UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.116790852C>A | CA382738693 | APOA5 | c.377G>T (p.Arg126Leu) c.461G>T (p.Arg154Leu) | |
| 11 | g.116790852C>G | CA382738696 | APOA5 | c.377G>C (p.Arg126Pro) c.461G>C (p.Arg154Pro) | |
| 11 | g.116790852C>T | CA382738699 | APOA5 | c.377G>A (p.Arg126Gln) c.461G>A (p.Arg154Gln) | COSMIC |
| 11 | g.116790853G>A | CA382738708 | APOA5 | c.376C>T (p.Arg126Trp) c.460C>T (p.Arg154Trp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790853G>C | CA382738706 | APOA5 | c.376C>G (p.Arg126Gly) c.460C>G (p.Arg154Gly) | |
| 11 | g.116790853G= | CA2002741004 | APOA5 | c.376C= (p.Arg126=) c.460C= (p.Arg154=) | |
| 11 | g.116790853G>T | CA6289087 | APOA5 | c.376C>A (p.Arg126=) c.460C>A (p.Arg154=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790854C>A | CA382738712 | APOA5 | c.375G>T (p.Leu125Phe) c.459G>T (p.Leu153Phe) | |
| 11 | g.116790854C>G | CA382738714 | APOA5 | c.375G>C (p.Leu125Phe) c.459G>C (p.Leu153Phe) | |
| 11 | g.116790854C>T | CA477047691 | APOA5 | c.375G>A (p.Leu125=) c.459G>A (p.Leu153=) | |
| 11 | g.116790855A>C | CA382738718 | APOA5 | c.374T>G (p.Leu125Trp) c.458T>G (p.Leu153Trp) | |
| 11 | g.116790855A>G | CA382738720 | APOA5 | c.374T>C (p.Leu125Ser) c.458T>C (p.Leu153Ser) | |
| 11 | g.116790855A>T | CA382738723 | APOA5 | c.374T>A (p.Leu125Ter) c.458T>A (p.Leu153Ter) | |
| 11 | g.116790856A>C | CA382738727 | APOA5 | c.373T>G (p.Leu125Val) c.457T>G (p.Leu153Val) | |
| 11 | g.116790856A>G | CA477047693 | APOA5 | c.373T>C (p.Leu125=) c.457T>C (p.Leu153=) | |
| 11 | g.116790856A>T | CA382738730 | APOA5 | c.373T>A (p.Leu125Met) c.457T>A (p.Leu153Met) | |
| 11 | g.116790857G>A | CA477047695 | APOA5 | c.372C>T (p.Gly124=) c.456C>T (p.Gly152=) | gnomAD v4 |
| 11 | g.116790857G>C | CA477047697 | APOA5 | c.372C>G (p.Gly124=) c.456C>G (p.Gly152=) | |
| 11 | g.116790857G>T | CA477047699 | APOA5 | c.372C>A (p.Gly124=) c.456C>A (p.Gly152=) | |
| 11 | g.116790858C>A | CA382738734 | APOA5 | c.371G>T (p.Gly124Val) c.455G>T (p.Gly152Val) | |
| 11 | g.116790858C>G | CA382738737 | APOA5 | c.371G>C (p.Gly124Ala) c.455G>C (p.Gly152Ala) | |
| 11 | g.116790858C>T | CA382738741 | APOA5 | c.371G>A (p.Gly124Asp) c.455G>A (p.Gly152Asp) | gnomAD v4 COSMIC |
| 11 | g.116790859C>A | CA382738745 | APOA5 | c.370G>T (p.Gly124Cys) c.454G>T (p.Gly152Cys) | |
| 11 | g.116790859C>G | CA382738746 | APOA5 | c.370G>C (p.Gly124Arg) c.454G>C (p.Gly152Arg) | |
| 11 | g.116790859C>T | CA382738749 | APOA5 | c.370G>A (p.Gly124Ser) c.454G>A (p.Gly152Ser) | |
| 11 | g.116790860C>A | CA382738752 | APOA5 | c.369G>T (p.Glu123Asp) c.453G>T (p.Glu151Asp) | |
| 11 | g.116790860C>G | CA382738756 | APOA5 | c.369G>C (p.Glu123Asp) c.453G>C (p.Glu151Asp) | |
| 11 | g.116790860C>T | CA477047708 | APOA5 | c.369G>A (p.Glu123=) c.453G>A (p.Glu151=) | |
| 11 | g.116790861T>A | CA382738759 | APOA5 | c.368A>T (p.Glu123Val) c.452A>T (p.Glu151Val) | |
| 11 | g.116790861T>C | CA382738762 | APOA5 | c.368A>G (p.Glu123Gly) c.452A>G (p.Glu151Gly) | |
| 11 | g.116790861T>G | CA382738764 | APOA5 | c.368A>C (p.Glu123Ala) c.452A>C (p.Glu151Ala) | |
| 11 | g.116790862C>A | CA382738767 | APOA5 | c.367G>T (p.Glu123Ter) c.451G>T (p.Glu151Ter) | |
| 11 | g.116790862C>G | CA382738770 | APOA5 | c.367G>C (p.Glu123Gln) c.451G>C (p.Glu151Gln) | |
| 11 | g.116790862C>T | CA382738773 | APOA5 | c.367G>A (p.Glu123Lys) c.451G>A (p.Glu151Lys) | |
| 11 | g.116790863C>A | CA382738777 | APOA5 | c.366G>T (p.Leu122Phe) c.450G>T (p.Leu150Phe) | |
| 11 | g.116790863C= | CA2002741008 | APOA5 | c.366G= (p.Leu122=) c.450G= (p.Leu150=) | |
| 11 | g.116790863C>G | CA382738779 | APOA5 | c.366G>C (p.Leu122Phe) c.450G>C (p.Leu150Phe) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790863C>T | CA477047715 | APOA5 | c.366G>A (p.Leu122=) c.450G>A (p.Leu150=) | |
| 11 | g.116790863_116790864delinsCA | CA2002741009 | APOA5 | c.365_366delinsTG (p.Leu122=) c.449_450delinsTG (p.Leu150=) | |
| 11 | g.116790864A>C | CA382738783 | APOA5 | c.365T>G (p.Leu122Trp) c.449T>G (p.Leu150Trp) | |
| 11 | g.116790864A>G | CA382738789 | APOA5 | c.365T>C (p.Leu122Ser) c.449T>C (p.Leu150Ser) | |
| 11 | g.116790864A>T | CA382738785 | APOA5 | c.365T>A (p.Leu122Ter) c.449T>A (p.Leu150Ter) | |
| 11 | g.116790866del | CA2002741011 | APOA5 | c.365del (p.Leu122TrpfsTer8) c.449del (p.Leu150TrpfsTer8) | dbSNP |
