ClinVar Miner

List of variants reported as uncertain significance for Fanconi anemia complementation group G by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 40
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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.1453C>T (p.Arg485Trp) rs201884798 0.00022
NM_004629.2(FANCG):c.-1C>T rs587777946 0.00014
NM_004629.2(FANCG):c.881G>A (p.Gly294Glu) rs17880082 0.00014
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.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.704C>T (p.Ala235Val) rs574975594 0.00005
NM_004629.2(FANCG):c.769C>T (p.Arg257Cys) rs759314410 0.00005
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.1156C>G (p.Pro386Ala) rs375757497 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.934G>A (p.Val312Ile) rs530535955 0.00003
NM_004629.2(FANCG):c.1702A>G (p.Thr568Ala) rs750212705 0.00002
NM_004629.2(FANCG):c.635C>T (p.Ala212Val) rs375754266 0.00002
NM_004629.2(FANCG):c.1298G>C (p.Arg433Pro) rs748738986 0.00001
NM_004629.2(FANCG):c.1354G>A (p.Val452Ile) rs756069860 0.00001
NM_004629.2(FANCG):c.1492A>C (p.Asn498His) rs748364103 0.00001
NM_004629.2(FANCG):c.1519G>A (p.Ala507Thr) rs373151602 0.00001
NM_004629.2(FANCG):c.1688G>A (p.Arg563Gln) rs1309056736 0.00001
NM_004629.2(FANCG):c.500A>G (p.Asn167Ser) rs749946550 0.00001
NM_004629.2(FANCG):c.682G>A (p.Ala228Thr) rs765095688 0.00001
NM_004629.2(FANCG):c.905G>T (p.Ser302Ile) rs61757386 0.00001
NM_004629.2(FANCG):c.1085A>G (p.Asp362Gly) rs1829076408
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.1157C>G (p.Pro386Arg) rs141147618
NM_004629.2(FANCG):c.1474G>C (p.Glu492Gln) rs1018027137
NM_004629.2(FANCG):c.1657C>T (p.His553Tyr) rs1251259584
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.770G>A (p.Arg257His) rs372234656
NM_004629.2(FANCG):c.787C>G (p.Gln263Glu) rs149721361
NM_004629.2(FANCG):c.833C>T (p.Ala278Val) rs771395169

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