Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.116830247_116836307delinsAGACAGAGGGCCTGAGGCAGGAGATGAGCAAGGATCTGGAGGAGGTGAAGGCCAAGGTGCAGCCCTACCTGGACGACTTCCAGAAGAAGTGGCAGGAGGAGATGGAGCTCTACCGCCAGAAGGTGGAGCCGCTGCGCGCAGAGCTCCAAGAGGGCGCGCGCCAGAAGCTGCACGAGCTGCAAGAGAAGCTGAGCCCACTGGGCGAGGAGATGCGCGACCGCGCGCGCGCCCATGTGGACGCGCTGCGCACGCATCTGGCCCCCTACAGCGACGAGCTGCGCCAGCGCTTGGCCGCGCGCCTTGAGGCTCTCAAGGAGAACGGCGGCGCCAGACTGGCCGAGTACCACGCCAAGGCCACCGAGCATCTGAGCACGCTCAGCGAGAAGGCCAAGCCCGCGCTCGAGGACCTCCGCCAAGGCCTGCTGCCCGTGCTGGAGAGCTTCAAGGTCAGCTTCCTGAGCGCTCTCGAGGAGTACACTAAGAAGCTCAACACCCAGTGAGGCGCCCGCCGCCGCCCCCCTTCCCGGTGCTCAGAATAAACGTTTCCAAAGTGGGAAGCAGCTTCTTTCTTTTGGGAGAATAGAGGGGGGTGCGGGGACATCCGGGGGAGCCCGGGTGGGGCCTTTGGCCCTGGAGCAGGGACTTCCTGCCGGATCTCAACAACTCCGTGCCCAGACTGGACGTCTTAGGGCCAAGATCGACGTTGGAGGACCTGCTGGACGCCTGGCTGCTTACGAGTGAGGGAGTAGAGTCTGCCTTAGCAAGGCTCAAGTAGAAAGGAAGTCACAGCGGACCAGGCAAAGCCACAGACAATCCAAGGCCAGGTGCCCTGAAAGGGGCTCAAACAAGGCCTGCAGCCCTGTCTGAGGCGGGCCAGGAAACAGGGTTGCTTTAGCTGGGAGCAGTGGGTTCCCCGTCCCCAGAGGTGTGTCCGTATAGAGCCTTCTCCAGCCCAGCCGCTGTCAGCGGGGCGGGACGGAGCGGGGCGGCCTCAGGGAGCCAGCCACTGGGATTGGGGTTTGGTCCCGGGTGCAAGTGAAGCGCTTGGAGTTTGCGCCTGTCCTCCTTTACTAATTCAAAAACCTCTCAAACAGACACTTCCCTTTTCTTCTCACAAGGCCAGTATCCCCCTCCCACTACTCCCATCCCGCCCAGAAACAGCCGCGGCTTCCTCAGGCACAGCAGTGGAAGCCAGTCCTCCACCCCCTGCGGCTCCATGCCATGCCACCCCCTCTTTCTGCCAGCCCTGGCAGAAGCTGGCCTGAGTAAGAAAATTCACCACCACCTCTTGCAGGTACATTTTTATTTCCAAGATGCTCTCATATCTGTGCTCTCACTGCATCCTCCCTTCCCCACATCCTGGCTAGATTGCCATCAGACGCAGAGCATGGATGAGGACACTGAAGCCTGGACCTGTGACGTCGCTTGCCCAGTGAACAGCAGGATGGGCTAGGCCGCGCTTTTTAGACCCTGCACCCCTGGCCATCCATGATTATTGAAAAGAGTGCGCGGGTCGGGTGCGGTGGCTCAAGCCTGTAATCCCAGCACTTTGGGAGGCTGAGGTGGGCGTATCACTTCAGGCCAGGAGTTTGAGACCAGCCTGGCCAATATGGTGAAACCCTGTCTCTACTAAAAATACAAAAAAAATCAGCTGGGCATGGTGGCTTGCACCCGTAATCCCAGCTACTAGGAAGGCTGAGGCAGGAGAATCGCTTGAACCTGGGAGGCAGAGGTCACAGTGAGCCGAAATCATGCCACTGCACTCCAGCCTGGGCGACGGAGCAAGACTCCAGCTAAAAAAAAAAAAAAAAAAAAAAGAGTGTGTGGCCTGGCACTCAAGTTCACATGGGTGTGCAGGCATGCCTGTGTATTCTCACATGACCTCCCTGCTCACGGTCCCTCCTTGCACTCATGTCTGAATGTCCCCGCGTGCACGCACATGGCTTCACAGATCTGGGCAGTGCCTTCCCTACCCTCTCTCTGCAGGGCCTTTTGCCCCCTCATGCAGGCCCCTGGATAATCGGCCCCATCCCCATGTCCCCATCTCCAGTGTATCTTAGCTACCCTAGGTAAAGGAGTGGGCTTTTTAGTTCCTAACCTTCCAGAGCTACAACAGCAGTCATCCAGCCAGGTCTGGGTGGGAACATTTTCTAGATACGGGTGCTGAGATCTCTCAGCCCAGAGAGAAGCCCTGGGGAATTTTCAGAGAGAAAGCAGTCTCCAGGTGGGGCTGGATGTACTGATGCCACTGAGATCTGTAAAGGAGTCCCTAACACCTGACATAGGAGTGACAAAACTGTTTTCTGCACCAACTGAGCAGAATACACGCAGCTGACCTGGGCTCAAGGTCTGGCCCTGCCACGTGCTGGCTCTGTGATGCTGGCCAAGTGCCTTCGCCTCTCCGGGCCACAGTTTTTTGATCTGAAGAGTGGAGCCCTACTCAAGCCATCTGCAGCTCTCGGGCTCTCTGACCTGACATCTTTCGGGTGGTGGGGACACAAAGGAAGCAGCCTCTATTGGGAGACCTTGTGCTTCTTTTTGGTCCCAGGACACTGCCCCCCACCACTCCAGTCCGGGTCCCAAGGGCCCAGTCAGCTCAACTGTAATCATGACAACATTGATCAAGCATCTTTACGTGCAGGTGCTGTGCCAAACGGTTCGAACGCTCTCTCATTTCAATCTCACGGCAAACCTACGGTGGAGGGGGTACGGTTGTATCCACTTTACATGTAAGAAACTGAGGCTGATATCAAGTGGTGGAGCCAAGAATAGTGCCTCGTTGCATCTTACTCCAACCTCTAGCCCATCCGGCCTCCTCCCTTCACGTGCGCCTAAGAGGGCTAGGGGGCCTGGATAGGGGAGGTCAGCTCCACAGTTTTGAGTAAACACACACAGTCTCAACTCTGATGACAACTTAAGTGCCAGGCATAGTGGCTGGCATGGGGCACACACTCAAGTCATGTTGTGCAGCACCTAACAGTTTATCAAAGTATCAGCAAACTTATTGTCCTGTTTGACCTTCCGCACAAAGCTGTCAAGGAAGGCAGGGTACGGAGGGTGATTCCTACCTTAGAGATGAAGAAACTGAGGCCCAGAGACTGCCCAGCTACCAGAAGGTGGATAGAGCGCTGGCCTCCATGCCTGCCTGACCTGGAGTCTGTCCAGTGCCCACCCACAGAACAGCCTCGGCCCTTTCCCATGCCCAGACACAGATGGCACACTTGCGACGGCCCACTCATAGCAGCTTCTTGTCCAGCTTTATTGGGAGGCCAGCATGCCTGGAGGGGGGCCAGGCATGAGGTGGGGTAGGAGAGCACTGAGAATACTGTCCCTTTTAAGCAACCTACAGGGGCAGCCCTGGAGATTGCAGGACCCAAGGAGCTCGCAGGATGGATAGGCAGGTGGACTTGGGGTATTGAGGTCTCAGGCAGCCACGGCTGAAGTTGGTCTGACCTCAGGGTCCAAATCCCAGAACTCAGAGAACTTGTCCTTAACGGTGCTCCAGTAGTCTTTCAGGGAACTGAAGCCATCGGTCACCCAGCCCCTAAATCAGTCAGGGGAAGCAACAGAGCAGGGCATGAGAACTCCTCTGTAGGCAACCATGGGACCCACACCCATGTCCCCACTGGACGACACCAGTCAGGACCACACCACCCTCTCAACTTCACTGGACGACAGCCCTGAGACCTCAGGCAGGAATCCCCCACAGCTGCCACCCTGGGAGAAGAGATATCCTTGCAGGAACCCCAGCACAAGTCAAACCCTGCCATCTCCAGGTCACCTCAGATGTTTATGCCCCTGGGCCTGAGGCACAAAGTGACAGGGTGGGGAGATGTGAAAGGTCAAGGCTGTCATTGTTTTCTGTGCAAACAGCACCGCCTGGAGTTGCACAACCTGGTGGCTCTGAGCAGGGTAGGACAGAGGGAGGCAGCCTCTCATTTGGAAAGTCATTGGAGGATTGATTAGTTGTGTGATCTGGGGCAGGTCACCTAATCGCTCTGAGCCTCAATTTTCTCATCTGCAAAGTGAGAAAATAACACCTACCCCAAAGCCGGTTCTGGGGACTAAGAATGTTTATGAACACCTCTGCTATGCCAGCTAATGCCAGTCAGGGTGAGGTGGAGAAGGGAGTAGGGGAGAGGAGAGTACTGATGGGCAGGGGCAGGATGGGAGAGGAAGGACACACTTCTGCTCACACTGGCCCCAGGTCTTAGAACAAAGCAGAAGCACTCACGGGCTTGAATTGGGTCAGGTGGGGCCTCCCAAGGCAAACCCCTAGCCCAGGGGTCCCCAACCCCCAAGTCATAGATAGGTACTGGTCCATGGACTGTTAGGAGCCGGGCTGCACAGCACGAAGTGAGTGGTGGGTGAGTGAGCAATACCGCCTGAGCTCCGCCTCCTGTCAGATCAAGTGGCCTTACATTCTCATAGGAGTGTGAACCCTATTGTGAACTGCACATGCCAGGGATCTAGGTGGAGGGCTCCTTATGAGAATCTAATGCCTGATGATCTGAGGTGGAACAGCTTCATCCCAAAACCATCCCCGCTGGCCCATGGAAAAATTGTCCACCACAAAACTGGTCCCTGGTGCCAAAAAGGCTGAGGACCACTGCTCTAGCCAGACCTTCAGAAAAGGAAAATGGGGCCAGGCGCAGTGGCTCATGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGAGGATCCCCTGAGGTCAGGAATTCAAGACCAACCTGGCCAACATGGTGAAACCCCATCTCTGCTAAAAATACAAAAATTAGCTGGGTGTGGTGGCGCGTGCCTGTAATCCCAGCTACTTGGGAGGCTGAGGCAGGAGAATGGGTTGAACCCGGGAGACGGAGGTTGCAGTGAGCCGAGATGGCACCACTGCACTCCAGCCTAGGTGACAGAGGGAGACTCCATTAAAAAAAAAAGAAGAAGAAAGAAAGAGAGAAAGGAAGAGAGGGAAAGAAAGAAAAAGGAAAGAAAGAAAGAAAGAGAAAGAAAGGAAAGAAAGAAAGAAAGGAAAGAAAGAAAGGAAAGAAAGAAAGGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAAGAAATAGAAAGAGAAAGAAAGGGAAAGGAAAGGAAAATGGAAATGAGGGCTAAAACGGCACGCCCTAGGACTGCTCCGGGGAGAAAGGAGGGACCTGGGAGGAATGCAGTCTCAACTCTGTCATCTCTCCCGCAGCAGCCTGACAAAGGCCCTGTGAGGAAAGAGGAGGCTGAAGAGGCACAGGCCCAGGGGAGGCTGGAGCACCTCCATTCCATTGTTGGGATCTCACCAGGGCAGGGGCGGGTGGGAATGGAGGCAGCTGGCAGGGGGGATGGGGAGGGAGGCCAGCGGGTGTACCTGGCCTGCTGGGCCACCTGGGACTCCTGCACGCTGCTCAGTGCATCCTTGGCGGTCTTGGTGGCGTGCTTCATGTAACCCTGCATGAAGCTGAGAAGGGAGGCATCCTCGGCCTCTGAAGCTCCTGAGGAAAGAGCAGGGCTGAGTGGGGTGGATCGGCCTCTGGACGAGCCCTGGGCTCCTGCTTGACCACCCATTGGGACTGGGATCCCCAAGTTGCCTCCACCCTGCCCCCAGCCCAGTCCCACCAAGTGCTTACGGGCAGAGGCCAGGAGCGCCAGGAGGGCAACAACAAGGAGTACCCGGGGCTGCATGGCACCTCTGTTCCTGCAAGGAAGTGTCCTGTGAGGGGCACCCCAGGTCCCCATGCCTCTGGACCCCTCCCTGGGGAGGTGGCGTGGCCCCTAAGGTAGAACCTTAGCTGGGTCTGCCAGAAGGAGTAGGGGCCGGCTCCCTGCTAATACGGGCTCTCAGAAGGGGGACTGGTGAGGGGCGAGGGATCGAGGCCCAAAGGGAGGTGGGTGGGATGGAGCAGAAAACCCACCAGACTGAACATCAAGGCACCTGCGGTCTGGACTGATCTCCGTCCAGTCCAGCCAACATGCTGTGTGTCTTTGGGTGATTTCTGGCCCTCTCCAGGCCTCAGTTTCCA2697558960 ClinVar
