ClinVar Miner

List of variants in gene APC reported by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 236
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HGVS dbSNP
NM_000038.5(APC):c.1177T>C (p.Ser393Pro) rs1060503352
NM_000038.5(APC):c.1192A>C (p.Lys398Gln) rs765196085
NM_000038.5(APC):c.120G>A (p.Glu40=) rs142720069
NM_000038.5(APC):c.1213C>T (p.Arg405Ter) rs587779780
NM_000038.5(APC):c.1240C>T (p.Arg414Cys) rs137854567
NM_000038.5(APC):c.1279C>A (p.His427Asn) rs587779781
NM_000038.5(APC):c.1291A>G (p.Met431Val) rs730881235
NM_000038.5(APC):c.1333C>T (p.Gln445Ter) rs876658802
NM_000038.5(APC):c.135+1G>T rs750508765
NM_000038.5(APC):c.1419G>A (p.Gln473=) rs141579422
NM_000038.5(APC):c.1488A>T (p.Thr496=) rs9282599
NM_000038.5(APC):c.1495C>G (p.Arg499Gly) rs137854580
NM_000038.5(APC):c.1604C>T (p.Ser535Phe) rs75870842
NM_000038.5(APC):c.1606G>A (p.Glu536Lys) rs138098808
NM_000038.5(APC):c.1626+1G>A rs1554081934
NM_000038.5(APC):c.1626+4C>A rs1202435147
NM_000038.5(APC):c.1626_1626+6del rs1554081930
NM_000038.5(APC):c.1631T>C (p.Ile544Thr) rs144056494
NM_000038.5(APC):c.1690C>T (p.Arg564Ter) rs137854574
NM_000038.5(APC):c.1697T>A (p.Val566Asp) rs1554082127
NM_000038.5(APC):c.1744-2A>T rs587783035
NM_000038.5(APC):c.1925T>C (p.Val642Ala) rs759528091
NM_000038.5(APC):c.1941T>C (p.Ala647=) rs1554083247
NM_000038.5(APC):c.1951dup (p.Asp651Glyfs) rs1554083255
NM_000038.5(APC):c.1958+3A>G rs879254032
NM_000038.5(APC):c.1958G>A (p.Arg653Lys) rs1060503318
NM_000038.5(APC):c.2026A>G (p.Ile676Val) rs745529713
NM_000038.5(APC):c.2031_2034delCAGT (p.Ser678Metfs) rs878853422
NM_000038.5(APC):c.2090C>T (p.Ala697Val) rs761733547
NM_000038.5(APC):c.2094A>G (p.Leu698=) rs1426881729
NM_000038.5(APC):c.2107delG (p.Ala703Glnfs) rs587783030
NM_000038.5(APC):c.2110G>A (p.Val704Ile) rs367804502
NM_000038.5(APC):c.211C>A (p.Arg71Ser) rs767741687
NM_000038.5(APC):c.220+2T>A rs587781809
NM_000038.5(APC):c.2205G>A (p.Ala735=) rs141001261
NM_000038.5(APC):c.2262T>G (p.Val754=) rs148987776
NM_000038.5(APC):c.2485A>G (p.Thr829Ala) rs768810807
NM_000038.5(APC):c.2593C>T (p.Pro865Ser) rs192620988
NM_000038.5(APC):c.2621C>G (p.Ser874Ter) rs1554084318
NM_000038.5(APC):c.2640C>T (p.Ile880=) rs200184105
NM_000038.5(APC):c.2725A>G (p.Thr909Ala) rs878853430
NM_000038.5(APC):c.2778T>C (p.Ser926=) rs371526966
NM_000038.5(APC):c.277C>G (p.Leu93Val) rs201567345
NM_000038.5(APC):c.2795C>A (p.Ser932Ter) rs878853432
NM_000038.5(APC):c.2802_2805delTTAC (p.Tyr935Ilefs) rs1131691143
NM_000038.5(APC):c.2805C>A (p.Tyr935Ter) rs137854575
