| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.116790730C>A | CA382738284 | APOA5 | c.499G>T (p.Asp167Tyr) c.583G>T (p.Asp195Tyr) | |
| 11 | g.116790730C>G | CA382738283 | APOA5 | c.499G>C (p.Asp167His) c.583G>C (p.Asp195His) | gnomAD v4 |
| 11 | g.116790730C>T | CA382738282 | APOA5 | c.499G>A (p.Asp167Asn) c.583G>A (p.Asp195Asn) | |
| 11 | g.116790731C>A | CA477047942 | APOA5 | c.498G>T (p.Val166=) c.582G>T (p.Val194=) | |
| 11 | g.116790731C>G | CA477047943 | APOA5 | c.498G>C (p.Val166=) c.582G>C (p.Val194=) | |
| 11 | g.116790731C>T | CA477047945 | APOA5 | c.498G>A (p.Val166=) c.582G>A (p.Val194=) | |
| 11 | g.116790732A>C | CA382738285 | APOA5 | c.497T>G (p.Val166Gly) c.581T>G (p.Val194Gly) | |
| 11 | g.116790732A>G | CA382738286 | APOA5 | c.497T>C (p.Val166Ala) c.581T>C (p.Val194Ala) | |
| 11 | g.116790732A>T | CA382738287 | APOA5 | c.497T>A (p.Val166Glu) c.581T>A (p.Val194Glu) | |
| 11 | g.116790733C>A | CA382738288 | APOA5 | c.496G>T (p.Val166Leu) c.580G>T (p.Val194Leu) | |
| 11 | g.116790733C= | CA2002740820 | APOA5 | c.496G= (p.Val166=) c.580G= (p.Val194=) | |
| 11 | g.116790733C>G | CA382738289 | APOA5 | c.496G>C (p.Val166Leu) c.580G>C (p.Val194Leu) | |
| 11 | g.116790733C>T | CA382738290 | APOA5 | c.496G>A (p.Val166Met) c.580G>A (p.Val194Met) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790734G>A | CA477047951 | APOA5 | c.495C>T (p.Gly165=) c.579C>T (p.Gly193=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790734G>C | CA477047952 | APOA5 | c.495C>G (p.Gly165=) c.579C>G (p.Gly193=) | |
| 11 | g.116790734G= | CA2002740822 | APOA5 | c.495C= (p.Gly165=) c.579C= (p.Gly193=) | |
| 11 | g.116790734G>T | CA6289069 | APOA5 | c.495C>A (p.Gly165=) c.579C>A (p.Gly193=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790735C>A | CA382738291 | APOA5 | c.494G>T (p.Gly165Val) c.578G>T (p.Gly193Val) | |
| 11 | g.116790735C= | CA2002740830 | APOA5 | c.494G= (p.Gly165=) c.578G= (p.Gly193=) | |
| 11 | g.116790735C>G | CA382738292 | APOA5 | c.494G>C (p.Gly165Ala) c.578G>C (p.Gly193Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790735C>T | CA382738293 | APOA5 | c.494G>A (p.Gly165Asp) c.578G>A (p.Gly193Asp) | dbSNP gnomAD v2 |
| 11 | g.116790740dup | CA6289070 | APOA5 | c.494dup (p.Val166ArgfsTer?) c.578dup (p.Val194ArgfsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790740del | CA2616086364 | APOA5 | c.494del (p.Gly165AlafsTer?) c.578del (p.Gly193AlafsTer?) | gnomAD v4 |
| 11 | g.116790736C>A | CA382738294 | APOA5 | c.493G>T (p.Gly165Cys) c.577G>T (p.Gly193Cys) | |
| 11 | g.116790736C= | CA2002740837 | APOA5 | c.493G= (p.Gly165=) c.577G= (p.Gly193=) | |
| 11 | g.116790736C>G | CA6289071 | APOA5 | c.493G>C (p.Gly165Arg) c.577G>C (p.Gly193Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790736C>T | CA382738295 | APOA5 | c.493G>A (p.Gly165Ser) c.577G>A (p.Gly193Ser) | gnomAD v4 |
| 11 | g.116790737C>A | CA477047967 | APOA5 | c.492G>T (p.Gly164=) c.576G>T (p.Gly192=) | |
| 11 | g.116790737C= | CA2002740839 | APOA5 | c.492G= (p.Gly164=) c.576G= (p.Gly192=) | |
| 11 | g.116790737C>G | CA477047968 | APOA5 | c.492G>C (p.Gly164=) c.576G>C (p.Gly192=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790737C>T | CA477047969 | APOA5 | c.492G>A (p.Gly164=) c.576G>A (p.Gly192=) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790738C>A | CA382738297 | APOA5 | c.491G>T (p.Gly164Val) c.575G>T (p.Gly192Val) | |
| 11 | g.116790738C>G | CA382738298 | APOA5 | c.491G>C (p.Gly164Ala) c.575G>C (p.Gly192Ala) | |
| 11 | g.116790738C>T | CA382738296 | APOA5 | c.491G>A (p.Gly164Glu) c.575G>A (p.Gly192Glu) | |
| 11 | g.116790739C>A | CA382738299 | APOA5 | c.490G>T (p.Gly164Trp) c.574G>T (p.Gly192Trp) | |
| 11 | g.116790739C= | CA2002740844 | APOA5 | c.490G= (p.Gly164=) c.574G= (p.Gly192=) | |
| 11 | g.116790739C>G | CA6289073 | APOA5 | c.490G>C (p.Gly164Arg) c.574G>C (p.Gly192Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790739C>T | CA6289072 | APOA5 | c.490G>A (p.Gly164Arg) c.574G>A (p.Gly192Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790740C>A | CA477047979 | APOA5 | c.489G>T (p.Leu163=) c.573G>T (p.Leu191=) | |
| 11 | g.116790740C>G | CA477047980 | APOA5 | c.489G>C (p.Leu163=) c.573G>C (p.Leu191=) | |
| 11 | g.116790740C>T | CA477047981 | APOA5 | c.489G>A (p.Leu163=) c.573G>A (p.Leu191=) | |
| 11 | g.116790741A= | CA2002740850 | APOA5 | c.488T= (p.Leu163=) c.572T= (p.Leu191=) | |
| 11 | g.116790741A>C | CA382738300 | APOA5 | c.488T>G (p.Leu163Arg) c.572T>G (p.Leu191Arg) | dbSNP |
| 11 | g.116790741A>G | CA382738301 | APOA5 | c.488T>C (p.Leu163Pro) c.572T>C (p.Leu191Pro) | |
