Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.56975122_56975132delinsTTCAACACCAACA2224400094CETPc.952_962delinsTTCAACACCAA (p.Phe318=)
c.772_782delinsTTCAACACCAA (p.Phe258=)
c.757_767delinsTTCAACACCAA (p.Phe253=)
16g.56975123T>ACA396004119CETPc.953T>A (p.Phe318Tyr)
c.773T>A (p.Phe258Tyr)
c.758T>A (p.Phe253Tyr)
16g.56975123T>CCA396004120CETPc.953T>C (p.Phe318Ser)
c.773T>C (p.Phe258Ser)
c.758T>C (p.Phe253Ser)
16g.56975123T>GCA396004121CETPc.953T>G (p.Phe318Cys)
c.773T>G (p.Phe258Cys)
c.758T>G (p.Phe253Cys)
16g.56975123_56975132delCA8071166CETPc.953_962del (p.Phe318SerfsTer?)
c.773_782del (p.Phe258SerfsTer?)
c.758_767del (p.Phe253SerfsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975124C>ACA396004122CETPc.954C>A (p.Phe318Leu)
c.774C>A (p.Phe258Leu)
c.759C>A (p.Phe253Leu)
16g.56975124C>GCA396004123CETPc.954C>G (p.Phe318Leu)
c.774C>G (p.Phe258Leu)
c.759C>G (p.Phe253Leu)
16g.56975124C>TCA495620073CETPc.954C>T (p.Phe318=)
c.774C>T (p.Phe258=)
c.759C>T (p.Phe253=)
16g.56975125A>CCA396004126CETPc.955A>C (p.Asn319His)
c.775A>C (p.Asn259His)
c.760A>C (p.Asn254His)
16g.56975125A>GCA396004125CETPc.955A>G (p.Asn319Asp)
c.775A>G (p.Asn259Asp)
c.760A>G (p.Asn254Asp)
16g.56975125A>TCA396004124CETPc.955A>T (p.Asn319Tyr)
c.775A>T (p.Asn259Tyr)
c.760A>T (p.Asn254Tyr)
16g.56975126A>CCA396004127CETPc.956A>C (p.Asn319Thr)
c.776A>C (p.Asn259Thr)
c.761A>C (p.Asn254Thr)
16g.56975126A>GCA396004128CETPc.956A>G (p.Asn319Ser)
c.776A>G (p.Asn259Ser)
c.761A>G (p.Asn254Ser)
16g.56975126A>TCA396004129CETPc.956A>T (p.Asn319Ile)
c.776A>T (p.Asn259Ile)
c.761A>T (p.Asn254Ile)
16g.56975127C>ACA8071167CETPc.957C>A (p.Asn319Lys)
c.777C>A (p.Asn259Lys)
c.762C>A (p.Asn254Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975127C=CA2224400095CETPc.957C= (p.Asn319=)
c.777C= (p.Asn259=)
c.762C= (p.Asn254=)
16g.56975127C>GCA396004130CETPc.957C>G (p.Asn319Lys)
c.777C>G (p.Asn259Lys)
c.762C>G (p.Asn254Lys)
16g.56975127C>TCA495620076CETPc.957C>T (p.Asn319=)
c.777C>T (p.Asn259=)
c.762C>T (p.Asn254=)
16g.56975128A>CCA396004131CETPc.958A>C (p.Thr320Pro)
c.778A>C (p.Thr260Pro)
c.763A>C (p.Thr255Pro)
16g.56975128A>GCA396004132CETPc.958A>G (p.Thr320Ala)
c.778A>G (p.Thr260Ala)
c.763A>G (p.Thr255Ala)
16g.56975128A>TCA396004133CETPc.958A>T (p.Thr320Ser)
c.778A>T (p.Thr260Ser)
c.763A>T (p.Thr255Ser)
16g.56975129C>ACA396004134CETPc.959C>A (p.Thr320Asn)
c.779C>A (p.Thr260Asn)
c.764C>A (p.Thr255Asn)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56975129C=CA2224400096CETPc.959C= (p.Thr320=)
c.779C= (p.Thr260=)
c.764C= (p.Thr255=)
16g.56975129C>GCA396004135CETPc.959C>G (p.Thr320Ser)
c.779C>G (p.Thr260Ser)
c.764C>G (p.Thr255Ser)
16g.56975129C>TCA396004136CETPc.959C>T (p.Thr320Ile)
c.779C>T (p.Thr260Ile)
c.764C>T (p.Thr255Ile)
 dbSNP gnomAD v2 gnomAD v4
16g.56975130C>ACA495620077CETPc.960C>A (p.Thr320=)
c.780C>A (p.Thr260=)
c.765C>A (p.Thr255=)
16g.56975130C=CA2224400097CETPc.960C= (p.Thr320=)
c.780C= (p.Thr260=)
c.765C= (p.Thr255=)
16g.56975130C>GCA495620078CETPc.960C>G (p.Thr320=)
c.780C>G (p.Thr260=)
c.765C>G (p.Thr255=)
16g.56975130C>TCA495620079CETPc.960C>T (p.Thr320=)
c.780C>T (p.Thr260=)
c.765C>T (p.Thr255=)
 dbSNP gnomAD v4
16g.56975131A>CCA396004139CETPc.961A>C (p.Asn321His)
