Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.240873932_240873936dup | CA766964118 | AGXT | c.596-46_596-42dup (n.596-46_596-42dup) n.332+883_332+887dup | dbSNP |
2 | g.240873936G>A | CA2754892281 | AGXT | c.596-42G>A (n.596-42G>A) n.332+887G>A | |
2 | g.240873936G>C | CA2209160 | AGXT | c.596-42G>C (n.596-42G>C) n.332+887G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873936G= | CA1339333521 | AGXT | c.596-42G= (n.596-42G=) n.332+887G= | |
2 | g.240873936G>T | CA2209161 | AGXT | c.596-42G>T (n.596-42G>T) n.332+887G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240873938G>A | CA2754892282 | AGXT | c.596-40G>A (n.596-40G>A) n.332+889G>A | |
2 | g.240873939G= | CA1339333523 | AGXT | c.596-39G= (n.596-39G=) n.332+890G= | |
2 | g.240873939G>T | CA1339333522 | AGXT | c.596-39G>T (n.596-39G>T) n.332+890G>T | dbSNP gnomAD v4 |
2 | g.240873941G>A | CA1339333525 | AGXT | c.596-37G>A (n.596-37G>A) n.332+892G>A | dbSNP gnomAD v4 |
2 | g.240873941G= | CA1339333524 | AGXT | c.596-37G= (n.596-37G=) n.332+892G= | |
2 | g.240873943dup | CA2701856366 | AGXT | c.596-35dup (n.596-35dup) n.332+894dup | dbSNP |
2 | g.240873942G>A | CA1339333527 | AGXT | c.596-36G>A (n.596-36G>A) n.332+893G>A | dbSNP gnomAD v4 |
2 | g.240873942G= | CA1339333526 | AGXT | c.596-36G= (n.596-36G=) n.332+893G= | |
2 | g.240873943G>A | CA540536287 | AGXT | c.596-35G>A (n.596-35G>A) n.332+894G>A | dbSNP gnomAD v2 |
2 | g.240873943G= | CA1339333528 | AGXT | c.596-35G= (n.596-35G=) n.332+894G= | |
2 | g.240873943G>T | CA2664007616 | AGXT | c.596-35G>T (n.596-35G>T) n.332+894G>T | gnomAD v4 |
2 | g.240873944A>G | CA2701856543 | AGXT | c.596-34A>G (n.596-34A>G) n.332+895A>G | dbSNP |
2 | g.240873945C= | CA1339333529 | AGXT | c.596-33C= (n.596-33C=) n.332+896C= | |
2 | g.240873945C>T | CA766964135 | AGXT | c.596-33C>T (n.596-33C>T) n.332+896C>T | dbSNP |
2 | g.240873946_240873964delinsTCACCCGTCCCGAGCAAAC | CA1339333530 | AGXT | c.596-32_596-14delinsTCACCCGTCCCGAGCAAAC (n.596-32_596-14delinsTCACCCGTCCCGAGCAAAC) n.332+897_332+915delinsTCACCCGTCCCGAGCAAAC | |
2 | g.240873947C= | CA1339333531 | AGXT | c.596-31C= (n.596-31C=) n.332+898C= | |
2 | g.240873947C>T | CA540536288 | AGXT | c.596-31C>T (n.596-31C>T) n.332+898C>T | dbSNP gnomAD v2 |
2 | g.240873952_240873969del | CA2209162 | AGXT | c.596-26_596-9del (n.596-26_596-9del) n.332+903_332+920del | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240873948A= | CA1339333532 | AGXT | c.596-30A= (n.596-30A=) n.332+899A= | |
2 | g.240873948A>C | CA1339333533 | AGXT | c.596-30A>C (n.596-30A>C) n.332+899A>C | dbSNP |
2 | g.240873949C>A | CA2664007622 | AGXT | c.596-29C>A (n.596-29C>A) n.332+900C>A | gnomAD v4 |
2 | g.240873949C>G | CA2701856556 | AGXT | c.596-29C>G (n.596-29C>G) n.332+900C>G | dbSNP |
2 | g.240873953_240873957dup | CA2664007621 | AGXT | c.596-25_596-21dup (n.596-25_596-21dup) n.332+904_332+908dup | gnomAD v4 |
2 | g.240873950C>G | CA2701856558 | AGXT | c.596-28C>G (n.596-28C>G) n.332+901C>G | dbSNP |
2 | g.240873950C>T | CA2664007625 | AGXT | c.596-28C>T (n.596-28C>T) n.332+901C>T | gnomAD v4 |
2 | g.240873951C= | CA1339333534 | AGXT | c.596-27C= (n.596-27C=) n.332+902C= | |