| 11 | g.116790741A>T | CA382738302 | APOA5 | c.488T>A (p.Leu163Gln) c.572T>A (p.Leu191Gln) | |
| 11 | g.116790742G>A | CA477047985 | APOA5 | c.487C>T (p.Leu163=) c.571C>T (p.Leu191=) | gnomAD v4 |
| 11 | g.116790742G>C | CA382738303 | APOA5 | c.487C>G (p.Leu163Val) c.571C>G (p.Leu191Val) | |
| 11 | g.116790742G>T | CA382738304 | APOA5 | c.487C>A (p.Leu163Met) c.571C>A (p.Leu191Met) | |
| 11 | g.116790743C>A | CA382738305 | APOA5 | c.486G>T (p.Leu162Phe) c.570G>T (p.Leu190Phe) | |
| 11 | g.116790743C>G | CA382738306 | APOA5 | c.486G>C (p.Leu162Phe) c.570G>C (p.Leu190Phe) | |
| 11 | g.116790743C>T | CA477047988 | APOA5 | c.486G>A (p.Leu162=) c.570G>A (p.Leu190=) | |
| 11 | g.116790744A= | CA2002740854 | APOA5 | c.485T= (p.Leu162=) c.569T= (p.Leu190=) | |
| 11 | g.116790744A>C | CA382738307 | APOA5 | c.485T>G (p.Leu162Trp) c.569T>G (p.Leu190Trp) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790744A>G | CA382738308 | APOA5 | c.485T>C (p.Leu162Ser) c.569T>C (p.Leu190Ser) | |
| 11 | g.116790744A>T | CA382738309 | APOA5 | c.485T>A (p.Leu162Ter) c.569T>A (p.Leu190Ter) | |
| 11 | g.116790745A>C | CA382738311 | APOA5 | c.484T>G (p.Leu162Val) c.568T>G (p.Leu190Val) | |
| 11 | g.116790745A>G | CA477047993 | APOA5 | c.484T>C (p.Leu162=) c.568T>C (p.Leu190=) | dbSNP gnomAD v4 |
| 11 | g.116790745A>T | CA382738310 | APOA5 | c.484T>A (p.Leu162Met) c.568T>A (p.Leu190Met) | gnomAD v4 |
| 11 | g.116790746C>A | CA382738312 | APOA5 | c.483G>T (p.Gln161His) c.567G>T (p.Gln189His) | COSMIC |
| 11 | g.116790746C>G | CA382738313 | APOA5 | c.483G>C (p.Gln161His) c.567G>C (p.Gln189His) | |
| 11 | g.116790746C>T | CA477047995 | APOA5 | c.483G>A (p.Gln161=) c.567G>A (p.Gln189=) | |
| 11 | g.116790747T>A | CA382738314 | APOA5 | c.482A>T (p.Gln161Leu) c.566A>T (p.Gln189Leu) | |
| 11 | g.116790747T>C | CA382738315 | APOA5 | c.482A>G (p.Gln161Arg) c.566A>G (p.Gln189Arg) | |
| 11 | g.116790747T>G | CA382738316 | APOA5 | c.482A>C (p.Gln161Pro) c.566A>C (p.Gln189Pro) | |
| 11 | g.116790748G>A | CA382738317 | APOA5 | c.481C>T (p.Gln161Ter) c.565C>T (p.Gln189Ter) | |
| 11 | g.116790748G>C | CA382738318 | APOA5 | c.481C>G (p.Gln161Glu) c.565C>G (p.Gln189Glu) | |
| 11 | g.116790748G>T | CA382738319 | APOA5 | c.481C>A (p.Gln161Lys) c.565C>A (p.Gln189Lys) | |
| 11 | g.116790749G>A | CA6289074 | APOA5 | c.480C>T (p.Ala160=) c.564C>T (p.Ala188=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790749G>C | CA477047999 | APOA5 | c.480C>G (p.Ala160=) c.564C>G (p.Ala188=) | |
| 11 | g.116790749G= | CA2002740856 | APOA5 | c.480C= (p.Ala160=) c.564C= (p.Ala188=) | |
| 11 | g.116790749G>T | CA477047997 | APOA5 | c.480C>A (p.Ala160=) c.564C>A (p.Ala188=) | ClinVar gnomAD v4 |
| 11 | g.116790750G>A | CA382738320 | APOA5 | c.479C>T (p.Ala160Val) c.563C>T (p.Ala188Val) | gnomAD v4 |
| 11 | g.116790750G>C | CA382738321 | APOA5 | c.479C>G (p.Ala160Gly) c.563C>G (p.Ala188Gly) | |
| 11 | g.116790750G>T | CA382738322 | APOA5 | c.479C>A (p.Ala160Asp) c.563C>A (p.Ala188Asp) | gnomAD v4 |
| 11 | g.116790751C>A | CA382738323 | APOA5 | c.478G>T (p.Ala160Ser) c.562G>T (p.Ala188Ser) | |
| 11 | g.116790751C= | CA2002740858 | APOA5 | c.478G= (p.Ala160=) c.562G= (p.Ala188=) | |
| 11 | g.116790751C>G | CA382738325 | APOA5 | c.478G>C (p.Ala160Pro) c.562G>C (p.Ala188Pro) | |
| 11 | g.116790751C>T | CA382738324 | APOA5 | c.478G>A (p.Ala160Thr) c.562G>A (p.Ala188Thr) | dbSNP |
| 11 | g.116790752C>A | CA382738326 | APOA5 | c.477G>T (p.Lys159Asn) c.561G>T (p.Lys187Asn) | |
| 11 | g.116790752C= | CA2002740860 | APOA5 | c.477G= (p.Lys159=) c.561G= (p.Lys187=) | |
| 11 | g.116790752C>G | CA382738327 | APOA5 | c.477G>C (p.Lys159Asn) c.561G>C (p.Lys187Asn) | |
| 11 | g.116790752C>T | CA477048013 | APOA5 | c.477G>A (p.Lys159=) c.561G>A (p.Lys187=) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790753T>A | CA382738328 | APOA5 | c.476A>T (p.Lys159Met) c.560A>T (p.Lys187Met) | |
| 11 | g.116790753T>C | CA382738329 | APOA5 | c.476A>G (p.Lys159Arg) c.560A>G (p.Lys187Arg) | dbSNP |
| 11 | g.116790753T>G | CA382738330 | APOA5 | c.476A>C (p.Lys159Thr) c.560A>C (p.Lys187Thr) | |
| 11 | g.116790753T= | CA2002740862 | APOA5 | c.476A= (p.Lys159=) c.560A= (p.Lys187=) | |
| 11 | g.116790754T>A | CA382738331 | APOA5 | c.475A>T (p.Lys159Ter) c.559A>T (p.Lys187Ter) | |
| 11 | g.116790754T>C | CA382738332 | APOA5 | c.475A>G (p.Lys159Glu) c.559A>G (p.Lys187Glu) | |
| 11 | g.116790754T>G | CA382738333 | APOA5 | c.475A>C (p.Lys159Gln) c.559A>C (p.Lys187Gln) | |
| 11 | g.116790755G>A | CA477048018 | APOA5 | c.474C>T (p.Thr158=) c.558C>T (p.Thr186=) | dbSNP gnomAD v4 |
| 11 | g.116790755G>C | CA477048019 | APOA5 | c.474C>G (p.Thr158=) c.558C>G (p.Thr186=) | dbSNP gnomAD v2 |
