ClinVar Miner

List of variants in gene FANCG reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
NM_004629.2(FANCG):c.511-45A>G rs554098 0.75732
NM_004629.2(FANCG):c.478G>A (p.Ala160Thr) rs140534765 0.00051
NM_004629.2(FANCG):c.881G>A (p.Gly294Glu) rs17880082 0.00014
NM_004629.2(FANCG):c.1433+9G>A rs187315404 0.00006
NM_004629.2(FANCG):c.705G>A (p.Ala235=) rs148910563 0.00006
NM_004629.2(FANCG):c.77A>G (p.Gln26Arg) rs200677800 0.00004
NM_004629.2(FANCG):c.1677G>A (p.Lys559=) rs779403243 0.00002
NM_004629.2(FANCG):c.176-10G>A rs376273679 0.00002
NM_004629.2(FANCG):c.1422T>C (p.Ser474=) rs144369518 0.00001
NM_004629.1(FANCG):c.1795_1804del (p.Trp599Profs) rs397507560
NM_004629.2(FANCG):c.*7C>T
NM_004629.2(FANCG):c.1581C>A (p.Ser527Arg)
NM_004629.2(FANCG):c.1689G>C (p.Arg563=) rs138855718
NM_004629.2(FANCG):c.298C>T (p.Leu100=)
NM_004629.2(FANCG):c.725G>A (p.Arg242Gln)
NM_004629.2(FANCG):c.777+10G>A rs374991414
NM_004629.2(FANCG):c.85-21A>C rs886038550
NM_004629.2(FANCG):c.922G>T (p.Glu308Ter)
NM_004629.2(FANCG):c.938C>G (p.Pro313Arg)
NM_004629.2(FANCG):c.941del (p.Cys314fs)

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