ClinVar Miner

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

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Gene type:
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Total variants: 55
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HGVS dbSNP
NM_144997.7(FLCN):c.-176G>A rs117215381
NM_144997.7(FLCN):c.1021C>T (p.Arg341Trp) rs770396757
NM_144997.7(FLCN):c.1149C>T (p.Leu383=) rs150752548
NM_144997.7(FLCN):c.1188C>T (p.Pro396=) rs1025539940
NM_144997.7(FLCN):c.1236C>G (p.Ala412=) rs769968368
NM_144997.7(FLCN):c.1242G>A (p.Arg414=) rs376836624
NM_144997.7(FLCN):c.1269C>T (p.His423=) rs41464156
NM_144997.7(FLCN):c.1278C>T (p.Ile426=) rs41459448
NM_144997.7(FLCN):c.1311C>A (p.Val437=) rs1002586963
NM_144997.7(FLCN):c.1314C>T (p.Ile438=) rs771247255
NM_144997.7(FLCN):c.1353T>C (p.Pro451=) rs1597580172
NM_144997.7(FLCN):c.1416T>C (p.Pro472=) rs1420039293
NM_144997.7(FLCN):c.1432+10C>G rs1216451293
NM_144997.7(FLCN):c.1432+9C>T rs751683346
NM_144997.7(FLCN):c.1509C>T (p.Cys503=) rs927844338
NM_144997.7(FLCN):c.1538+235G>A rs141383036
NM_144997.7(FLCN):c.1614C>T (p.Ile538=) rs1597574133
NM_144997.7(FLCN):c.1641C>A (p.Val547=) rs1235496125
NM_144997.7(FLCN):c.1707C>T (p.Val569=) rs1597573624
NM_144997.7(FLCN):c.1737C>T (p.Asn579=) rs767345167
NM_144997.7(FLCN):c.186C>T (p.Ser62=) rs1060504593
NM_144997.7(FLCN):c.189C>T (p.Pro63=) rs750047828
NM_144997.7(FLCN):c.198G>A (p.Gly66=) rs1369491093
NM_144997.7(FLCN):c.207C>T (p.Val69=) rs759772780
NM_144997.7(FLCN):c.210G>A (p.Glu70=) rs771202158
NM_144997.7(FLCN):c.222G>A (p.Pro74=) rs770311645
NM_144997.7(FLCN):c.225G>A (p.Gly75=) rs1555611381
NM_144997.7(FLCN):c.246C>T (p.Cys82=) rs150712346
NM_144997.7(FLCN):c.249+7G>A rs1597617052
NM_144997.7(FLCN):c.297T>C (p.Asp99=) rs1597613086
NM_144997.7(FLCN):c.306C>T (p.Thr102=) rs762265819
NM_144997.7(FLCN):c.327C>T (p.His109=) rs1597612898
NM_144997.7(FLCN):c.357C>T (p.Ser119=) rs878855216
NM_144997.7(FLCN):c.366C>G (p.Arg122=) rs1597612729
NM_144997.7(FLCN):c.384C>T (p.Ser128=) rs1597612670
NM_144997.7(FLCN):c.474C>T (p.Ile158=) rs1597607110
NM_144997.7(FLCN):c.480C>T (p.Asp160=) rs1597607089
NM_144997.7(FLCN):c.489C>A (p.Ala163=) rs775176038
NM_144997.7(FLCN):c.48C>G (p.Pro16=) rs1597618480
NM_144997.7(FLCN):c.534C>T (p.Asp178=) rs1597606800
NM_144997.7(FLCN):c.57C>T (p.Leu19=) rs1597618395
NM_144997.7(FLCN):c.630A>G (p.Ala210=) rs1305220357
NM_144997.7(FLCN):c.669C>T (p.Asn223=) rs938971627
NM_144997.7(FLCN):c.681G>A (p.Thr227=) rs781035304
NM_144997.7(FLCN):c.690A>C (p.Leu230=) rs373977390
NM_144997.7(FLCN):c.702C>T (p.Asn234=) rs1471089893
NM_144997.7(FLCN):c.720G>A (p.Ser240=) rs186366202
NM_144997.7(FLCN):c.779+8G>T rs1260972155
NM_144997.7(FLCN):c.822G>A (p.Leu274=) rs777731843
NM_144997.7(FLCN):c.837C>G (p.Thr279=) rs751877389
NM_144997.7(FLCN):c.871+47G>A rs142934950
NM_144997.7(FLCN):c.90T>C (p.Pro30=) rs766122649
NM_144997.7(FLCN):c.937T>C (p.Leu313=) rs1432138522
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu) rs138031155
NM_144997.7(FLCN):c.981A>G (p.Ala327=) rs763078516

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