ClinVar Miner

List of variants in gene combination AOPEP, FANCC reported as likely benign

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Gene type:
ClinVar version:
Total variants: 100
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HGVS dbSNP
NM_000136.2(FANCC):c.*10A>C rs1015228314
NM_000136.2(FANCC):c.*116A>C rs7048910
NM_000136.2(FANCC):c.*14C>T rs760413505
NM_000136.2(FANCC):c.*2085C>A rs4647559
NM_000136.2(FANCC):c.*2552T>C rs9673
NM_000136.2(FANCC):c.*359A>G rs4647551
NM_000136.2(FANCC):c.*42G>A rs7029888
NM_000136.2(FANCC):c.*604_*605delGT rs56271854
NM_000136.2(FANCC):c.*723_*726delAGTT rs56250966
NM_000136.2(FANCC):c.1023T>C (p.Phe341=) rs758439579
NM_000136.2(FANCC):c.1035T>G (p.Ser345=) rs1057522277
NM_000136.2(FANCC):c.1071A>G (p.Gln357=) rs1057522128
NM_000136.2(FANCC):c.1072+14G>C rs763466918
NM_000136.2(FANCC):c.1072+20G>A rs773767586
NM_000136.2(FANCC):c.1073-13T>C rs1057522472
NM_000136.2(FANCC):c.1073-18A>C rs876661081
NM_000136.2(FANCC):c.1073-20G>A rs781438798
NM_000136.2(FANCC):c.1073-4G>A rs147695697
NM_000136.2(FANCC):c.1073-5C>T rs375613884
NM_000136.2(FANCC):c.1095C>G (p.Leu365=) rs1057521687
NM_000136.2(FANCC):c.1095C>T (p.Leu365=) rs1057521687
NM_000136.2(FANCC):c.1107G>A (p.Lys369=) rs1321399501
NM_000136.2(FANCC):c.1155-13G>C rs747142087
NM_000136.2(FANCC):c.1155-16T>G rs1202931082
NM_000136.2(FANCC):c.1156T>C (p.Ser386Pro) rs41281202
NM_000136.2(FANCC):c.1161C>T (p.Cys387=) rs548998258
NM_000136.2(FANCC):c.1179C>T (p.Ser393=) rs1328914149
NM_000136.2(FANCC):c.1200C>T (p.Phe400=) rs767215159
NM_000136.2(FANCC):c.1242G>A (p.Ser414=) rs587780939
NM_000136.2(FANCC):c.1248C>T (p.Ala416=) rs747051975
NM_000136.2(FANCC):c.1254C>T (p.Pro418=) rs1057521431
NM_000136.2(FANCC):c.1257C>A (p.Pro419=) rs878853669
NM_000136.2(FANCC):c.1275C>G (p.Leu425=) rs767126985
NM_000136.2(FANCC):c.1281C>T (p.Ala427=) rs754604606
NM_000136.2(FANCC):c.1290C>T (p.Tyr430=) rs766105286
NM_000136.2(FANCC):c.1305G>C (p.Gly435=) rs765092951
NM_000136.2(FANCC):c.1317A>G (p.Arg439=) rs1554829450
NM_000136.2(FANCC):c.1329+10A>G rs977427150
NM_000136.2(FANCC):c.1329+181_1329+183delCCT rs587778328
NM_000136.2(FANCC):c.1329+238C>T rs768988593
NM_000136.2(FANCC):c.1329+246delC rs542091036
NM_000136.2(FANCC):c.1330-11C>T rs1057523289
NM_000136.2(FANCC):c.1330-3C>T rs4647542
NM_000136.2(FANCC):c.1330-4C>G rs762141353
NM_000136.2(FANCC):c.1330-6G>T rs1223668739
NM_000136.2(FANCC):c.1330-9A>G rs1264460608
NM_000136.2(FANCC):c.1344C>T (p.Ala448=) rs760983825
NM_000136.2(FANCC):c.1345G>A (p.Val449Met) rs1800367
NM_000136.2(FANCC):c.1394A>G (p.Gln465Arg) rs1800368
