
NM_000038.6(APC):c.8017A>G (p.Arg2673Gly) rs767286063 0.00002
NM_004360.5(CDH1):c.1004G>A (p.Arg335Gln) rs373364873 0.00002
NM_004360.5(CDH1):c.2098C>A (p.Pro700Thr) rs878854681 0.00002
NM_004360.5(CDH1):c.2371C>T (p.Leu791Phe) rs786202598 0.00002
NM_004360.5(CDH1):c.2558C>T (p.Ser853Leu) rs569928380 0.00002
NM_004360.5(CDH1):c.2595G>C (p.Trp865Cys) rs778019174 0.00002
NM_000038.6(APC):c.1121G>A (p.Arg374Gln) rs141582813 0.00001
NM_000038.6(APC):c.1192A>C (p.Lys398Gln) rs765196085 0.00001
NM_000038.6(APC):c.1498T>C (p.Tyr500His) rs762019672 0.00001
NM_000038.6(APC):c.1585C>T (p.Leu529Phe) rs1428025300 0.00001
NM_000038.6(APC):c.2114G>A (p.Ser705Asn) rs752874220 0.00001
NM_000038.6(APC):c.212G>A (p.Arg71His) rs750503329 0.00001
NM_000038.6(APC):c.2933A>C (p.Gln978Pro) rs730881223 0.00001
NM_000038.6(APC):c.3218C>T (p.Thr1073Ile) rs773354366 0.00001
NM_000038.6(APC):c.3313C>T (p.Arg1105Trp) rs768454793 0.00001
NM_000038.6(APC):c.3445G>A (p.Glu1149Lys) rs371117193 0.00001
NM_000038.6(APC):c.3515A>T (p.His1172Leu) rs1024630299 0.00001
NM_000038.6(APC):c.3964G>A (p.Glu1322Lys) rs752926571 0.00001
NM_000038.6(APC):c.4100A>G (p.Gln1367Arg) rs1399790840 0.00001
NM_000038.6(APC):c.4207A>G (p.Ser1403Gly) rs759317924 0.00001
NM_000038.6(APC):c.4213G>A (p.Val1405Ile) rs761966904 0.00001
NM_000038.6(APC):c.4430A>G (p.Gln1477Arg) rs1479009365 0.00001
NM_000038.6(APC):c.447C>A (p.Asp149Glu) rs750821213 0.00001
NM_000038.6(APC):c.468C>G (p.Asp156Glu) rs752627126 0.00001
NM_000038.6(APC):c.4963A>G (p.Thr1655Ala) rs759441332 0.00001
NM_000038.6(APC):c.5282A>C (p.Asn1761Thr) rs752038930 0.00001
NM_000038.6(APC):c.5399A>G (p.Asn1800Ser) rs865782682 0.00001
NM_000038.6(APC):c.5615T>A (p.Val1872Asp) rs748389037 0.00001
NM_000038.6(APC):c.5627G>T (p.Arg1876Met) rs773201570 0.00001
NM_000038.6(APC):c.5794A>T (p.Thr1932Ser) rs777604445 0.00001
NM_000038.6(APC):c.6383C>T (p.Ala2128Val) rs753228011 0.00001
NM_000038.6(APC):c.7136C>G (p.Thr2379Ser) rs767691072 0.00001
NM_000038.6(APC):c.7397C>T (p.Ser2466Phe) rs765669629 0.00001
NM_000038.6(APC):c.7541C>G (p.Thr2514Ser) rs747833393 0.00001
NM_000038.6(APC):c.7558G>A (p.Gly2520Arg) rs746138566 0.00001
NM_000038.6(APC):c.8057T>C (p.Val2686Ala) rs757901425 0.00001
NM_000038.6(APC):c.8282C>T (p.Pro2761Leu) rs757874563 0.00001
NM_004360.5(CDH1):c.1003C>T (p.Arg335Ter) rs587780784 0.00001
NM_004360.5(CDH1):c.1136C>T (p.Thr379Met) rs587782856 0.00001
NM_004360.5(CDH1):c.1171G>A (p.Val391Ile) rs556110297 0.00001
NM_004360.5(CDH1):c.1250A>G (p.Asn417Ser) rs773441320 0.00001
NM_004360.5(CDH1):c.1370C>T (p.Thr457Met) rs587778170 0.00001
NM_004360.5(CDH1):c.1843A>G (p.Ile615Val) rs1003012321 0.00001
NM_004360.5(CDH1):c.2358C>T (p.Asp786=) rs760701558 0.00001
NM_004360.5(CDH1):c.2380G>A (p.Val794Ile) rs587782466 0.00001
NM_004360.5(CDH1):c.2398C>T (p.Arg800Cys) rs587782162 0.00001
NM_004360.5(CDH1):c.2603G>A (p.Arg868His) rs369126891 0.00001
NM_004360.5(CDH1):c.322A>G (p.Arg108Gly) rs587778172 0.00001
