ClinVar Miner

List of variants in gene FLCN reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_144997.7(FLCN):c.1433-38A>G rs34235236 0.21634
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514 0.02907
NM_144997.7(FLCN):c.872-13A>G rs114970273 0.01651
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545 0.00217
NM_144997.7(FLCN):c.619-20C>T rs202217257 0.00037
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415 0.00029
NM_144997.7(FLCN):c.246C>T (p.Cys82=) rs150712346 0.00020
NM_144997.7(FLCN):c.1278C>T (p.Ile426=) rs41459448 0.00016
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741 0.00015
NM_144997.7(FLCN):c.396+7C>T rs781155484 0.00006
NM_144997.7(FLCN):c.396+19G>A rs767495491 0.00005
NM_144997.7(FLCN):c.779+10G>A rs376357696 0.00005
NM_144997.7(FLCN):c.43G>A (p.Gly15Ser) rs539468848 0.00004
NM_144997.7(FLCN):c.1174C>T (p.Arg392Trp) rs1060502374 0.00002
NM_144997.7(FLCN):c.1419A>C (p.Val473=) rs141036419 0.00001
NM_144997.7(FLCN):c.779+1G>T rs758175953 0.00001
NM_144997.7(FLCN):c.1177-5_1177-3del rs767671406
NM_144997.7(FLCN):c.1188del (p.Val397fs) rs1567809782
NM_144997.7(FLCN):c.1285del (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1285dup (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1301-2A>G rs1555607296
NM_144997.7(FLCN):c.1318_1334dup (p.Leu449fs) rs879255677
NM_144997.7(FLCN):c.1429C>T (p.Arg477Ter) rs879255678
NM_144997.7(FLCN):c.1432+1G>A rs755959303
NM_144997.7(FLCN):c.1532G>A (p.Trp511Ter) rs879255682
NM_144997.7(FLCN):c.1697T>C (p.Met566Thr) rs756302545
NM_144997.7(FLCN):c.189del (p.Ala64fs) rs876660611
NM_144997.7(FLCN):c.235_238del (p.Ser79fs) rs750146811
NM_144997.7(FLCN):c.296del (p.Asp99fs) rs398124534
NM_144997.7(FLCN):c.33C>G (p.Cys11Trp) rs754616167
NM_144997.7(FLCN):c.507G>A (p.Trp169Ter) rs1555610290
NM_144997.7(FLCN):c.594_596del (p.Asp198del) rs1567819459
NM_144997.7(FLCN):c.665T>G (p.Met222Arg) rs1555609889
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612
NM_144997.7(FLCN):c.871+170_871+178del rs750424403
NM_144997.7(FLCN):c.871+22C>T
NM_144997.7(FLCN):c.890_893del (p.Glu297fs) rs398124541
NM_144997.7(FLCN):c.89del (p.Pro30fs)

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