Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47733851G>A | CA400059348 | TBX21 | c.397G>A (p.Val133Met) n.427G>A | dbSNP gnomAD v4 |
17 | g.47733851G>C | CA400059352 | TBX21 | c.397G>C (p.Val133Leu) n.427G>C | |
17 | g.47733851G= | CA2262805825 | TBX21 | c.397G= (p.Val133=) n.427G= | |
17 | g.47733851G>T | CA400059355 | TBX21 | c.397G>T (p.Val133Leu) n.427G>T | gnomAD v4 |
17 | g.47733852T>A | CA400059359 | TBX21 | c.398T>A (p.Val133Glu) n.428T>A | |
17 | g.47733852T>C | CA400059362 | TBX21 | c.398T>C (p.Val133Ala) n.428T>C | |
17 | g.47733852T>G | CA400059366 | TBX21 | c.398T>G (p.Val133Gly) n.428T>G | dbSNP gnomAD v4 |
17 | g.47733852T= | CA2262805826 | TBX21 | c.398T= (p.Val133=) n.428T= | |
17 | g.47733853G>A | CA500652442 | TBX21 | c.399G>A (p.Val133=) n.429G>A | |
17 | g.47733853G>C | CA500652444 | TBX21 | c.399G>C (p.Val133=) n.429G>C | |
17 | g.47733853G>T | CA500652445 | TBX21 | c.399G>T (p.Val133=) n.429G>T | gnomAD v4 |
17 | g.47733854T>A | CA400059375 | TBX21 | c.400T>A (p.Ser134Thr) n.430T>A | |
17 | g.47733854T>C | CA400059368 | TBX21 | c.400T>C (p.Ser134Pro) n.430T>C | |
17 | g.47733854T>G | CA400059373 | TBX21 | c.400T>G (p.Ser134Ala) n.430T>G | |
17 | g.47733855C>A | CA400059378 | TBX21 | c.401C>A (p.Ser134Ter) n.431C>A | |
17 | g.47733855C>G | CA400059380 | TBX21 | c.401C>G (p.Ser134Trp) n.431C>G | |
17 | g.47733855C>T | CA400059382 | TBX21 | c.401C>T (p.Ser134Leu) n.431C>T | gnomAD v4 |
17 | g.47733856G>A | CA500652446 | TBX21 | c.402G>A (p.Ser134=) n.432G>A | gnomAD v4 |
17 | g.47733856G>C | CA500652447 | TBX21 | c.402G>C (p.Ser134=) n.432G>C | |
17 | g.47733856G>T | CA500652448 | TBX21 | c.402G>T (p.Ser134=) n.432G>T | gnomAD v4 |
17 | g.47733857G>A | CA400059383 | TBX21 | c.403G>A (p.Gly135Arg) n.433G>A | gnomAD v4 |
17 | g.47733857G>C | CA400059385 | TBX21 | c.403G>C (p.Gly135Arg) n.433G>C | gnomAD v4 |
17 | g.47733857G>T | CA400059386 | TBX21 | c.403G>T (p.Gly135Trp) n.433G>T | |
17 | g.47733858G>A | CA400059392 | TBX21 | c.404G>A (p.Gly135Glu) n.434G>A | |
17 | g.47733858G>C | CA400059395 | TBX21 | c.404G>C (p.Gly135Ala) n.434G>C | |
17 | g.47733858G>T | CA400059397 | TBX21 | c.404G>T (p.Gly135Val) n.434G>T | |
17 | g.47733859G>A | CA500652454 | TBX21 | c.405G>A (p.Gly135=) n.435G>A | |
17 | g.47733859G>C | CA500652452 | TBX21 | c.405G>C (p.Gly135=) n.435G>C | |
17 | g.47733859G>T | CA500652453 | TBX21 | c.405G>T (p.Gly135=) n.435G>T | |
17 | g.47733860A= | CA2262805827 | TBX21 | c.406A= (p.Lys136=) n.436A= | |
17 | g.47733860A>C | CA400059401 | TBX21 | c.406A>C (p.Lys136Gln) n.436A>C | |
17 | g.47733860A>G | CA8626261 | TBX21 | c.406A>G (p.Lys136Glu) n.436A>G | dbSNP ExAC gnomAD v2 |
17 | g.47733860A>T | CA400059409 | TBX21 | c.406A>T (p.Lys136Ter) n.436A>T | |
