ClinVar Miner

List of variants in gene combination AOPEP, FANCC reported as likely benign for not specified

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Gene type:
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Total variants: 56
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HGVS dbSNP
NM_000136.2(FANCC):c.1534-5delT rs748342368
NM_000136.3(FANCC):c.*10A>C rs1015228314
NM_000136.3(FANCC):c.*14C>T rs760413505
NM_000136.3(FANCC):c.1035T>G (p.Ser345=) rs1057522277
NM_000136.3(FANCC):c.1071A>G (p.Gln357=) rs1057522128
NM_000136.3(FANCC):c.1072+14G>C rs763466918
NM_000136.3(FANCC):c.1072+20G>A rs773767586
NM_000136.3(FANCC):c.1073-13T>C rs1057522472
NM_000136.3(FANCC):c.1073-18A>C rs876661081
NM_000136.3(FANCC):c.1073-20G>A rs781438798
NM_000136.3(FANCC):c.1073-4G>A rs147695697
NM_000136.3(FANCC):c.1095C>G (p.Leu365=) rs1057521687
NM_000136.3(FANCC):c.1095C>T (p.Leu365=) rs1057521687
NM_000136.3(FANCC):c.1107G>A (p.Lys369=) rs1321399501
NM_000136.3(FANCC):c.1155-13G>C rs747142087
NM_000136.3(FANCC):c.1155-16T>G rs1202931082
NM_000136.3(FANCC):c.1161C>T (p.Cys387=) rs548998258
NM_000136.3(FANCC):c.1248C>T (p.Ala416=) rs747051975
NM_000136.3(FANCC):c.1254C>T (p.Pro418=) rs1057521431
NM_000136.3(FANCC):c.1257C>A (p.Pro419=) rs878853669
NM_000136.3(FANCC):c.1305G>C (p.Gly435=) rs765092951
NM_000136.3(FANCC):c.1317A>G (p.Arg439=) rs1554829450
NM_000136.3(FANCC):c.1330-11C>T rs1057523289
NM_000136.3(FANCC):c.1330-4C>G rs762141353
NM_000136.3(FANCC):c.1330-6G>T rs1223668739
NM_000136.3(FANCC):c.1330-9A>G rs1264460608
NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg) rs1800368
NM_000136.3(FANCC):c.1425A>G (p.Thr475=) rs199739450
NM_000136.3(FANCC):c.1485G>A (p.Leu495=) rs56082100
NM_000136.3(FANCC):c.1485G>C (p.Leu495=) rs56082100
NM_000136.3(FANCC):c.1488C>G (p.Leu496=) rs1057520505
NM_000136.3(FANCC):c.1524C>T (p.Val508=) rs765766432
NM_000136.3(FANCC):c.1527C>T (p.Ile509=) rs1554828322
NM_000136.3(FANCC):c.1534-16T>C rs1057522372
NM_000136.3(FANCC):c.1560C>T (p.His520=) rs150020474
NM_000136.3(FANCC):c.1604G>A (p.Arg535His) rs587779902
NM_000136.3(FANCC):c.1611C>A (p.Gly537=) rs1027358273
NM_000136.3(FANCC):c.1623T>G (p.Pro541=) rs375362894
NM_000136.3(FANCC):c.738C>T (p.His246=) rs1414558793
NM_000136.3(FANCC):c.816C>T (p.Ile272=) rs55719336
NM_000136.3(FANCC):c.843+14T>A rs1554835055
NM_000136.3(FANCC):c.844-14T>C rs759280421
NM_000136.3(FANCC):c.896+13_896+48del rs749142233
NM_000136.3(FANCC):c.896+6C>T rs199525333
NM_000136.3(FANCC):c.897-18T>C rs1057523054
NM_000136.3(FANCC):c.897-3C>T rs1057521714
NM_000136.3(FANCC):c.897-8T>C rs878853673
NM_000136.3(FANCC):c.906C>G (p.Leu302=) rs766079351
NM_000136.3(FANCC):c.934A>G (p.Ile312Val) rs1800366
NM_000136.3(FANCC):c.957G>A (p.Thr319=) rs1060504647
NM_000136.3(FANCC):c.973G>A (p.Ala325Thr) rs201407189
NM_000136.3(FANCC):c.993G>A (p.Lys331=) rs748582850
NM_000136.3(FANCC):c.996+12C>A rs764979509
NM_000136.3(FANCC):c.996+9dup rs781108327
NM_000136.3(FANCC):c.997-15T>C rs922997650
NM_000136.3(FANCC):c.997-6T>C rs1057524604

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