Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.855536C=CA2317361322ELANEc.367-28C= (n.367-28C=)
19g.855536C>GCA9026030ELANEc.367-28C>G (n.367-28C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855536C>TCA9026029ELANEc.367-28C>T (n.367-28C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855537G>ACA631295187ELANEc.367-27G>A (n.367-27G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855537G=CA2317361323ELANEc.367-27G= (n.367-27G=)
19g.855537G>TCA9026031ELANEc.367-27G>T (n.367-27G>T)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855538C>ACA2587805300ELANEc.367-26C>A (n.367-26C>A)
gnomAD v4
19g.855539T>CCA2735524955ELANEc.367-25T>C (n.367-25T>C)
dbSNP
19g.855540G>TCA2587805301ELANEc.367-24G>T (n.367-24G>T)
gnomAD v4
19g.855541A>GCA2587805302ELANEc.367-23A>G (n.367-23A>G)
gnomAD v4
19g.855542C=CA2317361324ELANEc.367-22C= (n.367-22C=)
19g.855542C>GCA2317361325ELANEc.367-22C>G (n.367-22C>G)
dbSNP
19g.855542C>TCA9026032ELANEc.367-22C>T (n.367-22C>T)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
19g.855543G>ACA303944645ELANEc.367-21G>A (n.367-21G>A)
dbSNP gnomAD v2 gnomAD v4
19g.855543G>CCA2576540506ELANEc.367-21G>C (n.367-21G>C)
19g.855543G=CA2317361326ELANEc.367-21G= (n.367-21G=)
19g.855543G>TCA884314827ELANEc.367-21G>T (n.367-21G>T)
dbSNP gnomAD v3 gnomAD v4
19g.855545T>CCA9026033ELANEc.367-19T>C (n.367-19T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855545T=CA2317361327ELANEc.367-19T= (n.367-19T=)
19g.855546C=CA2317361328ELANEc.367-18C= (n.367-18C=)
19g.855546C>GCA2587805303ELANEc.367-18C>G (n.367-18C>G)
gnomAD v4
19g.855546C>TCA303944658ELANEc.367-18C>T (n.367-18C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855547T>CCA2587805304ELANEc.367-17T>C (n.367-17T>C)
gnomAD v4
19g.855548G>ACA658799087ELANEc.367-16G>A (n.367-16G>A)
ClinVar dbSNP
19g.855548G=CA2317361329ELANEc.367-16G= (n.367-16G=)
19g.855548G>TCA2587805305ELANEc.367-16G>T (n.367-16G>T)
gnomAD v4
19g.855549T>ACA2813227118ELANEc.367-15T>A (n.367-15T>A)
19g.855549T>CCA657480007ELANEc.367-15T>C (n.367-15T>C)
dbSNP COSMIC
19g.855549T=CA2317361330ELANEc.367-15T= (n.367-15T=)
19g.855551C=CA2317361331ELANEc.367-13C= (n.367-13C=)
19g.855551C>TCA631295188ELANEc.367-13C>T (n.367-13C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855552C>ACA884314837ELANEc.367-12C>A (n.367-12C>A)
dbSNP gnomAD v3 gnomAD v4
19g.855552C=CA2317361332ELANEc.367-12C= (n.367-12C=)
19g.855552C>TCA2580096962ELANEc.367-12C>T (n.367-12C>T)
ClinVar dbSNP gnomAD v4
19g.855553C>TCA2573155743ELANEc.367-11C>T (n.367-11C>T)
ClinVar dbSNP
19g.855554_855555dupCA9026034ELANEc.367-10_367-9dup (n.367-10_367-9dup)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855554A=CA2317361333ELANEc.367-10A= (n.367-10A=)
19g.855554A>CCA2317361334ELANEc.367-10A>C (n.367-10A>C)
dbSNP
19g.855554A>GCA2587805306ELANEc.367-10A>G (n.367-10A>G)
gnomAD v4
19g.855555C>TCA2587805307ELANEc.367-9C>T (n.367-9C>T)
gnomAD v4
19g.855556C>ACA501167ELANEc.367-8C>A (n.367-8C>A)
ClinVar dbSNP gnomAD v4
19g.855556C=CA2317361335ELANEc.367-8C= (n.367-8C=)
19g.855556C>GCA631295189ELANEc.367-8C>G (n.367-8C>G)
dbSNP gnomAD v2 gnomAD v4
19g.855556C>TCA9026035ELANEc.367-8C>T (n.367-8C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855557G>ACA9026036ELANEc.367-7G>A (n.367-7G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855557G=CA2317361336ELANEc.367-7G= (n.367-7G=)
19g.855557G>TCA2576540507ELANEc.367-7G>T (n.367-7G>T)
gnomAD v4
19g.855559C>ACA2587805308ELANEc.367-5C>A (n.367-5C>A)
