Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.3595776_3595780del | CA2584493820 | TBXA2R | c.942_946del (p.Val315ProfsTer?) c.553_557del (p.Arg185SerfsTer?) | gnomAD v4 |
19 | g.3595779G>A | CA403330441 | TBXA2R | c.941C>T (p.Ala314Val) c.552C>T (p.Arg184=) | gnomAD v4 |
19 | g.3595779G>C | CA403330443 | TBXA2R | c.941C>G (p.Ala314Gly) c.552C>G (p.Arg184=) | |
19 | g.3595779G>T | CA403330449 | TBXA2R | c.941C>A (p.Ala314Asp) c.552C>A (p.Arg184=) | |
19 | g.3595780_3595783dup | CA631712353 | TBXA2R | c.938_941dup (p.Val315ArgfsTer?) c.549_552dup (p.Arg185AlafsTer?) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595780C>A | CA403330452 | TBXA2R | c.940G>T (p.Ala314Ser) c.551G>T (p.Arg184Leu) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
19 | g.3595780C= | CA2318945847 | TBXA2R | c.940G= (p.Ala314=) c.551G= (p.Arg184=) | |
19 | g.3595780C>G | CA403330453 | TBXA2R | c.940G>C (p.Ala314Pro) c.551G>C (p.Arg184Pro) | |
19 | g.3595780C>T | CA403330456 | TBXA2R | c.940G>A (p.Ala314Thr) c.551G>A (p.Arg184His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595781G>A | CA9080738 | TBXA2R | c.939C>T (p.Arg313=) c.550C>T (p.Arg184Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC |
19 | g.3595781G>C | CA403330460 | TBXA2R | c.939C>G (p.Arg313=) c.550C>G (p.Arg184Gly) | |
19 | g.3595781G= | CA2318945848 | TBXA2R | c.939C= (p.Arg313=) c.550C= (p.Arg184=) | |
19 | g.3595781G>T | CA403330459 | TBXA2R | c.939C>A (p.Arg313=) c.550C>A (p.Arg184Ser) | |
19 | g.3595782C>A | CA403330464 | TBXA2R | c.938G>T (p.Arg313Leu) c.549G>T (p.Pro183=) | gnomAD v4 |
19 | g.3595782C= | CA2318945849 | TBXA2R | c.938G= (p.Arg313=) c.549G= (p.Pro183=) | |
19 | g.3595782C>G | CA403330466 | TBXA2R | c.938G>C (p.Arg313Pro) c.549G>C (p.Pro183=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595782C>T | CA403330467 | TBXA2R | c.938G>A (p.Arg313His) c.549G>A (p.Pro183=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595783G>A | CA304367902 | TBXA2R | c.937C>T (p.Arg313Cys) c.548C>T (p.Pro183Leu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595783G>C | CA403330471 | TBXA2R | c.937C>G (p.Arg313Gly) c.548C>G (p.Pro183Arg) | |
19 | g.3595783G= | CA2318945850 | TBXA2R | c.937C= (p.Arg313=) c.548C= (p.Pro183=) | |
19 | g.3595783G>T | CA403330474 | TBXA2R | c.937C>A (p.Arg313Ser) c.548C>A (p.Pro183Gln) | |
19 | g.3595784G>A | CA403330477 | TBXA2R | c.936C>T (p.Arg312=) c.547C>T (p.Pro183Ser) | COSMIC COSMIC |
19 | g.3595784G>C | CA403330482 | TBXA2R | c.936C>G (p.Arg312=) c.547C>G (p.Pro183Ala) | |
19 | g.3595784G>T | CA403330483 | TBXA2R | c.936C>A (p.Arg312=) c.547C>A (p.Pro183Thr) | |
19 | g.3595784_3595785delinsGC | CA2318945851 | TBXA2R | c.935_936delinsGC (p.Arg312=) c.546_547delinsGC (p.Pro182=) | |
19 | g.3595785del | CA920042087 | TBXA2R | c.935del (p.Arg312ProfsTer?) c.546del (p.Pro183ArgfsTer?) | dbSNP |
19 | g.3595785C>A | CA403330484 | TBXA2R | c.935G>T (p.Arg312Leu) c.546G>T (p.Pro182=) | gnomAD v4 |
19 | g.3595785C= | CA2318945852 | TBXA2R | c.935G= (p.Arg312=) c.546G= (p.Pro182=) | |
19 | g.3595785C>G | CA403330487 | TBXA2R | c.935G>C (p.Arg312Pro) c.546G>C (p.Pro182=) | |
19 | g.3595785C>T | CA9080739 | TBXA2R | c.935G>A (p.Arg312His) c.546G>A (p.Pro182=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595786G>A | CA403330496 | TBXA2R | c.934C>T (p.Arg312Cys) c.545C>T (p.Pro182Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595786G>C | CA403330492 | TBXA2R | c.934C>G (p.Arg312Gly) c.545C>G (p.Pro182Arg) | |
19 | g.3595786G= | CA2318945853 | TBXA2R | c.934C= (p.Arg312=) c.545C= (p.Pro182=) | |
19 | g.3595786G>T | CA403330494 | TBXA2R | c.934C>A (p.Arg312Ser) c.545C>A (p.Pro182Gln) | |
19 | g.3595787G>A | CA403330498 | TBXA2R | c.933C>T (p.Phe311=) c.544C>T (p.Pro182Ser) | |
19 | g.3595787G>C | CA403330499 | TBXA2R | c.933C>G (p.Phe311Leu) c.544C>G (p.Pro182Ala) | gnomAD v4 |
19 | g.3595787G>T | CA403330504 | TBXA2R | c.933C>A (p.Phe311Leu) c.544C>A (p.Pro182Thr) | gnomAD v4 |
19 | g.3595788A>C | CA403330505 | TBXA2R | c.932T>G (p.Phe311Cys) c.543T>G (p.Val181=) | |
19 | g.3595788A>G | CA403330507 | TBXA2R | c.932T>C (p.Phe311Ser) c.543T>C (p.Val181=) | |
19 | g.3595788A>T | CA403330508 | TBXA2R | c.932T>A (p.Phe311Tyr) c.543T>A (p.Val181=) | |
19 | g.3595789A= | CA2318945854 | TBXA2R | c.931T= (p.Phe311=) c.542T= (p.Val181=) | |
19 | g.3595789A>C | CA403330514 | TBXA2R | c.931T>G (p.Phe311Val) c.542T>G (p.Val181Gly) | |
19 | g.3595789A>G | CA403330510 | TBXA2R | c.931T>C (p.Phe311Leu) c.542T>C (p.Val181Ala) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595789A>T | CA403330509 | TBXA2R | c.931T>A (p.Phe311Ile) c.542T>A (p.Val181Asp) | |