NM_000136.2(FANCC):c.1407G>A (p.Thr469=) rs79722116
NM_000136.2(FANCC):c.1414G>A (p.Gly472Arg) rs201063698
NM_000136.2(FANCC):c.1425A>G (p.Thr475=) rs199739450
NM_000136.2(FANCC):c.1467C>T (p.His489=) rs1554828385
NM_000136.2(FANCC):c.1485G>A (p.Leu495=) rs56082100
NM_000136.2(FANCC):c.1485G>C (p.Leu495=) rs56082100
NM_000136.2(FANCC):c.1488C>G (p.Leu496=) rs1057520505
NM_000136.2(FANCC):c.1494T>C (p.Ala498=) rs76895298
NM_000136.2(FANCC):c.1509G>A (p.Thr503=) rs144278080
NM_000136.2(FANCC):c.1524C>T (p.Val508=) rs765766432
NM_000136.2(FANCC):c.1527C>T (p.Ile509=) rs1554828322
NM_000136.2(FANCC):c.1530C>T (p.Thr510=) rs372199352
NM_000136.2(FANCC):c.1533+50G>A rs4647544
NM_000136.2(FANCC):c.1533+9C>T rs863224323
NM_000136.2(FANCC):c.1534-16T>C rs1057522372
NM_000136.2(FANCC):c.1534-5delT rs748342368
NM_000136.2(FANCC):c.1560C>T (p.His520=) rs150020474
NM_000136.2(FANCC):c.1594A>C (p.Arg532=) rs764649916
NM_000136.2(FANCC):c.1604G>A (p.Arg535His) rs587779902
NM_000136.2(FANCC):c.1611C>A (p.Gly537=) rs1027358273
NM_000136.2(FANCC):c.1623T>G (p.Pro541=) rs375362894
NM_000136.2(FANCC):c.705C>T (p.Pro235=) rs141828876
NM_000136.2(FANCC):c.738C>T (p.His246=) rs1414558793
NM_000136.2(FANCC):c.783A>C (p.Leu261=) rs1060504646
NM_000136.2(FANCC):c.816C>T (p.Ile272=) rs55719336
NM_000136.2(FANCC):c.817G>A (p.Glu273Lys) rs143181565
NM_000136.2(FANCC):c.840G>A (p.Ser280=) rs34671520
NM_000136.2(FANCC):c.843+14T>A rs1554835055
NM_000136.2(FANCC):c.843+4C>T rs4647506
NM_000136.2(FANCC):c.844-10_844-8delCCT rs758617953
NM_000136.2(FANCC):c.844-14T>C rs759280421
NM_000136.2(FANCC):c.882T>C (p.Val294=) rs750639831
NM_000136.2(FANCC):c.896+13_896+48del36 rs749142233
NM_000136.2(FANCC):c.896+6C>T rs199525333
NM_000136.2(FANCC):c.896+7G>A rs1554833182
NM_000136.2(FANCC):c.897-10C>T rs955495354
NM_000136.2(FANCC):c.897-18T>C rs1057523054
NM_000136.2(FANCC):c.897-3C>T rs1057521714
NM_000136.2(FANCC):c.897-8T>C rs878853673
NM_000136.2(FANCC):c.906C>G (p.Leu302=) rs766079351
NM_000136.2(FANCC):c.906C>T (p.Leu302=) rs766079351
NM_000136.2(FANCC):c.915C>T (p.Thr305=) rs138132690
NM_000136.2(FANCC):c.924C>G (p.Ala308=) rs864622225
NM_000136.2(FANCC):c.934A>G (p.Ile312Val) rs1800366
NM_000136.2(FANCC):c.957G>A (p.Thr319=) rs1060504647
NM_000136.2(FANCC):c.973G>A (p.Ala325Thr) rs201407189
NM_000136.2(FANCC):c.993G>A (p.Lys331=) rs748582850
NM_000136.2(FANCC):c.996+12C>A rs764979509
NM_000136.2(FANCC):c.996+9dupT rs781108327
NM_000136.2(FANCC):c.997-15T>C rs922997650
NM_000136.2(FANCC):c.997-6T>C rs1057524604

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