| 11 | g.116790755G= | CA2002740865 | APOA5 | c.474C= (p.Thr158=) c.558C= (p.Thr186=) | |
| 11 | g.116790755G>T | CA477048016 | APOA5 | c.474C>A (p.Thr158=) c.558C>A (p.Thr186=) | |
| 11 | g.116790756G>A | CA382738334 | APOA5 | c.473C>T (p.Thr158Ile) c.557C>T (p.Thr186Ile) | gnomAD v4 |
| 11 | g.116790756G>C | CA382738335 | APOA5 | c.473C>G (p.Thr158Ser) c.557C>G (p.Thr186Ser) | |
| 11 | g.116790756G>T | CA382738336 | APOA5 | c.473C>A (p.Thr158Asn) c.557C>A (p.Thr186Asn) | gnomAD v4 |
| 11 | g.116790757T>A | CA382738337 | APOA5 | c.472A>T (p.Thr158Ser) c.556A>T (p.Thr186Ser) | |
| 11 | g.116790757T>C | CA382738338 | APOA5 | c.472A>G (p.Thr158Ala) c.556A>G (p.Thr186Ala) | |
| 11 | g.116790757T>G | CA382738339 | APOA5 | c.472A>C (p.Thr158Pro) c.556A>C (p.Thr186Pro) | dbSNP |
| 11 | g.116790757T= | CA2002740868 | APOA5 | c.472A= (p.Thr158=) c.556A= (p.Thr186=) | |
| 11 | g.116790758G>A | CA477048030 | APOA5 | c.471C>T (p.Asp157=) c.555C>T (p.Asp185=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790758G>C | CA382738340 | APOA5 | c.471C>G (p.Asp157Glu) c.555C>G (p.Asp185Glu) | |
| 11 | g.116790758G= | CA2002740872 | APOA5 | c.471C= (p.Asp157=) c.555C= (p.Asp185=) | |
| 11 | g.116790758G>T | CA382738341 | APOA5 | c.471C>A (p.Asp157Glu) c.555C>A (p.Asp185Glu) | gnomAD v4 |
| 11 | g.116790759T>A | CA382738342 | APOA5 | c.470A>T (p.Asp157Val) c.554A>T (p.Asp185Val) | |
| 11 | g.116790759T>C | CA382738343 | APOA5 | c.470A>G (p.Asp157Gly) c.554A>G (p.Asp185Gly) | |
| 11 | g.116790759T>G | CA382738344 | APOA5 | c.470A>C (p.Asp157Ala) c.554A>C (p.Asp185Ala) | |
| 11 | g.116790760C>A | CA382738345 | APOA5 | c.469G>T (p.Asp157Tyr) c.553G>T (p.Asp185Tyr) | |
| 11 | g.116790760C>G | CA382738346 | APOA5 | c.469G>C (p.Asp157His) c.553G>C (p.Asp185His) | |
| 11 | g.116790760C>T | CA382738347 | APOA5 | c.469G>A (p.Asp157Asn) c.553G>A (p.Asp185Asn) | |
| 11 | g.116790761T>A | CA382738348 | APOA5 | c.468A>T (p.Glu156Asp) c.552A>T (p.Glu184Asp) | |
| 11 | g.116790761T>C | CA477048038 | APOA5 | c.468A>G (p.Glu156=) c.552A>G (p.Glu184=) | dbSNP |
| 11 | g.116790761T>G | CA382738349 | APOA5 | c.468A>C (p.Glu156Asp) c.552A>C (p.Glu184Asp) | |
| 11 | g.116790761T= | CA2002740874 | APOA5 | c.468A= (p.Glu156=) c.552A= (p.Glu184=) | |
| 11 | g.116790761_116790790delinsTTCCCCCACCACGCGCAACTGCTCCTGCAG | CA2002740875 | APOA5 | c.439_468delinsCTGCAGGAGCAGTTGCGCGTGGTGGGGGAA (p.Leu147=) c.523_552delinsCTGCAGGAGCAGTTGCGCGTGGTGGGGGAA (p.Leu175=) | |
| 11 | g.116790762T>A | CA382738350 | APOA5 | c.467A>T (p.Glu156Val) c.551A>T (p.Glu184Val) | |
| 11 | g.116790762T>C | CA382738351 | APOA5 | c.467A>G (p.Glu156Gly) c.551A>G (p.Glu184Gly) | |
| 11 | g.116790762T>G | CA382738352 | APOA5 | c.467A>C (p.Glu156Ala) c.551A>C (p.Glu184Ala) | |
| 11 | g.116790762_116790790del | CA2002740876 | APOA5 | c.439_467del (p.Leu147ArgfsTer?) c.523_551del (p.Leu175ArgfsTer?) | dbSNP |
| 11 | g.116790763C>A | CA6289075 | APOA5 | c.466G>T (p.Glu156Ter) c.550G>T (p.Glu184Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 11 | g.116790763C= | CA2002740879 | APOA5 | c.466G= (p.Glu156=) c.550G= (p.Glu184=) | |
| 11 | g.116790763C>G | CA382738354 | APOA5 | c.466G>C (p.Glu156Gln) c.550G>C (p.Glu184Gln) | |
| 11 | g.116790763C>T | CA382738353 | APOA5 | c.466G>A (p.Glu156Lys) c.550G>A (p.Glu184Lys) | dbSNP gnomAD v4 COSMIC |
| 11 | g.116790767del | CA645571761 | APOA5 | c.466del (p.Glu156LysfsTer?) c.550del (p.Glu184LysfsTer?) | gnomAD v4 COSMIC |
| 11 | g.116790764C>A | CA477047457 | APOA5 | c.465G>T (p.Gly155=) c.549G>T (p.Gly183=) | |
| 11 | g.116790764C= | CA2002740884 | APOA5 | c.465G= (p.Gly155=) c.549G= (p.Gly183=) | |
| 11 | g.116790764C>G | CA477047455 | APOA5 | c.465G>C (p.Gly155=) c.549G>C (p.Gly183=) | |
| 11 | g.116790764C>T | CA477047453 | APOA5 | c.465G>A (p.Gly155=) c.549G>A (p.Gly183=) | ClinVar dbSNP |
| 11 | g.116790765C>A | CA382738355 | APOA5 | c.464G>T (p.Gly155Val) c.548G>T (p.Gly183Val) | gnomAD v4 |
| 11 | g.116790765C>G | CA382738356 | APOA5 | c.464G>C (p.Gly155Ala) c.548G>C (p.Gly183Ala) | |
| 11 | g.116790765C>T | CA382738357 | APOA5 | c.464G>A (p.Gly155Glu) c.548G>A (p.Gly183Glu) | ClinVar gnomAD v4 |
| 11 | g.116790766_116790772dup | CA2616086397 | APOA5 | c.458_464dup (p.Glu156GlyfsTer?) c.542_548dup (p.Glu184GlyfsTer?) | gnomAD v4 |
| 11 | g.116790766C>A | CA382738358 | APOA5 | c.463G>T (p.Gly155Trp) c.547G>T (p.Gly183Trp) | |
| 11 | g.116790766C>G | CA382738359 | APOA5 | c.463G>C (p.Gly155Arg) c.547G>C (p.Gly183Arg) | gnomAD v4 |
| 11 | g.116790766C>T | CA382738360 | APOA5 | c.463G>A (p.Gly155Arg) c.547G>A (p.Gly183Arg) | |
| 11 | g.116790767C>A | CA477047459 | APOA5 | c.462G>T (p.Val154=) c.546G>T (p.Val182=) | |
