ClinVar Miner

List of variants in gene FLCN reported as uncertain significance by Illumina Clinical Services Laboratory,Illumina

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Gene type:
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Total variants: 27
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HGVS dbSNP
NM_144997.7(FLCN):c.*1179T>A rs540609895
NM_144997.7(FLCN):c.*1179dup rs397932764
NM_144997.7(FLCN):c.*1273C>T rs886052654
NM_144997.7(FLCN):c.*224G>A rs541003301
NM_144997.7(FLCN):c.*290C>T rs886052660
NM_144997.7(FLCN):c.*333C>T rs750896108
NM_144997.7(FLCN):c.*340G>A rs886052659
NM_144997.7(FLCN):c.*379G>A rs117436649
NM_144997.7(FLCN):c.*695C>T rs775700421
NM_144997.7(FLCN):c.*695_*696del rs886052658
NM_144997.7(FLCN):c.*739C>T rs558952732
NM_144997.7(FLCN):c.*887T>C rs886052657
NM_144997.7(FLCN):c.*967T>C rs886052656
NM_144997.7(FLCN):c.-143C>A rs560968516
NM_144997.7(FLCN):c.-17dup rs886052662
NM_144997.7(FLCN):c.-437C>T rs886052663
NM_144997.7(FLCN):c.1281C>G (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1428C>G (p.Asp476Glu) rs756944795
NM_144997.7(FLCN):c.1430G>A (p.Arg477Gln) rs748878853
NM_144997.7(FLCN):c.250-7T>C rs748857550
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415
NM_144997.7(FLCN):c.536G>A (p.Arg179Gln) rs369906553
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn) rs200168437
NM_144997.7(FLCN):c.617A>G (p.Lys206Arg) rs886052661
NM_144997.7(FLCN):c.791C>T (p.Ala264Val) rs372304384
NM_144997.7(FLCN):c.82C>T (p.Pro28Ser) rs749758787
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu) rs138031155

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