ClinVar Miner

List of variants in gene FLCN reported as likely benign for not specified

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Total variants: 82
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HGVS dbSNP gnomAD frequency
NM_144997.7(FLCN):c.1538+14T>G rs112111994 0.00721
NM_144997.7(FLCN):c.*17G>T rs115885284 0.00549
NM_144997.7(FLCN):c.1177-21G>A rs150687840 0.00276
NM_144997.7(FLCN):c.779+50G>T rs112496006 0.00242
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545 0.00217
NM_144997.7(FLCN):c.-29G>A rs151144873 0.00213
NM_144997.7(FLCN):c.618+23G>A rs201373940 0.00162
NM_144997.7(FLCN):c.871+16T>A rs116643153 0.00146
NM_144997.7(FLCN):c.-45A>G rs571154058 0.00087
NM_144997.7(FLCN):c.871+47G>A rs142934950 0.00058
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156 0.00053
NM_144997.7(FLCN):c.397-21G>C rs149414632 0.00038
NM_144997.7(FLCN):c.619-20C>T rs202217257 0.00037
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415 0.00029
NM_144997.7(FLCN):c.1149C>T (p.Leu383=) rs150752548 0.00028
NM_144997.7(FLCN):c.246C>T (p.Cys82=) rs150712346 0.00020
NM_144997.7(FLCN):c.1300+48C>G rs565858485 0.00018
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834 0.00018
NM_144997.7(FLCN):c.1062+7G>A rs540198776 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.1281C>G (p.Pro427=) rs372207262 0.00014
NM_144997.7(FLCN):c.1539-6C>T rs779028759 0.00009
NM_144997.7(FLCN):c.687C>T (p.Phe229=) rs754710935 0.00008
NM_144997.7(FLCN):c.1287C>T (p.His429=) rs374707789 0.00005
NM_144997.7(FLCN):c.1387T>C (p.Tyr463His) rs770077517 0.00005
NM_144997.7(FLCN):c.1692C>T (p.His564=) rs201810397 0.00005
NM_144997.7(FLCN):c.249+13G>C rs200103733 0.00005
NM_144997.7(FLCN):c.708C>T (p.Asn236=) rs750394475 0.00005
NM_144997.7(FLCN):c.779+10G>A rs376357696 0.00005
NM_144997.7(FLCN):c.1300+12C>T rs565983064 0.00004
NM_144997.7(FLCN):c.-12C>T rs779391001 0.00003
NM_144997.7(FLCN):c.12C>T (p.Ile4=) rs752123350 0.00003
NM_144997.7(FLCN):c.1433-36C>T rs564294188 0.00003
NM_144997.7(FLCN):c.429C>T (p.Phe143=) rs773792624 0.00003
NM_144997.7(FLCN):c.1101C>T (p.His367=) rs1451481907 0.00002
NM_144997.7(FLCN):c.1509C>T (p.Cys503=) rs927844338 0.00002
NM_144997.7(FLCN):c.204C>T (p.Ser68=) rs371947198 0.00002
NM_144997.7(FLCN):c.1047C>T (p.Leu349=) rs1460704611 0.00001
NM_144997.7(FLCN):c.1059G>A (p.Arg353=) rs751513488 0.00001
NM_144997.7(FLCN):c.1176+14T>A rs757366854 0.00001
NM_144997.7(FLCN):c.1227C>T (p.Tyr409=) rs561236067 0.00001
NM_144997.7(FLCN):c.1266G>A (p.Pro422=) rs751013842 0.00001
NM_144997.7(FLCN):c.1300+15G>A rs751264915 0.00001
NM_144997.7(FLCN):c.1301-18G>A rs186967236 0.00001
NM_144997.7(FLCN):c.1557T>C (p.Phe519=) rs1555606453 0.00001
NM_144997.7(FLCN):c.42C>T (p.His14=) rs766288960 0.00001
NM_144997.7(FLCN):c.681G>A (p.Thr227=) rs781035304 0.00001
NM_144997.7(FLCN):c.871+35C>T rs370794931 0.00001
NM_144997.7(FLCN):c.*2C>T
NM_144997.7(FLCN):c.-8A>G
NM_144997.7(FLCN):c.1062+46A>C
NM_144997.7(FLCN):c.1071T>C (p.Gly357=)
NM_144997.7(FLCN):c.1301-38G>T
NM_144997.7(FLCN):c.1301-40A>G
NM_144997.7(FLCN):c.1432+42C>T
NM_144997.7(FLCN):c.1432+47G>A
NM_144997.7(FLCN):c.1494T>C (p.Asp498=) rs1555606990
NM_144997.7(FLCN):c.1538+40del
NM_144997.7(FLCN):c.1539-27dup
NM_144997.7(FLCN):c.180G>C (p.Ala60=) rs1203041436
NM_144997.7(FLCN):c.205G>A (p.Val69Ile) rs567617762
NM_144997.7(FLCN):c.249+14G>C
NM_144997.7(FLCN):c.249+16G>T rs372318505
NM_144997.7(FLCN):c.250-47C>T
NM_144997.7(FLCN):c.333C>T (p.His111=) rs1555610924
NM_144997.7(FLCN):c.372C>G (p.Ala124=) rs2145010585
NM_144997.7(FLCN):c.397-16G>A rs201100388
NM_144997.7(FLCN):c.618+15G>T rs1057522057
NM_144997.7(FLCN):c.618+28G>A
NM_144997.7(FLCN):c.618+29G>A
NM_144997.7(FLCN):c.618+36G>A
NM_144997.7(FLCN):c.735A>G (p.Thr245=) rs150175875
NM_144997.7(FLCN):c.756G>A (p.Ala252=) rs746664975
NM_144997.7(FLCN):c.75G>A (p.Leu25=) rs200350612
NM_144997.7(FLCN):c.779+46_779+47del
NM_144997.7(FLCN):c.779+50G>A
NM_144997.7(FLCN):c.871+22C>T
NM_144997.7(FLCN):c.871+32G>A
NM_144997.7(FLCN):c.871+34C>T rs1007272111
NM_144997.7(FLCN):c.871+44G>T rs757688846
NM_144997.7(FLCN):c.954A>G (p.Glu318=) rs1555608573

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