ClinVar Miner

List of variants in gene FANCG studied for not provided

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Total variants: 63
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HGVS dbSNP gnomAD frequency
NM_004629.2(FANCG):c.511-45A>G rs554098 0.75732
NM_004629.2(FANCG):c.84+77C>A rs504082 0.54871
NM_004629.2(FANCG):c.646+58C>T rs17885726 0.17456
NM_004629.1(FANCG):c.-453_-452insT rs16935545 0.12501
NM_004629.1(FANCG):c.-490G>T rs10972303 0.07883
NM_004629.2(FANCG):c.-392A>G rs10972302 0.06369
NC_000009.12:g.35080213C>T rs17885617 0.06112
NM_004629.1(FANCG):c.-504A>T rs17885140 0.05593
NM_004629.2(FANCG):c.511-81A>C rs12350245 0.02369
NM_004629.2(FANCG):c.778-39G>C rs17885376 0.01915
NM_004629.2(FANCG):c.510+38C>T rs17885506 0.01191
NM_004629.2(FANCG):c.307+126T>C rs17880162 0.01002
NM_004629.2(FANCG):c.176-112G>A rs17879399 0.00785
NM_004629.2(FANCG):c.1637-210G>A rs17879075 0.00671
NM_004629.2(FANCG):c.988C>T (p.Pro330Ser) rs4986940 0.00670
NC_000009.12:g.35080109T>C rs144749991 0.00661
NM_004629.2(FANCG):c.20C>T (p.Ser7Phe) rs35984312 0.00138
NM_004629.2(FANCG):c.739C>A (p.Gln247Lys) rs145613634 0.00103
NM_004629.2(FANCG):c.478G>A (p.Ala160Thr) rs140534765 0.00051
NM_004629.2(FANCG):c.794C>T (p.Ala265Val) rs764992007 0.00031
NM_004629.2(FANCG):c.1545C>T (p.Ala515=) rs201422773 0.00028
NM_004629.2(FANCG):c.722C>T (p.Pro241Leu) rs201438531 0.00010
NM_004629.2(FANCG):c.705G>A (p.Ala235=) rs148910563 0.00006
NM_004629.2(FANCG):c.77A>G (p.Gln26Arg) rs200677800 0.00004
NM_004629.2(FANCG):c.1156C>G (p.Pro386Ala) rs375757497 0.00003
NM_004629.2(FANCG):c.1077-2A>G rs769547477 0.00002
NM_004629.2(FANCG):c.1480+1G>C rs149616199 0.00002
NM_004629.2(FANCG):c.1642C>T (p.Arg548Ter) rs779834525 0.00002
NM_004629.2(FANCG):c.176-10G>A rs376273679 0.00002
NM_004629.2(FANCG):c.109C>G (p.Leu37Val) rs754229788 0.00001
NM_004629.2(FANCG):c.1203G>A (p.Ala401=) rs770325434 0.00001
NM_004629.2(FANCG):c.1626G>C (p.Gln542His) rs1060501867 0.00001
NM_004629.2(FANCG):c.1838G>A (p.Arg613Gln) rs748634605 0.00001
NM_004629.2(FANCG):c.308-11A>G rs371822998 0.00001
NM_004629.2(FANCG):c.313G>T (p.Glu105Ter) rs121434425 0.00001
NM_004629.2(FANCG):c.500A>G (p.Asn167Ser) rs749946550 0.00001
NM_004629.2(FANCG):c.541C>G (p.Leu181Val) rs778413747 0.00001
NM_004629.2(FANCG):c.634G>A (p.Ala212Thr) rs775291829 0.00001
NM_004629.2(FANCG):c.652C>T (p.Gln218Ter) rs1209807088 0.00001
NM_004629.2(FANCG):c.761C>T (p.Ser254Phe) rs376825957 0.00001
NM_004629.2(FANCG):c.976G>T (p.Glu326Ter) rs754484649 0.00001
NM_004629.2(FANCG):c.999C>T (p.Asp333=) rs762238437 0.00001
NM_004629.1(FANCG):c.1795_1804del (p.Trp599Profs) rs397507560
NM_004629.2(FANCG):c.1077-6C>T rs1587140760
NM_004629.2(FANCG):c.1143+5G>C rs778328620
NM_004629.2(FANCG):c.1157C>G (p.Pro386Arg) rs141147618
NM_004629.2(FANCG):c.1158del (p.Ser387fs) rs757418016
NM_004629.2(FANCG):c.1400del (p.Gly467fs) rs2131053777
NM_004629.2(FANCG):c.1433+1G>A rs1829065047
NM_004629.2(FANCG):c.1544C>T (p.Ala515Val)
NM_004629.2(FANCG):c.1636+9A>T rs1587139329
NM_004629.2(FANCG):c.1637-189G>C rs2237856
NM_004629.2(FANCG):c.1653C>T (p.Tyr551=)
NM_004629.2(FANCG):c.1657C>T (p.His553Tyr) rs1251259584
NM_004629.2(FANCG):c.1664T>G (p.Leu555Arg)
NM_004629.2(FANCG):c.1718G>T (p.Arg573Met) rs200466062
NM_004629.2(FANCG):c.176-127dup rs147608096
NM_004629.2(FANCG):c.511-301C>T rs17885008
NM_004629.2(FANCG):c.60T>A (p.Asn20Lys) rs1829144538
NM_004629.2(FANCG):c.620del (p.Leu207fs) rs753727461
NM_004629.2(FANCG):c.637_643del (p.Tyr213fs) rs587776640
NM_004629.2(FANCG):c.777+45G>A rs17885935
NM_004629.2(FANCG):c.84+3A>C rs1829143957

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