c.781A>C (p.Asn261His)
c.766A>C (p.Asn256His)
16g.56975131A>GCA396004138CETPc.961A>G (p.Asn321Asp)
c.781A>G (p.Asn261Asp)
c.766A>G (p.Asn256Asp)
16g.56975131A>TCA396004137CETPc.961A>T (p.Asn321Tyr)
c.781A>T (p.Asn261Tyr)
c.766A>T (p.Asn256Tyr)
16g.56975132A=CA2224400098CETPc.962A= (p.Asn321=)
c.782A= (p.Asn261=)
c.767A= (p.Asn256=)
16g.56975132A>CCA396004140CETPc.962A>C (p.Asn321Thr)
c.782A>C (p.Asn261Thr)
c.767A>C (p.Asn256Thr)
 gnomAD v4
16g.56975132A>GCA396004141CETPc.962A>G (p.Asn321Ser)
c.782A>G (p.Asn261Ser)
c.767A>G (p.Asn256Ser)
 dbSNP
16g.56975132A>TCA396004142CETPc.962A>T (p.Asn321Ile)
c.782A>T (p.Asn261Ile)
c.767A>T (p.Asn256Ile)
16g.56975133C>ACA396004143CETPc.963C>A (p.Asn321Lys)
c.783C>A (p.Asn261Lys)
c.768C>A (p.Asn256Lys)
 dbSNP gnomAD v2 gnomAD v4
16g.56975133C=CA2224400099CETPc.963C= (p.Asn321=)
c.783C= (p.Asn261=)
c.768C= (p.Asn256=)
16g.56975133C>GCA396004144CETPc.963C>G (p.Asn321Lys)
c.783C>G (p.Asn261Lys)
c.768C>G (p.Asn256Lys)
16g.56975133C>TCA495620081CETPc.963C>T (p.Asn321=)
c.783C>T (p.Asn261=)
c.768C>T (p.Asn256=)
 dbSNP gnomAD v3 gnomAD v4
16g.56975134C>ACA281525411CETPc.964C>A (p.Gln322Lys)
c.784C>A (p.Gln262Lys)
c.769C>A (p.Gln257Lys)
 dbSNP
16g.56975134C=CA2224400100CETPc.964C= (p.Gln322=)
c.784C= (p.Gln262=)
c.769C= (p.Gln257=)
16g.56975134C>GCA396004145CETPc.964C>G (p.Gln322Glu)
c.784C>G (p.Gln262Glu)
c.769C>G (p.Gln257Glu)
 gnomAD v4
16g.56975134C>TCA8071168CETPc.964C>T (p.Gln322Ter)
c.784C>T (p.Gln262Ter)
c.769C>T (p.Gln257Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975135A>CCA396004146CETPc.965A>C (p.Gln322Pro)
c.785A>C (p.Gln262Pro)
c.770A>C (p.Gln257Pro)
16g.56975135A>GCA396004147CETPc.965A>G (p.Gln322Arg)
c.785A>G (p.Gln262Arg)
c.770A>G (p.Gln257Arg)
16g.56975135A>TCA396004148CETPc.965A>T (p.Gln322Leu)
c.785A>T (p.Gln262Leu)
c.770A>T (p.Gln257Leu)
16g.56975135_56975136delCA2576002911CETPc.965_966del (p.Gln322ArgfsTer?)
c.785_786del (p.Gln262ArgfsTer?)
c.770_771del (p.Gln257ArgfsTer?)
16g.56975136G>ACA495620082CETPc.966G>A (p.Gln322=)
c.786G>A (p.Gln262=)
c.771G>A (p.Gln257=)
16g.56975136G>CCA396004149CETPc.966G>C (p.Gln322His)
c.786G>C (p.Gln262His)
c.771G>C (p.Gln257His)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56975136G=CA2224400101CETPc.966G= (p.Gln322=)
c.786G= (p.Gln262=)
c.771G= (p.Gln257=)
16g.56975136G>TCA396004150CETPc.966G>T (p.Gln322His)
c.786G>T (p.Gln262His)
c.771G>T (p.Gln257His)
16g.56975137delCA2633389168CETPc.967del (p.Glu323LysfsTer?)
c.787del (p.Glu263LysfsTer?)
c.772del (p.Glu258LysfsTer?)
 gnomAD v4
16g.56975137G>ACA396004151CETPc.967G>A (p.Glu323Lys)
c.787G>A (p.Glu263Lys)
c.772G>A (p.Glu258Lys)
 dbSNP COSMIC
16g.56975137G>CCA396004152CETPc.967G>C (p.Glu323Gln)
c.787G>C (p.Glu263Gln)
c.772G>C (p.Glu258Gln)
16g.56975137G=CA2224400102CETPc.967G= (p.Glu323=)
c.787G= (p.Glu263=)
c.772G= (p.Glu258=)
16g.56975137G>TCA8071169CETPc.967G>T (p.Glu323Ter)
c.787G>T (p.Glu263Ter)
c.772G>T (p.Glu258Ter)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56975138A=CA2224400103CETPc.968A= (p.Glu323=)
c.788A= (p.Glu263=)
c.773A= (p.Glu258=)
16g.56975138A>CCA396004153CETPc.968A>C (p.Glu323Ala)
c.788A>C (p.Glu263Ala)
c.773A>C (p.Glu258Ala)
16g.56975138A>GCA396004154CETPc.968A>G (p.Glu323Gly)
