ClinVar Miner

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

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Gene type:
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Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_000136.3(FANCC):c.1155-38T>C rs4647534 0.48457
NM_000136.3(FANCC):c.1330-141T>C rs2282216 0.48441
NM_000136.3(FANCC):c.*1288T>C rs4647554 0.45294
NM_000136.3(FANCC):c.1329+406C>T rs879492 0.37157
NM_000136.3(FANCC):c.*1871G>A rs4647558 0.36840
NM_000136.3(FANCC):c.1329+310C>T rs2404457 0.36786
NM_000136.3(FANCC):c.896+81G>A rs4647512 0.03851
NM_000136.3(FANCC):c.687-288C>T rs4647505 0.03615
NM_000136.3(FANCC):c.*116A>C rs7048910 0.03439
NM_000136.3(FANCC):c.*2552T>C rs9673 0.02750
NM_000136.3(FANCC):c.843+125G>A rs4647507 0.02279
NM_000136.3(FANCC):c.1345G>A (p.Val449Met) rs1800367 0.02254
NM_000136.3(FANCC):c.*2085C>A rs4647559 0.01780
NM_000136.3(FANCC):c.*359A>G rs4647551 0.01505
NM_000136.3(FANCC):c.843+4C>T rs4647506 0.01468
NM_000136.3(FANCC):c.686+30C>T rs1800363 0.01287
NM_000136.3(FANCC):c.*96A>G rs55687573 0.00893
NM_000136.3(FANCC):c.1330-3C>T rs4647542 0.00811
NM_000136.3(FANCC):c.*1968G>A rs114827984 0.00409
NM_000136.3(FANCC):c.1329+175C>T rs112446681 0.00401
NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg) rs1800368 0.00361
NM_000136.3(FANCC):c.584A>T (p.Asp195Val) rs1800365 0.00275
NM_000136.3(FANCC):c.1156T>C (p.Ser386Pro) rs41281202 0.00236
NM_000136.3(FANCC):c.840G>A (p.Ser280=) rs34671520 0.00154
NM_000136.3(FANCC):c.632C>G (p.Pro211Arg) rs140781259 0.00126
NM_000136.3(FANCC):c.816C>T (p.Ile272=) rs55719336 0.00074
NM_000136.3(FANCC):c.1329+212C>T rs41281200 0.00061
NM_000136.3(FANCC):c.1329+111C>T rs527823099 0.00056
NM_000136.3(FANCC):c.672C>T (p.Asn224=) rs150647141 0.00046
NM_000136.3(FANCC):c.705C>T (p.Pro235=) rs141828876 0.00046
NM_000136.3(FANCC):c.*5C>T rs117175949 0.00033
NM_000136.3(FANCC):c.973G>A (p.Ala325Thr) rs201407189 0.00028
NM_000136.3(FANCC):c.1407G>A (p.Thr469=) rs79722116 0.00020
NM_000136.3(FANCC):c.1290C>T (p.Tyr430=) rs766105286 0.00011
NM_000136.3(FANCC):c.1509G>A (p.Thr503=) rs144278080 0.00011
NM_000136.3(FANCC):c.522-4A>G rs371422485 0.00011
NM_000136.3(FANCC):c.1073-5C>T rs375613884 0.00009
NM_000136.3(FANCC):c.1533+13G>A rs200515307 0.00008
NM_000136.3(FANCC):c.531C>T (p.Pro177=) rs150070473 0.00007
NM_000136.3(FANCC):c.1242G>A (p.Ser414=) rs587780939 0.00006
NM_000136.3(FANCC):c.1329+306C>T rs185023012 0.00005
NM_000136.3(FANCC):c.1494T>C (p.Ala498=) rs76895298 0.00005
NM_000136.3(FANCC):c.*7C>T rs372511678 0.00004
NM_000136.3(FANCC):c.1414G>A (p.Gly472Arg) rs201063698 0.00002
NM_000136.3(FANCC):c.897-19C>T rs368830981 0.00002
NM_000136.3(FANCC):c.915C>T (p.Thr305=) rs138132690 0.00002
NM_000136.3(FANCC):c.1281C>T (p.Ala427=) rs754604606 0.00001
NM_000136.3(FANCC):c.1530C>T (p.Thr510=) rs372199352 0.00001
NM_000136.3(FANCC):c.1534-18C>T rs1289718209 0.00001
NM_000136.3(FANCC):c.687-15A>C rs765327075 0.00001
NM_000136.3(FANCC):c.882T>C (p.Val294=) rs750639831 0.00001
NM_000136.3(FANCC):c.*1662C>T rs4647556
NM_000136.3(FANCC):c.*1727T>A rs4647557
NM_000136.3(FANCC):c.*42G>A rs7029888
NM_000136.3(FANCC):c.1329+16del
NM_000136.3(FANCC):c.1485G>A (p.Leu495=) rs56082100
NM_000136.3(FANCC):c.1529C>A (p.Thr510Asn) rs1233501553
NM_000136.3(FANCC):c.567A>C (p.Pro189=) rs2135428194
NM_000136.3(FANCC):c.816C>G (p.Ile272Met) rs55719336
NM_000136.3(FANCC):c.997-216_997-215insATTTATT rs5899245

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