ClinVar Miner

List of variants in gene APC studied for gastric cancer

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 183
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000038.6(APC):c.4479G>A (p.Thr1493=) rs41115 0.59177
NM_000038.6(APC):c.4326T>A (p.Pro1442=) rs67622085 0.00705
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_000038.6(APC):c.5801C>T (p.Pro1934Leu) rs587780600 0.00012
NM_000038.6(APC):c.4918C>T (p.Arg1640Trp) rs373440614 0.00010
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_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.6977G>A (p.Arg2326Gln) rs531178000 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_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.70C>T (p.Arg24Ter) rs145945630 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_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_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.3149del (p.Ala1050fs) rs730882135 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.646C>T (p.Arg216Ter) rs62619935 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
GRCh37/hg19 5q22.2(chr5:112173249-112173448)x1
GRCh37/hg19 5q22.2(chr5:112175002-112177352)x1
NM_000038.6(APC):c.1015A>G (p.Ser339Gly) rs1060503301
NM_000038.6(APC):c.1042C>T (p.Arg348Ter) rs1314843920
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.1380del (p.Glu461fs)
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.147_150del (p.Lys49fs) rs587781694
NM_000038.6(APC):c.1552A>G (p.Thr518Ala)
NM_000038.6(APC):c.1612G>T (p.Glu538Ter)
NM_000038.6(APC):c.1660C>T (p.Arg554Ter) rs137854573
NM_000038.6(APC):c.1664C>G (p.Ala555Gly)
NM_000038.6(APC):c.1779G>A (p.Trp593Ter) rs1554083132
NM_000038.6(APC):c.1809dup (p.Ala604fs)
NM_000038.6(APC):c.212G>C (p.Arg71Pro)
NM_000038.6(APC):c.2160G>A (p.Met720Ile) rs1283428855
NM_000038.6(APC):c.2206A>T (p.Lys736Ter)
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.2413C>T (p.Arg805Ter) rs587779783
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.2658G>T (p.Gln886His) rs587780593
NM_000038.6(APC):c.2783C>T (p.Ala928Val)
NM_000038.6(APC):c.2805C>G (p.Tyr935Ter) rs137854575
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.3199C>T (p.Gln1067Ter) rs137854571
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.3359G>A (p.Gly1120Glu) rs28933379
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.3927_3931del (p.Glu1309fs) rs121913224
NM_000038.6(APC):c.3982C>T (p.Gln1328Ter) rs398123121
NM_000038.6(APC):c.406G>T (p.Glu136Ter)
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.4549C>T (p.Gln1517Ter) rs1114167596
NM_000038.6(APC):c.4612_4613del (p.Glu1538fs) rs387906236
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.4670T>A (p.Ile1557Asn) rs769121879
NM_000038.6(APC):c.4708G>A (p.Asp1570Asn)
NM_000038.6(APC):c.4782_4785del (p.Ala1595fs) rs1554086196
NM_000038.6(APC):c.4813G>A (p.Val1605Met) rs1554086219
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.4dup (p.Ala2fs)
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.5572C>T (p.Arg1858Ter) rs1270783041
NM_000038.6(APC):c.5696A>T (p.Glu1899Val)
NM_000038.6(APC):c.5818del (p.Ile1940fs)
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.6503dup (p.Pro2170fs)
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.8246C>G (p.Ser2749Ter)
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

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.