ClinVar Miner

List of variants in gene FANCG reported as pathogenic for DNA repair disease

Included ClinVar conditions (95):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
FANCG, IVS13, G-C, -1
NM_004629.1(FANCG):c.1066C>T (p.Gln356Ter) rs121434426
NM_004629.1(FANCG):c.1077-2A>G rs769547477
NM_004629.1(FANCG):c.1153dup (p.Ser387Leufs)
NM_004629.1(FANCG):c.1183_1192delGAGGTGTTTT (p.Glu395Trpfs) rs397507559
NM_004629.1(FANCG):c.1480+1G>C rs149616199
NM_004629.1(FANCG):c.156dupG (p.Leu53Alafs) rs863224506
NM_004629.1(FANCG):c.1642C>T (p.Arg548Ter)
NM_004629.1(FANCG):c.1795_1804del (p.Trp599Profs) rs397507560
NM_004629.1(FANCG):c.307+1G>C rs200479612
NM_004629.1(FANCG):c.313G>T (p.Glu105Ter) rs121434425
NM_004629.1(FANCG):c.637_643del (p.Tyr213Lysfs) rs587776640
NM_004629.1(FANCG):c.652C>T (p.Gln218Ter)
NM_004629.1(FANCG):c.925-2A>G rs397507561
NM_004629.1:c.1158delC

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