gnomAD v4
19g.855560A>GCA2519541806ELANEc.367-4A>G (n.367-4A>G)
19g.855561C=CA2317361337ELANEc.367-3C= (n.367-3C=)
19g.855561C>TCA303944666ELANEc.367-3C>T (n.367-3C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855562A>CCA402917673ELANEc.367-2A>C (n.367-2A>C)
19g.855562A>GCA402917677ELANEc.367-2A>G (n.367-2A>G)
gnomAD v4
19g.855562A>TCA402917674ELANEc.367-2A>T (n.367-2A>T)
19g.855563G>ACA402917680ELANEc.367-1G>A (n.367-1G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855563G>CCA402917683ELANEc.367-1G>C (n.367-1G>C)
ClinVar dbSNP
19g.855563G=CA2317361338ELANEc.367-1G= (n.367-1G=)
19g.855563G>TCA402917682ELANEc.367-1G>T (n.367-1G>T)
gnomAD v4
19g.855564C>ACA402917687ELANEc.367C>A (p.Leu123Ile)
gnomAD v4
19g.855564C=CA2317361339ELANEc.367C= (p.Leu123=)
19g.855564C>GCA402917690ELANEc.367C>G (p.Leu123Val)
ClinVar dbSNP
19g.855564C>TCA402917692ELANEc.367C>T (p.Leu123Phe)
gnomAD v4
19g.855565T>ACA402917696ELANEc.368T>A (p.Leu123His)
19g.855565T>CCA402917698ELANEc.368T>C (p.Leu123Pro)
ClinVar dbSNP
19g.855565T>GCA402917700ELANEc.368T>G (p.Leu123Arg)
19g.855566C>ACA504881741ELANEc.369C>A (p.Leu123=)
19g.855566C=CA2317361340ELANEc.369C= (p.Leu123=)
19g.855566C>GCA504881742ELANEc.369C>G (p.Leu123=)
dbSNP
19g.855566C>TCA504881743ELANEc.369C>T (p.Leu123=)
19g.855567A=CA2317361341ELANEc.370A= (p.Asn124=)
19g.855567A>CCA402917703ELANEc.370A>C (p.Asn124His)
gnomAD v4
19g.855567A>GCA9026037ELANEc.370A>G (p.Asn124Asp)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855567A>TCA402917706ELANEc.370A>T (p.Asn124Tyr)
19g.855568A>CCA402917710ELANEc.371A>C (p.Asn124Thr)
19g.855568A>GCA402917712ELANEc.371A>G (p.Asn124Ser)
19g.855568A>TCA402917713ELANEc.371A>T (p.Asn124Ile)
19g.855569C>ACA402917721ELANEc.372C>A (p.Asn124Lys)
ClinVar dbSNP gnomAD v4
19g.855569C=CA2317361342ELANEc.372C= (p.Asn124=)
19g.855569C>GCA402917716ELANEc.372C>G (p.Asn124Lys)
19g.855569C>TCA9026038ELANEc.372C>T (p.Asn124=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855570G>ACA9026039ELANEc.373G>A (p.Gly125Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855570G>CCA402917725ELANEc.373G>C (p.Gly125Arg)
19g.855570G=CA2317361343ELANEc.373G= (p.Gly125=)
19g.855570G>TCA402917728ELANEc.373G>T (p.Gly125Trp)
gnomAD v4
19g.855571G>ACA402917733ELANEc.374G>A (p.Gly125Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855571G>CCA402917734ELANEc.374G>C (p.Gly125Ala)
19g.855571G=CA2317361344ELANEc.374G= (p.Gly125=)
19g.855571G>TCA402917736ELANEc.374G>T (p.Gly125Val)
19g.855572G>ACA303944677ELANEc.375G>A (p.Gly125=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855572G>CCA504881744ELANEc.375G>C (p.Gly125=)
19g.855572G=CA2317361345ELANEc.375G= (p.Gly125=)
19g.855572G>TCA504881745ELANEc.375G>T (p.Gly125=)
19g.855573T>ACA402917742ELANEc.376T>A (p.Ser126Thr)
19g.855573T>CCA402917747ELANEc.376T>C (p.Ser126Pro)
19g.855573T>GCA402917750ELANEc.376T>G (p.Ser126Ala)
19g.855574C>ACA303944686ELANEc.377C>A (p.Ser126Ter)
dbSNP gnomAD v3 gnomAD v4
19g.855574C=CA2317361346ELANEc.377C= (p.Ser126=)
19g.855574C>GCA402917752ELANEc.377C>G (p.Ser126Trp)
ClinVar dbSNP
19g.855574C>TCA281055ELANEc.377C>T (p.Ser126Leu)
ClinVar dbSNP gnomAD v4
19g.855575G>ACA9026040ELANEc.378G>A (p.Ser126=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855575G>CCA504881746ELANEc.378G>C (p.Ser126=)
19g.855575G=CA2317361347ELANEc.378G= (p.Ser126=)
19g.855575G>TCA504881747ELANEc.378G>T (p.Ser126=)
gnomAD v4
19g.855575_855576delCA2587805309ELANEc.378_379del (p.Ala127HisfsTer?)