| 11 | g.116790865A>C | CA382738791 | APOA5 | c.364T>G (p.Leu122Val) c.448T>G (p.Leu150Val) | |
| 11 | g.116790865A>G | CA477047723 | APOA5 | c.364T>C (p.Leu122=) c.448T>C (p.Leu150=) | |
| 11 | g.116790865A>T | CA382738794 | APOA5 | c.364T>A (p.Leu122Met) c.448T>A (p.Leu150Met) | |
| 11 | g.116790866A>C | CA382738797 | APOA5 | c.363T>G (p.Asn121Lys) c.447T>G (p.Asn149Lys) | |
| 11 | g.116790866A>G | CA477047724 | APOA5 | c.363T>C (p.Asn121=) c.447T>C (p.Asn149=) | |
| 11 | g.116790866A>T | CA382738801 | APOA5 | c.363T>A (p.Asn121Lys) c.447T>A (p.Asn149Lys) | |
| 11 | g.116790867T>A | CA382738802 | APOA5 | c.362A>T (p.Asn121Ile) c.446A>T (p.Asn149Ile) | |
| 11 | g.116790867T>C | CA382738807 | APOA5 | c.362A>G (p.Asn121Ser) c.446A>G (p.Asn149Ser) | |
| 11 | g.116790867T>G | CA382738804 | APOA5 | c.362A>C (p.Asn121Thr) c.446A>C (p.Asn149Thr) | |
| 11 | g.116790868T>A | CA382738812 | APOA5 | c.361A>T (p.Asn121Tyr) c.445A>T (p.Asn149Tyr) | gnomAD v4 |
| 11 | g.116790868T>C | CA382738814 | APOA5 | c.361A>G (p.Asn121Asp) c.445A>G (p.Asn149Asp) | |
| 11 | g.116790868T>G | CA382738817 | APOA5 | c.361A>C (p.Asn121His) c.445A>C (p.Asn149His) | |
| 11 | g.116790869C>A | CA382738820 | APOA5 | c.360G>T (p.Trp120Cys) c.444G>T (p.Trp148Cys) | |
| 11 | g.116790869C= | CA2002741016 | APOA5 | c.360G= (p.Trp120=) c.444G= (p.Trp148=) | |
| 11 | g.116790869C>G | CA6289088 | APOA5 | c.360G>C (p.Trp120Cys) c.444G>C (p.Trp148Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790869C>T | CA382738826 | APOA5 | c.360G>A (p.Trp120Ter) c.444G>A (p.Trp148Ter) | COSMIC |
| 11 | g.116790870C>A | CA382738829 | APOA5 | c.359G>T (p.Trp120Leu) c.443G>T (p.Trp148Leu) | |
| 11 | g.116790870C>G | CA382738832 | APOA5 | c.359G>C (p.Trp120Ser) c.443G>C (p.Trp148Ser) | |
| 11 | g.116790870C>T | CA382738835 | APOA5 | c.359G>A (p.Trp120Ter) c.443G>A (p.Trp148Ter) | |
| 11 | g.116790871A>C | CA382738838 | APOA5 | c.358T>G (p.Trp120Gly) c.442T>G (p.Trp148Gly) | |
| 11 | g.116790871A>G | CA382738840 | APOA5 | c.358T>C (p.Trp120Arg) c.442T>C (p.Trp148Arg) | |
| 11 | g.116790871A>T | CA382738843 | APOA5 | c.358T>A (p.Trp120Arg) c.442T>A (p.Trp148Arg) | |
| 11 | g.116790872G>A | CA477047745 | APOA5 | c.357C>T (p.Gly119=) c.441C>T (p.Gly147=) | |
| 11 | g.116790872G>C | CA477047746 | APOA5 | c.357C>G (p.Gly119=) c.441C>G (p.Gly147=) | |
| 11 | g.116790872G>T | CA477047747 | APOA5 | c.357C>A (p.Gly119=) c.441C>A (p.Gly147=) | |
| 11 | g.116790873C>A | CA382738847 | APOA5 | c.356G>T (p.Gly119Val) c.440G>T (p.Gly147Val) | |
| 11 | g.116790873C>G | CA382738852 | APOA5 | c.356G>C (p.Gly119Ala) c.440G>C (p.Gly147Ala) | |
| 11 | g.116790873C>T | CA382738850 | APOA5 | c.356G>A (p.Gly119Asp) c.440G>A (p.Gly147Asp) | |
| 11 | g.116790874C>A | CA382738856 | APOA5 | c.355G>T (p.Gly119Cys) c.439G>T (p.Gly147Cys) | |
| 11 | g.116790874C>G | CA382738859 | APOA5 | c.355G>C (p.Gly119Arg) c.439G>C (p.Gly147Arg) | |
| 11 | g.116790874C>T | CA382738862 | APOA5 | c.355G>A (p.Gly119Ser) c.439G>A (p.Gly147Ser) | |
| 11 | g.116790875C>A | CA477047759 | APOA5 | c.354G>T (p.Val118=) c.438G>T (p.Val146=) | COSMIC |
| 11 | g.116790875C>G | CA477047760 | APOA5 | c.354G>C (p.Val118=) c.438G>C (p.Val146=) | |
| 11 | g.116790875C>T | CA477047758 | APOA5 | c.354G>A (p.Val118=) c.438G>A (p.Val146=) | |
| 11 | g.116790876A>C | CA382738865 | APOA5 | c.353T>G (p.Val118Gly) c.437T>G (p.Val146Gly) | |
| 11 | g.116790876A>G | CA382738868 | APOA5 | c.353T>C (p.Val118Ala) c.437T>C (p.Val146Ala) | |
| 11 | g.116790876A>T | CA382738870 | APOA5 | c.353T>A (p.Val118Glu) c.437T>A (p.Val146Glu) | gnomAD v4 |
| 11 | g.116790877C>A | CA382738876 | APOA5 | c.352G>T (p.Val118Leu) c.436G>T (p.Val146Leu) | gnomAD v4 |
| 11 | g.116790877C= | CA2002741019 | APOA5 | c.352G= (p.Val118=) c.436G= (p.Val146=) | |
| 11 | g.116790877C>G | CA382738878 | APOA5 | c.352G>C (p.Val118Leu) c.436G>C (p.Val146Leu) | |
| 11 | g.116790877C>T | CA6289089 | APOA5 | c.352G>A (p.Val118Met) c.436G>A (p.Val146Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790878C>A | CA477047763 | APOA5 | c.351G>T (p.Leu117=) c.435G>T (p.Leu145=) | COSMIC |
| 11 | g.116790878C>G | CA477047764 | APOA5 | c.351G>C (p.Leu117=) c.435G>C (p.Leu145=) | |
| 11 | g.116790878C>T | CA477047765 | APOA5 | c.351G>A (p.Leu117=) c.435G>A (p.Leu145=) | |