19 | g.3595790C>A | CA403330516 | TBXA2R | c.930G>T (p.Leu310=) c.541G>T (p.Val181Phe) | gnomAD v4 |
19 | g.3595790C>G | CA403330518 | TBXA2R | c.930G>C (p.Leu310=) c.541G>C (p.Val181Leu) | |
19 | g.3595790C>T | CA403330519 | TBXA2R | c.930G>A (p.Leu310=) c.541G>A (p.Val181Ile) | |
19 | g.3595791A>C | CA403330521 | TBXA2R | c.929T>G (p.Leu310Arg) c.540T>G (p.Pro180=) | |
19 | g.3595791A>G | CA403330523 | TBXA2R | c.929T>C (p.Leu310Pro) c.540T>C (p.Pro180=) | |
19 | g.3595791A>T | CA403330525 | TBXA2R | c.929T>A (p.Leu310Gln) c.540T>A (p.Pro180=) | |
19 | g.3595792G>A | CA403330528 | TBXA2R | c.928C>T (p.Leu310=) c.539C>T (p.Pro180Leu) | |
19 | g.3595792G>C | CA403330534 | TBXA2R | c.928C>G (p.Leu310Val) c.539C>G (p.Pro180Arg) | |
19 | g.3595792G>T | CA403330530 | TBXA2R | c.928C>A (p.Leu310Met) c.539C>A (p.Pro180His) | |
19 | g.3595793G>A | CA403330536 | TBXA2R | c.927C>T (p.Ile309=) c.538C>T (p.Pro180Ser) | gnomAD v4 COSMIC COSMIC |
19 | g.3595793G>C | CA403330538 | TBXA2R | c.927C>G (p.Ile309Met) c.538C>G (p.Pro180Ala) | |
19 | g.3595793G= | CA2318945855 | TBXA2R | c.927C= (p.Ile309=) c.538C= (p.Pro180=) | |
19 | g.3595793G>T | CA403330540 | TBXA2R | c.927C>A (p.Ile309=) c.538C>A (p.Pro180Thr) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595794A>C | CA403330541 | TBXA2R | c.926T>G (p.Ile309Ser) c.537T>G (p.Tyr179Ter) | gnomAD v4 |
19 | g.3595794A>G | CA403330542 | TBXA2R | c.926T>C (p.Ile309Thr) c.537T>C (p.Tyr179=) | |
19 | g.3595794A>T | CA403330544 | TBXA2R | c.926T>A (p.Ile309Asn) c.537T>A (p.Tyr179Ter) | |
19 | g.3595795T>A | CA403330546 | TBXA2R | c.925A>T (p.Ile309Phe) c.536A>T (p.Tyr179Phe) | gnomAD v4 |
19 | g.3595795T>C | CA403330549 | TBXA2R | c.925A>G (p.Ile309Val) c.536A>G (p.Tyr179Cys) | |
19 | g.3595795T>G | CA403330551 | TBXA2R | c.925A>C (p.Ile309Leu) c.536A>C (p.Tyr179Ser) | |
19 | g.3595796A= | CA2318945856 | TBXA2R | c.924T= (p.Tyr308=) c.535T= (p.Tyr179=) | |
19 | g.3595796A>C | CA403330552 | TBXA2R | c.924T>G (p.Tyr308Ter) c.535T>G (p.Tyr179Asp) | |
19 | g.3595796A>G | CA9080740 | TBXA2R | c.924T>C (p.Tyr308=) c.535T>C (p.Tyr179His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595796A>T | CA403330554 | TBXA2R | c.924T>A (p.Tyr308Ter) c.535T>A (p.Tyr179Asn) | |
19 | g.3595796_3595797insCACCCAGGGGTCCACCTGGAACCAGATCCTGGACCCCTGCGGAACAGGATG | CA992743728 | TBXA2R | c.923_924insCATCCTGTTCCGCAGGGGTCCAGGATCTGGTTCCAGGTGGACCCCTGGGTG (p.Tyr308_Ile309insIleLeuPheArgArgGlyProGlySerGlySerArgTrpThrProGlyCys) c.534_535insCATCCTGTTCCGCAGGGGTCCAGGATCTGGTTCCAGGTGGACCCCTGGGTG (p.Val178_Tyr179insHisProValProGlnGlySerArgIleTrpPheGlnValAspProTrpVal) | gnomAD v3 gnomAD v4 |
19 | g.3595797T>A | CA403330558 | TBXA2R | c.923A>T (p.Tyr308Phe) c.534A>T (p.Val178=) | |
19 | g.3595797T>C | CA403330555 | TBXA2R | c.923A>G (p.Tyr308Cys) c.534A>G (p.Val178=) | |
19 | g.3595797T>G | CA403330556 | TBXA2R | c.923A>C (p.Tyr308Ser) c.534A>C (p.Val178=) | |
19 | g.3595798A>C | CA403330559 | TBXA2R | c.922T>G (p.Tyr308Asp) c.533T>G (p.Val178Gly) | |
19 | g.3595798A>G | CA403330560 | TBXA2R | c.922T>C (p.Tyr308His) c.533T>C (p.Val178Ala) | |
19 | g.3595798A>T | CA403330562 | TBXA2R | c.922T>A (p.Tyr308Asn) c.533T>A (p.Val178Glu) | |
19 | g.3595799C>A | CA403330563 | TBXA2R | c.921G>T (p.Val307=) c.532G>T (p.Val178Leu) | |
19 | g.3595799C>G | CA403330565 | TBXA2R | c.921G>C (p.Val307=) c.532G>C (p.Val178Leu) | |
19 | g.3595799C>T | CA403330567 | TBXA2R | c.921G>A (p.Val307=) c.532G>A (p.Val178Ile) | |
19 | g.3595800A>C | CA403330573 | TBXA2R | c.920T>G (p.Val307Gly) c.531T>G (p.Gly177=) | gnomAD v4 |
19 | g.3595800A>G | CA403330571 | TBXA2R | c.920T>C (p.Val307Ala) c.531T>C (p.Gly177=) | |
19 | g.3595800A>T | CA403330570 | TBXA2R | c.920T>A (p.Val307Glu) c.531T>A (p.Gly177=) | |
19 | g.3595801C>A | CA403330574 | TBXA2R | c.919G>T (p.Val307Leu) c.530G>T (p.Gly177Val) | |
19 | g.3595801C= | CA2318945857 | TBXA2R | c.919G= (p.Val307=) c.530G= (p.Gly177=) | |
19 | g.3595801C>G | CA403330575 | TBXA2R | c.919G>C (p.Val307Leu) c.530G>C (p.Gly177Ala) | dbSNP |
19 | g.3595801C>T | CA403330576 | TBXA2R | c.919G>A (p.Val307Met) c.530G>A (p.Gly177Asp) | dbSNP gnomAD v4 |
19 | g.3595802C>A | CA403330578 | TBXA2R | c.918G>T (p.Trp306Cys) c.529G>T (p.Gly177Cys) | |
19 | g.3595802C= | CA2318945858 | TBXA2R | c.918G= (p.Trp306=) c.529G= (p.Gly177=) | |
19 | g.3595802C>G | CA403330580 | TBXA2R | c.918G>C (p.Trp306Cys) c.529G>C (p.Gly177Arg) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595802C>T | CA403330582 | TBXA2R | c.918G>A (p.Trp306Ter) c.529G>A (p.Gly177Ser) | dbSNP gnomAD v4 |
19 | g.3595803C>A | CA403330584 | TBXA2R | c.917G>T (p.Trp306Leu) c.528G>T (p.Leu176=) | |
