ClinVar Miner

List of variants in gene FANCG reported as likely benign for Fanconi anemia

Included ClinVar conditions (38):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 39
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HGVS dbSNP
NM_004629.1(FANCG):c.-450G>C rs535301610
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.1365C>A (p.Thr455=) rs767385265
NM_004629.1(FANCG):c.1433+9G>A rs187315404
NM_004629.1(FANCG):c.1545C>T (p.Ala515=) rs201422773
NM_004629.1(FANCG):c.1689G>C (p.Arg563=) rs138855718
NM_004629.1(FANCG):c.177G>A (p.Gly59=) rs1554670511
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.238C>T (p.Leu80=) rs115131067
NM_004629.1(FANCG):c.333G>A (p.Gly111=) rs1060504370
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.399G>A (p.Pro133=) rs200278002
NM_004629.1(FANCG):c.558C>G (p.Pro186=) rs1554670415
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.739C>A (p.Gln247Lys) rs145613634
NM_004629.1(FANCG):c.881G>A (p.Gly294Glu) rs17880082
NM_004629.1(FANCG):c.927C>G (p.Ala309=) rs370002843
NM_004629.1(FANCG):c.957G>A (p.Pro319=) rs145092954
NM_004629.2(FANCG):c.-342G>T
NM_004629.2(FANCG):c.1002A>G (p.Leu334=)
NM_004629.2(FANCG):c.1048C>T (p.Leu350=)
NM_004629.2(FANCG):c.1086C>T (p.Asp362=)
NM_004629.2(FANCG):c.1158C>G (p.Pro386=)
NM_004629.2(FANCG):c.1233A>G (p.Gln411=)
NM_004629.2(FANCG):c.1521G>A (p.Ala507=)
NM_004629.2(FANCG):c.1677G>A (p.Lys559=)
NM_004629.2(FANCG):c.18C>T (p.Thr6=)
NM_004629.2(FANCG):c.510+7G>C
NM_004629.2(FANCG):c.511-6dup
NM_004629.2(FANCG):c.729T>C (p.Pro243=)
NM_004629.2(FANCG):c.84+9G>T
NM_004629.2(FANCG):c.933T>C (p.Asn311=)

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