17 | g.47733861A>C | CA400059413 | TBX21 | c.407A>C (p.Lys136Thr) n.437A>C | gnomAD v4 |
17 | g.47733861A>G | CA400059416 | TBX21 | c.407A>G (p.Lys136Arg) n.437A>G | |
17 | g.47733861A>T | CA400059415 | TBX21 | c.407A>T (p.Lys136Ile) n.437A>T | |
17 | g.47733862A= | CA2262805828 | TBX21 | c.408A= (p.Lys136=) n.438A= | |
17 | g.47733862A>C | CA400059420 | TBX21 | c.408A>C (p.Lys136Asn) n.438A>C | |
17 | g.47733862A>G | CA8626262 | TBX21 | c.408A>G (p.Lys136=) n.438A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47733862A>T | CA400059429 | TBX21 | c.408A>T (p.Lys136Asn) n.438A>T | |
17 | g.47733863C>A | CA400059431 | TBX21 | c.409C>A (p.Leu137Met) n.439C>A | |
17 | g.47733863C>G | CA400059434 | TBX21 | c.409C>G (p.Leu137Val) n.439C>G | |
17 | g.47733863C>T | CA500652456 | TBX21 | c.409C>T (p.Leu137=) n.439C>T | |
17 | g.47733864T>A | CA400059442 | TBX21 | c.410T>A (p.Leu137Gln) n.440T>A | |
17 | g.47733864T>C | CA400059443 | TBX21 | c.410T>C (p.Leu137Pro) n.440T>C | |
17 | g.47733864T>G | CA400059459 | TBX21 | c.410T>G (p.Leu137Arg) n.440T>G | |
17 | g.47733865G>A | CA500652458 | TBX21 | c.411G>A (p.Leu137=) n.441G>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.47733865G>C | CA500652459 | TBX21 | c.411G>C (p.Leu137=) n.441G>C | |
17 | g.47733865G= | CA2262805829 | TBX21 | c.411G= (p.Leu137=) n.441G= | |
17 | g.47733865G>T | CA500652457 | TBX21 | c.411G>T (p.Leu137=) n.441G>T | |
17 | g.47733866A>C | CA500652460 | TBX21 | c.412A>C (p.Arg138=) n.442A>C | |
17 | g.47733866A>G | CA400059463 | TBX21 | c.412A>G (p.Arg138Gly) n.442A>G | |
17 | g.47733866A>T | CA400059469 | TBX21 | c.412A>T (p.Arg138Trp) n.442A>T | |
17 | g.47733867G>A | CA400059471 | TBX21 | c.413G>A (p.Arg138Lys) n.443G>A | |
17 | g.47733867G>C | CA400059473 | TBX21 | c.413G>C (p.Arg138Thr) n.443G>C | |
17 | g.47733867G>T | CA400059475 | TBX21 | c.413G>T (p.Arg138Met) n.443G>T | COSMIC |
17 | g.47733868G>A | CA500652462 | TBX21 | c.414G>A (p.Arg138=) n.444G>A | gnomAD v4 |
17 | g.47733868G>C | CA400059479 | TBX21 | c.414G>C (p.Arg138Ser) n.444G>C | |
17 | g.47733868G>T | CA400059480 | TBX21 | c.414G>T (p.Arg138Ser) n.444G>T | gnomAD v4 COSMIC |
17 | g.47733869G>A | CA400059482 | TBX21 | c.415G>A (p.Val139Ile) n.445G>A | |
17 | g.47733869G>C | CA400059485 | TBX21 | c.415G>C (p.Val139Leu) n.445G>C | |
17 | g.47733869G>T | CA400059484 | TBX21 | c.415G>T (p.Val139Phe) n.445G>T | |
17 | g.47733870T>A | CA400059486 | TBX21 | c.416T>A (p.Val139Asp) n.446T>A | |
17 | g.47733870T>C | CA400059489 | TBX21 | c.416T>C (p.Val139Ala) n.446T>C | |
17 | g.47733870T>G | CA400059492 | TBX21 | c.416T>G (p.Val139Gly) n.446T>G | |