c.788A>G (p.Glu263Gly)
c.773A>G (p.Glu258Gly)
 dbSNP gnomAD v4
16g.56975138A>TCA396004155CETPc.968A>T (p.Glu323Val)
c.788A>T (p.Glu263Val)
c.773A>T (p.Glu258Val)
16g.56975139A>CCA396004156CETPc.969A>C (p.Glu323Asp)
c.789A>C (p.Glu263Asp)
c.774A>C (p.Glu258Asp)
 COSMIC
16g.56975139A>GCA495620083CETPc.969A>G (p.Glu323=)
c.789A>G (p.Glu263=)
c.774A>G (p.Glu258=)
16g.56975139A>TCA396004157CETPc.969A>T (p.Glu323Asp)
c.789A>T (p.Glu263Asp)
c.774A>T (p.Glu258Asp)
16g.56975140A>CCA396004158CETPc.970A>C (p.Ile324Leu)
c.790A>C (p.Ile264Leu)
c.775A>C (p.Ile259Leu)
16g.56975140A>GCA396004159CETPc.970A>G (p.Ile324Val)
c.790A>G (p.Ile264Val)
c.775A>G (p.Ile259Val)
16g.56975140A>TCA396004160CETPc.970A>T (p.Ile324Phe)
c.790A>T (p.Ile264Phe)
c.775A>T (p.Ile259Phe)
16g.56975141T>ACA396004161CETPc.971T>A (p.Ile324Asn)
c.791T>A (p.Ile264Asn)
c.776T>A (p.Ile259Asn)
16g.56975141T>CCA396004162CETPc.971T>C (p.Ile324Thr)
c.791T>C (p.Ile264Thr)
c.776T>C (p.Ile259Thr)
16g.56975141T>GCA396004163CETPc.971T>G (p.Ile324Ser)
c.791T>G (p.Ile264Ser)
c.776T>G (p.Ile259Ser)
16g.56975142C>ACA8071170CETPc.972C>A (p.Ile324=)
c.792C>A (p.Ile264=)
c.777C>A (p.Ile259=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56975142C=CA2224400104CETPc.972C= (p.Ile324=)
c.792C= (p.Ile264=)
c.777C= (p.Ile259=)
16g.56975142C>GCA396004164CETPc.972C>G (p.Ile324Met)
c.792C>G (p.Ile264Met)
c.777C>G (p.Ile259Met)
16g.56975142C>TCA495620084CETPc.972C>T (p.Ile324=)
c.792C>T (p.Ile264=)
c.777C>T (p.Ile259=)
16g.56975143T>ACA396004165CETPc.973T>A (p.Phe325Ile)
c.793T>A (p.Phe265Ile)
c.778T>A (p.Phe260Ile)
16g.56975143T>CCA396004167CETPc.973T>C (p.Phe325Leu)
c.793T>C (p.Phe265Leu)
c.778T>C (p.Phe260Leu)
16g.56975143T>GCA396004166CETPc.973T>G (p.Phe325Val)
c.793T>G (p.Phe265Val)
c.778T>G (p.Phe260Val)
16g.56975144T>ACA396004168CETPc.974T>A (p.Phe325Tyr)
c.794T>A (p.Phe265Tyr)
c.779T>A (p.Phe260Tyr)
16g.56975144T>CCA396004169CETPc.974T>C (p.Phe325Ser)
c.794T>C (p.Phe265Ser)
c.779T>C (p.Phe260Ser)
16g.56975144T>GCA396004170CETPc.974T>G (p.Phe325Cys)
c.794T>G (p.Phe265Cys)
c.779T>G (p.Phe260Cys)
16g.56975145C>ACA396004171CETPc.975C>A (p.Phe325Leu)
c.795C>A (p.Phe265Leu)
c.780C>A (p.Phe260Leu)
16g.56975145C>GCA396004172CETPc.975C>G (p.Phe325Leu)
c.795C>G (p.Phe265Leu)
c.780C>G (p.Phe260Leu)
16g.56975145C>TCA495620085CETPc.975C>T (p.Phe325=)
c.795C>T (p.Phe265=)
c.780C>T (p.Phe260=)
16g.56975146C>ACA396004173CETPc.976C>A (p.Gln326Lys)
c.796C>A (p.Gln266Lys)
c.781C>A (p.Gln261Lys)
16g.56975146C=CA2224400105CETPc.976C= (p.Gln326=)
c.796C= (p.Gln266=)
c.781C= (p.Gln261=)
16g.56975146C>GCA396004174CETPc.976C>G (p.Gln326Glu)
c.796C>G (p.Gln266Glu)
c.781C>G (p.Gln261Glu)
16g.56975146C>TCA396004175CETPc.976C>T (p.Gln326Ter)
c.796C>T (p.Gln266Ter)
c.781C>T (p.Gln261Ter)
 dbSNP gnomAD v2 gnomAD v4
16g.56975147A>CCA396004176CETPc.977A>C (p.Gln326Pro)
c.797A>C (p.Gln266Pro)
c.782A>C (p.Gln261Pro)
16g.56975147A>GCA396004177CETPc.977A>G (p.Gln326Arg)
c.797A>G (p.Gln266Arg)
c.782A>G (p.Gln261Arg)
16g.56975147A>TCA396004178CETPc.977A>T (p.Gln326Leu)
c.797A>T (p.Gln266Leu)
c.782A>T (p.Gln261Leu)
16g.56975148delCA2807162148CETPc.978del (p.Glu327ArgfsTer?)
c.798del (p.Glu267ArgfsTer?)
c.783del (p.Glu262ArgfsTer?)
