Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.79921664A=CA1640824968ELOVL4c.502T= (p.Leu168=)
6g.79921664A>CCA364656516ELOVL4c.502T>G (p.Leu168Val)
6g.79921664A>GCA10627695ELOVL4c.502T>C (p.Leu168=)
ClinVar dbSNP gnomAD v4
6g.79921664A>TCA364656517ELOVL4c.502T>A (p.Leu168Met)
6g.79921665G>ACA451068508ELOVL4c.501C>T (p.Thr167=)
COSMIC
6g.79921665G>CCA451068510ELOVL4c.501C>G (p.Thr167=)
6g.79921665G>TCA451068509ELOVL4c.501C>A (p.Thr167=)
6g.79921666G>ACA364656518ELOVL4c.500C>T (p.Thr167Ile)
6g.79921666G>CCA364656519ELOVL4c.500C>G (p.Thr167Ser)
6g.79921666G>TCA364656520ELOVL4c.500C>A (p.Thr167Asn)
6g.79921667T>ACA364656521ELOVL4c.499A>T (p.Thr167Ser)
6g.79921667T>CCA364656522ELOVL4c.499A>G (p.Thr167Ala)
6g.79921667T>GCA364656523ELOVL4c.499A>C (p.Thr167Pro)
gnomAD v4
6g.79921668A>CCA364656524ELOVL4c.498T>G (p.Phe166Leu)
6g.79921668A>GCA451068511ELOVL4c.498T>C (p.Phe166=)
6g.79921668A>TCA364656525ELOVL4c.498T>A (p.Phe166Leu)
6g.79921669A>CCA364656526ELOVL4c.497T>G (p.Phe166Cys)
6g.79921669A>GCA364656527ELOVL4c.497T>C (p.Phe166Ser)
6g.79921669A>TCA364656528ELOVL4c.497T>A (p.Phe166Tyr)
6g.79921670A=CA1640824969ELOVL4c.496T= (p.Phe166=)
6g.79921670A>CCA364656529ELOVL4c.496T>G (p.Phe166Val)
dbSNP gnomAD v2
6g.79921670A>GCA364656531ELOVL4c.496T>C (p.Phe166Leu)
6g.79921670A>TCA364656530ELOVL4c.496T>A (p.Phe166Ile)
6g.79921671C>ACA364656532ELOVL4c.495G>T (p.Met165Ile)
6g.79921671C=CA1640824970ELOVL4c.495G= (p.Met165=)
6g.79921671C>GCA364656534ELOVL4c.495G>C (p.Met165Ile)
6g.79921671C>TCA364656533ELOVL4c.495G>A (p.Met165Ile)
dbSNP gnomAD v3 gnomAD v4
6g.79921672A>CCA364656535ELOVL4c.494T>G (p.Met165Arg)
6g.79921672A>GCA364656536ELOVL4c.494T>C (p.Met165Thr)
6g.79921672A>TCA364656537ELOVL4c.494T>A (p.Met165Lys)
6g.79921673T>ACA364656538ELOVL4c.493A>T (p.Met165Leu)
6g.79921673T>CCA364656539ELOVL4c.493A>G (p.Met165Val)
gnomAD v4
6g.79921673T>GCA364656540ELOVL4c.493A>C (p.Met165Leu)
6g.79921674C>ACA451068512ELOVL4c.492G>T (p.Thr164=)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.79921674C=CA1640824971ELOVL4c.492G= (p.Thr164=)
6g.79921674C>GCA451068513ELOVL4c.492G>C (p.Thr164=)
dbSNP
6g.79921674C>TCA142271130ELOVL4c.492G>A (p.Thr164=)
ClinVar dbSNP gnomAD v4
6g.79921675G>ACA3901526ELOVL4c.491C>T (p.Thr164Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.79921675G>CCA364656541ELOVL4c.491C>G (p.Thr164Arg)
6g.79921675G=CA1640824972ELOVL4c.491C= (p.Thr164=)
6g.79921675G>TCA364656542ELOVL4c.491C>A (p.Thr164Lys)
6g.79921676T>ACA364656543ELOVL4c.490A>T (p.Thr164Ser)
6g.79921676T>CCA142271131ELOVL4c.490A>G (p.Thr164Ala)
dbSNP
6g.79921676T>GCA364656544ELOVL4c.490A>C (p.Thr164Pro)
