ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 70
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HGVS dbSNP
NM_144997.6(FLCN):c.-487G>C rs1736209
NM_144997.7(FLCN):c.*1179T>A rs540609895
NM_144997.7(FLCN):c.*1179dup rs397932764
NM_144997.7(FLCN):c.*1182dup rs199535675
NM_144997.7(FLCN):c.*1273C>T rs886052654
NM_144997.7(FLCN):c.*1336G>T rs7218992
NM_144997.7(FLCN):c.*1403T>C rs7218795
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.*333C>T rs750896108
NM_144997.7(FLCN):c.*340G>A rs886052659
NM_144997.7(FLCN):c.*356G>T rs7224474
NM_144997.7(FLCN):c.*379G>A rs117436649
NM_144997.7(FLCN):c.*393G>A rs12602675
NM_144997.7(FLCN):c.*425G>A rs7224335
NM_144997.7(FLCN):c.*442T>C rs7224213
NM_144997.7(FLCN):c.*526T>C rs574547835
NM_144997.7(FLCN):c.*528G>A rs184006653
NM_144997.7(FLCN):c.*557T>C rs3803761
NM_144997.7(FLCN):c.*634A>C rs199572622
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.*911G>A rs571893996
NM_144997.7(FLCN):c.*914C>T rs7223831
NM_144997.7(FLCN):c.*956A>G rs141650706
NM_144997.7(FLCN):c.*967T>C rs886052656
NM_144997.7(FLCN):c.-134C>T rs116581458
NM_144997.7(FLCN):c.-141G>T rs541105214
NM_144997.7(FLCN):c.-143C>A rs560968516
NM_144997.7(FLCN):c.-176G>A rs117215381
NM_144997.7(FLCN):c.-17dup rs886052662
NM_144997.7(FLCN):c.-299C>T rs1708629
NM_144997.7(FLCN):c.-29G>A rs151144873
NM_144997.7(FLCN):c.-302G>A rs41345949
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.-480G>C rs564584154
NM_144997.7(FLCN):c.-78G>C rs147598893
NM_144997.7(FLCN):c.-90A>G rs8069957
NM_144997.7(FLCN):c.-93C>T rs115413827
NM_144997.7(FLCN):c.-97C>T rs114481741
NM_144997.7(FLCN):c.1062+6C>T rs8065832
NM_144997.7(FLCN):c.1233G>A (p.Glu411=) rs61750032
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156
NM_144997.7(FLCN):c.1281C>G (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1300+14C>T rs200823760
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
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.1538+14T>G rs112111994
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.397-13G>A rs3744123
NM_144997.7(FLCN):c.397-14C>T rs1736219
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.715C>T (p.Arg239Cys) rs78683075
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514
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.872-13A>G rs114970273
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu) rs138031155

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