ClinVar Miner

List of variants in gene FLCN reported as uncertain significance for Pneumothorax, primary spontaneous

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Total variants: 56
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HGVS dbSNP
NM_144997.7(FLCN):c.*1035T>C
NM_144997.7(FLCN):c.*1101C>G
NM_144997.7(FLCN):c.*1179T>A rs540609895
NM_144997.7(FLCN):c.*1273C>T rs886052654
NM_144997.7(FLCN):c.*140C>T
NM_144997.7(FLCN):c.*178A>C
NM_144997.7(FLCN):c.*178A>G rs145430714
NM_144997.7(FLCN):c.*224G>A rs541003301
NM_144997.7(FLCN):c.*290C>T rs886052660
NM_144997.7(FLCN):c.*29G>A
NM_144997.7(FLCN):c.*333C>T rs750896108
NM_144997.7(FLCN):c.*339C>T
NM_144997.7(FLCN):c.*340G>A rs886052659
NM_144997.7(FLCN):c.*379G>A rs117436649
NM_144997.7(FLCN):c.*4G>A
NM_144997.7(FLCN):c.*528G>A rs184006653
NM_144997.7(FLCN):c.*634A>C rs199572622
NM_144997.7(FLCN):c.*695C>T rs775700421
NM_144997.7(FLCN):c.*739C>T rs558952732
NM_144997.7(FLCN):c.*846C>T
NM_144997.7(FLCN):c.*887T>C rs886052657
NM_144997.7(FLCN):c.*915G>T
NM_144997.7(FLCN):c.*967T>C rs886052656
NM_144997.7(FLCN):c.-143C>A rs560968516
NM_144997.7(FLCN):c.-173G>A
NM_144997.7(FLCN):c.-29G>A rs151144873
NM_144997.7(FLCN):c.-342G>A
NM_144997.7(FLCN):c.-431C>T rs138847774
NM_144997.7(FLCN):c.-437C>T rs886052663
NM_144997.7(FLCN):c.-45A>G rs571154058
NM_144997.7(FLCN):c.-65A>G
NM_144997.7(FLCN):c.1084C>T (p.Arg362Cys) rs557336321
NM_144997.7(FLCN):c.10A>G (p.Ile4Val) rs1555611575
NM_144997.7(FLCN):c.1281C>G (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1300+14C>T rs200823760
NM_144997.7(FLCN):c.135G>A (p.Ala45=) rs759930161
NM_144997.7(FLCN):c.1428C>G (p.Asp476Glu) rs756944795
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val) rs200660337
NM_144997.7(FLCN):c.1482C>T (p.Asn494=) rs1597578831
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1559A>G (p.Lys520Arg) rs142288285
NM_144997.7(FLCN):c.1580G>A (p.Arg527Gln) rs777826268
NM_144997.7(FLCN):c.205G>A (p.Val69Ile) rs567617762
NM_144997.7(FLCN):c.249+13G>C rs200103733
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.552C>A (p.Asn184Lys) rs143525924
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn) rs200168437
NM_144997.7(FLCN):c.598C>T (p.Leu200Phe) rs1229735191
NM_144997.7(FLCN):c.617A>G (p.Lys206Arg) rs886052661
NM_144997.7(FLCN):c.708C>T (p.Asn236=) rs750394475
NM_144997.7(FLCN):c.791C>T (p.Ala264Val) rs372304384
NM_144997.7(FLCN):c.798C>T (p.Gly266=)
NM_144997.7(FLCN):c.82C>T (p.Pro28Ser) rs749758787
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu) rs138031155

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