ClinVar Miner

List of variants in gene APC reported as uncertain significance by Integrated Genetics/Laboratory Corporation of America

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Gene type:
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Total variants: 176
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HGVS dbSNP
NM_000038.6(APC):c.1009A>G (p.Met337Val) rs1438780449
NM_000038.6(APC):c.1100C>G (p.Ser367Cys) rs1554080012
NM_000038.6(APC):c.1110G>A (p.Leu370=) rs1439967202
NM_000038.6(APC):c.1234C>G (p.Gln412Glu) rs876660802
NM_000038.6(APC):c.1241G>A (p.Arg414His) rs730881233
NM_000038.6(APC):c.1291A>G (p.Met431Val) rs730881235
NM_000038.6(APC):c.1318G>A (p.Ala440Thr) rs1064793023
NM_000038.6(APC):c.1319C>G (p.Ala440Gly) rs1561545834
NM_000038.6(APC):c.1333C>G (p.Gln445Glu) rs876658802
NM_000038.6(APC):c.1366C>T (p.Leu456Phe) rs876660195
NM_000038.6(APC):c.1392T>C (p.His464=) rs1057524073
NM_000038.6(APC):c.1405C>T (p.Leu469=) rs746293695
NM_000038.6(APC):c.1440A>T (p.Gln480His) rs863224537
NM_000038.6(APC):c.1441G>A (p.Val481Met) rs587780542
NM_000038.6(APC):c.1481G>A (p.Ser494Asn) rs1554081691
NM_000038.6(APC):c.1495C>G (p.Arg499Gly) rs137854580
NM_000038.6(APC):c.14C>T (p.Ser5Leu) rs373718658
NM_000038.6(APC):c.1579A>G (p.Arg527Gly) rs751120046
NM_000038.6(APC):c.1589T>C (p.Val530Ala) rs202199891
NM_000038.6(APC):c.1626+4C>A rs1202435147
NM_000038.6(APC):c.1626+6A>G rs1197354854
NM_000038.6(APC):c.1691G>A (p.Arg564Gln) rs747418061
NM_000038.6(APC):c.193C>A (p.Gln65Lys) rs863225320
NM_000038.6(APC):c.195G>C (p.Gln65His) rs1554069548
NM_000038.6(APC):c.2031C>T (p.Val677=) rs769363082
NM_000038.6(APC):c.2110G>A (p.Val704Ile) rs367804502
NM_000038.6(APC):c.211C>A (p.Arg71Ser) rs767741687
NM_000038.6(APC):c.211C>T (p.Arg71Cys) rs767741687
NM_000038.6(APC):c.2204C>T (p.Ala735Val) rs147655929
NM_000038.6(APC):c.221-5T>C rs1057524155
NM_000038.6(APC):c.2297C>T (p.Ala766Val) rs200339830
NM_000038.6(APC):c.2346G>A (p.Lys782=) rs1554084084
NM_000038.6(APC):c.234T>G (p.Asp78Glu) rs765434321
NM_000038.6(APC):c.2434G>C (p.Asp812His) rs761178697
NM_000038.6(APC):c.2438A>G (p.Asn813Ser) rs201522866
NM_000038.6(APC):c.2461G>A (p.Val821Ile) rs138498551
NM_000038.6(APC):c.2677G>A (p.Glu893Lys) rs199740875
NM_000038.6(APC):c.268A>G (p.Lys90Glu) rs763184444
NM_000038.6(APC):c.2707G>A (p.Asp903Asn) rs587782610
NM_000038.6(APC):c.2764C>T (p.Leu922Phe) rs150543576
NM_000038.6(APC):c.2775C>T (p.Ser925=) rs864622701
NM_000038.6(APC):c.2780C>G (p.Ala927Gly) rs587781500
NM_000038.6(APC):c.2812A>G (p.Thr938Ala) rs965844436
NM_000038.6(APC):c.2840G>T (p.Cys947Phe) rs997271472
NM_000038.6(APC):c.2847G>T (p.Met949Ile) rs147394539
NM_000038.6(APC):c.2860T>C (p.Leu954=) rs863224278
NM_000038.6(APC):c.2870A>G (p.Lys957Arg) rs777881096
NM_000038.6(APC):c.2903G>A (p.Ser968Asn) rs1554084581
NM_000038.6(APC):c.2942C>G (p.Pro981Arg) rs587779784
NM_000038.6(APC):c.2952A>G (p.Glu984=) rs772562489
NM_000038.6(APC):c.296G>A (p.Arg99Gln) rs199842850
NM_000038.6(APC):c.3125G>C (p.Ser1042Thr) rs786203919
NM_000038.6(APC):c.3415A>C (p.Lys1139Gln) rs201550951
NM_000038.6(APC):c.3479C>A (p.Thr1160Lys) rs201004111
NM_000038.6(APC):c.3529A>G (p.Ile1177Val) rs369834416