17 | g.47733871C>A | CA500652466 | TBX21 | c.417C>A (p.Val139=) n.447C>A | gnomAD v4 |
17 | g.47733871C= | CA2262805830 | TBX21 | c.417C= (p.Val139=) n.447C= | |
17 | g.47733871C>G | CA500652465 | TBX21 | c.417C>G (p.Val139=) n.447C>G | |
17 | g.47733871C>T | CA8626263 | TBX21 | c.417C>T (p.Val139=) n.447C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47733872G>A | CA400059496 | TBX21 | c.418G>A (p.Ala140Thr) n.448G>A | |
17 | g.47733872G>C | CA400059499 | TBX21 | c.418G>C (p.Ala140Pro) n.448G>C | |
17 | g.47733872G>T | CA400059501 | TBX21 | c.418G>T (p.Ala140Ser) n.448G>T | |
17 | g.47733873C>A | CA400059503 | TBX21 | c.419C>A (p.Ala140Glu) n.449C>A | |
17 | g.47733873C>G | CA400059506 | TBX21 | c.419C>G (p.Ala140Gly) n.449C>G | |
17 | g.47733873C>T | CA400059508 | TBX21 | c.419C>T (p.Ala140Val) n.449C>T | |
17 | g.47733874G>A | CA8626265 | TBX21 | c.420G>A (p.Ala140=) n.450G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47733874G>C | CA8626264 | TBX21 | c.420G>C (p.Ala140=) n.450G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47733874G= | CA2262805831 | TBX21 | c.420G= (p.Ala140=) n.450G= | |
17 | g.47733874G>T | CA500652467 | TBX21 | c.420G>T (p.Ala140=) n.450G>T | |
17 | g.47733875C>A | CA400059512 | TBX21 | c.421C>A (p.Leu141Ile) n.451C>A | |
17 | g.47733875C>G | CA400059519 | TBX21 | c.421C>G (p.Leu141Val) n.451C>G | |
17 | g.47733875C>T | CA400059516 | TBX21 | c.421C>T (p.Leu141Phe) n.451C>T | |
17 | g.47733876T>A | CA400059523 | TBX21 | c.422T>A (p.Leu141His) n.452T>A | |
17 | g.47733876T>C | CA400059526 | TBX21 | c.422T>C (p.Leu141Pro) n.452T>C | |
17 | g.47733876T>G | CA400059529 | TBX21 | c.422T>G (p.Leu141Arg) n.452T>G | |
17 | g.47733877C>A | CA500652468 | TBX21 | c.423C>A (p.Leu141=) n.453C>A | |
17 | g.47733877C>G | CA500652469 | TBX21 | c.423C>G (p.Leu141=) n.453C>G | |
17 | g.47733877C>T | CA500652470 | TBX21 | c.423C>T (p.Leu141=) n.453C>T | gnomAD v4 |
17 | g.47733878A>C | CA400059540 | TBX21 | c.424A>C (p.Asn142His) n.454A>C | |
17 | g.47733878A>G | CA400059541 | TBX21 | c.424A>G (p.Asn142Asp) n.454A>G | |
17 | g.47733878A>T | CA400059546 | TBX21 | c.424A>T (p.Asn142Tyr) n.454A>T | |
17 | g.47733879A= | CA2262805832 | TBX21 | c.425A= (p.Asn142=) n.455A= | |
17 | g.47733879A>C | CA400059551 | TBX21 | c.425A>C (p.Asn142Thr) n.455A>C | |
17 | g.47733879A>G | CA291302310 | TBX21 | c.425A>G (p.Asn142Ser) n.455A>G | dbSNP gnomAD v4 |
17 | g.47733879A>T | CA400059558 | TBX21 | c.425A>T (p.Asn142Ile) n.455A>T | |
17 | g.47733880C>A | CA400059562 | TBX21 | c.426C>A (p.Asn142Lys) n.456C>A | |
17 | g.47733880C>G | CA400059564 | TBX21 | c.426C>G (p.Asn142Lys) n.456C>G | |
17 | g.47733880C>T | CA500652474 | TBX21 | c.426C>T (p.Asn142=) n.456C>T | |
