ClinVar Miner

List of variants in gene FLCN reported as not provided

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Total variants: 21
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HGVS dbSNP
NM_144606.5(FLCN):c.971C>T (p.Ala324Val) rs587778368
NM_144606.5(FLCN):c.992C>T (p.Thr331Met) rs149863088
NM_144997.5(FLCN):c.1283C>T (p.Pro428Leu) rs199889477
NM_144997.5(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.5(FLCN):c.202A>G (p.Ser68Gly) rs587778365
NM_144997.5(FLCN):c.296delA (p.Asp99Valfs) rs398124534
NM_144997.5(FLCN):c.396+55G>T rs587777930
NM_144997.5(FLCN):c.502C>T (p.Arg168Cys) rs587778367
NM_144997.5(FLCN):c.584delG (p.Gly195Glufs) rs878855217
NM_144997.5(FLCN):c.715C>T (p.Arg239Cys) rs78683075
NM_144997.5(FLCN):c.871+16T>A rs116643153
NM_144997.5(FLCN):c.871+47G>A rs142934950
NM_144997.5(FLCN):c.95G>A (p.Gly32Glu) rs587778366
NM_144997.6(FLCN):c.1049G>A (p.Arg350Gln) rs190786280
NM_144997.6(FLCN):c.1198G>A (p.Val400Ile) rs148257120
NM_144997.6(FLCN):c.134C>G (p.Ala45Gly) rs556510460
NM_144997.6(FLCN):c.268G>T (p.Ala90Ser) rs141140415
NM_144997.6(FLCN):c.396+59T>C rs41525346
NM_144997.6(FLCN):c.592G>A (p.Asp198Asn) rs200168437
NM_144997.6(FLCN):c.871+36G>A rs3744124
NM_144997.6(FLCN):c.959G>A (p.Arg320Gln) rs143483053

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