Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.855622delCA2587805314ELANEc.425del (p.Gly142AspfsTer?)
gnomAD v4
19g.855621G>ACA402917983ELANEc.424G>A (p.Gly142Arg)
19g.855621G>CCA402917984ELANEc.424G>C (p.Gly142Arg)
19g.855621G>TCA402917986ELANEc.424G>T (p.Gly142Ter)
gnomAD v4
19g.855622G>ACA402917988ELANEc.425G>A (p.Gly142Glu)
19g.855622G>CCA402917992ELANEc.425G>C (p.Gly142Ala)
19g.855622G>TCA402917990ELANEc.425G>T (p.Gly142Val)
gnomAD v4
19g.855623A=CA2317361374ELANEc.426A= (p.Gly142=)
19g.855623A>CCA504881865ELANEc.426A>C (p.Gly142=)
19g.855623A>GCA303944760ELANEc.426A>G (p.Gly142=)
dbSNP
19g.855623A>TCA504881864ELANEc.426A>T (p.Gly142=)
19g.855624C>ACA402917994ELANEc.427C>A (p.Arg143Ser)
19g.855624C=CA2317361375ELANEc.427C= (p.Arg143=)
19g.855624C>GCA402917996ELANEc.427C>G (p.Arg143Gly)
19g.855624C>TCA9026055ELANEc.427C>T (p.Arg143Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855628_855630delCA2587805315ELANEc.431_433del (p.Arg144del)
gnomAD v4
19g.855625G>ACA9026056ELANEc.428G>A (p.Arg143His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855625G>CCA402918003ELANEc.428G>C (p.Arg143Pro)
19g.855625G=CA2317361376ELANEc.428G= (p.Arg143=)
19g.855625G>TCA9026057ELANEc.428G>T (p.Arg143Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855626C>ACA504881866ELANEc.429C>A (p.Arg143=)
dbSNP gnomAD v4
19g.855626C=CA2317361377ELANEc.429C= (p.Arg143=)
19g.855626C>GCA504881868ELANEc.429C>G (p.Arg143=)
19g.855626C>TCA504881870ELANEc.429C>T (p.Arg143=)
dbSNP gnomAD v2 gnomAD v4
19g.855627C>ACA402918006ELANEc.430C>A (p.Arg144Ser)
19g.855627C=CA2317361378ELANEc.430C= (p.Arg144=)
19g.855627C>GCA402918008ELANEc.430C>G (p.Arg144Gly)
19g.855627C>TCA9026058ELANEc.430C>T (p.Arg144Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855628G>ACA9026059ELANEc.431G>A (p.Arg144His)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855628G>CCA402918014ELANEc.431G>C (p.Arg144Pro)
19g.855628G=CA2317361379ELANEc.431G= (p.Arg144=)
19g.855628G>TCA402918011ELANEc.431G>T (p.Arg144Leu)
gnomAD v4
19g.855634_855654dupCA2573155744ELANEc.437_457dup (p.Leu152_Ala153insGlyAsnGlyValGlnCysLeu)
ClinVar dbSNP
19g.855629C>ACA504881872ELANEc.432C>A (p.Arg144=)
19g.855629C=CA2317361380ELANEc.432C= (p.Arg144=)
19g.855629C>GCA504881873ELANEc.432C>G (p.Arg144=)
19g.855629C>TCA504881874ELANEc.432C>T (p.Arg144=)
dbSNP gnomAD v3 gnomAD v4
19g.855630C>ACA402918015ELANEc.433C>A (p.Leu145Met)
19g.855630C=CA2317361381ELANEc.433C= (p.Leu145=)
19g.855630C>GCA402918016ELANEc.433C>G (p.Leu145Val)
gnomAD v4
19g.855630C>TCA9026060ELANEc.433C>T (p.Leu145=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855631T>ACA402918018ELANEc.434T>A (p.Leu145Gln)
