ClinVar Miner

List of variants in gene FLCN reported as likely benign for Hereditary cancer-predisposing syndrome

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Total variants: 56
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HGVS dbSNP
NM_144997.7(FLCN):c.1059G>A (p.Arg353=) rs751513488
NM_144997.7(FLCN):c.1107C>T (p.Leu369=) rs786202175
NM_144997.7(FLCN):c.1149C>T (p.Leu383=) rs150752548
NM_144997.7(FLCN):c.1155G>T (p.Gln385His) rs141250189
NM_144997.7(FLCN):c.1198G>A (p.Val400Ile) rs148257120
NM_144997.7(FLCN):c.1201C>T (p.Arg401Cys) rs143183215
NM_144997.7(FLCN):c.120C>T (p.Gly40=) rs1555611501
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156
NM_144997.7(FLCN):c.1278C>T (p.Ile426=) rs41459448
NM_144997.7(FLCN):c.1281C>G (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1282C>G (p.Pro428Ala) rs368880414
NM_144997.7(FLCN):c.1284C>G (p.Pro428=) rs942763423
NM_144997.7(FLCN):c.1287C>T (p.His429=) rs374707789
NM_144997.7(FLCN):c.1326C>T (p.His442=) rs145004158
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.7(FLCN):c.135G>A (p.Ala45=) rs759930161
NM_144997.7(FLCN):c.1418T>C (p.Val473Ala) rs144883828
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) rs747029882
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1632G>A (p.Glu544=) rs763688092
NM_144997.7(FLCN):c.1647G>T (p.Leu549=) rs978355107
NM_144997.7(FLCN):c.1692C>T (p.His564=) rs201810397
NM_144997.7(FLCN):c.1704G>A (p.Thr568=) rs147554296
NM_144997.7(FLCN):c.204C>T (p.Ser68=) rs371947198
NM_144997.7(FLCN):c.207C>T (p.Val69=) rs759772780
NM_144997.7(FLCN):c.222G>A (p.Pro74=) rs770311645
NM_144997.7(FLCN):c.246C>T (p.Cys82=) rs150712346
NM_144997.7(FLCN):c.247G>A (p.Glu83Lys) rs757060348
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415
NM_144997.7(FLCN):c.279G>A (p.Pro93=) rs138688941
NM_144997.7(FLCN):c.318C>T (p.Tyr106=) rs773946854
NM_144997.7(FLCN):c.33C>T (p.Cys11=) rs754616167
NM_144997.7(FLCN):c.42C>T (p.His14=) rs766288960
NM_144997.7(FLCN):c.450T>C (p.Phe150=) rs200672897
NM_144997.7(FLCN):c.561C>G (p.Pro187=) rs1267713990
NM_144997.7(FLCN):c.580C>T (p.Arg194Trp) rs138070947
NM_144997.7(FLCN):c.591C>T (p.Ile197=) rs763617124
NM_144997.7(FLCN):c.687C>T (p.Phe229=) rs754710935
NM_144997.7(FLCN):c.711C>T (p.Ala237=) rs111258744
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys) rs78683075
NM_144997.7(FLCN):c.720G>A (p.Ser240=) rs186366202
NM_144997.7(FLCN):c.729G>A (p.Ser243=) rs377261933
NM_144997.7(FLCN):c.735A>C (p.Thr245=) rs150175875
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612
NM_144997.7(FLCN):c.804G>T (p.Arg268=) rs771424902
NM_144997.7(FLCN):c.810C>A (p.Thr270=) rs372342796
NM_144997.7(FLCN):c.81C>T (p.Ala27=) rs876659348
NM_144997.7(FLCN):c.834G>A (p.Pro278=) rs146801028
NM_144997.7(FLCN):c.837C>G (p.Thr279=) rs751877389
NM_144997.7(FLCN):c.874T>C (p.Leu292=) rs759503601
NM_144997.7(FLCN):c.915A>G (p.Glu305=) rs551034228
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu) rs138031155
NM_144997.7(FLCN):c.978G>A (p.Pro326=) rs920594920
NM_144997.7(FLCN):c.9C>T (p.Ala3=) rs1555611576

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