11g.116835994C>ACA382714935APOA1c.618G>T (p.Lys206Asn)
c.552G>T (p.Lys184Asn)
c.291G>T (p.Lys97Asn)
11g.116835994C=CA2002761832APOA1c.618G= (p.Lys206=)
c.552G= (p.Lys184=)
c.291G= (p.Lys97=)
11g.116835994C>GCA382714937APOA1c.618G>C (p.Lys206Asn)
c.552G>C (p.Lys184Asn)
c.291G>C (p.Lys97Asn)
11g.116835994C>TCA229324050APOA1c.618G>A (p.Lys206=)
c.552G>A (p.Lys184=)
c.291G>A (p.Lys97=)
dbSNP gnomAD v4
11g.116835994_116835996delCA2616112002APOA1c.616_618del (p.Lys206del)
c.550_552del (p.Lys184del)
c.289_291del (p.Lys97del)
gnomAD v4
11g.116835995T>ACA382714940APOA1c.617A>T (p.Lys206Met)
c.551A>T (p.Lys184Met)
c.290A>T (p.Lys97Met)
11g.116835995T>CCA6289772APOA1c.617A>G (p.Lys206Arg)
c.551A>G (p.Lys184Arg)
c.290A>G (p.Lys97Arg)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116835995T>GCA382714944APOA1c.617A>C (p.Lys206Thr)
c.551A>C (p.Lys184Thr)
c.290A>C (p.Lys97Thr)
11g.116835995T=CA2002761833APOA1c.617A= (p.Lys206=)
c.551A= (p.Lys184=)
c.290A= (p.Lys97=)
11g.116835996T>ACA382714946APOA1c.616A>T (p.Lys206Ter)
c.550A>T (p.Lys184Ter)
c.289A>T (p.Lys97Ter)
11g.116835996T>CCA382714948APOA1c.616A>G (p.Lys206Glu)
c.550A>G (p.Lys184Glu)
c.289A>G (p.Lys97Glu)
gnomAD v4
11g.116835996T>GCA382714950APOA1c.616A>C (p.Lys206Gln)
c.550A>C (p.Lys184Gln)
c.289A>C (p.Lys97Gln)
11g.116835997G>ACA477048627APOA1c.615C>T (p.Leu205=)
c.549C>T (p.Leu183=)
c.288C>T (p.Leu96=)
11g.116835997G>CCA477048628APOA1c.615C>G (p.Leu205=)
c.549C>G (p.Leu183=)
c.288C>G (p.Leu96=)
11g.116835997G>TCA477048629APOA1c.615C>A (p.Leu205=)
c.549C>A (p.Leu183=)
c.288C>A (p.Leu96=)
gnomAD v4
11g.116836000_116836001delCA2695215579APOA1c.614_615del (p.Leu205GlnfsTer?)
c.548_549del (p.Leu183GlnfsTer?)
c.287_288del (p.Leu96GlnfsTer?)
11g.116835998A>CCA382714952APOA1c.614T>G (p.Leu205Arg)
c.548T>G (p.Leu183Arg)
c.287T>G (p.Leu96Arg)
11g.116835998A>GCA382714953APOA1c.614T>C (p.Leu205Pro)
c.548T>C (p.Leu183Pro)
c.287T>C (p.Leu96Pro)
11g.116835998A>TCA382714954APOA1c.614T>A (p.Leu205His)
c.548T>A (p.Leu183His)
c.287T>A (p.Leu96His)
11g.116835999G>ACA382714955APOA1c.613C>T (p.Leu205Phe)
c.547C>T (p.Leu183Phe)
c.286C>T (p.Leu96Phe)
11g.116835999G>CCA382714956APOA1c.613C>G (p.Leu205Val)
c.547C>G (p.Leu183Val)
c.286C>G (p.Leu96Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116835999G=CA2002761834APOA1c.613C= (p.Leu205=)
c.547C= (p.Leu183=)
c.286C= (p.Leu96=)
11g.116835999G>TCA382714957APOA1c.613C>A (p.Leu205Ile)
c.547C>A (p.Leu183Ile)
c.286C>A (p.Leu96Ile)
11g.116836000A=CA2002761835APOA1c.612T= (p.Ala204=)
c.546T= (p.Ala182=)
c.285T= (p.Ala95=)
11g.116836000A>CCA477048630APOA1c.612T>G (p.Ala204=)
c.546T>G (p.Ala182=)
c.285T>G (p.Ala95=)
11g.116836000A>GCA477048631APOA1c.612T>C (p.Ala204=)
c.546T>C (p.Ala182=)
c.285T>C (p.Ala95=)
dbSNP gnomAD v3 gnomAD v4
11g.116836000A>TCA477048632APOA1c.612T>A (p.Ala204=)
c.546T>A (p.Ala182=)
c.285T>A (p.Ala95=)
gnomAD v4
11g.116836001G>ACA6289773APOA1c.611C>T (p.Ala204Val)
c.545C>T (p.Ala182Val)
c.284C>T (p.Ala95Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836001G>CCA382714962APOA1c.611C>G (p.Ala204Gly)
c.545C>G (p.Ala182Gly)
c.284C>G (p.Ala95Gly)
11g.116836001G=CA2002761836APOA1c.611C= (p.Ala204=)
c.545C= (p.Ala182=)
c.284C= (p.Ala95=)
11g.116836001G>TCA382714959APOA1c.611C>A (p.Ala204Asp)
c.545C>A (p.Ala182Asp)
c.284C>A (p.Ala95Asp)
11g.116836002C>ACA382714965APOA1c.610G>T (p.Ala204Ser)
c.544G>T (p.Ala182Ser)
c.283G>T (p.Ala95Ser)
gnomAD v4
11g.116836002C>GCA382714967APOA1c.610G>C (p.Ala204Pro)
c.544G>C (p.Ala182Pro)
c.283G>C (p.Ala95Pro)
11g.116836002C>TCA382714968APOA1c.610G>A (p.Ala204Thr)
c.544G>A (p.Ala182Thr)
c.283G>A (p.Ala95Thr)
gnomAD v4
11g.116836003C>ACA382714972APOA1c.609G>T (p.Glu203Asp)
c.543G>T (p.Glu181Asp)
c.282G>T (p.Glu94Asp)
11g.116836003C=CA2002761837APOA1c.609G= (p.Glu203=)
c.543G= (p.Glu181=)
c.282G= (p.Glu94=)
11g.116836003C>GCA382714980APOA1c.609G>C (p.Glu203Asp)
c.543G>C (p.Glu181Asp)
c.282G>C (p.Glu94Asp)
gnomAD v4
11g.116836003C>TCA477048633APOA1c.609G>A (p.Glu203=)
c.543G>A (p.Glu181=)
c.282G>A (p.Glu94=)
dbSNP
11g.116836004T>ACA382714988APOA1c.608A>T (p.Glu203Val)
c.542A>T (p.Glu181Val)
c.281A>T (p.Glu94Val)
11g.116836004T>CCA382714986APOA1c.608A>G (p.Glu203Gly)
c.542A>G (p.Glu181Gly)
c.281A>G (p.Glu94Gly)
11g.116836004T>GCA382714983APOA1c.608A>C (p.Glu203Ala)
c.542A>C (p.Glu181Ala)
c.281A>C (p.Glu94Ala)
11g.116836005C>ACA382714991APOA1c.607G>T (p.Glu203Ter)
c.541G>T (p.Glu181Ter)
c.280G>T (p.Glu94Ter)
11g.116836005C=CA2002761838APOA1c.607G= (p.Glu203=)
c.541G= (p.Glu181=)
c.280G= (p.Glu94=)
11g.116836005C>GCA382714993APOA1c.607G>C (p.Glu203Gln)
c.541G>C (p.Glu181Gln)
c.280G>C (p.Glu94Gln)
dbSNP
11g.116836005C>TCA382714995APOA1c.607G>A (p.Glu203Lys)
c.541G>A (p.Glu181Lys)
c.280G>A (p.Glu94Lys)
11g.116836006A>CCA477048634APOA1c.606T>G (p.Leu202=)
c.540T>G (p.Leu180=)
c.279T>G (p.Leu93=)
11g.116836006A>GCA477048635APOA1c.606T>C (p.Leu202=)
c.540T>C (p.Leu180=)
c.279T>C (p.Leu93=)
gnomAD v4
11g.116836006A>TCA477048636APOA1c.606T>A (p.Leu202=)
c.540T>A (p.Leu180=)
c.279T>A (p.Leu93=)
