ClinVar Miner

List of variants in gene APC studied for APC-Associated Polyposis Disorders

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Gene type:
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Total variants: 191
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HGVS dbSNP
NM_000038.6(APC):c.*1050T>C rs17135042
NM_000038.6(APC):c.*1098T>C rs41116
NM_000038.6(APC):c.*1127C>A
NM_000038.6(APC):c.*1132C>A rs886059811
NM_000038.6(APC):c.*1164G>A rs576186544
NM_000038.6(APC):c.*1203A>C rs6594650
NM_000038.6(APC):c.*1233_*1235TAT[1] rs886059812
NM_000038.6(APC):c.*1294A>G rs886059813
NM_000038.6(APC):c.*1304G>A rs112588804
NM_000038.6(APC):c.*1320T>A rs373883680
NM_000038.6(APC):c.*142C>T rs6875894
NM_000038.6(APC):c.*1460C>T rs3733961
NM_000038.6(APC):c.*1497C>T rs138754620
NM_000038.6(APC):c.*1555C>T rs886059814
NM_000038.6(APC):c.*1556C>G rs448475
NM_000038.6(APC):c.*1609T>A
NM_000038.6(APC):c.*1609T>C rs767384752
NM_000038.6(APC):c.*1753G>A rs397768
NM_000038.6(APC):c.*1818A>G
NM_000038.6(APC):c.*1834T>G rs886059815
NM_000038.6(APC):c.*1840A>G rs886059816
NM_000038.6(APC):c.*1918G>C
NM_000038.6(APC):c.*1937G>T rs886059817
NM_000038.6(APC):c.*1960C>G rs886059818
NM_000038.6(APC):c.*1970T>G rs886059819
NM_000038.6(APC):c.*1986C>T
NM_000038.6(APC):c.*2005T>G rs559244186
NM_000038.6(APC):c.*2087C>A rs886059820
NM_000038.6(APC):c.*210_*213del rs763673039
NM_000038.6(APC):c.*2111G>A
NM_000038.6(APC):c.*248A>G rs186777258
NM_000038.6(APC):c.*266C>A rs191347307
NM_000038.6(APC):c.*275A>G
NM_000038.6(APC):c.*404_*405insA rs1554089340
NM_000038.6(APC):c.*405C>A rs79379053
NM_000038.6(APC):c.*414dup rs397817775
NM_000038.6(APC):c.*434C>T rs12189
NM_000038.6(APC):c.*505C>A rs886059803
NM_000038.6(APC):c.*551T>C rs886059804
NM_000038.6(APC):c.*574T>C rs886059805
NM_000038.6(APC):c.*582C>T
NM_000038.6(APC):c.*624A>C rs886059806
NM_000038.6(APC):c.*645A>G rs886059807
NM_000038.6(APC):c.*650T>C
NM_000038.6(APC):c.*655G>T
NM_000038.6(APC):c.*714G>T rs886059808
NM_000038.6(APC):c.*86C>A rs1804197
NM_000038.6(APC):c.*913T>C rs886059809
NM_000038.6(APC):c.*928_*929del rs555618339
NM_000038.6(APC):c.120G>A (p.Glu40=) rs142720069
NM_000038.6(APC):c.1240C>T (p.Arg414Cys) rs137854567
NM_000038.6(APC):c.1312+12A>G rs372970635
NM_000038.6(APC):c.1398G>A (p.Met466Ile) rs878853417
NM_000038.6(APC):c.1458T>C (p.Tyr486=) rs2229992
NM_000038.6(APC):c.1488A>T (p.Thr496=) rs9282599
NM_000038.6(APC):c.1562C>G (p.Ser521Cys) rs1554081882
NM_000038.6(APC):c.1631T>C (p.Ile544Thr) rs144056494
NM_000038.6(APC):c.1635G>A (p.Ala545=) rs351771
NM_000038.6(APC):c.1695A>G (p.Glu565=) rs77921116
NM_000038.6(APC):c.1722A>G (p.Glu574=) rs786201277
NM_000038.6(APC):c.1958+10G>T rs375175370
NM_000038.6(APC):c.1958+8T>C rs62626346
NM_000038.6(APC):c.1959G>A (p.Arg653=) rs72541809
NM_000038.6(APC):c.2110G>A (p.Val704Ile) rs367804502
NM_000038.6(APC):c.2205G>A (p.Ala735=) rs141001261
NM_000038.6(APC):c.2223T>C (p.Asn741=) rs1554084025
NM_000038.6(APC):c.2258A>G (p.His753Arg) rs1580619903
NM_000038.6(APC):c.2322C>T (p.Asp774=) rs145792879
NM_000038.6(APC):c.2444A>C (p.Asn815Thr) rs762990578
NM_000038.6(APC):c.2481T>C (p.Asn827=) rs749477816