16g.56975148A>CCA396004179CETPc.978A>C (p.Gln326His)
c.798A>C (p.Gln266His)
c.783A>C (p.Gln261His)
16g.56975148A>GCA495620086CETPc.978A>G (p.Gln326=)
c.798A>G (p.Gln266=)
c.783A>G (p.Gln261=)
16g.56975148A>TCA396004180CETPc.978A>T (p.Gln326His)
c.798A>T (p.Gln266His)
c.783A>T (p.Gln261His)
16g.56975149G>ACA396004181CETPc.979G>A (p.Glu327Lys)
c.799G>A (p.Glu267Lys)
c.784G>A (p.Glu262Lys)
16g.56975149G>CCA396004183CETPc.979G>C (p.Glu327Gln)
c.799G>C (p.Glu267Gln)
c.784G>C (p.Glu262Gln)
16g.56975149G>TCA396004182CETPc.979G>T (p.Glu327Ter)
c.799G>T (p.Glu267Ter)
c.784G>T (p.Glu262Ter)
16g.56975150A>CCA396004184CETPc.980A>C (p.Glu327Ala)
c.800A>C (p.Glu267Ala)
c.785A>C (p.Glu262Ala)
16g.56975150A>GCA396004185CETPc.980A>G (p.Glu327Gly)
c.800A>G (p.Glu267Gly)
c.785A>G (p.Glu262Gly)
16g.56975150A>TCA396004186CETPc.980A>T (p.Glu327Val)
c.800A>T (p.Glu267Val)
c.785A>T (p.Glu262Val)
16g.56975151G>ACA495620087CETPc.981G>A (p.Glu327=)
c.801G>A (p.Glu267=)
c.786G>A (p.Glu262=)
16g.56975151G>CCA396004187CETPc.981G>C (p.Glu327Asp)
c.801G>C (p.Glu267Asp)
c.786G>C (p.Glu262Asp)
16g.56975151G>TCA396004188CETPc.981G>T (p.Glu327Asp)
c.801G>T (p.Glu267Asp)
c.786G>T (p.Glu262Asp)
 gnomAD v4
16g.56975152G>ACA396004189CETPc.981+1G>A (n.981+1G>A)
c.801+1G>A (n.801+1G>A)
c.786+1G>A (n.786+1G>A)
16g.56975152G>CCA396004190CETPc.981+1G>C (n.981+1G>C)
c.801+1G>C (n.801+1G>C)
c.786+1G>C (n.786+1G>C)
16g.56975152G>TCA396004191CETPc.981+1G>T (n.981+1G>T)
c.801+1G>T (n.801+1G>T)
c.786+1G>T (n.786+1G>T)
16g.56975153T>ACA396004192CETPc.981+2T>A (n.981+2T>A)
c.801+2T>A (n.801+2T>A)
c.786+2T>A (n.786+2T>A)
16g.56975153T>CCA396004193CETPc.981+2T>C (n.981+2T>C)
c.801+2T>C (n.801+2T>C)
c.786+2T>C (n.786+2T>C)
 ClinVar dbSNP gnomAD v4
16g.56975153T>GCA396004194CETPc.981+2T>G (n.981+2T>G)
c.801+2T>G (n.801+2T>G)
c.786+2T>G (n.786+2T>G)
16g.56975157T>ACA2224400107CETPc.981+6T>A (n.981+6T>A)
c.801+6T>A (n.801+6T>A)
c.786+6T>A (n.786+6T>A)
 dbSNP
16g.56975157T>CCA2576002912CETPc.981+6T>C (n.981+6T>C)
c.801+6T>C (n.801+6T>C)
c.786+6T>C (n.786+6T>C)
 gnomAD v4
16g.56975157T=CA2224400106CETPc.981+6T= (n.981+6T=)
c.801+6T= (n.801+6T=)
c.786+6T= (n.786+6T=)
16g.56975158G>ACA622342476CETPc.981+7G>A (n.981+7G>A)
c.801+7G>A (n.801+7G>A)
c.786+7G>A (n.786+7G>A)
 dbSNP gnomAD v2 gnomAD v4
16g.56975158G=CA2224400108CETPc.981+7G= (n.981+7G=)
c.801+7G= (n.801+7G=)
c.786+7G= (n.786+7G=)
16g.56975158G>TCA8071171CETPc.981+7G>T (n.981+7G>T)
c.801+7G>T (n.801+7G>T)
c.786+7G>T (n.786+7G>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56975159C>ACA2224400109CETPc.981+8C>A (n.981+8C>A)
c.801+8C>A (n.801+8C>A)
c.786+8C>A (n.786+8C>A)
 dbSNP
16g.56975159C=CA2224400110CETPc.981+8C= (n.981+8C=)
c.801+8C= (n.801+8C=)
c.786+8C= (n.786+8C=)
16g.56975159C>TCA8071172CETPc.981+8C>T (n.981+8C>T)
c.801+8C>T (n.801+8C>T)
c.786+8C>T (n.786+8C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975163dupCA2807162150CETPc.981+12dup (n.981+12dup)
c.801+12dup (n.801+12dup)
c.786+12dup (n.786+12dup)
16g.56975160C>GCA2633389190CETPc.981+9C>G (n.981+9C>G)
c.801+9C>G (n.801+9C>G)
c.786+9C>G (n.786+9C>G)
 gnomAD v4
16g.56975162C=CA2224400111CETPc.981+11C= (n.981+11C=)
c.801+11C= (n.801+11C=)
c.786+11C= (n.786+11C=)
16g.56975162C>TCA622342481CETPc.981+11C>T (n.981+11C>T)
c.801+11C>T (n.801+11C>T)
c.786+11C>T (n.786+11C>T)
 dbSNP gnomAD v2 gnomAD v4
16g.56975163C>TCA2633389193CETPc.981+12C>T (n.981+12C>T)
c.801+12C>T (n.801+12C>T)
c.786+12C>T (n.786+12C>T)
 gnomAD v4
16g.56975164T>CCA2224400113CETPc.981+13T>C (n.981+13T>C)
c.801+13T>C (n.801+13T>C)
c.786+13T>C (n.786+13T>C)
 dbSNP gnomAD v4
16g.56975164T>GCA2633389195CETPc.981+13T>G (n.981+13T>G)
c.801+13T>G (n.801+13T>G)
c.786+13T>G (n.786+13T>G)
 gnomAD v4
16g.56975164T=CA2224400112CETPc.981+13T= (n.981+13T=)
c.801+13T= (n.801+13T=)
c.786+13T= (n.786+13T=)
16g.56975165G>ACA2224400115CETPc.981+14G>A (n.981+14G>A)
c.801+14G>A (n.801+14G>A)