19 | g.3595803C>G | CA403330587 | TBXA2R | c.917G>C (p.Trp306Ser) c.528G>C (p.Leu176=) | |
19 | g.3595803C>T | CA403330586 | TBXA2R | c.917G>A (p.Trp306Ter) c.528G>A (p.Leu176=) | ClinVar gnomAD v4 |
19 | g.3595804A>C | CA403330589 | TBXA2R | c.916T>G (p.Trp306Gly) c.527T>G (p.Leu176Arg) | |
19 | g.3595804A>G | CA403330590 | TBXA2R | c.916T>C (p.Trp306Arg) c.527T>C (p.Leu176Pro) | |
19 | g.3595804A>T | CA403330592 | TBXA2R | c.916T>A (p.Trp306Arg) c.527T>A (p.Leu176Gln) | gnomAD v4 |
19 | g.3595805G>A | CA505155054 | TBXA2R | c.915C>T (p.Pro305=) c.526C>T (p.Leu176=) | |
19 | g.3595805G>C | CA403330593 | TBXA2R | c.915C>G (p.Pro305=) c.526C>G (p.Leu176Val) | |
19 | g.3595805G>T | CA403330594 | TBXA2R | c.915C>A (p.Pro305=) c.526C>A (p.Leu176Met) | gnomAD v4 |
19 | g.3595806G>A | CA9080741 | TBXA2R | c.914C>T (p.Pro305Leu) c.525C>T (p.Pro175=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595806G>C | CA403330603 | TBXA2R | c.914C>G (p.Pro305Arg) c.525C>G (p.Pro175=) | |
19 | g.3595806G= | CA2318945859 | TBXA2R | c.914C= (p.Pro305=) c.525C= (p.Pro175=) | |
19 | g.3595806G>T | CA403330604 | TBXA2R | c.914C>A (p.Pro305His) c.525C>A (p.Pro175=) | |
19 | g.3595807G>A | CA403330608 | TBXA2R | c.913C>T (p.Pro305Ser) c.524C>T (p.Pro175Leu) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595807G>C | CA403330609 | TBXA2R | c.913C>G (p.Pro305Ala) c.524C>G (p.Pro175Arg) | |
19 | g.3595807G= | CA2318945860 | TBXA2R | c.913C= (p.Pro305=) c.524C= (p.Pro175=) | |
19 | g.3595807G>T | CA403330612 | TBXA2R | c.913C>A (p.Pro305Thr) c.524C>A (p.Pro175His) | |
19 | g.3595808G>A | CA403330622 | TBXA2R | c.912C>T (p.Asp304=) c.523C>T (p.Pro175Ser) | |
19 | g.3595808G>C | CA403330616 | TBXA2R | c.912C>G (p.Asp304Glu) c.523C>G (p.Pro175Ala) | gnomAD v4 |
19 | g.3595808G>T | CA403330620 | TBXA2R | c.912C>A (p.Asp304Glu) c.523C>A (p.Pro175Thr) | |
19 | g.3595809T>A | CA403330625 | TBXA2R | c.911A>T (p.Asp304Val) c.522A>T (p.Gly174=) | |
19 | g.3595809T>C | CA403330626 | TBXA2R | c.911A>G (p.Asp304Gly) c.522A>G (p.Gly174=) | gnomAD v4 |
19 | g.3595809T>G | CA403330627 | TBXA2R | c.911A>C (p.Asp304Ala) c.522A>C (p.Gly174=) | |
19 | g.3595810C>A | CA403330628 | TBXA2R | c.910G>T (p.Asp304Tyr) c.521G>T (p.Gly174Val) | |
19 | g.3595810C= | CA2318945861 | TBXA2R | c.910G= (p.Asp304=) c.521G= (p.Gly174=) | |
19 | g.3595810C>G | CA403330629 | TBXA2R | c.910G>C (p.Asp304His) c.521G>C (p.Gly174Ala) | |
19 | g.3595810C>T | CA128736 | TBXA2R | c.910G>A (p.Asp304Asn) c.521G>A (p.Gly174Glu) | ClinVar dbSNP gnomAD v4 |
19 | g.3595811C>A | CA403330639 | TBXA2R | c.909G>T (p.Leu303=) c.520G>T (p.Gly174Ter) | gnomAD v4 |
19 | g.3595811C>G | CA403330637 | TBXA2R | c.909G>C (p.Leu303=) c.520G>C (p.Gly174Arg) | |
19 | g.3595811C>T | CA403330635 | TBXA2R | c.909G>A (p.Leu303=) c.520G>A (p.Gly174Arg) | gnomAD v4 |
19 | g.3595812A= | CA2318945862 | TBXA2R | c.908T= (p.Leu303=) c.519T= (p.Pro173=) | |
19 | g.3595812A>C | CA403330643 | TBXA2R | c.908T>G (p.Leu303Arg) c.519T>G (p.Pro173=) | |
19 | g.3595812A>G | CA403330646 | TBXA2R | c.908T>C (p.Leu303Pro) c.519T>C (p.Pro173=) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595812A>T | CA403330649 | TBXA2R | c.908T>A (p.Leu303Gln) c.519T>A (p.Pro173=) | |
19 | g.3595813G>A | CA403330651 | TBXA2R | c.907C>T (p.Leu303=) c.518C>T (p.Pro173Leu) | |
19 | g.3595813G>C | CA403330654 | TBXA2R | c.907C>G (p.Leu303Val) c.518C>G (p.Pro173Arg) | |
19 | g.3595813G>T | CA403330656 | TBXA2R | c.907C>A (p.Leu303Met) c.518C>A (p.Pro173His) | gnomAD v4 |
19 | g.3595814G>A | CA403330659 | TBXA2R | c.906C>T (p.Ile302=) c.517C>T (p.Pro173Ser) | COSMIC COSMIC |
19 | g.3595814G>C | CA403330665 | TBXA2R | c.906C>G (p.Ile302Met) c.517C>G (p.Pro173Ala) | |
19 | g.3595814G>T | CA403330662 | TBXA2R | c.906C>A (p.Ile302=) c.517C>A (p.Pro173Thr) | |
19 | g.3595815A= | CA2318945863 | TBXA2R | c.905T= (p.Ile302=) c.516T= (p.Asp172=) | |
19 | g.3595815A>C | CA403330667 | TBXA2R | c.905T>G (p.Ile302Ser) c.516T>G (p.Asp172Glu) | |
19 | g.3595815A>G | CA403330668 | TBXA2R | c.905T>C (p.Ile302Thr) c.516T>C (p.Asp172=) | |
19 | g.3595815A>T | CA403330670 | TBXA2R | c.905T>A (p.Ile302Asn) c.516T>A (p.Asp172Glu) | dbSNP |
19 | g.3595816T>A | CA403330673 | TBXA2R | c.904A>T (p.Ile302Phe) c.515A>T (p.Asp172Val) | |
19 | g.3595816T>C | CA403330680 | TBXA2R | c.904A>G (p.Ile302Val) c.515A>G (p.Asp172Gly) | |
19 | g.3595816T>G | CA403330681 | TBXA2R | c.904A>C (p.Ile302Leu) c.515A>C (p.Asp172Ala) | |
19 | g.3595817C>A | CA403330684 | TBXA2R | c.903G>T (p.Gln301His) c.514G>T (p.Asp172Tyr) | |