| 11 | g.116790767C>G | CA477047461 | APOA5 | c.462G>C (p.Val154=) c.546G>C (p.Val182=) | |
| 11 | g.116790767C>T | CA477047460 | APOA5 | c.462G>A (p.Val154=) c.546G>A (p.Val182=) | |
| 11 | g.116790768A>C | CA382738361 | APOA5 | c.461T>G (p.Val154Gly) c.545T>G (p.Val182Gly) | |
| 11 | g.116790768A>G | CA382738362 | APOA5 | c.461T>C (p.Val154Ala) c.545T>C (p.Val182Ala) | |
| 11 | g.116790768A>T | CA382738363 | APOA5 | c.461T>A (p.Val154Glu) c.545T>A (p.Val182Glu) | |
| 11 | g.116790769C>A | CA382738364 | APOA5 | c.460G>T (p.Val154Leu) c.544G>T (p.Val182Leu) | |
| 11 | g.116790769C= | CA2002740887 | APOA5 | c.460G= (p.Val154=) c.544G= (p.Val182=) | |
| 11 | g.116790769C>G | CA382738365 | APOA5 | c.460G>C (p.Val154Leu) c.544G>C (p.Val182Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790769C>T | CA229337938 | APOA5 | c.460G>A (p.Val154Met) c.544G>A (p.Val182Met) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790770C>A | CA477047465 | APOA5 | c.459G>T (p.Val153=) c.543G>T (p.Val181=) | |
| 11 | g.116790770C= | CA2002740889 | APOA5 | c.459G= (p.Val153=) c.543G= (p.Val181=) | |
| 11 | g.116790770C>G | CA477047467 | APOA5 | c.459G>C (p.Val153=) c.543G>C (p.Val181=) | ClinVar dbSNP gnomAD v4 |
| 11 | g.116790770C>T | CA477047469 | APOA5 | c.459G>A (p.Val153=) c.543G>A (p.Val181=) | |
| 11 | g.116790771A>C | CA382738367 | APOA5 | c.458T>G (p.Val153Gly) c.542T>G (p.Val181Gly) | |
| 11 | g.116790771A>G | CA382738368 | APOA5 | c.458T>C (p.Val153Ala) c.542T>C (p.Val181Ala) | |
| 11 | g.116790771A>T | CA382738366 | APOA5 | c.458T>A (p.Val153Glu) c.542T>A (p.Val181Glu) | |
| 11 | g.116790772C>A | CA382738369 | APOA5 | c.457G>T (p.Val153Leu) c.541G>T (p.Val181Leu) | |
| 11 | g.116790772C= | CA1630855369 | APOA5 | c.457G= (p.Val153=) c.541G= (p.Val181=) | |
| 11 | g.116790772C>G | CA382738370 | APOA5 | c.457G>C (p.Val153Leu) c.541G>C (p.Val181Leu) | gnomAD v4 |
| 11 | g.116790772C>T | CA6289076 | APOA5 | c.457G>A (p.Val153Met) c.541G>A (p.Val181Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790773G>A | CA477047474 | APOA5 | c.456C>T (p.Arg152=) c.540C>T (p.Arg180=) | dbSNP gnomAD v4 |
| 11 | g.116790773G>C | CA477047475 | APOA5 | c.456C>G (p.Arg152=) c.540C>G (p.Arg180=) | gnomAD v4 |
| 11 | g.116790773G= | CA2002740897 | APOA5 | c.456C= (p.Arg152=) c.540C= (p.Arg180=) | |
| 11 | g.116790773G>T | CA229337944 | APOA5 | c.456C>A (p.Arg152=) c.540C>A (p.Arg180=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790774C>A | CA382738371 | APOA5 | c.455G>T (p.Arg152Leu) c.539G>T (p.Arg180Leu) | gnomAD v4 |
| 11 | g.116790774C= | CA2002740904 | APOA5 | c.455G= (p.Arg152=) c.539G= (p.Arg180=) | |
| 11 | g.116790774C>G | CA382738372 | APOA5 | c.455G>C (p.Arg152Pro) c.539G>C (p.Arg180Pro) | |
| 11 | g.116790774C>T | CA6289077 | APOA5 | c.455G>A (p.Arg152His) c.539G>A (p.Arg180His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 11 | g.116790775G>A | CA229337960 | APOA5 | c.454C>T (p.Arg152Cys) c.538C>T (p.Arg180Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790775G>C | CA382738374 | APOA5 | c.454C>G (p.Arg152Gly) c.538C>G (p.Arg180Gly) | |
| 11 | g.116790775G= | CA2002740908 | APOA5 | c.454C= (p.Arg152=) c.538C= (p.Arg180=) | |
| 11 | g.116790775G>T | CA382738373 | APOA5 | c.454C>A (p.Arg152Ser) c.538C>A (p.Arg180Ser) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790776C>A | CA382738375 | APOA5 | c.453G>T (p.Leu151Phe) c.537G>T (p.Leu179Phe) | |
| 11 | g.116790776C>G | CA382738376 | APOA5 | c.453G>C (p.Leu151Phe) c.537G>C (p.Leu179Phe) | |
| 11 | g.116790776C>T | CA477047481 | APOA5 | c.453G>A (p.Leu151=) c.537G>A (p.Leu179=) | |
| 11 | g.116790777A>C | CA382738377 | APOA5 | c.452T>G (p.Leu151Trp) c.536T>G (p.Leu179Trp) | |
| 11 | g.116790777A>G | CA382738378 | APOA5 | c.452T>C (p.Leu151Ser) c.536T>C (p.Leu179Ser) | gnomAD v4 |
| 11 | g.116790777A>T | CA382738379 | APOA5 | c.452T>A (p.Leu151Ter) c.536T>A (p.Leu179Ter) | |
| 11 | g.116790778A>C | CA382738381 | APOA5 | c.451T>G (p.Leu151Val) c.535T>G (p.Leu179Val) | |
| 11 | g.116790778A>G | CA477047485 | APOA5 | c.451T>C (p.Leu151=) c.535T>C (p.Leu179=) | COSMIC |
| 11 | g.116790778A>T | CA382738380 | APOA5 | c.451T>A (p.Leu151Met) c.535T>A (p.Leu179Met) | |
| 11 | g.116790779C>A | CA382738382 | APOA5 | c.450G>T (p.Gln150His) c.534G>T (p.Gln178His) | |
| 11 | g.116790779C>G | CA382738383 | APOA5 | c.450G>C (p.Gln150His) c.534G>C (p.Gln178His) | |
| 11 | g.116790779C>T | CA477047487 | APOA5 | c.450G>A (p.Gln150=) c.534G>A (p.Gln178=) | |
| 11 | g.116790779_116790782del | CA2695215434 | APOA5 | c.447_450del (p.Glu149AspfsTer?) c.531_534del (p.Glu177AspfsTer?) | |
