ClinVar Miner

List of variants in gene FLCN reported as uncertain significance for not provided

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Total variants: 20
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HGVS dbSNP
NM_144997.7(FLCN):c.1149C>T (p.Leu383=) rs150752548
NM_144997.7(FLCN):c.1198G>T (p.Val400Phe) rs148257120
NM_144997.7(FLCN):c.1253T>C (p.Leu418Pro) rs879255674
NM_144997.7(FLCN):c.1333G>A (p.Ala445Thr) rs41419545
NM_144997.7(FLCN):c.1430G>A (p.Arg477Gln) rs748878853
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1539-16_1539-12del rs398124531
NM_144997.7(FLCN):c.247G>A (p.Glu83Lys) rs757060348
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser) rs141140415
NM_144997.7(FLCN):c.429C>G (p.Phe143Leu) rs773792624
NM_144997.7(FLCN):c.451G>A (p.Val151Met) rs147164515
NM_144997.7(FLCN):c.50G>C (p.Arg17Pro) rs398124537
NM_144997.7(FLCN):c.552C>A (p.Asn184Lys) rs143525924
NM_144997.7(FLCN):c.586A>G (p.Ile196Val) rs201078144
NM_144997.7(FLCN):c.594_596del (p.Asp198del) rs1567819459
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys) rs78683075
NM_144997.7(FLCN):c.871+16T>A rs116643153
NM_144997.7(FLCN):c.871+47G>A rs142934950
NM_144997.7(FLCN):c.959G>A (p.Arg320Gln) rs143483053
NM_144997.7(FLCN):c.97G>C (p.Asp33His) rs386833401

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