6g.79921676T=CA1640824973ELOVL4c.490A= (p.Thr164=)
6g.79921677A=CA1640824974ELOVL4c.489T= (p.Cys163=)
6g.79921677A>CCA364656546ELOVL4c.489T>G (p.Cys163Trp)
6g.79921677A>GCA3901527ELOVL4c.489T>C (p.Cys163=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921677A>TCA364656545ELOVL4c.489T>A (p.Cys163Ter)
6g.79921678_79921679delCA2679489855ELOVL4c.488_489del (p.Cys163TyrfsTer11)
gnomAD v4
6g.79921678C>ACA364656547ELOVL4c.488G>T (p.Cys163Phe)
6g.79921678C=CA1640824975ELOVL4c.488G= (p.Cys163=)
6g.79921678C>GCA364656548ELOVL4c.488G>C (p.Cys163Ser)
6g.79921678C>TCA3901528ELOVL4c.488G>A (p.Cys163Tyr)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921679A=CA1640824976ELOVL4c.487T= (p.Cys163=)
6g.79921679A>CCA364656549ELOVL4c.487T>G (p.Cys163Gly)
dbSNP
6g.79921679A>GCA364656550ELOVL4c.487T>C (p.Cys163Arg)
6g.79921679A>TCA3901529ELOVL4c.487T>A (p.Cys163Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921680G>ACA3901530ELOVL4c.486C>T (p.His162=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921680G>CCA364656551ELOVL4c.486C>G (p.His162Gln)
6g.79921680G=CA1640824977ELOVL4c.486C= (p.His162=)
6g.79921680G>TCA364656552ELOVL4c.486C>A (p.His162Gln)
6g.79921681T>ACA364656553ELOVL4c.485A>T (p.His162Leu)
6g.79921681T>CCA364656554ELOVL4c.485A>G (p.His162Arg)
6g.79921681T>GCA364656555ELOVL4c.485A>C (p.His162Pro)
6g.79921682G>ACA364656556ELOVL4c.484C>T (p.His162Tyr)
6g.79921682G>CCA364656558ELOVL4c.484C>G (p.His162Asp)
6g.79921682G>TCA364656557ELOVL4c.484C>A (p.His162Asn)
6g.79921683A>CCA364656559ELOVL4c.483T>G (p.His161Gln)
6g.79921683A>GCA451068514ELOVL4c.483T>C (p.His161=)
6g.79921683A>TCA364656560ELOVL4c.483T>A (p.His161Gln)
6g.79921684T>ACA364656561ELOVL4c.482A>T (p.His161Leu)
6g.79921684T>CCA364656562ELOVL4c.482A>G (p.His161Arg)
ClinVar
6g.79921684T>GCA364656563ELOVL4c.482A>C (p.His161Pro)
6g.79921685G>ACA364656564ELOVL4c.481C>T (p.His161Tyr)
6g.79921685G>CCA364656565ELOVL4c.481C>G (p.His161Asp)
6g.79921685G>TCA364656566ELOVL4c.481C>A (p.His161Asn)
6g.79921686A>CCA364656567ELOVL4c.480T>G (p.Tyr160Ter)
6g.79921686A>GCA451068515ELOVL4c.480T>C (p.Tyr160=)
6g.79921686A>TCA364656568ELOVL4c.480T>A (p.Tyr160Ter)
6g.79921687T>ACA364656571ELOVL4c.479A>T (p.Tyr160Phe)
6g.79921687T>CCA364656570ELOVL4c.479A>G (p.Tyr160Cys)
gnomAD v4
6g.79921687T>GCA364656569ELOVL4c.479A>C (p.Tyr160Ser)
6g.79921688A>CCA364656572ELOVL4c.478T>G (p.Tyr160Asp)
6g.79921688A>GCA364656573ELOVL4c.478T>C (p.Tyr160His)
6g.79921688A>TCA364656574ELOVL4c.478T>A (p.Tyr160Asn)
6g.79921689C>ACA451068516ELOVL4c.477G>T (p.Val159=)
6g.79921689C>GCA451068517ELOVL4c.477G>C (p.Val159=)