| 11 | g.116790879A>C | CA382738883 | APOA5 | c.350T>G (p.Leu117Arg) c.434T>G (p.Leu145Arg) | gnomAD v4 |
| 11 | g.116790879A>G | CA382738884 | APOA5 | c.350T>C (p.Leu117Pro) c.434T>C (p.Leu145Pro) | |
| 11 | g.116790879A>T | CA382738887 | APOA5 | c.350T>A (p.Leu117Gln) c.434T>A (p.Leu145Gln) | |
| 11 | g.116790880G>A | CA477047766 | APOA5 | c.349C>T (p.Leu117=) c.433C>T (p.Leu145=) | |
| 11 | g.116790880G>C | CA382738891 | APOA5 | c.349C>G (p.Leu117Val) c.433C>G (p.Leu145Val) | |
| 11 | g.116790880G>T | CA382738893 | APOA5 | c.349C>A (p.Leu117Met) c.433C>A (p.Leu145Met) | |
| 11 | g.116790881C>A | CA382738897 | APOA5 | c.348G>T (p.Glu116Asp) c.432G>T (p.Glu144Asp) | |
| 11 | g.116790881C= | CA2002741022 | APOA5 | c.348G= (p.Glu116=) c.432G= (p.Glu144=) | |
| 11 | g.116790881C>G | CA382738899 | APOA5 | c.348G>C (p.Glu116Asp) c.432G>C (p.Glu144Asp) | |
| 11 | g.116790881C>T | CA477047769 | APOA5 | c.348G>A (p.Glu116=) c.432G>A (p.Glu144=) | dbSNP gnomAD v4 |
| 11 | g.116790882T>A | CA382738905 | APOA5 | c.347A>T (p.Glu116Val) c.431A>T (p.Glu144Val) | gnomAD v4 |
| 11 | g.116790882T>C | CA382738908 | APOA5 | c.347A>G (p.Glu116Gly) c.431A>G (p.Glu144Gly) | |
| 11 | g.116790882T>G | CA382738910 | APOA5 | c.347A>C (p.Glu116Ala) c.431A>C (p.Glu144Ala) | |
| 11 | g.116790883C>A | CA382738914 | APOA5 | c.346G>T (p.Glu116Ter) c.430G>T (p.Glu144Ter) | gnomAD v4 |
| 11 | g.116790883C= | CA2002741024 | APOA5 | c.346G= (p.Glu116=) c.430G= (p.Glu144=) | |
| 11 | g.116790883C>G | CA382738917 | APOA5 | c.346G>C (p.Glu116Gln) c.430G>C (p.Glu144Gln) | dbSNP gnomAD v4 |
| 11 | g.116790883C>T | CA229338010 | APOA5 | c.346G>A (p.Glu116Lys) c.430G>A (p.Glu144Lys) | dbSNP gnomAD v4 COSMIC |
| 11 | g.116790884G>A | CA477047770 | APOA5 | c.345C>T (p.His115=) c.429C>T (p.His143=) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790884G>C | CA382738922 | APOA5 | c.345C>G (p.His115Gln) c.429C>G (p.His143Gln) | |
| 11 | g.116790884G= | CA2002741028 | APOA5 | c.345C= (p.His115=) c.429C= (p.His143=) | |
| 11 | g.116790884G>T | CA382738928 | APOA5 | c.345C>A (p.His115Gln) c.429C>A (p.His143Gln) | |
| 11 | g.116790885T>A | CA382738932 | APOA5 | c.344A>T (p.His115Leu) c.428A>T (p.His143Leu) | gnomAD v4 |
| 11 | g.116790885T>C | CA382738934 | APOA5 | c.344A>G (p.His115Arg) c.428A>G (p.His143Arg) | |
| 11 | g.116790885T>G | CA382738937 | APOA5 | c.344A>C (p.His115Pro) c.428A>C (p.His143Pro) | |
| 11 | g.116790886G>A | CA382738947 | APOA5 | c.343C>T (p.His115Tyr) c.427C>T (p.His143Tyr) | |
| 11 | g.116790886G>C | CA382738940 | APOA5 | c.343C>G (p.His115Asp) c.427C>G (p.His143Asp) | |
| 11 | g.116790886G>T | CA382738944 | APOA5 | c.343C>A (p.His115Asn) c.427C>A (p.His143Asn) | |
| 11 | g.116790887C>A | CA477047779 | APOA5 | c.342G>T (p.Ala114=) c.426G>T (p.Ala142=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790887C= | CA2002741032 | APOA5 | c.342G= (p.Ala114=) c.426G= (p.Ala142=) | |
| 11 | g.116790887C>G | CA477047775 | APOA5 | c.342G>C (p.Ala114=) c.426G>C (p.Ala142=) | |
| 11 | g.116790887C>T | CA6289090 | APOA5 | c.342G>A (p.Ala114=) c.426G>A (p.Ala142=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790888G>A | CA382738959 | APOA5 | c.341C>T (p.Ala114Val) c.425C>T (p.Ala142Val) | COSMIC |
| 11 | g.116790888G>C | CA382738954 | APOA5 | c.341C>G (p.Ala114Gly) c.425C>G (p.Ala142Gly) | |
| 11 | g.116790888G>T | CA382738956 | APOA5 | c.341C>A (p.Ala114Glu) c.425C>A (p.Ala142Glu) | gnomAD v4 |
| 11 | g.116790889C>A | CA382738965 | APOA5 | c.340G>T (p.Ala114Ser) c.424G>T (p.Ala142Ser) | |
| 11 | g.116790889C= | CA2002741035 | APOA5 | c.340G= (p.Ala114=) c.424G= (p.Ala142=) | |
| 11 | g.116790889C>G | CA382738968 | APOA5 | c.340G>C (p.Ala114Pro) c.424G>C (p.Ala142Pro) | |
| 11 | g.116790889C>T | CA382738969 | APOA5 | c.340G>A (p.Ala114Thr) c.424G>A (p.Ala142Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790890C>A | CA382738974 | APOA5 | c.339G>T (p.Glu113Asp) c.423G>T (p.Glu141Asp) | |
| 11 | g.116790890C>G | CA382738975 | APOA5 | c.339G>C (p.Glu113Asp) c.423G>C (p.Glu141Asp) | |
| 11 | g.116790890C>T | CA477047785 | APOA5 | c.339G>A (p.Glu113=) c.423G>A (p.Glu141=) | |
| 11 | g.116790891T>A | CA382738979 | APOA5 | c.338A>T (p.Glu113Val) c.422A>T (p.Glu141Val) | |
| 11 | g.116790891T>C | CA382738981 | APOA5 | c.338A>G (p.Glu113Gly) c.422A>G (p.Glu141Gly) | |
