ClinVar Miner

List of variants in gene APC reported by ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories

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Total variants: 64
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HGVS dbSNP
NM_000038.5(APC):c.1213C>T (p.Arg405Ter) rs587779780
NM_000038.5(APC):c.1370C>G (p.Ser457Ter) rs1060503333
NM_000038.5(APC):c.1458T>C (p.Tyr486=) rs2229992
NM_000038.5(APC):c.1635G>A (p.Ala545=) rs351771
NM_000038.5(APC):c.1695A>G (p.Glu565=) rs77921116
NM_000038.5(APC):c.1866C>A (p.Tyr622Ter) rs876658355
NM_000038.5(APC):c.1958+8T>C rs62626346
NM_000038.5(APC):c.2232T>G (p.Ser744=) rs145751759
NM_000038.5(APC):c.2485delA (p.Thr829Glnfs)
NM_000038.5(APC):c.2608C>T (p.Pro870Ser) rs33974176
NM_000038.5(APC):c.2739T>C (p.His913=) rs553363502
NM_000038.5(APC):c.2805C>T (p.Tyr935=) rs137854575
NM_000038.5(APC):c.295C>T (p.Arg99Trp) rs139196838
NM_000038.5(APC):c.311C>G (p.Ser104Ter) rs74953290
NM_000038.5(APC):c.3146G>A (p.Trp1049Ter) rs876658667
NM_000038.5(APC):c.3165A>T (p.Ile1055=) rs61734287
NM_000038.5(APC):c.3279T>G (p.Phe1093Leu) rs199539973
NM_000038.5(APC):c.3386T>C (p.Leu1129Ser) rs143638171
NM_000038.5(APC):c.3468_3470delAGA (p.Glu1157del) rs386833391
NM_000038.5(APC):c.3732A>G (p.Gln1244=) rs74380081
NM_000038.5(APC):c.3920T>A (p.Ile1307Lys) rs1801155
NM_000038.5(APC):c.3949G>C (p.Glu1317Gln) rs1801166
NM_000038.5(APC):c.426_427delAT (p.Leu143Alafs) rs587782557
NM_000038.5(APC):c.4326T>A (p.Pro1442=) rs67622085
NM_000038.5(APC):c.4420G>A (p.Ala1474Thr) rs139387758
NM_000038.5(APC):c.4479G>A (p.Thr1493=) rs41115
NM_000038.5(APC):c.4732T>G (p.Cys1578Gly) rs138367627
NM_000038.5(APC):c.5034G>A (p.Gly1678=) rs42427
NM_000038.5(APC):c.5250C>G (p.Val1750=) rs2229997
NM_000038.5(APC):c.5265G>A (p.Ala1755=) rs34506289
NM_000038.5(APC):c.5268T>G (p.Ser1756=) rs866006
NM_000038.5(APC):c.5880G>A (p.Pro1960=) rs465899
NM_000038.5(APC):c.6117G>T (p.Leu2039Phe) rs372418435
NM_000038.5(APC):c.643C>T (p.Gln215Ter) rs137854577
NM_000038.5(APC):c.645+32C>T rs2909961
NM_000038.5(APC):c.6669A>G (p.Ser2223=) rs372680843
NM_000038.5(APC):c.6821C>T (p.Ala2274Val) rs34919187
NM_000038.5(APC):c.705A>G (p.Leu235=) rs147036141
NM_000038.5(APC):c.70C>T (p.Arg24Ter) rs145945630
NM_000038.5(APC):c.7201C>T (p.Leu2401=) rs2229994
NM_000038.5(APC):c.7415C>T (p.Ala2472Val) rs200399245
NM_000038.5(APC):c.7704A>G (p.Gly2568=) rs35043160
NM_000038.5(APC):c.7786T>G (p.Ser2596Ala) rs138137162
NM_000038.5(APC):c.7862C>G (p.Ser2621Cys) rs72541816
NM_000038.5(APC):c.933+30A>G rs145211300
NM_000038.6(APC):c.2651C>T (p.Ala884Val)
NM_000038.6(APC):c.5465T>A (p.Val1822Asp) rs459552
NM_000038.6(APC):c.5839A>C (p.Thr1947Pro)
NM_000038.6(APC):c.8465G>C (p.Ser2822Thr)
NM_000038.6(APC):c.8466C>A (p.Ser2822Arg)
NM_001127510.2(APC):c.-18-13T>G rs1554067089
NM_001127510.2(APC):c.1312+27G>A rs74975092
NM_001127510.2(APC):c.1512T>C (p.Ala504=)
NM_001127510.2(APC):c.1937T>G (p.Ile646Arg) rs1554083243
NM_001127510.2(APC):c.2589C>A (p.Tyr863Ter)
NM_001127510.2(APC):c.532-1G>A rs1554072547
NM_001127510.2(APC):c.6281_6282delCT (p.Pro2094Argfs) rs1554087314
NM_001127510.2(APC):c.834+1G>A rs1554076225
NM_001127510.2:c.2100dupC
NM_001127510.2:c.4638_4639delTG
NM_001127510.2:c.5971_5972insGCAGCATCTGATGAAAAGTTACAGAATTTTGCTATTGAAAATACTCCGGTTTGCTTTTCTCATAATTCCTCTCTGAGTTCTCTCAGTGACATTGACCAAGAAAACAACAATAAAGAAAATGAACCTATCAAAGAGACTGG
NM_001127511.2(APC):c.-31T>G rs78429131
NM_001127511.2(APC):c.5211_5214delGTCTinsATCG (p.Ala1737_Ser1738=) rs1554086584
NM_001127511.2(APC):c.78C>A (p.Ser26Arg) rs113782655

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