ClinVar Miner

List of variants in gene FLCN reported by PreventionGenetics, part of Exact Sciences

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Gene type:
ClinVar version:
Total variants: 96
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HGVS dbSNP gnomAD frequency
NM_144997.7(FLCN):c.1062+6C>T rs8065832 0.47076
NM_144997.7(FLCN):c.397-14C>T rs1736219 0.40309
NM_144997.7(FLCN):c.397-13G>A rs3744123 0.07012
NM_144997.7(FLCN):c.1233G>A (p.Glu411=) rs61750032 0.03557
NM_144997.7(FLCN):c.726A>T (p.Thr242=) rs113938514 0.02907
NM_144997.7(FLCN):c.872-13A>G rs114970273 0.01651
NM_144997.7(FLCN):c.871+16T>A rs116643153 0.00146
NM_144997.7(FLCN):c.1414C>G (p.Pro472Ala) rs151312899 0.00080
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053 0.00071
NM_144997.7(FLCN):c.871+98C>T rs144832463 0.00061
NM_144997.7(FLCN):c.871+47G>A rs142934950 0.00058
NM_144997.7(FLCN):c.1155G>T (p.Gln385His) rs141250189 0.00038
NM_144997.7(FLCN):c.619-20C>T rs202217257 0.00037
NM_144997.7(FLCN):c.735A>C (p.Thr245=) rs150175875 0.00032
NM_144997.7(FLCN):c.931C>T (p.Pro311Ser) rs140246224 0.00029
NM_144997.7(FLCN):c.871+158A>C rs201282009 0.00028
NM_144997.7(FLCN):c.871+121C>T rs149863088 0.00025
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys) rs78683075 0.00024
NM_144997.7(FLCN):c.1326C>T (p.His442=) rs145004158 0.00023
NM_144997.7(FLCN):c.246C>T (p.Cys82=) rs150712346 0.00020
NM_144997.7(FLCN):c.396+4A>G rs370353839 0.00020
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn) rs200168437 0.00019
NM_144997.7(FLCN):c.-431C>T rs138847774 0.00018
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834 0.00018
NM_144997.7(FLCN):c.113G>T (p.Ser38Ile) rs139418842 0.00016
NM_144997.7(FLCN):c.1278C>T (p.Ile426=) rs41459448 0.00016
NM_144997.7(FLCN):c.1332C>T (p.Ala444=) rs141283741 0.00015
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val) rs200660337 0.00014
NM_144997.7(FLCN):c.1704G>A (p.Thr568=) rs147554296 0.00011
NM_144997.7(FLCN):c.1538+10A>C rs12451312 0.00010
NM_144997.7(FLCN):c.779+9C>T rs373504780 0.00009
NM_144997.7(FLCN):c.802C>T (p.Arg268Trp) rs762370059 0.00007
NM_144997.7(FLCN):c.867C>T (p.Leu289=) rs367562964 0.00007
NM_144997.7(FLCN):c.1274A>G (p.Gln425Arg) rs786203348 0.00006
NM_144997.7(FLCN):c.189C>T (p.Pro63=) rs750047828 0.00006
NM_144997.7(FLCN):c.396+7C>T rs781155484 0.00006
NM_144997.7(FLCN):c.444C>T (p.His148=) rs376825814 0.00006
NM_144997.7(FLCN):c.78C>T (p.His26=) rs746222481 0.00006
NM_144997.7(FLCN):c.871+100C>T rs587778368 0.00006
NM_144997.7(FLCN):c.1287C>T (p.His429=) rs374707789 0.00005
NM_144997.7(FLCN):c.346C>A (p.Gln116Lys) rs398124536 0.00005
NM_144997.7(FLCN):c.779+10G>A rs376357696 0.00005
