ClinVar Miner

List of variants in gene FANCG reported as uncertain significance for Fanconi anemia

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 225
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HGVS dbSNP gnomAD frequency
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.1453C>T (p.Arg485Trp) rs201884798 0.00022
NM_004629.2(FANCG):c.1367A>T (p.His456Leu) rs148808709 0.00013
NM_004629.2(FANCG):c.1454G>A (p.Arg485Gln) rs77152961 0.00010
NM_004629.2(FANCG):c.373_375dup (p.Val125dup) rs750843326 0.00009
NM_004629.2(FANCG):c.421C>T (p.Arg141Cys) rs201153812 0.00007
NM_004629.2(FANCG):c.1297C>T (p.Arg433Trp) rs183777537 0.00006
NM_004629.2(FANCG):c.1801C>T (p.Arg601Cys) rs368098479 0.00006
NM_004629.2(FANCG):c.464G>A (p.Arg155His) rs201099560 0.00006
NM_004629.2(FANCG):c.724C>T (p.Arg242Trp) rs574511407 0.00006
NM_004629.2(FANCG):c.766C>T (p.His256Tyr) rs753955326 0.00006
NM_004629.2(FANCG):c.968T>C (p.Ile323Thr) rs752346718 0.00006
NM_004629.2(FANCG):c.55A>G (p.Lys19Glu) rs186641344 0.00005
NM_004629.2(FANCG):c.704C>T (p.Ala235Val) rs574975594 0.00005
NM_004629.2(FANCG):c.769C>T (p.Arg257Cys) rs759314410 0.00005
NM_004629.2(FANCG):c.1510A>C (p.Lys504Gln) rs1304316655 0.00004
NM_004629.2(FANCG):c.293G>A (p.Arg98Gln) rs372854981 0.00004
NM_004629.2(FANCG):c.366G>C (p.Trp122Cys) rs546023787 0.00004
NM_004629.2(FANCG):c.422G>A (p.Arg141His) rs775719850 0.00004
NM_004629.2(FANCG):c.880G>A (p.Gly294Arg) rs886063897 0.00004
NM_004629.2(FANCG):c.992C>G (p.Pro331Arg) rs765722724 0.00004
NM_004629.2(FANCG):c.1156C>G (p.Pro386Ala) rs375757497 0.00003
NM_004629.2(FANCG):c.1298G>A (p.Arg433Gln) rs748738986 0.00003
NM_004629.2(FANCG):c.1441G>C (p.Glu481Gln) rs772460728 0.00003
NM_004629.2(FANCG):c.1459A>C (p.Thr487Pro) rs1414696119 0.00003
NM_004629.2(FANCG):c.1718G>C (p.Arg573Thr) rs200466062 0.00003
NM_004629.2(FANCG):c.1768C>G (p.Pro590Ala) rs541868979 0.00003
NM_004629.2(FANCG):c.1805C>A (p.Pro602His) rs370950631 0.00003
NM_004629.2(FANCG):c.181C>T (p.Pro61Ser) rs931163229 0.00003
NM_004629.2(FANCG):c.380G>A (p.Arg127His) rs780985218 0.00003
NM_004629.2(FANCG):c.398C>T (p.Pro133Leu) rs1270561172 0.00003
NM_004629.2(FANCG):c.730G>A (p.Val244Met) rs746248064 0.00003
NM_004629.2(FANCG):c.934G>A (p.Val312Ile) rs530535955 0.00003
NM_004629.2(FANCG):c.1292T>G (p.Met431Arg) rs759285011 0.00002
NM_004629.2(FANCG):c.1346C>T (p.Pro449Leu) rs757442131 0.00002
