Chr Mutation (hg38) CAid Gene Transcript Linkouts
6g.79921614A=CA1640824954ELOVL4c.541+11T= (n.541+11T=)
6g.79921614A>GCA2771859718ELOVL4c.541+11T>C (n.541+11T>C)
6g.79921615A=CA1640824955ELOVL4c.541+10T= (n.541+10T=)
6g.79921615A>TCA1090954888ELOVL4c.541+10T>A (n.541+10T>A)
dbSNP gnomAD v3 gnomAD v4
6g.79921615_79921616insTACA142271126ELOVL4c.541+10_541+11insAT (n.541+10_541+11insAT)
dbSNP
6g.79921616A=CA1640824956ELOVL4c.541+9T= (n.541+9T=)
6g.79921616A>TCA142271127ELOVL4c.541+9T>A (n.541+9T>A)
dbSNP
6g.79921618T>GCA3901521ELOVL4c.541+7A>C (n.541+7A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921618T=CA1640824957ELOVL4c.541+7A= (n.541+7A=)
6g.79921619G=CA1640824958ELOVL4c.541+6C= (n.541+6C=)
6g.79921619G>TCA3901522ELOVL4c.541+6C>A (n.541+6C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921620C>TCA2578677066ELOVL4c.541+5G>A (n.541+5G>A)
ClinVar
6g.79921623A>CCA364656419ELOVL4c.541+2T>G (n.541+2T>G)
gnomAD v4
6g.79921623A>GCA364656420ELOVL4c.541+2T>C (n.541+2T>C)
6g.79921623A>TCA364656421ELOVL4c.541+2T>A (n.541+2T>A)
6g.79921624C>ACA364656422ELOVL4c.541+1G>T (n.541+1G>T)
6g.79921624C>GCA364656423ELOVL4c.541+1G>C (n.541+1G>C)
6g.79921624C>TCA364656424ELOVL4c.541+1G>A (n.541+1G>A)
6g.79921625C>ACA364656427ELOVL4c.541G>T (p.Ala181Ser)
6g.79921625C>GCA364656425ELOVL4c.541G>C (p.Ala181Pro)
6g.79921625C>TCA364656426ELOVL4c.541G>A (p.Ala181Thr)
6g.79921626T>ACA364656428ELOVL4c.540A>T (p.Gln180His)
6g.79921626T>CCA3901523ELOVL4c.540A>G (p.Gln180=)
dbSNP ExAC gnomAD v2 gnomAD v4
6g.79921626T>GCA364656429ELOVL4c.540A>C (p.Gln180His)
6g.79921626T=CA1640824959ELOVL4c.540A= (p.Gln180=)
6g.79921627T>ACA364656430ELOVL4c.539A>T (p.Gln180Leu)
6g.79921627T>CCA364656431ELOVL4c.539A>G (p.Gln180Arg)
6g.79921627T>GCA364656432ELOVL4c.539A>C (p.Gln180Pro)
ClinVar dbSNP
6g.79921628_79921629delCA2531281113ELOVL4c.538_539del (p.Gln180SerfsTer?)
6g.79921628G>ACA364656433ELOVL4c.538C>T (p.Gln180Ter)
6g.79921628G>CCA364656434ELOVL4c.538C>G (p.Gln180Glu)
6g.79921628G>TCA364656435ELOVL4c.538C>A (p.Gln180Lys)
6g.79921629T>ACA451068487ELOVL4c.537A>T (p.Gly179=)
6g.79921629T>CCA3901524ELOVL4c.537A>G (p.Gly179=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
6g.79921629T>GCA451068488ELOVL4c.537A>C (p.Gly179=)
6g.79921629T=CA1640824960ELOVL4c.537A= (p.Gly179=)
6g.79921630C>ACA364656436ELOVL4c.536G>T (p.Gly179Val)
6g.79921630C>GCA364656437ELOVL4c.536G>C (p.Gly179Ala)
6g.79921630C>TCA364656438ELOVL4c.536G>A (p.Gly179Glu)
6g.79921631C>ACA364656441ELOVL4c.535G>T (p.Gly179Ter)
gnomAD v4
6g.79921631C>GCA364656439ELOVL4c.535G>C (p.Gly179Arg)
6g.79921631C>TCA364656440ELOVL4c.535G>A (p.Gly179Arg)
6g.79921632T>ACA451068490ELOVL4c.534A>T (p.Gly178=)
6g.79921632T>CCA451068491ELOVL4c.534A>G (p.Gly178=)
6g.79921632T>GCA451068492ELOVL4c.534A>C (p.Gly178=)
6g.79921633C>ACA364656442ELOVL4c.533G>T (p.Gly178Val)
6g.79921633C>GCA364656443ELOVL4c.533G>C (p.Gly178Ala)