| 11 | g.116790891T>G | CA382738984 | APOA5 | c.338A>C (p.Glu113Ala) c.422A>C (p.Glu141Ala) | |
| 11 | g.116790892C>A | CA382738988 | APOA5 | c.337G>T (p.Glu113Ter) c.421G>T (p.Glu141Ter) | |
| 11 | g.116790892C>G | CA382738990 | APOA5 | c.337G>C (p.Glu113Gln) c.421G>C (p.Glu141Gln) | |
| 11 | g.116790892C>T | CA382738993 | APOA5 | c.337G>A (p.Glu113Lys) c.421G>A (p.Glu141Lys) | gnomAD v4 |
| 11 | g.116790893T>A | CA477047795 | APOA5 | c.336A>T (p.Ala112=) c.420A>T (p.Ala140=) | |
| 11 | g.116790893T>C | CA477047796 | APOA5 | c.336A>G (p.Ala112=) c.420A>G (p.Ala140=) | |
| 11 | g.116790893T>G | CA477047797 | APOA5 | c.336A>C (p.Ala112=) c.420A>C (p.Ala140=) | |
| 11 | g.116790894G>A | CA382739002 | APOA5 | c.335C>T (p.Ala112Val) c.419C>T (p.Ala140Val) | gnomAD v4 |
| 11 | g.116790894G>C | CA382738999 | APOA5 | c.335C>G (p.Ala112Gly) c.419C>G (p.Ala140Gly) | |
| 11 | g.116790894G>T | CA382738997 | APOA5 | c.335C>A (p.Ala112Glu) c.419C>A (p.Ala140Glu) | |
| 11 | g.116790895C>A | CA382739006 | APOA5 | c.334G>T (p.Ala112Ser) c.418G>T (p.Ala140Ser) | |
| 11 | g.116790895C= | CA2002741037 | APOA5 | c.334G= (p.Ala112=) c.418G= (p.Ala140=) | |
| 11 | g.116790895C>G | CA382739008 | APOA5 | c.334G>C (p.Ala112Pro) c.418G>C (p.Ala140Pro) | |
| 11 | g.116790895C>T | CA229338038 | APOA5 | c.334G>A (p.Ala112Thr) c.418G>A (p.Ala140Thr) | dbSNP |
| 11 | g.116790896C>A | CA6289091 | APOA5 | c.333G>T (p.Met111Ile) c.417G>T (p.Met139Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790896C= | CA2002741040 | APOA5 | c.333G= (p.Met111=) c.417G= (p.Met139=) | |
| 11 | g.116790896C>G | CA382739017 | APOA5 | c.333G>C (p.Met111Ile) c.417G>C (p.Met139Ile) | |
| 11 | g.116790896C>T | CA382739025 | APOA5 | c.333G>A (p.Met111Ile) c.417G>A (p.Met139Ile) | ClinVar |
| 11 | g.116790897A= | CA2002741043 | APOA5 | c.332T= (p.Met111=) c.416T= (p.Met139=) | |
| 11 | g.116790897A>C | CA382739029 | APOA5 | c.332T>G (p.Met111Arg) c.416T>G (p.Met139Arg) | |
| 11 | g.116790897A>G | CA382739031 | APOA5 | c.332T>C (p.Met111Thr) c.416T>C (p.Met139Thr) | |
| 11 | g.116790897A>T | CA382739035 | APOA5 | c.332T>A (p.Met111Lys) c.416T>A (p.Met139Lys) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790898T>A | CA382739038 | APOA5 | c.331A>T (p.Met111Leu) c.415A>T (p.Met139Leu) | |
| 11 | g.116790898T>C | CA6289092 | APOA5 | c.331A>G (p.Met111Val) c.415A>G (p.Met139Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790898T>G | CA382739042 | APOA5 | c.331A>C (p.Met111Leu) c.415A>C (p.Met139Leu) | |
| 11 | g.116790898T= | CA2002741046 | APOA5 | c.331A= (p.Met111=) c.415A= (p.Met139=) | |
| 11 | g.116790899G>A | CA477047811 | APOA5 | c.330C>T (p.Tyr110=) c.414C>T (p.Tyr138=) | |
| 11 | g.116790899G>C | CA382739046 | APOA5 | c.330C>G (p.Tyr110Ter) c.414C>G (p.Tyr138Ter) | |
| 11 | g.116790899G>T | CA382739049 | APOA5 | c.330C>A (p.Tyr110Ter) c.414C>A (p.Tyr138Ter) | |
| 11 | g.116790900T>A | CA382739059 | APOA5 | c.329A>T (p.Tyr110Phe) c.413A>T (p.Tyr138Phe) | |
| 11 | g.116790900T>C | CA382739061 | APOA5 | c.329A>G (p.Tyr110Cys) c.413A>G (p.Tyr138Cys) | gnomAD v4 |
| 11 | g.116790900T>G | CA382739057 | APOA5 | c.329A>C (p.Tyr110Ser) c.413A>C (p.Tyr138Ser) | |
| 11 | g.116790901A= | CA2002741048 | APOA5 | c.328T= (p.Tyr110=) c.412T= (p.Tyr138=) | |
| 11 | g.116790901A>C | CA382739064 | APOA5 | c.328T>G (p.Tyr110Asp) c.412T>G (p.Tyr138Asp) | |
| 11 | g.116790901A>G | CA382739067 | APOA5 | c.328T>C (p.Tyr110His) c.412T>C (p.Tyr138His) | |
| 11 | g.116790901A>T | CA382739070 | APOA5 | c.328T>A (p.Tyr110Asn) c.412T>A (p.Tyr138Asn) | |
| 11 | g.116790902G>A | CA477047814 | APOA5 | c.327C>T (p.Pro109=) c.411C>T (p.Pro137=) | |
| 11 | g.116790902G>C | CA477047812 | APOA5 | c.327C>G (p.Pro109=) c.411C>G (p.Pro137=) | |
| 11 | g.116790902G>T | CA477047813 | APOA5 | c.327C>A (p.Pro109=) c.411C>A (p.Pro137=) | |
| 11 | g.116790904dup | CA477047815 | APOA5 | c.327dup (p.Tyr110LeufsTer?) c.411dup (p.Tyr138LeufsTer?) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790903G>A | CA382739075 | APOA5 | c.326C>T (p.Pro109Leu) c.410C>T (p.Pro137Leu) | |
| 11 | g.116790903G>C | CA382739082 | APOA5 | c.326C>G (p.Pro109Arg) c.410C>G (p.Pro137Arg) | |
| 11 | g.116790903G>T | CA382739084 | APOA5 | c.326C>A (p.Pro109His) c.410C>A (p.Pro137His) | |
