ClinVar Miner

List of variants in gene FANCG studied for Fanconi anemia

Included ClinVar conditions (38):
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Gene type:
ClinVar version:
Total variants: 117
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HGVS dbSNP
FANCG, IVS13, G-C, -1
NM_004629.1(FANCG):c.*101A>G rs751616369
NM_004629.1(FANCG):c.*250C>T rs535188841
NM_004629.1(FANCG):c.-182delG rs886063899
NM_004629.1(FANCG):c.-311T>A rs886063900
NM_004629.1(FANCG):c.-348A>G rs376750755
NM_004629.1(FANCG):c.-392A>G rs10972302
NM_004629.1(FANCG):c.-450G>C rs535301610
NM_004629.1(FANCG):c.-453_-452insT rs16935545
NM_004629.1(FANCG):c.-488G>A rs752617227
NM_004629.1(FANCG):c.-490G>T rs10972303
NM_004629.1(FANCG):c.-491G>A rs886063901
NM_004629.1(FANCG):c.-504A>T rs17885140
NM_004629.1(FANCG):c.-93C>G rs532840867
NM_004629.1(FANCG):c.1017T>C (p.His339=) rs764465471
NM_004629.1(FANCG):c.1066C>T (p.Gln356Ter) rs121434426
NM_004629.1(FANCG):c.1077-2A>G rs769547477
NM_004629.1(FANCG):c.107C>T (p.Thr36Ile)
NM_004629.1(FANCG):c.1126G>T (p.Asp376Tyr)
NM_004629.1(FANCG):c.1153C>G (p.Pro385Ala) rs1288516919
NM_004629.1(FANCG):c.1155_1163del (p.Ser387_Pro389del) rs1554670228
NM_004629.1(FANCG):c.1156C>G (p.Pro386Ala)
NM_004629.1(FANCG):c.1157C>G (p.Pro386Arg) rs141147618
NM_004629.1(FANCG):c.1158del (p.Ser387fs) rs757418016
NM_004629.1(FANCG):c.1158dup (p.Ser387fs) rs757418016
NM_004629.1(FANCG):c.1183_1192del (p.Glu395fs) rs397507559
NM_004629.1(FANCG):c.1189T>C (p.Phe397Leu) rs1060501868
NM_004629.1(FANCG):c.1216del (p.Gln406fs)
NM_004629.1(FANCG):c.1252G>A (p.Glu418Lys) rs886063896
NM_004629.1(FANCG):c.1268G>A (p.Arg423His) rs757276792
NM_004629.1(FANCG):c.1298G>A (p.Arg433Gln)
NM_004629.1(FANCG):c.1365C>A (p.Thr455=) rs767385265
NM_004629.1(FANCG):c.1367A>T (p.His456Leu)
NM_004629.1(FANCG):c.1433+9G>A rs187315404
NM_004629.1(FANCG):c.1441G>C (p.Glu481Gln) rs772460728
NM_004629.1(FANCG):c.1453C>T (p.Arg485Trp) rs201884798
NM_004629.1(FANCG):c.1454G>A (p.Arg485Gln) rs77152961
NM_004629.1(FANCG):c.1459A>C (p.Thr487Pro) rs1414696119
NM_004629.1(FANCG):c.1474G>C (p.Glu492Gln)
NM_004629.1(FANCG):c.1480+1G>C rs149616199
NM_004629.1(FANCG):c.1480+5T>G rs1554670176
NM_004629.1(FANCG):c.1510A>C (p.Lys504Gln) rs1304316655
NM_004629.1(FANCG):c.1545C>T (p.Ala515=) rs201422773
NM_004629.1(FANCG):c.156dup (p.Leu53fs) rs863224506
NM_004629.1(FANCG):c.1573del (p.Trp524_Val525insTer)
NM_004629.1(FANCG):c.1578C>T (p.Ala526=) rs1060504371
NM_004629.1(FANCG):c.158T>G (p.Leu53Arg) rs756388446
NM_004629.1(FANCG):c.1595A>G (p.Lys532Arg)
NM_004629.1(FANCG):c.161dup (p.His55fs) rs886063898
NM_004629.1(FANCG):c.1626G>C (p.Gln542His) rs1060501867
NM_004629.1(FANCG):c.1636+5G>A rs748961871
NM_004629.1(FANCG):c.1642C>T (p.Arg548Ter)
NM_004629.1(FANCG):c.1648A>G (p.Thr550Ala) rs1255677446
NM_004629.1(FANCG):c.1689G>C (p.Arg563=) rs138855718
NM_004629.1(FANCG):c.1718G>C (p.Arg573Thr) rs200466062
NM_004629.1(FANCG):c.1747G>T (p.Glu583Ter) rs786204205
NM_004629.1(FANCG):c.175+4G>C rs1060501869
NM_004629.1(FANCG):c.1767C>T (p.Leu589=) rs1060504369
NM_004629.1(FANCG):c.1768C>G (p.Pro590Ala)
NM_004629.1(FANCG):c.1774T>C (p.Tyr592His) rs768325047
NM_004629.1(FANCG):c.177G>A (p.Gly59=) rs1554670511
NM_004629.1(FANCG):c.1795_1804del (p.Trp599Profs) rs397507560
NM_004629.1(FANCG):c.1801C>T (p.Arg601Cys)
NM_004629.1(FANCG):c.1806C>T (p.Pro602=) rs756632525
NM_004629.1(FANCG):c.1808C>T (p.Ser603Phe) rs17878854
NM_004629.1(FANCG):c.1814G>A (p.Arg605His)
NM_004629.1(FANCG):c.181C>T (p.Pro61Ser)
NM_004629.1(FANCG):c.1852_1853del (p.Lys618fs) rs532302967
NM_004629.1(FANCG):c.20C>T (p.Ser7Phe) rs35984312
NM_004629.1(FANCG):c.238C>T (p.Leu80=) rs115131067
NM_004629.1(FANCG):c.293G>A (p.Arg98Gln) rs372854981
NM_004629.1(FANCG):c.307+1G>C rs200479612
NM_004629.1(FANCG):c.313G>T (p.Glu105Ter) rs121434425
NM_004629.1(FANCG):c.333G>A (p.Gly111=) rs1060504370
NM_004629.1(FANCG):c.338G>A (p.Arg113Lys) rs778894219
NM_004629.1(FANCG):c.345A>G (p.Glu115=) rs1213271836
NM_004629.1(FANCG):c.366G>C (p.Trp122Cys) rs546023787
NM_004629.1(FANCG):c.373_375dup (p.Val125dup) rs750843326
NM_004629.1(FANCG):c.375C>A (p.Val125=) rs199754122
NM_004629.1(FANCG):c.375C>G (p.Val125=) rs199754122
NM_004629.1(FANCG):c.380G>A (p.Arg127His)
NM_004629.1(FANCG):c.399G>A (p.Pro133=) rs200278002
NM_004629.1(FANCG):c.421C>T (p.Arg141Cys) rs201153812
NM_004629.1(FANCG):c.458C>G (p.Ala153Gly)
NM_004629.1(FANCG):c.464G>A (p.Arg155His) rs201099560
NM_004629.1(FANCG):c.478G>A (p.Ala160Thr) rs140534765
NM_004629.1(FANCG):c.500A>G (p.Asn167Ser) rs749946550
NM_004629.1(FANCG):c.520_523delinsC (p.Ser174_Lys175delinsGln) rs1554670417
NM_004629.1(FANCG):c.54A>C (p.Glu18Asp) rs1563987701
NM_004629.1(FANCG):c.558C>G (p.Pro186=) rs1554670415
NM_004629.1(FANCG):c.55A>G (p.Lys19Glu)
NM_004629.1(FANCG):c.580C>T (p.Pro194Ser) rs1554670412
NM_004629.1(FANCG):c.635C>T (p.Ala212Val)
NM_004629.1(FANCG):c.637_643del (p.Tyr213fs) rs587776640
NM_004629.1(FANCG):c.652C>T (p.Gln218Ter) rs1209807088
NM_004629.1(FANCG):c.682G>A (p.Ala228Thr) rs765095688
NM_004629.1(FANCG):c.705G>A (p.Ala235=) rs148910563
NM_004629.1(FANCG):c.722C>T (p.Pro241Leu) rs201438531
NM_004629.1(FANCG):c.730G>A (p.Val244Met) rs746248064
NM_004629.1(FANCG):c.739C>A (p.Gln247Lys) rs145613634
NM_004629.1(FANCG):c.743T>C (p.Val248Ala) rs1221668009
NM_004629.1(FANCG):c.766C>T (p.His256Tyr)
NM_004629.1(FANCG):c.777+1G>A rs1060501862
NM_004629.1(FANCG):c.778-1G>A rs767518932
NM_004629.1(FANCG):c.787C>G (p.Gln263Glu)
NM_004629.1(FANCG):c.81C>T (p.Ala27=) rs1060504372
NM_004629.1(FANCG):c.84+53G>T rs1563987651
NM_004629.1(FANCG):c.85-2A>T
NM_004629.1(FANCG):c.880G>A (p.Gly294Arg) rs886063897
NM_004629.1(FANCG):c.881G>A (p.Gly294Glu) rs17880082
NM_004629.1(FANCG):c.908T>C (p.Leu303Pro) rs1563986439
NM_004629.1(FANCG):c.925-2A>G rs397507561
NM_004629.1(FANCG):c.927C>G (p.Ala309=) rs370002843
NM_004629.1(FANCG):c.957G>A (p.Pro319=) rs145092954
NM_004629.1(FANCG):c.968T>C (p.Ile323Thr) rs752346718
NM_004629.1(FANCG):c.988C>T (p.Pro330Ser) rs4986940
Single allele

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