c.786+14G>A (n.786+14G>A)
 dbSNP
16g.56975165G=CA2224400114CETPc.981+14G= (n.981+14G=)
c.801+14G= (n.801+14G=)
c.786+14G= (n.786+14G=)
16g.56975166C>ACA622342482CETPc.981+15C>A (n.981+15C>A)
c.801+15C>A (n.801+15C>A)
c.786+15C>A (n.786+15C>A)
 dbSNP gnomAD v2 gnomAD v4
16g.56975166C=CA2224400116CETPc.981+15C= (n.981+15C=)
c.801+15C= (n.801+15C=)
c.786+15C= (n.786+15C=)
16g.56975166C>TCA2224400117CETPc.981+15C>T (n.981+15C>T)
c.801+15C>T (n.801+15C>T)
c.786+15C>T (n.786+15C>T)
 dbSNP
16g.56975167C>ACA622342483CETPc.981+16C>A (n.981+16C>A)
c.801+16C>A (n.801+16C>A)
c.786+16C>A (n.786+16C>A)
 dbSNP gnomAD v2 gnomAD v4
16g.56975167C=CA2224400118CETPc.981+16C= (n.981+16C=)
c.801+16C= (n.801+16C=)
c.786+16C= (n.786+16C=)
16g.56975167C>GCA8071173CETPc.981+16C>G (n.981+16C>G)
c.801+16C>G (n.801+16C>G)
c.786+16C>G (n.786+16C>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56975167C>TCA2633389204CETPc.981+16C>T (n.981+16C>T)
c.801+16C>T (n.801+16C>T)
c.786+16C>T (n.786+16C>T)
 gnomAD v4
16g.56975168C=CA2224400119CETPc.981+17C= (n.981+17C=)
c.801+17C= (n.801+17C=)
c.786+17C= (n.786+17C=)
16g.56975168C>GCA2633389207CETPc.981+17C>G (n.981+17C>G)
c.801+17C>G (n.801+17C>G)
c.786+17C>G (n.786+17C>G)
 gnomAD v4
16g.56975168C>TCA2224400120CETPc.981+17C>T (n.981+17C>T)
c.801+17C>T (n.801+17C>T)
c.786+17C>T (n.786+17C>T)
 dbSNP gnomAD v4
16g.56975169C=CA2224400121CETPc.981+18C= (n.981+18C=)
c.801+18C= (n.801+18C=)
c.786+18C= (n.786+18C=)
16g.56975169C>GCA8071174CETPc.981+18C>G (n.981+18C>G)
c.801+18C>G (n.801+18C>G)
c.786+18C>G (n.786+18C>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56975170T>CCA8071175CETPc.981+19T>C (n.981+19T>C)
c.801+19T>C (n.801+19T>C)
c.786+19T>C (n.786+19T>C)
 dbSNP ExAC gnomAD v3 gnomAD v4
16g.56975170T=CA2224400122CETPc.981+19T= (n.981+19T=)
c.801+19T= (n.801+19T=)
c.786+19T= (n.786+19T=)
16g.56975171G>ACA8071176CETPc.981+20G>A (n.981+20G>A)
c.801+20G>A (n.801+20G>A)
c.786+20G>A (n.786+20G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975171G=CA2224400123CETPc.981+20G= (n.981+20G=)
c.801+20G= (n.801+20G=)
c.786+20G= (n.786+20G=)
16g.56975173G>ACA2633389212CETPc.981+22G>A (n.981+22G>A)
c.801+22G>A (n.801+22G>A)
c.786+22G>A (n.786+22G>A)
 gnomAD v4
16g.56975173G>TCA2807162151CETPc.981+22G>T (n.981+22G>T)
c.801+22G>T (n.801+22G>T)
c.786+22G>T (n.786+22G>T)
16g.56975174T>CCA8071177CETPc.981+23T>C (n.981+23T>C)
c.801+23T>C (n.801+23T>C)
c.786+23T>C (n.786+23T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975174T>GCA2633389213CETPc.981+23T>G (n.981+23T>G)
c.801+23T>G (n.801+23T>G)
c.786+23T>G (n.786+23T>G)
 gnomAD v4
16g.56975174T=CA2224400124CETPc.981+23T= (n.981+23T=)
c.801+23T= (n.801+23T=)
c.786+23T= (n.786+23T=)
16g.56975175G>TCA2807162152CETPc.981+24G>T (n.981+24G>T)
c.801+24G>T (n.801+24G>T)
c.786+24G>T (n.786+24G>T)
16g.56975176G>ACA2633389214CETPc.981+25G>A (n.981+25G>A)
c.801+25G>A (n.801+25G>A)
c.786+25G>A (n.786+25G>A)
 gnomAD v4
16g.56975177G>ACA2633389215CETPc.981+26G>A (n.981+26G>A)
c.801+26G>A (n.801+26G>A)
c.786+26G>A (n.786+26G>A)
 gnomAD v4
16g.56975177G=CA2224400125CETPc.981+26G= (n.981+26G=)
c.801+26G= (n.801+26G=)
c.786+26G= (n.786+26G=)
16g.56975177G>TCA2224400126CETPc.981+26G>T (n.981+26G>T)
c.801+26G>T (n.801+26G>T)
c.786+26G>T (n.786+26G>T)
 dbSNP
16g.56975178G>ACA2633389218CETPc.981+27G>A (n.981+27G>A)
c.801+27G>A (n.801+27G>A)
c.786+27G>A (n.786+27G>A)
 gnomAD v4
16g.56975178G=CA2224400127CETPc.981+27G= (n.981+27G=)
c.801+27G= (n.801+27G=)
c.786+27G= (n.786+27G=)
16g.56975178G>TCA622342494CETPc.981+27G>T (n.981+27G>T)
c.801+27G>T (n.801+27G>T)
c.786+27G>T (n.786+27G>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56975179T>ACA2633389220CETPc.981+28T>A (n.981+28T>A)
c.801+28T>A (n.801+28T>A)
c.786+28T>A (n.786+28T>A)
 gnomAD v4
16g.56975181delCA2576002913CETPc.981+30del (n.981+30del)
c.801+30del (n.801+30del)
c.786+30del (n.786+30del)
16g.56975180T>GCA2807162153CETPc.981+29T>G (n.981+29T>G)