17 | g.47733881A>C | CA400059569 | TBX21 | c.427A>C (p.Asn143His) n.457A>C | |
17 | g.47733881A>G | CA400059567 | TBX21 | c.427A>G (p.Asn143Asp) n.457A>G | |
17 | g.47733881A>T | CA400059565 | TBX21 | c.427A>T (p.Asn143Tyr) n.457A>T | |
17 | g.47733882A= | CA2262805833 | TBX21 | c.428A= (p.Asn143=) n.458A= | |
17 | g.47733882A>C | CA291302312 | TBX21 | c.428A>C (p.Asn143Thr) n.458A>C | dbSNP |
17 | g.47733882A>G | CA400059573 | TBX21 | c.428A>G (p.Asn143Ser) n.458A>G | |
17 | g.47733882A>T | CA400059574 | TBX21 | c.428A>T (p.Asn143Ile) n.458A>T | |
17 | g.47733883C>A | CA400059577 | TBX21 | c.429C>A (p.Asn143Lys) n.459C>A | |
17 | g.47733883C>G | CA400059583 | TBX21 | c.429C>G (p.Asn143Lys) n.459C>G | |
17 | g.47733883C>T | CA500652475 | TBX21 | c.429C>T (p.Asn143=) n.459C>T | gnomAD v4 |
17 | g.47733884C>A | CA400059586 | TBX21 | c.430C>A (p.His144Asn) n.460C>A | |
17 | g.47733884C= | CA2262805834 | TBX21 | c.430C= (p.His144=) n.460C= | |
17 | g.47733884C>G | CA400059588 | TBX21 | c.430C>G (p.His144Asp) n.460C>G | |
17 | g.47733884C>T | CA8626266 | TBX21 | c.430C>T (p.His144Tyr) n.460C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47733885A>C | CA400059604 | TBX21 | c.431A>C (p.His144Pro) n.461A>C | |
17 | g.47733885A>G | CA400059608 | TBX21 | c.431A>G (p.His144Arg) n.461A>G | |
17 | g.47733885A>T | CA400059613 | TBX21 | c.431A>T (p.His144Leu) n.461A>T | |
17 | g.47733886C>A | CA400059616 | TBX21 | c.432C>A (p.His144Gln) n.462C>A | ClinVar |
17 | g.47733886C= | CA2262805835 | TBX21 | c.432C= (p.His144=) n.462C= | |
17 | g.47733886C>G | CA400059627 | TBX21 | c.432C>G (p.His144Gln) n.462C>G | |
17 | g.47733886C>T | CA500652479 | TBX21 | c.432C>T (p.His144=) n.462C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47733887C>A | CA400059633 | TBX21 | c.433C>A (p.Leu145Met) n.463C>A | |
17 | g.47733887C= | CA2262805836 | TBX21 | c.433C= (p.Leu145=) n.463C= | |
17 | g.47733887C>G | CA400059630 | TBX21 | c.433C>G (p.Leu145Val) n.463C>G | |
17 | g.47733887C>T | CA291302319 | TBX21 | c.433C>T (p.Leu145=) n.463C>T | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47733888T>A | CA400059653 | TBX21 | c.434T>A (p.Leu145Gln) n.464T>A | |
17 | g.47733888T>C | CA400059661 | TBX21 | c.434T>C (p.Leu145Pro) n.464T>C | |
17 | g.47733888T>G | CA400059655 | TBX21 | c.434T>G (p.Leu145Arg) n.464T>G | |
17 | g.47733889G>A | CA500652483 | TBX21 | c.435G>A (p.Leu145=) n.465G>A | |
17 | g.47733889G>C | CA500652484 | TBX21 | c.435G>C (p.Leu145=) n.465G>C | |
17 | g.47733889G>T | CA500652485 | TBX21 | c.435G>T (p.Leu145=) n.465G>T | |
17 | g.47733890T>A | CA400059672 | TBX21 | c.436T>A (p.Leu146Met) n.466T>A | |
17 | g.47733890T>C | CA500652486 | TBX21 | c.436T>C (p.Leu146=) n.466T>C | gnomAD v4 |