11g.116836007A>CCA382714996APOA1c.605T>G (p.Leu202Arg)
c.539T>G (p.Leu180Arg)
c.278T>G (p.Leu93Arg)
11g.116836007A>GCA382714997APOA1c.605T>C (p.Leu202Pro)
c.539T>C (p.Leu180Pro)
c.278T>C (p.Leu93Pro)
ClinVar dbSNP
11g.116836007A>TCA382714999APOA1c.605T>A (p.Leu202His)
c.539T>A (p.Leu180His)
c.278T>A (p.Leu93His)
11g.116836008G>ACA382715002APOA1c.604C>T (p.Leu202Phe)
c.538C>T (p.Leu180Phe)
c.277C>T (p.Leu93Phe)
gnomAD v4
11g.116836008G>CCA382715005APOA1c.604C>G (p.Leu202Val)
c.538C>G (p.Leu180Val)
c.277C>G (p.Leu93Val)
11g.116836008G>TCA382715003APOA1c.604C>A (p.Leu202Ile)
c.538C>A (p.Leu180Ile)
c.277C>A (p.Leu93Ile)
11g.116836009G>ACA477048638APOA1c.603C>T (p.Arg201=)
c.537C>T (p.Arg179=)
c.276C>T (p.Arg92=)
11g.116836009G>CCA477048639APOA1c.603C>G (p.Arg201=)
c.537C>G (p.Arg179=)
c.276C>G (p.Arg92=)
11g.116836009G>TCA477048637APOA1c.603C>A (p.Arg201=)
c.537C>A (p.Arg179=)
c.276C>A (p.Arg92=)
gnomAD v4
11g.116836010C>ACA382715006APOA1c.602G>T (p.Arg201Leu)
c.536G>T (p.Arg179Leu)
c.275G>T (p.Arg92Leu)
dbSNP gnomAD v3 gnomAD v4
11g.116836010C=CA2002761839APOA1c.602G= (p.Arg201=)
c.536G= (p.Arg179=)
c.275G= (p.Arg92=)
11g.116836010C>GCA382715010APOA1c.602G>C (p.Arg201Pro)
c.536G>C (p.Arg179Pro)
c.275G>C (p.Arg92Pro)
ClinVar dbSNP
11g.116836010C>TCA6289774APOA1c.602G>A (p.Arg201His)
c.536G>A (p.Arg179His)
c.275G>A (p.Arg92His)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836011G>ACA382715012APOA1c.601C>T (p.Arg201Cys)
c.535C>T (p.Arg179Cys)
c.274C>T (p.Arg92Cys)
11g.116836011G>CCA382715013APOA1c.601C>G (p.Arg201Gly)
c.535C>G (p.Arg179Gly)
c.274C>G (p.Arg92Gly)
dbSNP gnomAD v4
11g.116836011G=CA2002761840APOA1c.601C= (p.Arg201=)
c.535C= (p.Arg179=)
c.274C= (p.Arg92=)
11g.116836011G>TCA6289775APOA1c.601C>A (p.Arg201Ser)
c.535C>A (p.Arg179Ser)
c.274C>A (p.Arg92Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836012C>ACA477048642APOA1c.600G>T (p.Ala200=)
c.534G>T (p.Ala178=)
c.273G>T (p.Ala91=)
gnomAD v4
11g.116836012C>GCA477048640APOA1c.600G>C (p.Ala200=)
c.534G>C (p.Ala178=)
c.273G>C (p.Ala91=)
11g.116836012C>TCA477048641APOA1c.600G>A (p.Ala200=)
c.534G>A (p.Ala178=)
c.273G>A (p.Ala91=)
11g.116836013G>ACA382715014APOA1c.599C>T (p.Ala200Val)
c.533C>T (p.Ala178Val)
c.272C>T (p.Ala91Val)
ClinVar gnomAD v4
11g.116836013G>CCA382715016APOA1c.599C>G (p.Ala200Gly)
c.533C>G (p.Ala178Gly)
c.272C>G (p.Ala91Gly)
11g.116836013G>TCA382715015APOA1c.599C>A (p.Ala200Glu)
c.533C>A (p.Ala178Glu)
c.272C>A (p.Ala91Glu)
gnomAD v4
11g.116836014C>ACA382715017APOA1c.598G>T (p.Ala200Ser)
c.532G>T (p.Ala178Ser)
c.271G>T (p.Ala91Ser)
11g.116836014C>GCA382715019APOA1c.598G>C (p.Ala200Pro)
c.532G>C (p.Ala178Pro)
c.271G>C (p.Ala91Pro)
11g.116836014C>TCA382715018APOA1c.598G>A (p.Ala200Thr)
c.532G>A (p.Ala178Thr)
c.271G>A (p.Ala91Thr)
gnomAD v4
11g.116836015G>ACA477048643APOA1c.597C>T (p.Ala199=)
c.531C>T (p.Ala177=)
c.270C>T (p.Ala90=)
dbSNP gnomAD v2 gnomAD v4
11g.116836015G>CCA6289776APOA1c.597C>G (p.Ala199=)
c.531C>G (p.Ala177=)
c.270C>G (p.Ala90=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836015G=CA2002761841APOA1c.597C= (p.Ala199=)
c.531C= (p.Ala177=)
c.270C= (p.Ala90=)
11g.116836015G>TCA477048644APOA1c.597C>A (p.Ala199=)
c.531C>A (p.Ala177=)
c.270C>A (p.Ala90=)
11g.116836020_116836052delCA2695215580APOA1c.565_597del (p.Pro189_Ala199del)
c.499_531del (p.Pro167_Ala177del)
c.238_270del (p.Pro80_Ala90del)
11g.116836016G>ACA382715024APOA1c.596C>T (p.Ala199Val)
c.530C>T (p.Ala177Val)
c.269C>T (p.Ala90Val)
gnomAD v4
11g.116836016G>CCA382715022APOA1c.596C>G (p.Ala199Gly)
c.530C>G (p.Ala177Gly)
c.269C>G (p.Ala90Gly)
11g.116836016G>TCA382715028APOA1c.596C>A (p.Ala199Asp)
c.530C>A (p.Ala177Asp)
c.269C>A (p.Ala90Asp)
gnomAD v4
11g.116836017C>ACA382715031APOA1c.595G>T (p.Ala199Ser)
c.529G>T (p.Ala177Ser)
c.268G>T (p.Ala90Ser)
11g.116836017C=CA2002761842APOA1c.595G= (p.Ala199=)
c.529G= (p.Ala177=)
c.268G= (p.Ala90=)
11g.116836017C>GCA127592APOA1c.595G>C (p.Ala199Pro)
c.529G>C (p.Ala177Pro)
c.268G>C (p.Ala90Pro)
ClinVar dbSNP gnomAD v4
11g.116836017C>TCA6289777APOA1c.595G>A (p.Ala199Thr)
c.529G>A (p.Ala177Thr)
c.268G>A (p.Ala90Thr)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836018C>ACA382715038APOA1c.594G>T (p.Leu198Phe)
c.528G>T (p.Leu176Phe)
c.267G>T (p.Leu89Phe)
gnomAD v4
11g.116836018C=CA2002761843APOA1c.594G= (p.Leu198=)
c.528G= (p.Leu176=)
c.267G= (p.Leu89=)
11g.116836018C>GCA382715040APOA1c.594G>C (p.Leu198Phe)
c.528G>C (p.Leu176Phe)
c.267G>C (p.Leu89Phe)
11g.116836018C>TCA477048645APOA1c.594G>A (p.Leu198=)
c.528G>A (p.Leu176=)
c.267G>A (p.Leu89=)
dbSNP gnomAD v2
11g.116836019A=CA2002761844APOA1c.593T= (p.Leu198=)
c.527T= (p.Leu176=)
c.266T= (p.Leu89=)
11g.116836019A>CCA382715043APOA1c.593T>G (p.Leu198Trp)
c.527T>G (p.Leu176Trp)
c.266T>G (p.Leu89Trp)
11g.116836019A>GCA127589APOA1c.593T>C (p.Leu198Ser)
c.527T>C (p.Leu176Ser)
c.266T>C (p.Leu89Ser)
ClinVar dbSNP
11g.116836019A>TCA382715049APOA1c.593T>A (p.Leu198Ter)
c.527T>A (p.Leu176Ter)
c.266T>A (p.Leu89Ter)
11g.116836020A>CCA382715050APOA1c.592T>G (p.Leu198Val)
c.526T>G (p.Leu176Val)
c.265T>G (p.Leu89Val)
11g.116836020A>GCA477048646APOA1c.592T>C (p.Leu198=)
c.526T>C (p.Leu176=)
c.265T>C (p.Leu89=)
11g.116836020A>TCA382715051APOA1c.592T>A (p.Leu198Met)
c.526T>A (p.Leu176Met)
c.265T>A (p.Leu89Met)
11g.116836020_116836035dupCA2580083483APOA1c.577_592dup (p.Leu198Ter)
c.511_526dup (p.Leu176Ter)
c.250_265dup (p.Leu89Ter)
ClinVar
11g.116836021G>ACA477048647APOA1c.591C>T (p.Arg197=)
c.525C>T (p.Arg175=)
c.264C>T (p.Arg88=)
dbSNP gnomAD v4
11g.116836021G>CCA477048648APOA1c.591C>G (p.Arg197=)
c.525C>G (p.Arg175=)
c.264C>G (p.Arg88=)
11g.116836021G=CA2002761845APOA1c.591C= (p.Arg197=)