NM_000038.6(APC):c.3612A>G (p.Gln1204=) rs864622196
NM_000038.6(APC):c.3775A>T (p.Ile1259Leu) rs762391822
NM_000038.6(APC):c.3807A>G (p.Ile1269Met) rs876658536
NM_000038.6(APC):c.3837T>G (p.Ser1279=) rs1057522493
NM_000038.6(APC):c.3837_3845dup (p.1277_1279LSS[3]) rs1561587936
NM_000038.6(APC):c.3909A>G (p.Gln1303=) rs746289994
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.6(APC):c.4072G>A (p.Ala1358Thr) rs139618756
NM_000038.6(APC):c.4091_4093GTG[1] (p.Gly1365del)
NM_000038.6(APC):c.4147A>G (p.Met1383Val) rs1064793836
NM_000038.6(APC):c.4213G>A (p.Val1405Ile) rs761966904
NM_000038.6(APC):c.4225C>A (p.Pro1409Thr) rs1554085637
NM_000038.6(APC):c.4252A>T (p.Ile1418Leu) rs777386397
NM_000038.6(APC):c.4320A>T (p.Pro1440=) rs1561591372
NM_000038.6(APC):c.4349G>A (p.Arg1450Gln) rs587782678
NM_000038.6(APC):c.437C>T (p.Ala146Val) rs1305794169
NM_000038.6(APC):c.4416A>T (p.Val1472=) rs773352404
NM_000038.6(APC):c.4478C>T (p.Thr1493Met) rs374892194
NM_000038.6(APC):c.449A>G (p.Lys150Arg) rs371085910
NM_000038.6(APC):c.4533C>T (p.Leu1511=) rs150089434
NM_000038.6(APC):c.4693G>A (p.Asp1565Asn) rs767138124
NM_000038.6(APC):c.4693G>T (p.Asp1565Tyr) rs767138124
NM_000038.6(APC):c.4732T>G (p.Cys1578Gly) rs138367627
NM_000038.6(APC):c.4902G>A (p.Pro1634=) rs876659202
NM_000038.6(APC):c.4913T>C (p.Met1638Thr) rs201797422
NM_000038.6(APC):c.4918C>T (p.Arg1640Trp) rs373440614
NM_000038.6(APC):c.4963A>G (p.Thr1655Ala) rs759441332
NM_000038.6(APC):c.4973G>C (p.Ser1658Thr) rs1561596738
NM_000038.6(APC):c.5026A>G (p.Arg1676Gly) rs370560998
NM_000038.6(APC):c.5026_5028del (p.Arg1676del) rs768369050
NM_000038.6(APC):c.5097G>A (p.Glu1699=) rs1561597648
NM_000038.6(APC):c.5181C>T (p.Cys1727=) rs1554086499
NM_000038.6(APC):c.5194A>G (p.Met1732Val) rs752065261
NM_000038.6(APC):c.5197C>T (p.Pro1733Ser) rs1441448668
NM_000038.6(APC):c.5216A>G (p.Lys1739Arg) rs769558291
NM_000038.6(APC):c.5282A>C (p.Asn1761Thr) rs752038930
NM_000038.6(APC):c.5304G>A (p.Lys1768=) rs863224285
NM_000038.6(APC):c.531+9C>G rs1554071622
NM_000038.6(APC):c.5315C>G (p.Pro1772Arg) rs1554086633
NM_000038.6(APC):c.5363G>A (p.Arg1788His) rs201472075
NM_000038.6(APC):c.537C>A (p.Ser179=) rs149736402
NM_000038.6(APC):c.5465T>G (p.Val1822Gly) rs459552
NM_000038.6(APC):c.5528C>T (p.Pro1843Leu) rs368080169
NM_000038.6(APC):c.5540C>T (p.Thr1847Met) rs371686531
NM_000038.6(APC):c.5571A>C (p.Ser1857=) rs376624613
NM_000038.6(APC):c.5635G>T (p.Ala1879Ser) rs587779799
NM_000038.6(APC):c.565T>C (p.Leu189=) rs762146761
NM_000038.6(APC):c.566T>G (p.Leu189Trp) rs1554072581
NM_000038.6(APC):c.5688C>G (p.Ser1896Arg) rs1561601778
NM_000038.6(APC):c.5734G>A (p.Ala1912Thr) rs1554086930
NM_000038.6(APC):c.5759G>A (p.Arg1920Gln) rs587780599
NM_000038.6(APC):c.5779C>A (p.Leu1927Ile) rs730881253
NM_000038.6(APC):c.5784G>A (p.Gln1928=) rs761186363
NM_000038.6(APC):c.5839A>G (p.Thr1947Ala) rs746346292
NM_000038.6(APC):c.5866A>G (p.Ile1956Val) rs749597014
NM_000038.6(APC):c.5912C>A (p.Ser1971Tyr) rs754691867
NM_000038.6(APC):c.5914C>T (p.Leu1972Phe) rs1222940653
NM_000038.6(APC):c.5998A>G (p.Ser2000Gly) rs587782271
NM_000038.6(APC):c.6019T>C (p.Tyr2007His) rs745811356
NM_000038.6(APC):c.6127A>G (p.Ile2043Val) rs876660233
NM_000038.6(APC):c.6446A>C (p.His2149Pro) rs749230730