| 11 | g.116790780T>A | CA382738384 | APOA5 | c.449A>T (p.Gln150Leu) c.533A>T (p.Gln178Leu) | |
| 11 | g.116790780T>C | CA382738385 | APOA5 | c.449A>G (p.Gln150Arg) c.533A>G (p.Gln178Arg) | |
| 11 | g.116790780T>G | CA382738386 | APOA5 | c.449A>C (p.Gln150Pro) c.533A>C (p.Gln178Pro) | |
| 11 | g.116790780T= | CA2002740914 | APOA5 | c.449A= (p.Gln150=) c.533A= (p.Gln178=) | |
| 11 | g.116790781G>A | CA382738387 | APOA5 | c.448C>T (p.Gln150Ter) c.532C>T (p.Gln178Ter) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790781G>C | CA382738388 | APOA5 | c.448C>G (p.Gln150Glu) c.532C>G (p.Gln178Glu) | |
| 11 | g.116790781G= | CA2002740917 | APOA5 | c.448C= (p.Gln150=) c.532C= (p.Gln178=) | |
| 11 | g.116790781G>T | CA382738389 | APOA5 | c.448C>A (p.Gln150Lys) c.532C>A (p.Gln178Lys) | gnomAD v4 |
| 11 | g.116790790_116790798dup | CA942583221 | APOA5 | c.440_448dup (p.Glu149_Gln150insLeuGlnGlu) c.524_532dup (p.Glu177_Gln178insLeuGlnGlu) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790781_116790782insGA | CA2616086424 | APOA5 | c.447_448insTC (p.Gln150SerfsTer?) c.531_532insTC (p.Gln178SerfsTer?) | gnomAD v4 |
| 11 | g.116790782C>A | CA382738390 | APOA5 | c.447G>T (p.Glu149Asp) c.531G>T (p.Glu177Asp) | |
| 11 | g.116790782C= | CA2002740923 | APOA5 | c.447G= (p.Glu149=) c.531G= (p.Glu177=) | |
| 11 | g.116790782C>G | CA382738391 | APOA5 | c.447G>C (p.Glu149Asp) c.531G>C (p.Glu177Asp) | gnomAD v4 |
| 11 | g.116790782C>T | CA477047494 | APOA5 | c.447G>A (p.Glu149=) c.531G>A (p.Glu177=) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790782delinsGAG | CA2695215435 | APOA5 | c.447delinsCTC (p.Glu149AspfsTer?) c.531delinsCTC (p.Glu177AspfsTer?) | |
| 11 | g.116790783T>A | CA382738392 | APOA5 | c.446A>T (p.Glu149Val) c.530A>T (p.Glu177Val) | |
| 11 | g.116790783T>C | CA382738393 | APOA5 | c.446A>G (p.Glu149Gly) c.530A>G (p.Glu177Gly) | |
| 11 | g.116790783T>G | CA382738394 | APOA5 | c.446A>C (p.Glu149Ala) c.530A>C (p.Glu177Ala) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790783T= | CA2002740927 | APOA5 | c.446A= (p.Glu149=) c.530A= (p.Glu177=) | |
| 11 | g.116790784C>A | CA382738395 | APOA5 | c.445G>T (p.Glu149Ter) c.529G>T (p.Glu177Ter) | |
| 11 | g.116790784C>G | CA382738396 | APOA5 | c.445G>C (p.Glu149Gln) c.529G>C (p.Glu177Gln) | |
| 11 | g.116790784C>T | CA382738397 | APOA5 | c.445G>A (p.Glu149Lys) c.529G>A (p.Glu177Lys) | COSMIC |
| 11 | g.116790785C>A | CA382738398 | APOA5 | c.444G>T (p.Gln148His) c.528G>T (p.Gln176His) | |
| 11 | g.116790785C= | CA2002740930 | APOA5 | c.444G= (p.Gln148=) c.528G= (p.Gln176=) | |
| 11 | g.116790785C>G | CA382738399 | APOA5 | c.444G>C (p.Gln148His) c.528G>C (p.Gln176His) | |
| 11 | g.116790785C>T | CA477047497 | APOA5 | c.444G>A (p.Gln148=) c.528G>A (p.Gln176=) | dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790786T>A | CA382738400 | APOA5 | c.443A>T (p.Gln148Leu) c.527A>T (p.Gln176Leu) | |
| 11 | g.116790786T>C | CA382738401 | APOA5 | c.443A>G (p.Gln148Arg) c.527A>G (p.Gln176Arg) | |
| 11 | g.116790786T>G | CA382738402 | APOA5 | c.443A>C (p.Gln148Pro) c.527A>C (p.Gln176Pro) | |
| 11 | g.116790787G>A | CA382738403 | APOA5 | c.442C>T (p.Gln148Ter) c.526C>T (p.Gln176Ter) | |
| 11 | g.116790787G>C | CA382738404 | APOA5 | c.442C>G (p.Gln148Glu) c.526C>G (p.Gln176Glu) | |
| 11 | g.116790787G>T | CA382738405 | APOA5 | c.442C>A (p.Gln148Lys) c.526C>A (p.Gln176Lys) | gnomAD v4 |
| 11 | g.116790788C>A | CA477047500 | APOA5 | c.441G>T (p.Leu147=) c.525G>T (p.Leu175=) | |
| 11 | g.116790788C>G | CA477047503 | APOA5 | c.441G>C (p.Leu147=) c.525G>C (p.Leu175=) | |
| 11 | g.116790788C>T | CA477047501 | APOA5 | c.441G>A (p.Leu147=) c.525G>A (p.Leu175=) | |
| 11 | g.116790789A>C | CA382738406 | APOA5 | c.440T>G (p.Leu147Arg) c.524T>G (p.Leu175Arg) | |
| 11 | g.116790789A>G | CA382738407 | APOA5 | c.440T>C (p.Leu147Pro) c.524T>C (p.Leu175Pro) | |
| 11 | g.116790789A>T | CA382738408 | APOA5 | c.440T>A (p.Leu147Gln) c.524T>A (p.Leu175Gln) | |
| 11 | g.116790789_116790799delinsAGCTCCTGCAC | CA2002740933 | APOA5 | c.430_440delinsGTGCAGGAGCT (p.Val144=) c.514_524delinsGTGCAGGAGCT (p.Val172=) | |
| 11 | g.116790790G>A | CA477047507 | APOA5 | c.439C>T (p.Leu147=) c.523C>T (p.Leu175=) | |
| 11 | g.116790790G>C | CA382738409 | APOA5 | c.439C>G (p.Leu147Val) c.523C>G (p.Leu175Val) | |
| 11 | g.116790790G>T | CA382738410 | APOA5 | c.439C>A (p.Leu147Met) c.523C>A (p.Leu175Met) | |
| 11 | g.116790792_116790801del | CA2002740935 | APOA5 | c.430_439del (p.Val144CysfsTer?) c.514_523del (p.Val172CysfsTer?) | dbSNP |
