ClinVar Miner

List of variants in gene FLCN reported as likely benign by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 117
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HGVS dbSNP
NM_144997.7(FLCN):c.1021C>T (p.Arg341Trp) rs770396757
NM_144997.7(FLCN):c.1022G>A (p.Arg341Gln) rs375352888
NM_144997.7(FLCN):c.1030C>T (p.Pro344Ser) rs1597591391
NM_144997.7(FLCN):c.1047C>T (p.Leu349=) rs1460704611
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.1140C>T (p.Asp380=) rs768454196
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.1227C>T (p.Tyr409=) rs561236067
NM_144997.7(FLCN):c.1252C>T (p.Leu418=) rs1060504595
NM_144997.7(FLCN):c.1266G>A (p.Pro422=) rs751013842
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.1281C>T (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1282C>G (p.Pro428Ala) rs368880414
NM_144997.7(FLCN):c.1283C>G (p.Pro428Arg) rs199889477
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.12C>T (p.Ile4=) rs752123350
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.1362T>C (p.Cys454=) rs1597580072
NM_144997.7(FLCN):c.1380C>T (p.Leu460=) rs773581294
NM_144997.7(FLCN):c.1389C>T (p.Tyr463=) rs137852929
NM_144997.7(FLCN):c.138A>G (p.Glu46=) rs1597617874
NM_144997.7(FLCN):c.1416T>C (p.Pro472=) rs1420039293
NM_144997.7(FLCN):c.1418T>C (p.Val473Ala) rs144883828
NM_144997.7(FLCN):c.1440C>T (p.Pro480=) rs1597579041
NM_144997.7(FLCN):c.1461A>G (p.Glu487=) rs1597578928
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val) rs200660337
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) rs747029882
NM_144997.7(FLCN):c.1476C>T (p.Asn492=) rs779837933
NM_144997.7(FLCN):c.1482C>T (p.Asn494=) rs1597578831
NM_144997.7(FLCN):c.1512C>T (p.Leu504=) rs757471403
NM_144997.7(FLCN):c.1515C>T (p.Val505=) rs1388452217
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1602G>A (p.Lys534=) rs1597574143
NM_144997.7(FLCN):c.1623G>A (p.Ala541=) rs185419942
NM_144997.7(FLCN):c.1626C>T (p.Ser542=) rs1433647771
NM_144997.7(FLCN):c.1632G>A (p.Glu544=) rs763688092
NM_144997.7(FLCN):c.1647G>A (p.Leu549=) rs978355107
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.180G>A (p.Ala60=) rs1203041436
NM_144997.7(FLCN):c.198G>T (p.Gly66=) rs1369491093
NM_144997.7(FLCN):c.204C>T (p.Ser68=) rs371947198
NM_144997.7(FLCN):c.205G>A (p.Val69Ile) rs567617762
NM_144997.7(FLCN):c.207C>T (p.Val69=) rs759772780
NM_144997.7(FLCN):c.210G>A (p.Glu70=) rs771202158
NM_144997.7(FLCN):c.222G>A (p.Pro74=) rs770311645
NM_144997.7(FLCN):c.228C>T (p.Pro76=) rs1597617304
NM_144997.7(FLCN):c.231A>G (p.Lys77=) rs1597617272
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.252C>T (p.Gly84=) rs1597613345
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.315A>G (p.Lys105=) rs759011359
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.346C>A (p.Gln116Lys) rs398124536
NM_144997.7(FLCN):c.366C>A (p.Arg122=) rs1597612729
NM_144997.7(FLCN):c.396+4A>G rs370353839
NM_144997.7(FLCN):c.429C>T (p.Phe143=) rs773792624
NM_144997.7(FLCN):c.42C>T (p.His14=) rs766288960
NM_144997.7(FLCN):c.444C>T (p.His148=) rs376825814
NM_144997.7(FLCN):c.450T>C (p.Phe150=) rs200672897
NM_144997.7(FLCN):c.489C>A (p.Ala163=) rs775176038
NM_144997.7(FLCN):c.552C>A (p.Asn184Lys) rs143525924
NM_144997.7(FLCN):c.555C>A (p.Ser185=) rs748363919
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.586A>G (p.Ile196Val) rs201078144
NM_144997.7(FLCN):c.591C>T (p.Ile197=) rs763617124
NM_144997.7(FLCN):c.612G>A (p.Ala204=) rs763168749
NM_144997.7(FLCN):c.615C>G (p.Leu205=) rs1555610191
NM_144997.7(FLCN):c.687C>T (p.Phe229=) rs754710935
NM_144997.7(FLCN):c.702C>T (p.Asn234=) rs1471089893
NM_144997.7(FLCN):c.708C>T (p.Asn236=) rs750394475
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.717C>T (p.Arg239=) rs1597602140
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.735A>G (p.Thr245=) rs150175875
NM_144997.7(FLCN):c.756G>A (p.Ala252=) rs746664975
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612
NM_144997.7(FLCN):c.78C>T (p.His26=) rs746222481
NM_144997.7(FLCN):c.792G>A (p.Ala264=) rs140500421
NM_144997.7(FLCN):c.792G>T (p.Ala264=) rs140500421
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.810C>T (p.Thr270=) rs372342796
NM_144997.7(FLCN):c.816G>A (p.Lys272=) rs1597599277
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.867C>G (p.Leu289=) rs367562964
NM_144997.7(FLCN):c.867C>T (p.Leu289=) rs367562964
NM_144997.7(FLCN):c.872-4G>A rs752727873
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.957G>A (p.Gly319=) rs1428171261
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.996C>G (p.Leu332=) rs980011580
NM_144997.7(FLCN):c.9C>T (p.Ala3=) rs1555611576

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