c.525C= (p.Arg175=)
c.264C= (p.Arg88=)
11g.116836021G>TCA477048649APOA1c.591C>A (p.Arg197=)
c.525C>A (p.Arg175=)
c.264C>A (p.Arg88=)
11g.116836022C>ACA382715054APOA1c.590G>T (p.Arg197Leu)
c.524G>T (p.Arg175Leu)
c.263G>T (p.Arg88Leu)
gnomAD v4
11g.116836022C=CA2002761846APOA1c.590G= (p.Arg197=)
c.524G= (p.Arg175=)
c.263G= (p.Arg88=)
11g.116836022C>GCA229324102APOA1c.590G>C (p.Arg197Pro)
c.524G>C (p.Arg175Pro)
c.263G>C (p.Arg88Pro)
ClinVar dbSNP
11g.116836022C>TCA382715052APOA1c.590G>A (p.Arg197His)
c.524G>A (p.Arg175His)
c.263G>A (p.Arg88His)
dbSNP gnomAD v4
11g.116836023G>ACA127537APOA1c.589C>T (p.Arg197Cys)
c.523C>T (p.Arg175Cys)
c.262C>T (p.Arg88Cys)
ClinVar dbSNP
11g.116836023G>CCA382715057APOA1c.589C>G (p.Arg197Gly)
c.523C>G (p.Arg175Gly)
c.262C>G (p.Arg88Gly)
11g.116836023G=CA2002761847APOA1c.589C= (p.Arg197=)
c.523C= (p.Arg175=)
c.262C= (p.Arg88=)
11g.116836023G>TCA382715059APOA1c.589C>A (p.Arg197Ser)
c.523C>A (p.Arg175Ser)
c.262C>A (p.Arg88Ser)
dbSNP gnomAD v2 gnomAD v4
11g.116836024C>ACA382715062APOA1c.588G>T (p.Gln196His)
c.522G>T (p.Gln174His)
c.261G>T (p.Gln87His)
11g.116836024C>GCA382715065APOA1c.588G>C (p.Gln196His)
c.522G>C (p.Gln174His)
c.261G>C (p.Gln87His)
11g.116836024C>TCA477048650APOA1c.588G>A (p.Gln196=)
c.522G>A (p.Gln174=)
c.261G>A (p.Gln87=)
11g.116836024_116836025delinsGGCA2695215581APOA1c.587_588delinsCC (p.Gln196Pro)
c.521_522delinsCC (p.Gln174Pro)
c.260_261delinsCC (p.Gln87Pro)
11g.116836025T>ACA382715069APOA1c.587A>T (p.Gln196Leu)
c.521A>T (p.Gln174Leu)
c.260A>T (p.Gln87Leu)
11g.116836025T>CCA382715071APOA1c.587A>G (p.Gln196Arg)
c.521A>G (p.Gln174Arg)
c.260A>G (p.Gln87Arg)
gnomAD v4
11g.116836025T>GCA6289778APOA1c.587A>C (p.Gln196Pro)
c.521A>C (p.Gln174Pro)
c.260A>C (p.Gln87Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836025T=CA2002761848APOA1c.587A= (p.Gln196=)
c.521A= (p.Gln174=)
c.260A= (p.Gln87=)
11g.116836026G>ACA382715072APOA1c.586C>T (p.Gln196Ter)
c.520C>T (p.Gln174Ter)
c.259C>T (p.Gln87Ter)
gnomAD v4
11g.116836026G>CCA382715073APOA1c.586C>G (p.Gln196Glu)
c.520C>G (p.Gln174Glu)
c.259C>G (p.Gln87Glu)
11g.116836026G>TCA382715075APOA1c.586C>A (p.Gln196Lys)
c.520C>A (p.Gln174Lys)
c.259C>A (p.Gln87Lys)
gnomAD v4
11g.116836027G>ACA477048651APOA1c.585C>T (p.Arg195=)
c.519C>T (p.Arg173=)
c.258C>T (p.Arg86=)
dbSNP
11g.116836027G>CCA477048652APOA1c.585C>G (p.Arg195=)
c.519C>G (p.Arg173=)
c.258C>G (p.Arg86=)
gnomAD v4
11g.116836027G=CA2002761849APOA1c.585C= (p.Arg195=)
c.519C= (p.Arg173=)
c.258C= (p.Arg86=)
11g.116836027G>TCA477048653APOA1c.585C>A (p.Arg195=)
c.519C>A (p.Arg173=)
c.258C>A (p.Arg86=)
11g.116836028C>ACA382715080APOA1c.584G>T (p.Arg195Leu)
c.518G>T (p.Arg173Leu)
c.257G>T (p.Arg86Leu)
gnomAD v4
11g.116836028C=CA2002761850APOA1c.584G= (p.Arg195=)
c.518G= (p.Arg173=)
c.257G= (p.Arg86=)
11g.116836028C>GCA382715085APOA1c.584G>C (p.Arg195Pro)
c.518G>C (p.Arg173Pro)
c.257G>C (p.Arg86Pro)
11g.116836028C>TCA382715078APOA1c.584G>A (p.Arg195His)
c.518G>A (p.Arg173His)
c.257G>A (p.Arg86His)
dbSNP
11g.116836029G>ACA382715091APOA1c.583C>T (p.Arg195Cys)
c.517C>T (p.Arg173Cys)
c.256C>T (p.Arg86Cys)
11g.116836029G>CCA382715095APOA1c.583C>G (p.Arg195Gly)
c.517C>G (p.Arg173Gly)
c.256C>G (p.Arg86Gly)
11g.116836029G>TCA382715097APOA1c.583C>A (p.Arg195Ser)
c.517C>A (p.Arg173Ser)
c.256C>A (p.Arg86Ser)
11g.116836030C>ACA477048654APOA1c.582G>T (p.Leu194=)
c.516G>T (p.Leu172=)
c.255G>T (p.Leu85=)
11g.116836030C=CA2002761851APOA1c.582G= (p.Leu194=)
c.516G= (p.Leu172=)
c.255G= (p.Leu85=)
11g.116836030C>GCA6289779APOA1c.582G>C (p.Leu194=)
c.516G>C (p.Leu172=)
c.255G>C (p.Leu85=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836030C>TCA477048655APOA1c.582G>A (p.Leu194=)
c.516G>A (p.Leu172=)
c.255G>A (p.Leu85=)
11g.116836031A>CCA382715102APOA1c.581T>G (p.Leu194Arg)
c.515T>G (p.Leu172Arg)
c.254T>G (p.Leu85Arg)
11g.116836031A>GCA382715107APOA1c.581T>C (p.Leu194Pro)
c.515T>C (p.Leu172Pro)
c.254T>C (p.Leu85Pro)
11g.116836031A>TCA382715109APOA1c.581T>A (p.Leu194Gln)
c.515T>A (p.Leu172Gln)
c.254T>A (p.Leu85Gln)
gnomAD v4
11g.116836032G>ACA477048656APOA1c.580C>T (p.Leu194=)
c.514C>T (p.Leu172=)
c.253C>T (p.Leu85=)
11g.116836032G>CCA382715112APOA1c.580C>G (p.Leu194Val)
c.514C>G (p.Leu172Val)
c.253C>G (p.Leu85Val)
gnomAD v4
11g.116836032G>TCA382715118APOA1c.580C>A (p.Leu194Met)
c.514C>A (p.Leu172Met)
c.253C>A (p.Leu85Met)
11g.116836033C>ACA382715121APOA1c.579G>T (p.Glu193Asp)
c.513G>T (p.Glu171Asp)
c.252G>T (p.Glu84Asp)
11g.116836033C>GCA382715129APOA1c.579G>C (p.Glu193Asp)
c.513G>C (p.Glu171Asp)
c.252G>C (p.Glu84Asp)
11g.116836033C>TCA477048657APOA1c.579G>A (p.Glu193=)
c.513G>A (p.Glu171=)
c.252G>A (p.Glu84=)
11g.116836034T>ACA382715138APOA1c.578A>T (p.Glu193Val)
c.512A>T (p.Glu171Val)
c.251A>T (p.Glu84Val)
11g.116836034T>CCA382715134APOA1c.578A>G (p.Glu193Gly)
c.512A>G (p.Glu171Gly)
c.251A>G (p.Glu84Gly)
11g.116836034T>GCA382715133APOA1c.578A>C (p.Glu193Ala)
c.512A>C (p.Glu171Ala)
c.251A>C (p.Glu84Ala)
11g.116836035C>ACA382715141APOA1c.577G>T (p.Glu193Ter)
c.511G>T (p.Glu171Ter)
c.250G>T (p.Glu84Ter)
ClinVar gnomAD v4
11g.116836035C=CA2002761852APOA1c.577G= (p.Glu193=)
c.511G= (p.Glu171=)
c.250G= (p.Glu84=)
11g.116836035C>GCA382715144APOA1c.577G>C (p.Glu193Gln)
c.511G>C (p.Glu171Gln)
c.250G>C (p.Glu84Gln)
gnomAD v4
11g.116836035C>TCA6289780APOA1c.577G>A (p.Glu193Lys)
c.511G>A (p.Glu171Lys)
c.250G>A (p.Glu84Lys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
11g.116836036G>ACA477048658APOA1c.576C>T (p.Asp192=)
c.510C>T (p.Asp170=)
c.249C>T (p.Asp83=)
gnomAD v4
11g.116836036G>CCA6289781APOA1c.576C>G (p.Asp192Glu)
c.510C>G (p.Asp170Glu)