NM_000038.6(APC):c.2547T>C (p.Asp849=) rs766086010
NM_000038.6(APC):c.2555T>G (p.Leu852Trp) rs1405022793
NM_000038.6(APC):c.2586C>G (p.Asn862Lys) rs147972247
NM_000038.6(APC):c.2593C>T (p.Pro865Ser) rs192620988
NM_000038.6(APC):c.2608C>T (p.Pro870Ser) rs33974176
NM_000038.6(APC):c.2654C>T (p.Ala885Val)
NM_000038.6(APC):c.2658G>T (p.Gln886His) rs587780593
NM_000038.6(APC):c.2805C>T (p.Tyr935=) rs137854575
NM_000038.6(APC):c.2958T>C (p.Tyr986=) rs746581330
NM_000038.6(APC):c.3165A>T (p.Ile1055=) rs61734287
NM_000038.6(APC):c.3173A>G (p.Asp1058Gly) rs148725540
NM_000038.6(APC):c.3210T>C (p.Asn1070=) rs886059794
NM_000038.6(APC):c.3341G>A (p.Arg1114Gln) rs753209586
NM_000038.6(APC):c.336T>A (p.Pro112=) rs886059793
NM_000038.6(APC):c.3374T>C (p.Val1125Ala) rs377278397
NM_000038.6(APC):c.3378C>G (p.Ser1126Arg) rs149353082
NM_000038.6(APC):c.3386T>C (p.Leu1129Ser) rs143638171
NM_000038.6(APC):c.3462_3464AGA[2] (p.Glu1157del) rs386833391
NM_000038.6(APC):c.3471G>A (p.Glu1157=) rs143927847
NM_000038.6(APC):c.3625G>A (p.Glu1209Lys) rs201185479
NM_000038.6(APC):c.3653C>T (p.Thr1218Met) rs377640390
NM_000038.6(APC):c.3732A>G (p.Gln1244=) rs74380081
NM_000038.6(APC):c.388A>G (p.Ser130Gly) rs150973053
NM_000038.6(APC):c.3901A>T (p.Thr1301Ser)
NM_000038.6(APC):c.3949G>C (p.Glu1317Gln) rs1801166
NM_000038.6(APC):c.4049A>C (p.Lys1350Thr)
NM_000038.6(APC):c.4201A>G (p.Ile1401Val) rs1554085612
NM_000038.6(APC):c.422G>A (p.Arg141Lys) rs1359881085
NM_000038.6(APC):c.4326T>A (p.Pro1442=) rs67622085
NM_000038.6(APC):c.4343C>T (p.Thr1448Ile) rs907886109
NM_000038.6(APC):c.4360A>G (p.Lys1454Glu) rs111866410
NM_000038.6(APC):c.4420G>A (p.Ala1474Thr) rs139387758
NM_000038.6(APC):c.4479G>A (p.Thr1493=) rs41115
NM_000038.6(APC):c.450A>G (p.Lys150=) rs116020626
NM_000038.6(APC):c.4534G>A (p.Asp1512Asn) rs778699501
NM_000038.6(APC):c.4594G>A (p.Asp1532Asn) rs730881251
NM_000038.6(APC):c.4765C>G (p.Arg1589Gly) rs72541813
NM_000038.6(APC):c.4833G>A (p.Gln1611=) rs762030106
NM_000038.6(APC):c.4893T>C (p.Ser1631=) rs35634377
NM_000038.6(APC):c.4905G>A (p.Gly1635=) rs137988845
NM_000038.6(APC):c.4913T>C (p.Met1638Thr) rs201797422
NM_000038.6(APC):c.5034G>A (p.Gly1678=) rs42427
NM_000038.6(APC):c.5050T>C (p.Phe1684Leu) rs886059795
NM_000038.6(APC):c.5078A>G (p.Glu1693Gly) rs533667536
NM_000038.6(APC):c.5140G>A (p.Asp1714Asn) rs148275069
NM_000038.6(APC):c.5194A>G (p.Met1732Val) rs752065261
NM_000038.6(APC):c.5224C>T (p.Arg1742Cys) rs876658835
NM_000038.6(APC):c.5225G>A (p.Arg1742His) rs199775075
NM_000038.6(APC):c.5250C>G (p.Val1750=) rs2229997
NM_000038.6(APC):c.5265G>A (p.Ala1755=) rs34506289
NM_000038.6(APC):c.5268T>A (p.Ser1756=) rs866006
NM_000038.6(APC):c.5268T>G (p.Ser1756=) rs866006
NM_000038.6(APC):c.5363G>A (p.Arg1788His) rs201472075
NM_000038.6(APC):c.5399A>G (p.Asn1800Ser) rs865782682
NM_000038.6(APC):c.5424C>T (p.Asn1808=) rs747721259
NM_000038.6(APC):c.5465T>A (p.Val1822Asp) rs459552
NM_000038.6(APC):c.5524T>A (p.Ser1842Thr) rs754648125
NM_000038.6(APC):c.5658A>G (p.Glu1886=) rs1417046511
NM_000038.6(APC):c.5712A>G (p.Gln1904=) rs755851369
NM_000038.6(APC):c.573T>C (p.Tyr191=) rs185154886
NM_000038.6(APC):c.5790A>G (p.Gln1930=) rs141152252