c.801+29T>G (n.801+29T>G)
c.786+29T>G (n.786+29T>G)
16g.56975182A>CCA2633389222CETPc.981+31A>C (n.981+31A>C)
c.801+31A>C (n.801+31A>C)
c.786+31A>C (n.786+31A>C)
 gnomAD v4
16g.56975182A>GCA2732294081CETPc.981+31A>G (n.981+31A>G)
c.801+31A>G (n.801+31A>G)
c.786+31A>G (n.786+31A>G)
 dbSNP
16g.56975184C>ACA2633389223CETPc.981+33C>A (n.981+33C>A)
c.801+33C>A (n.801+33C>A)
c.786+33C>A (n.786+33C>A)
 gnomAD v4
16g.56975185T>CCA2224400129CETPc.981+34T>C (n.981+34T>C)
c.801+34T>C (n.801+34T>C)
c.786+34T>C (n.786+34T>C)
 dbSNP
16g.56975185T=CA2224400128CETPc.981+34T= (n.981+34T=)
c.801+34T= (n.801+34T=)
c.786+34T= (n.786+34T=)
16g.56975186C>ACA2633389227CETPc.981+35C>A (n.981+35C>A)
c.801+35C>A (n.801+35C>A)
c.786+35C>A (n.786+35C>A)
 gnomAD v4
16g.56975186C=CA2224400130CETPc.981+35C= (n.981+35C=)
c.801+35C= (n.801+35C=)
c.786+35C= (n.786+35C=)
16g.56975186C>TCA622342496CETPc.981+35C>T (n.981+35C>T)
c.801+35C>T (n.801+35C>T)
c.786+35C>T (n.786+35C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56975188C>ACA2633389230CETPc.981+37C>A (n.981+37C>A)
c.801+37C>A (n.801+37C>A)
c.786+37C>A (n.786+37C>A)
 gnomAD v4
16g.56975188C=CA2224400131CETPc.981+37C= (n.981+37C=)
c.801+37C= (n.801+37C=)
c.786+37C= (n.786+37C=)
16g.56975188C>TCA8071178CETPc.981+37C>T (n.981+37C>T)
c.801+37C>T (n.801+37C>T)
c.786+37C>T (n.786+37C>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975189G>ACA8071179CETPc.981+38G>A (n.981+38G>A)
c.801+38G>A (n.801+38G>A)
c.786+38G>A (n.786+38G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975189G>CCA2633389235CETPc.981+38G>C (n.981+38G>C)
c.801+38G>C (n.801+38G>C)
c.786+38G>C (n.786+38G>C)
 gnomAD v4
16g.56975189G=CA2224400132CETPc.981+38G= (n.981+38G=)
c.801+38G= (n.801+38G=)
c.786+38G= (n.786+38G=)
16g.56975190T>CCA2732294084CETPc.981+39T>C (n.981+39T>C)
c.801+39T>C (n.801+39T>C)
c.786+39T>C (n.786+39T>C)
 dbSNP
16g.56975191A=CA2224400133CETPc.981+40A= (n.981+40A=)
c.801+40A= (n.801+40A=)
c.786+40A= (n.786+40A=)
16g.56975191A>CCA2224400134CETPc.981+40A>C (n.981+40A>C)
c.801+40A>C (n.801+40A>C)
c.786+40A>C (n.786+40A>C)
 dbSNP
16g.56975192C>ACA2633389237CETPc.981+41C>A (n.981+41C>A)
c.801+41C>A (n.801+41C>A)
c.786+41C>A (n.786+41C>A)
 gnomAD v4
16g.56975192C>TCA2633389239CETPc.981+41C>T (n.981+41C>T)
c.801+41C>T (n.801+41C>T)
c.786+41C>T (n.786+41C>T)
 gnomAD v4
16g.56975193C>ACA2633389241CETPc.981+42C>A (n.981+42C>A)
c.801+42C>A (n.801+42C>A)
c.786+42C>A (n.786+42C>A)
 gnomAD v4
16g.56975193C=CA2224400135CETPc.981+42C= (n.981+42C=)
c.801+42C= (n.801+42C=)
c.786+42C= (n.786+42C=)
16g.56975193C>TCA281525473CETPc.981+42C>T (n.981+42C>T)
c.801+42C>T (n.801+42C>T)
c.786+42C>T (n.786+42C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56975194C>ACA2633389243CETPc.981+43C>A (n.981+43C>A)
c.801+43C>A (n.801+43C>A)
c.786+43C>A (n.786+43C>A)
 gnomAD v4
16g.56975194C=CA2224400136CETPc.981+43C= (n.981+43C=)
c.801+43C= (n.801+43C=)
c.786+43C= (n.786+43C=)
16g.56975194C>GCA8071180CETPc.981+43C>G (n.981+43C>G)
c.801+43C>G (n.801+43C>G)
c.786+43C>G (n.786+43C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975194_56975195insAGAGCA2807162154CETPc.981+43_981+44insAGAG (n.981+43_981+44insAGAG)
c.801+43_801+44insAGAG (n.801+43_801+44insAGAG)
c.786+43_786+44insAGAG (n.786+43_786+44insAGAG)
16g.56975195C>ACA2633389246CETPc.981+44C>A (n.981+44C>A)
c.801+44C>A (n.801+44C>A)
c.786+44C>A (n.786+44C>A)
 gnomAD v4
16g.56975195C=CA2224400137CETPc.981+44C= (n.981+44C=)
c.801+44C= (n.801+44C=)
c.786+44C= (n.786+44C=)
16g.56975195C>TCA2224400138CETPc.981+44C>T (n.981+44C>T)
c.801+44C>T (n.801+44C>T)
c.786+44C>T (n.786+44C>T)
 dbSNP gnomAD v4
16g.56975196A=CA2224400139CETPc.981+45A= (n.981+45A=)
c.801+45A= (n.801+45A=)
c.786+45A= (n.786+45A=)
16g.56975196A>GCA8071181CETPc.981+45A>G (n.981+45A>G)
c.801+45A>G (n.801+45A>G)
c.786+45A>G (n.786+45A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.56975196_56975197insGGCA2807162155CETPc.981+45_981+46insGG (n.981+45_981+46insGG)