NM_000038.5(APC):c.2805C>T (p.Tyr935=) rs137854575
NM_000038.5(APC):c.2876C>T (p.Ser959Phe) rs757526267
NM_000038.5(APC):c.288T>A (p.Tyr96Ter) rs376213437
NM_000038.5(APC):c.288T>C (p.Tyr96=) rs376213437
NM_000038.5(APC):c.295C>T (p.Arg99Trp) rs139196838
NM_000038.5(APC):c.2966A>G (p.Asp989Gly) rs770976457
NM_000038.5(APC):c.298delG (p.Glu100Lysfs) rs1064794224
NM_000038.5(APC):c.3006C>T (p.Ala1002=) rs72541810
NM_000038.5(APC):c.3049_3051delAAT (p.Asn1017del) rs730881229
NM_000038.5(APC):c.3079T>G (p.Tyr1027Asp) rs587781605
NM_000038.5(APC):c.3113C>T (p.Ser1038Phe) rs1375326078
NM_000038.5(APC):c.3149delC (p.Ala1050Glufs) rs730882135
NM_000038.5(APC):c.3164_3168delTAATA (p.Ile1055Argfs) rs1554084772
NM_000038.5(APC):c.3173A>G (p.Asp1058Gly) rs148725540
NM_000038.5(APC):c.317G>A (p.Arg106His) rs201764637
NM_000038.5(APC):c.3183_3187delACAAA (p.Gln1062Terfs) rs587779352
NM_000038.5(APC):c.3205A>G (p.Arg1069Gly) rs375408871
NM_000038.5(APC):c.3211C>T (p.Gln1071Ter) rs876659539
NM_000038.5(APC):c.3249T>G (p.Asp1083Glu) rs201629780
NM_000038.5(APC):c.3264G>A (p.Lys1088=) rs114774495
NM_000038.5(APC):c.3352A>G (p.Asn1118Asp) rs140493115
NM_000038.5(APC):c.3378C>G (p.Ser1126Arg) rs149353082
NM_000038.5(APC):c.3425A>G (p.Asn1142Ser) rs138410865
NM_000038.5(APC):c.3436C>T (p.Arg1146Cys) rs202168805
NM_000038.5(APC):c.3468_3470delAGA (p.Glu1157del) rs386833391
NM_000038.5(APC):c.3479C>A (p.Thr1160Lys) rs201004111
NM_000038.5(APC):c.3511C>T (p.Arg1171Cys) rs201830995
NM_000038.5(APC):c.3535T>G (p.Tyr1179Asp) rs751249843
NM_000038.5(APC):c.3555A>G (p.Thr1185=) rs786201125
NM_000038.5(APC):c.3623C>T (p.Thr1208Ile) rs752590375
NM_000038.5(APC):c.3632T>C (p.Met1211Thr) rs575268622
NM_000038.5(APC):c.3632T>G (p.Met1211Arg) rs575268622
NM_000038.5(APC):c.3774A>G (p.Thr1258=) rs542928573
NM_000038.5(APC):c.3786T>C (p.Tyr1262=) rs147411334
NM_000038.5(APC):c.3810T>A (p.Cys1270Ter) rs863225347
NM_000038.5(APC):c.3875C>T (p.Thr1292Met) rs371113837
NM_000038.5(APC):c.3887C>T (p.Ala1296Val) rs1291513037
NM_000038.5(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.5(APC):c.3927_3931delAAAGA (p.Glu1309Aspfs) rs121913224
NM_000038.5(APC):c.3949G>C (p.Glu1317Gln) rs1801166
NM_000038.5(APC):c.3963C>T (p.Ser1321=) rs150595875
NM_000038.5(APC):c.4055T>C (p.Val1352Ala) rs528724202
NM_000038.5(APC):c.4072G>A (p.Ala1358Thr) rs139618756
NM_000038.5(APC):c.4073C>T (p.Ala1358Val) rs730881249
NM_000038.5(APC):c.4207A>G (p.Ser1403Gly) rs759317924
NM_000038.5(APC):c.4249A>C (p.Ile1417Leu) rs200166878