NM_004629.2(FANCG):c.1702A>G (p.Thr568Ala) rs750212705 0.00002
NM_004629.2(FANCG):c.458C>G (p.Ala153Gly) rs200074432 0.00002
NM_004629.2(FANCG):c.635C>T (p.Ala212Val) rs375754266 0.00002
NM_004629.2(FANCG):c.944G>A (p.Ser315Asn) rs745833004 0.00002
NM_004629.2(FANCG):c.1077G>A (p.Arg359=) rs901079231 0.00001
NM_004629.2(FANCG):c.1162C>G (p.Pro388Ala) rs1356114266 0.00001
NM_004629.2(FANCG):c.1189T>C (p.Phe397Leu) rs1060501868 0.00001
NM_004629.2(FANCG):c.1222G>A (p.Gly408Ser) rs371171892 0.00001
NM_004629.2(FANCG):c.1252G>A (p.Glu418Lys) rs886063896 0.00001
NM_004629.2(FANCG):c.1268G>A (p.Arg423His) rs757276792 0.00001
NM_004629.2(FANCG):c.1298G>C (p.Arg433Pro) rs748738986 0.00001
NM_004629.2(FANCG):c.1492A>C (p.Asn498His) rs748364103 0.00001
NM_004629.2(FANCG):c.1519G>A (p.Ala507Thr) rs373151602 0.00001
NM_004629.2(FANCG):c.1567G>C (p.Glu523Gln) rs761993636 0.00001
NM_004629.2(FANCG):c.158T>G (p.Leu53Arg) rs756388446 0.00001
NM_004629.2(FANCG):c.1595A>G (p.Lys532Arg) rs1587139402 0.00001
NM_004629.2(FANCG):c.1615C>G (p.Leu539Val) rs1486862292 0.00001
NM_004629.2(FANCG):c.1626G>C (p.Gln542His) rs1060501867 0.00001
NM_004629.2(FANCG):c.1662G>A (p.Leu554=) rs750982155 0.00001
NM_004629.2(FANCG):c.1687C>T (p.Arg563Trp) rs754258080 0.00001
NM_004629.2(FANCG):c.1688G>A (p.Arg563Gln) rs1309056736 0.00001
NM_004629.2(FANCG):c.176G>A (p.Gly59Glu) rs538555981 0.00001
NM_004629.2(FANCG):c.1814G>A (p.Arg605His) rs751710424 0.00001
NM_004629.2(FANCG):c.338G>A (p.Arg113Lys) rs778894219 0.00001
NM_004629.2(FANCG):c.463C>T (p.Arg155Cys) rs200926249 0.00001
NM_004629.2(FANCG):c.500A>G (p.Asn167Ser) rs749946550 0.00001
NM_004629.2(FANCG):c.634G>A (p.Ala212Thr) rs775291829 0.00001
NM_004629.2(FANCG):c.646+5G>A rs1453133047 0.00001
NM_004629.2(FANCG):c.682G>A (p.Ala228Thr) rs765095688 0.00001
NM_004629.2(FANCG):c.73C>G (p.Arg25Gly) rs752839554 0.00001
NM_004629.2(FANCG):c.869A>G (p.Tyr290Cys) rs779840229 0.00001
NM_004629.2(FANCG):c.8G>T (p.Arg3Leu) rs770674344 0.00001
NM_004629.2(FANCG):c.905G>T (p.Ser302Ile) rs61757386 0.00001
NM_004629.2(FANCG):c.924+3A>G rs1338383222 0.00001
NM_004629.2(FANCG):c.933_938dup (p.Val312_Pro313dup) rs1199832786 0.00001
NM_004629.1(FANCG):c.520_523delinsC (p.Ser174_Lys175delinsGln) rs1554670417
NM_004629.2(FANCG):c.-182del rs886063899
NM_004629.2(FANCG):c.1017T>A (p.His339Gln) rs764465471