c.801+45_801+46insGG (n.801+45_801+46insGG)
c.786+45_786+46insGG (n.786+45_786+46insGG)
16g.56975197A=CA2224400140CETPc.981+46A= (n.981+46A=)
c.801+46A= (n.801+46A=)
c.786+46A= (n.786+46A=)
16g.56975197A>GCA8071182CETPc.981+46A>G (n.981+46A>G)
c.801+46A>G (n.801+46A>G)
c.786+46A>G (n.786+46A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.56975197A>TCA495620088CETPc.981+46A>T (n.981+46A>T)
c.801+46A>T (n.801+46A>T)
c.786+46A>T (n.786+46A>T)
16g.56975198T>ACA2807162156CETPc.981+47T>A (n.981+47T>A)
c.801+47T>A (n.801+47T>A)
c.786+47T>A (n.786+47T>A)
16g.56975198T>CCA2224400142CETPc.981+47T>C (n.981+47T>C)
c.801+47T>C (n.801+47T>C)
c.786+47T>C (n.786+47T>C)
 dbSNP gnomAD v4
16g.56975198T=CA2224400141CETPc.981+47T= (n.981+47T=)
c.801+47T= (n.801+47T=)
c.786+47T= (n.786+47T=)
16g.56975199C>ACA2633389250CETPc.981+48C>A (n.981+48C>A)
c.801+48C>A (n.801+48C>A)
c.786+48C>A (n.786+48C>A)
 gnomAD v4
16g.56975199C>TCA2633389251CETPc.981+48C>T (n.981+48C>T)
c.801+48C>T (n.801+48C>T)
c.786+48C>T (n.786+48C>T)
 gnomAD v4
16g.56975199_56975200delCA2807162157CETPc.981+48_981+49del (n.981+48_981+49del)
c.801+48_801+49del (n.801+48_801+49del)
c.786+48_786+49del (n.786+48_786+49del)
16g.56975200C>ACA2633389252CETPc.981+49C>A (n.981+49C>A)
c.801+49C>A (n.801+49C>A)
c.786+49C>A (n.786+49C>A)
 gnomAD v4
16g.56975200C>GCA2807162158CETPc.981+49C>G (n.981+49C>G)
c.801+49C>G (n.801+49C>G)
c.786+49C>G (n.786+49C>G)
16g.56975200C>TCA2633389253CETPc.981+49C>T (n.981+49C>T)
c.801+49C>T (n.801+49C>T)
c.786+49C>T (n.786+49C>T)
 gnomAD v4
16g.56975200_56975210delCA2807162159CETPc.981+49_981+59del (n.981+49_981+59del)
c.801+49_801+59del (n.801+49_801+59del)
c.786+49_786+59del (n.786+49_786+59del)
16g.56975203C>ACA2633389254CETPc.981+52C>A (n.981+52C>A)
c.801+52C>A (n.801+52C>A)
c.786+52C>A (n.786+52C>A)
 gnomAD v4
16g.56975203C=CA2224400143CETPc.981+52C= (n.981+52C=)
c.801+52C= (n.801+52C=)
c.786+52C= (n.786+52C=)
16g.56975203C>TCA2224400144CETPc.981+52C>T (n.981+52C>T)
c.801+52C>T (n.801+52C>T)
c.786+52C>T (n.786+52C>T)
 dbSNP
16g.56975203_56975206delCA2807162160CETPc.981+52_981+55del (n.981+52_981+55del)
c.801+52_801+55del (n.801+52_801+55del)
c.786+52_786+55del (n.786+52_786+55del)
16g.56975205C>ACA2633389255CETPc.981+54C>A (n.981+54C>A)
c.801+54C>A (n.801+54C>A)
c.786+54C>A (n.786+54C>A)
 gnomAD v4
16g.56975205C>GCA2633389256CETPc.981+54C>G (n.981+54C>G)
c.801+54C>G (n.801+54C>G)
c.786+54C>G (n.786+54C>G)
 gnomAD v4
16g.56975206dupCA2633389258CETPc.981+55dup (n.981+55dup)
c.801+55dup (n.801+55dup)
c.786+55dup (n.786+55dup)
 gnomAD v4
16g.56975206_56975207insTGAAGCCAGAGCACA2633389259CETPc.981+55_981+56insTGAAGCCAGAGCA (n.981+55_981+56insTGAAGCCAGAGCA)
c.801+55_801+56insTGAAGCCAGAGCA (n.801+55_801+56insTGAAGCCAGAGCA)
c.786+55_786+56insTGAAGCCAGAGCA (n.786+55_786+56insTGAAGCCAGAGCA)
 gnomAD v4
16g.56975207_56975208insAACA2633389260CETPc.981+56_981+57insAA (n.981+56_981+57insAA)
c.801+56_801+57insAA (n.801+56_801+57insAA)
c.786+56_786+57insAA (n.786+56_786+57insAA)
 gnomAD v4
16g.56975208G>ACA2576002914CETPc.981+57G>A (n.981+57G>A)
c.801+57G>A (n.801+57G>A)
c.786+57G>A (n.786+57G>A)
16g.56975208G>TCA2633389262CETPc.981+57G>T (n.981+57G>T)
c.801+57G>T (n.801+57G>T)
c.786+57G>T (n.786+57G>T)
 gnomAD v4
16g.56975209C>ACA2576002915CETPc.981+58C>A (n.981+58C>A)
c.801+58C>A (n.801+58C>A)
c.786+58C>A (n.786+58C>A)
 gnomAD v4
16g.56975209C=CA2224400145CETPc.981+58C= (n.981+58C=)
c.801+58C= (n.801+58C=)
c.786+58C= (n.786+58C=)
16g.56975209C>GCA2807162161CETPc.981+58C>G (n.981+58C>G)
c.801+58C>G (n.801+58C>G)
c.786+58C>G (n.786+58C>G)
16g.56975209C>TCA2224400146CETPc.981+58C>T (n.981+58C>T)
c.801+58C>T (n.801+58C>T)
c.786+58C>T (n.786+58C>T)
 dbSNP
16g.56975210_56975211delCA2633389264CETPc.981+59_981+60del (n.981+59_981+60del)
c.801+59_801+60del (n.801+59_801+60del)