| 11 | g.116790791C>A | CA6289078 | APOA5 | c.438G>T (p.Glu146Asp) c.522G>T (p.Glu174Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790791C= | CA2002740936 | APOA5 | c.438G= (p.Glu146=) c.522G= (p.Glu174=) | |
| 11 | g.116790791C>G | CA382738411 | APOA5 | c.438G>C (p.Glu146Asp) c.522G>C (p.Glu174Asp) | |
| 11 | g.116790791C>T | CA477047516 | APOA5 | c.438G>A (p.Glu146=) c.522G>A (p.Glu174=) | |
| 11 | g.116790792T>A | CA382738414 | APOA5 | c.437A>T (p.Glu146Val) c.521A>T (p.Glu174Val) | |
| 11 | g.116790792T>C | CA382738412 | APOA5 | c.437A>G (p.Glu146Gly) c.521A>G (p.Glu174Gly) | |
| 11 | g.116790792T>G | CA382738413 | APOA5 | c.437A>C (p.Glu146Ala) c.521A>C (p.Glu174Ala) | |
| 11 | g.116790792_116790793delinsTC | CA2002740939 | APOA5 | c.436_437delinsGA (p.Glu146=) c.520_521delinsGA (p.Glu174=) | |
| 11 | g.116790793C>A | CA382738415 | APOA5 | c.436G>T (p.Glu146Ter) c.520G>T (p.Glu174Ter) | |
| 11 | g.116790793C>G | CA382738416 | APOA5 | c.436G>C (p.Glu146Gln) c.520G>C (p.Glu174Gln) | |
| 11 | g.116790793C>T | CA382738417 | APOA5 | c.436G>A (p.Glu146Lys) c.520G>A (p.Glu174Lys) | |
| 11 | g.116790794del | CA2002740941 | APOA5 | c.436del (p.Glu146SerfsTer?) c.520del (p.Glu174SerfsTer?) | dbSNP |
| 11 | g.116790794C>A | CA382738418 | APOA5 | c.435G>T (p.Gln145His) c.519G>T (p.Gln173His) | |
| 11 | g.116790794C= | CA2002740945 | APOA5 | c.435G= (p.Gln145=) c.519G= (p.Gln173=) | |
| 11 | g.116790794C>G | CA382738419 | APOA5 | c.435G>C (p.Gln145His) c.519G>C (p.Gln173His) | |
| 11 | g.116790794C>T | CA477047524 | APOA5 | c.435G>A (p.Gln145=) c.519G>A (p.Gln173=) | dbSNP |
| 11 | g.116790795T>A | CA382738421 | APOA5 | c.434A>T (p.Gln145Leu) c.518A>T (p.Gln173Leu) | |
| 11 | g.116790795T>C | CA6289079 | APOA5 | c.434A>G (p.Gln145Arg) c.518A>G (p.Gln173Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790795T>G | CA382738420 | APOA5 | c.434A>C (p.Gln145Pro) c.518A>C (p.Gln173Pro) | |
| 11 | g.116790795T= | CA2002740949 | APOA5 | c.434A= (p.Gln145=) c.518A= (p.Gln173=) | |
| 11 | g.116790796G>A | CA382738422 | APOA5 | c.433C>T (p.Gln145Ter) c.517C>T (p.Gln173Ter) | COSMIC |
| 11 | g.116790796G>C | CA382738423 | APOA5 | c.433C>G (p.Gln145Glu) c.517C>G (p.Gln173Glu) | |
| 11 | g.116790796G>T | CA382738424 | APOA5 | c.433C>A (p.Gln145Lys) c.517C>A (p.Gln173Lys) | |
| 11 | g.116790797C>A | CA477047534 | APOA5 | c.432G>T (p.Val144=) c.516G>T (p.Val172=) | dbSNP |
| 11 | g.116790797C= | CA2002740951 | APOA5 | c.432G= (p.Val144=) c.516G= (p.Val172=) | |
| 11 | g.116790797C>G | CA477047530 | APOA5 | c.432G>C (p.Val144=) c.516G>C (p.Val172=) | |
| 11 | g.116790797C>T | CA477047532 | APOA5 | c.432G>A (p.Val144=) c.516G>A (p.Val172=) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790798A>C | CA382738425 | APOA5 | c.431T>G (p.Val144Gly) c.515T>G (p.Val172Gly) | dbSNP |
| 11 | g.116790798A>G | CA382738426 | APOA5 | c.431T>C (p.Val144Ala) c.515T>C (p.Val172Ala) | |
| 11 | g.116790798A>T | CA382738427 | APOA5 | c.431T>A (p.Val144Glu) c.515T>A (p.Val172Glu) | |
| 11 | g.116790799C>A | CA382738429 | APOA5 | c.430G>T (p.Val144Leu) c.514G>T (p.Val172Leu) | |
| 11 | g.116790799C= | CA2002740955 | APOA5 | c.430G= (p.Val144=) c.514G= (p.Val172=) | |
| 11 | g.116790799C>G | CA382738428 | APOA5 | c.430G>C (p.Val144Leu) c.514G>C (p.Val172Leu) | gnomAD v4 |
| 11 | g.116790799C>T | CA6289080 | APOA5 | c.430G>A (p.Val144Met) c.514G>A (p.Val172Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790800G>A | CA6289081 | APOA5 | c.429C>T (p.Arg143=) c.513C>T (p.Arg171=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790800G>C | CA477047539 | APOA5 | c.429C>G (p.Arg143=) c.513C>G (p.Arg171=) | |
| 11 | g.116790800G= | CA2002740958 | APOA5 | c.429C= (p.Arg143=) c.513C= (p.Arg171=) | |
| 11 | g.116790800G>T | CA477047541 | APOA5 | c.429C>A (p.Arg143=) c.513C>A (p.Arg171=) | |
| 11 | g.116790801C>A | CA382738430 | APOA5 | c.428G>T (p.Arg143Leu) c.512G>T (p.Arg171Leu) | |
| 11 | g.116790801C= | CA2002740962 | APOA5 | c.428G= (p.Arg143=) c.512G= (p.Arg171=) | |
| 11 | g.116790801C>G | CA382738431 | APOA5 | c.428G>C (p.Arg143Pro) c.512G>C (p.Arg171Pro) | |
| 11 | g.116790801C>T | CA382738432 | APOA5 | c.428G>A (p.Arg143His) c.512G>A (p.Arg171His) | ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
| 11 | g.116790801_116790802delinsCG | CA2002740961 | APOA5 | c.427_428delinsCG (p.Arg143=) c.511_512delinsCG (p.Arg171=) | |
| 11 | g.116790802del | CA6289082 | APOA5 | c.427del (p.Arg143AlafsTer?) c.511del (p.Arg171AlafsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790802G>A | CA382738433 | APOA5 | c.427C>T (p.Arg143Cys) c.511C>T (p.Arg171Cys) | gnomAD v4 |
| 11 | g.116790802G>C | CA382738434 | APOA5 | c.427C>G (p.Arg143Gly) c.511C>G (p.Arg171Gly) | |