6g.79921633C>TCA364656444ELOVL4c.533G>A (p.Gly178Glu)
6g.79921634C>ACA364656445ELOVL4c.532G>T (p.Gly178Ter)
gnomAD v4
6g.79921634C>GCA364656446ELOVL4c.532G>C (p.Gly178Arg)
6g.79921634C>TCA364656447ELOVL4c.532G>A (p.Gly178Arg)
6g.79921635T>ACA451068493ELOVL4c.531A>T (p.Ala177=)
6g.79921635T>CCA451068495ELOVL4c.531A>G (p.Ala177=)
6g.79921635T>GCA451068494ELOVL4c.531A>C (p.Ala177=)
6g.79921636G>ACA364656450ELOVL4c.530C>T (p.Ala177Val)
dbSNP gnomAD v2 gnomAD v4
6g.79921636G>CCA364656449ELOVL4c.530C>G (p.Ala177Gly)
6g.79921636G=CA1640824961ELOVL4c.530C= (p.Ala177=)
6g.79921636G>TCA364656448ELOVL4c.530C>A (p.Ala177Glu)
6g.79921637C>ACA364656451ELOVL4c.529G>T (p.Ala177Ser)
gnomAD v4
6g.79921637C>GCA364656452ELOVL4c.529G>C (p.Ala177Pro)
6g.79921637C>TCA364656453ELOVL4c.529G>A (p.Ala177Thr)
COSMIC
6g.79921638A>CCA451068497ELOVL4c.528T>G (p.Val176=)
6g.79921638A>GCA451068498ELOVL4c.528T>C (p.Val176=)
6g.79921638A>TCA451068499ELOVL4c.528T>A (p.Val176=)
6g.79921639A>CCA364656454ELOVL4c.527T>G (p.Val176Gly)
6g.79921639A>GCA364656455ELOVL4c.527T>C (p.Val176Ala)
6g.79921639A>TCA364656456ELOVL4c.527T>A (p.Val176Asp)
6g.79921640C>ACA364656457ELOVL4c.526G>T (p.Val176Phe)
6g.79921640C>GCA364656459ELOVL4c.526G>C (p.Val176Leu)
COSMIC
6g.79921640C>TCA364656458ELOVL4c.526G>A (p.Val176Ile)
6g.79921641C>ACA364656460ELOVL4c.525G>T (p.Trp175Cys)
gnomAD v4
6g.79921641C>GCA364656461ELOVL4c.525G>C (p.Trp175Cys)
6g.79921641C>TCA364656462ELOVL4c.525G>A (p.Trp175Ter)
6g.79921642C>ACA364656463ELOVL4c.524G>T (p.Trp175Leu)
6g.79921642C>GCA364656464ELOVL4c.524G>C (p.Trp175Ser)
6g.79921642C>TCA364656465ELOVL4c.524G>A (p.Trp175Ter)
6g.79921643A=CA1640824962ELOVL4c.523T= (p.Trp175=)
6g.79921643A>CCA364656466ELOVL4c.523T>G (p.Trp175Gly)
6g.79921643A>GCA3901525ELOVL4c.523T>C (p.Trp175Arg)
dbSNP ExAC gnomAD v2
6g.79921643A>TCA364656467ELOVL4c.523T>A (p.Trp175Arg)
6g.79921644C>ACA364656468ELOVL4c.522G>T (p.Lys174Asn)
6g.79921644C=CA1640824963ELOVL4c.522G= (p.Lys174=)
6g.79921644C>GCA142271128ELOVL4c.522G>C (p.Lys174Asn)
dbSNP
6g.79921644C>TCA451068500ELOVL4c.522G>A (p.Lys174=)
gnomAD v4
6g.79921645T>ACA364656469ELOVL4c.521A>T (p.Lys174Met)
6g.79921645T>CCA364656471ELOVL4c.521A>G (p.Lys174Arg)
6g.79921645T>GCA364656470ELOVL4c.521A>C (p.Lys174Thr)
6g.79921646T>ACA364656472ELOVL4c.520A>T (p.Lys174Ter)
6g.79921646T>CCA364656474ELOVL4c.520A>G (p.Lys174Glu)
6g.79921646T>GCA364656473ELOVL4c.520A>C (p.Lys174Gln)
6g.79921647A>CCA364656475ELOVL4c.519T>G (p.Ile173Met)
6g.79921647A>GCA451068501ELOVL4c.519T>C (p.Ile173=)
6g.79921647A>TCA451068502ELOVL4c.519T>A (p.Ile173=)
6g.79921648A>CCA364656476ELOVL4c.518T>G (p.Ile173Ser)
6g.79921648A>GCA364656477ELOVL4c.518T>C (p.Ile173Thr)
6g.79921648A>TCA364656478ELOVL4c.518T>A (p.Ile173Asn)
6g.79921649T>ACA364656479ELOVL4c.517A>T (p.Ile173Phe)
6g.79921649T>CCA364656480ELOVL4c.517A>G (p.Ile173Val)