c.786+59_786+60del (n.786+59_786+60del)
 gnomAD v4
16g.56975211T>ACA2807162162CETPc.981+60T>A (n.981+60T>A)
c.801+60T>A (n.801+60T>A)
c.786+60T>A (n.786+60T>A)
16g.56975211T>CCA2633389266CETPc.981+60T>C (n.981+60T>C)
c.801+60T>C (n.801+60T>C)
c.786+60T>C (n.786+60T>C)
 gnomAD v4
16g.56975212C>GCA2633389268CETPc.981+61C>G (n.981+61C>G)
c.801+61C>G (n.801+61C>G)
c.786+61C>G (n.786+61C>G)
 gnomAD v4
16g.56975213A=CA2224400147CETPc.981+62A= (n.981+62A=)
c.801+62A= (n.801+62A=)
c.786+62A= (n.786+62A=)
16g.56975213A>CCA281525500CETPc.981+62A>C (n.981+62A>C)
c.801+62A>C (n.801+62A>C)
c.786+62A>C (n.786+62A>C)
 dbSNP gnomAD v3 gnomAD v4
16g.56975213A>GCA2807162163CETPc.981+62A>G (n.981+62A>G)
c.801+62A>G (n.801+62A>G)
c.786+62A>G (n.786+62A>G)
16g.56975214delCA2633389270CETPc.981+63del (n.981+63del)
c.801+63del (n.801+63del)
c.786+63del (n.786+63del)
 gnomAD v4
16g.56975214A>GCA2633389273CETPc.981+63A>G (n.981+63A>G)
c.801+63A>G (n.801+63A>G)
c.786+63A>G (n.786+63A>G)
 gnomAD v4
16g.56975214A>TCA2807162165CETPc.981+63A>T (n.981+63A>T)
c.801+63A>T (n.801+63A>T)
c.786+63A>T (n.786+63A>T)
16g.56975214_56975218delCA2807162164CETPc.981+63_981+67del (n.981+63_981+67del)
c.801+63_801+67del (n.801+63_801+67del)
c.786+63_786+67del (n.786+63_786+67del)
16g.56975215G>ACA622342503CETPc.981+64G>A (n.981+64G>A)
c.801+64G>A (n.801+64G>A)
c.786+64G>A (n.786+64G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56975215G=CA2224400148CETPc.981+64G= (n.981+64G=)
c.801+64G= (n.801+64G=)
c.786+64G= (n.786+64G=)
16g.56975217G>ACA622342505CETPc.981+66G>A (n.981+66G>A)
c.801+66G>A (n.801+66G>A)
c.786+66G>A (n.786+66G>A)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
16g.56975217G>CCA2633389276CETPc.981+66G>C (n.981+66G>C)
c.801+66G>C (n.801+66G>C)
c.786+66G>C (n.786+66G>C)
 gnomAD v4
16g.56975217G=CA2224400149CETPc.981+66G= (n.981+66G=)
c.801+66G= (n.801+66G=)
c.786+66G= (n.786+66G=)
16g.56975217_56975218insATAACA2807162167CETPc.981+66_981+67insATAA (n.981+66_981+67insATAA)
c.801+66_801+67insATAA (n.801+66_801+67insATAA)
c.786+66_786+67insATAA (n.786+66_786+67insATAA)
16g.56975218C>ACA2576002917CETPc.981+67C>A (n.981+67C>A)
c.801+67C>A (n.801+67C>A)
c.786+67C>A (n.786+67C>A)
 gnomAD v4
16g.56975218C>TCA2576002918CETPc.981+67C>T (n.981+67C>T)
c.801+67C>T (n.801+67C>T)
c.786+67C>T (n.786+67C>T)
 gnomAD v4
16g.56975222dupCA2633389278CETPc.981+71dup (n.981+71dup)
c.801+71dup (n.801+71dup)
c.786+71dup (n.786+71dup)
 gnomAD v4
16g.56975222delCA2576002916CETPc.981+71del (n.981+71del)
c.801+71del (n.801+71del)
c.786+71del (n.786+71del)
 gnomAD v4
16g.56975219C>ACA2224400151CETPc.981+68C>A (n.981+68C>A)
c.801+68C>A (n.801+68C>A)
c.786+68C>A (n.786+68C>A)
 dbSNP gnomAD v4
16g.56975219C=CA2224400150CETPc.981+68C= (n.981+68C=)
c.801+68C= (n.801+68C=)
c.786+68C= (n.786+68C=)
16g.56975220C>ACA2576002919CETPc.981+69C>A (n.981+69C>A)
c.801+69C>A (n.801+69C>A)
c.786+69C>A (n.786+69C>A)
16g.56975220C>GCA2633389281CETPc.981+69C>G (n.981+69C>G)
c.801+69C>G (n.801+69C>G)
c.786+69C>G (n.786+69C>G)
 gnomAD v4
16g.56975220C>TCA2633389282CETPc.981+69C>T (n.981+69C>T)
c.801+69C>T (n.801+69C>T)
c.786+69C>T (n.786+69C>T)
 gnomAD v4
16g.56975221C>ACA2560706577CETPc.981+70C>A (n.981+70C>A)
c.801+70C>A (n.801+70C>A)
c.786+70C>A (n.786+70C>A)
16g.56975222C>ACA2576002920CETPc.981+71C>A (n.981+71C>A)
c.801+71C>A (n.801+71C>A)
c.786+71C>A (n.786+71C>A)
16g.56975226_56975227delCA2633389283CETPc.981+75_981+76del (n.981+75_981+76del)
c.801+75_801+76del (n.801+75_801+76del)
c.786+75_786+76del (n.786+75_786+76del)
 gnomAD v4
16g.56975223A=CA2224400152CETPc.981+72A= (n.981+72A=)
c.801+72A= (n.801+72A=)
c.786+72A= (n.786+72A=)
16g.56975223A>CCA281525502CETPc.981+72A>C (n.981+72A>C)
c.801+72A>C (n.801+72A>C)
c.786+72A>C (n.786+72A>C)
 dbSNP gnomAD v4
16g.56975223A>GCA2633389284CETPc.981+72A>G (n.981+72A>G)
c.801+72A>G (n.801+72A>G)
c.786+72A>G (n.786+72A>G)
 gnomAD v4

Number of alleles fetched