ClinVar Miner

List of variants in gene FLCN reported as uncertain significance for Birt-Hogg-Dube syndrome 1

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_144997.7(FLCN):c.707A>G (p.Asn236Ser) rs1194767470 0.00004
NM_144997.7(FLCN):c.1066C>G (p.Leu356Val) rs757313788 0.00003
NM_144997.7(FLCN):c.1270G>A (p.Val424Met) rs1264775833 0.00003
NM_144997.7(FLCN):c.1376C>T (p.Ser459Phe) rs377468280 0.00003
NM_144997.7(FLCN):c.197G>A (p.Gly66Glu) rs753787458 0.00003
NM_144997.7(FLCN):c.604G>A (p.Gly202Ser) rs774491699 0.00003
NM_144997.7(FLCN):c.62G>A (p.Cys21Tyr) rs1025567379 0.00002
NM_144997.7(FLCN):c.1022G>A (p.Arg341Gln) rs375352888 0.00001
NM_144997.7(FLCN):c.1315G>A (p.Val439Met) rs112980409 0.00001
NM_144997.7(FLCN):c.1363G>A (p.Glu455Lys) rs759637055 0.00001
NM_144997.7(FLCN):c.1453A>G (p.Lys485Glu) rs1448703959 0.00001
NM_144997.7(FLCN):c.1700C>T (p.Ser567Phe) rs1466102804 0.00001
NM_144997.7(FLCN):c.1702A>G (p.Thr568Ala) rs748337450 0.00001
NM_144997.7(FLCN):c.256C>T (p.Arg86Trp) rs1327627870 0.00001
NM_144997.7(FLCN):c.278C>T (p.Pro93Leu) rs766548696 0.00001
NM_144997.7(FLCN):c.284A>G (p.Tyr95Cys) rs1555610947 0.00001
NM_144997.7(FLCN):c.502C>T (p.Arg168Cys) rs587778367 0.00001
NM_144997.7(FLCN):c.544C>T (p.Leu182Phe) rs749368513 0.00001
NM_144997.7(FLCN):c.734C>A (p.Thr245Lys) rs371401039 0.00001
NM_144997.7(FLCN):c.838G>A (p.Glu280Lys) rs1060502367 0.00001
NM_144997.7(FLCN):c.958C>T (p.Arg320Trp) rs777456756 0.00001
NM_144997.7(FLCN):c.1085G>A (p.Arg362His) rs559055296
NM_144997.7(FLCN):c.1085G>T (p.Arg362Leu) rs559055296
NM_144997.7(FLCN):c.1099C>T (p.His367Tyr)
NM_144997.7(FLCN):c.1100A>G (p.His367Arg) rs1555607981
NM_144997.7(FLCN):c.1105C>G (p.Leu369Val) rs2144870384
NM_144997.7(FLCN):c.1150G>A (p.Val384Ile) rs779913370
NM_144997.7(FLCN):c.1283C>A (p.Pro428His) rs199889477
NM_144997.7(FLCN):c.1285C>G (p.His429Asp) rs375082054
NM_144997.7(FLCN):c.12C>G (p.Ile4Met)
NM_144997.7(FLCN):c.1360T>G (p.Cys454Gly) rs767762804
NM_144997.7(FLCN):c.1375T>G (p.Ser459Ala) rs1229110607
NM_144997.7(FLCN):c.1465G>A (p.Ala489Thr) rs757222242
NM_144997.7(FLCN):c.1487C>G (p.Ser496Cys) rs750535468
NM_144997.7(FLCN):c.1508G>A (p.Cys503Tyr)
NM_144997.7(FLCN):c.1527G>T (p.Glu509Asp) rs1597578623
NM_144997.7(FLCN):c.1544T>C (p.Val515Ala)
NM_144997.7(FLCN):c.1627G>C (p.Glu543Gln)
NM_144997.7(FLCN):c.1697T>C (p.Met566Thr) rs756302545
NM_144997.7(FLCN):c.1709G>T (p.Arg570Leu) rs201056799
NM_144997.7(FLCN):c.176G>T (p.Arg59Leu) rs374969279
NM_144997.7(FLCN):c.183C>A (p.His61Gln)
NM_144997.7(FLCN):c.424TTC[1] (p.Phe143del) rs764153620
NM_144997.7(FLCN):c.451G>T (p.Val151Leu) rs147164515
NM_144997.7(FLCN):c.53C>G (p.Thr18Ser)
NM_144997.7(FLCN):c.53C>T (p.Thr18Ile) rs2047314341
NM_144997.7(FLCN):c.574A>G (p.Lys192Glu) rs2047173108
NM_144997.7(FLCN):c.659A>T (p.Gln220Leu) rs2047129363
NM_144997.7(FLCN):c.695A>G (p.Gln232Arg)
NM_144997.7(FLCN):c.719C>T (p.Ser240Leu) rs2047125657
NM_144997.7(FLCN):c.820C>A (p.Leu274Met)
NM_144997.7(FLCN):c.82C>G (p.Pro28Ala) rs749758787
NM_144997.7(FLCN):c.842_850del (p.Asp281_Leu283del)
NM_144997.7(FLCN):c.94G>C (p.Gly32Arg)

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