19g.855631T>CCA402918021ELANEc.434T>C (p.Leu145Pro)
19g.855631T>GCA402918023ELANEc.434T>G (p.Leu145Arg)
19g.855632G>ACA504881878ELANEc.435G>A (p.Leu145=)
19g.855632G>CCA303944780ELANEc.435G>C (p.Leu145=)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855632G=CA2317361382ELANEc.435G= (p.Leu145=)
19g.855632G>TCA504881879ELANEc.435G>T (p.Leu145=)
gnomAD v4
19g.855634delCA2587805316ELANEc.437del (p.Gly146AlafsTer29)
gnomAD v4
19g.855633G>ACA402918029ELANEc.436G>A (p.Gly146Ser)
19g.855633G>CCA402918025ELANEc.436G>C (p.Gly146Arg)
19g.855633G>TCA402918028ELANEc.436G>T (p.Gly146Cys)
gnomAD v4
19g.855634G>ACA10583961ELANEc.437G>A (p.Gly146Asp)
ClinVar dbSNP gnomAD v4
19g.855634G>CCA402918033ELANEc.437G>C (p.Gly146Ala)
19g.855634G=CA2317361383ELANEc.437G= (p.Gly146=)
19g.855634G>TCA402918035ELANEc.437G>T (p.Gly146Val)
19g.855635C>ACA9026062ELANEc.438C>A (p.Gly146=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855635C=CA2317361384ELANEc.438C= (p.Gly146=)
19g.855635C>GCA504881882ELANEc.438C>G (p.Gly146=)
19g.855635C>TCA9026061ELANEc.438C>T (p.Gly146=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855636A>CCA402918042ELANEc.439A>C (p.Asn147His)
19g.855636A>GCA402918047ELANEc.439A>G (p.Asn147Asp)
19g.855636A>TCA402918045ELANEc.439A>T (p.Asn147Tyr)
19g.855637A=CA2317361385ELANEc.440A= (p.Asn147=)
19g.855637A>CCA402918049ELANEc.440A>C (p.Asn147Thr)
19g.855637A>GCA402918052ELANEc.440A>G (p.Asn147Ser)
dbSNP gnomAD v2 gnomAD v4
19g.855637A>TCA402918054ELANEc.440A>T (p.Asn147Ile)
dbSNP
19g.855638C>ACA402918058ELANEc.441C>A (p.Asn147Lys)
dbSNP gnomAD v2 gnomAD v4
19g.855638C=CA2317361386ELANEc.441C= (p.Asn147=)
19g.855638C>GCA402918061ELANEc.441C>G (p.Asn147Lys)
ClinVar
19g.855638C>TCA9026063ELANEc.441C>T (p.Asn147=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855639G>ACA9026064ELANEc.442G>A (p.Gly148Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855639G>CCA402918066ELANEc.442G>C (p.Gly148Arg)
gnomAD v4
19g.855639G=CA2317361387ELANEc.442G= (p.Gly148=)
19g.855639G>TCA402918069ELANEc.442G>T (p.Gly148Trp)
dbSNP gnomAD v4
19g.855640G>ACA402918072ELANEc.443G>A (p.Gly148Glu)
ClinVar dbSNP gnomAD v2
19g.855640G>CCA402918074ELANEc.443G>C (p.Gly148Ala)
19g.855640G=CA2317361388ELANEc.443G= (p.Gly148=)
19g.855640G>TCA402918077ELANEc.443G>T (p.Gly148Val)
gnomAD v4
19g.855641G>ACA504881887ELANEc.444G>A (p.Gly148=)
gnomAD v4
19g.855641G>CCA504881888ELANEc.444G>C (p.Gly148=)
19g.855641G>TCA504881889ELANEc.444G>T (p.Gly148=)
gnomAD v4
19g.855642G>ACA402918082ELANEc.445G>A (p.Val149Met)
gnomAD v4