| 11 | g.116790802G= | CA2002740966 | APOA5 | c.427C= (p.Arg143=) c.511C= (p.Arg171=) | |
| 11 | g.116790802G>T | CA6289083 | APOA5 | c.427C>A (p.Arg143Ser) c.511C>A (p.Arg171Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790803C>A | CA477047549 | APOA5 | c.426G>T (p.Leu142=) c.510G>T (p.Leu170=) | |
| 11 | g.116790803C>G | CA477047548 | APOA5 | c.426G>C (p.Leu142=) c.510G>C (p.Leu170=) | |
| 11 | g.116790803C>T | CA477047550 | APOA5 | c.426G>A (p.Leu142=) c.510G>A (p.Leu170=) | |
| 11 | g.116790804A>C | CA382738435 | APOA5 | c.425T>G (p.Leu142Arg) c.509T>G (p.Leu170Arg) | |
| 11 | g.116790804A>G | CA382738436 | APOA5 | c.425T>C (p.Leu142Pro) c.509T>C (p.Leu170Pro) | |
| 11 | g.116790804A>T | CA382738437 | APOA5 | c.425T>A (p.Leu142Gln) c.509T>A (p.Leu170Gln) | |
| 11 | g.116790805G>A | CA477047551 | APOA5 | c.424C>T (p.Leu142=) c.508C>T (p.Leu170=) | |
| 11 | g.116790805G>C | CA382738438 | APOA5 | c.424C>G (p.Leu142Val) c.508C>G (p.Leu170Val) | |
| 11 | g.116790805G>T | CA382738439 | APOA5 | c.424C>A (p.Leu142Met) c.508C>A (p.Leu170Met) | |
| 11 | g.116790807del | CA2616086448 | APOA5 | c.424del (p.Leu142CysfsTer?) c.508del (p.Leu170CysfsTer?) | gnomAD v4 |
| 11 | g.116790806G>A | CA477047553 | APOA5 | c.423C>T (p.Ala141=) c.507C>T (p.Ala169=) | |
| 11 | g.116790806G>C | CA477047554 | APOA5 | c.423C>G (p.Ala141=) c.507C>G (p.Ala169=) | |
| 11 | g.116790806G>T | CA477047555 | APOA5 | c.423C>A (p.Ala141=) c.507C>A (p.Ala169=) | |
| 11 | g.116790807G>A | CA382738440 | APOA5 | c.422C>T (p.Ala141Val) c.506C>T (p.Ala169Val) | |
| 11 | g.116790807G>C | CA382738442 | APOA5 | c.422C>G (p.Ala141Gly) c.506C>G (p.Ala169Gly) | |
| 11 | g.116790807G>T | CA382738441 | APOA5 | c.422C>A (p.Ala141Asp) c.506C>A (p.Ala169Asp) | gnomAD v4 |
| 11 | g.116790808C>A | CA382738443 | APOA5 | c.421G>T (p.Ala141Ser) c.505G>T (p.Ala169Ser) | gnomAD v4 |
| 11 | g.116790808C>G | CA382738445 | APOA5 | c.421G>C (p.Ala141Pro) c.505G>C (p.Ala169Pro) | COSMIC |
| 11 | g.116790808C>T | CA382738444 | APOA5 | c.421G>A (p.Ala141Thr) c.505G>A (p.Ala169Thr) | |
| 11 | g.116790809C>A | CA477047564 | APOA5 | c.420G>T (p.Val140=) c.504G>T (p.Val168=) | |
| 11 | g.116790809C= | CA2002740970 | APOA5 | c.420G= (p.Val140=) c.504G= (p.Val168=) | |
| 11 | g.116790809C>G | CA477047565 | APOA5 | c.420G>C (p.Val140=) c.504G>C (p.Val168=) | |
| 11 | g.116790809C>T | CA6289084 | APOA5 | c.420G>A (p.Val140=) c.504G>A (p.Val168=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790810A>C | CA382738449 | APOA5 | c.419T>G (p.Val140Gly) c.503T>G (p.Val168Gly) | |
| 11 | g.116790810A>G | CA382738450 | APOA5 | c.419T>C (p.Val140Ala) c.503T>C (p.Val168Ala) | |
| 11 | g.116790810A>T | CA382738452 | APOA5 | c.419T>A (p.Val140Glu) c.503T>A (p.Val168Glu) | |
| 11 | g.116790811C>A | CA382738454 | APOA5 | c.418G>T (p.Val140Leu) c.502G>T (p.Val168Leu) | |
| 11 | g.116790811C>G | CA382738456 | APOA5 | c.418G>C (p.Val140Leu) c.502G>C (p.Val168Leu) | |
| 11 | g.116790811C>T | CA382738459 | APOA5 | c.418G>A (p.Val140Met) c.502G>A (p.Val168Met) | |
| 11 | g.116790812C>A | CA382738461 | APOA5 | c.417G>T (p.Gln139His) c.501G>T (p.Gln167His) | |
| 11 | g.116790812C>G | CA382738463 | APOA5 | c.417G>C (p.Gln139His) c.501G>C (p.Gln167His) | |
| 11 | g.116790812C>T | CA477047570 | APOA5 | c.417G>A (p.Gln139=) c.501G>A (p.Gln167=) | |
| 11 | g.116790813T>A | CA382738466 | APOA5 | c.416A>T (p.Gln139Leu) c.500A>T (p.Gln167Leu) | |
| 11 | g.116790813T>C | CA382738467 | APOA5 | c.416A>G (p.Gln139Arg) c.500A>G (p.Gln167Arg) | |
| 11 | g.116790813T>G | CA382738469 | APOA5 | c.416A>C (p.Gln139Pro) c.500A>C (p.Gln167Pro) | |
| 11 | g.116790814G>A | CA116847 | APOA5 | c.415C>T (p.Gln139Ter) c.499C>T (p.Gln167Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 11 | g.116790814G>C | CA382738472 | APOA5 | c.415C>G (p.Gln139Glu) c.499C>G (p.Gln167Glu) | |
| 11 | g.116790814G= | CA2002740972 | APOA5 | c.415C= (p.Gln139=) c.499C= (p.Gln167=) | |
| 11 | g.116790814G>T | CA382738474 | APOA5 | c.415C>A (p.Gln139Lys) c.499C>A (p.Gln167Lys) | gnomAD v4 |
| 11 | g.116790815C>A | CA382738478 | APOA5 | c.414G>T (p.Glu138Asp) c.498G>T (p.Glu166Asp) | |
| 11 | g.116790815C>G | CA382738479 | APOA5 | c.414G>C (p.Glu138Asp) c.498G>C (p.Glu166Asp) | |
| 11 | g.116790815C>T | CA477047578 | APOA5 | c.414G>A (p.Glu138=) c.498G>A (p.Glu166=) | |
| 11 | g.116790816T>A | CA382738481 | APOA5 | c.413A>T (p.Glu138Val) c.497A>T (p.Glu166Val) | |
| 11 | g.116790816T>C | CA382738483 | APOA5 | c.413A>G (p.Glu138Gly) c.497A>G (p.Glu166Gly) | gnomAD v4 |
| 11 | g.116790816T>G | CA382738485 | APOA5 | c.413A>C (p.Glu138Ala) c.497A>C (p.Glu166Ala) | |