6g.79921689C>TCA451068518ELOVL4c.477G>A (p.Val159=)
6g.79921690A>CCA364656575ELOVL4c.476T>G (p.Val159Gly)
6g.79921690A>GCA364656576ELOVL4c.476T>C (p.Val159Ala)
6g.79921690A>TCA364656577ELOVL4c.476T>A (p.Val159Glu)
6g.79921691C>ACA364656578ELOVL4c.475G>T (p.Val159Leu)
dbSNP gnomAD v2 gnomAD v4
6g.79921691C=CA1640824978ELOVL4c.475G= (p.Val159=)
6g.79921691C>GCA364656579ELOVL4c.475G>C (p.Val159Leu)
6g.79921691C>TCA364656580ELOVL4c.475G>A (p.Val159Met)
ClinVar
6g.79921692A=CA1640824979ELOVL4c.474T= (p.His158=)
6g.79921692A>CCA364656581ELOVL4c.474T>G (p.His158Gln)
6g.79921692A>GCA3901531ELOVL4c.474T>C (p.His158=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921692A>TCA364656582ELOVL4c.474T>A (p.His158Gln)
gnomAD v4
6g.79921693T>ACA364656583ELOVL4c.473A>T (p.His158Leu)
6g.79921693T>CCA364656584ELOVL4c.473A>G (p.His158Arg)
ClinVar dbSNP
6g.79921693T>GCA3901532ELOVL4c.473A>C (p.His158Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921693T=CA1640824980ELOVL4c.473A= (p.His158=)
6g.79921694G>ACA364656587ELOVL4c.472C>T (p.His158Tyr)
6g.79921694G>CCA364656585ELOVL4c.472C>G (p.His158Asp)
6g.79921694G>TCA364656586ELOVL4c.472C>A (p.His158Asn)
6g.79921697_79921700delCA2771859720ELOVL4c.469_472del (p.Leu157MetfsTer30)
6g.79921695A>CCA451068519ELOVL4c.471T>G (p.Leu157=)
6g.79921695A>GCA451068520ELOVL4c.471T>C (p.Leu157=)
6g.79921695A>TCA451068521ELOVL4c.471T>A (p.Leu157=)
6g.79921696A>CCA364656588ELOVL4c.470T>G (p.Leu157Arg)
6g.79921696A>GCA364656589ELOVL4c.470T>C (p.Leu157Pro)
6g.79921696A>TCA364656590ELOVL4c.470T>A (p.Leu157His)
6g.79921697G>ACA364656591ELOVL4c.469C>T (p.Leu157Phe)
6g.79921697G>CCA364656592ELOVL4c.469C>G (p.Leu157Val)
6g.79921697G>TCA364656593ELOVL4c.469C>A (p.Leu157Ile)
6g.79921698G>ACA451068522ELOVL4c.468C>T (p.Phe156=)
6g.79921698G>CCA364656594ELOVL4c.468C>G (p.Phe156Leu)
6g.79921698G=CA1640824981ELOVL4c.468C= (p.Phe156=)
6g.79921698G>TCA3901533ELOVL4c.468C>A (p.Phe156Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.79921699A=CA1640824982ELOVL4c.467T= (p.Phe156=)
6g.79921699A>CCA364656595ELOVL4c.467T>G (p.Phe156Cys)
6g.79921699A>GCA233951ELOVL4c.467T>C (p.Phe156Ser)
ClinVar dbSNP gnomAD v4
6g.79921699A>TCA364656596ELOVL4c.467T>A (p.Phe156Tyr)
6g.79921700A>CCA364656599ELOVL4c.466T>G (p.Phe156Val)
gnomAD v4
6g.79921700A>GCA364656597ELOVL4c.466T>C (p.Phe156Leu)
6g.79921700A>TCA364656598ELOVL4c.466T>A (p.Phe156Ile)
6g.79921701A>CCA451068525ELOVL4c.465T>G (p.Ser155=)
6g.79921701A>GCA451068524ELOVL4c.465T>C (p.Ser155=)
6g.79921701A>TCA451068523ELOVL4c.465T>A (p.Ser155=)
6g.79921702G>ACA364656600ELOVL4c.464C>T (p.Ser155Phe)
COSMIC
6g.79921702G>CCA364656601ELOVL4c.464C>G (p.Ser155Cys)