19g.855642G>CCA402918084ELANEc.445G>C (p.Val149Leu)
gnomAD v4
19g.855642G>TCA402918080ELANEc.445G>T (p.Val149Leu)
gnomAD v4
19g.855643T>ACA402918087ELANEc.446T>A (p.Val149Glu)
19g.855643T>CCA402918092ELANEc.446T>C (p.Val149Ala)
19g.855643T>GCA402918090ELANEc.446T>G (p.Val149Gly)
19g.855644G>ACA504881895ELANEc.447G>A (p.Val149=)
dbSNP gnomAD v2 gnomAD v4
19g.855644G>CCA504881894ELANEc.447G>C (p.Val149=)
19g.855644G=CA2317361389ELANEc.447G= (p.Val149=)
19g.855644G>TCA504881892ELANEc.447G>T (p.Val149=)
gnomAD v4
19g.855645C>ACA402918095ELANEc.448C>A (p.Gln150Lys)
19g.855645C=CA2317361390ELANEc.448C= (p.Gln150=)
19g.855645C>GCA402918101ELANEc.448C>G (p.Gln150Glu)
COSMIC
19g.855645C>TCA402918098ELANEc.448C>T (p.Gln150Ter)
dbSNP gnomAD v2 gnomAD v4
19g.855646A>CCA402918103ELANEc.449A>C (p.Gln150Pro)
gnomAD v4
19g.855646A>GCA402918107ELANEc.449A>G (p.Gln150Arg)
19g.855646A>TCA402918105ELANEc.449A>T (p.Gln150Leu)
19g.855647G>ACA9026065ELANEc.450G>A (p.Gln150=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855647G>CCA402918110ELANEc.450G>C (p.Gln150His)
gnomAD v4
19g.855647G=CA2317361391ELANEc.450G= (p.Gln150=)
19g.855647G>TCA402918109ELANEc.450G>T (p.Gln150His)
gnomAD v4
19g.855648_855649dupCA2587805317ELANEc.451_452dup (p.Leu152AlafsTer24)
gnomAD v4
19g.855648T>ACA402918114ELANEc.451T>A (p.Cys151Ser)
19g.855648T>CCA402918115ELANEc.451T>C (p.Cys151Arg)
19g.855648T>GCA402918117ELANEc.451T>G (p.Cys151Gly)
19g.855649G>ACA303944794ELANEc.452G>A (p.Cys151Tyr)
ClinVar dbSNP gnomAD v2
19g.855649G>CCA402918122ELANEc.452G>C (p.Cys151Ser)
ClinVar dbSNP
19g.855649G=CA2317361392ELANEc.452G= (p.Cys151=)
19g.855649G>TCA10583962ELANEc.452G>T (p.Cys151Phe)
ClinVar dbSNP gnomAD v4
19g.855650C>ACA402918126ELANEc.453C>A (p.Cys151Ter)
gnomAD v4
19g.855650C=CA2317361393ELANEc.453C= (p.Cys151=)
19g.855650C>GCA402918128ELANEc.453C>G (p.Cys151Trp)
19g.855650C>TCA504881899ELANEc.453C>T (p.Cys151=)
ClinVar dbSNP gnomAD v4
19g.855651delCA2587805318ELANEc.454del (p.Leu152TrpfsTer23)
gnomAD v4
19g.855651C>ACA402918130ELANEc.454C>A (p.Leu152Met)
19g.855651C=CA2317361394ELANEc.454C= (p.Leu152=)
19g.855651C>GCA402918132ELANEc.454C>G (p.Leu152Val)
19g.855651C>TCA9026066ELANEc.454C>T (p.Leu152=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855652T>ACA402918140ELANEc.455T>A (p.Leu152Gln)
19g.855652T>CCA402918135ELANEc.455T>C (p.Leu152Pro)
19g.855652T>GCA402918137ELANEc.455T>G (p.Leu152Arg)
19g.855653G>ACA9026067ELANEc.456G>A (p.Leu152=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855653G>CCA504881902ELANEc.456G>C (p.Leu152=)
19g.855653G=CA2317361395ELANEc.456G= (p.Leu152=)
19g.855653G>TCA504881903ELANEc.456G>T (p.Leu152=)