NM_000038.5(APC):c.4260C>A (p.Pro1420=) rs770579741
NM_000038.5(APC):c.4260dup (p.Ser1421Glnfs) rs1554085679
NM_000038.5(APC):c.426_427delAT (p.Leu143Alafs) rs587782557
NM_000038.5(APC):c.4395T>A (p.Ser1465Arg) rs779898882
NM_000038.5(APC):c.4413A>G (p.Ala1471=) rs964029262
NM_000038.5(APC):c.4420G>A (p.Ala1474Thr) rs139387758
NM_000038.5(APC):c.450A>G (p.Lys150=) rs116020626
NM_000038.5(APC):c.4533C>T (p.Leu1511=) rs150089434
NM_000038.5(APC):c.4765C>T (p.Arg1589Cys) rs72541813
NM_000038.5(APC):c.4766G>A (p.Arg1589His) rs374048423
NM_000038.5(APC):c.4813G>A (p.Val1605Met) rs1554086219
NM_000038.5(APC):c.4893T>C (p.Ser1631=) rs35634377
NM_000038.5(APC):c.4905G>A (p.Gly1635=) rs137988845
NM_000038.5(APC):c.4918C>T (p.Arg1640Trp) rs373440614
NM_000038.5(APC):c.4963A>G (p.Thr1655Ala) rs759441332
NM_000038.5(APC):c.5017G>A (p.Glu1673Lys) rs587779796
NM_000038.5(APC):c.5025T>G (p.Val1675=) rs876658169
NM_000038.5(APC):c.5038C>T (p.Gln1680Ter) rs754122018
NM_000038.5(APC):c.5105G>A (p.Gly1702Glu) rs769273526
NM_000038.5(APC):c.5140G>A (p.Asp1714Asn) rs148275069
NM_000038.5(APC):c.5179T>C (p.Cys1727Arg) rs758815860
NM_000038.5(APC):c.5250C>G (p.Val1750=) rs2229997
NM_000038.5(APC):c.5268T>A (p.Ser1756=) rs866006
NM_000038.5(APC):c.5274T>A (p.Ser1758=) rs199600387
NM_000038.5(APC):c.5282A>C (p.Asn1761Thr) rs752038930
NM_000038.5(APC):c.5363G>A (p.Arg1788His) rs201472075
NM_000038.5(APC):c.5392A>C (p.Asn1798His) rs200794097
NM_000038.5(APC):c.5392A>G (p.Asn1798Asp) rs200794097
NM_000038.5(APC):c.5399A>G (p.Asn1800Ser) rs865782682
NM_000038.5(APC):c.5431T>C (p.Ser1811Pro) rs777788406
NM_000038.5(APC):c.5501_5506delTCAGAG (p.Val1834_Arg1835del) rs587778029
NM_000038.5(APC):c.5635G>T (p.Ala1879Ser) rs587779799
NM_000038.5(APC):c.5708A>G (p.Asn1903Ser) rs750404000
NM_000038.5(APC):c.573T>C (p.Tyr191=) rs185154886
NM_000038.5(APC):c.5790A>G (p.Gln1930=) rs141152252
NM_000038.5(APC):c.5801C>T (p.Pro1934Leu) rs587780600
NM_000038.5(APC):c.5826_5829delCAGA (p.Asp1942Glufs) rs864622228
NM_000038.5(APC):c.583C>T (p.Gln195Ter) rs749479682
NM_000038.5(APC):c.5879_5880delCGinsTA (p.Pro1960Leu) rs587779801
NM_000038.5(APC):c.5912C>G (p.Ser1971Cys) rs754691867
NM_000038.5(APC):c.6059_6062delGTTT (p.Cys2020Serfs) rs876660174
NM_000038.5(APC):c.607C>G (p.Gln203Glu) rs141576417
NM_000038.5(APC):c.6117G>T (p.Leu2039Phe) rs372418435
NM_000038.5(APC):c.6136G>A (p.Ala2046Thr) rs770406711
NM_000038.5(APC):c.6162A>G (p.Ser2054=) rs776160547
NM_000038.5(APC):c.6173G>A (p.Gly2058Asp) rs150140908
NM_000038.5(APC):c.6245A>G (p.Asp2082Gly) rs554370603