19 | g.3595817C>G | CA403330685 | TBXA2R | c.903G>C (p.Gln301His) c.514G>C (p.Asp172His) | |
19 | g.3595817C>T | CA403330687 | TBXA2R | c.903G>A (p.Gln301=) c.514G>A (p.Asp172Asn) | |
19 | g.3595818T>A | CA403330689 | TBXA2R | c.902A>T (p.Gln301Leu) c.513A>T (p.Pro171=) | |
19 | g.3595818T>C | CA403330691 | TBXA2R | c.902A>G (p.Gln301Arg) c.513A>G (p.Pro171=) | gnomAD v4 |
19 | g.3595818T>G | CA403330694 | TBXA2R | c.902A>C (p.Gln301Pro) c.513A>C (p.Pro171=) | |
19 | g.3595819G>A | CA403330697 | TBXA2R | c.901C>T (p.Gln301Ter) c.512C>T (p.Pro171Leu) | |
19 | g.3595819G>C | CA403330703 | TBXA2R | c.901C>G (p.Gln301Glu) c.512C>G (p.Pro171Arg) | |
19 | g.3595819G= | CA2318945864 | TBXA2R | c.901C= (p.Gln301=) c.512C= (p.Pro171=) | |
19 | g.3595819G>T | CA403330701 | TBXA2R | c.901C>A (p.Gln301Lys) c.512C>A (p.Pro171Gln) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595820G>A | CA403330708 | TBXA2R | c.900C>T (p.Asn300=) c.511C>T (p.Pro171Ser) | |
19 | g.3595820G>C | CA403330709 | TBXA2R | c.900C>G (p.Asn300Lys) c.511C>G (p.Pro171Ala) | |
19 | g.3595820G>T | CA403330711 | TBXA2R | c.900C>A (p.Asn300Lys) c.511C>A (p.Pro171Thr) | |
19 | g.3595821T>A | CA403330712 | TBXA2R | c.899A>T (p.Asn300Ile) c.510A>T (p.Glu170Asp) | |
19 | g.3595821T>C | CA403330715 | TBXA2R | c.899A>G (p.Asn300Ser) c.510A>G (p.Glu170=) | |
19 | g.3595821T>G | CA403330717 | TBXA2R | c.899A>C (p.Asn300Thr) c.510A>C (p.Glu170Asp) | |
19 | g.3595822T>A | CA403330721 | TBXA2R | c.898A>T (p.Asn300Tyr) c.509A>T (p.Glu170Val) | |
19 | g.3595822T>C | CA403330723 | TBXA2R | c.898A>G (p.Asn300Asp) c.509A>G (p.Glu170Gly) | |
19 | g.3595822T>G | CA403330726 | TBXA2R | c.898A>C (p.Asn300His) c.509A>C (p.Glu170Ala) | |
19 | g.3595823C>A | CA403330728 | TBXA2R | c.897G>T (p.Trp299Cys) c.508G>T (p.Glu170Ter) | |
19 | g.3595823C>G | CA403330731 | TBXA2R | c.897G>C (p.Trp299Cys) c.508G>C (p.Glu170Gln) | |
19 | g.3595823C>T | CA403330732 | TBXA2R | c.897G>A (p.Trp299Ter) c.508G>A (p.Glu170Lys) | |
19 | g.3595824C>A | CA403330739 | TBXA2R | c.896G>T (p.Trp299Leu) c.507G>T (p.Leu169=) | |
19 | g.3595824C= | CA2318945866 | TBXA2R | c.896G= (p.Trp299=) c.507G= (p.Leu169=) | |
19 | g.3595824C>G | CA403330736 | TBXA2R | c.896G>C (p.Trp299Ser) c.507G>C (p.Leu169=) | |
19 | g.3595824C>T | CA9080742 | TBXA2R | c.896G>A (p.Trp299Ter) c.507G>A (p.Leu169=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595824_3595847delinsCAGGTGGCCACGCGCAAGTAGATG | CA2318945865 | TBXA2R | c.873_896delinsCATCTACTTGCGCGTGGCCACCTG (p.Leu291=) c.484_507delinsCATCTACTTGCGCGTGGCCACCTG (p.His162=) | |
19 | g.3595825A>C | CA403330744 | TBXA2R | c.895T>G (p.Trp299Gly) c.506T>G (p.Leu169Arg) | |
19 | g.3595825A>G | CA403330748 | TBXA2R | c.895T>C (p.Trp299Arg) c.506T>C (p.Leu169Pro) | |
19 | g.3595825A>T | CA403330751 | TBXA2R | c.895T>A (p.Trp299Arg) c.506T>A (p.Leu169Gln) | |
19 | g.3595827_3595849del | CA9080743 | TBXA2R | c.873_895del (p.Ile292GlufsTer?) c.484_506del (p.His162GlyfsTer?) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595826G>A | CA505155014 | TBXA2R | c.894C>T (p.Thr298=) c.505C>T (p.Leu169=) | |
19 | g.3595826G>C | CA403330755 | TBXA2R | c.894C>G (p.Thr298=) c.505C>G (p.Leu169Val) | |
19 | g.3595826G>T | CA403330756 | TBXA2R | c.894C>A (p.Thr298=) c.505C>A (p.Leu169Met) | COSMIC COSMIC |
19 | g.3595827G>A | CA403330760 | TBXA2R | c.893C>T (p.Thr298Ile) c.504C>T (p.His168=) | dbSNP gnomAD v4 |
19 | g.3595827G>C | CA403330763 | TBXA2R | c.893C>G (p.Thr298Ser) c.504C>G (p.His168Gln) | dbSNP |
19 | g.3595827G= | CA2318945867 | TBXA2R | c.893C= (p.Thr298=) c.504C= (p.His168=) | |
19 | g.3595827G>T | CA403330766 | TBXA2R | c.893C>A (p.Thr298Asn) c.504C>A (p.His168Gln) | |
19 | g.3595828T>A | CA403330770 | TBXA2R | c.892A>T (p.Thr298Ser) c.503A>T (p.His168Leu) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595828T>C | CA403330771 | TBXA2R | c.892A>G (p.Thr298Ala) c.503A>G (p.His168Arg) | gnomAD v4 |
19 | g.3595828T>G | CA403330773 | TBXA2R | c.892A>C (p.Thr298Pro) c.503A>C (p.His168Pro) | |
19 | g.3595828T= | CA2318945868 | TBXA2R | c.892A= (p.Thr298=) c.503A= (p.His168=) | |
19 | g.3595829G>A | CA304367908 | TBXA2R | c.891C>T (p.Ala297=) c.502C>T (p.His168Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.3595829G>C | CA403330780 | TBXA2R | c.891C>G (p.Ala297=) c.502C>G (p.His168Asp) | |
19 | g.3595829G= | CA2318945869 | TBXA2R | c.891C= (p.Ala297=) c.502C= (p.His168=) | |
19 | g.3595829G>T | CA403330777 | TBXA2R | c.891C>A (p.Ala297=) c.502C>A (p.His168Asn) | |
19 | g.3595830G>A | CA403330783 | TBXA2R | c.890C>T (p.Ala297Val) c.501C>T (p.Gly167=) | |
19 | g.3595830G>C | CA403330785 | TBXA2R | c.890C>G (p.Ala297Gly) c.501C>G (p.Gly167=) | |