gnomAD v4
19g.855654G>ACA402918144ELANEc.457G>A (p.Ala153Thr)
gnomAD v4
19g.855654G>CCA402918145ELANEc.457G>C (p.Ala153Pro)
ClinVar
19g.855654G>TCA402918146ELANEc.457G>T (p.Ala153Ser)
gnomAD v4
19g.855655C>ACA402918149ELANEc.458C>A (p.Ala153Asp)
ClinVar
19g.855655C>GCA402918151ELANEc.458C>G (p.Ala153Gly)
19g.855655C>TCA402918154ELANEc.458C>T (p.Ala153Val)
gnomAD v4
19g.855656C>ACA504881905ELANEc.459C>A (p.Ala153=)
gnomAD v4
19g.855656C=CA2317361396ELANEc.459C= (p.Ala153=)
19g.855656C>GCA504881906ELANEc.459C>G (p.Ala153=)
19g.855656C>TCA504881908ELANEc.459C>T (p.Ala153=)
dbSNP
19g.855657A>CCA402918156ELANEc.460A>C (p.Met154Leu)
19g.855657A>GCA402918159ELANEc.460A>G (p.Met154Val)
19g.855657A>TCA402918163ELANEc.460A>T (p.Met154Leu)
19g.855658T>ACA402918173ELANEc.461T>A (p.Met154Lys)
19g.855658T>CCA402918172ELANEc.461T>C (p.Met154Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855658T>GCA402918170ELANEc.461T>G (p.Met154Arg)
ClinVar dbSNP
19g.855658T=CA2317361397ELANEc.461T= (p.Met154=)
19g.855659G>ACA402918175ELANEc.462G>A (p.Met154Ile)
gnomAD v4
19g.855659G>CCA402918176ELANEc.462G>C (p.Met154Ile)
19g.855659G=CA2317361398ELANEc.462G= (p.Met154=)
19g.855659G>TCA402918179ELANEc.462G>T (p.Met154Ile)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855660G>ACA402918181ELANEc.463G>A (p.Gly155Ser)
dbSNP gnomAD v2 gnomAD v4
19g.855660G>CCA402918183ELANEc.463G>C (p.Gly155Arg)
19g.855660G=CA2317361399ELANEc.463G= (p.Gly155=)
19g.855660G>TCA402918186ELANEc.463G>T (p.Gly155Cys)
gnomAD v4
19g.855661G>ACA402918190ELANEc.464G>A (p.Gly155Asp)
gnomAD v4
19g.855661G>CCA402918192ELANEc.464G>C (p.Gly155Ala)
COSMIC
19g.855661G>TCA402918195ELANEc.464G>T (p.Gly155Val)
gnomAD v4
19g.855662C>ACA504881912ELANEc.465C>A (p.Gly155=)
19g.855662C>GCA504881913ELANEc.465C>G (p.Gly155=)
19g.855662C>TCA504881914ELANEc.465C>T (p.Gly155=)
gnomAD v4
19g.855662_855685delinsCTGGGGCCTTCTGGGCAGGAACCGCA2317361400ELANEc.465_488delinsCTGGGGCCTTCTGGGCAGGAACCG (p.Gly155=)
19g.855663T>ACA402918196ELANEc.466T>A (p.Trp156Arg)
ClinVar
19g.855663T>CCA402918199ELANEc.466T>C (p.Trp156Arg)
19g.855663T>GCA402918201ELANEc.466T>G (p.Trp156Gly)
19g.855663T=CA2317361401ELANEc.466T= (p.Trp156=)
19g.855667_855689delCA631295190ELANEc.470_492del (p.Gly157AspfsTer?)
dbSNP gnomAD v2 gnomAD v4
19g.855664G>ACA402918207ELANEc.467G>A (p.Trp156Ter)
dbSNP gnomAD v4
19g.855664G>CCA402918203ELANEc.467G>C (p.Trp156Ser)
ClinVar dbSNP
19g.855664G=CA2317361403ELANEc.467G= (p.Trp156=)
19g.855664G>TCA402918205ELANEc.467G>T (p.Trp156Leu)
gnomAD v4 COSMIC
19g.855667dupCA2317361402ELANEc.470dup (p.Leu158ProfsTer?)
