ClinVar Miner

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

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Gene type:
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Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_000136.3(FANCC):c.686+169G>A rs139424828 0.01483
NM_000136.3(FANCC):c.843+4C>T rs4647506 0.01468
NM_000136.3(FANCC):c.686+310C>T rs116104972 0.01181
NM_000136.3(FANCC):c.897-221C>A rs114222721 0.01137
NM_000136.3(FANCC):c.686+197C>T rs146354746 0.01120
NM_000136.3(FANCC):c.*96A>G rs55687573 0.00893
NM_000136.3(FANCC):c.1329+554A>G rs151242485 0.00823
NM_000136.3(FANCC):c.1330-3C>T rs4647542 0.00811
NM_000136.3(FANCC):c.897-234A>G rs56140833 0.00778
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.686+135T>G rs530439883 0.00246
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.934A>G (p.Ile312Val) rs1800366 0.00051
NM_000136.3(FANCC):c.1533+50G>A rs4647544 0.00046
NM_000136.3(FANCC):c.705C>T (p.Pro235=) rs141828876 0.00046
NM_000136.3(FANCC):c.1407G>A (p.Thr469=) rs79722116 0.00020
NM_000136.3(FANCC):c.817G>A (p.Glu273Lys) rs143181565 0.00011
NM_000136.3(FANCC):c.*9C>T rs370270817 0.00007
NM_000136.3(FANCC):c.531C>T (p.Pro177=) rs150070473 0.00007
NM_000136.3(FANCC):c.1155-13G>T rs747142087 0.00006
NM_000136.3(FANCC):c.609C>T (p.Leu203=) rs567226063 0.00006
NM_000136.3(FANCC):c.1425A>G (p.Thr475=) rs199739450 0.00005
NM_000136.3(FANCC):c.1494T>C (p.Ala498=) rs76895298 0.00005
NM_000136.3(FANCC):c.1560C>T (p.His520=) rs150020474 0.00005
NM_000136.3(FANCC):c.897-8T>C rs878853673 0.00005
NM_000136.3(FANCC):c.*8G>A rs753428914 0.00004
NM_000136.3(FANCC):c.1073-4G>A rs147695697 0.00004
NM_000136.3(FANCC):c.1623T>G (p.Pro541=) rs375362894 0.00004
NM_000136.3(FANCC):c.1353C>T (p.Gly451=) rs745338413 0.00003
NM_000136.3(FANCC):c.1611C>A (p.Gly537=) rs1027358273 0.00003
NM_000136.3(FANCC):c.1161C>T (p.Cys387=) rs548998258 0.00002
NM_000136.3(FANCC):c.1414G>A (p.Gly472Arg) rs201063698 0.00002
NM_000136.3(FANCC):c.654G>A (p.Glu218=) rs754705988 0.00002
NM_000136.3(FANCC):c.783A>T (p.Leu261=) rs1060504646 0.00002
NM_000136.3(FANCC):c.993G>A (p.Lys331=) rs748582850 0.00002
NM_000136.3(FANCC):c.1588T>C (p.Leu530=) rs988780618 0.00001
NM_000136.3(FANCC):c.576C>T (p.Thr192=) rs759392396 0.00001
NM_000136.3(FANCC):c.897-3C>T rs1057521714 0.00001
NM_000136.3(FANCC):c.957G>A (p.Thr319=) rs1060504647 0.00001
NM_000136.3(FANCC):c.1155-11C>T rs2134552343
NM_000136.3(FANCC):c.1260G>A (p.Thr420=) rs749709412
NM_000136.3(FANCC):c.1264C>T (p.Leu422=) rs756716463
NM_000136.3(FANCC):c.1302T>C (p.Asp434=) rs2134546972
NM_000136.3(FANCC):c.1317A>G (p.Arg439=) rs1554829450
NM_000136.3(FANCC):c.1329+192C>T
NM_000136.3(FANCC):c.1329+213G>A
NM_000136.3(FANCC):c.1329+246del rs542091036
NM_000136.3(FANCC):c.1329+255C>T
NM_000136.3(FANCC):c.1485G>C (p.Leu495=) rs56082100
NM_000136.3(FANCC):c.1534-5del rs748342368
NM_000136.3(FANCC):c.1534-8G>T rs2071090579
NM_000136.3(FANCC):c.1663C>A (p.Arg555=) rs370974124
NM_000136.3(FANCC):c.558T>G (p.Val186=) rs1588181909
NM_000136.3(FANCC):c.642C>A (p.Ile214=) rs777274497
NM_000136.3(FANCC):c.686+157_686+159del rs202175311
NM_000136.3(FANCC):c.844-10C>G rs1588106888
NM_000136.3(FANCC):c.996+9T>C rs757984397
NM_000136.3(FANCC):c.997-9C>G rs774886992

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