ClinVar Miner

List of variants in gene FLCN reported as not provided

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Total variants: 27
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HGVS dbSNP gnomAD frequency
NM_144997.7(FLCN):c.871+36G>A rs3744124 0.07420
NM_144997.7(FLCN):c.396+59T>C rs41525346 0.06134
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545 0.00217
NM_144997.7(FLCN):c.871+16T>A rs116643153 0.00146
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053 0.00071
NM_144997.7(FLCN):c.871+47G>A rs142934950 0.00058
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415 0.00029
NM_144997.7(FLCN):c.871+121C>T rs149863088 0.00025
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys) rs78683075 0.00024
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn) rs200168437 0.00019
NM_144997.7(FLCN):c.1283C>T (p.Pro428Leu) rs199889477 0.00006
NM_144997.7(FLCN):c.871+100C>T rs587778368 0.00006
NM_144997.7(FLCN):c.1198G>A (p.Val400Ile) rs148257120 0.00003
NM_144997.7(FLCN):c.134C>G (p.Ala45Gly) rs556510460 0.00003
NM_144997.7(FLCN):c.1049G>A (p.Arg350Gln) rs190786280 0.00002
NM_144997.7(FLCN):c.396+55G>T rs587777930 0.00001
NM_144997.7(FLCN):c.502C>T (p.Arg168Cys) rs587778367 0.00001
NM_144997.7(FLCN):c.95G>A (p.Gly32Glu) rs587778366 0.00001
NM_144997.7(FLCN):c.1085G>A (p.Arg362His) rs559055296
NM_144997.7(FLCN):c.1285del (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1285dup (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1389C>G (p.Tyr463Ter) rs137852929
NM_144997.7(FLCN):c.1420G>A (p.Ala474Thr) rs2046876810
NM_144997.7(FLCN):c.202A>G (p.Ser68Gly) rs587778365
NM_144997.7(FLCN):c.296del (p.Asp99fs) rs398124534
NM_144997.7(FLCN):c.584del (p.Gly195fs) rs878855217
NM_144997.7(FLCN):c.610_611delinsTA (p.Ala204Ter) rs398124538

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