19 | g.3595830G>T | CA403330787 | TBXA2R | c.890C>A (p.Ala297Asp) c.501C>A (p.Gly167=) | gnomAD v4 |
19 | g.3595831C>A | CA403330790 | TBXA2R | c.889G>T (p.Ala297Ser) c.500G>T (p.Gly167Val) | |
19 | g.3595831C= | CA2318945870 | TBXA2R | c.889G= (p.Ala297=) c.500G= (p.Gly167=) | |
19 | g.3595831C>G | CA403330792 | TBXA2R | c.889G>C (p.Ala297Pro) c.500G>C (p.Gly167Ala) | |
19 | g.3595831C>T | CA304367910 | TBXA2R | c.889G>A (p.Ala297Thr) c.500G>A (p.Gly167Asp) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595832C>A | CA403330801 | TBXA2R | c.888G>T (p.Val296=) c.499G>T (p.Gly167Cys) | dbSNP gnomAD v2 |
19 | g.3595832C= | CA2318945871 | TBXA2R | c.888G= (p.Val296=) c.499G= (p.Gly167=) | |
19 | g.3595832C>G | CA403330798 | TBXA2R | c.888G>C (p.Val296=) c.499G>C (p.Gly167Arg) | |
19 | g.3595832C>T | CA9080744 | TBXA2R | c.888G>A (p.Val296=) c.499G>A (p.Gly167Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595833A= | CA2318945872 | TBXA2R | c.887T= (p.Val296=) c.498T= (p.Arg166=) | |
19 | g.3595833A>C | CA403330805 | TBXA2R | c.887T>G (p.Val296Gly) c.498T>G (p.Arg166=) | |
19 | g.3595833A>G | CA403330807 | TBXA2R | c.887T>C (p.Val296Ala) c.498T>C (p.Arg166=) | dbSNP gnomAD v4 |
19 | g.3595833A>T | CA403330810 | TBXA2R | c.887T>A (p.Val296Glu) c.498T>A (p.Arg166=) | |
19 | g.3595834C>A | CA403330814 | TBXA2R | c.886G>T (p.Val296Leu) c.497G>T (p.Arg166Leu) | |
19 | g.3595834C= | CA2318945873 | TBXA2R | c.886G= (p.Val296=) c.497G= (p.Arg166=) | |
19 | g.3595834C>G | CA403330816 | TBXA2R | c.886G>C (p.Val296Leu) c.497G>C (p.Arg166Pro) | |
19 | g.3595834C>T | CA9080745 | TBXA2R | c.886G>A (p.Val296Met) c.497G>A (p.Arg166His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595835G>A | CA403330819 | TBXA2R | c.885C>T (p.Arg295=) c.496C>T (p.Arg166Cys) | dbSNP gnomAD v4 COSMIC COSMIC |
19 | g.3595835G>C | CA304367913 | TBXA2R | c.885C>G (p.Arg295=) c.496C>G (p.Arg166Gly) | dbSNP |
19 | g.3595835G= | CA2318945874 | TBXA2R | c.885C= (p.Arg295=) c.496C= (p.Arg166=) | |
19 | g.3595835G>T | CA403330822 | TBXA2R | c.885C>A (p.Arg295=) c.496C>A (p.Arg166Ser) | |
19 | g.3595836C>A | CA403330825 | TBXA2R | c.884G>T (p.Arg295Leu) c.495G>T (p.Ala165=) | gnomAD v4 |
19 | g.3595836C= | CA2318945875 | TBXA2R | c.884G= (p.Arg295=) c.495G= (p.Ala165=) | |
19 | g.3595836C>G | CA403330828 | TBXA2R | c.884G>C (p.Arg295Pro) c.495G>C (p.Ala165=) | |
19 | g.3595836C>T | CA9080746 | TBXA2R | c.884G>A (p.Arg295His) c.495G>A (p.Ala165=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595837del | CA2584493821 | TBXA2R | c.883del (p.Arg295AlafsTer?) c.494del (p.Ala165GlyfsTer?) | gnomAD v4 |
19 | g.3595837G>A | CA9080747 | TBXA2R | c.883C>T (p.Arg295Cys) c.494C>T (p.Ala165Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595837G>C | CA403330833 | TBXA2R | c.883C>G (p.Arg295Gly) c.494C>G (p.Ala165Gly) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595837G= | CA2318945876 | TBXA2R | c.883C= (p.Arg295=) c.494C= (p.Ala165=) | |
19 | g.3595837G>T | CA403330834 | TBXA2R | c.883C>A (p.Arg295Ser) c.494C>A (p.Ala165Glu) | |
19 | g.3595838C>A | CA403330837 | TBXA2R | c.882G>T (p.Leu294Phe) c.493G>T (p.Ala165Ser) | |
19 | g.3595838C= | CA2318945877 | TBXA2R | c.882G= (p.Leu294=) c.493G= (p.Ala165=) | |
19 | g.3595838C>G | CA403330839 | TBXA2R | c.882G>C (p.Leu294Phe) c.493G>C (p.Ala165Pro) | |
19 | g.3595838C>T | CA9080748 | TBXA2R | c.882G>A (p.Leu294=) c.493G>A (p.Ala165Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595838dup | CA2584493822 | TBXA2R | c.882dup (p.Arg295AlafsTer?) c.493dup (p.Ala165GlyfsTer?) | gnomAD v4 |
19 | g.3595839A>C | CA403330842 | TBXA2R | c.881T>G (p.Leu294Trp) c.492T>G (p.Leu164=) | |
19 | g.3595839A>G | CA403330843 | TBXA2R | c.881T>C (p.Leu294Ser) c.492T>C (p.Leu164=) | |
19 | g.3595839A>T | CA403330844 | TBXA2R | c.881T>A (p.Leu294Ter) c.492T>A (p.Leu164=) | |
19 | g.3595840A>C | CA403330853 | TBXA2R | c.880T>G (p.Leu294Val) c.491T>G (p.Leu164Arg) | |
19 | g.3595840A>G | CA403330849 | TBXA2R | c.880T>C (p.Leu294=) c.491T>C (p.Leu164Pro) | |
19 | g.3595840A>T | CA403330851 | TBXA2R | c.880T>A (p.Leu294Met) c.491T>A (p.Leu164His) | |
19 | g.3595841G>A | CA9080749 | TBXA2R | c.879C>T (p.Tyr293=) c.490C>T (p.Leu164Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595841G>C | CA403330858 | TBXA2R | c.879C>G (p.Tyr293Ter) c.490C>G (p.Leu164Val) | |
19 | g.3595841G= | CA2318945878 | TBXA2R | c.879C= (p.Tyr293=) c.490C= (p.Leu164=) | |
19 | g.3595841G>T | CA403330861 | TBXA2R | c.879C>A (p.Tyr293Ter) c.490C>A (p.Leu164Ile) | |
19 | g.3595842T>A | CA403330863 | TBXA2R | c.878A>T (p.Tyr293Phe) c.489A>T (p.Leu163=) | |
