ClinVar Miner

List of variants in gene ELOVL4 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 95
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_022726.4(ELOVL4):c.541+60G>A rs45466000 0.02757
NM_022726.4(ELOVL4):c.669+58A>T rs114247663 0.00971
NM_022726.4(ELOVL4):c.814G>C (p.Glu272Gln) rs148919174 0.00936
NM_022726.4(ELOVL4):c.101-268G>A rs10223474 0.00834
NM_022726.4(ELOVL4):c.101-4A>G rs140639896 0.00267
NM_022726.4(ELOVL4):c.931G>A (p.Ala311Thr) rs189898207 0.00084
NM_022726.4(ELOVL4):c.351T>A (p.Asn117Lys) rs148018494 0.00031
NM_022726.4(ELOVL4):c.651C>T (p.Tyr217=) rs199860277 0.00024
NM_022726.4(ELOVL4):c.315A>T (p.Gly105=) rs149577942 0.00013
NM_022726.4(ELOVL4):c.541+17A>G rs367615182 0.00005
NM_022726.4(ELOVL4):c.108T>C (p.Arg36=) rs762319799 0.00004
NM_022726.4(ELOVL4):c.693G>A (p.Gly231=) rs771190061 0.00004
NM_022726.4(ELOVL4):c.105G>A (p.Lys35=) rs750472407 0.00003
NM_022726.4(ELOVL4):c.273C>G (p.Leu91=) rs762598733 0.00003
NM_022726.4(ELOVL4):c.289-11T>G rs751200164 0.00003
NM_022726.4(ELOVL4):c.370-11C>T rs954200666 0.00003
NM_022726.4(ELOVL4):c.370-19A>G rs775098373 0.00003
NM_022726.4(ELOVL4):c.100+13A>G rs763149475 0.00002
NM_022726.4(ELOVL4):c.303A>T (p.Ser101=) rs1282310555 0.00002
NM_022726.4(ELOVL4):c.312G>A (p.Ala104=) rs768561554 0.00002
NM_022726.4(ELOVL4):c.192A>C (p.Pro64=) rs201014417 0.00001
NM_022726.4(ELOVL4):c.333G>A (p.Gln111=) rs749538550 0.00001
NM_022726.4(ELOVL4):c.370-17G>A rs1386642150 0.00001
NM_022726.4(ELOVL4):c.486C>T (p.His162=) rs747560791 0.00001
NM_022726.4(ELOVL4):c.633T>C (p.Tyr211=) rs1486924167 0.00001
NM_022726.4(ELOVL4):c.654G>A (p.Leu218=) rs771331626 0.00001
NM_022726.4(ELOVL4):c.735A>G (p.Lys245=) rs769435926 0.00001
NM_022726.4(ELOVL4):c.762T>C (p.Tyr254=) rs1774170778 0.00001
NM_022726.4(ELOVL4):c.924T>C (p.Asn308=) rs528228676 0.00001
NC_000006.12:g.79947706G>C
NC_000006.12:g.79947729C>T rs555010506
NM_022726.4(ELOVL4):c.-272_-260dup rs200403099
NM_022726.4(ELOVL4):c.100+152G>A rs78496216
NM_022726.4(ELOVL4):c.100+8C>G rs2127703522
NM_022726.4(ELOVL4):c.101-20G>A
NM_022726.4(ELOVL4):c.101-5T>C rs1561985668
NM_022726.4(ELOVL4):c.101-8C>G rs2127699423
NM_022726.4(ELOVL4):c.111G>A (p.Val37=)
NM_022726.4(ELOVL4):c.126G>A (p.Leu42=)
NM_022726.4(ELOVL4):c.168T>C (p.Tyr56=)
NM_022726.4(ELOVL4):c.174G>A (p.Leu58=)
NM_022726.4(ELOVL4):c.189T>A (p.Gly63=)