dbSNP
19g.855667delCA2587805319ELANEc.470del (p.Gly157AlafsTer18)
gnomAD v4
19g.855665G>ACA402918210ELANEc.468G>A (p.Trp156Ter)
19g.855665G>CCA402918211ELANEc.468G>C (p.Trp156Cys)
19g.855665G>TCA402918215ELANEc.468G>T (p.Trp156Cys)
gnomAD v4
19g.855666G>ACA402918218ELANEc.469G>A (p.Gly157Ser)
ClinVar
19g.855666G>CCA402918220ELANEc.469G>C (p.Gly157Arg)
19g.855666G=CA2317361404ELANEc.469G= (p.Gly157=)
19g.855666G>TCA303944803ELANEc.469G>T (p.Gly157Cys)
dbSNP gnomAD v4
19g.855667G>ACA402918226ELANEc.470G>A (p.Gly157Asp)
gnomAD v4
19g.855667G>CCA402918228ELANEc.470G>C (p.Gly157Ala)
19g.855667G>TCA402918230ELANEc.470G>T (p.Gly157Val)
gnomAD v4
19g.855668C>ACA504881920ELANEc.471C>A (p.Gly157=)
19g.855668C>GCA504881919ELANEc.471C>G (p.Gly157=)
19g.855668C>TCA504881918ELANEc.471C>T (p.Gly157=)
gnomAD v4
19g.855669C>ACA402918233ELANEc.472C>A (p.Leu158Ile)
19g.855669C=CA2317361405ELANEc.472C= (p.Leu158=)
19g.855669C>GCA9026068ELANEc.472C>G (p.Leu158Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855669C>TCA402918237ELANEc.472C>T (p.Leu158Phe)
ClinVar dbSNP
19g.855670T>ACA402918247ELANEc.473T>A (p.Leu158His)
19g.855670T>CCA402918243ELANEc.473T>C (p.Leu158Pro)
19g.855670T>GCA402918241ELANEc.473T>G (p.Leu158Arg)
19g.855671T>ACA504881921ELANEc.474T>A (p.Leu158=)
19g.855671T>CCA504881922ELANEc.474T>C (p.Leu158=)
19g.855671T>GCA504881923ELANEc.474T>G (p.Leu158=)
19g.855672C>ACA402918252ELANEc.475C>A (p.Leu159Met)
19g.855672C=CA2317361406ELANEc.475C= (p.Leu159=)
19g.855672C>GCA402918249ELANEc.475C>G (p.Leu159Val)
19g.855672C>TCA504881924ELANEc.475C>T (p.Leu159=)
dbSNP gnomAD v4
19g.855673T>ACA402918254ELANEc.476T>A (p.Leu159Gln)
19g.855673T>CCA402918257ELANEc.476T>C (p.Leu159Pro)
19g.855673T>GCA9026069ELANEc.476T>G (p.Leu159Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855673T=CA2317361407ELANEc.476T= (p.Leu159=)
19g.855674G>ACA504881925ELANEc.477G>A (p.Leu159=)
19g.855674G>CCA9026070ELANEc.477G>C (p.Leu159=)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.855674G=CA2317361408ELANEc.477G= (p.Leu159=)
19g.855674G>TCA504881926ELANEc.477G>T (p.Leu159=)
gnomAD v4
19g.855675G>ACA402918262ELANEc.478G>A (p.Gly160Ser)
19g.855675G>CCA402918265ELANEc.478G>C (p.Gly160Arg)
19g.855675G=CA2317361409ELANEc.478G= (p.Gly160=)
19g.855675G>TCA303944813ELANEc.478G>T (p.Gly160Cys)
dbSNP gnomAD v3 gnomAD v4
19g.855676G>ACA402918269ELANEc.479G>A (p.Gly160Asp)
gnomAD v4
19g.855676G>CCA402918274ELANEc.479G>C (p.Gly160Ala)
19g.855676G=CA2317361410ELANEc.479G= (p.Gly160=)
19g.855676G>TCA402918277ELANEc.479G>T (p.Gly160Val)
dbSNP
19g.855677C>ACA504881927ELANEc.480C>A (p.Gly160=)
19g.855677C>GCA504881928ELANEc.480C>G (p.Gly160=)
19g.855677C>TCA504881929ELANEc.480C>T (p.Gly160=)
gnomAD v4
19g.855678A=CA2317361411ELANEc.481A= (p.Arg161=)
19g.855678A>CCA303944815ELANEc.481A>C (p.Arg161=)
dbSNP gnomAD v3 gnomAD v4
19g.855678A>GCA402918280ELANEc.481A>G (p.Arg161Gly)
gnomAD v4
19g.855678A>TCA402918283ELANEc.481A>T (p.Arg161Trp)
19g.855679G>ACA402918293ELANEc.482G>A (p.Arg161Lys)
ClinVar dbSNP gnomAD v4
19g.855679G>CCA402918290ELANEc.482G>C (p.Arg161Thr)