NM_004629.2(FANCG):c.1019G>A (p.Cys340Tyr) rs2131055383
NM_004629.2(FANCG):c.1032C>A (p.Ser344Arg)
NM_004629.2(FANCG):c.1045A>T (p.Ile349Leu)
NM_004629.2(FANCG):c.1070C>T (p.Thr357Met)
NM_004629.2(FANCG):c.1076+3_1076+7del rs780410457
NM_004629.2(FANCG):c.1076+4A>G rs1829084813
NM_004629.2(FANCG):c.107C>T (p.Thr36Ile) rs1587144550
NM_004629.2(FANCG):c.1082G>A (p.Gly361Glu) rs1276088946
NM_004629.2(FANCG):c.1087G>A (p.Ala363Thr)
NM_004629.2(FANCG):c.10C>G (p.Gln4Glu) rs1326382443
NM_004629.2(FANCG):c.1100A>C (p.Tyr367Ser)
NM_004629.2(FANCG):c.1113G>A (p.Leu371=) rs1829075976
NM_004629.2(FANCG):c.1125G>A (p.Leu375=)
NM_004629.2(FANCG):c.1126G>T (p.Asp376Tyr) rs1587140699
NM_004629.2(FANCG):c.1129A>G (p.Ser377Gly)
NM_004629.2(FANCG):c.1143+4G>A rs2131054635
NM_004629.2(FANCG):c.1143+5G>C rs778328620
NM_004629.2(FANCG):c.1144-3C>T
NM_004629.2(FANCG):c.1153C>A (p.Pro385Thr) rs1288516919
NM_004629.2(FANCG):c.1153C>G (p.Pro385Ala) rs1288516919
NM_004629.2(FANCG):c.1155_1163del (p.Ser387_Pro389del) rs1554670228
NM_004629.2(FANCG):c.1156C>A (p.Pro386Thr)
NM_004629.2(FANCG):c.1157C>A (p.Pro386His) rs141147618
NM_004629.2(FANCG):c.1157C>G (p.Pro386Arg) rs141147618
NM_004629.2(FANCG):c.1161_1163dup (p.Pro389_Gly390insPro)
NM_004629.2(FANCG):c.1199C>T (p.Ala400Val)
NM_004629.2(FANCG):c.119A>C (p.Gln40Pro)
NM_004629.2(FANCG):c.1228G>A (p.Ala410Thr) rs1829068737
NM_004629.2(FANCG):c.123G>C (p.Gln41His)
NM_004629.2(FANCG):c.1277C>G (p.Ser426Cys)
NM_004629.2(FANCG):c.1292T>C (p.Met431Thr)
NM_004629.2(FANCG):c.1377G>A (p.Gln459=) rs1587140019
NM_004629.2(FANCG):c.1385C>A (p.Ala462Asp) rs2131053797
NM_004629.2(FANCG):c.1400G>A (p.Gly467Asp)
NM_004629.2(FANCG):c.1403C>T (p.Ala468Val) rs1829065605
NM_004629.2(FANCG):c.1408A>G (p.Lys470Glu)
NM_004629.2(FANCG):c.1433+5G>T
NM_004629.2(FANCG):c.1437C>G (p.Cys479Trp) rs904322133
NM_004629.2(FANCG):c.1441G>A (p.Glu481Lys)
NM_004629.2(FANCG):c.1448T>C (p.Leu483Pro) rs1829061760
NM_004629.2(FANCG):c.1460C>T (p.Thr487Ile) rs2131053434
NM_004629.2(FANCG):c.1462C>T (p.Pro488Ser)
NM_004629.2(FANCG):c.1474G>C (p.Glu492Gln) rs1018027137
NM_004629.2(FANCG):c.1480+5T>C rs1554670176
NM_004629.2(FANCG):c.1480+5T>G rs1554670176
NM_004629.2(FANCG):c.1481G>T (p.Gly494Val) rs770011456
NM_004629.2(FANCG):c.1495T>G (p.Cys499Gly)
NM_004629.2(FANCG):c.1498G>A (p.Glu500Lys)
NM_004629.2(FANCG):c.1505G>T (p.Gly502Val)