c.249C>G (p.Asp83Glu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836036G=CA2002761853APOA1c.576C= (p.Asp192=)
c.510C= (p.Asp170=)
c.249C= (p.Asp83=)
11g.116836036G>TCA382715146APOA1c.576C>A (p.Asp192Glu)
c.510C>A (p.Asp170Glu)
c.249C>A (p.Asp83Glu)
11g.116836037T>ACA229324113APOA1c.575A>T (p.Asp192Val)
c.509A>T (p.Asp170Val)
c.248A>T (p.Asp83Val)
dbSNP
11g.116836037T>CCA382715147APOA1c.575A>G (p.Asp192Gly)
c.509A>G (p.Asp170Gly)
c.248A>G (p.Asp83Gly)
11g.116836037T>GCA382715149APOA1c.575A>C (p.Asp192Ala)
c.509A>C (p.Asp170Ala)
c.248A>C (p.Asp83Ala)
11g.116836037T=CA2002761854APOA1c.575A= (p.Asp192=)
c.509A= (p.Asp170=)
c.248A= (p.Asp83=)
11g.116836038C>ACA382715151APOA1c.574G>T (p.Asp192Tyr)
c.508G>T (p.Asp170Tyr)
c.247G>T (p.Asp83Tyr)
11g.116836038C=CA2002761855APOA1c.574G= (p.Asp192=)
c.508G= (p.Asp170=)
c.247G= (p.Asp83=)
11g.116836038C>GCA382715153APOA1c.574G>C (p.Asp192His)
c.508G>C (p.Asp170His)
c.247G>C (p.Asp83His)
dbSNP gnomAD v3 gnomAD v4
11g.116836038C>TCA6289782APOA1c.574G>A (p.Asp192Asn)
c.508G>A (p.Asp170Asn)
c.247G>A (p.Asp83Asn)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836039G>ACA477048659APOA1c.573C>T (p.Ser191=)
c.507C>T (p.Ser169=)
c.246C>T (p.Ser82=)
11g.116836039G>CCA382715156APOA1c.573C>G (p.Ser191Arg)
c.507C>G (p.Ser169Arg)
c.246C>G (p.Ser82Arg)
dbSNP gnomAD v3 gnomAD v4
11g.116836039G=CA2002761856APOA1c.573C= (p.Ser191=)
c.507C= (p.Ser169=)
c.246C= (p.Ser82=)
11g.116836039G>TCA382715157APOA1c.573C>A (p.Ser191Arg)
c.507C>A (p.Ser169Arg)
c.246C>A (p.Ser82Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116836040C>ACA382715162APOA1c.572G>T (p.Ser191Ile)
c.506G>T (p.Ser169Ile)
c.245G>T (p.Ser82Ile)
gnomAD v4
11g.116836040C=CA2002761857APOA1c.572G= (p.Ser191=)
c.506G= (p.Ser169=)
c.245G= (p.Ser82=)
11g.116836040C>GCA382715163APOA1c.572G>C (p.Ser191Thr)
c.506G>C (p.Ser169Thr)
c.245G>C (p.Ser82Thr)
11g.116836040C>TCA382715160APOA1c.572G>A (p.Ser191Asn)
c.506G>A (p.Ser169Asn)
c.245G>A (p.Ser82Asn)
dbSNP gnomAD v3 gnomAD v4
11g.116836041T>ACA382715169APOA1c.571A>T (p.Ser191Cys)
c.505A>T (p.Ser169Cys)
c.244A>T (p.Ser82Cys)
11g.116836041T>CCA382715165APOA1c.571A>G (p.Ser191Gly)
c.505A>G (p.Ser169Gly)
c.244A>G (p.Ser82Gly)
11g.116836041T>GCA382715167APOA1c.571A>C (p.Ser191Arg)
c.505A>C (p.Ser169Arg)
c.244A>C (p.Ser82Arg)
dbSNP gnomAD v3 gnomAD v4
11g.116836041T=CA2002761858APOA1c.571A= (p.Ser191=)
c.505A= (p.Ser169=)
c.244A= (p.Ser82=)
11g.116836042G>ACA477048661APOA1c.570C>T (p.Tyr190=)
c.504C>T (p.Tyr168=)
c.243C>T (p.Tyr81=)
11g.116836042G>CCA382715171APOA1c.570C>G (p.Tyr190Ter)
c.504C>G (p.Tyr168Ter)
c.243C>G (p.Tyr81Ter)
11g.116836042G>TCA382715172APOA1c.570C>A (p.Tyr190Ter)
c.504C>A (p.Tyr168Ter)
c.243C>A (p.Tyr81Ter)
gnomAD v4
11g.116836043T>ACA382715174APOA1c.569A>T (p.Tyr190Phe)
c.503A>T (p.Tyr168Phe)
c.242A>T (p.Tyr81Phe)
11g.116836043T>CCA382715175APOA1c.569A>G (p.Tyr190Cys)
c.503A>G (p.Tyr168Cys)
c.242A>G (p.Tyr81Cys)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116836043T>GCA382715177APOA1c.569A>C (p.Tyr190Ser)
c.503A>C (p.Tyr168Ser)
c.242A>C (p.Tyr81Ser)
11g.116836043T=CA2002761859APOA1c.569A= (p.Tyr190=)
c.503A= (p.Tyr168=)
c.242A= (p.Tyr81=)
11g.116836044A>CCA382715180APOA1c.568T>G (p.Tyr190Asp)
c.502T>G (p.Tyr168Asp)
c.241T>G (p.Tyr81Asp)
11g.116836044A>GCA382715181APOA1c.568T>C (p.Tyr190His)
c.502T>C (p.Tyr168His)
c.241T>C (p.Tyr81His)
gnomAD v4
11g.116836044A>TCA382715182APOA1c.568T>A (p.Tyr190Asn)
c.502T>A (p.Tyr168Asn)
c.241T>A (p.Tyr81Asn)
11g.116836044_116836045delinsAGCA2002761860APOA1c.567_568delinsCT (p.Pro189=)
c.501_502delinsCT (p.Pro167=)
c.240_241delinsCT (p.Pro80=)
11g.116836045G>ACA477048664APOA1c.567C>T (p.Pro189=)
c.501C>T (p.Pro167=)
c.240C>T (p.Pro80=)
dbSNP gnomAD v2 gnomAD v4
11g.116836045G>CCA477048665APOA1c.567C>G (p.Pro189=)
c.501C>G (p.Pro167=)
c.240C>G (p.Pro80=)
dbSNP gnomAD v2
11g.116836045G=CA2002761861APOA1c.567C= (p.Pro189=)
c.501C= (p.Pro167=)
c.240C= (p.Pro80=)
11g.116836045G>TCA477048666APOA1c.567C>A (p.Pro189=)
c.501C>A (p.Pro167=)
c.240C>A (p.Pro80=)
11g.116836049delCA2002761862APOA1c.567del (p.Tyr190ThrfsTer?)
c.501del (p.Tyr168ThrfsTer?)
c.240del (p.Tyr81ThrfsTer?)
dbSNP gnomAD v4
11g.116836046G>ACA382715185APOA1c.566C>T (p.Pro189Leu)
c.500C>T (p.Pro167Leu)
c.239C>T (p.Pro80Leu)
11g.116836046G>CCA127558APOA1c.566C>G (p.Pro189Arg)
c.500C>G (p.Pro167Arg)
c.239C>G (p.Pro80Arg)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116836046G=CA2002761863APOA1c.566C= (p.Pro189=)
c.500C= (p.Pro167=)
c.239C= (p.Pro80=)
11g.116836046G>TCA382715187APOA1c.566C>A (p.Pro189His)
c.500C>A (p.Pro167His)
c.239C>A (p.Pro80His)
11g.116836047G>ACA382715189APOA1c.565C>T (p.Pro189Ser)
c.499C>T (p.Pro167Ser)
c.238C>T (p.Pro80Ser)
dbSNP gnomAD v4
11g.116836047G>CCA382715192APOA1c.565C>G (p.Pro189Ala)
c.499C>G (p.Pro167Ala)
c.238C>G (p.Pro80Ala)
11g.116836047G=CA2002761864APOA1c.565C= (p.Pro189=)
c.499C= (p.Pro167=)
c.238C= (p.Pro80=)
11g.116836047G>TCA382715190APOA1c.565C>A (p.Pro189Thr)
c.499C>A (p.Pro167Thr)
c.238C>A (p.Pro80Thr)
dbSNP gnomAD v4
11g.116836048G>ACA477048670APOA1c.564C>T (p.Ala188=)
c.498C>T (p.Ala166=)
c.237C>T (p.Ala79=)
dbSNP gnomAD v3 gnomAD v4
11g.116836048G>CCA6289783APOA1c.564C>G (p.Ala188=)
c.498C>G (p.Ala166=)
c.237C>G (p.Ala79=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836048G=CA2002761865APOA1c.564C= (p.Ala188=)
c.498C= (p.Ala166=)
c.237C= (p.Ala79=)
11g.116836048G>TCA229324124APOA1c.564C>A (p.Ala188=)
c.498C>A (p.Ala166=)
c.237C>A (p.Ala79=)
dbSNP gnomAD v2 gnomAD v4
11g.116836049_116836062dupCA2739271021APOA1c.551_564dup (p.Pro189AlafsTer?)
c.485_498dup (p.Pro167AlafsTer?)
c.224_237dup (p.Pro80AlafsTer?)