2 | g.240873951C>G | CA2209164 | AGXT | c.596-27C>G (n.596-27C>G) n.332+902C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240873951C>T | CA2209163 | AGXT | c.596-27C>T (n.596-27C>T) n.332+902C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240873952G>A | CA2209165 | AGXT | c.596-26G>A (n.596-26G>A) n.332+903G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873952G= | CA1339333535 | AGXT | c.596-26G= (n.596-26G=) n.332+903G= | |
2 | g.240873952G>T | CA766964143 | AGXT | c.596-26G>T (n.596-26G>T) n.332+903G>T | dbSNP gnomAD v3 gnomAD v4 |
2 | g.240873955C>A | CA2577302624 | AGXT | c.596-23C>A (n.596-23C>A) n.332+906C>A | gnomAD v4 |
2 | g.240873956C= | CA1339333536 | AGXT | c.596-22C= (n.596-22C=) n.332+907C= | |
2 | g.240873956C>T | CA540536289 | AGXT | c.596-22C>T (n.596-22C>T) n.332+907C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873957G>A | CA2209166 | AGXT | c.596-21G>A (n.596-21G>A) n.332+908G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873957G>C | CA1044068523 | AGXT | c.596-21G>C (n.596-21G>C) n.332+908G>C | dbSNP gnomAD v3 gnomAD v4 |
2 | g.240873957G= | CA1339333537 | AGXT | c.596-21G= (n.596-21G=) n.332+908G= | |
2 | g.240873959G>A | CA68179236 | AGXT | c.596-19G>A (n.596-19G>A) n.332+910G>A | dbSNP gnomAD v4 |
2 | g.240873959G= | CA1339333538 | AGXT | c.596-19G= (n.596-19G=) n.332+910G= | |
2 | g.240873959G>T | CA2209167 | AGXT | c.596-19G>T (n.596-19G>T) n.332+910G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873960C>A | CA2577302625 | AGXT | c.596-18C>A (n.596-18C>A) n.332+911C>A | gnomAD v4 |
2 | g.240873963A= | CA1339333539 | AGXT | c.596-15A= (n.596-15A=) n.332+914A= | |
2 | g.240873963A>T | CA1044068524 | AGXT | c.596-15A>T (n.596-15A>T) n.332+914A>T | dbSNP gnomAD v3 gnomAD v4 |
2 | g.240873966A= | CA1339333540 | AGXT | c.596-12A= (n.596-12A=) n.332+917A= | |
2 | g.240873966A>C | CA1339333541 | AGXT | c.596-12A>C (n.596-12A>C) n.332+917A>C | dbSNP |
2 | g.240873966A>G | CA2209168 | AGXT | c.596-12A>G (n.596-12A>G) n.332+917A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873967C>A | CA1339333543 | AGXT | c.596-11C>A (n.596-11C>A) n.332+918C>A | dbSNP gnomAD v4 |
2 | g.240873967C= | CA1339333542 | AGXT | c.596-11C= (n.596-11C=) n.332+918C= | |
2 | g.240873968C>A | CA2580068027 | AGXT | c.596-10C>A (n.596-10C>A) n.332+919C>A | ClinVar |
2 | g.240873968C= | CA1339333544 | AGXT | c.596-10C= (n.596-10C=) n.332+919C= | |
2 | g.240873968C>T | CA68179239 | AGXT | c.596-10C>T (n.596-10C>T) n.332+919C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873969C= | CA1339333546 | AGXT | c.596-9C= (n.596-9C=) n.332+920C= | |
2 | g.240873969C>T | CA1339333545 | AGXT | c.596-9C>T (n.596-9C>T) n.332+920C>T | ClinVar dbSNP gnomAD v4 |
2 | g.240873970A= | CA1339333547 | AGXT | c.596-8A= (n.596-8A=) n.332+921A= | |
2 | g.240873970A>G | CA1339333548 | AGXT | c.596-8A>G (n.596-8A>G) n.332+921A>G | ClinVar dbSNP gnomAD v4 |
2 | g.240873971T>A | CA2664007657 | AGXT | c.596-7T>A (n.596-7T>A) n.332+922T>A | gnomAD v4 |
2 | g.240873971T>C | CA2209169 | AGXT | c.596-7T>C (n.596-7T>C) n.332+922T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873971T= | CA1339333549 | AGXT | c.596-7T= (n.596-7T=) n.332+922T= | |
2 | g.240873972C>G | CA2577302626 | AGXT | c.596-6C>G (n.596-6C>G) n.332+923C>G | |
2 | g.240873974A= | CA1339333550 | AGXT | c.596-4A= (n.596-4A=) n.332+925A= | |
2 | g.240873974A>G | CA68179242 | AGXT | c.596-4A>G (n.596-4A>G) n.332+925A>G | ClinVar dbSNP |