| 11 | g.116790904G>A | CA6289093 | APOA5 | c.325C>T (p.Pro109Ser) c.409C>T (p.Pro137Ser) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.116790904G>C | CA382739095 | APOA5 | c.325C>G (p.Pro109Ala) c.409C>G (p.Pro137Ala) | |
| 11 | g.116790904G= | CA2002741053 | APOA5 | c.325C= (p.Pro109=) c.409C= (p.Pro137=) | |
| 11 | g.116790904G>T | CA382739100 | APOA5 | c.325C>A (p.Pro109Thr) c.409C>A (p.Pro137Thr) | |
| 11 | g.116790905C>A | CA382739105 | APOA5 | c.324G>T (p.Gln108His) c.408G>T (p.Gln136His) | |
| 11 | g.116790905C>G | CA382739106 | APOA5 | c.324G>C (p.Gln108His) c.408G>C (p.Gln136His) | |
| 11 | g.116790905C>T | CA477047817 | APOA5 | c.324G>A (p.Gln108=) c.408G>A (p.Gln136=) | |
| 11 | g.116790906T>A | CA382739119 | APOA5 | c.323A>T (p.Gln108Leu) c.407A>T (p.Gln136Leu) | |
| 11 | g.116790906T>C | CA382739111 | APOA5 | c.323A>G (p.Gln108Arg) c.407A>G (p.Gln136Arg) | dbSNP |
| 11 | g.116790906T>G | CA382739108 | APOA5 | c.323A>C (p.Gln108Pro) c.407A>C (p.Gln136Pro) | |
| 11 | g.116790907G>A | CA382739125 | APOA5 | c.322C>T (p.Gln108Ter) c.406C>T (p.Gln136Ter) | dbSNP gnomAD v4 |
| 11 | g.116790907G>C | CA382739129 | APOA5 | c.322C>G (p.Gln108Glu) c.406C>G (p.Gln136Glu) | |
| 11 | g.116790907G= | CA2002741056 | APOA5 | c.322C= (p.Gln108=) c.406C= (p.Gln136=) | |
| 11 | g.116790907G>T | CA382739148 | APOA5 | c.322C>A (p.Gln108Lys) c.406C>A (p.Gln136Lys) | |
| 11 | g.116790908G>A | CA6289094 | APOA5 | c.321C>T (p.Leu107=) c.405C>T (p.Leu135=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790908G>C | CA477047818 | APOA5 | c.321C>G (p.Leu107=) c.405C>G (p.Leu135=) | gnomAD v4 |
| 11 | g.116790908G= | CA2002741062 | APOA5 | c.321C= (p.Leu107=) c.405C= (p.Leu135=) | |
| 11 | g.116790908G>T | CA477047819 | APOA5 | c.321C>A (p.Leu107=) c.405C>A (p.Leu135=) | |
| 11 | g.116790909A>C | CA382739155 | APOA5 | c.320T>G (p.Leu107Arg) c.404T>G (p.Leu135Arg) | |
| 11 | g.116790909A>G | CA382739158 | APOA5 | c.320T>C (p.Leu107Pro) c.404T>C (p.Leu135Pro) | |
| 11 | g.116790909A>T | CA382739160 | APOA5 | c.320T>A (p.Leu107His) c.404T>A (p.Leu135His) | |
| 11 | g.116790910G>A | CA382739168 | APOA5 | c.319C>T (p.Leu107Phe) c.403C>T (p.Leu135Phe) | dbSNP gnomAD v4 |
| 11 | g.116790910G>C | CA382739172 | APOA5 | c.319C>G (p.Leu107Val) c.403C>G (p.Leu135Val) | |
| 11 | g.116790910G= | CA2002741066 | APOA5 | c.319C= (p.Leu107=) c.403C= (p.Leu135=) | |
| 11 | g.116790910G>T | CA382739175 | APOA5 | c.319C>A (p.Leu107Ile) c.403C>A (p.Leu135Ile) | |
| 11 | g.116790911G>A | CA477047824 | APOA5 | c.318C>T (p.Arg106=) c.402C>T (p.Arg134=) | gnomAD v4 |
| 11 | g.116790911G>C | CA477047825 | APOA5 | c.318C>G (p.Arg106=) c.402C>G (p.Arg134=) | |
| 11 | g.116790911G>T | CA477047826 | APOA5 | c.318C>A (p.Arg106=) c.402C>A (p.Arg134=) | |
| 11 | g.116790912C>A | CA382739179 | APOA5 | c.317G>T (p.Arg106Leu) c.401G>T (p.Arg134Leu) | |
| 11 | g.116790912C= | CA2002741069 | APOA5 | c.317G= (p.Arg106=) c.401G= (p.Arg134=) | |
| 11 | g.116790912C>G | CA382739183 | APOA5 | c.317G>C (p.Arg106Pro) c.401G>C (p.Arg134Pro) | |
| 11 | g.116790912C>T | CA382739189 | APOA5 | c.317G>A (p.Arg106His) c.401G>A (p.Arg134His) | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.116790913G>A | CA382739200 | APOA5 | c.316C>T (p.Arg106Cys) c.400C>T (p.Arg134Cys) | gnomAD v4 COSMIC |
| 11 | g.116790913G>C | CA382739199 | APOA5 | c.316C>G (p.Arg106Gly) c.400C>G (p.Arg134Gly) | |
| 11 | g.116790913G>T | CA382739195 | APOA5 | c.316C>A (p.Arg106Ser) c.400C>A (p.Arg134Ser) | |
| 11 | g.116790914A>C | CA477047833 | APOA5 | c.315T>G (p.Ala105=) c.399T>G (p.Ala133=) | |
| 11 | g.116790914A>G | CA477047834 | APOA5 | c.315T>C (p.Ala105=) c.399T>C (p.Ala133=) | |
| 11 | g.116790914A>T | CA477047836 | APOA5 | c.315T>A (p.Ala105=) c.399T>A (p.Ala133=) | |
| 11 | g.116790915G>A | CA382739207 | APOA5 | c.314C>T (p.Ala105Val) c.398C>T (p.Ala133Val) | |
| 11 | g.116790915G>C | CA382739201 | APOA5 | c.314C>G (p.Ala105Gly) c.398C>G (p.Ala133Gly) | |
| 11 | g.116790915G>T | CA382739213 | APOA5 | c.314C>A (p.Ala105Asp) c.398C>A (p.Ala133Asp) | |
| 11 | g.116790916C>A | CA6289095 | APOA5 | c.313G>T (p.Ala105Ser) c.397G>T (p.Ala133Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790916C= | CA2002741073 | APOA5 | c.313G= (p.Ala105=) c.397G= (p.Ala133=) | |
