ClinVar Miner

List of variants in gene APC reported by PreventionGenetics

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Gene type:
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Total variants: 134
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HGVS dbSNP
NM_000038.6(APC):c.*86C>A rs1804197
NM_000038.6(APC):c.1139G>A (p.Arg380Gln) rs587782886
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.1241G>A (p.Arg414His) rs730881233
NM_000038.6(APC):c.1408+792A>T rs77551834
NM_000038.6(APC):c.1419G>A (p.Gln473=) rs141579422
NM_000038.6(APC):c.1458T>C (p.Tyr486=) rs2229992
NM_000038.6(APC):c.1557A>G (p.Leu519=) rs765537673
NM_000038.6(APC):c.1635G>A (p.Ala545=) rs351771
NM_000038.6(APC):c.1686G>A (p.Thr562=) rs770256026
NM_000038.6(APC):c.1695A>G (p.Glu565=) rs77921116
NM_000038.6(APC):c.1825G>A (p.Val609Ile) rs147863331
NM_000038.6(APC):c.1958+8T>C rs62626346
NM_000038.6(APC):c.1959G>A (p.Arg653=) rs72541809
NM_000038.6(APC):c.2026A>G (p.Ile676Val) rs745529713
NM_000038.6(APC):c.2031C>T (p.Val677=) rs769363082
NM_000038.6(APC):c.2222A>G (p.Asn741Ser) rs150209825
NM_000038.6(APC):c.2262T>G (p.Val754=) rs148987776
NM_000038.6(APC):c.2297C>T (p.Ala766Val) rs200339830
NM_000038.6(APC):c.2322C>T (p.Asp774=) rs145792879
NM_000038.6(APC):c.2438A>G (p.Asn813Ser) rs201522866
NM_000038.6(APC):c.2444A>C (p.Asn815Thr) rs762990578
NM_000038.6(APC):c.2503T>C (p.Ser835Pro) rs748302469
NM_000038.6(APC):c.2552G>A (p.Ser851Asn) rs1554084260
NM_000038.6(APC):c.2608C>T (p.Pro870Ser) rs33974176
NM_000038.6(APC):c.2805C>T (p.Tyr935=) rs137854575
NM_000038.6(APC):c.2946G>A (p.Ser982=) rs377384463
NM_000038.6(APC):c.3049_3051del (p.Asn1017del) rs730881229
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.317G>A (p.Arg106His) rs201764637
NM_000038.6(APC):c.3249T>G (p.Asp1083Glu) rs201629780
NM_000038.6(APC):c.3264G>A (p.Lys1088=) rs114774495
NM_000038.6(APC):c.3368A>C (p.Gln1123Pro) rs587779789
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.3511C>T (p.Arg1171Cys) rs201830995
NM_000038.6(APC):c.3555A>G (p.Thr1185=) rs786201125
NM_000038.6(APC):c.358A>G (p.Arg120Gly) rs876659470
NM_000038.6(APC):c.3624C>T (p.Thr1208=) rs730882125
NM_000038.6(APC):c.3650A>C (p.Asn1217Thr) rs138933660
NM_000038.6(APC):c.3732A>G (p.Gln1244=) rs74380081
NM_000038.6(APC):c.3798T>C (p.Asp1266=) rs1488397941
NM_000038.6(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.6(APC):c.3949G>C (p.Glu1317Gln) rs1801166
NM_000038.6(APC):c.4005C>T (p.Ser1335=) rs751729992
NM_000038.6(APC):c.4326T>A (p.Pro1442=) rs67622085
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.449A>G (p.Lys150Arg) rs371085910
NM_000038.6(APC):c.4765C>G (p.Arg1589Gly) rs72541813
NM_000038.6(APC):c.4828A>G (p.Ser1610Gly) rs587781512
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.4963A>G (p.Thr1655Ala) rs759441332
NM_000038.6(APC):c.5009C>T (p.Ala1670Val) rs202228932
NM_000038.6(APC):c.5026A>G (p.Arg1676Gly) rs370560998
NM_000038.6(APC):c.5034G>A (p.Gly1678=) rs42427
NM_000038.6(APC):c.5113A>G (p.Thr1705Ala) rs1554086453
NM_000038.6(APC):c.5140G>A (p.Asp1714Asn) rs148275069
NM_000038.6(APC):c.5147A>G (p.Asn1716Ser) rs141298709
NM_000038.6(APC):c.5178A>G (p.Glu1726=) rs368494571
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>G (p.Ser1756=) rs866006
NM_000038.6(APC):c.5271T>C (p.Ser1757=) rs752875511