2 | g.240873975C>A | CA68179245 | AGXT | c.596-3C>A (n.596-3C>A) n.332+926C>A | dbSNP |
2 | g.240873975C= | CA1339333551 | AGXT | c.596-3C= (n.596-3C=) n.332+926C= | |
2 | g.240873976A= | CA1339333552 | AGXT | c.596-2A= (n.596-2A=) n.332+927A= | |
2 | g.240873976A>C | CA351316724 | AGXT | c.596-2A>C (n.596-2A>C) n.332+927A>C | |
2 | g.240873976A>G | CA275806 | AGXT | c.596-2A>G (n.596-2A>G) n.332+927A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.240873976A>T | CA351316727 | AGXT | c.596-2A>T (n.596-2A>T) n.332+927A>T | |
2 | g.240873977G>A | CA351316732 | AGXT | c.596-1G>A (n.596-1G>A) n.332+928G>A | ClinVar |
2 | g.240873977G>C | CA351316737 | AGXT | c.596-1G>C (n.596-1G>C) n.332+928G>C | |
2 | g.240873977G>T | CA351316730 | AGXT | c.596-1G>T (n.596-1G>T) n.332+928G>T | |
2 | g.240873977_240873982delinsGGCATC | CA1339333553 | AGXT | c.596-1_600delinsGGCATC n.332+928_332+933delinsGGCATC | |
2 | g.240873978G>A | CA351316739 | AGXT | c.596G>A (p.Gly199Asp) n.332+929G>A | |
2 | g.240873978G>C | CA351316741 | AGXT | c.596G>C (p.Gly199Ala) n.332+929G>C | |
2 | g.240873978G>T | CA351316743 | AGXT | c.596G>T (p.Gly199Val) n.332+929G>T | |
2 | g.240873979_240873983del | CA540536290 | AGXT | c.597_601del (p.Ile200HisfsTer23) n.332+930_332+934del | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.240873979C>A | CA432024091 | AGXT | c.597C>A (p.Gly199=) n.332+930C>A | |
2 | g.240873979C>G | CA432024092 | AGXT | c.597C>G (p.Gly199=) n.332+930C>G | |
2 | g.240873979C>T | CA432024093 | AGXT | c.597C>T (p.Gly199=) n.332+930C>T | |
2 | g.240873980A= | CA1339333554 | AGXT | c.598A= (p.Ile200=) n.332+931A= | |
2 | g.240873980A>C | CA351316745 | AGXT | c.598A>C (p.Ile200Leu) n.332+931A>C | |
2 | g.240873980A>G | CA68179247 | AGXT | c.598A>G (p.Ile200Val) n.332+931A>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.240873980A>T | CA351316748 | AGXT | c.598A>T (p.Ile200Phe) n.332+931A>T | |
2 | g.240873981T>A | CA351316755 | AGXT | c.599T>A (p.Ile200Asn) n.332+932T>A | |
2 | g.240873981T>C | CA351316751 | AGXT | c.599T>C (p.Ile200Thr) n.332+932T>C | gnomAD v4 |
2 | g.240873981T>G | CA351316753 | AGXT | c.599T>G (p.Ile200Ser) n.332+932T>G | |
2 | g.240873982C>A | CA432024095 | AGXT | c.600C>A (p.Ile200=) n.332+933C>A | |
2 | g.240873982C= | CA1339333555 | AGXT | c.600C= (p.Ile200=) n.332+933C= | |
2 | g.240873982C>G | CA351316757 | AGXT | c.600C>G (p.Ile200Met) n.332+933C>G | |
2 | g.240873982C>T | CA2209170 | AGXT | c.600C>T (p.Ile200=) n.332+933C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.240873983G>A | CA10612912 | AGXT | c.601G>A (p.Asp201Asn) n.332+934G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873983G>C | CA351316761 | AGXT | c.601G>C (p.Asp201His) n.332+934G>C | |
2 | g.240873983G= | CA1339333556 | AGXT | c.601G= (p.Asp201=) n.332+934G= | |
2 | g.240873983G>T | CA351316763 | AGXT | c.601G>T (p.Asp201Tyr) n.332+934G>T | |
2 | g.240873984A= | CA1339333557 | AGXT | c.602A= (p.Asp201=) n.332+935A= | |
2 | g.240873984A>C | CA351316765 | AGXT | c.602A>C (p.Asp201Ala) n.332+935A>C | |
2 | g.240873984A>G | CA351316769 | AGXT | c.602A>G (p.Asp201Gly) n.332+935A>G | dbSNP |
2 | g.240873984A>T | CA351316767 | AGXT | c.602A>T (p.Asp201Val) n.332+935A>T | ClinVar |