6g.79921702G>TCA364656602ELOVL4c.464C>A (p.Ser155Tyr)
gnomAD v4
6g.79921703A>CCA364656603ELOVL4c.463T>G (p.Ser155Ala)
6g.79921703A>GCA364656604ELOVL4c.463T>C (p.Ser155Pro)
gnomAD v4
6g.79921703A>TCA364656605ELOVL4c.463T>A (p.Ser155Thr)
6g.79921704A>CCA451068526ELOVL4c.462T>G (p.Val154=)
6g.79921704A>GCA451068528ELOVL4c.462T>C (p.Val154=)
6g.79921704A>TCA451068527ELOVL4c.462T>A (p.Val154=)
6g.79921705A>CCA364656606ELOVL4c.461T>G (p.Val154Gly)
6g.79921705A>GCA364656607ELOVL4c.461T>C (p.Val154Ala)
6g.79921705A>TCA364656608ELOVL4c.461T>A (p.Val154Asp)
6g.79921706C>ACA364656609ELOVL4c.460G>T (p.Val154Phe)
6g.79921706C=CA1640824983ELOVL4c.460G= (p.Val154=)
6g.79921706C>GCA364656610ELOVL4c.460G>C (p.Val154Leu)
dbSNP
6g.79921706C>TCA364656611ELOVL4c.460G>A (p.Val154Ile)
6g.79921707T>ACA364656613ELOVL4c.459A>T (p.Gln153His)
6g.79921707T>CCA451068529ELOVL4c.459A>G (p.Gln153=)
gnomAD v4
6g.79921707T>GCA364656612ELOVL4c.459A>C (p.Gln153His)
6g.79921708T>ACA364656614ELOVL4c.458A>T (p.Gln153Leu)
6g.79921708T>CCA364656615ELOVL4c.458A>G (p.Gln153Arg)
gnomAD v4
6g.79921708T>GCA364656616ELOVL4c.458A>C (p.Gln153Pro)
6g.79921709G>ACA364656617ELOVL4c.457C>T (p.Gln153Ter)
6g.79921709G>CCA364656618ELOVL4c.457C>G (p.Gln153Glu)
6g.79921709G=CA1640824984ELOVL4c.457C= (p.Gln153=)
6g.79921709G>TCA364656619ELOVL4c.457C>A (p.Gln153Lys)
6g.79921709_79921710insCGTTTAATTGCATATATGTCA1640824985ELOVL4c.456_457insACATATATGCAATTAAACG (p.Gln153ThrfsTer28)
dbSNP
6g.79921710G>ACA451068530ELOVL4c.456C>T (p.Asn152=)
6g.79921710G>CCA364656620ELOVL4c.456C>G (p.Asn152Lys)
6g.79921710G>TCA364656621ELOVL4c.456C>A (p.Asn152Lys)
6g.79921711T>ACA364656622ELOVL4c.455A>T (p.Asn152Ile)
6g.79921711T>CCA364656623ELOVL4c.455A>G (p.Asn152Ser)
gnomAD v4
6g.79921711T>GCA364656624ELOVL4c.455A>C (p.Asn152Thr)
6g.79921712T>ACA364656625ELOVL4c.454A>T (p.Asn152Tyr)
6g.79921712T>CCA364656626ELOVL4c.454A>G (p.Asn152Asp)
6g.79921712T>GCA364656627ELOVL4c.454A>C (p.Asn152His)
gnomAD v4
6g.79921713G>ACA451068531ELOVL4c.453C>T (p.Asn151=)
dbSNP gnomAD v4
6g.79921713G>CCA364656629ELOVL4c.453C>G (p.Asn151Lys)
6g.79921713G=CA1640824986ELOVL4c.453C= (p.Asn151=)
6g.79921713G>TCA364656628ELOVL4c.453C>A (p.Asn151Lys)
6g.79921714T>ACA364656630ELOVL4c.452A>T (p.Asn151Ile)
6g.79921714T>CCA364656631ELOVL4c.452A>G (p.Asn151Ser)
gnomAD v4
6g.79921714T>GCA364656632ELOVL4c.452A>C (p.Asn151Thr)
6g.79921717_79921718delCA2679489857ELOVL4c.451_452del (p.Asn151GlnfsTer23)
gnomAD v4
6g.79921715T>ACA364656633ELOVL4c.451A>T (p.Asn151Tyr)
6g.79921715T>CCA364656634ELOVL4c.451A>G (p.Asn151Asp)
6g.79921715T>GCA364656635ELOVL4c.451A>C (p.Asn151His)