| 11 | g.116790916C>G | CA382739231 | APOA5 | c.313G>C (p.Ala105Pro) c.397G>C (p.Ala133Pro) | |
| 11 | g.116790916C>T | CA382739238 | APOA5 | c.313G>A (p.Ala105Thr) c.397G>A (p.Ala133Thr) | dbSNP gnomAD v4 |
| 11 | g.116790917C>A | CA382739243 | APOA5 | c.312G>T (p.Lys104Asn) c.396G>T (p.Lys132Asn) | |
| 11 | g.116790917C= | CA2002741079 | APOA5 | c.312G= (p.Lys104=) c.396G= (p.Lys132=) | |
| 11 | g.116790917C>G | CA229338107 | APOA5 | c.312G>C (p.Lys104Asn) c.396G>C (p.Lys132Asn) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790917C>T | CA477047838 | APOA5 | c.312G>A (p.Lys104=) c.396G>A (p.Lys132=) | |
| 11 | g.116790918T>A | CA382739260 | APOA5 | c.311A>T (p.Lys104Met) c.395A>T (p.Lys132Met) | |
| 11 | g.116790918T>C | CA382739256 | APOA5 | c.311A>G (p.Lys104Arg) c.395A>G (p.Lys132Arg) | |
| 11 | g.116790918T>G | CA382739254 | APOA5 | c.311A>C (p.Lys104Thr) c.395A>C (p.Lys132Thr) | |
| 11 | g.116790919T>A | CA382739265 | APOA5 | c.310A>T (p.Lys104Ter) c.394A>T (p.Lys132Ter) | |
| 11 | g.116790919T>C | CA382739270 | APOA5 | c.310A>G (p.Lys104Glu) c.394A>G (p.Lys132Glu) | |
| 11 | g.116790919T>G | CA382739274 | APOA5 | c.310A>C (p.Lys104Gln) c.394A>C (p.Lys132Gln) | |
| 11 | g.116790920C>A | CA477047847 | APOA5 | c.309G>T (p.Val103=) c.393G>T (p.Val131=) | |
| 11 | g.116790920C= | CA2002741082 | APOA5 | c.309G= (p.Val103=) c.393G= (p.Val131=) | |
| 11 | g.116790920C>G | CA477047848 | APOA5 | c.309G>C (p.Val103=) c.393G>C (p.Val131=) | |
| 11 | g.116790920C>T | CA477047849 | APOA5 | c.309G>A (p.Val103=) c.393G>A (p.Val131=) | dbSNP COSMIC |
| 11 | g.116790921A>C | CA382739278 | APOA5 | c.308T>G (p.Val103Gly) c.392T>G (p.Val131Gly) | |
| 11 | g.116790921A>G | CA382739281 | APOA5 | c.308T>C (p.Val103Ala) c.392T>C (p.Val131Ala) | gnomAD v4 |
| 11 | g.116790921A>T | CA382739286 | APOA5 | c.308T>A (p.Val103Glu) c.392T>A (p.Val131Glu) | |
| 11 | g.116790922C>A | CA382739292 | APOA5 | c.307G>T (p.Val103Leu) c.391G>T (p.Val131Leu) | |
| 11 | g.116790922C>G | CA382739299 | APOA5 | c.307G>C (p.Val103Leu) c.391G>C (p.Val131Leu) | |
| 11 | g.116790922C>T | CA382739296 | APOA5 | c.307G>A (p.Val103Met) c.391G>A (p.Val131Met) | |
| 11 | g.116790927_116790929del | CA2616086534 | APOA5 | c.305_307del (p.Glu102del) c.389_391del (p.Glu130del) | gnomAD v4 |
| 11 | g.116790923C>A | CA382739303 | APOA5 | c.306G>T (p.Glu102Asp) c.390G>T (p.Glu130Asp) | |
| 11 | g.116790923C>G | CA382739307 | APOA5 | c.306G>C (p.Glu102Asp) c.390G>C (p.Glu130Asp) | |
| 11 | g.116790923C>T | CA477047857 | APOA5 | c.306G>A (p.Glu102=) c.390G>A (p.Glu130=) | gnomAD v4 |
| 11 | g.116790930_116790938del | CA2616086537 | APOA5 | c.298_306del (p.Leu100_Glu102del) c.382_390del (p.Leu128_Glu130del) | gnomAD v4 |
| 11 | g.116790924T>A | CA382739313 | APOA5 | c.305A>T (p.Glu102Val) c.389A>T (p.Glu130Val) | |
| 11 | g.116790924T>C | CA382739318 | APOA5 | c.305A>G (p.Glu102Gly) c.389A>G (p.Glu130Gly) | |
| 11 | g.116790924T>G | CA382739321 | APOA5 | c.305A>C (p.Glu102Ala) c.389A>C (p.Glu130Ala) | |
| 11 | g.116790925C>A | CA382739325 | APOA5 | c.304G>T (p.Glu102Ter) c.388G>T (p.Glu130Ter) | |
| 11 | g.116790925C= | CA2002741086 | APOA5 | c.304G= (p.Glu102=) c.388G= (p.Glu130=) | |
| 11 | g.116790925C>G | CA382739329 | APOA5 | c.304G>C (p.Glu102Gln) c.388G>C (p.Glu130Gln) | |
| 11 | g.116790925C>T | CA6289096 | APOA5 | c.304G>A (p.Glu102Lys) c.388G>A (p.Glu130Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790926C>A | CA382739338 | APOA5 | c.303G>T (p.Glu101Asp) c.387G>T (p.Glu129Asp) | |
| 11 | g.116790926C= | CA2002741090 | APOA5 | c.303G= (p.Glu101=) c.387G= (p.Glu129=) | |
| 11 | g.116790926C>G | CA382739339 | APOA5 | c.303G>C (p.Glu101Asp) c.387G>C (p.Glu129Asp) | |
| 11 | g.116790926C>T | CA477047863 | APOA5 | c.303G>A (p.Glu101=) c.387G>A (p.Glu129=) | dbSNP gnomAD v2 |
| 11 | g.116790927T>A | CA382739347 | APOA5 | c.302A>T (p.Glu101Val) c.386A>T (p.Glu129Val) | |
| 11 | g.116790927T>C | CA382739344 | APOA5 | c.302A>G (p.Glu101Gly) c.386A>G (p.Glu129Gly) | |
| 11 | g.116790927T>G | CA382739342 | APOA5 | c.302A>C (p.Glu101Ala) c.386A>C (p.Glu129Ala) | |
| 11 | g.116790928C>A | CA382739352 | APOA5 | c.301G>T (p.Glu101Ter) c.385G>T (p.Glu129Ter) | |
| 11 | g.116790928C>G | CA382739358 | APOA5 | c.301G>C (p.Glu101Gln) c.385G>C (p.Glu129Gln) | |