NM_004629.2(FANCG):c.1519G>T (p.Ala507Ser)
NM_004629.2(FANCG):c.1520C>T (p.Ala507Val)
NM_004629.2(FANCG):c.1546G>A (p.Ala516Thr)
NM_004629.2(FANCG):c.1556G>A (p.Ser519Asn) rs1209146448
NM_004629.2(FANCG):c.1582G>A (p.Gly528Ser)
NM_004629.2(FANCG):c.1586A>G (p.Gln529Arg)
NM_004629.2(FANCG):c.1592C>T (p.Thr531Ile)
NM_004629.2(FANCG):c.1633C>G (p.Pro545Ala) rs1315654777
NM_004629.2(FANCG):c.1635A>G (p.Pro545=)
NM_004629.2(FANCG):c.1636+5G>A rs748961871
NM_004629.2(FANCG):c.1636+7_1636+8delinsGA
NM_004629.2(FANCG):c.1642C>G (p.Arg548Gly)
NM_004629.2(FANCG):c.1643G>A (p.Arg548Gln) rs1587138702
NM_004629.2(FANCG):c.1648A>G (p.Thr550Ala) rs1255677446
NM_004629.2(FANCG):c.1651T>C (p.Tyr551His)
NM_004629.2(FANCG):c.1663C>T (p.Leu555Phe) rs2131051917
NM_004629.2(FANCG):c.1668G>T (p.Gln556His) rs1829042320
NM_004629.2(FANCG):c.1708C>T (p.Leu570Phe)
NM_004629.2(FANCG):c.1718G>T (p.Arg573Met) rs200466062
NM_004629.2(FANCG):c.1727C>T (p.Ala576Val)
NM_004629.2(FANCG):c.1745A>G (p.His582Arg) rs1196002404
NM_004629.2(FANCG):c.175+4G>C rs1060501869
NM_004629.2(FANCG):c.1760+4A>T
NM_004629.2(FANCG):c.1772del (p.Leu591fs)
NM_004629.2(FANCG):c.1774T>C (p.Tyr592His) rs768325047
NM_004629.2(FANCG):c.1782A>C (p.Glu594Asp)
NM_004629.2(FANCG):c.1785C>G (p.Ser595Arg)
NM_004629.2(FANCG):c.178C>T (p.Leu60Phe) rs1026058105
NM_004629.2(FANCG):c.1793G>A (p.Ser598Asn)
NM_004629.2(FANCG):c.1794C>G (p.Ser598Arg)
NM_004629.2(FANCG):c.1804C>T (p.Pro602Ser)
NM_004629.2(FANCG):c.1810G>C (p.Asp604His)
NM_004629.2(FANCG):c.1820C>A (p.Ala607Asp)
NM_004629.2(FANCG):c.1825del (p.Glu610fs)
NM_004629.2(FANCG):c.1837C>T (p.Arg613Trp)
NM_004629.2(FANCG):c.1852_1853del (p.Lys618fs) rs532302967
NM_004629.2(FANCG):c.193C>T (p.Pro65Ser) rs2131059151
NM_004629.2(FANCG):c.244G>A (p.Ala82Thr)
NM_004629.2(FANCG):c.263T>G (p.Phe88Cys)
NM_004629.2(FANCG):c.293G>T (p.Arg98Leu) rs372854981
NM_004629.2(FANCG):c.308-12T>G
NM_004629.2(FANCG):c.308-25_308-12del rs1563987234
NM_004629.2(FANCG):c.322G>A (p.Glu108Lys)
NM_004629.2(FANCG):c.335_352del (p.Pro112_Gly117del)
NM_004629.2(FANCG):c.337A>G (p.Arg113Gly) rs2131058590
NM_004629.2(FANCG):c.355A>C (p.Arg119=)
NM_004629.2(FANCG):c.403C>A (p.Leu135Met)
NM_004629.2(FANCG):c.410C>G (p.Ser137Cys) rs1203036492
NM_004629.2(FANCG):c.412G>C (p.Ala138Pro)
NM_004629.2(FANCG):c.420C>A (p.His140Gln)
NM_004629.2(FANCG):c.431G>C (p.Gly144Ala) rs767880403