NM_000038.5(APC):c.6249A>G (p.Ile2083Met) rs374625279
NM_000038.5(APC):c.6387G>A (p.Ser2129=) rs374310157
NM_000038.5(APC):c.6446A>C (p.His2149Pro) rs749230730
NM_000038.5(APC):c.646C>T (p.Arg216Ter) rs62619935
NM_000038.5(APC):c.6496C>T (p.Arg2166Ter) rs764527706
NM_000038.5(APC):c.64A>G (p.Asn22Asp) rs1415062077
NM_000038.5(APC):c.6510A>C (p.Pro2170=) rs138571760
NM_000038.5(APC):c.6510delA (p.Glu2172Argfs) rs1554087474
NM_000038.5(APC):c.6525A>G (p.Thr2175=) rs200151646
NM_000038.5(APC):c.6526T>C (p.Leu2176=) rs183468041
NM_000038.5(APC):c.6609T>C (p.Val2203=) rs149328018
NM_000038.5(APC):c.6610C>T (p.Arg2204Ter) rs752654519
NM_000038.5(APC):c.6658A>G (p.Asn2220Asp) rs374464049
NM_000038.5(APC):c.6662T>C (p.Met2221Thr) rs730881255
NM_000038.5(APC):c.6669A>G (p.Ser2223=) rs372680843
NM_000038.5(APC):c.6679G>T (p.Gly2227Cys) rs367905430
NM_000038.5(APC):c.6694C>G (p.His2232Asp) rs730881256
NM_000038.5(APC):c.6724A>G (p.Ser2242Gly) rs201375478
NM_000038.5(APC):c.6750C>T (p.Gly2250=) rs555799753
NM_000038.5(APC):c.6821C>T (p.Ala2274Val) rs34919187
NM_000038.5(APC):c.6850C>A (p.Pro2284Thr) rs1554087789
NM_000038.5(APC):c.6873A>T (p.Gln2291His) rs148878262
NM_000038.5(APC):c.688C>T (p.Arg230Cys) rs587779805
NM_000038.5(APC):c.6896C>T (p.Pro2299Leu) rs876658800
NM_000038.5(APC):c.6918T>A (p.Asp2306Glu) rs1060503350
NM_000038.5(APC):c.694C>T (p.Arg232Ter) rs397515734
NM_000038.5(APC):c.7036C>T (p.Pro2346Ser) rs200756935
NM_000038.5(APC):c.7055G>A (p.Ser2352Asn) rs1554087958
NM_000038.5(APC):c.7099A>G (p.Thr2367Ala) rs772778630
NM_000038.5(APC):c.7193C>T (p.Ser2398Phe) rs150882838
NM_000038.5(APC):c.7194C>T (p.Ser2398=) rs565688379
NM_000038.5(APC):c.7223A>G (p.Asn2408Ser) rs1554088139
NM_000038.5(APC):c.7264A>G (p.Thr2422Ala) rs730881260
NM_000038.5(APC):c.7395T>C (p.Leu2465=) rs369906346
NM_000038.5(APC):c.7415C>T (p.Ala2472Val) rs200399245
NM_000038.5(APC):c.7443T>A (p.Thr2481=) rs147757080
NM_000038.5(APC):c.7467_7468dup (p.Asp2490Valfs) rs1554088383
NM_000038.5(APC):c.7471A>G (p.Met2491Val) rs375674083
NM_000038.5(APC):c.7477_7478delCT (p.Leu2493Ilefs) rs1554088391
NM_000038.5(APC):c.7495G>C (p.Val2499Leu) rs33941929
NM_000038.5(APC):c.7514G>A (p.Arg2505Gln) rs147549623
NM_000038.5(APC):c.7533C>T (p.Leu2511=) rs1057522957
NM_000038.5(APC):c.7536T>C (p.Ser2512=) rs587780604
NM_000038.5(APC):c.7550A>G (p.Tyr2517Cys) rs587783036
NM_000038.5(APC):c.756C>T (p.Thr252=) rs771535363
NM_000038.5(APC):c.7588C>T (p.Arg2530Trp) rs730881265
NM_000038.5(APC):c.7589G>A (p.Arg2530Gln) rs587778043
