List of variants in gene FLCN reported as uncertain significance by Quest Diagnostics Nichols Institute San Juan Capistrano

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 50

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.715C>T (p.Arg239Cys)	rs78683075	0.00024
NM_144997.7(FLCN):c.1432+8C>T	rs201898226	0.00009
NM_144997.7(FLCN):c.552C>A (p.Asn184Lys)	rs143525924	0.00007
NM_144997.7(FLCN):c.*4G>A	rs770795599	0.00004
NM_144997.7(FLCN):c.1216A>G (p.Ser406Gly)	rs528541881	0.00004
NM_144997.7(FLCN):c.1373A>G (p.Gln458Arg)	rs150439088	0.00003
NM_144997.7(FLCN):c.139G>C (p.Glu47Gln)	rs369115472	0.00003
NM_144997.7(FLCN):c.1430G>A (p.Arg477Gln)	rs748878853	0.00003
NM_144997.7(FLCN):c.1432+3G>T	rs752730139	0.00003
NM_144997.7(FLCN):c.1580G>A (p.Arg527Gln)	rs777826268	0.00003
NM_144997.7(FLCN):c.429C>G (p.Phe143Leu)	rs773792624	0.00003
NM_144997.7(FLCN):c.955G>C (p.Gly319Arg)	rs753491072	0.00003
NM_144997.7(FLCN):c.971A>G (p.Gln324Arg)	rs767368450	0.00003
NM_144997.7(FLCN):c.1049G>A (p.Arg350Gln)	rs190786280	0.00002
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.249+2C>T	rs939223011	0.00002
NM_144997.7(FLCN):c.249+4A>G	rs753648691	0.00002
NM_144997.7(FLCN):c.1124T>C (p.Ile375Thr)	rs2046950265	0.00001
NM_144997.7(FLCN):c.1193G>C (p.Gly398Ala)	rs766801011	0.00001
NM_144997.7(FLCN):c.1254G>A (p.Leu418=)	rs1226366288	0.00001
NM_144997.7(FLCN):c.1301A>G (p.Glu434Gly)	rs1286890611	0.00001
NM_144997.7(FLCN):c.1336C>T (p.Arg446Cys)	rs200724468	0.00001
NM_144997.7(FLCN):c.1415C>T (p.Pro472Leu)	rs1180118315	0.00001
NM_144997.7(FLCN):c.1635C>G (p.Asp545Glu)	rs760329266	0.00001
NM_144997.7(FLCN):c.1700C>T (p.Ser567Phe)	rs1466102804	0.00001
NM_144997.7(FLCN):c.1732C>T (p.Arg578Trp)	rs775107483	0.00001
NM_144997.7(FLCN):c.175C>T (p.Arg59Cys)	rs778275358	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.286A>G (p.Ile96Val)	rs2544283170	0.00001
NM_144997.7(FLCN):c.549C>T (p.Ile183=)	rs1278501001	0.00001
NM_144997.7(FLCN):c.748C>A (p.Leu250Met)	rs898441209	0.00001
NM_144997.7(FLCN):c.791C>T (p.Ala264Val)	rs372304384	0.00001
NM_144997.7(FLCN):c.908A>G (p.Glu303Gly)	rs773482946	0.00001
NM_144997.7(FLCN):c.1067T>C (p.Leu356Pro)	rs879255671
NM_144997.7(FLCN):c.1198G>T (p.Val400Phe)	rs148257120
NM_144997.7(FLCN):c.1382G>A (p.Ser461Asn)	rs1397579538
NM_144997.7(FLCN):c.1433-5C>A	rs781046590
NM_144997.7(FLCN):c.1451A>G (p.Asn484Ser)	rs1010980331
NM_144997.7(FLCN):c.1719A>G (p.Thr573=)	rs2544121194
NM_144997.7(FLCN):c.233A>G (p.Lys78Arg)	rs1209539424
NM_144997.7(FLCN):c.250-5G>A
NM_144997.7(FLCN):c.464_475del (p.Thr155_Ile158del)	rs2047178513
NM_144997.7(FLCN):c.516C>T (p.Ile172=)	rs2047176639
NM_144997.7(FLCN):c.565C>G (p.Leu189Val)	rs781433539
NM_144997.7(FLCN):c.779+8G>A	rs1260972155
NM_144997.7(FLCN):c.787_789dup (p.Lys263_Ala264insLys)
NM_144997.7(FLCN):c.976C>T (p.Pro326Ser)	rs751478971

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