6g.79921716T>ACA364656636ELOVL4c.450A>T (p.Lys150Asn)
6g.79921716T>CCA451068532ELOVL4c.450A>G (p.Lys150=)
6g.79921716T>GCA364656637ELOVL4c.450A>C (p.Lys150Asn)
6g.79921717T>ACA364656638ELOVL4c.449A>T (p.Lys150Ile)
6g.79921717T>CCA364656639ELOVL4c.449A>G (p.Lys150Arg)
6g.79921717T>GCA364656640ELOVL4c.449A>C (p.Lys150Thr)
6g.79921718T>ACA364656641ELOVL4c.448A>T (p.Lys150Ter)
6g.79921718T>CCA364656642ELOVL4c.448A>G (p.Lys150Glu)
6g.79921718T>GCA364656643ELOVL4c.448A>C (p.Lys150Gln)
6g.79921719C>ACA364656645ELOVL4c.447G>T (p.Lys149Asn)
6g.79921719C>GCA364656644ELOVL4c.447G>C (p.Lys149Asn)
6g.79921719C>TCA451068533ELOVL4c.447G>A (p.Lys149=)
gnomAD v4
6g.79921720T>ACA364656646ELOVL4c.446A>T (p.Lys149Met)
6g.79921720T>CCA364656648ELOVL4c.446A>G (p.Lys149Arg)
ClinVar dbSNP gnomAD v4 COSMIC
6g.79921720T>GCA364656647ELOVL4c.446A>C (p.Lys149Thr)
6g.79921721T>ACA364656649ELOVL4c.445A>T (p.Lys149Ter)
6g.79921721T>CCA364656651ELOVL4c.445A>G (p.Lys149Glu)
6g.79921721T>GCA364656650ELOVL4c.445A>C (p.Lys149Gln)
6g.79921722T>ACA364656652ELOVL4c.444A>T (p.Arg148Ser)
6g.79921722T>CCA451068534ELOVL4c.444A>G (p.Arg148=)
COSMIC
6g.79921722T>GCA364656653ELOVL4c.444A>C (p.Arg148Ser)
6g.79921723C>ACA364656654ELOVL4c.443G>T (p.Arg148Ile)
ClinVar dbSNP
6g.79921723C=CA1640824987ELOVL4c.443G= (p.Arg148=)
6g.79921723C>GCA364656655ELOVL4c.443G>C (p.Arg148Thr)
6g.79921723C>TCA364656656ELOVL4c.443G>A (p.Arg148Lys)
6g.79921724T>ACA364656657ELOVL4c.442A>T (p.Arg148Ter)
6g.79921724T>CCA364656658ELOVL4c.442A>G (p.Arg148Gly)
6g.79921724T>GCA451068535ELOVL4c.442A>C (p.Arg148=)
6g.79921725C>ACA451068536ELOVL4c.441G>T (p.Leu147=)
6g.79921725C>GCA451068538ELOVL4c.441G>C (p.Leu147=)
6g.79921725C>TCA451068537ELOVL4c.441G>A (p.Leu147=)
gnomAD v4
6g.79921726A>CCA364656659ELOVL4c.440T>G (p.Leu147Arg)
6g.79921726A>GCA364656660ELOVL4c.440T>C (p.Leu147Pro)
6g.79921726A>TCA364656661ELOVL4c.440T>A (p.Leu147Gln)
6g.79921727G>ACA451068539ELOVL4c.439C>T (p.Leu147=)
6g.79921727G>CCA364656662ELOVL4c.439C>G (p.Leu147Val)
6g.79921727G=CA1640824988ELOVL4c.439C= (p.Leu147=)
6g.79921727G>TCA364656663ELOVL4c.439C>A (p.Leu147Met)
dbSNP
6g.79921728A=CA1640824989ELOVL4c.438T= (p.Ile146=)
6g.79921728A>CCA364656664ELOVL4c.438T>G (p.Ile146Met)
6g.79921728A>GCA451068540ELOVL4c.438T>C (p.Ile146=)
dbSNP gnomAD v4
6g.79921728A>TCA451068541ELOVL4c.438T>A (p.Ile146=)
6g.79921729A>CCA364656667ELOVL4c.437T>G (p.Ile146Ser)
6g.79921729A>GCA364656665ELOVL4c.437T>C (p.Ile146Thr)
6g.79921729A>TCA364656666ELOVL4c.437T>A (p.Ile146Asn)
6g.79921730T>ACA364656668ELOVL4c.436A>T (p.Ile146Phe)
6g.79921730T>CCA364656669ELOVL4c.436A>G (p.Ile146Val)