ClinVar
11g.116836049G>ACA229324129APOA1c.563C>T (p.Ala188Val)
c.497C>T (p.Ala166Val)
c.236C>T (p.Ala79Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116836049G>CCA382715195APOA1c.563C>G (p.Ala188Gly)
c.497C>G (p.Ala166Gly)
c.236C>G (p.Ala79Gly)
dbSNP gnomAD v2 gnomAD v4
11g.116836049G=CA2002761866APOA1c.563C= (p.Ala188=)
c.497C= (p.Ala166=)
c.236C= (p.Ala79=)
11g.116836049G>TCA382715197APOA1c.563C>A (p.Ala188Asp)
c.497C>A (p.Ala166Asp)
c.236C>A (p.Ala79Asp)
gnomAD v4
11g.116836050C>ACA6289784APOA1c.562G>T (p.Ala188Ser)
c.496G>T (p.Ala166Ser)
c.235G>T (p.Ala79Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836050C=CA2002761867APOA1c.562G= (p.Ala188=)
c.496G= (p.Ala166=)
c.235G= (p.Ala79=)
11g.116836050C>GCA382715199APOA1c.562G>C (p.Ala188Pro)
c.496G>C (p.Ala166Pro)
c.235G>C (p.Ala79Pro)
11g.116836050C>TCA382715201APOA1c.562G>A (p.Ala188Thr)
c.496G>A (p.Ala166Thr)
c.235G>A (p.Ala79Thr)
11g.116836051C>ACA477048674APOA1c.561G>T (p.Leu187=)
c.495G>T (p.Leu165=)
c.234G>T (p.Leu78=)
11g.116836051C=CA2002761868APOA1c.561G= (p.Leu187=)
c.495G= (p.Leu165=)
c.234G= (p.Leu78=)
11g.116836051C>GCA229324130APOA1c.561G>C (p.Leu187=)
c.495G>C (p.Leu165=)
c.234G>C (p.Leu78=)
dbSNP gnomAD v4
11g.116836051C>TCA477048675APOA1c.561G>A (p.Leu187=)
c.495G>A (p.Leu165=)
c.234G>A (p.Leu78=)
11g.116836052A=CA2002761869APOA1c.560T= (p.Leu187=)
c.494T= (p.Leu165=)
c.233T= (p.Leu78=)
11g.116836052A>CCA382715203APOA1c.560T>G (p.Leu187Arg)
c.494T>G (p.Leu165Arg)
c.233T>G (p.Leu78Arg)
11g.116836052A>GCA382715205APOA1c.560T>C (p.Leu187Pro)
c.494T>C (p.Leu165Pro)
c.233T>C (p.Leu78Pro)
dbSNP
11g.116836052A>TCA382715206APOA1c.560T>A (p.Leu187Gln)
c.494T>A (p.Leu165Gln)
c.233T>A (p.Leu78Gln)
11g.116836053G>ACA229324137APOA1c.559C>T (p.Leu187=)
c.493C>T (p.Leu165=)
c.232C>T (p.Leu78=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116836053G>CCA382715210APOA1c.559C>G (p.Leu187Val)
c.493C>G (p.Leu165Val)
c.232C>G (p.Leu78Val)
gnomAD v4
11g.116836053G=CA2002761870APOA1c.559C= (p.Leu187=)
c.493C= (p.Leu165=)
c.232C= (p.Leu78=)
11g.116836053G>TCA382715208APOA1c.559C>A (p.Leu187Met)
c.493C>A (p.Leu165Met)
c.232C>A (p.Leu78Met)
11g.116836054A>CCA382715212APOA1c.558T>G (p.His186Gln)
c.492T>G (p.His164Gln)
c.231T>G (p.His77Gln)
11g.116836054A>GCA477048679APOA1c.558T>C (p.His186=)
c.492T>C (p.His164=)
c.231T>C (p.His77=)
11g.116836054A>TCA382715214APOA1c.558T>A (p.His186Gln)
c.492T>A (p.His164Gln)
c.231T>A (p.His77Gln)
11g.116836055T>ACA382715216APOA1c.557A>T (p.His186Leu)
c.491A>T (p.His164Leu)
c.230A>T (p.His77Leu)
gnomAD v4
11g.116836055T>CCA229324150APOA1c.557A>G (p.His186Arg)
c.491A>G (p.His164Arg)
c.230A>G (p.His77Arg)
dbSNP
11g.116836055T>GCA382715219APOA1c.557A>C (p.His186Pro)
c.491A>C (p.His164Pro)
c.230A>C (p.His77Pro)
11g.116836055T=CA2002761871APOA1c.557A= (p.His186=)
c.491A= (p.His164=)
c.230A= (p.His77=)
11g.116836056G>ACA382715223APOA1c.556C>T (p.His186Tyr)
c.490C>T (p.His164Tyr)
c.229C>T (p.His77Tyr)
11g.116836056G>CCA382715224APOA1c.556C>G (p.His186Asp)
c.490C>G (p.His164Asp)
c.229C>G (p.His77Asp)
11g.116836056G>TCA382715226APOA1c.556C>A (p.His186Asn)
c.490C>A (p.His164Asn)
c.229C>A (p.His77Asn)
11g.116836059_116836081dupCA602136490APOA1c.534_556dup (p.His186ProfsTer?)
c.468_490dup (p.His164ProfsTer?)
c.207_229dup (p.His77ProfsTer?)
dbSNP gnomAD v2 gnomAD v4
11g.116836057C>ACA477048681APOA1c.555G>T (p.Thr185=)
c.489G>T (p.Thr163=)
c.228G>T (p.Thr76=)
gnomAD v4
11g.116836057C=CA2002761872APOA1c.555G= (p.Thr185=)
c.489G= (p.Thr163=)
c.228G= (p.Thr76=)
11g.116836057C>GCA6289785APOA1c.555G>C (p.Thr185=)
c.489G>C (p.Thr163=)
c.228G>C (p.Thr76=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836057C>TCA477048682APOA1c.555G>A (p.Thr185=)
c.489G>A (p.Thr163=)
c.228G>A (p.Thr76=)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.116836058G>ACA382715229APOA1c.554C>T (p.Thr185Met)
c.488C>T (p.Thr163Met)
c.227C>T (p.Thr76Met)
ClinVar gnomAD v4
11g.116836058G>CCA382715231APOA1c.554C>G (p.Thr185Arg)
c.488C>G (p.Thr163Arg)
c.227C>G (p.Thr76Arg)
11g.116836058G>TCA382715233APOA1c.554C>A (p.Thr185Lys)
c.488C>A (p.Thr163Lys)
c.227C>A (p.Thr76Lys)
11g.116836059T>ACA382715236APOA1c.553A>T (p.Thr185Ser)
c.487A>T (p.Thr163Ser)
c.226A>T (p.Thr76Ser)
11g.116836059T>CCA382715238APOA1c.553A>G (p.Thr185Ala)
c.487A>G (p.Thr163Ala)
c.226A>G (p.Thr76Ala)
11g.116836059T>GCA382715234APOA1c.553A>C (p.Thr185Pro)
c.487A>C (p.Thr163Pro)
c.226A>C (p.Thr76Pro)
11g.116836060G>ACA477048686APOA1c.552C>T (p.Arg184=)
c.486C>T (p.Arg162=)
c.225C>T (p.Arg75=)
11g.116836060G>CCA477048687APOA1c.552C>G (p.Arg184=)
c.486C>G (p.Arg162=)
c.225C>G (p.Arg75=)
11g.116836060G>TCA477048688APOA1c.552C>A (p.Arg184=)
c.486C>A (p.Arg162=)
c.225C>A (p.Arg75=)
11g.116836062_116836106delCA2695215582APOA1c.508_552del (p.Glu170_Arg184del)
c.442_486del (p.Glu148_Arg162del)
c.181_225del (p.Glu61_Arg75del)
11g.116836061C>ACA6289786APOA1c.551G>T (p.Arg184Leu)
c.485G>T (p.Arg162Leu)
c.224G>T (p.Arg75Leu)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836061C=CA2002761873APOA1c.551G= (p.Arg184=)
c.485G= (p.Arg162=)
c.224G= (p.Arg75=)
11g.116836061C>GCA229324152APOA1c.551G>C (p.Arg184Pro)
c.485G>C (p.Arg162Pro)
c.224G>C (p.Arg75Pro)
dbSNP
11g.116836061C>TCA382715242APOA1c.551G>A (p.Arg184His)
c.485G>A (p.Arg162His)
c.224G>A (p.Arg75His)
dbSNP
11g.116836062G>ACA382715244APOA1c.550C>T (p.Arg184Cys)
c.484C>T (p.Arg162Cys)
c.223C>T (p.Arg75Cys)
11g.116836062G>CCA382715246APOA1c.550C>G (p.Arg184Gly)
c.484C>G (p.Arg162Gly)
c.223C>G (p.Arg75Gly)
11g.116836062G>TCA382715248APOA1c.550C>A (p.Arg184Ser)
c.484C>A (p.Arg162Ser)
c.223C>A (p.Arg75Ser)
11g.116836063C>ACA477048689APOA1c.549G>T (p.Leu183=)
c.483G>T (p.Leu161=)
c.222G>T (p.Leu74=)
11g.116836063C=CA2002761874APOA1c.549G= (p.Leu183=)
c.483G= (p.Leu161=)
c.222G= (p.Leu74=)
11g.116836063C>GCA477048690APOA1c.549G>C (p.Leu183=)
c.483G>C (p.Leu161=)
c.222G>C (p.Leu74=)
11g.116836063C>TCA6289787APOA1c.549G>A (p.Leu183=)
c.483G>A (p.Leu161=)
c.222G>A (p.Leu74=)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836064A>CCA382715251APOA1c.548T>G (p.Leu183Arg)
c.482T>G (p.Leu161Arg)
c.221T>G (p.Leu74Arg)
11g.116836064A>GCA382715255APOA1c.548T>C (p.Leu183Pro)
c.482T>C (p.Leu161Pro)
c.221T>C (p.Leu74Pro)
ClinVar
11g.116836064A>TCA382715253APOA1c.548T>A (p.Leu183Gln)
c.482T>A (p.Leu161Gln)
c.221T>A (p.Leu74Gln)
11g.116836064_116836074delinsAGCGCGTCCACCA2002761875APOA1c.538_548delinsGTGGACGCGCT (p.Val180=)
c.472_482delinsGTGGACGCGCT (p.Val158=)
c.211_221delinsGTGGACGCGCT (p.Val71=)
11g.116836065G>ACA477048691APOA1c.547C>T (p.Leu183=)
c.481C>T (p.Leu161=)
c.220C>T (p.Leu74=)
11g.116836065G>CCA382715257APOA1c.547C>G (p.Leu183Val)
c.481C>G (p.Leu161Val)
c.220C>G (p.Leu74Val)
gnomAD v4
11g.116836065G>TCA382715259APOA1c.547C>A (p.Leu183Met)
c.481C>A (p.Leu161Met)
c.220C>A (p.Leu74Met)
11g.116836068_116836069delCA2695215583APOA1c.546_547del (p.Leu183AlafsTer20)
c.480_481del (p.Leu161AlafsTer20)
c.219_220del (p.Leu74AlafsTer20)
11g.116836065_116836074delCA942609942APOA1c.538_547del (p.Val180CysfsTer?)