19g.855679G>TCA402918287ELANEc.482G>T (p.Arg161Met)
gnomAD v4
19g.855680G>ACA504881930ELANEc.483G>A (p.Arg161=)
19g.855680G>CCA402918295ELANEc.483G>C (p.Arg161Ser)
19g.855680G>TCA402918297ELANEc.483G>T (p.Arg161Ser)
gnomAD v4
19g.855681A>CCA402918299ELANEc.484A>C (p.Asn162His)
19g.855681A>GCA402918301ELANEc.484A>G (p.Asn162Asp)
19g.855681A>TCA402918303ELANEc.484A>T (p.Asn162Tyr)
19g.855682A>CCA402918308ELANEc.485A>C (p.Asn162Thr)
19g.855682A>GCA402918310ELANEc.485A>G (p.Asn162Ser)
gnomAD v4
19g.855682A>TCA402918313ELANEc.485A>T (p.Asn162Ile)
gnomAD v4
19g.855683C>ACA402918317ELANEc.486C>A (p.Asn162Lys)
19g.855683C=CA2317361412ELANEc.486C= (p.Asn162=)
19g.855683C>GCA402918322ELANEc.486C>G (p.Asn162Lys)
dbSNP gnomAD v3 gnomAD v4
19g.855683C>TCA504881931ELANEc.486C>T (p.Asn162=)
19g.855684C>ACA402918324ELANEc.487C>A (p.Arg163Ser)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855684C=CA2317361413ELANEc.487C= (p.Arg163=)
19g.855684C>GCA402918328ELANEc.487C>G (p.Arg163Gly)
dbSNP gnomAD v3 gnomAD v4
19g.855684C>TCA9026071ELANEc.487C>T (p.Arg163Cys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.855685G>ACA402918332ELANEc.488G>A (p.Arg163His)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855685G>CCA402918334ELANEc.488G>C (p.Arg163Pro)
19g.855685G=CA2317361414ELANEc.488G= (p.Arg163=)
19g.855685G>TCA402918330ELANEc.488G>T (p.Arg163Leu)
gnomAD v4
19g.855686T>ACA504881933ELANEc.489T>A (p.Arg163=)
19g.855686T>CCA504881934ELANEc.489T>C (p.Arg163=)
19g.855686T>GCA504881935ELANEc.489T>G (p.Arg163=)
19g.855687G>ACA303944823ELANEc.490G>A (p.Gly164Arg)
dbSNP COSMIC
19g.855687G>CCA9026072ELANEc.490G>C (p.Gly164Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855687G=CA2317361415ELANEc.490G= (p.Gly164=)
19g.855687G>TCA402918342ELANEc.490G>T (p.Gly164Trp)
gnomAD v4
19g.855688G>ACA402918344ELANEc.491G>A (p.Gly164Glu)
gnomAD v4
19g.855688G>CCA402918347ELANEc.491G>C (p.Gly164Ala)
19g.855688G>TCA402918350ELANEc.491G>T (p.Gly164Val)
gnomAD v4
19g.855689G>ACA504881939ELANEc.492G>A (p.Gly164=)
dbSNP COSMIC
19g.855689G>CCA303944826ELANEc.492G>C (p.Gly164=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855689G=CA2317361416ELANEc.492G= (p.Gly164=)
19g.855689G>TCA504881940ELANEc.492G>T (p.Gly164=)
gnomAD v4
19g.855690A=CA2317361417ELANEc.493A= (p.Ile165=)
19g.855690A>CCA402918354ELANEc.493A>C (p.Ile165Leu)
19g.855690A>GCA402918357ELANEc.493A>G (p.Ile165Val)
ClinVar dbSNP
19g.855690A>TCA402918358ELANEc.493A>T (p.Ile165Phe)
19g.855691T>ACA402918359ELANEc.494T>A (p.Ile165Asn)
19g.855691T>CCA402918360ELANEc.494T>C (p.Ile165Thr)
19g.855691T>GCA402918363ELANEc.494T>G (p.Ile165Ser)
gnomAD v4
19g.855692C>ACA504881941ELANEc.495C>A (p.Ile165=)
gnomAD v4
19g.855692C=CA2317361418ELANEc.495C= (p.Ile165=)
19g.855692C>GCA9026074ELANEc.495C>G (p.Ile165Met)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855692C>TCA9026073ELANEc.495C>T (p.Ile165=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.855693G>ACA9026075ELANEc.496G>A (p.Ala166Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855693G>CCA402918368ELANEc.496G>C (p.Ala166Pro)