2 | g.240873985C>A | CA275715 | AGXT | c.603C>A (p.Asp201Glu) n.332+936C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873985C= | CA1339333558 | AGXT | c.603C= (p.Asp201=) n.332+936C= | |
2 | g.240873985C>G | CA351316771 | AGXT | c.603C>G (p.Asp201Glu) n.332+936C>G | |
2 | g.240873985C>T | CA432024100 | AGXT | c.603C>T (p.Asp201=) n.332+936C>T | gnomAD v4 |
2 | g.240873986A>C | CA351316774 | AGXT | c.604A>C (p.Ile202Leu) n.332+937A>C | gnomAD v4 |
2 | g.240873986A>G | CA351316776 | AGXT | c.604A>G (p.Ile202Val) n.332+937A>G | |
2 | g.240873986A>T | CA351316778 | AGXT | c.604A>T (p.Ile202Phe) n.332+937A>T | |
2 | g.240873987T>A | CA275716 | AGXT | c.605T>A (p.Ile202Asn) n.332+938T>A | ClinVar dbSNP |
2 | g.240873987T>C | CA68179251 | AGXT | c.605T>C (p.Ile202Thr) n.332+938T>C | dbSNP gnomAD v3 gnomAD v4 |
2 | g.240873987T>G | CA351316782 | AGXT | c.605T>G (p.Ile202Ser) n.332+938T>G | |
2 | g.240873987T= | CA1339333559 | AGXT | c.605T= (p.Ile202=) n.332+938T= | |
2 | g.240873988C>A | CA68179253 | AGXT | c.606C>A (p.Ile202=) n.332+939C>A | dbSNP |
2 | g.240873988C= | CA1339333560 | AGXT | c.606C= (p.Ile202=) n.332+939C= | |
2 | g.240873988C>G | CA351316784 | AGXT | c.606C>G (p.Ile202Met) n.332+939C>G | |
2 | g.240873988C>T | CA432024107 | AGXT | c.606C>T (p.Ile202=) n.332+939C>T | |
2 | g.240873989del | CA2664007702 | AGXT | c.607del (p.Leu203CysfsTer9) n.332+940del | gnomAD v4 |
2 | g.240873989C>A | CA351316787 | AGXT | c.607C>A (p.Leu203Met) n.332+940C>A | |
2 | g.240873989C= | CA1339333561 | AGXT | c.607C= (p.Leu203=) n.332+940C= | |
2 | g.240873989C>G | CA351316789 | AGXT | c.607C>G (p.Leu203Val) n.332+940C>G | |
2 | g.240873989C>T | CA2209171 | AGXT | c.607C>T (p.Leu203=) n.332+940C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873990del | CA2664007711 | AGXT | c.608del (p.Leu203ArgfsTer9) n.332+941del | gnomAD v4 |
2 | g.240873990T>A | CA351316794 | AGXT | c.608T>A (p.Leu203Gln) n.332+941T>A | |
2 | g.240873990T>C | CA351316796 | AGXT | c.608T>C (p.Leu203Pro) n.332+941T>C | |
2 | g.240873990T>G | CA351316792 | AGXT | c.608T>G (p.Leu203Arg) n.332+941T>G | |
2 | g.240873991G>A | CA432024114 | AGXT | c.609G>A (p.Leu203=) n.332+942G>A | |
2 | g.240873991G>C | CA2209172 | AGXT | c.609G>C (p.Leu203=) n.332+942G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873991G= | CA1339333562 | AGXT | c.609G= (p.Leu203=) n.332+942G= | |
2 | g.240873991G>T | CA432024116 | AGXT | c.609G>T (p.Leu203=) n.332+942G>T | |
2 | g.240873992T>A | CA351316799 | AGXT | c.610T>A (p.Tyr204Asn) n.332+943T>A | gnomAD v4 |
2 | g.240873992T>C | CA351316802 | AGXT | c.610T>C (p.Tyr204His) n.332+943T>C | |
2 | g.240873992T>G | CA351316800 | AGXT | c.610T>G (p.Tyr204Asp) n.332+943T>G | |
2 | g.240873993A>C | CA351316805 | AGXT | c.611A>C (p.Tyr204Ser) n.332+944A>C | |
2 | g.240873993A>G | CA351316809 | AGXT | c.611A>G (p.Tyr204Cys) n.332+944A>G | gnomAD v4 |
2 | g.240873993A>T | CA351316806 | AGXT | c.611A>T (p.Tyr204Phe) n.332+944A>T | |
2 | g.240873994C>A | CA275718 | AGXT | c.612C>A (p.Tyr204Ter) n.332+945C>A | ClinVar dbSNP gnomAD v4 |
2 | g.240873994C= | CA1339333563 | AGXT | c.612C= (p.Tyr204=) n.332+945C= | |
2 | g.240873994C>G | CA351316812 | AGXT | c.612C>G (p.Tyr204Ter) n.332+945C>G | |
2 | g.240873994C>T | CA432024119 | AGXT | c.612C>T (p.Tyr204=) n.332+945C>T | ClinVar dbSNP gnomAD v4 |