c.472_481del (p.Val158CysfsTer?)
c.211_220del (p.Val71CysfsTer?)
dbSNP gnomAD v3 gnomAD v4
11g.116836066C>ACA477048692APOA1c.546G>T (p.Ala182=)
c.480G>T (p.Ala160=)
c.219G>T (p.Ala73=)
11g.116836066C=CA2002761876APOA1c.546G= (p.Ala182=)
c.480G= (p.Ala160=)
c.219G= (p.Ala73=)
11g.116836066C>GCA477048693APOA1c.546G>C (p.Ala182=)
c.480G>C (p.Ala160=)
c.219G>C (p.Ala73=)
11g.116836066C>TCA477048694APOA1c.546G>A (p.Ala182=)
c.480G>A (p.Ala160=)
c.219G>A (p.Ala73=)
dbSNP gnomAD v2 gnomAD v4
11g.116836067G>ACA382715261APOA1c.545C>T (p.Ala182Val)
c.479C>T (p.Ala160Val)
c.218C>T (p.Ala73Val)
dbSNP gnomAD v2 gnomAD v4
11g.116836067G>CCA382715263APOA1c.545C>G (p.Ala182Gly)
c.479C>G (p.Ala160Gly)
c.218C>G (p.Ala73Gly)
11g.116836067G=CA2002761877APOA1c.545C= (p.Ala182=)
c.479C= (p.Ala160=)
c.218C= (p.Ala73=)
11g.116836067G>TCA229324164APOA1c.545C>A (p.Ala182Glu)
c.479C>A (p.Ala160Glu)
c.218C>A (p.Ala73Glu)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116836068C>ACA382715269APOA1c.544G>T (p.Ala182Ser)
c.478G>T (p.Ala160Ser)
c.217G>T (p.Ala73Ser)
11g.116836068C=CA2002761878APOA1c.544G= (p.Ala182=)
c.478G= (p.Ala160=)
c.217G= (p.Ala73=)
11g.116836068C>GCA382715268APOA1c.544G>C (p.Ala182Pro)
c.478G>C (p.Ala160Pro)
c.217G>C (p.Ala73Pro)
11g.116836068C>TCA382715266APOA1c.544G>A (p.Ala182Thr)
c.478G>A (p.Ala160Thr)
c.217G>A (p.Ala73Thr)
ClinVar dbSNP gnomAD v2 gnomAD v4
11g.116836069G>ACA477048696APOA1c.543C>T (p.Asp181=)
c.477C>T (p.Asp159=)
c.216C>T (p.Asp72=)
dbSNP gnomAD v2 gnomAD v4
11g.116836069G>CCA382715272APOA1c.543C>G (p.Asp181Glu)
c.477C>G (p.Asp159Glu)
c.216C>G (p.Asp72Glu)
11g.116836069G=CA2002761879APOA1c.543C= (p.Asp181=)
c.477C= (p.Asp159=)
c.216C= (p.Asp72=)
11g.116836069G>TCA382715270APOA1c.543C>A (p.Asp181Glu)
c.477C>A (p.Asp159Glu)
c.216C>A (p.Asp72Glu)
11g.116836070T>ACA382715277APOA1c.542A>T (p.Asp181Val)
c.476A>T (p.Asp159Val)
c.215A>T (p.Asp72Val)
11g.116836070T>CCA382715274APOA1c.542A>G (p.Asp181Gly)
c.476A>G (p.Asp159Gly)
c.215A>G (p.Asp72Gly)
ClinVar dbSNP
11g.116836070T>GCA382715275APOA1c.542A>C (p.Asp181Ala)
c.476A>C (p.Asp159Ala)
c.215A>C (p.Asp72Ala)
11g.116836071C>ACA382715279APOA1c.541G>T (p.Asp181Tyr)
c.475G>T (p.Asp159Tyr)
c.214G>T (p.Asp72Tyr)
11g.116836071C>GCA382715281APOA1c.541G>C (p.Asp181His)
c.475G>C (p.Asp159His)
c.214G>C (p.Asp72His)
11g.116836071C>TCA382715282APOA1c.541G>A (p.Asp181Asn)
c.475G>A (p.Asp159Asn)
c.214G>A (p.Asp72Asn)
gnomAD v4
11g.116836071_116836088dupCA2695215584APOA1c.524_541dup (p.Val180_Asp181insGlyAlaArgAlaHisVal)
c.458_475dup (p.Val158_Asp159insGlyAlaArgAlaHisVal)
c.197_214dup (p.Val71_Asp72insGlyAlaArgAlaHisVal)
11g.116836072C>ACA477048699APOA1c.540G>T (p.Val180=)
c.474G>T (p.Val158=)
c.213G>T (p.Val71=)
11g.116836072C=CA2002761880APOA1c.540G= (p.Val180=)
c.474G= (p.Val158=)
c.213G= (p.Val71=)
11g.116836072C>GCA477048701APOA1c.540G>C (p.Val180=)
c.474G>C (p.Val158=)
c.213G>C (p.Val71=)
dbSNP gnomAD v2
11g.116836072C>TCA477048698APOA1c.540G>A (p.Val180=)
c.474G>A (p.Val158=)
c.213G>A (p.Val71=)
11g.116836073A=CA2002761881APOA1c.539T= (p.Val180=)
c.473T= (p.Val158=)
c.212T= (p.Val71=)
11g.116836073A>CCA382715283APOA1c.539T>G (p.Val180Gly)
c.473T>G (p.Val158Gly)
c.212T>G (p.Val71Gly)
11g.116836073A>GCA382715286APOA1c.539T>C (p.Val180Ala)
c.473T>C (p.Val158Ala)
c.212T>C (p.Val71Ala)
ClinVar gnomAD v4
11g.116836073A>TCA127580APOA1c.539T>A (p.Val180Glu)
c.473T>A (p.Val158Glu)
c.212T>A (p.Val71Glu)
ClinVar dbSNP
11g.116836074C>ACA382715289APOA1c.538G>T (p.Val180Leu)
c.472G>T (p.Val158Leu)
c.211G>T (p.Val71Leu)
11g.116836074C>GCA382715290APOA1c.538G>C (p.Val180Leu)
c.472G>C (p.Val158Leu)
c.211G>C (p.Val71Leu)
11g.116836074C>TCA382715292APOA1c.538G>A (p.Val180Met)
c.472G>A (p.Val158Met)
c.211G>A (p.Val71Met)
gnomAD v4
11g.116836075A=CA2002761882APOA1c.537T= (p.His179=)
c.471T= (p.His157=)
c.210T= (p.His70=)
11g.116836075A>CCA382715294APOA1c.537T>G (p.His179Gln)
c.471T>G (p.His157Gln)
c.210T>G (p.His70Gln)
ClinVar gnomAD v4
11g.116836075A>GCA477048660APOA1c.537T>C (p.His179=)
c.471T>C (p.His157=)
c.210T>C (p.His70=)
11g.116836075A>TCA382715295APOA1c.537T>A (p.His179Gln)
c.471T>A (p.His157Gln)
c.210T>A (p.His70Gln)
dbSNP
11g.116836076T>ACA382715300APOA1c.536A>T (p.His179Leu)
c.470A>T (p.His157Leu)
c.209A>T (p.His70Leu)
11g.116836076T>CCA229324176APOA1c.536A>G (p.His179Arg)
c.470A>G (p.His157Arg)
c.209A>G (p.His70Arg)
dbSNP gnomAD v3 gnomAD v4
11g.116836076T>GCA382715298APOA1c.536A>C (p.His179Pro)
c.470A>C (p.His157Pro)
c.209A>C (p.His70Pro)
11g.116836076T=CA2002761883APOA1c.536A= (p.His179=)
c.470A= (p.His157=)
c.209A= (p.His70=)
11g.116836077G>ACA382715302APOA1c.535C>T (p.His179Tyr)
c.469C>T (p.His157Tyr)
c.208C>T (p.His70Tyr)
11g.116836077G>CCA382715304APOA1c.535C>G (p.His179Asp)
c.469C>G (p.His157Asp)
c.208C>G (p.His70Asp)
11g.116836077G>TCA382715305APOA1c.535C>A (p.His179Asn)
c.469C>A (p.His157Asn)
c.208C>A (p.His70Asn)
11g.116836079delCA2616112004APOA1c.535del (p.His179MetfsTer?)
c.469del (p.His157MetfsTer?)
c.208del (p.His70MetfsTer?)
gnomAD v4
11g.116836079_116836090dupCA672204755APOA1c.524_535dup (p.Ala178_His179insArgAlaArgAla)
c.458_469dup (p.Ala156_His157insArgAlaArgAla)
c.197_208dup (p.Ala69_His70insArgAlaArgAla)
ClinVar dbSNP gnomAD v3 gnomAD v4
11g.116836078G>ACA477048662APOA1c.534C>T (p.Ala178=)
c.468C>T (p.Ala156=)
c.207C>T (p.Ala69=)
11g.116836078G>CCA229324177APOA1c.534C>G (p.Ala178=)
c.468C>G (p.Ala156=)
c.207C>G (p.Ala69=)
dbSNP gnomAD v3 gnomAD v4
11g.116836078G=CA2002761885APOA1c.534C= (p.Ala178=)
c.468C= (p.Ala156=)
c.207C= (p.Ala69=)
11g.116836078G>TCA477048663APOA1c.534C>A (p.Ala178=)
c.468C>A (p.Ala156=)
c.207C>A (p.Ala69=)
11g.116836078_116836080delinsGGCCA2002761884APOA1c.532_534delinsGCC (p.Ala178=)
c.466_468delinsGCC (p.Ala156=)
c.205_207delinsGCC (p.Ala69=)
11g.116836079G>ACA382715308APOA1c.533C>T (p.Ala178Val)
c.467C>T (p.Ala156Val)
c.206C>T (p.Ala69Val)
dbSNP gnomAD v4
11g.116836079G>CCA382715310APOA1c.533C>G (p.Ala178Gly)
c.467C>G (p.Ala156Gly)
c.206C>G (p.Ala69Gly)
11g.116836079G=CA2002761886APOA1c.533C= (p.Ala178=)
c.467C= (p.Ala156=)
c.206C= (p.Ala69=)
11g.116836079G>TCA382715311APOA1c.533C>A (p.Ala178Asp)
c.467C>A (p.Ala156Asp)
c.206C>A (p.Ala69Asp)
11g.116836088_116836089dupCA658821170APOA1c.532_533dup (p.His179ProfsTer?)
c.466_467dup (p.His157ProfsTer?)
c.205_206dup (p.His70ProfsTer?)
