ClinVar Miner

List of variants in gene APC reported by Illumina Clinical Services Laboratory,Illumina

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Gene type:
ClinVar version:
Total variants: 117
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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.*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>C rs767384752
NM_000038.6(APC):c.*1753G>A rs397768
NM_000038.6(APC):c.*1834T>G rs886059815
NM_000038.6(APC):c.*1840A>G rs886059816
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.*2005T>G rs559244186
NM_000038.6(APC):c.*2087C>A rs886059820
NM_000038.6(APC):c.*210_*213del rs763673039
NM_000038.6(APC):c.*248A>G rs186777258
NM_000038.6(APC):c.*266C>A rs191347307
NM_000038.6(APC):c.*404_*405insA rs1554089340
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.*624A>C rs886059806
NM_000038.6(APC):c.*645A>G rs886059807
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.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.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.2322C>T (p.Asp774=) rs145792879
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.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.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.3732A>G (p.Gln1244=) rs74380081
NM_000038.6(APC):c.3949G>C (p.Glu1317Gln) rs1801166
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.4594G>A (p.Asp1532Asn) rs730881251
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.5194A>G (p.Met1732Val) rs752065261
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.5363G>A (p.Arg1788His) rs201472075
NM_000038.6(APC):c.5399A>G (p.Asn1800Ser) rs865782682
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.573T>C (p.Tyr191=) rs185154886
NM_000038.6(APC):c.5790A>G (p.Gln1930=) rs141152252
NM_000038.6(APC):c.5840C>G (p.Thr1947Ser) rs575724078
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.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.6821C>T (p.Ala2274Val) rs34919187
NM_000038.6(APC):c.6921G>A (p.Ser2307=) rs2229993
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.7415C>T (p.Ala2472Val) rs200399245
NM_000038.6(APC):c.7504G>A (p.Gly2502Ser) rs2229995
NM_000038.6(APC):c.7704A>G (p.Gly2568=) rs35043160
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.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.8389A>G (p.Ser2797Gly) rs147287751
NM_000038.6(APC):c.8425G>A (p.Val2809Met) rs886059801
NM_001127511.3(APC):c.166-28452G>C rs115242894

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