ClinVar Miner

List of variants in gene FLCN reported as benign for Multiple fibrofolliculomas

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Total variants: 58
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HGVS dbSNP
NM_144997.6(FLCN):c.-487G>C rs1736209
NM_144997.7(FLCN):c.*1182dup rs199535675
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.*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.*4G>A
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.*911G>A rs571893996
NM_144997.7(FLCN):c.*914C>T rs7223831
NM_144997.7(FLCN):c.*956A>G rs141650706
NM_144997.7(FLCN):c.-134C>T rs116581458
NM_144997.7(FLCN):c.-176G>A rs117215381
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.-430C>T
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.1149C>T (p.Leu383=) rs150752548
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.1433-38A>G rs34235236
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val) rs200660337
NM_144997.7(FLCN):c.1464G>A (p.Ala488=) rs747029882
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1538+10A>C rs12451312
NM_144997.7(FLCN):c.1538+14T>G rs112111994
NM_144997.7(FLCN):c.1580G>A (p.Arg527Gln) rs777826268
NM_144997.7(FLCN):c.249+13G>C rs200103733
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.450T>C (p.Phe150=) rs200672897
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn) rs200168437
NM_144997.7(FLCN):c.708C>T (p.Asn236=) rs750394475
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514
NM_144997.7(FLCN):c.735A>C (p.Thr245=) rs150175875
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612
NM_144997.7(FLCN):c.779+9C>T rs373504780
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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