ClinVar Miner

List of variants in gene FASN reported as benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
Download table as spreadsheet
HGVS dbSNP
NM_004104.4(FASN):c.1230G>A (p.Pro410=) rs376870564
NM_004104.4(FASN):c.1236C>T (p.Pro412=) rs558030339
NM_004104.4(FASN):c.1436G>T (p.Gly479Val) rs149982597
NM_004104.4(FASN):c.1455G>A (p.Val485=) rs190389710
NM_004104.4(FASN):c.1465G>A (p.Glu489Lys) rs62642482
NM_004104.4(FASN):c.1968C>T (p.Ala656=) rs45540245
NM_004104.4(FASN):c.2034C>T (p.Gly678=) rs148923081
NM_004104.4(FASN):c.2155G>A (p.Glu719Lys) rs12946178
NM_004104.4(FASN):c.2187G>A (p.Thr729=) rs17848930
NM_004104.4(FASN):c.2721C>T (p.Val907=) rs140477777
NM_004104.4(FASN):c.2757G>A (p.Leu919=) rs147904451
NM_004104.4(FASN):c.2815G>A (p.Glu939Lys) rs142371324
NM_004104.4(FASN):c.2937C>T (p.Pro979=) rs62642479
NM_004104.4(FASN):c.3186C>T (p.His1062=) rs45493497
NM_004104.4(FASN):c.3306C>G (p.Ala1102=) rs34179714
NM_004104.4(FASN):c.3427+8C>T rs565758653
NM_004104.4(FASN):c.3636C>T (p.Asp1212=) rs144326994
NM_004104.4(FASN):c.3669A>C (p.Ala1223=) rs45444299
NM_004104.4(FASN):c.3682C>T (p.Leu1228=) rs146800506
NM_004104.4(FASN):c.3829C>G (p.Pro1277Ala) rs764159372
NM_004104.4(FASN):c.3974C>T (p.Pro1325Leu) rs150915750
NM_004104.4(FASN):c.4128G>A (p.Ala1376=) rs201599707
NM_004104.4(FASN):c.4188C>T (p.Tyr1396=) rs45506801
NM_004104.4(FASN):c.4455G>A (p.Glu1485=) rs181585755
NM_004104.4(FASN):c.4578G>A (p.Glu1526=) rs45483502
NM_004104.4(FASN):c.4617G>C (p.Gly1539=) rs143566258
NM_004104.4(FASN):c.463A>G (p.Ile155Val) rs548430047
NM_004104.4(FASN):c.4999C>T (p.Pro1667Ser) rs45557233
NM_004104.4(FASN):c.5259G>A (p.Leu1753=) rs75603975
NM_004104.4(FASN):c.5336C>T (p.Pro1779Leu) rs2229426
NM_004104.4(FASN):c.5337G>A (p.Pro1779=) rs115708196
NM_004104.4(FASN):c.5412T>A (p.Ser1804Arg) rs140221463
NM_004104.4(FASN):c.552C>T (p.Ile184=) rs143728093
NM_004104.4(FASN):c.5535A>G (p.Gln1845=) rs2229421
NM_004104.4(FASN):c.5662A>G (p.Ile1888Val) rs2228307
NM_004104.4(FASN):c.5767+9G>A rs140072817
NM_004104.4(FASN):c.5768-4G>A rs369059351
NM_004104.4(FASN):c.5809G>A (p.Val1937Ile) rs17848945
NM_004104.4(FASN):c.5872G>A (p.Glu1958Lys) rs145688025
NM_004104.4(FASN):c.591C>T (p.Ser197=) rs141843553
NM_004104.4(FASN):c.6012-10G>A rs45491595
NM_004104.4(FASN):c.6014T>C (p.Val2005Ala) rs2228306
NM_004104.4(FASN):c.6118G>T (p.Ala2040Ser) rs150748779
NM_004104.4(FASN):c.6164-8C>G rs76966965
NM_004104.4(FASN):c.624C>T (p.Pro208=) rs45624241
NM_004104.4(FASN):c.6374G>A (p.Arg2125Gln) rs145866788
NM_004104.4(FASN):c.6477C>T (p.Ser2159=) rs146570982
NM_004104.4(FASN):c.6554G>A (p.Arg2185Gln) rs45507397
NM_004104.4(FASN):c.6765C>T (p.Thr2255=) rs148481729
NM_004104.4(FASN):c.694C>T (p.Leu232=) rs143618212
NM_004104.4(FASN):c.7167G>A (p.Pro2389=) rs143485066
NM_004104.4(FASN):c.7169T>G (p.Leu2390Arg) rs138021210
NM_004104.4(FASN):c.7192G>T (p.Ala2398Ser) rs200842352
NM_004104.4(FASN):c.747C>T (p.Ala249=) rs115212667
NM_004104.4(FASN):c.894+8C>A rs759051221
NM_004104.4(FASN):c.966C>T (p.Ile322=) rs200366210

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.