| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 11 | g.116790761_116790790delinsTTCCCCCACCACGCGCAACTGCTCCTGCAG | CA2002740875 | APOA5 | c.439_468delinsCTGCAGGAGCAGTTGCGCGTGGTGGGGGAA (p.Leu147=) c.523_552delinsCTGCAGGAGCAGTTGCGCGTGGTGGGGGAA (p.Leu175=) | |
| 11 | g.116790762_116790790del | CA2002740876 | APOA5 | c.439_467del (p.Leu147ArgfsTer?) c.523_551del (p.Leu175ArgfsTer?) | dbSNP |
| 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.116790831G>A | CA382738559 | APOA5 | c.398C>T (p.Thr133Met) c.482C>T (p.Thr161Met) | |
| 11 | g.116790831G>C | CA382738561 | APOA5 | c.398C>G (p.Thr133Arg) c.482C>G (p.Thr161Arg) | |
| 11 | g.116790831G>T | CA382738562 | APOA5 | c.398C>A (p.Thr133Lys) c.482C>A (p.Thr161Lys) | |
| 11 | g.116790832T>A | CA382738565 | APOA5 | c.397A>T (p.Thr133Ser) c.481A>T (p.Thr161Ser) | |
| 11 | g.116790832T>C | CA382738570 | APOA5 | c.397A>G (p.Thr133Ala) c.481A>G (p.Thr161Ala) | dbSNP gnomAD v4 |
| 11 | g.116790832T>G | CA382738567 | APOA5 | c.397A>C (p.Thr133Pro) c.481A>C (p.Thr161Pro) | |
| 11 | g.116790832T= | CA2002740987 | APOA5 | c.397A= (p.Thr133=) c.481A= (p.Thr161=) | |
| 11 | g.116790833G>A | CA477047625 | APOA5 | c.396C>T (p.Tyr132=) c.480C>T (p.Tyr160=) | |
| 11 | g.116790833G>C | CA382738574 | APOA5 | c.396C>G (p.Tyr132Ter) c.480C>G (p.Tyr160Ter) | |
| 11 | g.116790833G>T | CA382738575 | APOA5 | c.396C>A (p.Tyr132Ter) c.480C>A (p.Tyr160Ter) | |
| 11 | g.116790834T>A | CA382738580 | APOA5 | c.395A>T (p.Tyr132Phe) c.479A>T (p.Tyr160Phe) | |
| 11 | g.116790834T>C | CA382738583 | APOA5 | c.395A>G (p.Tyr132Cys) c.479A>G (p.Tyr160Cys) | |
| 11 | g.116790834T>G | CA382738587 | APOA5 | c.395A>C (p.Tyr132Ser) c.479A>C (p.Tyr160Ser) | |
| 11 | g.116790835A>C | CA382738589 | APOA5 | c.394T>G (p.Tyr132Asp) c.478T>G (p.Tyr160Asp) | |
| 11 | g.116790835A>G | CA382738590 | APOA5 | c.394T>C (p.Tyr132His) c.478T>C (p.Tyr160His) | |
| 11 | g.116790835A>T | CA382738591 | APOA5 | c.394T>A (p.Tyr132Asn) c.478T>A (p.Tyr160Asn) | |
| 11 | g.116790835_116790838dup | CA2574986398 | APOA5 | c.391_394dup (p.Tyr132SerfsTer?) c.475_478dup (p.Tyr160SerfsTer?) | |
| 11 | g.116790836G>A | CA477047630 | APOA5 | c.393C>T (p.Pro131=) c.477C>T (p.Pro159=) | gnomAD v4 |
| 11 | g.116790836G>C | CA477047631 | APOA5 | c.393C>G (p.Pro131=) c.477C>G (p.Pro159=) | |
| 11 | g.116790836G>T | CA477047633 | APOA5 | c.393C>A (p.Pro131=) c.477C>A (p.Pro159=) | |
| 11 | g.116790837G>A | CA382738596 | APOA5 | c.392C>T (p.Pro131Leu) c.476C>T (p.Pro159Leu) | gnomAD v4 |
| 11 | g.116790837G>C | CA382738592 | APOA5 | c.392C>G (p.Pro131Arg) c.476C>G (p.Pro159Arg) | gnomAD v4 |
| 11 | g.116790837G>T | CA382738594 | APOA5 | c.392C>A (p.Pro131His) c.476C>A (p.Pro159His) | |
| 11 | g.116790838G>A | CA382738599 | APOA5 | c.391C>T (p.Pro131Ser) c.475C>T (p.Pro159Ser) | |
| 11 | g.116790838G>C | CA382738602 | APOA5 | c.391C>G (p.Pro131Ala) c.475C>G (p.Pro159Ala) | |
| 11 | g.116790838G>T | CA382738605 | APOA5 | c.391C>A (p.Pro131Thr) c.475C>A (p.Pro159Thr) | |
| 11 | g.116790839C>A | CA382738609 | APOA5 | c.390G>T (p.Lys130Asn) c.474G>T (p.Lys158Asn) | |
| 11 | g.116790839C>G | CA382738612 | APOA5 | c.390G>C (p.Lys130Asn) c.474G>C (p.Lys158Asn) | |
| 11 | g.116790839C>T | CA477047640 | APOA5 | c.390G>A (p.Lys130=) c.474G>A (p.Lys158=) | |
| 11 | g.116790840T>A | CA382738620 | APOA5 | c.389A>T (p.Lys130Met) c.473A>T (p.Lys158Met) | |
| 11 | g.116790840T>C | CA382738616 | APOA5 | c.389A>G (p.Lys130Arg) c.473A>G (p.Lys158Arg) | |
| 11 | g.116790840T>G | CA382738618 | APOA5 | c.389A>C (p.Lys130Thr) c.473A>C (p.Lys158Thr) | |
| 11 | g.116790841T>A | CA382738623 | APOA5 | c.388A>T (p.Lys130Ter) c.472A>T (p.Lys158Ter) | |
| 11 | g.116790841T>C | CA382738625 | APOA5 | c.388A>G (p.Lys130Glu) c.472A>G (p.Lys158Glu) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790841T>G | CA382738626 | APOA5 | c.388A>C (p.Lys130Gln) c.472A>C (p.Lys158Gln) | |
| 11 | g.116790841T= | CA2002740990 | APOA5 | c.388A= (p.Lys130=) c.472A= (p.Lys158=) | |
| 11 | g.116790842C>A | CA477047653 | APOA5 | c.387G>T (p.Leu129=) c.471G>T (p.Leu157=) | |
| 11 | g.116790842C= | CA2002740992 | APOA5 | c.387G= (p.Leu129=) c.471G= (p.Leu157=) | |
| 11 | g.116790842C>G | CA477047655 | APOA5 | c.387G>C (p.Leu129=) c.471G>C (p.Leu157=) | |
| 11 | g.116790842C>T | CA477047656 | APOA5 | c.387G>A (p.Leu129=) c.471G>A (p.Leu157=) | dbSNP gnomAD v3 gnomAD v4 |
| 11 | g.116790843A>C | CA382738627 | APOA5 | c.386T>G (p.Leu129Arg) c.470T>G (p.Leu157Arg) | |
| 11 | g.116790843A>G | CA382738628 | APOA5 | c.386T>C (p.Leu129Pro) c.470T>C (p.Leu157Pro) | ClinVar |
| 11 | g.116790843A>T | CA382738629 | APOA5 | c.386T>A (p.Leu129Gln) c.470T>A (p.Leu157Gln) | |
| 11 | g.116790844G>A | CA477047661 | APOA5 | c.385C>T (p.Leu129=) c.469C>T (p.Leu157=) | |
| 11 | g.116790844G>C | CA382738631 | APOA5 | c.385C>G (p.Leu129Val) c.469C>G (p.Leu157Val) | |
| 11 | g.116790844G= | CA2002740993 | APOA5 | c.385C= (p.Leu129=) c.469C= (p.Leu157=) | |
| 11 | g.116790844G>T | CA6289086 | APOA5 | c.385C>A (p.Leu129Met) c.469C>A (p.Leu157Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790845T>A | CA382738636 | APOA5 | c.384A>T (p.Gln128His) c.468A>T (p.Gln156His) | |
| 11 | g.116790845T>C | CA477047663 | APOA5 | c.384A>G (p.Gln128=) c.468A>G (p.Gln156=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 11 | g.116790845T>G | CA382738637 | APOA5 | c.384A>C (p.Gln128His) c.468A>C (p.Gln156His) | |
| 11 | g.116790845T= | CA2002740997 | APOA5 | c.384A= (p.Gln128=) c.468A= (p.Gln156=) | |
| 11 | g.116790846T>A | CA382738641 | APOA5 | c.383A>T (p.Gln128Leu) c.467A>T (p.Gln156Leu) | |
| 11 | g.116790846T>C | CA382738644 | APOA5 | c.383A>G (p.Gln128Arg) c.467A>G (p.Gln156Arg) | gnomAD v4 |
| 11 | g.116790846T>G | CA382738648 | APOA5 | c.383A>C (p.Gln128Pro) c.467A>C (p.Gln156Pro) | |
| 11 | g.116790847G>A | CA382738652 | APOA5 | c.382C>T (p.Gln128Ter) c.466C>T (p.Gln156Ter) | |
| 11 | g.116790847G>C | CA382738658 | APOA5 | c.382C>G (p.Gln128Glu) c.466C>G (p.Gln156Glu) | |
| 11 | g.116790847G>T | CA382738655 | APOA5 | c.382C>A (p.Gln128Lys) c.466C>A (p.Gln156Lys) | gnomAD v4 |
| 11 | g.116790848C>A | CA382738661 | APOA5 | c.381G>T (p.Gln127His) c.465G>T (p.Gln155His) | |
| 11 | g.116790848C>G | CA382738663 | APOA5 | c.381G>C (p.Gln127His) c.465G>C (p.Gln155His) | |
| 11 | g.116790848C>T | CA477047676 | APOA5 | c.381G>A (p.Gln127=) c.465G>A (p.Gln155=) | |
| 11 | g.116790849T>A | CA382738667 | APOA5 | c.380A>T (p.Gln127Leu) c.464A>T (p.Gln155Leu) | |
| 11 | g.116790849T>C | CA382738671 | APOA5 | c.380A>G (p.Gln127Arg) c.464A>G (p.Gln155Arg) | |
| 11 | g.116790849T>G | CA382738673 | APOA5 | c.380A>C (p.Gln127Pro) c.464A>C (p.Gln155Pro) | |
| 11 | g.116790850G>A | CA382738678 | APOA5 | c.379C>T (p.Gln127Ter) c.463C>T (p.Gln155Ter) | |
| 11 | g.116790850G>C | CA382738680 | APOA5 | c.379C>G (p.Gln127Glu) c.463C>G (p.Gln155Glu) | |
| 11 | g.116790850G>T | CA382738689 | APOA5 | c.379C>A (p.Gln127Lys) c.463C>A (p.Gln155Lys) | |
| 11 | g.116790851C>A | CA477047684 | APOA5 | c.378G>T (p.Arg126=) c.462G>T (p.Arg154=) | |
| 11 | g.116790851C>G | CA477047686 | APOA5 | c.378G>C (p.Arg126=) c.462G>C (p.Arg154=) | |
| 11 | g.116790851C>T | CA477047685 | APOA5 | c.378G>A (p.Arg126=) c.462G>A (p.Arg154=) | gnomAD v4 |
| 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=) |