2 | g.240873995T>A | CA351316814 | AGXT | c.613T>A (p.Ser205Thr) n.332+946T>A | |
2 | g.240873995T>C | CA340441 | AGXT | c.613T>C (p.Ser205Pro) n.332+946T>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873995T>G | CA351316816 | AGXT | c.613T>G (p.Ser205Ala) n.332+946T>G | |
2 | g.240873995T= | CA1339333564 | AGXT | c.613T= (p.Ser205=) n.332+946T= | |
2 | g.240873996C>A | CA275723 | AGXT | c.614C>A (p.Ser205Ter) n.332+947C>A | ClinVar dbSNP |
2 | g.240873996C= | CA1339333565 | AGXT | c.614C= (p.Ser205=) n.332+947C= | |
2 | g.240873996C>G | CA351316819 | AGXT | c.614C>G (p.Ser205Trp) n.332+947C>G | dbSNP |
2 | g.240873996C>T | CA275721 | AGXT | c.614C>T (p.Ser205Leu) n.332+947C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
2 | g.240873997G>A | CA2209173 | AGXT | c.615G>A (p.Ser205=) n.332+948G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240873997G>C | CA432024124 | AGXT | c.615G>C (p.Ser205=) n.332+948G>C | ClinVar dbSNP gnomAD v2 |
2 | g.240873997G= | CA1339333566 | AGXT | c.615G= (p.Ser205=) n.332+948G= | |
2 | g.240873997G>T | CA432024125 | AGXT | c.615G>T (p.Ser205=) n.332+948G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.240873998G>A | CA351316823 | AGXT | c.616G>A (p.Gly206Ser) n.332+949G>A | |
2 | g.240873998G>C | CA351316825 | AGXT | c.616G>C (p.Gly206Arg) n.332+949G>C | |
2 | g.240873998G>T | CA351316827 | AGXT | c.616G>T (p.Gly206Cys) n.332+949G>T | |
2 | g.240873999G>A | CA351316829 | AGXT | c.617G>A (p.Gly206Asp) n.332+950G>A | |
2 | g.240873999G>C | CA351316831 | AGXT | c.617G>C (p.Gly206Ala) n.332+950G>C | |
2 | g.240873999G>T | CA351316833 | AGXT | c.617G>T (p.Gly206Val) n.332+950G>T | |
2 | g.240874000C>A | CA432024127 | AGXT | c.618C>A (p.Gly206=) n.332+951C>A | |
2 | g.240874000C= | CA1339333567 | AGXT | c.618C= (p.Gly206=) n.332+951C= | |
2 | g.240874000C>G | CA432024128 | AGXT | c.618C>G (p.Gly206=) n.332+951C>G | |
2 | g.240874000C>T | CA432024129 | AGXT | c.618C>T (p.Gly206=) n.332+951C>T | dbSNP gnomAD v2 gnomAD v4 |
2 | g.240874001T>A | CA351316834 | AGXT | c.619T>A (p.Ser207Thr) n.332+952T>A | |
2 | g.240874001T>C | CA351316839 | AGXT | c.619T>C (p.Ser207Pro) n.332+952T>C | |
2 | g.240874001T>G | CA351316837 | AGXT | c.619T>G (p.Ser207Ala) n.332+952T>G | |
2 | g.240874002C>A | CA351316841 | AGXT | c.620C>A (p.Ser207Tyr) n.332+953C>A | |
2 | g.240874002C>G | CA351316843 | AGXT | c.620C>G (p.Ser207Cys) n.332+953C>G | |
2 | g.240874002C>T | CA351316845 | AGXT | c.620C>T (p.Ser207Phe) n.332+953C>T | |
2 | g.240874003C>A | CA432024133 | AGXT | c.621C>A (p.Ser207=) n.332+954C>A | |
2 | g.240874003C>G | CA432024134 | AGXT | c.621C>G (p.Ser207=) n.332+954C>G | |
2 | g.240874003C>T | CA432024136 | AGXT | c.621C>T (p.Ser207=) n.332+954C>T | |
2 | g.240874004C>A | CA2209174 | AGXT | c.622C>A (p.Gln208Lys) n.332+955C>A | dbSNP ExAC gnomAD v2 |
2 | g.240874004C= | CA1339333568 | AGXT | c.622C= (p.Gln208=) n.332+955C= | |
2 | g.240874004C>G | CA351316848 | AGXT | c.622C>G (p.Gln208Glu) n.332+955C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874004C>T | CA351316850 | AGXT | c.622C>T (p.Gln208Ter) n.332+955C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874005A= | CA1339333569 | AGXT | c.623A= (p.Gln208=) n.332+956A= | |
2 | g.240874005A>C | CA351316852 | AGXT | c.623A>C (p.Gln208Pro) n.332+956A>C | |