6g.79921730T>GCA364656670ELOVL4c.436A>C (p.Ile146Leu)
6g.79921730dupCA2573141259ELOVL4c.436dup (p.Ile146AsnfsTer29)
ClinVar dbSNP
6g.79921730_79921731delinsTACA1640824990ELOVL4c.435_436delinsTA (p.Phe145=)
6g.79921731A>CCA364656671ELOVL4c.435T>G (p.Phe145Leu)
6g.79921731A>GCA451068542ELOVL4c.435T>C (p.Phe145=)
6g.79921731A>TCA364656672ELOVL4c.435T>A (p.Phe145Leu)
6g.79921736dupCA1640824991ELOVL4c.435dup (p.Ile146TyrfsTer29)
ClinVar dbSNP
6g.79921736delCA3901534ELOVL4c.435del (p.Phe145LeufsTer3)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921732A>CCA364656673ELOVL4c.434T>G (p.Phe145Cys)
6g.79921732A>GCA364656674ELOVL4c.434T>C (p.Phe145Ser)
6g.79921732A>TCA364656675ELOVL4c.434T>A (p.Phe145Tyr)
6g.79921733A>CCA364656676ELOVL4c.433T>G (p.Phe145Val)
6g.79921733A>GCA364656677ELOVL4c.433T>C (p.Phe145Leu)
6g.79921733A>TCA364656678ELOVL4c.433T>A (p.Phe145Ile)
6g.79921734A>CCA364656680ELOVL4c.432T>G (p.Phe144Leu)
6g.79921734A>GCA451068543ELOVL4c.432T>C (p.Phe144=)
6g.79921734A>TCA364656679ELOVL4c.432T>A (p.Phe144Leu)
6g.79921735A=CA1640824992ELOVL4c.431T= (p.Phe144=)
6g.79921735A>CCA142271132ELOVL4c.431T>G (p.Phe144Cys)
dbSNP gnomAD v4
6g.79921735A>GCA364656681ELOVL4c.431T>C (p.Phe144Ser)
6g.79921735A>TCA364656682ELOVL4c.431T>A (p.Phe144Tyr)
6g.79921736A>CCA364656683ELOVL4c.430T>G (p.Phe144Val)
6g.79921736A>GCA364656684ELOVL4c.430T>C (p.Phe144Leu)
6g.79921736A>TCA364656685ELOVL4c.430T>A (p.Phe144Ile)
6g.79921737C>ACA451068544ELOVL4c.429G>T (p.Val143=)
6g.79921737C=CA1640824993ELOVL4c.429G= (p.Val143=)
6g.79921737C>GCA451068545ELOVL4c.429G>C (p.Val143=)
dbSNP gnomAD v2 gnomAD v4
6g.79921737C>TCA142271133ELOVL4c.429G>A (p.Val143=)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.79921738A=CA1640824994ELOVL4c.428T= (p.Val143=)
6g.79921738A>CCA364656686ELOVL4c.428T>G (p.Val143Gly)
6g.79921738A>GCA364656687ELOVL4c.428T>C (p.Val143Ala)
ClinVar dbSNP gnomAD v3 gnomAD v4
6g.79921738A>TCA364656688ELOVL4c.428T>A (p.Val143Glu)
6g.79921739C>ACA364656689ELOVL4c.427G>T (p.Val143Leu)
dbSNP gnomAD v2 gnomAD v4 COSMIC
6g.79921739C=CA1640824996ELOVL4c.427G= (p.Val143=)
6g.79921739C>GCA364656690ELOVL4c.427G>C (p.Val143Leu)
6g.79921739C>TCA364656691ELOVL4c.427G>A (p.Val143Met)
dbSNP
6g.79921739_79921741delinsCTGCA1640824995ELOVL4c.425_427delinsCAG (p.Thr142=)
6g.79921740T>ACA451068547ELOVL4c.426A>T (p.Thr142=)
6g.79921740T>CCA3901535ELOVL4c.426A>G (p.Thr142=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921740T>GCA451068546ELOVL4c.426A>C (p.Thr142=)
6g.79921740T=CA1640824997ELOVL4c.426A= (p.Thr142=)
6g.79921743_79921744delCA568600871ELOVL4c.425_426del (p.Thr142SerfsTer?)