19 | g.3595842T>C | CA9080750 | TBXA2R | c.878A>G (p.Tyr293Cys) c.489A>G (p.Leu163=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595842T>G | CA403330867 | TBXA2R | c.878A>C (p.Tyr293Ser) c.489A>C (p.Leu163=) | |
19 | g.3595842T= | CA2318945879 | TBXA2R | c.878A= (p.Tyr293=) c.489A= (p.Leu163=) | |
19 | g.3595843A= | CA2318945880 | TBXA2R | c.877T= (p.Tyr293=) c.488T= (p.Leu163=) | |
19 | g.3595843A>C | CA403330874 | TBXA2R | c.877T>G (p.Tyr293Asp) c.488T>G (p.Leu163Arg) | dbSNP |
19 | g.3595843A>G | CA403330869 | TBXA2R | c.877T>C (p.Tyr293His) c.488T>C (p.Leu163Pro) | gnomAD v4 |
19 | g.3595843A>T | CA403330871 | TBXA2R | c.877T>A (p.Tyr293Asn) c.488T>A (p.Leu163Gln) | |
19 | g.3595844G>A | CA505155028 | TBXA2R | c.876C>T (p.Ile292=) c.487C>T (p.Leu163=) | gnomAD v4 |
19 | g.3595844G>C | CA403330876 | TBXA2R | c.876C>G (p.Ile292Met) c.487C>G (p.Leu163Val) | |
19 | g.3595844G= | CA2318945881 | TBXA2R | c.876C= (p.Ile292=) c.487C= (p.Leu163=) | |
19 | g.3595844G>T | CA304367918 | TBXA2R | c.876C>A (p.Ile292=) c.487C>A (p.Leu163Ile) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595845A>C | CA403330889 | TBXA2R | c.875T>G (p.Ile292Ser) c.486T>G (p.His162Gln) | |
19 | g.3595845A>G | CA403330891 | TBXA2R | c.875T>C (p.Ile292Thr) c.486T>C (p.His162=) | |
19 | g.3595845A>T | CA403330893 | TBXA2R | c.875T>A (p.Ile292Asn) c.486T>A (p.His162Gln) | |
19 | g.3595846T>A | CA403330900 | TBXA2R | c.874A>T (p.Ile292Phe) c.485A>T (p.His162Leu) | |
19 | g.3595846T>C | CA403330895 | TBXA2R | c.874A>G (p.Ile292Val) c.485A>G (p.His162Arg) | gnomAD v4 |
19 | g.3595846T>G | CA403330898 | TBXA2R | c.874A>C (p.Ile292Leu) c.485A>C (p.His162Pro) | |
19 | g.3595847G>A | CA403330903 | TBXA2R | c.873C>T (p.Leu291=) c.484C>T (p.His162Tyr) | gnomAD v4 |
19 | g.3595847G>C | CA403330906 | TBXA2R | c.873C>G (p.Leu291=) c.484C>G (p.His162Asp) | |
19 | g.3595847G= | CA2318945882 | TBXA2R | c.873C= (p.Leu291=) c.484C= (p.His162=) | |
19 | g.3595847G>T | CA403330908 | TBXA2R | c.873C>A (p.Leu291=) c.484C>A (p.His162Asn) | |
19 | g.3595848A>C | CA403330912 | TBXA2R | c.872T>G (p.Leu291Arg) c.483T>G (p.Ala161=) | |
19 | g.3595848A>G | CA403330914 | TBXA2R | c.872T>C (p.Leu291Pro) c.483T>C (p.Ala161=) | |
19 | g.3595848A>T | CA403330916 | TBXA2R | c.872T>A (p.Leu291His) c.483T>A (p.Ala161=) | |
19 | g.3595851_3595853dup | CA881804184 | TBXA2R | c.870_872dup (p.Leu291_Ile292insLeu) c.481_483dup (p.Ala161_His162insAla) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595849G>A | CA403330919 | TBXA2R | c.871C>T (p.Leu291Phe) c.482C>T (p.Ala161Val) | |
19 | g.3595849G>C | CA403330921 | TBXA2R | c.871C>G (p.Leu291Val) c.482C>G (p.Ala161Gly) | |
19 | g.3595849G>T | CA403330922 | TBXA2R | c.871C>A (p.Leu291Ile) c.482C>A (p.Ala161Asp) | |
19 | g.3595850C>A | CA403330925 | TBXA2R | c.870G>T (p.Leu290=) c.481G>T (p.Ala161Ser) | |
19 | g.3595850C= | CA2318945883 | TBXA2R | c.870G= (p.Leu290=) c.481G= (p.Ala161=) | |
19 | g.3595850C>G | CA403330928 | TBXA2R | c.870G>C (p.Leu290=) c.481G>C (p.Ala161Pro) | |
19 | g.3595850C>T | CA9080751 | TBXA2R | c.870G>A (p.Leu290=) c.481G>A (p.Ala161Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595851A>C | CA403330936 | TBXA2R | c.869T>G (p.Leu290Arg) c.480T>G (p.Ala160=) | |
19 | g.3595851A>G | CA403330932 | TBXA2R | c.869T>C (p.Leu290Pro) c.480T>C (p.Ala160=) | |
19 | g.3595851A>T | CA403330933 | TBXA2R | c.869T>A (p.Leu290Gln) c.480T>A (p.Ala160=) | |
19 | g.3595852G>A | CA403330938 | TBXA2R | c.868C>T (p.Leu290=) c.479C>T (p.Ala160Val) | dbSNP gnomAD v2 |
19 | g.3595852G>C | CA403330940 | TBXA2R | c.868C>G (p.Leu290Val) c.479C>G (p.Ala160Gly) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595852G= | CA2318945884 | TBXA2R | c.868C= (p.Leu290=) c.479C= (p.Ala160=) | |
19 | g.3595852G>T | CA403330942 | TBXA2R | c.868C>A (p.Leu290Met) c.479C>A (p.Ala160Asp) | |
19 | g.3595853C>A | CA403330945 | TBXA2R | c.867G>T (p.Glu289Asp) c.478G>T (p.Ala160Ser) | |
19 | g.3595853C= | CA2318945885 | TBXA2R | c.867G= (p.Glu289=) c.478G= (p.Ala160=) | |
19 | g.3595853C>G | CA403330948 | TBXA2R | c.867G>C (p.Glu289Asp) c.478G>C (p.Ala160Pro) | |
19 | g.3595853C>T | CA403330950 | TBXA2R | c.867G>A (p.Glu289=) c.478G>A (p.Ala160Thr) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595854T>A | CA403330959 | TBXA2R | c.866A>T (p.Glu289Val) c.477A>T (p.Gly159=) | |
19 | g.3595854T>C | CA403330955 | TBXA2R | c.866A>G (p.Glu289Gly) c.477A>G (p.Gly159=) | |
19 | g.3595854T>G | CA403330954 | TBXA2R | c.866A>C (p.Glu289Ala) c.477A>C (p.Gly159=) | |
19 | g.3595855C>A | CA403330962 | TBXA2R | c.865G>T (p.Glu289Ter) c.476G>T (p.Gly159Val) | |