19g.855693G=CA2317361419ELANEc.496G= (p.Ala166=)
19g.855693G>TCA402918369ELANEc.496G>T (p.Ala166Ser)
gnomAD v4
19g.855694C>ACA402918373ELANEc.497C>A (p.Ala166Asp)
19g.855694C=CA2317361420ELANEc.497C= (p.Ala166=)
19g.855694C>GCA402918376ELANEc.497C>G (p.Ala166Gly)
19g.855694C>TCA303944836ELANEc.497C>T (p.Ala166Val)
dbSNP gnomAD v4
19g.855695C>ACA504881942ELANEc.498C>A (p.Ala166=)
19g.855695C>GCA504881943ELANEc.498C>G (p.Ala166=)
19g.855695C>TCA504881944ELANEc.498C>T (p.Ala166=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.855696A>CCA402918381ELANEc.499A>C (p.Ser167Arg)
19g.855696A>GCA402918382ELANEc.499A>G (p.Ser167Gly)
19g.855696A>TCA402918384ELANEc.499A>T (p.Ser167Cys)
19g.855697G>ACA9026076ELANEc.500G>A (p.Ser167Asn)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855697G>CCA402918389ELANEc.500G>C (p.Ser167Thr)
19g.855697G=CA2317361421ELANEc.500G= (p.Ser167=)
19g.855697G>TCA402918391ELANEc.500G>T (p.Ser167Ile)
gnomAD v4
19g.855698C>ACA402918396ELANEc.501C>A (p.Ser167Arg)
dbSNP gnomAD v2 gnomAD v4
19g.855698C=CA2317361422ELANEc.501C= (p.Ser167=)
19g.855698C>GCA402918399ELANEc.501C>G (p.Ser167Arg)
dbSNP gnomAD v4
19g.855698C>TCA9026077ELANEc.501C>T (p.Ser167=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855699G>ACA9026078ELANEc.502G>A (p.Val168Ile)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.855699G>CCA402918404ELANEc.502G>C (p.Val168Leu)
19g.855699G=CA2317361423ELANEc.502G= (p.Val168=)
19g.855699G>TCA402918403ELANEc.502G>T (p.Val168Phe)
gnomAD v4
19g.855700T>ACA402918408ELANEc.503T>A (p.Val168Asp)
19g.855700T>CCA402918411ELANEc.503T>C (p.Val168Ala)
19g.855700T>GCA402918413ELANEc.503T>G (p.Val168Gly)
19g.855701C>ACA504881945ELANEc.504C>A (p.Val168=)
19g.855701C>GCA504881946ELANEc.504C>G (p.Val168=)
19g.855701C>TCA504881947ELANEc.504C>T (p.Val168=)
19g.855702C>ACA9026079ELANEc.505C>A (p.Leu169Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855702C=CA2317361424ELANEc.505C= (p.Leu169=)
19g.855702C>GCA402918416ELANEc.505C>G (p.Leu169Val)
19g.855702C>TCA504881948ELANEc.505C>T (p.Leu169=)
19g.855703T>ACA402918418ELANEc.506T>A (p.Leu169Gln)
19g.855703T>CCA402918421ELANEc.506T>C (p.Leu169Pro)
19g.855703T>GCA402918424ELANEc.506T>G (p.Leu169Arg)
19g.855704G>ACA504881951ELANEc.507G>A (p.Leu169=)
gnomAD v4
19g.855704G>CCA504881950ELANEc.507G>C (p.Leu169=)
19g.855704G=CA2317361425ELANEc.507G= (p.Leu169=)
19g.855704G>TCA504881949ELANEc.507G>T (p.Leu169=)
dbSNP gnomAD v4
19g.855705C>ACA402918427ELANEc.508C>A (p.Gln170Lys)
19g.855705C=CA2317361426ELANEc.508C= (p.Gln170=)
19g.855705C>GCA402918428ELANEc.508C>G (p.Gln170Glu)
19g.855705C>TCA303944847ELANEc.508C>T (p.Gln170Ter)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.855706A=CA2317361427ELANEc.509A= (p.Gln170=)
19g.855706A>CCA402918432ELANEc.509A>C (p.Gln170Pro)
19g.855706A>GCA402918433ELANEc.509A>G (p.Gln170Arg)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855706A>TCA402918434ELANEc.509A>T (p.Gln170Leu)
gnomAD v4
19g.855707G>ACA504881952ELANEc.510G>A (p.Gln170=)
gnomAD v4
19g.855707G>CCA402918437ELANEc.510G>C (p.Gln170His)