2 | g.240874005A>G | CA2209175 | AGXT | c.623A>G (p.Gln208Arg) n.332+956A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240874005A>T | CA351316854 | AGXT | c.623A>T (p.Gln208Leu) n.332+956A>T | |
2 | g.240874006G>A | CA432024140 | AGXT | c.624G>A (p.Gln208=) n.332+957G>A | ClinVar dbSNP |
2 | g.240874006G>C | CA351316856 | AGXT | c.624G>C (p.Gln208His) n.332+957G>C | COSMIC |
2 | g.240874006G>T | CA351316858 | AGXT | c.624G>T (p.Gln208His) n.332+957G>T | |
2 | g.240874007A>C | CA351316861 | AGXT | c.625A>C (p.Lys209Gln) n.332+958A>C | |
2 | g.240874007A>G | CA351316865 | AGXT | c.625A>G (p.Lys209Glu) n.332+958A>G | gnomAD v4 COSMIC |
2 | g.240874007A>T | CA351316862 | AGXT | c.625A>T (p.Lys209Ter) n.332+958A>T | |
2 | g.240874008del | CA2697550616 | AGXT | c.626del (p.Lys209ArgfsTer3) n.332+959del | ClinVar |
2 | g.240874008A>C | CA351316867 | AGXT | c.626A>C (p.Lys209Thr) n.332+959A>C | gnomAD v4 |
2 | g.240874008A>G | CA351316869 | AGXT | c.626A>G (p.Lys209Arg) n.332+959A>G | COSMIC |
2 | g.240874008A>T | CA351316871 | AGXT | c.626A>T (p.Lys209Met) n.332+959A>T | |
2 | g.240874009G>A | CA432024144 | AGXT | c.627G>A (p.Lys209=) n.332+960G>A | ClinVar COSMIC |
2 | g.240874009G>C | CA351316873 | AGXT | c.627G>C (p.Lys209Asn) n.332+960G>C | |
2 | g.240874009G= | CA1339333570 | AGXT | c.627G= (p.Lys209=) n.332+960G= | |
2 | g.240874009G>T | CA351316875 | AGXT | c.627G>T (p.Lys209Asn) n.332+960G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.240874010G>A | CA351316878 | AGXT | c.628G>A (p.Ala210Thr) n.332+961G>A | gnomAD v4 |
2 | g.240874010G>C | CA275726 | AGXT | c.628G>C (p.Ala210Pro) n.332+961G>C | ClinVar dbSNP |
2 | g.240874010G= | CA1339333571 | AGXT | c.628G= (p.Ala210=) n.332+961G= | |
2 | g.240874010G>T | CA351316881 | AGXT | c.628G>T (p.Ala210Ser) n.332+961G>T | |
2 | g.240874011C>A | CA351316883 | AGXT | c.629C>A (p.Ala210Asp) n.332+962C>A | |
2 | g.240874011C>G | CA351316885 | AGXT | c.629C>G (p.Ala210Gly) n.332+962C>G | |
2 | g.240874011C>T | CA351316887 | AGXT | c.629C>T (p.Ala210Val) n.332+962C>T | gnomAD v4 |
2 | g.240874012C>A | CA432024154 | AGXT | c.630C>A (p.Ala210=) n.332+963C>A | |
2 | g.240874012C= | CA1339333572 | AGXT | c.630C= (p.Ala210=) n.332+963C= | |
2 | g.240874012C>G | CA432024155 | AGXT | c.630C>G (p.Ala210=) n.332+963C>G | gnomAD v4 |
2 | g.240874012C>T | CA432024156 | AGXT | c.630C>T (p.Ala210=) n.332+963C>T | ClinVar dbSNP gnomAD v4 |
2 | g.240874013C>A | CA351316889 | AGXT | c.631C>A (p.Leu211Met) n.332+964C>A | |
2 | g.240874013C>G | CA351316890 | AGXT | c.631C>G (p.Leu211Val) n.332+964C>G | |
2 | g.240874013C>T | CA432024157 | AGXT | c.631C>T (p.Leu211=) n.332+964C>T | COSMIC |
2 | g.240874014T>A | CA351316893 | AGXT | c.632T>A (p.Leu211Gln) n.332+965T>A | |
2 | g.240874014T>C | CA351316897 | AGXT | c.632T>C (p.Leu211Pro) n.332+965T>C | |
2 | g.240874014T>G | CA351316895 | AGXT | c.632T>G (p.Leu211Arg) n.332+965T>G | ClinVar |
2 | g.240874015G>A | CA432024159 | AGXT | c.633G>A (p.Leu211=) n.332+966G>A | |
2 | g.240874015G>C | CA432024160 | AGXT | c.633G>C (p.Leu211=) n.332+966G>C | |
2 | g.240874015G>T | CA432024162 | AGXT | c.633G>T (p.Leu211=) n.332+966G>T | |
2 | g.240874016A>C | CA351316899 | AGXT | c.634A>C (p.Asn212His) n.332+967A>C | gnomAD v4 |
2 | g.240874016A>G | CA351316901 | AGXT | c.634A>G (p.Asn212Asp) n.332+967A>G | |