| 11 | g.116790928C>T | CA382739362 | APOA5 | c.301G>A (p.Glu101Lys) c.385G>A (p.Glu129Lys) | COSMIC |
| 11 | g.116790929C>A | CA382739364 | APOA5 | c.300G>T (p.Leu100Phe) c.384G>T (p.Leu128Phe) | |
| 11 | g.116790929C>G | CA382739368 | APOA5 | c.300G>C (p.Leu100Phe) c.384G>C (p.Leu128Phe) | |
| 11 | g.116790929C>T | CA477047866 | APOA5 | c.300G>A (p.Leu100=) c.384G>A (p.Leu128=) | |
| 11 | g.116790930A>C | CA382739373 | APOA5 | c.299T>G (p.Leu100Trp) c.383T>G (p.Leu128Trp) | |
| 11 | g.116790930A>G | CA382739376 | APOA5 | c.299T>C (p.Leu100Ser) c.383T>C (p.Leu128Ser) | |
| 11 | g.116790930A>T | CA382739378 | APOA5 | c.299T>A (p.Leu100Ter) c.383T>A (p.Leu128Ter) | |
| 11 | g.116790931A>C | CA382739380 | APOA5 | c.298T>G (p.Leu100Val) c.382T>G (p.Leu128Val) | |
| 11 | g.116790931A>G | CA477047876 | APOA5 | c.298T>C (p.Leu100=) c.382T>C (p.Leu128=) | |
| 11 | g.116790931A>T | CA382739382 | APOA5 | c.298T>A (p.Leu100Met) c.382T>A (p.Leu128Met) | |
| 11 | g.116790931_116790934delinsACTC | CA2002741093 | APOA5 | c.295_298delinsGAGT (p.Glu99=) c.379_382delinsGAGT (p.Glu127=) | |
| 11 | g.116790932C>A | CA382739385 | APOA5 | c.297G>T (p.Glu99Asp) c.381G>T (p.Glu127Asp) | |
| 11 | g.116790932C>G | CA382739387 | APOA5 | c.297G>C (p.Glu99Asp) c.381G>C (p.Glu127Asp) | |
| 11 | g.116790932C>T | CA477047877 | APOA5 | c.297G>A (p.Glu99=) c.381G>A (p.Glu127=) | |
| 11 | g.116790937_116790939del | CA915948263 | APOA5 | c.295_297del (p.Glu99del) c.379_381del (p.Glu127del) | ClinVar dbSNP |
| 11 | g.116790933T>A | CA382739401 | APOA5 | c.296A>T (p.Glu99Val) c.380A>T (p.Glu127Val) | |
| 11 | g.116790933T>C | CA229338113 | APOA5 | c.296A>G (p.Glu99Gly) c.380A>G (p.Glu127Gly) | dbSNP |
| 11 | g.116790933T>G | CA382739395 | APOA5 | c.296A>C (p.Glu99Ala) c.380A>C (p.Glu127Ala) | |
| 11 | g.116790933T= | CA2002741105 | APOA5 | c.296A= (p.Glu99=) c.380A= (p.Glu127=) | |
| 11 | g.116790934C>A | CA382739425 | APOA5 | c.295G>T (p.Glu99Ter) c.379G>T (p.Glu127Ter) | |
| 11 | g.116790934C= | CA2002741109 | APOA5 | c.295G= (p.Glu99=) c.379G= (p.Glu127=) | |
| 11 | g.116790934C>G | CA382739426 | APOA5 | c.295G>C (p.Glu99Gln) c.379G>C (p.Glu127Gln) | |
| 11 | g.116790934C>T | CA6289097 | APOA5 | c.295G>A (p.Glu99Lys) c.379G>A (p.Glu127Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790935C>A | CA229338117 | APOA5 | c.294G>T (p.Glu98Asp) c.378G>T (p.Glu126Asp) | dbSNP |
| 11 | g.116790935C= | CA2002741113 | APOA5 | c.294G= (p.Glu98=) c.378G= (p.Glu126=) | |
| 11 | g.116790935C>G | CA6289098 | APOA5 | c.294G>C (p.Glu98Asp) c.378G>C (p.Glu126Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790935C>T | CA6289099 | APOA5 | c.294G>A (p.Glu98=) c.378G>A (p.Glu126=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790936T>A | CA382739441 | APOA5 | c.293A>T (p.Glu98Val) c.377A>T (p.Glu126Val) | |
| 11 | g.116790936T>C | CA382739445 | APOA5 | c.293A>G (p.Glu98Gly) c.377A>G (p.Glu126Gly) | |
| 11 | g.116790936T>G | CA382739444 | APOA5 | c.293A>C (p.Glu98Ala) c.377A>C (p.Glu126Ala) | gnomAD v4 |
| 11 | g.116790937C>A | CA382739446 | APOA5 | c.292G>T (p.Glu98Ter) c.376G>T (p.Glu126Ter) | |
| 11 | g.116790937C>G | CA382739448 | APOA5 | c.292G>C (p.Glu98Gln) c.376G>C (p.Glu126Gln) | |
| 11 | g.116790937C>T | CA382739452 | APOA5 | c.292G>A (p.Glu98Lys) c.376G>A (p.Glu126Lys) | |
| 11 | g.116790938C>A | CA382739454 | APOA5 | c.291G>T (p.Gln97His) c.375G>T (p.Gln125His) | |
| 11 | g.116790938C>G | CA382739460 | APOA5 | c.291G>C (p.Gln97His) c.375G>C (p.Gln125His) | |
| 11 | g.116790938C>T | CA477047885 | APOA5 | c.291G>A (p.Gln97=) c.375G>A (p.Gln125=) | |
| 11 | g.116790939T>A | CA382739464 | APOA5 | c.290A>T (p.Gln97Leu) c.374A>T (p.Gln125Leu) | |
| 11 | g.116790939T>C | CA382739465 | APOA5 | c.290A>G (p.Gln97Arg) c.374A>G (p.Gln125Arg) | |
| 11 | g.116790939T>G | CA382739463 | APOA5 | c.290A>C (p.Gln97Pro) c.374A>C (p.Gln125Pro) | |
| 11 | g.116790940G>A | CA6289100 | APOA5 | c.289C>T (p.Gln97Ter) c.373C>T (p.Gln125Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790940G>C | CA382739471 | APOA5 | c.289C>G (p.Gln97Glu) c.373C>G (p.Gln125Glu) | |
| 11 | g.116790940G= | CA2002741121 | APOA5 | c.289C= (p.Gln97=) c.373C= (p.Gln125=) | |
| 11 | g.116790940G>T | CA6289101 | APOA5 | c.289C>A (p.Gln97Lys) c.373C>A (p.Gln125Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