19g.855707G>TCA402918439ELANEc.510G>T (p.Gln170His)
gnomAD v4
19g.855708G>ACA9026080ELANEc.511G>A (p.Glu171Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855708G>CCA402918444ELANEc.511G>C (p.Glu171Gln)
gnomAD v4
19g.855708G=CA2317361428ELANEc.511G= (p.Glu171=)
19g.855708G>TCA402918446ELANEc.511G>T (p.Glu171Ter)
gnomAD v4
19g.855709A>CCA402918449ELANEc.512A>C (p.Glu171Ala)
19g.855709A>GCA402918452ELANEc.512A>G (p.Glu171Gly)
19g.855709A>TCA402918455ELANEc.512A>T (p.Glu171Val)
19g.855710G>ACA504881953ELANEc.513G>A (p.Glu171=)
19g.855710G>CCA402918456ELANEc.513G>C (p.Glu171Asp)
19g.855710G=CA2317361429ELANEc.513G= (p.Glu171=)
19g.855710G>TCA9026081ELANEc.513G>T (p.Glu171Asp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855711C>ACA402918463ELANEc.514C>A (p.Leu172Ile)
gnomAD v4
19g.855711C>GCA402918464ELANEc.514C>G (p.Leu172Val)
19g.855711C>TCA402918466ELANEc.514C>T (p.Leu172Phe)
19g.855712T>ACA402918469ELANEc.515T>A (p.Leu172His)
gnomAD v4
19g.855712T>CCA402918474ELANEc.515T>C (p.Leu172Pro)
19g.855712T>GCA402918471ELANEc.515T>G (p.Leu172Arg)
19g.855713C>ACA504881954ELANEc.516C>A (p.Leu172=)
19g.855713C>GCA504881955ELANEc.516C>G (p.Leu172=)
ClinVar
19g.855713C>TCA504881956ELANEc.516C>T (p.Leu172=)
19g.855714A=CA2317361430ELANEc.517A= (p.Asn173=)
19g.855714A>CCA402918476ELANEc.517A>C (p.Asn173His)
dbSNP
19g.855714A>GCA402918479ELANEc.517A>G (p.Asn173Asp)
gnomAD v4
19g.855714A>TCA402918482ELANEc.517A>T (p.Asn173Tyr)
19g.855715A=CA2317361431ELANEc.518A= (p.Asn173=)
19g.855715A>CCA402918485ELANEc.518A>C (p.Asn173Thr)
19g.855715A>GCA9026082ELANEc.518A>G (p.Asn173Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855715A>TCA402918490ELANEc.518A>T (p.Asn173Ile)
19g.855716C>ACA402918492ELANEc.519C>A (p.Asn173Lys)
ClinVar dbSNP gnomAD v4
19g.855716C=CA2317361432ELANEc.519C= (p.Asn173=)
19g.855716C>GCA402918496ELANEc.519C>G (p.Asn173Lys)
19g.855716C>TCA9026083ELANEc.519C>T (p.Asn173=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855717G>ACA402918501ELANEc.520G>A (p.Val174Met)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.855717G>CCA402918503ELANEc.520G>C (p.Val174Leu)
19g.855717G=CA2317361433ELANEc.520G= (p.Val174=)
19g.855717G>TCA402918506ELANEc.520G>T (p.Val174Leu)
gnomAD v4
19g.855718T>ACA402918507ELANEc.521T>A (p.Val174Glu)
19g.855718T>CCA402918509ELANEc.521T>C (p.Val174Ala)
19g.855718T>GCA402918508ELANEc.521T>G (p.Val174Gly)
19g.855719G>ACA504881957ELANEc.522G>A (p.Val174=)
19g.855719G>CCA504881958ELANEc.522G>C (p.Val174=)
19g.855719G>TCA504881959ELANEc.522G>T (p.Val174=)
gnomAD v4
19g.855720A=CA2317361434ELANEc.523A= (p.Thr175=)
19g.855720A>CCA402918510ELANEc.523A>C (p.Thr175Pro)
19g.855720A>GCA402918512ELANEc.523A>G (p.Thr175Ala)
19g.855720A>TCA402918520ELANEc.523A>T (p.Thr175Ser)
dbSNP gnomAD v4
19g.855721C>ACA402918525ELANEc.524C>A (p.Thr175Lys)
19g.855721C=CA2317361435ELANEc.524C= (p.Thr175=)
19g.855721C>GCA402918527ELANEc.524C>G (p.Thr175Arg)
19g.855721C>TCA9026084ELANEc.524C>T (p.Thr175Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC

Number of alleles fetched