ClinVar Miner

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

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 67
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HGVS dbSNP
NM_004629.1(FANCG):c.*101A>G rs751616369
NM_004629.1(FANCG):c.*250C>T rs535188841
NM_004629.1(FANCG):c.-182del rs886063899
NM_004629.1(FANCG):c.-311T>A rs886063900
NM_004629.1(FANCG):c.-348A>G rs376750755
NM_004629.1(FANCG):c.-450G>C rs535301610
NM_004629.1(FANCG):c.-488G>A rs752617227
NM_004629.1(FANCG):c.-491G>A rs886063901
NM_004629.1(FANCG):c.-93C>G rs532840867
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.1189T>C (p.Phe397Leu) rs1060501868
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.1367A>T (p.His456Leu)
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+5T>G rs1554670176
NM_004629.1(FANCG):c.1510A>C (p.Lys504Gln) rs1304316655
NM_004629.1(FANCG):c.158T>G (p.Leu53Arg) rs756388446
NM_004629.1(FANCG):c.1595A>G (p.Lys532Arg)
NM_004629.1(FANCG):c.1626G>C (p.Gln542His) rs1060501867
NM_004629.1(FANCG):c.1636+5G>A rs748961871
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.175+4G>C rs1060501869
NM_004629.1(FANCG):c.1768C>G (p.Pro590Ala)
NM_004629.1(FANCG):c.1774T>C (p.Tyr592His) rs768325047
NM_004629.1(FANCG):c.1801C>T (p.Arg601Cys)
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.238C>T (p.Leu80=) rs115131067
NM_004629.1(FANCG):c.293G>A (p.Arg98Gln) rs372854981
NM_004629.1(FANCG):c.338G>A (p.Arg113Lys) rs778894219
NM_004629.1(FANCG):c.380G>A (p.Arg127His)
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.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.682G>A (p.Ala228Thr) rs765095688
NM_004629.1(FANCG):c.730G>A (p.Val244Met) rs746248064
NM_004629.1(FANCG):c.743T>C (p.Val248Ala) rs1221668009
NM_004629.1(FANCG):c.766C>T (p.His256Tyr)
NM_004629.1(FANCG):c.787C>G (p.Gln263Glu)
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.957G>A (p.Pro319=) rs145092954
NM_004629.1(FANCG):c.968T>C (p.Ile323Thr) rs752346718
Single allele

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