NM_000038.6(APC):c.6448C>G (p.Leu2150Val) rs1263640330
NM_000038.6(APC):c.646-8T>A rs879254149
NM_000038.6(APC):c.6473C>G (p.Pro2158Arg) rs587779804
NM_000038.6(APC):c.6487A>C (p.Lys2163Gln) rs759728732
NM_000038.6(APC):c.6488A>T (p.Lys2163Ile) rs1554087458
NM_000038.6(APC):c.6588A>C (p.Lys2196Asn) rs961108427
NM_000038.6(APC):c.6658A>G (p.Asn2220Asp) rs374464049
NM_000038.6(APC):c.6674C>G (p.Ser2225Cys) rs759307079
NM_000038.6(APC):c.6675T>C (p.Ser2225=) rs950337714
NM_000038.6(APC):c.6679G>T (p.Gly2227Cys) rs367905430
NM_000038.6(APC):c.6688A>G (p.Met2230Val) rs751547785
NM_000038.6(APC):c.6750C>T (p.Gly2250=) rs555799753
NM_000038.6(APC):c.6812C>G (p.Pro2271Arg) rs1561610413
NM_000038.6(APC):c.6853G>A (p.Val2285Ile) rs1554087794
NM_000038.6(APC):c.688C>T (p.Arg230Cys) rs587779805
NM_000038.6(APC):c.689G>A (p.Arg230His) rs587780545
NM_000038.6(APC):c.6952A>G (p.Ser2318Gly) rs747056590
NM_000038.6(APC):c.6958C>T (p.Pro2320Ser) rs587778036
NM_000038.6(APC):c.7166G>A (p.Ser2389Asn) rs779287035
NM_000038.6(APC):c.7182T>C (p.Ser2394=) rs777420141
NM_000038.6(APC):c.7264A>G (p.Thr2422Ala) rs730881260
NM_000038.6(APC):c.730-3C>A rs786203125
NM_000038.6(APC):c.730-3C>T rs786203125
NM_000038.6(APC):c.7400C>T (p.Pro2467Leu) rs758713824
NM_000038.6(APC):c.7402T>C (p.Ser2468Pro) rs375586273
NM_000038.6(APC):c.7415C>T (p.Ala2472Val) rs200399245
NM_000038.6(APC):c.7472T>C (p.Met2491Thr) rs369075403
NM_000038.6(APC):c.7478T>C (p.Leu2493Pro) rs769889352
NM_000038.6(APC):c.7573C>T (p.Arg2525Cys) rs774952444
NM_000038.6(APC):c.7594C>T (p.His2532Tyr) rs375080917
NM_000038.6(APC):c.7621A>G (p.Ile2541Val) rs587778033
NM_000038.6(APC):c.7625A>G (p.Asn2542Ser) rs151163793
NM_000038.6(APC):c.7696A>C (p.Arg2566=) rs1060504883
NM_000038.6(APC):c.775C>T (p.Arg259Trp) rs762117133
NM_000038.6(APC):c.776G>A (p.Arg259Gln) rs767457050
NM_000038.6(APC):c.7832C>T (p.Thr2611Ile) rs587778037
NM_000038.6(APC):c.7833A>G (p.Thr2611=) rs1057520909
NM_000038.6(APC):c.7863T>A (p.Ser2621=) rs1561618785
NM_000038.6(APC):c.7967A>G (p.Asp2656Gly) rs1463203731
NM_000038.6(APC):c.7986G>A (p.Glu2662=) rs571645304
NM_000038.6(APC):c.8008A>C (p.Arg2670=) rs756875223
NM_000038.6(APC):c.800G>C (p.Gly267Ala) rs747759906
NM_000038.6(APC):c.8010A>G (p.Arg2670=) rs786201524
NM_000038.6(APC):c.8038C>G (p.Pro2680Ala) rs587780553
NM_000038.6(APC):c.8057T>C (p.Val2686Ala) rs757901425
NM_000038.6(APC):c.8071A>G (p.Asn2691Asp) rs1060503281
NM_000038.6(APC):c.8128A>C (p.Ser2710Arg) rs760472102
NM_000038.6(APC):c.8138T>C (p.Met2713Thr) rs1479889029
NM_000038.6(APC):c.8213T>C (p.Ile2738Thr) rs863224552
NM_000038.6(APC):c.8233C>A (p.Pro2745Thr) rs587779809
NM_000038.6(APC):c.8251A>G (p.Thr2751Ala) rs1060503341
NM_000038.6(APC):c.8281C>G (p.Pro2761Ala) rs1060503332
NM_000038.6(APC):c.8321G>C (p.Ser2774Thr) rs863224553
NM_000038.6(APC):c.8416C>G (p.Pro2806Ala) rs587780608
NM_000038.6(APC):c.8440A>G (p.Lys2814Glu) rs756826512
NM_000038.6(APC):c.8441_8444del (p.Lys2814fs) rs879253985
NM_000038.6(APC):c.8462A>G (p.Asp2821Gly) rs780049836
NM_000038.6(APC):c.918T>G (p.Ser306Arg) rs730881231
NM_000038.6(APC):c.933+7G>A rs369087912
NM_000038.6(APC):c.95A>G (p.Asn32Ser) rs539108537

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