ClinVar dbSNP gnomAD v2 gnomAD v4
6g.79921741G>ACA364656694ELOVL4c.425C>T (p.Thr142Ile)
6g.79921741G>CCA364656693ELOVL4c.425C>G (p.Thr142Arg)
6g.79921741G>TCA364656692ELOVL4c.425C>A (p.Thr142Lys)
6g.79921742T>ACA364656695ELOVL4c.424A>T (p.Thr142Ser)
6g.79921742T>CCA364656696ELOVL4c.424A>G (p.Thr142Ala)
6g.79921742T>GCA364656697ELOVL4c.424A>C (p.Thr142Pro)
6g.79921743G>ACA451068548ELOVL4c.423C>T (p.Asp141=)
dbSNP
6g.79921743G>CCA364656698ELOVL4c.423C>G (p.Asp141Glu)
6g.79921743G=CA1640824998ELOVL4c.423C= (p.Asp141=)
6g.79921743G>TCA364656699ELOVL4c.423C>A (p.Asp141Glu)
6g.79921744T>ACA364656700ELOVL4c.422A>T (p.Asp141Val)
6g.79921744T>CCA364656701ELOVL4c.422A>G (p.Asp141Gly)
6g.79921744T>GCA364656702ELOVL4c.422A>C (p.Asp141Ala)
6g.79921745C>ACA364656703ELOVL4c.421G>T (p.Asp141Tyr)
6g.79921745C>GCA364656704ELOVL4c.421G>C (p.Asp141His)
6g.79921745C>TCA364656705ELOVL4c.421G>A (p.Asp141Asn)
6g.79921746C>ACA364656706ELOVL4c.420G>T (p.Leu140Phe)
6g.79921746C=CA1640824999ELOVL4c.420G= (p.Leu140=)
6g.79921746C>GCA364656707ELOVL4c.420G>C (p.Leu140Phe)
6g.79921746C>TCA3901536ELOVL4c.420G>A (p.Leu140=)
dbSNP ExAC gnomAD v2
6g.79921747A>CCA364656709ELOVL4c.419T>G (p.Leu140Trp)
6g.79921747A>GCA364656710ELOVL4c.419T>C (p.Leu140Ser)
6g.79921747A>TCA364656708ELOVL4c.419T>A (p.Leu140Ter)
6g.79921748A>CCA364656711ELOVL4c.418T>G (p.Leu140Val)
6g.79921748A>GCA451068549ELOVL4c.418T>C (p.Leu140=)
6g.79921748A>TCA364656712ELOVL4c.418T>A (p.Leu140Met)
6g.79921749A>CCA364656713ELOVL4c.417T>G (p.Tyr139Ter)
6g.79921749A>GCA451068550ELOVL4c.417T>C (p.Tyr139=)
6g.79921749A>TCA364656714ELOVL4c.417T>A (p.Tyr139Ter)
6g.79921750T>ACA364656715ELOVL4c.416A>T (p.Tyr139Phe)
6g.79921750T>CCA364656716ELOVL4c.416A>G (p.Tyr139Cys)
6g.79921750T>GCA364656717ELOVL4c.416A>C (p.Tyr139Ser)
6g.79921751A>CCA364656718ELOVL4c.415T>G (p.Tyr139Asp)
6g.79921751A>GCA364656719ELOVL4c.415T>C (p.Tyr139His)
6g.79921751A>TCA364656720ELOVL4c.415T>A (p.Tyr139Asn)
6g.79921752C>ACA364656721ELOVL4c.414G>T (p.Glu138Asp)
ClinVar
6g.79921752C>GCA364656722ELOVL4c.414G>C (p.Glu138Asp)
6g.79921752C>TCA451068551ELOVL4c.414G>A (p.Glu138=)
6g.79921752_79921754delCA2679489860ELOVL4c.412_414del (p.Glu138del)
gnomAD v4