NM_000038.6(APC):c.5801C>T (p.Pro1934Leu) rs587780600
NM_000038.6(APC):c.5840C>G (p.Thr1947Ser) rs575724078
NM_000038.6(APC):c.5879C>T (p.Pro1960Leu) rs587781546
NM_000038.6(APC):c.5880G>A (p.Pro1960=) rs465899
NM_000038.6(APC):c.5894A>C (p.His1965Pro) rs773776516
NM_000038.6(APC):c.5894A>G (p.His1965Arg) rs773776516
NM_000038.6(APC):c.5952T>C (p.Asn1984=) rs142019870
NM_000038.6(APC):c.6019T>C (p.Tyr2007His) rs745811356
NM_000038.6(APC):c.607C>G (p.Gln203Glu) rs141576417
NM_000038.6(APC):c.6316G>C (p.Glu2106Gln) rs886059796
NM_000038.6(APC):c.6387G>A (p.Ser2129=) rs374310157
NM_000038.6(APC):c.647G>A (p.Arg216Gln) rs76685252
NM_000038.6(APC):c.6492C>T (p.Gly2164=) rs765332758
NM_000038.6(APC):c.6525A>G (p.Thr2175=) rs200151646
NM_000038.6(APC):c.6526T>C (p.Leu2176=) rs183468041
NM_000038.6(APC):c.6556A>C (p.Lys2186Gln) rs886059797
NM_000038.6(APC):c.6609T>C (p.Val2203=) rs149328018
NM_000038.6(APC):c.6624A>G (p.Glu2208=) rs886059798
NM_000038.6(APC):c.6639G>A (p.Met2213Ile) rs35540155
NM_000038.6(APC):c.6724A>G (p.Ser2242Gly) rs201375478
NM_000038.6(APC):c.672C>A (p.Ile224=) rs367816013
NM_000038.6(APC):c.6741T>C (p.Ser2247=) rs878853464
NM_000038.6(APC):c.6814A>G (p.Arg2272Gly) rs1561610453
NM_000038.6(APC):c.6821C>T (p.Ala2274Val) rs34919187
NM_000038.6(APC):c.6873A>T (p.Gln2291His) rs148878262
NM_000038.6(APC):c.6887G>A (p.Ser2296Asn) rs919611781
NM_000038.6(APC):c.6921G>A (p.Ser2307=) rs2229993
NM_000038.6(APC):c.6985A>G (p.Ile2329Val) rs146048493
NM_000038.6(APC):c.6989C>T (p.Ser2330Phe) rs1554087891
NM_000038.6(APC):c.7036C>T (p.Pro2346Ser) rs200756935
NM_000038.6(APC):c.705A>G (p.Leu235=) rs147036141
NM_000038.6(APC):c.7201C>T (p.Leu2401=) rs2229994
NM_000038.6(APC):c.7209G>A (p.Gln2403=) rs769603145
NM_000038.6(APC):c.72A>T (p.Arg24=)
NM_000038.6(APC):c.7389A>C (p.Glu2463Asp) rs587782127
NM_000038.6(APC):c.7415C>T (p.Ala2472Val) rs200399245
NM_000038.6(APC):c.7490C>T (p.Ser2497Leu) rs141010008
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser) rs2229995
NM_000038.6(APC):c.757G>A (p.Gly253Ser) rs772806807
NM_000038.6(APC):c.7704A>G (p.Gly2568=) rs35043160
NM_000038.6(APC):c.772G>C (p.Glu258Gln) rs774604680
NM_000038.6(APC):c.777G>T (p.Arg259=) rs147704593
NM_000038.6(APC):c.7781C>G (p.Ser2594Cys) rs543396310
NM_000038.6(APC):c.7821C>T (p.Ser2607=) rs532235331
NM_000038.6(APC):c.7862C>G (p.Ser2621Cys) rs72541816
NM_000038.6(APC):c.7903A>G (p.Thr2635Ala) rs886059799
NM_000038.6(APC):c.7929A>G (p.Leu2643=) rs138796072
NM_000038.6(APC):c.7957A>G (p.Lys2653Glu) rs1554088788
NM_000038.6(APC):c.8033A>G (p.Asn2678Ser) rs886059800
NM_000038.6(APC):c.8043G>C (p.Pro2681=) rs149347068
NM_000038.6(APC):c.8100T>C (p.Asn2700=) rs761326128
NM_000038.6(APC):c.8107A>G (p.Lys2703Glu) rs730881270
NM_000038.6(APC):c.8212A>G (p.Ile2738Val) rs876658839
NM_000038.6(APC):c.8266A>G (p.Ile2756Val) rs146115809
NM_000038.6(APC):c.8298C>T (p.Ser2766=) rs876658523
NM_000038.6(APC):c.8389A>G (p.Ser2797Gly) rs147287751
NM_000038.6(APC):c.8425G>A (p.Val2809Met) rs886059801
NM_000038.6(APC):c.8454C>T (p.Ser2818=)
NM_000038.6(APC):c.934-14C>T rs778707022
NM_001127511.3(APC):c.166-28452G>C rs115242894

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