19 | g.3595855C>G | CA403330964 | TBXA2R | c.865G>C (p.Glu289Gln) c.476G>C (p.Gly159Ala) | gnomAD v4 |
19 | g.3595855C>T | CA403330965 | TBXA2R | c.865G>A (p.Glu289Lys) c.476G>A (p.Gly159Glu) | |
19 | g.3595855_3595858delinsCCTT | CA2318945886 | TBXA2R | c.862_865delinsAAGG (p.Lys288=) c.473_476delinsAAGG (p.Glu158=) | |
19 | g.3595856C>A | CA403330968 | TBXA2R | c.864G>T (p.Lys288Asn) c.475G>T (p.Gly159Ter) | gnomAD v4 |
19 | g.3595856C= | CA2318945887 | TBXA2R | c.864G= (p.Lys288=) c.475G= (p.Gly159=) | |
19 | g.3595856C>G | CA403330970 | TBXA2R | c.864G>C (p.Lys288Asn) c.475G>C (p.Gly159Arg) | |
19 | g.3595856C>T | CA403330973 | TBXA2R | c.864G>A (p.Lys288=) c.475G>A (p.Gly159Arg) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595858_3595860del | CA992743747 | TBXA2R | c.862_864del (p.Lys288del) c.473_475del (p.Glu158del) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595857T>A | CA403330980 | TBXA2R | c.863A>T (p.Lys288Met) c.474A>T (p.Glu158Asp) | |
19 | g.3595857T>C | CA9080752 | TBXA2R | c.863A>G (p.Lys288Arg) c.474A>G (p.Glu158=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595857T>G | CA403330982 | TBXA2R | c.863A>C (p.Lys288Thr) c.474A>C (p.Glu158Asp) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595857T= | CA2318945888 | TBXA2R | c.863A= (p.Lys288=) c.474A= (p.Glu158=) | |
19 | g.3595858T>A | CA403330987 | TBXA2R | c.862A>T (p.Lys288Ter) c.473A>T (p.Glu158Val) | COSMIC COSMIC |
19 | g.3595858T>C | CA403330990 | TBXA2R | c.862A>G (p.Lys288Glu) c.473A>G (p.Glu158Gly) | gnomAD v4 |
19 | g.3595858T>G | CA403330993 | TBXA2R | c.862A>C (p.Lys288Gln) c.473A>C (p.Glu158Ala) | |
19 | g.3595859C>A | CA403330996 | TBXA2R | c.861G>T (p.Glu287Asp) c.472G>T (p.Glu158Ter) | |
19 | g.3595859C>G | CA403330998 | TBXA2R | c.861G>C (p.Glu287Asp) c.472G>C (p.Glu158Gln) | gnomAD v4 |
19 | g.3595859C>T | CA403331000 | TBXA2R | c.861G>A (p.Glu287=) c.472G>A (p.Glu158Lys) | |
19 | g.3595860T>A | CA403331003 | TBXA2R | c.860A>T (p.Glu287Val) c.471A>T (p.Gly157=) | |
19 | g.3595860T>C | CA403331005 | TBXA2R | c.860A>G (p.Glu287Gly) c.471A>G (p.Gly157=) | |
19 | g.3595860T>G | CA403331006 | TBXA2R | c.860A>C (p.Glu287Ala) c.471A>C (p.Gly157=) | |
19 | g.3595861C>A | CA403331009 | TBXA2R | c.859G>T (p.Glu287Ter) c.470G>T (p.Gly157Val) | |
19 | g.3595861C>G | CA403331011 | TBXA2R | c.859G>C (p.Glu287Gln) c.470G>C (p.Gly157Ala) | |
19 | g.3595861C>T | CA403331014 | TBXA2R | c.859G>A (p.Glu287Lys) c.470G>A (p.Gly157Glu) | gnomAD v4 |
19 | g.3595862C>A | CA403331016 | TBXA2R | c.858G>T (p.Thr286=) c.469G>T (p.Gly157Ter) | |
19 | g.3595862C= | CA2318945889 | TBXA2R | c.858G= (p.Thr286=) c.469G= (p.Gly157=) | |
19 | g.3595862C>G | CA403331020 | TBXA2R | c.858G>C (p.Thr286=) c.469G>C (p.Gly157Arg) | |
19 | g.3595862C>T | CA304367921 | TBXA2R | c.858G>A (p.Thr286=) c.469G>A (p.Gly157Arg) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595863G>A | CA9080753 | TBXA2R | c.857C>T (p.Thr286Met) c.468C>T (p.His156=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595863G>C | CA403331023 | TBXA2R | c.857C>G (p.Thr286Arg) c.468C>G (p.His156Gln) | dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595863G= | CA2318945890 | TBXA2R | c.857C= (p.Thr286=) c.468C= (p.His156=) | |
19 | g.3595863G>T | CA403331026 | TBXA2R | c.857C>A (p.Thr286Lys) c.468C>A (p.His156Gln) | COSMIC COSMIC |
19 | g.3595864T>A | CA403331027 | TBXA2R | c.856A>T (p.Thr286Ser) c.467A>T (p.His156Leu) | |
19 | g.3595864T>C | CA403331029 | TBXA2R | c.856A>G (p.Thr286Ala) c.467A>G (p.His156Arg) | |
19 | g.3595864T>G | CA403331032 | TBXA2R | c.856A>C (p.Thr286Pro) c.467A>C (p.His156Pro) | |
19 | g.3595864_3595865delinsCA | CA645611085 | TBXA2R | c.855_856delinsTG (p.Thr286Ala) c.466_467delinsTG (p.His156Cys) | COSMIC |
19 | g.3595865G>A | CA9080754 | TBXA2R | c.855C>T (p.Thr285=) c.466C>T (p.His156Tyr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595865G>C | CA403331036 | TBXA2R | c.855C>G (p.Thr285=) c.466C>G (p.His156Asp) | |
19 | g.3595865G= | CA2318945891 | TBXA2R | c.855C= (p.Thr285=) c.466C= (p.His156=) | |
19 | g.3595865G>T | CA403331037 | TBXA2R | c.855C>A (p.Thr285=) c.466C>A (p.His156Asn) | |
19 | g.3595866G>A | CA403331039 | TBXA2R | c.854C>T (p.Thr285Ile) c.465C>T (p.His155=) | gnomAD v4 |
19 | g.3595866G>C | CA403331041 | TBXA2R | c.854C>G (p.Thr285Ser) c.465C>G (p.His155Gln) | |
19 | g.3595866G= | CA2318945892 | TBXA2R | c.854C= (p.Thr285=) c.465C= (p.His155=) | |
19 | g.3595866G>T | CA9080755 | TBXA2R | c.854C>A (p.Thr285Asn) c.465C>A (p.His155Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595867T>A | CA403331048 | TBXA2R | c.853A>T (p.Thr285Ser) c.464A>T (p.His155Leu) | |
