ClinVar Miner

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

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Gene type:
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Total variants: 31
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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.1329+406C>T rs879492 0.37157
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.843+125G>A rs4647507 0.02279
NM_000136.3(FANCC):c.1345G>A (p.Val449Met) rs1800367 0.02254
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.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.632C>G (p.Pro211Arg) rs140781259 0.00126
NM_000136.3(FANCC):c.816C>T (p.Ile272=) rs55719336 0.00074
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.1533+13G>A rs200515307 0.00008
NM_000136.3(FANCC):c.1494T>C (p.Ala498=) rs76895298 0.00005
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.882T>C (p.Val294=) rs750639831 0.00001
NM_000136.3(FANCC):c.*42G>A rs7029888
NM_000136.3(FANCC):c.567A>C (p.Pro189=) rs2135428194
NM_000136.3(FANCC):c.997-216_997-215insATTTATT rs5899245

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