| 11 | g.116790941C>A | CA477047890 | APOA5 | c.288G>T (p.Leu96=) c.372G>T (p.Leu124=) | |
| 11 | g.116790941C>G | CA477047892 | APOA5 | c.288G>C (p.Leu96=) c.372G>C (p.Leu124=) | |
| 11 | g.116790941C>T | CA477047891 | APOA5 | c.288G>A (p.Leu96=) c.372G>A (p.Leu124=) | |
| 11 | g.116790942A= | CA2002741123 | APOA5 | c.287T= (p.Leu96=) c.371T= (p.Leu124=) | |
| 11 | g.116790942A>C | CA382739474 | APOA5 | c.287T>G (p.Leu96Arg) c.371T>G (p.Leu124Arg) | dbSNP |
| 11 | g.116790942A>G | CA382739477 | APOA5 | c.287T>C (p.Leu96Pro) c.371T>C (p.Leu124Pro) | |
| 11 | g.116790942A>T | CA382739486 | APOA5 | c.287T>A (p.Leu96Gln) c.371T>A (p.Leu124Gln) | |
| 11 | g.116790943G>A | CA477047893 | APOA5 | c.286C>T (p.Leu96=) c.370C>T (p.Leu124=) | ClinVar |
| 11 | g.116790943G>C | CA382739490 | APOA5 | c.286C>G (p.Leu96Val) c.370C>G (p.Leu124Val) | |
| 11 | g.116790943G>T | CA382739491 | APOA5 | c.286C>A (p.Leu96Met) c.370C>A (p.Leu124Met) | |
| 11 | g.116790944C>A | CA382739492 | APOA5 | c.285G>T (p.Gln95His) c.369G>T (p.Gln123His) | |
| 11 | g.116790944C>G | CA382739493 | APOA5 | c.285G>C (p.Gln95His) c.369G>C (p.Gln123His) | |
| 11 | g.116790944C>T | CA477047897 | APOA5 | c.285G>A (p.Gln95=) c.369G>A (p.Gln123=) | |
| 11 | g.116790945T>A | CA382739495 | APOA5 | c.284A>T (p.Gln95Leu) c.368A>T (p.Gln123Leu) | |
| 11 | g.116790945T>C | CA382739498 | APOA5 | c.284A>G (p.Gln95Arg) c.368A>G (p.Gln123Arg) | |
| 11 | g.116790945T>G | CA382739500 | APOA5 | c.284A>C (p.Gln95Pro) c.368A>C (p.Gln123Pro) | |
| 11 | g.116790946G>A | CA6289102 | APOA5 | c.283C>T (p.Gln95Ter) c.367C>T (p.Gln123Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790946G>C | CA382739501 | APOA5 | c.283C>G (p.Gln95Glu) c.367C>G (p.Gln123Glu) | |
| 11 | g.116790946G= | CA2002741126 | APOA5 | c.283C= (p.Gln95=) c.367C= (p.Gln123=) | |
| 11 | g.116790946G>T | CA382739503 | APOA5 | c.283C>A (p.Gln95Lys) c.367C>A (p.Gln123Lys) | |
| 11 | g.116790947C>A | CA477047899 | APOA5 | c.282G>T (p.Arg94=) c.366G>T (p.Arg122=) | |
| 11 | g.116790947C= | CA2002741128 | APOA5 | c.282G= (p.Arg94=) c.366G= (p.Arg122=) | |
| 11 | g.116790947C>G | CA477047901 | APOA5 | c.282G>C (p.Arg94=) c.366G>C (p.Arg122=) | |
| 11 | g.116790947C>T | CA477047902 | APOA5 | c.282G>A (p.Arg94=) c.366G>A (p.Arg122=) | dbSNP gnomAD v4 |
| 11 | g.116790948C>A | CA6289103 | APOA5 | c.281G>T (p.Arg94Leu) c.365G>T (p.Arg122Leu) | dbSNP ExAC gnomAD v2 |
| 11 | g.116790948C= | CA2002741133 | APOA5 | c.281G= (p.Arg94=) c.365G= (p.Arg122=) | |
| 11 | g.116790948C>G | CA382739509 | APOA5 | c.281G>C (p.Arg94Pro) c.365G>C (p.Arg122Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790948C>T | CA382739507 | APOA5 | c.281G>A (p.Arg94Gln) c.365G>A (p.Arg122Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790949G>A | CA6289104 | APOA5 | c.280C>T (p.Arg94Trp) c.364C>T (p.Arg122Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790949G>C | CA382739518 | APOA5 | c.280C>G (p.Arg94Gly) c.364C>G (p.Arg122Gly) | |
| 11 | g.116790949G= | CA2002741138 | APOA5 | c.280C= (p.Arg94=) c.364C= (p.Arg122=) | |
| 11 | g.116790949G>T | CA477047905 | APOA5 | c.280C>A (p.Arg94=) c.364C>A (p.Arg122=) | |
| 11 | g.116790950C>A | CA477047906 | APOA5 | c.279G>T (p.Arg93=) c.363G>T (p.Arg121=) | |
| 11 | g.116790950C>G | CA477047907 | APOA5 | c.279G>C (p.Arg93=) c.363G>C (p.Arg121=) | |
| 11 | g.116790950C>T | CA477047908 | APOA5 | c.279G>A (p.Arg93=) c.363G>A (p.Arg121=) | |
| 11 | g.116790951C>A | CA382739520 | APOA5 | c.278G>T (p.Arg93Leu) c.362G>T (p.Arg121Leu) | dbSNP gnomAD v4 |
| 11 | g.116790951C= | CA2002741142 | APOA5 | c.278G= (p.Arg93=) c.362G= (p.Arg121=) | |
| 11 | g.116790951C>G | CA382739527 | APOA5 | c.278G>C (p.Arg93Pro) c.362G>C (p.Arg121Pro) | |
| 11 | g.116790951C>T | CA6289105 | APOA5 | c.278G>A (p.Arg93Gln) c.362G>A (p.Arg121Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790952G>A | CA229338148 | APOA5 | c.277C>T (p.Arg93Trp) c.361C>T (p.Arg121Trp) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790952G>C | CA382739532 | APOA5 | c.277C>G (p.Arg93Gly) c.361C>G (p.Arg121Gly) | |
| 11 | g.116790952G= | CA2002741145 | APOA5 | c.277C= (p.Arg93=) c.361C= (p.Arg121=) | |
| 11 | g.116790952G>T | CA229338135 | APOA5 | c.277C>A (p.Arg93=) c.361C>A (p.Arg121=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |