ClinVar Miner

List of variants in gene FLCN studied for not specified

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Total variants: 79
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HGVS dbSNP
NM_144997.7(FLCN):c.*17G>T rs115885284
NM_144997.7(FLCN):c.-134C>T rs116581458
NM_144997.7(FLCN):c.-29G>A rs151144873
NM_144997.7(FLCN):c.-45A>G rs571154058
NM_144997.7(FLCN):c.-93C>T rs115413827
NM_144997.7(FLCN):c.-97C>T rs114481741
NM_144997.7(FLCN):c.1049G>A (p.Arg350Gln) rs190786280
NM_144997.7(FLCN):c.1059G>A (p.Arg353=) rs751513488
NM_144997.7(FLCN):c.1062+6C>T rs8065832
NM_144997.7(FLCN):c.1062+7G>A rs540198776
NM_144997.7(FLCN):c.1149C>T (p.Leu383=) rs150752548
NM_144997.7(FLCN):c.1176+14T>A rs757366854
NM_144997.7(FLCN):c.1176+31G>A rs41340844
NM_144997.7(FLCN):c.1177-21G>A rs150687840
NM_144997.7(FLCN):c.1177-5_1177-3del rs767671406
NM_144997.7(FLCN):c.1198G>A (p.Val400Ile) rs148257120
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=) rs561236067
NM_144997.7(FLCN):c.1233G>A (p.Glu411=) rs61750032
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.1283C>T (p.Pro428Leu) rs199889477
NM_144997.7(FLCN):c.1285dup (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1287C>T (p.His429=) rs374707789
NM_144997.7(FLCN):c.1300+12C>T rs565983064
NM_144997.7(FLCN):c.1300+15G>A rs751264915
NM_144997.7(FLCN):c.1301-18G>A rs186967236
NM_144997.7(FLCN):c.1301-2A>G rs1555607296
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.134C>G (p.Ala45Gly) rs556510460
NM_144997.7(FLCN):c.135G>A (p.Ala45=) rs759930161
NM_144997.7(FLCN):c.1389C>T (p.Tyr463=) rs137852929
NM_144997.7(FLCN):c.1414C>G (p.Pro472Ala) rs151312899
NM_144997.7(FLCN):c.1418T>C (p.Val473Ala) rs144883828
NM_144997.7(FLCN):c.1429C>T (p.Arg477Ter) rs879255678
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) rs747029882
NM_144997.7(FLCN):c.1494T>C (p.Asp498=) rs1555606990
NM_144997.7(FLCN):c.1509C>T (p.Cys503=) rs927844338
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1538+14T>G rs112111994
NM_144997.7(FLCN):c.1557T>C (p.Phe519=) rs1555606453
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.202A>G (p.Ser68Gly) rs587778365
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.249+13G>C rs200103733
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415
NM_144997.7(FLCN):c.396+55G>T rs587777930
NM_144997.7(FLCN):c.396+59T>C rs41525346
NM_144997.7(FLCN):c.397-12G>T rs199958635
NM_144997.7(FLCN):c.397-13G>A rs3744123
NM_144997.7(FLCN):c.397-14C>T rs1736219
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.502C>T (p.Arg168Cys) rs587778367
NM_144997.7(FLCN):c.507G>A (p.Trp169Ter) rs1555610290
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn) rs200168437
NM_144997.7(FLCN):c.618+15G>T rs1057522057
NM_144997.7(FLCN):c.619-20C>T rs202217257
NM_144997.7(FLCN):c.665T>G (p.Met222Arg) rs1555609889
NM_144997.7(FLCN):c.687C>T (p.Phe229=) rs754710935
NM_144997.7(FLCN):c.708C>T (p.Asn236=) rs750394475
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys) rs78683075
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514
NM_144997.7(FLCN):c.729G>A (p.Ser243=) rs377261933
NM_144997.7(FLCN):c.779+10G>A rs376357696
NM_144997.7(FLCN):c.779+1G>T rs758175953
NM_144997.7(FLCN):c.871+100C>T rs587778368
NM_144997.7(FLCN):c.871+121C>T rs149863088
NM_144997.7(FLCN):c.871+16T>A rs116643153
NM_144997.7(FLCN):c.871+36G>A rs3744124
NM_144997.7(FLCN):c.871+47G>A rs142934950
NM_144997.7(FLCN):c.872-13A>G rs114970273
NM_144997.7(FLCN):c.954A>G (p.Glu318=) rs1555608573
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053
NM_144997.7(FLCN):c.95G>A (p.Gly32Glu) rs587778366
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu) rs138031155

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