NM_000038.5(APC):c.7615C>T (p.Leu2539Phe) rs876660819
NM_000038.5(APC):c.7625A>G (p.Asn2542Ser) rs151163793
NM_000038.5(APC):c.7645C>T (p.Arg2549Cys) rs199539353
NM_000038.5(APC):c.7717A>G (p.Ile2573Val) rs145444830
NM_000038.5(APC):c.7766A>G (p.Glu2589Gly) rs200406572
NM_000038.5(APC):c.777G>T (p.Arg259=) rs147704593
NM_000038.5(APC):c.7786T>G (p.Ser2596Ala) rs138137162
NM_000038.5(APC):c.7793C>A (p.Thr2598Asn) rs747339588
NM_000038.5(APC):c.7821C>T (p.Ser2607=) rs532235331
NM_000038.5(APC):c.7878T>G (p.Thr2626=) rs757020188
NM_000038.5(APC):c.791A>G (p.Gln264Arg) rs369345931
NM_000038.5(APC):c.8033A>G (p.Asn2678Ser) rs886059800
NM_000038.5(APC):c.8043G>C (p.Pro2681=) rs149347068
NM_000038.5(APC):c.8068G>A (p.Ala2690Thr) rs140868933
NM_000038.5(APC):c.8141G>A (p.Arg2714His) rs747362422
NM_000038.5(APC):c.8196C>A (p.Asp2732Glu) rs1554088957
NM_000038.5(APC):c.8234C>T (p.Pro2745Leu) rs759421641
NM_000038.5(APC):c.8325G>A (p.Gly2775=) rs770719841
NM_000038.5(APC):c.835G>T (p.Gly279Cys) rs1554079129
NM_000038.5(APC):c.8378G>A (p.Ser2793Asn) rs374853436
NM_000038.5(APC):c.8389A>G (p.Ser2797Gly) rs147287751
NM_000038.5(APC):c.8390G>A (p.Ser2797Asn) rs1060503339
NM_000038.5(APC):c.896_897delCT (p.Ser299Cysfs) rs397515735
NM_000038.5(APC):c.904C>T (p.Arg302Ter) rs137854568
NM_000038.5(APC):c.95A>G (p.Asn32Ser) rs539108537
NM_000038.5(APC):c.994C>T (p.Arg332Ter) rs775126020
NM_000038.6(APC):c.1198G>A (p.Gly400Ser)
NM_000038.6(APC):c.1479C>T (p.Tyr493=)
NM_000038.6(APC):c.1613A>T (p.Glu538Val)
NM_000038.6(APC):c.1643dup (p.Leu548Phefs)
NM_000038.6(APC):c.2074C>T (p.Pro692Ser)
NM_000038.6(APC):c.2109A>C (p.Ala703=)
NM_000038.6(APC):c.2114G>A (p.Ser705Asn) rs752874220
NM_000038.6(APC):c.3721G>A (p.Gly1241Ser)
NM_000038.6(APC):c.3724C>G (p.Gln1242Glu)
NM_000038.6(APC):c.4109A>G (p.Lys1370Arg)
NM_000038.6(APC):c.423-9A>C
NM_000038.6(APC):c.449A>T (p.Lys150Ile)
NM_000038.6(APC):c.5570C>A (p.Ser1857Ter)
NM_000038.6(APC):c.5912C>A (p.Ser1971Tyr)
NM_000038.6(APC):c.6361G>C (p.Ala2121Pro)
NM_000038.6(APC):c.636dup (p.Arg213Thrfs)
NM_000038.6(APC):c.6474C>T (p.Pro2158=) rs772027192
NM_000038.6(APC):c.6491G>A (p.Gly2164Asp)
NM_000038.6(APC):c.7897G>C (p.Gly2633Arg)
NM_000038.6(APC):c.990G>T (p.Met330Ile)
NM_001127510.2(APC):c.1240del (p.Arg414Alafs) rs1554080082
NM_001127510.2(APC):c.6542_6545del (p.Ile2181Asnfs) rs1554087515
NM_001127510.2(APC):c.7573C>T (p.Arg2525Cys) rs774952444
NM_001127511.2(APC):c.1954_1960delAAATCTCinsTAGTTTTGTA (p.Lys652_His988delinsTer) rs1554083888

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