ClinVar Miner

List of variants in gene FANCG reported as uncertain significance by Natera, Inc.

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
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HGVS dbSNP gnomAD frequency
NM_004629.2(FANCG):c.478G>A (p.Ala160Thr) rs140534765 0.00051
NM_004629.2(FANCG):c.794C>T (p.Ala265Val) rs764992007 0.00031
NM_004629.2(FANCG):c.1453C>T (p.Arg485Trp) rs201884798 0.00022
NM_004629.2(FANCG):c.1367A>T (p.His456Leu) rs148808709 0.00013
NM_004629.2(FANCG):c.1454G>A (p.Arg485Gln) rs77152961 0.00010
NM_004629.2(FANCG):c.421C>T (p.Arg141Cys) rs201153812 0.00007
NM_004629.2(FANCG):c.1297C>T (p.Arg433Trp) rs183777537 0.00006
NM_004629.2(FANCG):c.1801C>T (p.Arg601Cys) rs368098479 0.00006
NM_004629.2(FANCG):c.464G>A (p.Arg155His) rs201099560 0.00006
NM_004629.2(FANCG):c.766C>T (p.His256Tyr) rs753955326 0.00006
NM_004629.2(FANCG):c.968T>C (p.Ile323Thr) rs752346718 0.00006
NM_004629.2(FANCG):c.704C>T (p.Ala235Val) rs574975594 0.00005
NM_004629.2(FANCG):c.1510A>C (p.Lys504Gln) rs1304316655 0.00004
NM_004629.2(FANCG):c.1521G>A (p.Ala507=) rs373411028 0.00004
NM_004629.2(FANCG):c.293G>A (p.Arg98Gln) rs372854981 0.00004
NM_004629.2(FANCG):c.422G>A (p.Arg141His) rs775719850 0.00004
NM_004629.2(FANCG):c.880G>A (p.Gly294Arg) rs886063897 0.00004
NM_004629.2(FANCG):c.992C>G (p.Pro331Arg) rs765722724 0.00004
NM_004629.2(FANCG):c.1156C>G (p.Pro386Ala) rs375757497 0.00003
NM_004629.2(FANCG):c.1298G>A (p.Arg433Gln) rs748738986 0.00003
NM_004629.2(FANCG):c.1441G>C (p.Glu481Gln) rs772460728 0.00003
NM_004629.2(FANCG):c.1718G>C (p.Arg573Thr) rs200466062 0.00003
NM_004629.2(FANCG):c.1768C>G (p.Pro590Ala) rs541868979 0.00003
NM_004629.2(FANCG):c.181C>T (p.Pro61Ser) rs931163229 0.00003
NM_004629.2(FANCG):c.380G>A (p.Arg127His) rs780985218 0.00003
NM_004629.2(FANCG):c.398C>T (p.Pro133Leu) rs1270561172 0.00003
NM_004629.2(FANCG):c.730G>A (p.Val244Met) rs746248064 0.00003
NM_004629.2(FANCG):c.1292T>G (p.Met431Arg) rs759285011 0.00002
NM_004629.2(FANCG):c.1346C>T (p.Pro449Leu) rs757442131 0.00002
NM_004629.2(FANCG):c.1702A>G (p.Thr568Ala) rs750212705 0.00002
NM_004629.2(FANCG):c.458C>G (p.Ala153Gly) rs200074432 0.00002
NM_004629.2(FANCG):c.1189T>C (p.Phe397Leu) rs1060501868 0.00001
NM_004629.2(FANCG):c.1222G>A (p.Gly408Ser) rs371171892 0.00001
NM_004629.2(FANCG):c.1252G>A (p.Glu418Lys) rs886063896 0.00001
NM_004629.2(FANCG):c.1268G>A (p.Arg423His) rs757276792 0.00001
NM_004629.2(FANCG):c.1519G>A (p.Ala507Thr) rs373151602 0.00001
NM_004629.2(FANCG):c.158T>G (p.Leu53Arg) rs756388446 0.00001
NM_004629.2(FANCG):c.1595A>G (p.Lys532Arg) rs1587139402 0.00001
NM_004629.2(FANCG):c.1626G>C (p.Gln542His) rs1060501867 0.00001
NM_004629.2(FANCG):c.1688G>A (p.Arg563Gln) rs1309056736 0.00001
NM_004629.2(FANCG):c.1814G>A (p.Arg605His) rs751710424 0.00001
NM_004629.2(FANCG):c.338G>A (p.Arg113Lys) rs778894219 0.00001
NM_004629.2(FANCG):c.500A>G (p.Asn167Ser) rs749946550 0.00001
NM_004629.2(FANCG):c.634G>A (p.Ala212Thr) rs775291829 0.00001
NM_004629.2(FANCG):c.84+9G>T rs759504806 0.00001
NM_004629.2(FANCG):c.1082G>A (p.Gly361Glu) rs1276088946
NM_004629.2(FANCG):c.1153C>G (p.Pro385Ala) rs1288516919
NM_004629.2(FANCG):c.1157C>A (p.Pro386His) rs141147618
NM_004629.2(FANCG):c.1480+5T>G rs1554670176
NM_004629.2(FANCG):c.1648A>G (p.Thr550Ala) rs1255677446
NM_004629.2(FANCG):c.1745A>G (p.His582Arg) rs1196002404
NM_004629.2(FANCG):c.1777C>T (p.Leu593=) rs746613103
NM_004629.2(FANCG):c.178C>T (p.Leu60Phe) rs1026058105
NM_004629.2(FANCG):c.1852_1853del (p.Lys618fs) rs532302967
NM_004629.2(FANCG):c.293G>T (p.Arg98Leu) rs372854981
NM_004629.2(FANCG):c.448T>C (p.Trp150Arg) rs202114813
NM_004629.2(FANCG):c.511-6dup rs376732298
NM_004629.2(FANCG):c.580C>T (p.Pro194Ser) rs1554670412
NM_004629.2(FANCG):c.743T>C (p.Val248Ala) rs1221668009
NM_004629.2(FANCG):c.787C>G (p.Gln263Glu) rs149721361
NM_004629.2(FANCG):c.833C>T (p.Ala278Val) rs771395169

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