2 | g.240874016A>T | CA351316903 | AGXT | c.634A>T (p.Asn212Tyr) n.332+967A>T | |
2 | g.240874017A= | CA1339333573 | AGXT | c.635A= (p.Asn212=) n.332+968A= | |
2 | g.240874017A>C | CA351316908 | AGXT | c.635A>C (p.Asn212Thr) n.332+968A>C | |
2 | g.240874017A>G | CA2209176 | AGXT | c.635A>G (p.Asn212Ser) n.332+968A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240874017A>T | CA351316911 | AGXT | c.635A>T (p.Asn212Ile) n.332+968A>T | |
2 | g.240874018C>A | CA351316918 | AGXT | c.636C>A (p.Asn212Lys) n.332+969C>A | gnomAD v4 |
2 | g.240874018C= | CA1339333574 | AGXT | c.636C= (p.Asn212=) n.332+969C= | |
2 | g.240874018C>G | CA351316920 | AGXT | c.636C>G (p.Asn212Lys) n.332+969C>G | |
2 | g.240874018C>T | CA2209177 | AGXT | c.636C>T (p.Asn212=) n.332+969C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.240874019G>A | CA351316926 | AGXT | c.637G>A (p.Ala213Thr) n.332+970G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.240874019G>C | CA351316924 | AGXT | c.637G>C (p.Ala213Pro) n.332+970G>C | |
2 | g.240874019G= | CA1339333575 | AGXT | c.637G= (p.Ala213=) n.332+970G= | |
2 | g.240874019G>T | CA351316923 | AGXT | c.637G>T (p.Ala213Ser) n.332+970G>T | dbSNP gnomAD v3 gnomAD v4 |
2 | g.240874020C>A | CA351316927 | AGXT | c.638C>A (p.Ala213Asp) n.332+971C>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874020C= | CA1339333576 | AGXT | c.638C= (p.Ala213=) n.332+971C= | |
2 | g.240874020C>G | CA351316928 | AGXT | c.638C>G (p.Ala213Gly) n.332+971C>G | |
2 | g.240874020C>T | CA2209178 | AGXT | c.638C>T (p.Ala213Val) n.332+971C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.240874021C>A | CA432024174 | AGXT | c.639C>A (p.Ala213=) n.332+972C>A | gnomAD v4 |
2 | g.240874021C= | CA1339333577 | AGXT | c.639C= (p.Ala213=) n.332+972C= | |
2 | g.240874021C>G | CA432024175 | AGXT | c.639C>G (p.Ala213=) n.332+972C>G | |
2 | g.240874021C>T | CA2209179 | AGXT | c.639C>T (p.Ala213=) n.332+972C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874022C>A | CA351316931 | AGXT | c.640C>A (p.Pro214Thr) n.332+973C>A | |
2 | g.240874022C>G | CA351316933 | AGXT | c.640C>G (p.Pro214Ala) n.332+973C>G | |
2 | g.240874022C>T | CA351316935 | AGXT | c.640C>T (p.Pro214Ser) n.332+973C>T | |
2 | g.240874023C>A | CA351316937 | AGXT | c.641C>A (p.Pro214His) n.332+974C>A | |
2 | g.240874023C>G | CA351316939 | AGXT | c.641C>G (p.Pro214Arg) n.332+974C>G | |
2 | g.240874023C>T | CA351316941 | AGXT | c.641C>T (p.Pro214Leu) n.332+974C>T | |
2 | g.240874023_240874027delinsCTCCA | CA1339333578 | AGXT | c.641_645delinsCTCCA (p.Pro214=) n.332+974_332+978delinsCTCCA | |
2 | g.240874024del | CA2573051906 | AGXT | c.642del (p.Pro215GlnfsTer?) n.332+975del | ClinVar dbSNP |
2 | g.240874024T>A | CA432024179 | AGXT | c.642T>A (p.Pro214=) n.332+975T>A | |
2 | g.240874024T>C | CA432024180 | AGXT | c.642T>C (p.Pro214=) n.332+975T>C | |
2 | g.240874024T>G | CA432024181 | AGXT | c.642T>G (p.Pro214=) n.332+975T>G | |
2 | g.240874024_240874027del | CA275844 | AGXT | c.642_645del (p.Pro215GlyfsTer?) n.332+975_332+978del | ClinVar dbSNP |
2 | g.240874025C>A | CA351316944 | AGXT | c.643C>A (p.Pro215Thr) n.332+976C>A | |
2 | g.240874025C= | CA1339333579 | AGXT | c.643C= (p.Pro215=) n.332+976C= | |