19 | g.3595867T>C | CA403331046 | TBXA2R | c.853A>G (p.Thr285Ala) c.464A>G (p.His155Arg) | dbSNP |
19 | g.3595867T>G | CA403331044 | TBXA2R | c.853A>C (p.Thr285Pro) c.464A>C (p.His155Pro) | |
19 | g.3595868G>A | CA304367925 | TBXA2R | c.852C>T (p.Arg284=) c.463C>T (p.His155Tyr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595868G>C | CA9080756 | TBXA2R | c.852C>G (p.Arg284=) c.463C>G (p.His155Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595868G= | CA2318945893 | TBXA2R | c.852C= (p.Arg284=) c.463C= (p.His155=) | |
19 | g.3595868G>T | CA403331053 | TBXA2R | c.852C>A (p.Arg284=) c.463C>A (p.His155Asn) | |
19 | g.3595869C>A | CA403331056 | TBXA2R | c.851G>T (p.Arg284Leu) c.462G>T (p.Pro154=) | gnomAD v4 |
19 | g.3595869C= | CA2318945894 | TBXA2R | c.851G= (p.Arg284=) c.462G= (p.Pro154=) | |
19 | g.3595869C>G | CA403331059 | TBXA2R | c.851G>C (p.Arg284Pro) c.462G>C (p.Pro154=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595869C>T | CA9080757 | TBXA2R | c.851G>A (p.Arg284His) c.462G>A (p.Pro154=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595870G>A | CA9080758 | TBXA2R | c.850C>T (p.Arg284Cys) c.461C>T (p.Pro154Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.3595870G>C | CA403331065 | TBXA2R | c.850C>G (p.Arg284Gly) c.461C>G (p.Pro154Arg) | gnomAD v4 |
19 | g.3595870G= | CA2318945895 | TBXA2R | c.850C= (p.Arg284=) c.461C= (p.Pro154=) | |
19 | g.3595870G>T | CA403331068 | TBXA2R | c.850C>A (p.Arg284Ser) c.461C>A (p.Pro154Gln) | gnomAD v4 |
19 | g.3595871G>A | CA403331070 | TBXA2R | c.849C>T (p.Ser283=) c.460C>T (p.Pro154Ser) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595871G>C | CA403331071 | TBXA2R | c.849C>G (p.Ser283=) c.460C>G (p.Pro154Ala) | |
19 | g.3595871G= | CA2318945896 | TBXA2R | c.849C= (p.Ser283=) c.460C= (p.Pro154=) | |
19 | g.3595871G>T | CA403331073 | TBXA2R | c.849C>A (p.Ser283=) c.460C>A (p.Pro154Thr) | gnomAD v4 |
19 | g.3595872G>A | CA403331076 | TBXA2R | c.848C>T (p.Ser283Phe) c.459C>T (p.Val153=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595872G>C | CA304367929 | TBXA2R | c.848C>G (p.Ser283Cys) c.459C>G (p.Val153=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.3595872G= | CA2318945897 | TBXA2R | c.848C= (p.Ser283=) c.459C= (p.Val153=) | |
19 | g.3595872G>T | CA9080759 | TBXA2R | c.848C>A (p.Ser283Tyr) c.459C>A (p.Val153=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.3595873A>C | CA403331082 | TBXA2R | c.847T>G (p.Ser283Ala) c.458T>G (p.Val153Gly) | |
19 | g.3595873A>G | CA403331088 | TBXA2R | c.847T>C (p.Ser283Pro) c.458T>C (p.Val153Ala) | gnomAD v4 |
19 | g.3595873A>T | CA403331086 | TBXA2R | c.847T>A (p.Ser283Thr) c.458T>A (p.Val153Asp) | |
19 | g.3595874C>A | CA403331090 | TBXA2R | c.846G>T (p.Leu282=) c.457G>T (p.Val153Phe) | gnomAD v4 |
19 | g.3595874C= | CA2318945898 | TBXA2R | c.846G= (p.Leu282=) c.457G= (p.Val153=) | |
19 | g.3595874C>G | CA403331093 | TBXA2R | c.846G>C (p.Leu282=) c.457G>C (p.Val153Leu) | gnomAD v4 |
19 | g.3595874C>T | CA304367931 | TBXA2R | c.846G>A (p.Leu282=) c.457G>A (p.Val153Ile) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595875A>C | CA403331095 | TBXA2R | c.845T>G (p.Leu282Arg) c.456T>G (p.Ala152=) | |
19 | g.3595875A>G | CA403331097 | TBXA2R | c.845T>C (p.Leu282Pro) c.456T>C (p.Ala152=) | gnomAD v4 |
19 | g.3595875A>T | CA403331099 | TBXA2R | c.845T>A (p.Leu282Gln) c.456T>A (p.Ala152=) | |
19 | g.3595876G>A | CA403331101 | TBXA2R | c.844C>T (p.Leu282=) c.455C>T (p.Ala152Val) | |
19 | g.3595876G>C | CA403331103 | TBXA2R | c.844C>G (p.Leu282Val) c.455C>G (p.Ala152Gly) | |
19 | g.3595876G>T | CA403331104 | TBXA2R | c.844C>A (p.Leu282Met) c.455C>A (p.Ala152Asp) | |
19 | g.3595877C>A | CA403331106 | TBXA2R | c.843G>T (p.Gln281His) c.454G>T (p.Ala152Ser) | |
19 | g.3595877C>G | CA403331107 | TBXA2R | c.843G>C (p.Gln281His) c.454G>C (p.Ala152Pro) | |
19 | g.3595877C>T | CA403331109 | TBXA2R | c.843G>A (p.Gln281=) c.454G>A (p.Ala152Thr) | |
19 | g.3595878T>A | CA403331111 | TBXA2R | c.842A>T (p.Gln281Leu) c.453A>T (p.Ala151=) | |
19 | g.3595878T>C | CA403331113 | TBXA2R | c.842A>G (p.Gln281Arg) c.453A>G (p.Ala151=) | |
19 | g.3595878T>G | CA403331114 | TBXA2R | c.842A>C (p.Gln281Pro) c.453A>C (p.Ala151=) | dbSNP gnomAD v2 gnomAD v4 |
19 | g.3595878T= | CA2318945899 | TBXA2R | c.842A= (p.Gln281=) c.453A= (p.Ala151=) | |
19 | g.3595879G>A | CA403331115 | TBXA2R | c.841C>T (p.Gln281Ter) c.452C>T (p.Ala151Val) | |
19 | g.3595879G>C | CA403331118 | TBXA2R | c.841C>G (p.Gln281Glu) c.452C>G (p.Ala151Gly) | |
19 | g.3595879G>T | CA403331116 | TBXA2R | c.841C>A (p.Gln281Lys) c.452C>A (p.Ala151Glu) | gnomAD v4 |