NM_004360.5(CDH1):c.631A>G (p.Thr211Ala) rs587781766 0.00001
NM_000038.6(APC):c.1015A>G (p.Ser339Gly) rs1060503301
NM_000038.6(APC):c.1073A>G (p.Gln358Arg) rs1064793508
NM_000038.6(APC):c.1094A>G (p.Lys365Arg) rs1580529121
NM_000038.6(APC):c.1333C>G (p.Gln445Glu) rs876658802
NM_000038.6(APC):c.1462C>T (p.Leu488Phe) rs587779782
NM_000038.6(APC):c.1475A>G (p.His492Arg) rs1580565129
NM_000038.6(APC):c.1552A>G (p.Thr518Ala)
NM_000038.6(APC):c.1664C>G (p.Ala555Gly)
NM_000038.6(APC):c.212G>C (p.Arg71Pro)
NM_000038.6(APC):c.2160G>A (p.Met720Ile) rs1283428855
NM_000038.6(APC):c.232G>A (p.Asp78Asn) rs1253209514
NM_000038.6(APC):c.2383C>G (p.Leu795Val) rs1442780982
NM_000038.6(APC):c.2425A>G (p.Asn809Asp) rs1580621960
NM_000038.6(APC):c.2573T>C (p.Ile858Thr) rs1765215022
NM_000038.6(APC):c.2783C>T (p.Ala928Val)
NM_000038.6(APC):c.2845A>G (p.Met949Val) rs587781348
NM_000038.6(APC):c.2896A>T (p.Ser966Cys)
NM_000038.6(APC):c.3122A>G (p.Gln1041Arg) rs1554084709
NM_000038.6(APC):c.3209A>T (p.Asn1070Ile) rs1315959337
NM_000038.6(APC):c.3263A>C (p.Lys1088Thr) rs1580633119
NM_000038.6(APC):c.3309G>T (p.Arg1103Ser) rs1580633773
NM_000038.6(APC):c.3365A>G (p.Asn1122Ser) rs372855304
NM_000038.6(APC):c.3490A>G (p.Ile1164Val) rs1554085052
NM_000038.6(APC):c.3632T>C (p.Met1211Thr) rs575268622
NM_000038.6(APC):c.3773C>T (p.Thr1258Ile) rs1765517499
NM_000038.6(APC):c.3901dup (p.Thr1301fs) rs1554085382
NM_000038.6(APC):c.3982C>T (p.Gln1328Ter) rs398123121
NM_000038.6(APC):c.422+10C>G rs899376835
NM_000038.6(APC):c.423-4del rs730881230
NM_000038.6(APC):c.423-4dup rs730881230
NM_000038.6(APC):c.4261A>G (p.Ser1421Gly) rs1303200783
NM_000038.6(APC):c.4332A>T (p.Gln1444His) rs748342378
NM_000038.6(APC):c.461A>G (p.Glu154Gly) rs1561477912
NM_000038.6(APC):c.4638_4639del (p.Asn1546fs) rs1561594148
NM_000038.6(APC):c.4708G>A (p.Asp1570Asn)
NM_000038.6(APC):c.4831C>T (p.Gln1611Ter) rs774847203
NM_000038.6(APC):c.4987G>A (p.Glu1663Lys) rs758987855
NM_000038.6(APC):c.5011G>A (p.Ala1671Thr) rs587781600
NM_000038.6(APC):c.5042C>T (p.Ser1681Leu) rs876659056
NM_000038.6(APC):c.5265_5268delinsATCG (p.Ala1755_Ser1756=) rs1554086584
NM_000038.6(APC):c.5266TCT[2] (p.Ser1758del) rs780061589
NM_000038.6(APC):c.5287A>G (p.Asn1763Asp) rs1440736149
NM_000038.6(APC):c.5305A>C (p.Lys1769Gln)
NM_000038.6(APC):c.5378C>G (p.Ala1793Gly) rs764203580
NM_000038.6(APC):c.5459C>T (p.Ser1820Phe) rs879367927
NM_000038.6(APC):c.5696A>T (p.Glu1899Val)
NM_000038.6(APC):c.6218G>A (p.Gly2073Asp) rs1766164614
NM_000038.6(APC):c.6293A>G (p.Asn2098Ser) rs1766183030
NM_000038.6(APC):c.643C>T (p.Gln215Ter) rs137854577
NM_000038.6(APC):c.645+1G>T rs863225370
NM_000038.6(APC):c.646C>G (p.Arg216Gly) rs62619935
NM_000038.6(APC):c.6602G>A (p.Gly2201Glu)
NM_000038.6(APC):c.6634dup (p.Gln2212fs)
NM_000038.6(APC):c.6727A>G (p.Thr2243Ala) rs773539706
NM_000038.6(APC):c.6918T>A (p.Asp2306Glu) rs1060503350
NM_000038.6(APC):c.7085G>C (p.Gly2362Ala) rs756740976
NM_000038.6(APC):c.7097A>G (p.Tyr2366Cys) rs1561612604