2 | g.240874025C>G | CA68179273 | AGXT | c.643C>G (p.Pro215Ala) n.332+976C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.240874025C>T | CA351316946 | AGXT | c.643C>T (p.Pro215Ser) n.332+976C>T | |
2 | g.240874026C>A | CA351316953 | AGXT | c.644C>A (p.Pro215Gln) n.332+977C>A | |
2 | g.240874026C>G | CA351316950 | AGXT | c.644C>G (p.Pro215Arg) n.332+977C>G | |
2 | g.240874026C>T | CA351316948 | AGXT | c.644C>T (p.Pro215Leu) n.332+977C>T | |
2 | g.240874027A>C | CA432024185 | AGXT | c.645A>C (p.Pro215=) n.332+978A>C | |
2 | g.240874027A>G | CA432024187 | AGXT | c.645A>G (p.Pro215=) n.332+978A>G | ClinVar dbSNP |
2 | g.240874027A>T | CA432024189 | AGXT | c.645A>T (p.Pro215=) n.332+978A>T | |
2 | g.240874028G>A | CA275728 | AGXT | c.646G>A (p.Gly216Arg) n.332+979G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240874028G>C | CA351316956 | AGXT | c.646G>C (p.Gly216Arg) n.332+979G>C | |
2 | g.240874028G= | CA1339333580 | AGXT | c.646G= (p.Gly216=) n.332+979G= | |
2 | g.240874028G>T | CA351316958 | AGXT | c.646G>T (p.Gly216Trp) n.332+979G>T | |
2 | g.240874029G>A | CA2209180 | AGXT | c.647G>A (p.Gly216Glu) n.332+980G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.240874029G>C | CA351316960 | AGXT | c.647G>C (p.Gly216Ala) n.332+980G>C | |
2 | g.240874029G= | CA1339333581 | AGXT | c.647G= (p.Gly216=) n.332+980G= | |
2 | g.240874029G>T | CA351316962 | AGXT | c.647G>T (p.Gly216Val) n.332+980G>T | |
2 | g.240874029_240874030delinsAA | CA645538649 | AGXT | c.647_648delinsAA (p.Gly216Glu) n.332+980_332+981delinsAA | COSMIC |
2 | g.240874030G>A | CA432024194 | AGXT | c.648G>A (p.Gly216=) n.332+981G>A | |
2 | g.240874030G>C | CA2209181 | AGXT | c.648G>C (p.Gly216=) n.332+981G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874030G= | CA1339333582 | AGXT | c.648G= (p.Gly216=) n.332+981G= | |
2 | g.240874030G>T | CA432024195 | AGXT | c.648G>T (p.Gly216=) n.332+981G>T | |
2 | g.240874031A>C | CA351316966 | AGXT | c.649A>C (p.Thr217Pro) n.332+982A>C | |
2 | g.240874031A>G | CA351316968 | AGXT | c.649A>G (p.Thr217Ala) n.332+982A>G | |
2 | g.240874031A>T | CA351316970 | AGXT | c.649A>T (p.Thr217Ser) n.332+982A>T | |
2 | g.240874032C>A | CA351316972 | AGXT | c.650C>A (p.Thr217Asn) n.332+983C>A | |
2 | g.240874032C>G | CA351316974 | AGXT | c.650C>G (p.Thr217Ser) n.332+983C>G | |
2 | g.240874032C>T | CA351316978 | AGXT | c.650C>T (p.Thr217Ile) n.332+983C>T | |
2 | g.240874033C>A | CA432024205 | AGXT | c.651C>A (p.Thr217=) n.332+984C>A | |
2 | g.240874033C= | CA1339333583 | AGXT | c.651C= (p.Thr217=) n.332+984C= | |
2 | g.240874033C>G | CA432024206 | AGXT | c.651C>G (p.Thr217=) n.332+984C>G | |
2 | g.240874033C>T | CA2209182 | AGXT | c.651C>T (p.Thr217=) n.332+984C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.240874034T>A | CA351316983 | AGXT | c.652T>A (p.Ser218Thr) n.332+985T>A | |
2 | g.240874034T>C | CA351316980 | AGXT | c.652T>C (p.Ser218Pro) n.332+985T>C | |
2 | g.240874034T>G | CA351316981 | AGXT | c.652T>G (p.Ser218Ala) n.332+985T>G | |
2 | g.240874035C>A | CA351316985 | AGXT | c.653C>A (p.Ser218Ter) n.332+986C>A | ClinVar dbSNP |
2 | g.240874035C= | CA1339333584 | AGXT | c.653C= (p.Ser218=) n.332+986C= | |
2 | g.240874035C>G | CA351316987 | AGXT | c.653C>G (p.Ser218Trp) n.332+986C>G | |
2 | g.240874035C>T | CA274210 | AGXT | c.653C>T (p.Ser218Leu) n.332+986C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |