| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 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=) | |
| 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) |