List of variants in gene FLCN reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 58

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HGVS	dbSNP	gnomAD frequency
NM_144997.7(FLCN):c.-29G>A	rs151144873	0.00213
NM_144997.7(FLCN):c.-45A>G	rs571154058	0.00087
NM_144997.7(FLCN):c.*695C>T	rs775700421	0.00058
NM_144997.7(FLCN):c.*224G>A	rs541003301	0.00051
NM_144997.7(FLCN):c.268G>T (p.Ala90Ser)	rs141140415	0.00029
NM_144997.7(FLCN):c.*178A>G	rs145430714	0.00026
NM_144997.7(FLCN):c.*379G>A	rs117436649	0.00021
NM_144997.7(FLCN):c.592G>A (p.Asp198Asn)	rs200168437	0.00019
NM_144997.7(FLCN):c.*340G>A	rs886052659	0.00018
NM_144997.7(FLCN):c.-431C>T	rs138847774	0.00018
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg)	rs199643834	0.00018
NM_144997.7(FLCN):c.*528G>A	rs184006653	0.00017
NM_144997.7(FLCN):c.695_696del	rs886052658	0.00015
NM_144997.7(FLCN):c.*739C>T	rs558952732	0.00014
NM_144997.7(FLCN):c.1281C>G (p.Pro427=)	rs372207262	0.00014
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val)	rs200660337	0.00014
NM_144997.7(FLCN):c.977C>T (p.Pro326Leu)	rs138031155	0.00012
NM_144997.7(FLCN):c.*1035T>C	rs566019526	0.00009
NM_144997.7(FLCN):c.*1101C>G	rs543608114	0.00009
NM_144997.7(FLCN):c.*887T>C	rs886052657	0.00009
NM_144997.7(FLCN):c.-437C>T	rs886052663	0.00009
NM_144997.7(FLCN):c.*333C>T	rs750896108	0.00008
NM_144997.7(FLCN):c.552C>A (p.Asn184Lys)	rs143525924	0.00007
NM_144997.7(FLCN):c.*634A>C	rs199572622	0.00006
NM_144997.7(FLCN):c.1300+14C>T	rs200823760	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.*4G>A	rs770795599	0.00004
NM_144997.7(FLCN):c.-65A>G	rs145125741	0.00004
NM_144997.7(FLCN):c.1428C>G (p.Asp476Glu)	rs756944795	0.00004
NM_144997.7(FLCN):c.82C>T (p.Pro28Ser)	rs749758787	0.00004
NM_144997.7(FLCN):c.-173G>A	rs894893484	0.00003
NM_144997.7(FLCN):c.1430G>A (p.Arg477Gln)	rs748878853	0.00003
NM_144997.7(FLCN):c.1580G>A (p.Arg527Gln)	rs777826268	0.00003
NM_144997.7(FLCN):c.536G>A (p.Arg179Gln)	rs369906553	0.00003
NM_144997.7(FLCN):c.1084C>T (p.Arg362Cys)	rs557336321	0.00002
NM_144997.7(FLCN):c.135G>A (p.Ala45=)	rs759930161	0.00001
NM_144997.7(FLCN):c.791C>T (p.Ala264Val)	rs372304384	0.00001
NM_144997.7(FLCN):c.*1179T>A	rs540609895
NM_144997.7(FLCN):c.*1179dup	rs397932764
NM_144997.7(FLCN):c.*1273C>T	rs886052654
NM_144997.7(FLCN):c.*140C>T	rs2046810998
NM_144997.7(FLCN):c.*178A>C	rs145430714
NM_144997.7(FLCN):c.*290C>T	rs886052660
NM_144997.7(FLCN):c.*29G>A	rs1189817112
NM_144997.7(FLCN):c.*339C>T	rs1312482683
NM_144997.7(FLCN):c.*846C>T	rs2046796611
NM_144997.7(FLCN):c.*915G>T	rs1021480303
NM_144997.7(FLCN):c.*967T>C	rs886052656
NM_144997.7(FLCN):c.-143C>A	rs560968516
NM_144997.7(FLCN):c.-17dup	rs886052662
NM_144997.7(FLCN):c.-342G>A	rs2047601141
NM_144997.7(FLCN):c.10A>G (p.Ile4Val)	rs1555611575
NM_144997.7(FLCN):c.1482C>T (p.Asn494=)	rs1597578831
NM_144997.7(FLCN):c.250-7T>C	rs748857550
NM_144997.7(FLCN):c.598C>T (p.Leu200Phe)	rs1229735191
NM_144997.7(FLCN):c.617A>G (p.Lys206Arg)	rs886052661
NM_144997.7(FLCN):c.798C>T (p.Gly266=)	rs2047092959

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