NM_000038.6(APC):c.7117A>G (p.Met2373Val) rs879254221
NM_000038.6(APC):c.7264A>T (p.Thr2422Ser) rs730881260
NM_000038.6(APC):c.7273A>G (p.Ser2425Gly) rs730881261
NM_000038.6(APC):c.74_75del (p.Gln25fs) rs1554067124
NM_000038.6(APC):c.7583T>C (p.Ile2528Thr) rs730881264
NM_000038.6(APC):c.7757G>T (p.Ser2586Ile) rs199806334
NM_000038.6(APC):c.7769A>C (p.Lys2590Thr)
NM_000038.6(APC):c.7922A>C (p.Lys2641Thr) rs879254231
NM_000038.6(APC):c.7946C>T (p.Pro2649Leu) rs1766608503
NM_000038.6(APC):c.8065A>G (p.Lys2689Glu) rs1554088874
NM_000038.6(APC):c.8122A>G (p.Asn2708Asp) rs1580690269
NM_000038.6(APC):c.813G>A (p.Met271Ile) rs1064793903
NM_000038.6(APC):c.8146G>T (p.Val2716Leu) rs587778044
NM_000038.6(APC):c.8281C>T (p.Pro2761Ser) rs1060503332
NM_000038.6(APC):c.834+1G>A rs1554076225
NM_000038.6(APC):c.835-17A>G rs1580511131
NM_000038.6(APC):c.8391C>A (p.Ser2797Arg) rs1060503256
NM_000038.6(APC):c.847C>T (p.Arg283Ter) rs786201856
NM_000038.6(APC):c.887G>C (p.Ser296Thr) rs1762421045
NM_000038.6(APC):c.994C>T (p.Arg332Ter) rs775126020
NM_001127511.3(APC):c.-142G>A rs951500465
NM_001127511.3(APC):c.-93G>C
NM_001127511.3(APC):c.9C>T (p.Ala3=) rs1750602563
NM_004360.5(CDH1):c.1145del (p.Gly382fs) rs1555515863
NM_004360.5(CDH1):c.1147C>T (p.Gln383Ter) rs587782798
NM_004360.5(CDH1):c.1174G>C (p.Val392Leu) rs141864044
NM_004360.5(CDH1):c.1234G>A (p.Val412Ile) rs587782189
NM_004360.5(CDH1):c.1320G>T (p.Lys440Asn) rs1555515925
NM_004360.5(CDH1):c.1354_1357del (p.Leu452fs) rs886039612
NM_004360.5(CDH1):c.1376T>C (p.Val459Ala) rs1555516109
NM_004360.5(CDH1):c.1403C>T (p.Thr468Ile) rs876659141
NM_004360.5(CDH1):c.1430T>C (p.Val477Ala)
NM_004360.5(CDH1):c.1492G>A (p.Asp498Asn) rs2152135021
NM_004360.5(CDH1):c.1585A>G (p.Thr529Ala) rs776890776
NM_004360.5(CDH1):c.1649G>C (p.Arg550Thr) rs771649648
NM_004360.5(CDH1):c.1741C>T (p.Leu581Phe) rs1567512154
NM_004360.5(CDH1):c.1774G>T (p.Ala592Ser) rs35187787
NM_004360.5(CDH1):c.1927A>G (p.Asn643Asp) rs587781540
NM_004360.5(CDH1):c.202T>G (p.Tyr68Asp) rs1060501218
NM_004360.5(CDH1):c.2038A>G (p.Thr680Ala) rs876658936
NM_004360.5(CDH1):c.2064_2065del (p.Cys688_Glu689delinsTer) rs587781276
NM_004360.5(CDH1):c.2116C>G (p.Gln706Glu)
NM_004360.5(CDH1):c.220C>T (p.Arg74Ter) rs876658932
NM_004360.5(CDH1):c.2222T>C (p.Leu741Ser)
NM_004360.5(CDH1):c.2356G>A (p.Asp786Asn) rs876659218
NM_004360.5(CDH1):c.2435A>G (p.Asp812Gly) rs878854684
NM_004360.5(CDH1):c.2578G>C (p.Asp860His) rs1412506259
NM_004360.5(CDH1):c.2623A>G (p.Met875Val) rs1555518287
NM_004360.5(CDH1):c.320A>G (p.Tyr107Cys) rs1060501241
NM_004360.5(CDH1):c.321C>G (p.Tyr107Ter) rs765929630
NM_004360.5(CDH1):c.382del (p.His128fs) rs1555514492
NM_004360.5(CDH1):c.488G>C (p.Cys163Ser) rs748783182
NM_004360.5(CDH1):c.56C>G (p.Ser19Cys) rs1221633501
NM_004360.5(CDH1):c.715G>A (p.Gly239Arg) rs587780537
NM_004360.5(CDH1):c.946A>G (p.Met316Val) rs761182866
NM_004985.5(KRAS):c.458A>T (p.Asp153Val) rs104894360

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