NM_022726.4(ELOVL4):c.192A>G (p.Pro64=)
NM_022726.4(ELOVL4):c.204G>A (p.Lys68=)
NM_022726.4(ELOVL4):c.216T>G (p.Pro72=) rs1774340977
NM_022726.4(ELOVL4):c.231A>G (p.Leu77=)
NM_022726.4(ELOVL4):c.234G>A (p.Val78=) rs950684247
NM_022726.4(ELOVL4):c.279C>T (p.Ile93=) rs1477917919
NM_022726.4(ELOVL4):c.289-13A>G
NM_022726.4(ELOVL4):c.289-14T>C
NM_022726.4(ELOVL4):c.289-17T>A
NM_022726.4(ELOVL4):c.291A>G (p.Leu97=)
NM_022726.4(ELOVL4):c.309T>C (p.Asn103=)
NM_022726.4(ELOVL4):c.30T>C (p.Ser10=)
NM_022726.4(ELOVL4):c.324T>C (p.Tyr108=) rs200158201
NM_022726.4(ELOVL4):c.33C>T (p.Val11=)
NM_022726.4(ELOVL4):c.369+15A>T
NM_022726.4(ELOVL4):c.370-14T>C rs2127698536
NM_022726.4(ELOVL4):c.370-15T>C rs987467575
NM_022726.4(ELOVL4):c.370-6T>C
NM_022726.4(ELOVL4):c.375T>G (p.Ala125=)
NM_022726.4(ELOVL4):c.399A>G (p.Val133=) rs1275204469
NM_022726.4(ELOVL4):c.405A>G (p.Lys135=)
NM_022726.4(ELOVL4):c.426A>G (p.Thr142=)
NM_022726.4(ELOVL4):c.429G>A (p.Val143=) rs973821185
NM_022726.4(ELOVL4):c.492G>A (p.Thr164=) rs267601134
NM_022726.4(ELOVL4):c.492G>T (p.Thr164=)
NM_022726.4(ELOVL4):c.502T>C (p.Leu168=) rs886061802
NM_022726.4(ELOVL4):c.537A>G (p.Gly179=)
NM_022726.4(ELOVL4):c.541+14G>A rs2127698488
NM_022726.4(ELOVL4):c.542-15G>C
NM_022726.4(ELOVL4):c.542-18C>T
NM_022726.4(ELOVL4):c.54A>T (p.Ala18=)
NM_022726.4(ELOVL4):c.591A>G (p.Ser197=) rs1774216267
NM_022726.4(ELOVL4):c.597T>C (p.Tyr199=)
NM_022726.4(ELOVL4):c.609A>G (p.Ala203=)
NM_022726.4(ELOVL4):c.648A>T (p.Arg216=)
NM_022726.4(ELOVL4):c.652C>T (p.Leu218=)
NM_022726.4(ELOVL4):c.663G>A (p.Leu221=)
NM_022726.4(ELOVL4):c.669+50del rs200457540
NM_022726.4(ELOVL4):c.670-11C>G
NM_022726.4(ELOVL4):c.670-16C>T rs2127697616
NM_022726.4(ELOVL4):c.687C>A (p.Thr229=)
NM_022726.4(ELOVL4):c.6G>T (p.Gly2=)
NM_022726.4(ELOVL4):c.723C>T (p.Cys241=) rs2127697605
NM_022726.4(ELOVL4):c.732C>T (p.Pro244=) rs1055380093
NM_022726.4(ELOVL4):c.78C>T (p.Tyr26=) rs2127703538
NM_022726.4(ELOVL4):c.804G>A (p.Arg268=) rs1399239991
NM_022726.4(ELOVL4):c.810C>T (p.Tyr270=)
NM_022726.4(ELOVL4):c.81C>T (p.Arg27=) rs2127703535
NM_022726.4(ELOVL4):c.831A>G (p.Lys277=)
NM_022726.4(ELOVL4):c.834T>C (p.Ala278=) rs2127697582
NM_022726.4(ELOVL4):c.894_895inv (p.Met299Val)
NM_022726.4(ELOVL4):c.944A>G (p.Ter315=)
NM_022726.4(ELOVL4):c.9C>T (p.Leu3=)

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.