ClinVar dbSNP
11g.116836088_116836089delCA6289788APOA1c.532_533del (p.Ala178ProfsTer25)
c.466_467del (p.Ala156ProfsTer25)
c.205_206del (p.Ala69ProfsTer25)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836080C>ACA382715314APOA1c.532G>T (p.Ala178Ser)
c.466G>T (p.Ala156Ser)
c.205G>T (p.Ala69Ser)
gnomAD v4
11g.116836080C>GCA382715315APOA1c.532G>C (p.Ala178Pro)
c.466G>C (p.Ala156Pro)
c.205G>C (p.Ala69Pro)
COSMIC
11g.116836080C>TCA382715317APOA1c.532G>A (p.Ala178Thr)
c.466G>A (p.Ala156Thr)
c.205G>A (p.Ala69Thr)
gnomAD v4
11g.116836081G>ACA477048667APOA1c.531C>T (p.Arg177=)
c.465C>T (p.Arg155=)
c.204C>T (p.Arg68=)
gnomAD v4
11g.116836081G>CCA477048668APOA1c.531C>G (p.Arg177=)
c.465C>G (p.Arg155=)
c.204C>G (p.Arg68=)
11g.116836081G>TCA477048669APOA1c.531C>A (p.Arg177=)
c.465C>A (p.Arg155=)
c.204C>A (p.Arg68=)
gnomAD v4
11g.116836082C>ACA382715319APOA1c.530G>T (p.Arg177Leu)
c.464G>T (p.Arg155Leu)
c.203G>T (p.Arg68Leu)
dbSNP gnomAD v2 gnomAD v4
11g.116836082C=CA2002761887APOA1c.530G= (p.Arg177=)
c.464G= (p.Arg155=)
c.203G= (p.Arg68=)
11g.116836082C>GCA382715320APOA1c.530G>C (p.Arg177Pro)
c.464G>C (p.Arg155Pro)
c.203G>C (p.Arg68Pro)
ClinVar dbSNP
11g.116836082C>TCA382715322APOA1c.530G>A (p.Arg177His)
c.464G>A (p.Arg155His)
c.203G>A (p.Arg68His)
11g.116836083G>ACA382715326APOA1c.529C>T (p.Arg177Cys)
c.463C>T (p.Arg155Cys)
c.202C>T (p.Arg68Cys)
dbSNP gnomAD v2 COSMIC
11g.116836083G>CCA382715327APOA1c.529C>G (p.Arg177Gly)
c.463C>G (p.Arg155Gly)
c.202C>G (p.Arg68Gly)
11g.116836083G=CA2002761888APOA1c.529C= (p.Arg177=)
c.463C= (p.Arg155=)
c.202C= (p.Arg68=)
11g.116836083G>TCA382715325APOA1c.529C>A (p.Arg177Ser)
c.463C>A (p.Arg155Ser)
c.202C>A (p.Arg68Ser)
11g.116836084C>ACA477048671APOA1c.528G>T (p.Ala176=)
c.462G>T (p.Ala154=)
c.201G>T (p.Ala67=)
gnomAD v4
11g.116836084C>GCA477048672APOA1c.528G>C (p.Ala176=)
c.462G>C (p.Ala154=)
c.201G>C (p.Ala67=)
gnomAD v4
11g.116836084C>TCA477048673APOA1c.528G>A (p.Ala176=)
c.462G>A (p.Ala154=)
c.201G>A (p.Ala67=)
COSMIC
11g.116836085G>ACA6289789APOA1c.527C>T (p.Ala176Val)
c.461C>T (p.Ala154Val)
c.200C>T (p.Ala67Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836085G>CCA382715330APOA1c.527C>G (p.Ala176Gly)
c.461C>G (p.Ala154Gly)
c.200C>G (p.Ala67Gly)
11g.116836085G=CA2002761889APOA1c.527C= (p.Ala176=)
c.461C= (p.Ala154=)
c.200C= (p.Ala67=)
11g.116836085G>TCA382715332APOA1c.527C>A (p.Ala176Glu)
c.461C>A (p.Ala154Glu)
c.200C>A (p.Ala67Glu)
11g.116836086C>ACA6289791APOA1c.526G>T (p.Ala176Ser)
c.460G>T (p.Ala154Ser)
c.199G>T (p.Ala67Ser)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116836086C=CA2002761890APOA1c.526G= (p.Ala176=)
c.460G= (p.Ala154=)
c.199G= (p.Ala67=)
11g.116836086C>GCA382715335APOA1c.526G>C (p.Ala176Pro)
c.460G>C (p.Ala154Pro)
c.199G>C (p.Ala67Pro)
11g.116836086C>TCA6289790APOA1c.526G>A (p.Ala176Thr)
c.460G>A (p.Ala154Thr)
c.199G>A (p.Ala67Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116836087G>ACA477048676APOA1c.525C>T (p.Arg175=)
c.459C>T (p.Arg153=)
c.198C>T (p.Arg66=)
11g.116836087G>CCA477048677APOA1c.525C>G (p.Arg175=)
c.459C>G (p.Arg153=)
c.198C>G (p.Arg66=)
11g.116836087G>TCA477048678APOA1c.525C>A (p.Arg175=)
c.459C>A (p.Arg153=)
c.198C>A (p.Arg66=)
11g.116836088C>ACA382715338APOA1c.524G>T (p.Arg175Leu)
c.458G>T (p.Arg153Leu)
c.197G>T (p.Arg66Leu)
11g.116836088C>GCA382715340APOA1c.524G>C (p.Arg175Pro)
c.458G>C (p.Arg153Pro)
c.197G>C (p.Arg66Pro)
11g.116836088C>TCA382715342APOA1c.524G>A (p.Arg175His)
c.458G>A (p.Arg153His)
c.197G>A (p.Arg66His)
11g.116836089G>ACA382715344APOA1c.523C>T (p.Arg175Cys)
c.457C>T (p.Arg153Cys)
c.196C>T (p.Arg66Cys)
ClinVar gnomAD v4
11g.116836089G>CCA382715346APOA1c.523C>G (p.Arg175Gly)
c.457C>G (p.Arg153Gly)
c.196C>G (p.Arg66Gly)
ClinVar dbSNP gnomAD v4
11g.116836089G=CA2002761891APOA1c.523C= (p.Arg175=)
c.457C= (p.Arg153=)
c.196C= (p.Arg66=)
11g.116836089G>TCA382715347APOA1c.523C>A (p.Arg175Ser)
c.457C>A (p.Arg153Ser)
c.196C>A (p.Arg66Ser)
11g.116836090G>ACA477048680APOA1c.522C>T (p.Asp174=)
c.456C>T (p.Asp152=)
c.195C>T (p.Asp65=)
dbSNP gnomAD v2 gnomAD v4
11g.116836090G>CCA382715351APOA1c.522C>G (p.Asp174Glu)
c.456C>G (p.Asp152Glu)
c.195C>G (p.Asp65Glu)
11g.116836090G=CA2002761892APOA1c.522C= (p.Asp174=)
c.456C= (p.Asp152=)
c.195C= (p.Asp65=)
11g.116836090G>TCA382715349APOA1c.522C>A (p.Asp174Glu)
c.456C>A (p.Asp152Glu)
c.195C>A (p.Asp65Glu)
dbSNP
11g.116836091T>ACA382715353APOA1c.521A>T (p.Asp174Val)
c.455A>T (p.Asp152Val)
c.194A>T (p.Asp65Val)
11g.116836091T>CCA382715354APOA1c.521A>G (p.Asp174Gly)
c.455A>G (p.Asp152Gly)
c.194A>G (p.Asp65Gly)
11g.116836091T>GCA382715356APOA1c.521A>C (p.Asp174Ala)
c.455A>C (p.Asp152Ala)
c.194A>C (p.Asp65Ala)
11g.116836091_116836096delCA2575000170APOA1c.516_521del (p.Met172_Asp174delinsIle)
c.450_455del (p.Met150_Asp152delinsIle)
c.189_194del (p.Met63_Asp65delinsIle)
11g.116836092C>ACA382715358APOA1c.520G>T (p.Asp174Tyr)
c.454G>T (p.Asp152Tyr)
c.193G>T (p.Asp65Tyr)
11g.116836092C>GCA382715359APOA1c.520G>C (p.Asp174His)
c.454G>C (p.Asp152His)
c.193G>C (p.Asp65His)
11g.116836092C>TCA382715361APOA1c.520G>A (p.Asp174Asn)
c.454G>A (p.Asp152Asn)
c.193G>A (p.Asp65Asn)
ClinVar
11g.116836093G>ACA477048684APOA1c.519C>T (p.Arg173=)
c.453C>T (p.Arg151=)
c.192C>T (p.Arg64=)
dbSNP gnomAD v3 gnomAD v4
11g.116836093G>CCA477048685APOA1c.519C>G (p.Arg173=)
c.453C>G (p.Arg151=)
c.192C>G (p.Arg64=)
gnomAD v4
11g.116836093G=CA2002761893APOA1c.519C= (p.Arg173=)
c.453C= (p.Arg151=)
c.192C= (p.Arg64=)
11g.116836093G>TCA477048683APOA1c.519C>A (p.Arg173=)
c.453C>A (p.Arg151=)
c.192C>A (p.Arg64=)
11g.116836094C>ACA382715363APOA1c.518G>T (p.Arg173Leu)
c.452G>T (p.Arg151Leu)
c.191G>T (p.Arg64Leu)
gnomAD v4
11g.116836094C=CA2002761894APOA1c.518G= (p.Arg173=)
c.452G= (p.Arg151=)
c.191G= (p.Arg64=)
11g.116836094C>GCA127586APOA1c.518G>C (p.Arg173Pro)
c.452G>C (p.Arg151Pro)
c.191G>C (p.Arg64Pro)
ClinVar dbSNP
11g.116836094C>TCA382715366APOA1c.518G>A (p.Arg173His)
c.452G>A (p.Arg151His)
c.191G>A (p.Arg64His)
COSMIC

Number of alleles fetched