ClinVar Miner

List of variants in gene FANCG reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_004629.1(FANCG):c.-453_-452insT rs16935545 0.12501
NM_004629.1(FANCG):c.-490G>T rs10972303 0.07883
NM_004629.2(FANCG):c.-392A>G rs10972302 0.06369
NM_004629.1(FANCG):c.-504A>T rs17885140 0.05593
NM_004629.2(FANCG):c.988C>T (p.Pro330Ser) rs4986940 0.00670
NM_004629.2(FANCG):c.238C>T (p.Leu80=) rs115131067 0.00330
NM_004629.1(FANCG):c.-450G>C rs535301610 0.00283
NM_004629.2(FANCG):c.20C>T (p.Ser7Phe) rs35984312 0.00138
NM_004629.2(FANCG):c.478G>A (p.Ala160Thr) rs140534765 0.00051
NM_004629.1(FANCG):c.-488G>A rs752617227 0.00047
NM_004629.2(FANCG):c.794C>T (p.Ala265Val) rs764992007 0.00031
NM_004629.2(FANCG):c.1545C>T (p.Ala515=) rs201422773 0.00028
NM_004629.2(FANCG):c.-1C>T rs587777946 0.00014
NM_004629.2(FANCG):c.-56G>A rs967151809 0.00013
NM_004629.2(FANCG):c.*250C>T rs535188841 0.00010
NM_004629.2(FANCG):c.1808C>T (p.Ser603Phe) rs17878854 0.00006
NM_004629.2(FANCG):c.724C>T (p.Arg242Trp) rs574511407 0.00006
NM_004629.2(FANCG):c.-93C>G rs532840867 0.00004
NM_004629.2(FANCG):c.366G>C (p.Trp122Cys) rs546023787 0.00004
NM_004629.2(FANCG):c.77A>G (p.Gln26Arg) rs200677800 0.00004
NM_004629.2(FANCG):c.880G>A (p.Gly294Arg) rs886063897 0.00004
NM_004629.2(FANCG):c.*141A>G rs1323568562 0.00002
NM_004629.2(FANCG):c.1155C>T (p.Pro385=) rs1217203217 0.00002
NM_004629.2(FANCG):c.458C>G (p.Ala153Gly) rs200074432 0.00002
NM_004629.2(FANCG):c.944G>A (p.Ser315Asn) rs745833004 0.00002
NM_004629.1(FANCG):c.-491G>A rs886063901 0.00001
NM_004629.2(FANCG):c.*101A>G rs751616369 0.00001
NM_004629.2(FANCG):c.-276G>A rs1445799529 0.00001
NM_004629.2(FANCG):c.-311T>A rs886063900 0.00001
NM_004629.2(FANCG):c.-348A>G rs376750755 0.00001
NM_004629.2(FANCG):c.1252G>A (p.Glu418Lys) rs886063896 0.00001
NM_004629.2(FANCG):c.1434-6C>T rs1404150675 0.00001
NM_004629.2(FANCG):c.1652A>C (p.Tyr551Ser) rs1447816480 0.00001
NM_004629.2(FANCG):c.682G>A (p.Ala228Thr) rs765095688 0.00001
NM_004629.2(FANCG):c.999C>T (p.Asp333=) rs762238437 0.00001
NM_004629.2(FANCG):c.*77C>T rs1829028329
NM_004629.2(FANCG):c.-182del rs886063899
NM_004629.2(FANCG):c.-342G>T rs556082635
NM_004629.2(FANCG):c.1002A>T (p.Leu334=) rs984958735
NM_004629.2(FANCG):c.1027C>G (p.Gln343Glu) rs1829085768
NM_004629.2(FANCG):c.1152A>C (p.Pro384=) rs1487531031
NM_004629.2(FANCG):c.1157C>A (p.Pro386His) rs141147618
NM_004629.2(FANCG):c.1345C>T (p.Pro449Ser) rs1829066600
NM_004629.2(FANCG):c.1448T>C (p.Leu483Pro) rs1829061760
NM_004629.2(FANCG):c.161dup (p.His55fs) rs886063898
NM_004629.2(FANCG):c.1689G>C (p.Arg563=) rs138855718
NM_004629.2(FANCG):c.292C>A (p.Arg98=) rs532525154
NM_004629.2(FANCG):c.497T>C (p.Leu166Pro)
NM_004629.2(FANCG):c.736G>T (p.Val246Phe)
NM_004629.2(FANCG):c.957G>A (p.Pro319=) rs145092954

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