NM_144997.7(FLCN):c.1068G>T (p.Leu356=) rs534904034 0.00004
NM_144997.7(FLCN):c.1271T>C (p.Val424Ala) rs752170592 0.00004
NM_144997.7(FLCN):c.134C>G (p.Ala45Gly) rs556510460 0.00003
NM_144997.7(FLCN):c.1380C>T (p.Leu460=) rs773581294 0.00003
NM_144997.7(FLCN):c.429C>T (p.Phe143=) rs773792624 0.00003
NM_144997.7(FLCN):c.450T>C (p.Phe150=) rs200672897 0.00003
NM_144997.7(FLCN):c.804G>T (p.Arg268=) rs771424902 0.00003
NM_144997.7(FLCN):c.1084C>T (p.Arg362Cys) rs557336321 0.00002
NM_144997.7(FLCN):c.1102G>A (p.Val368Ile) rs767714543 0.00002
NM_144997.7(FLCN):c.204C>T (p.Ser68=) rs371947198 0.00002
NM_144997.7(FLCN):c.1176+14T>A rs757366854 0.00001
NM_144997.7(FLCN):c.1230G>A (p.Glu410=) rs749287631 0.00001
NM_144997.7(FLCN):c.1363G>A (p.Glu455Lys) rs759637055 0.00001
NM_144997.7(FLCN):c.1522_1524del (p.Lys508del) rs398124529 0.00001
NM_144997.7(FLCN):c.1599G>C (p.Gln533His) rs190965235 0.00001
NM_144997.7(FLCN):c.179C>T (p.Ala60Val) rs779900587 0.00001
NM_144997.7(FLCN):c.247G>A (p.Glu83Lys) rs757060348 0.00001
NM_144997.7(FLCN):c.42C>T (p.His14=) rs766288960 0.00001
NM_144997.7(FLCN):c.610G>A (p.Ala204Thr) rs1456509027 0.00001
NM_144997.7(FLCN):c.721C>G (p.Leu241Val) rs1337020636 0.00001
NM_144997.7(FLCN):c.729G>A (p.Ser243=) rs377261933 0.00001
NM_144997.7(FLCN):c.780-6C>T rs752746072 0.00001
NM_144997.7(FLCN):c.-161G>A
NM_144997.7(FLCN):c.-452C>A
NM_144997.7(FLCN):c.-8A>G
NM_144997.7(FLCN):c.1202G>A (p.Arg401His) rs771653740
NM_144997.7(FLCN):c.1285del (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1285dup (p.His429fs) rs80338682
NM_144997.7(FLCN):c.1287dup (p.Val430fs)
NM_144997.7(FLCN):c.1300+5G>C rs746264578
NM_144997.7(FLCN):c.1300+9C>T
NM_144997.7(FLCN):c.1389C>G (p.Tyr463Ter) rs137852929
NM_144997.7(FLCN):c.1433-20_1433-10del rs1380029891
NM_144997.7(FLCN):c.1647G>T (p.Leu549=) rs978355107
NM_144997.7(FLCN):c.227C>T (p.Pro76Leu) rs2047302894
NM_144997.7(FLCN):c.250-2A>G rs398124533
NM_144997.7(FLCN):c.289A>G (p.Ser97Gly)
NM_144997.7(FLCN):c.397-330C>T
NM_144997.7(FLCN):c.397-374T>C
NM_144997.7(FLCN):c.494G>C (p.Gly165Ala)
NM_144997.7(FLCN):c.615C>G (p.Leu205=) rs1555610191
NM_144997.7(FLCN):c.619-1G>A rs1131690840
NM_144997.7(FLCN):c.767CCT[1] (p.Ser257del)
NM_144997.7(FLCN):c.871+134A>G
NM_144997.7(FLCN):c.871+146G>A
NM_144997.7(FLCN):c.871+152G>A
NM_144997.7(FLCN):c.871+158A>G
NM_144997.7(FLCN):c.871+160del
NM_144997.7(FLCN):c.871+22C>T
NM_144997.7(FLCN):c.871+42C>T
NM_144997.7(FLCN):c.871+44G>A
NM_144997.7(FLCN):c.871+50C>T
NM_144997.7(FLCN):c.890_893del (p.Glu297fs) rs398124541
NM_144997.7(FLCN):c.918G>T (p.Glu306Asp)

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