| 11 | g.116790817C>A | CA382738487 | APOA5 | c.412G>T (p.Glu138Ter) c.496G>T (p.Glu166Ter) | |
| 11 | g.116790817C= | CA2002740976 | APOA5 | c.412G= (p.Glu138=) c.496G= (p.Glu166=) | |
| 11 | g.116790817C>G | CA6289085 | APOA5 | c.412G>C (p.Glu138Gln) c.496G>C (p.Glu166Gln) | dbSNP ExAC gnomAD v2 |
| 11 | g.116790817C>T | CA382738490 | APOA5 | c.412G>A (p.Glu138Lys) c.496G>A (p.Glu166Lys) | |
| 11 | g.116790818C>A | CA382738492 | APOA5 | c.411G>T (p.Met137Ile) c.495G>T (p.Met165Ile) | |
| 11 | g.116790818C>G | CA382738495 | APOA5 | c.411G>C (p.Met137Ile) c.495G>C (p.Met165Ile) | |
| 11 | g.116790818C>T | CA382738497 | APOA5 | c.411G>A (p.Met137Ile) c.495G>A (p.Met165Ile) | |
| 11 | g.116790819A>C | CA382738502 | APOA5 | c.410T>G (p.Met137Arg) c.494T>G (p.Met165Arg) | |
| 11 | g.116790819A>G | CA382738500 | APOA5 | c.410T>C (p.Met137Thr) c.494T>C (p.Met165Thr) | |
| 11 | g.116790819A>T | CA382738499 | APOA5 | c.410T>A (p.Met137Lys) c.494T>A (p.Met165Lys) | |
| 11 | g.116790820T>A | CA382738504 | APOA5 | c.409A>T (p.Met137Leu) c.493A>T (p.Met165Leu) | |
| 11 | g.116790820T>C | CA382738506 | APOA5 | c.409A>G (p.Met137Val) c.493A>G (p.Met165Val) | |
| 11 | g.116790820T>G | CA382738507 | APOA5 | c.409A>C (p.Met137Leu) c.493A>C (p.Met165Leu) | |
| 11 | g.116790821C>A | CA477047597 | APOA5 | c.408G>T (p.Leu136=) c.492G>T (p.Leu164=) | |
| 11 | g.116790821C>G | CA477047598 | APOA5 | c.408G>C (p.Leu136=) c.492G>C (p.Leu164=) | |
| 11 | g.116790821C>T | CA477047599 | APOA5 | c.408G>A (p.Leu136=) c.492G>A (p.Leu164=) | |
| 11 | g.116790822A>C | CA382738509 | APOA5 | c.407T>G (p.Leu136Arg) c.491T>G (p.Leu164Arg) | |
| 11 | g.116790822A>G | CA382738510 | APOA5 | c.407T>C (p.Leu136Pro) c.491T>C (p.Leu164Pro) | ClinVar dbSNP |
| 11 | g.116790822A>T | CA382738513 | APOA5 | c.407T>A (p.Leu136Gln) c.491T>A (p.Leu164Gln) | |
| 11 | g.116790823G>A | CA477047606 | APOA5 | c.406C>T (p.Leu136=) c.490C>T (p.Leu164=) | |
| 11 | g.116790823G>C | CA382738515 | APOA5 | c.406C>G (p.Leu136Val) c.490C>G (p.Leu164Val) | |
| 11 | g.116790823G>T | CA382738517 | APOA5 | c.406C>A (p.Leu136Met) c.490C>A (p.Leu164Met) | gnomAD v4 |
| 11 | g.116790824A>C | CA382738518 | APOA5 | c.405T>G (p.Asp135Glu) c.489T>G (p.Asp163Glu) | |
| 11 | g.116790824A>G | CA477047607 | APOA5 | c.405T>C (p.Asp135=) c.489T>C (p.Asp163=) | gnomAD v4 |
| 11 | g.116790824A>T | CA382738519 | APOA5 | c.405T>A (p.Asp135Glu) c.489T>A (p.Asp163Glu) | |
| 11 | g.116790825T>A | CA382738522 | APOA5 | c.404A>T (p.Asp135Val) c.488A>T (p.Asp163Val) | |
| 11 | g.116790825T>C | CA382738524 | APOA5 | c.404A>G (p.Asp135Gly) c.488A>G (p.Asp163Gly) | |
| 11 | g.116790825T>G | CA382738525 | APOA5 | c.404A>C (p.Asp135Ala) c.488A>C (p.Asp163Ala) | |
| 11 | g.116790826C>A | CA382738538 | APOA5 | c.403G>T (p.Asp135Tyr) c.487G>T (p.Asp163Tyr) | |
| 11 | g.116790826C= | CA2002740981 | APOA5 | c.403G= (p.Asp135=) c.487G= (p.Asp163=) | |
| 11 | g.116790826C>G | CA382738528 | APOA5 | c.403G>C (p.Asp135His) c.487G>C (p.Asp163His) | |
| 11 | g.116790826C>T | CA382738536 | APOA5 | c.403G>A (p.Asp135Asn) c.487G>A (p.Asp163Asn) | dbSNP gnomAD v4 |
| 11 | g.116790827C>A | CA382738541 | APOA5 | c.402G>T (p.Met134Ile) c.486G>T (p.Met162Ile) | |
| 11 | g.116790827C>G | CA382738543 | APOA5 | c.402G>C (p.Met134Ile) c.486G>C (p.Met162Ile) | |
| 11 | g.116790827C>T | CA382738545 | APOA5 | c.402G>A (p.Met134Ile) c.486G>A (p.Met162Ile) | |
| 11 | g.116790828A= | CA2002740984 | APOA5 | c.401T= (p.Met134=) c.485T= (p.Met162=) | |
| 11 | g.116790828A>C | CA382738549 | APOA5 | c.401T>G (p.Met134Arg) c.485T>G (p.Met162Arg) | |
| 11 | g.116790828A>G | CA229337981 | APOA5 | c.401T>C (p.Met134Thr) c.485T>C (p.Met162Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790828A>T | CA382738551 | APOA5 | c.401T>A (p.Met134Lys) c.485T>A (p.Met162Lys) | |
| 11 | g.116790829T>A | CA382738554 | APOA5 | c.400A>T (p.Met134Leu) c.484A>T (p.Met162Leu) | |
| 11 | g.116790829T>C | CA382738556 | APOA5 | c.400A>G (p.Met134Val) c.484A>G (p.Met162Val) | |
| 11 | g.116790829T>G | CA382738558 | APOA5 | c.400A>C (p.Met134Leu) c.484A>C (p.Met162Leu) | |
| 11 | g.116790830C>A | CA477047618 | APOA5 | c.399G>T (p.Thr133=) c.483G>T (p.Thr161=) | |
| 11 | g.116790830C>G | CA477047620 | APOA5 | c.399G>C (p.Thr133=) c.483G>C (p.Thr161=) | |
| 11 | g.116790830C>T | CA477047624 | APOA5 | c.399G>A (p.Thr133=) c.483G>A (p.Thr161=) | gnomAD v4 COSMIC |
| 11 | g.116790831_116790896dup | CA2831038860 | APOA5 | c.334_399dup (p.Thr133_Met134insAlaGluAlaHisGluLeuValGlyTrpAsnLeuGluGlyLeuArgGlnGlnLeuLysProTyrThr) c.418_483dup (p.Thr161_Met162insAlaGluAlaHisGluLeuValGlyTrpAsnLeuGluGlyLeuArgGlnGlnLeuLysProTyrThr) |