NM_004629.2(FANCG):c.443C>T (p.Ala148Val) rs1829121038
NM_004629.2(FANCG):c.448T>C (p.Trp150Arg) rs202114813
NM_004629.2(FANCG):c.486A>T (p.Leu162Phe) rs779677132
NM_004629.2(FANCG):c.497T>C (p.Leu166Pro)
NM_004629.2(FANCG):c.510+5T>C rs921564097
NM_004629.2(FANCG):c.517G>A (p.Ala173Thr)
NM_004629.2(FANCG):c.525G>C (p.Lys175Asn)
NM_004629.2(FANCG):c.52G>A (p.Glu18Lys) rs1829144761
NM_004629.2(FANCG):c.542_556del (p.Leu181_Ser185del)
NM_004629.2(FANCG):c.54A>C (p.Glu18Asp) rs1563987701
NM_004629.2(FANCG):c.560C>A (p.Pro187Gln)
NM_004629.2(FANCG):c.563C>T (p.Ala188Val)
NM_004629.2(FANCG):c.572T>C (p.Leu191Ser)
NM_004629.2(FANCG):c.580C>T (p.Pro194Ser) rs1554670412
NM_004629.2(FANCG):c.587C>T (p.Thr196Ile)
NM_004629.2(FANCG):c.595G>A (p.Asp199Asn)
NM_004629.2(FANCG):c.616G>A (p.Val206Ile) rs768648609
NM_004629.2(FANCG):c.626C>T (p.Thr209Ile) rs1382724792
NM_004629.2(FANCG):c.633T>A (p.Phe211Leu)
NM_004629.2(FANCG):c.63C>A (p.Asp21Glu)
NM_004629.2(FANCG):c.647-3C>T rs1311964497
NM_004629.2(FANCG):c.64C>T (p.Arg22Trp)
NM_004629.2(FANCG):c.65G>A (p.Arg22Gln) rs1829144428
NM_004629.2(FANCG):c.662T>A (p.Ile221Asn) rs1829099355
NM_004629.2(FANCG):c.665C>T (p.Thr222Ile)
NM_004629.2(FANCG):c.690C>A (p.Ser230Arg) rs1333976481
NM_004629.2(FANCG):c.706G>A (p.Ala236Thr) rs2131056564
NM_004629.2(FANCG):c.70G>C (p.Val24Leu)
NM_004629.2(FANCG):c.714C>T (p.Gly238=)
NM_004629.2(FANCG):c.725G>A (p.Arg242Gln)
NM_004629.2(FANCG):c.743T>C (p.Val248Ala) rs1221668009
NM_004629.2(FANCG):c.763T>C (p.Cys255Arg)
NM_004629.2(FANCG):c.764G>A (p.Cys255Tyr)
NM_004629.2(FANCG):c.769C>G (p.Arg257Gly) rs759314410
NM_004629.2(FANCG):c.787C>G (p.Gln263Glu) rs149721361
NM_004629.2(FANCG):c.801G>C (p.Leu267Phe) rs1482595465
NM_004629.2(FANCG):c.807G>C (p.Leu269Phe)
NM_004629.2(FANCG):c.833C>T (p.Ala278Val) rs771395169
NM_004629.2(FANCG):c.844C>T (p.Pro282Ser) rs770009374
NM_004629.2(FANCG):c.865C>A (p.Leu289Ile)
NM_004629.2(FANCG):c.889A>G (p.Thr297Ala)
NM_004629.2(FANCG):c.895G>A (p.Glu299Lys)
NM_004629.2(FANCG):c.906_907delinsAT (p.Ser302Arg)
NM_004629.2(FANCG):c.916C>A (p.Leu306Ile)
NM_004629.2(FANCG):c.917T>C (p.Leu306Pro)
NM_004629.2(FANCG):c.920T>G (p.Val307Gly) rs774982952
NM_004629.2(FANCG):c.955C>A (p.Pro319Thr)
NM_004629.2(FANCG):c.965T>G (p.Leu322Arg)
NM_004629.2(FANCG):c.978A>G (p.Glu326=)
Single allele

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