gnomAD v4
19g.855576G>ACA402917757ELANEc.379G>A (p.Ala127Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855576G>CCA402917760ELANEc.379G>C (p.Ala127Pro)
19g.855576G=CA2317361348ELANEc.379G= (p.Ala127=)
19g.855576G>TCA402917763ELANEc.379G>T (p.Ala127Ser)
19g.855576_855579delinsGCCACA2317361349ELANEc.379_382delinsGCCA (p.Ala127=)
19g.855577C>ACA402917766ELANEc.380C>A (p.Ala127Asp)
gnomAD v4
19g.855577C=CA2317361350ELANEc.380C= (p.Ala127=)
19g.855577C>GCA402917768ELANEc.380C>G (p.Ala127Gly)
19g.855577C>TCA9026041ELANEc.380C>T (p.Ala127Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855580_855582delCA915951612ELANEc.383_385del (p.Thr128del)
ClinVar dbSNP
19g.855578C>ACA504881750ELANEc.381C>A (p.Ala127=)
gnomAD v4
19g.855578C>GCA504881749ELANEc.381C>G (p.Ala127=)
19g.855578C>TCA504881748ELANEc.381C>T (p.Ala127=)
19g.855579A>CCA402917774ELANEc.382A>C (p.Thr128Pro)
19g.855579A>GCA402917777ELANEc.382A>G (p.Thr128Ala)
gnomAD v4
19g.855579A>TCA402917779ELANEc.382A>T (p.Thr128Ser)
19g.855579_855580insACAACAAACA2813227121ELANEc.382_383insACAACAAA (p.Thr128AsnfsTer?)
19g.855580C>ACA402917780ELANEc.383C>A (p.Thr128Asn)
19g.855580C>GCA402917782ELANEc.383C>G (p.Thr128Ser)
19g.855580C>TCA402917784ELANEc.383C>T (p.Thr128Ile)
19g.855581delCA2813227122ELANEc.384del (p.Ile129SerfsTer?)
19g.855581C>ACA504881751ELANEc.384C>A (p.Thr128=)
19g.855581C=CA2317361351ELANEc.384C= (p.Thr128=)
19g.855581C>GCA504881752ELANEc.384C>G (p.Thr128=)
19g.855581C>TCA9026042ELANEc.384C>T (p.Thr128=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855583_855585delCA2695227793ELANEc.386_388del (p.Ile129del)
19g.855582delCA2587805310ELANEc.385del (p.Ile129SerfsTer?)
gnomAD v4
19g.855582A=CA2317361352ELANEc.385A= (p.Ile129=)
19g.855582A>CCA402917788ELANEc.385A>C (p.Ile129Leu)
19g.855582A>GCA402917790ELANEc.385A>G (p.Ile129Val)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.855582A>TCA402917792ELANEc.385A>T (p.Ile129Phe)
gnomAD v4
19g.855583T>ACA402917794ELANEc.386T>A (p.Ile129Asn)
19g.855583T>CCA303944696ELANEc.386T>C (p.Ile129Thr)
dbSNP
19g.855583T>GCA402917796ELANEc.386T>G (p.Ile129Ser)
19g.855583T=CA2317361353ELANEc.386T= (p.Ile129=)
19g.855583_855584delCA2813227123ELANEc.386_387del (p.Ile129LysfsTer?)
19g.855584C>ACA504881753ELANEc.387C>A (p.Ile129=)
19g.855584C>GCA402917799ELANEc.387C>G (p.Ile129Met)
gnomAD v4
19g.855584C>TCA504881754ELANEc.387C>T (p.Ile129=)
gnomAD v4
19g.855584_855587delCA2587805311ELANEc.387_390del (p.Ile129MetfsTer?)
gnomAD v4
19g.855585A>CCA402917801ELANEc.388A>C (p.Asn130His)
19g.855585A>GCA402917803ELANEc.388A>G (p.Asn130Asp)
gnomAD v4
19g.855585A>TCA402917805ELANEc.388A>T (p.Asn130Tyr)
19g.855586A=CA2317361354ELANEc.389A= (p.Asn130=)
19g.855586A>CCA402917808ELANEc.389A>C (p.Asn130Thr)
19g.855586A>GCA9026043ELANEc.389A>G (p.Asn130Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855586A>TCA402917811ELANEc.389A>T (p.Asn130Ile)
19g.855587C>ACA402917814ELANEc.390C>A (p.Asn130Lys)
gnomAD v4
19g.855587C=CA2317361355ELANEc.390C= (p.Asn130=)
19g.855587C>GCA402917816ELANEc.390C>G (p.Asn130Lys)
19g.855587C>TCA9026044ELANEc.390C>T (p.Asn130=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855588G>ACA9026045ELANEc.391G>A (p.Ala131Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855588G>CCA402917820ELANEc.391G>C (p.Ala131Pro)
19g.855588G=CA2317361356ELANEc.391G= (p.Ala131=)
19g.855588G>TCA303944721ELANEc.391G>T (p.Ala131Ser)
dbSNP gnomAD v4
19g.855589C>ACA402917826ELANEc.392C>A (p.Ala131Asp)
gnomAD v4
19g.855589C=CA2317361357ELANEc.392C= (p.Ala131=)
19g.855589C>GCA402917827ELANEc.392C>G (p.Ala131Gly)
dbSNP gnomAD v3 gnomAD v4
19g.855589C>TCA402917829ELANEc.392C>T (p.Ala131Val)
ClinVar dbSNP
19g.855589_855590insACCCAACACA2813227124ELANEc.392_393insACCCAACA (p.Asn132ProfsTer?)
19g.855590C>ACA504881755ELANEc.393C>A (p.Ala131=)
19g.855590C>GCA504881756ELANEc.393C>G (p.Ala131=)
19g.855590C>TCA504881757ELANEc.393C>T (p.Ala131=)
19g.855591A>CCA402917835ELANEc.394A>C (p.Asn132His)
19g.855591A>GCA402917833ELANEc.394A>G (p.Asn132Asp)
19g.855591A>TCA402917832ELANEc.394A>T (p.Asn132Tyr)
19g.855592A>CCA402917837ELANEc.395A>C (p.Asn132Thr)
19g.855592A>GCA402917840ELANEc.395A>G (p.Asn132Ser)
gnomAD v4
19g.855592A>TCA402917842ELANEc.395A>T (p.Asn132Ile)
19g.855593C>ACA303944724ELANEc.396C>A (p.Asn132Lys)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855593C=CA2317361358ELANEc.396C= (p.Asn132=)
19g.855593C>GCA402917847ELANEc.396C>G (p.Asn132Lys)
19g.855593C>TCA9026046ELANEc.396C>T (p.Asn132=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
19g.855594G>ACA402917850ELANEc.397G>A (p.Val133Met)
gnomAD v4
19g.855594G>CCA402917855ELANEc.397G>C (p.Val133Leu)
dbSNP gnomAD v2
19g.855594G=CA2317361359ELANEc.397G= (p.Val133=)
19g.855594G>TCA402917853ELANEc.397G>T (p.Val133Leu)
gnomAD v4
19g.855595delCA2587805312ELANEc.398del (p.Val133GlyfsTer?)
gnomAD v4
19g.855595T>ACA402917857ELANEc.398T>A (p.Val133Glu)
19g.855595T>CCA402917858ELANEc.398T>C (p.Val133Ala)
19g.855595T>GCA402917859ELANEc.398T>G (p.Val133Gly)
19g.855596G>ACA504881758ELANEc.399G>A (p.Val133=)
19g.855596G>CCA504881759ELANEc.399G>C (p.Val133=)
19g.855596G>TCA504881760ELANEc.399G>T (p.Val133=)
gnomAD v4
19g.855597C>ACA402917862ELANEc.400C>A (p.Gln134Lys)
19g.855597C>GCA402917864ELANEc.400C>G (p.Gln134Glu)
19g.855597C>TCA402917866ELANEc.400C>T (p.Gln134Ter)
gnomAD v4
19g.855598A>CCA402917871ELANEc.401A>C (p.Gln134Pro)
19g.855598A>GCA402917873ELANEc.401A>G (p.Gln134Arg)
ClinVar
19g.855598A>TCA402917876ELANEc.401A>T (p.Gln134Leu)
19g.855599G>ACA504881764ELANEc.402G>A (p.Gln134=)
dbSNP gnomAD v2 gnomAD v4
19g.855599G>CCA402917879ELANEc.402G>C (p.Gln134His)
dbSNP
19g.855599G=CA2317361360ELANEc.402G= (p.Gln134=)
19g.855599G>TCA402917881ELANEc.402G>T (p.Gln134His)
gnomAD v4
19g.855600G>ACA9026047ELANEc.403G>A (p.Val135Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855600G>CCA402917885ELANEc.403G>C (p.Val135Leu)
19g.855600G=CA2317361361ELANEc.403G= (p.Val135=)
19g.855600G>TCA402917883ELANEc.403G>T (p.Val135Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
19g.855601T>ACA402917892ELANEc.404T>A (p.Val135Glu)
gnomAD v4
19g.855601T>CCA402917889ELANEc.404T>C (p.Val135Ala)
gnomAD v4
19g.855601T>GCA402917890ELANEc.404T>G (p.Val135Gly)
19g.855602G>ACA504881846ELANEc.405G>A (p.Val135=)
19g.855602G>CCA504881845ELANEc.405G>C (p.Val135=)
19g.855602G>TCA504881843ELANEc.405G>T (p.Val135=)
ClinVar gnomAD v4
19g.855603G>ACA402917894ELANEc.406G>A (p.Ala136Thr)
dbSNP gnomAD v2 gnomAD v4 COSMIC
19g.855603G>CCA402917897ELANEc.406G>C (p.Ala136Pro)
19g.855603G=CA2317361362ELANEc.406G= (p.Ala136=)
19g.855603G>TCA402917898ELANEc.406G>T (p.Ala136Ser)
gnomAD v4
19g.855603_855604insGACCAGCTGCCGGCGCA2695227794ELANEc.406_407insGACCAGCTGCCGGCG (p.Val135_Ala136insGlyProAlaAlaGly)
19g.855604C>ACA402917902ELANEc.407C>A (p.Ala136Asp)
gnomAD v4
19g.855604C=CA2317361363ELANEc.407C= (p.Ala136=)
19g.855604C>GCA402917904ELANEc.407C>G (p.Ala136Gly)
gnomAD v4
19g.855604C>TCA9026048ELANEc.407C>T (p.Ala136Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855606delCA2587805313ELANEc.409del (p.Gln137SerfsTer?)
gnomAD v4
19g.855605C>ACA504881849ELANEc.408C>A (p.Ala136=)
gnomAD v4
19g.855605C=CA2317361364ELANEc.408C= (p.Ala136=)
19g.855605C>GCA504881850ELANEc.408C>G (p.Ala136=)
19g.855605C>TCA504881851ELANEc.408C>T (p.Ala136=)
dbSNP gnomAD v2 gnomAD v4
19g.855607_855613delCA2740091832ELANEc.410_416del (p.Gln137ArgfsTer?)
ClinVar
19g.855606C>ACA402917908ELANEc.409C>A (p.Gln137Lys)
19g.855606C=CA2317361365ELANEc.409C= (p.Gln137=)
19g.855606C>GCA402917910ELANEc.409C>G (p.Gln137Glu)
19g.855606C>TCA402917913ELANEc.409C>T (p.Gln137Ter)
dbSNP
19g.855607A=CA2317361366ELANEc.410A= (p.Gln137=)
19g.855607A>CCA402917916ELANEc.410A>C (p.Gln137Pro)
19g.855607A>GCA402917917ELANEc.410A>G (p.Gln137Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.855607A>TCA402917919ELANEc.410A>T (p.Gln137Leu)
19g.855608G>ACA504881852ELANEc.411G>A (p.Gln137=)
gnomAD v4
19g.855608G>CCA402917923ELANEc.411G>C (p.Gln137His)
ClinVar
19g.855608G>TCA402917925ELANEc.411G>T (p.Gln137His)
gnomAD v4
19g.855609C>ACA402917927ELANEc.412C>A (p.Leu138Met)
gnomAD v4
19g.855609C>GCA402917929ELANEc.412C>G (p.Leu138Val)
19g.855609C>TCA504881854ELANEc.412C>T (p.Leu138=)
gnomAD v4
19g.855610T>ACA402917932ELANEc.413T>A (p.Leu138Gln)
ClinVar
19g.855610T>CCA402917933ELANEc.413T>C (p.Leu138Pro)
gnomAD v4
19g.855610T>GCA402917935ELANEc.413T>G (p.Leu138Arg)
19g.855611G>ACA504881856ELANEc.414G>A (p.Leu138=)
gnomAD v4
19g.855611G>CCA504881857ELANEc.414G>C (p.Leu138=)
19g.855611G>TCA504881858ELANEc.414G>T (p.Leu138=)
gnomAD v4
19g.855612C>ACA402917937ELANEc.415C>A (p.Pro139Thr)
gnomAD v4
19g.855612C>GCA402917940ELANEc.415C>G (p.Pro139Ala)
gnomAD v4
19g.855612C>TCA402917942ELANEc.415C>T (p.Pro139Ser)
gnomAD v4
19g.855613C>ACA402917943ELANEc.416C>A (p.Pro139Gln)
19g.855613C=CA2317361367ELANEc.416C= (p.Pro139=)
19g.855613C>GCA402917946ELANEc.416C>G (p.Pro139Arg)
ClinVar
19g.855613C>TCA281050ELANEc.416C>T (p.Pro139Leu)
ClinVar dbSNP gnomAD v4
19g.855614G>ACA9026049ELANEc.417G>A (p.Pro139=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855614G>CCA9026050ELANEc.417G>C (p.Pro139=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855614G=CA2317361368ELANEc.417G= (p.Pro139=)
19g.855614G>TCA504881860ELANEc.417G>T (p.Pro139=)
gnomAD v4
19g.855615G>ACA402917953ELANEc.418G>A (p.Ala140Thr)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.855615G>CCA402917956ELANEc.418G>C (p.Ala140Pro)
19g.855615G=CA2317361369ELANEc.418G= (p.Ala140=)
19g.855615G>TCA9026051ELANEc.418G>T (p.Ala140Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
19g.855616C>ACA402917959ELANEc.419C>A (p.Ala140Asp)
gnomAD v4
19g.855616C=CA2317361370ELANEc.419C= (p.Ala140=)
19g.855616C>GCA402917964ELANEc.419C>G (p.Ala140Gly)
19g.855616C>TCA9026052ELANEc.419C>T (p.Ala140Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.855617T>ACA9026053ELANEc.420T>A (p.Ala140=)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855617T>CCA504881861ELANEc.420T>C (p.Ala140=)
19g.855617T>GCA504881862ELANEc.420T>G (p.Ala140=)
19g.855617T=CA2317361371ELANEc.420T= (p.Ala140=)
19g.855618C>ACA402917966ELANEc.421C>A (p.Gln141Lys)
19g.855618C>GCA402917969ELANEc.421C>G (p.Gln141Glu)
COSMIC
19g.855618C>TCA402917972ELANEc.421C>T (p.Gln141Ter)
gnomAD v4
19g.855619A=CA2317361372ELANEc.422A= (p.Gln141=)
19g.855619A>CCA402917974ELANEc.422A>C (p.Gln141Pro)
19g.855619A>GCA402917975ELANEc.422A>G (p.Gln141Arg)
dbSNP
19g.855619A>TCA402917977ELANEc.422A>T (p.Gln141Leu)
19g.855620G>ACA504881863ELANEc.423G>A (p.Gln141=)
gnomAD v4
19g.855620G>CCA9026054ELANEc.423G>C (p.Gln141His)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.855620G=CA2317361373ELANEc.423G= (p.Gln141=)
19g.855620G>TCA402917981ELANEc.423G>T (p.Gln141His)
gnomAD v4
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)

Number of alleles fetched