ClinVar Miner

List of variants in gene FLCN reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
Download table as spreadsheet
HGVS dbSNP
NM_144997.6(FLCN):c.1433-25_1433-9dup rs778841914
NM_144997.6(FLCN):c.872-11_872-10delCT rs1555608679
NM_144997.7(FLCN):c.1059G>A (p.Arg353=) rs751513488
NM_144997.7(FLCN):c.1062+7G>A rs540198776
NM_144997.7(FLCN):c.1062+8G>C rs1317761101
NM_144997.7(FLCN):c.1063-6G>T rs1060504592
NM_144997.7(FLCN):c.1113G>A (p.Gly371=) rs1555607972
NM_144997.7(FLCN):c.1140C>T (p.Asp380=) rs768454196
NM_144997.7(FLCN):c.1155G>A (p.Gln385=) rs141250189
NM_144997.7(FLCN):c.1155G>T (p.Gln385His) rs141250189
NM_144997.7(FLCN):c.1176+8C>T rs1033129279
NM_144997.7(FLCN):c.1197C>T (p.Cys399=) rs750894316
NM_144997.7(FLCN):c.1252C>T (p.Leu418=) rs1060504595
NM_144997.7(FLCN):c.1275G>A (p.Gln425=) rs1555607680
NM_144997.7(FLCN):c.1278C>T (p.Ile426=) rs41459448
NM_144997.7(FLCN):c.1281C>T (p.Pro427=) rs372207262
NM_144997.7(FLCN):c.1284C>G (p.Pro428=) rs942763423
NM_144997.7(FLCN):c.1287C>T (p.His429=) rs374707789
NM_144997.7(FLCN):c.12C>T (p.Ile4=) rs752123350
NM_144997.7(FLCN):c.1300+8C>T rs936407961
NM_144997.7(FLCN):c.1314C>T (p.Ile438=) rs771247255
NM_144997.7(FLCN):c.1326C>T (p.His442=) rs145004158
NM_144997.7(FLCN):c.1350C>T (p.His450=) rs753685944
NM_144997.7(FLCN):c.1359G>A (p.Gly453=) rs752677061
NM_144997.7(FLCN):c.135G>A (p.Ala45=) rs759930161
NM_144997.7(FLCN):c.1389C>T (p.Tyr463=) rs137852929
NM_144997.7(FLCN):c.1414C>G (p.Pro472Ala) rs151312899
NM_144997.7(FLCN):c.1416T>C (p.Pro472=) rs1420039293
NM_144997.7(FLCN):c.1432+8C>T rs201898226
NM_144997.7(FLCN):c.1463C>T (p.Ala488Val) rs200660337
NM_144997.7(FLCN):c.1470G>A (p.Leu490=) rs1306737502
NM_144997.7(FLCN):c.1503C>T (p.Asp501=) rs1447641168
NM_144997.7(FLCN):c.1512C>T (p.Leu504=) rs757471403
NM_144997.7(FLCN):c.1523A>G (p.Lys508Arg) rs199643834
NM_144997.7(FLCN):c.1539-6C>T rs779028759
NM_144997.7(FLCN):c.1623G>A (p.Ala541=) rs185419942
NM_144997.7(FLCN):c.1641C>A (p.Val547=) rs1235496125
NM_144997.7(FLCN):c.1669C>T (p.Leu557=) rs878855215
NM_144997.7(FLCN):c.1692C>T (p.His564=) rs201810397
NM_144997.7(FLCN):c.1704G>A (p.Thr568=) rs147554296
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.198G>T (p.Gly66=) rs1369491093
NM_144997.7(FLCN):c.204C>T (p.Ser68=) rs371947198
NM_144997.7(FLCN):c.205G>A (p.Val69Ile) rs567617762
NM_144997.7(FLCN):c.207C>T (p.Val69=) rs759772780
NM_144997.7(FLCN):c.222G>A (p.Pro74=) rs770311645
NM_144997.7(FLCN):c.225G>T (p.Gly75=) rs1555611381
NM_144997.7(FLCN):c.246C>T (p.Cys82=) rs150712346
NM_144997.7(FLCN):c.250-8A>T rs770589774
NM_144997.7(FLCN):c.276C>T (p.His92=) rs1555610970
NM_144997.7(FLCN):c.318C>T (p.Tyr106=) rs773946854
NM_144997.7(FLCN):c.333C>T (p.His111=) rs1555610924
NM_144997.7(FLCN):c.354C>T (p.Phe118=) rs1555610913
NM_144997.7(FLCN):c.357C>T (p.Ser119=) rs878855216
NM_144997.7(FLCN):c.429C>T (p.Phe143=) rs773792624
NM_144997.7(FLCN):c.42C>T (p.His14=) rs766288960
NM_144997.7(FLCN):c.444C>T (p.His148=) rs376825814
NM_144997.7(FLCN):c.456C>T (p.Phe152=) rs763630763
NM_144997.7(FLCN):c.565C>T (p.Leu189=) rs781433539
NM_144997.7(FLCN):c.591C>T (p.Ile197=) rs763617124
NM_144997.7(FLCN):c.597G>A (p.Glu199=) rs1555610215
NM_144997.7(FLCN):c.615C>G (p.Leu205=) rs1555610191
NM_144997.7(FLCN):c.618+8C>G rs1555610185
NM_144997.7(FLCN):c.672A>G (p.Thr224=) rs1555609880
NM_144997.7(FLCN):c.687C>T (p.Phe229=) rs754710935
NM_144997.7(FLCN):c.708C>T (p.Asn236=) rs750394475
NM_144997.7(FLCN):c.729G>A (p.Ser243=) rs377261933
NM_144997.7(FLCN):c.735A>C (p.Thr245=) rs150175875
NM_144997.7(FLCN):c.735A>G (p.Thr245=) rs150175875
NM_144997.7(FLCN):c.75G>T (p.Leu25=) rs200350612
NM_144997.7(FLCN):c.779+10G>A rs376357696
NM_144997.7(FLCN):c.780-6C>T rs752746072
NM_144997.7(FLCN):c.789G>A (p.Lys263=) rs1483962771
NM_144997.7(FLCN):c.78C>T (p.His26=) rs746222481
NM_144997.7(FLCN):c.792G>A (p.Ala264=) rs140500421
NM_144997.7(FLCN):c.792G>T (p.Ala264=) rs140500421
NM_144997.7(FLCN):c.804G>T (p.Arg268=) rs771424902
NM_144997.7(FLCN):c.810C>A (p.Thr270=) rs372342796
NM_144997.7(FLCN):c.810C>G (p.Thr270=) rs372342796
NM_144997.7(FLCN):c.810C>T (p.Thr270=) rs372342796
NM_144997.7(FLCN):c.834G>A (p.Pro278=) rs146801028
NM_144997.7(FLCN):c.83C>G (p.Pro28Arg) rs780588085
NM_144997.7(FLCN):c.867C>T (p.Leu289=) rs367562964
NM_144997.7(FLCN):c.871+47G>A rs142934950
NM_144997.7(FLCN):c.872-4G>A rs752727873
NM_144997.7(FLCN):c.874T>C (p.Leu292=) rs759503601
NM_144997.7(FLCN):c.882G>A (p.Glu294=) rs1555608661
NM_144997.7(FLCN):c.939G>A (p.Leu313=) rs558365108
NM_144997.7(FLCN):c.951A>C (p.Thr317=) rs1060504594
NM_144997.7(FLCN):c.990C>T (p.Ser330=) rs761984486

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.