6g.79921649T>GCA364656481ELOVL4c.517A>C (p.Ile173Leu)
6g.79921650T>ACA451068503ELOVL4c.516A>T (p.Gly172=)
6g.79921650T>CCA451068504ELOVL4c.516A>G (p.Gly172=)
6g.79921650T>GCA451068505ELOVL4c.516A>C (p.Gly172=)
6g.79921651C>ACA364656482ELOVL4c.515G>T (p.Gly172Val)
COSMIC
6g.79921651C>GCA364656483ELOVL4c.515G>C (p.Gly172Ala)
6g.79921651C>TCA364656484ELOVL4c.515G>A (p.Gly172Glu)
6g.79921652delCA2679489853ELOVL4c.515del (p.Gly172GlufsTer16)
gnomAD v4
6g.79921652C>ACA364656485ELOVL4c.514G>T (p.Gly172Ter)
6g.79921652C>GCA364656486ELOVL4c.514G>C (p.Gly172Arg)
6g.79921652C>TCA364656487ELOVL4c.514G>A (p.Gly172Arg)
6g.79921653A>CCA364656488ELOVL4c.513T>G (p.Ile171Met)
6g.79921653A>GCA451068506ELOVL4c.513T>C (p.Ile171=)
6g.79921653A>TCA451068507ELOVL4c.513T>A (p.Ile171=)
6g.79921654A=CA1640824964ELOVL4c.512T= (p.Ile171=)
6g.79921654A>CCA364656489ELOVL4c.512T>G (p.Ile171Ser)
6g.79921654A>GCA364656490ELOVL4c.512T>C (p.Ile171Thr)
ClinVar dbSNP
6g.79921654A>TCA364656491ELOVL4c.512T>A (p.Ile171Asn)
6g.79921655T>ACA364656492ELOVL4c.511A>T (p.Ile171Phe)
6g.79921655T>CCA364656493ELOVL4c.511A>G (p.Ile171Val)
gnomAD v4
6g.79921655T>GCA364656494ELOVL4c.511A>C (p.Ile171Leu)
6g.79921656C>ACA364656495ELOVL4c.510G>T (p.Trp170Cys)
6g.79921656C>GCA364656496ELOVL4c.510G>C (p.Trp170Cys)
COSMIC
6g.79921656C>TCA364656497ELOVL4c.510G>A (p.Trp170Ter)
6g.79921657C>ACA364656498ELOVL4c.509G>T (p.Trp170Leu)
6g.79921657C=CA1640824965ELOVL4c.509G= (p.Trp170=)
6g.79921657C>GCA364656499ELOVL4c.509G>C (p.Trp170Ser)
6g.79921657C>TCA364656500ELOVL4c.509G>A (p.Trp170Ter)
6g.79921657_79921658insTTAATTCA568600870ELOVL4c.508_509insAATTAA (p.Trp170Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
6g.79921658A>CCA364656503ELOVL4c.508T>G (p.Trp170Gly)
6g.79921658A>GCA364656502ELOVL4c.508T>C (p.Trp170Arg)
6g.79921658A>TCA364656501ELOVL4c.508T>A (p.Trp170Arg)
6g.79921659C>ACA364656504ELOVL4c.507G>T (p.Trp169Cys)
COSMIC
6g.79921659C>GCA364656505ELOVL4c.507G>C (p.Trp169Cys)
6g.79921659C>TCA364656506ELOVL4c.507G>A (p.Trp169Ter)
6g.79921660C>ACA364656507ELOVL4c.506G>T (p.Trp169Leu)
6g.79921660C=CA1640824966ELOVL4c.506G= (p.Trp169=)
6g.79921660C>GCA364656508ELOVL4c.506G>C (p.Trp169Ser)
6g.79921660C>TCA16605161ELOVL4c.506G>A (p.Trp169Ter)
ClinVar dbSNP
6g.79921661A>CCA364656511ELOVL4c.505T>G (p.Trp169Gly)
6g.79921661A>GCA364656509ELOVL4c.505T>C (p.Trp169Arg)
6g.79921661A>TCA364656510ELOVL4c.505T>A (p.Trp169Arg)
6g.79921662C>ACA364656512ELOVL4c.504G>T (p.Leu168Phe)
6g.79921662C=CA1640824967ELOVL4c.504G= (p.Leu168=)
6g.79921662C>GCA170078ELOVL4c.504G>C (p.Leu168Phe)
ClinVar dbSNP
6g.79921662C>TCA142271129ELOVL4c.504G>A (p.Leu168=)
dbSNP gnomAD v4
6g.79921663A>CCA364656513ELOVL4c.503T>G (p.Leu168Trp)
6g.79921663A>GCA364656514ELOVL4c.503T>C (p.Leu168Ser)
6g.79921663A>TCA364656515ELOVL4c.503T>A (p.Leu168Ter)
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

Number of alleles fetched