6g.79921753T>ACA364656723ELOVL4c.413A>T (p.Glu138Val)
6g.79921753T>CCA364656724ELOVL4c.413A>G (p.Glu138Gly)
6g.79921753T>GCA364656725ELOVL4c.413A>C (p.Glu138Ala)
6g.79921753_79921755delCA2771859721ELOVL4c.411_413del (p.Glu138del)
6g.79921754C>ACA364656728ELOVL4c.412G>T (p.Glu138Ter)
6g.79921754C>GCA364656726ELOVL4c.412G>C (p.Glu138Gln)
6g.79921754C>TCA364656727ELOVL4c.412G>A (p.Glu138Lys)
6g.79921755A>CCA451068552ELOVL4c.411T>G (p.Val137=)
6g.79921755A>GCA451068553ELOVL4c.411T>C (p.Val137=)
6g.79921755A>TCA451068554ELOVL4c.411T>A (p.Val137=)
6g.79921756delCA2771859722ELOVL4c.411del (p.Glu138SerfsTer10)
6g.79921756A>CCA364656729ELOVL4c.410T>G (p.Val137Gly)
6g.79921756A>GCA364656730ELOVL4c.410T>C (p.Val137Ala)
6g.79921756A>TCA364656731ELOVL4c.410T>A (p.Val137Asp)
6g.79921757C>ACA364656732ELOVL4c.409G>T (p.Val137Phe)
6g.79921757C>GCA364656733ELOVL4c.409G>C (p.Val137Leu)
6g.79921757C>TCA364656734ELOVL4c.409G>A (p.Val137Ile)
ClinVar dbSNP gnomAD v4
6g.79921758T>ACA451068555ELOVL4c.408A>T (p.Gly136=)
6g.79921758T>CCA451068556ELOVL4c.408A>G (p.Gly136=)
gnomAD v4
6g.79921758T>GCA451068557ELOVL4c.408A>C (p.Gly136=)
6g.79921758_79921775delCA2771859723ELOVL4c.391_408del (p.Tyr131_Gly136del)
6g.79921759C>ACA364656735ELOVL4c.407G>T (p.Gly136Val)
6g.79921759C>GCA364656736ELOVL4c.407G>C (p.Gly136Ala)
6g.79921759C>TCA364656737ELOVL4c.407G>A (p.Gly136Glu)
6g.79921760C>ACA364656738ELOVL4c.406G>T (p.Gly136Ter)
6g.79921760C>GCA364656739ELOVL4c.406G>C (p.Gly136Arg)
6g.79921760C>TCA364656740ELOVL4c.406G>A (p.Gly136Arg)
6g.79921761T>ACA364656741ELOVL4c.405A>T (p.Lys135Asn)
6g.79921761T>CCA451068558ELOVL4c.405A>G (p.Lys135=)
ClinVar
6g.79921761T>GCA364656742ELOVL4c.405A>C (p.Lys135Asn)
6g.79921762T>ACA364656743ELOVL4c.404A>T (p.Lys135Ile)
6g.79921762T>CCA364656744ELOVL4c.404A>G (p.Lys135Arg)
6g.79921762T>GCA364656745ELOVL4c.404A>C (p.Lys135Thr)
6g.79921763T>ACA364656746ELOVL4c.403A>T (p.Lys135Ter)
6g.79921763T>CCA364656747ELOVL4c.403A>G (p.Lys135Glu)
6g.79921763T>GCA364656748ELOVL4c.403A>C (p.Lys135Gln)
6g.79921764A>CCA451068559ELOVL4c.402T>G (p.Ser134=)
6g.79921764A>GCA451068561ELOVL4c.402T>C (p.Ser134=)
6g.79921764A>TCA451068560ELOVL4c.402T>A (p.Ser134=)

Number of alleles fetched