NM_000038.6(APC):c.5274T>A (p.Ser1758=) rs199600387
NM_000038.6(APC):c.5282A>C (p.Asn1761Thr) rs752038930
NM_000038.6(APC):c.5298T>C (p.Asp1766=) rs781533317
NM_000038.6(APC):c.5421_5423CAA[1] (p.Asn1808del) rs587782002
NM_000038.6(APC):c.5465T>A (p.Val1822Asp) rs459552
NM_000038.6(APC):c.5478G>A (p.Lys1826=) rs768922376
NM_000038.6(APC):c.5500G>A (p.Val1834Ile) rs555944438
NM_000038.6(APC):c.5506G>A (p.Gly1836Arg) rs766739164
NM_000038.6(APC):c.5528C>T (p.Pro1843Leu) rs368080169
NM_000038.6(APC):c.5571A>C (p.Ser1857=) rs376624613
NM_000038.6(APC):c.5687G>A (p.Ser1896Asn) rs751088165
NM_000038.6(APC):c.5790A>G (p.Gln1930=) rs141152252
NM_000038.6(APC):c.5794A>T (p.Thr1932Ser) rs777604445
NM_000038.6(APC):c.5805G>A (p.Gln1935=) rs377040690
NM_000038.6(APC):c.5880G>A (p.Pro1960=) rs465899
NM_000038.6(APC):c.588C>T (p.Ile196=) rs147846364
NM_000038.6(APC):c.5908A>C (p.Ser1970Arg) rs1561603616
NM_000038.6(APC):c.607C>G (p.Gln203Glu) rs141576417
NM_000038.6(APC):c.608A>G (p.Gln203Arg) rs1554072626
NM_000038.6(APC):c.6135C>T (p.Ser2045=) rs187297940
NM_000038.6(APC):c.6150_6151del (p.Lys2052fs) rs1561605508
NM_000038.6(APC):c.6245A>G (p.Asp2082Gly) rs554370603
NM_000038.6(APC):c.626A>T (p.Asp209Val) rs1554072636
NM_000038.6(APC):c.6349C>A (p.Gln2117Lys) rs587780546
NM_000038.6(APC):c.6354_6356TGC[5] (p.Ala2122dup) rs587780602
NM_000038.6(APC):c.643C>T (p.Gln215Ter) rs137854577
NM_000038.6(APC):c.6446A>C (p.His2149Pro) rs749230730
NM_000038.6(APC):c.645+32C>T rs2909961
NM_000038.6(APC):c.6510A>C (p.Pro2170=) rs138571760
NM_000038.6(APC):c.6526T>C (p.Leu2176=) rs183468041
NM_000038.6(APC):c.6750C>T (p.Gly2250=) rs555799753
NM_000038.6(APC):c.6821C>T (p.Ala2274Val) rs34919187
NM_000038.6(APC):c.6921G>A (p.Ser2307=) rs2229993
NM_000038.6(APC):c.7026A>G (p.Leu2342=) rs766086022
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.7205A>G (p.Asn2402Ser) rs745843442
NM_000038.6(APC):c.7399C>A (p.Pro2467Thr) rs372305287
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser) rs2229995
NM_000038.6(APC):c.7514G>A (p.Arg2505Gln) rs147549623
NM_000038.6(APC):c.7621A>G (p.Ile2541Val) rs587778033
NM_000038.6(APC):c.7652A>T (p.His2551Leu) rs1060503314
NM_000038.6(APC):c.7704A>G (p.Gly2568=) rs35043160
NM_000038.6(APC):c.7717A>G (p.Ile2573Val) rs145444830
NM_000038.6(APC):c.7731A>G (p.Ser2577=) rs537187449
NM_000038.6(APC):c.7862C>G (p.Ser2621Cys) rs72541816
NM_000038.6(APC):c.789T>A (p.Gly263=) rs767053295
NM_000038.6(APC):c.8042C>T (p.Pro2681Leu) rs182456139
NM_000038.6(APC):c.8043G>C (p.Pro2681=) rs149347068
NM_000038.6(APC):c.8068G>A (p.Ala2690Thr) rs140868933
NM_000038.6(APC):c.8104G>A (p.Ala2702Thr) rs587779808
NM_000038.6(APC):c.8161C>T (p.Arg2721Cys) rs587782312
NM_000038.6(APC):c.8182G>A (p.Val2728Met) rs587778045
NM_000038.6(APC):c.8378G>A (p.Ser2793Asn) rs374853436
NM_000038.6(APC):c.8389A>G (p.Ser2797Gly) rs147287751
NM_000038.6(APC):c.8419A>G (p.Thr2807Ala) rs894164638
NM_000038.6(APC):c.8511T>C (p.Ser2837=) rs1010623341
NM_000038.6(APC):c.933+15C>T
NM_000038.6(APC):c.933+30A>G rs145211300
NM_000038.6(APC):c.934-17del rs762333924
NM_001127511.3(APC):c.-3C>A
NM_001127511.3(APC):c.125G>A (p.Gly42Asp) rs1057517570
NM_001127511.3(APC):c.16G>A (p.Gly6Ser) rs1043505718
NM_001127511.3(APC):c.78C>A (p.Ser26Arg) rs113782655

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