17 | g.47733890T>G | CA400059680 | TBX21 | c.436T>G (p.Leu146Val) n.466T>G | |
17 | g.47733891T>A | CA400059682 | TBX21 | c.437T>A (p.Leu146Ter) n.467T>A | |
17 | g.47733891T>C | CA400059687 | TBX21 | c.437T>C (p.Leu146Ser) n.467T>C | |
17 | g.47733891T>G | CA400059683 | TBX21 | c.437T>G (p.Leu146Trp) n.467T>G | |
17 | g.47733892G>A | CA500652487 | TBX21 | c.438G>A (p.Leu146=) n.468G>A | gnomAD v4 |
17 | g.47733892G>C | CA400059691 | TBX21 | c.438G>C (p.Leu146Phe) n.468G>C | |
17 | g.47733892G>T | CA400059697 | TBX21 | c.438G>T (p.Leu146Phe) n.468G>T | |
17 | g.47733893T>A | CA400059702 | TBX21 | c.439T>A (p.Trp147Arg) n.469T>A | |
17 | g.47733893T>C | CA400059703 | TBX21 | c.439T>C (p.Trp147Arg) n.469T>C | |
17 | g.47733893T>G | CA400059704 | TBX21 | c.439T>G (p.Trp147Gly) n.469T>G | |
17 | g.47733894G>A | CA400059709 | TBX21 | c.440G>A (p.Trp147Ter) n.470G>A | gnomAD v4 |
17 | g.47733894G>C | CA400059716 | TBX21 | c.440G>C (p.Trp147Ser) n.470G>C | |
17 | g.47733894G>T | CA400059719 | TBX21 | c.440G>T (p.Trp147Leu) n.470G>T | |
17 | g.47733895G>A | CA400059721 | TBX21 | c.441G>A (p.Trp147Ter) n.471G>A | |
17 | g.47733895G>C | CA400059722 | TBX21 | c.441G>C (p.Trp147Cys) n.471G>C | |
17 | g.47733895G>T | CA400059728 | TBX21 | c.441G>T (p.Trp147Cys) n.471G>T | |
17 | g.47733896T>A | CA400059740 | TBX21 | c.442T>A (p.Ser148Thr) n.472T>A | |
17 | g.47733896T>C | CA400059737 | TBX21 | c.442T>C (p.Ser148Pro) n.472T>C | |
17 | g.47733896T>G | CA400059731 | TBX21 | c.442T>G (p.Ser148Ala) n.472T>G | |
17 | g.47733897C>A | CA400059746 | TBX21 | c.443C>A (p.Ser148Tyr) n.473C>A | |
17 | g.47733897C>G | CA400059751 | TBX21 | c.443C>G (p.Ser148Cys) n.473C>G | |
17 | g.47733897C>T | CA400059753 | TBX21 | c.443C>T (p.Ser148Phe) n.473C>T | |
17 | g.47733898C>A | CA500652490 | TBX21 | c.444C>A (p.Ser148=) n.474C>A | |
17 | g.47733898C>G | CA500652491 | TBX21 | c.444C>G (p.Ser148=) n.474C>G | |
17 | g.47733898C>T | CA500652493 | TBX21 | c.444C>T (p.Ser148=) n.474C>T | |
17 | g.47733899A>C | CA400059759 | TBX21 | c.445A>C (p.Lys149Gln) n.475A>C | |
17 | g.47733899A>G | CA400059764 | TBX21 | c.445A>G (p.Lys149Glu) n.475A>G | |
17 | g.47733899A>T | CA400059765 | TBX21 | c.445A>T (p.Lys149Ter) n.475A>T | |
17 | g.47733900A>C | CA400059768 | TBX21 | c.446A>C (p.Lys149Thr) n.476A>C | |
17 | g.47733900A>G | CA400059771 | TBX21 | c.446A>G (p.Lys149Arg) n.476A>G | gnomAD v4 |
17 | g.47733900A>T | CA400059778 | TBX21 | c.446A>T (p.Lys149Met) n.476A>T | |
17 | g.47733901G>A | CA500652495 | TBX21 | c.447G>A (p.Lys149=) n.477G>A | |
17 | g.47733901G>C | CA400059780 | TBX21 | c.447G>C (p.Lys149Asn) n.477G>C | |
17 | g.47733901G>T | CA400059781 | TBX21 | c.447G>T (p.Lys149Asn) n.477G>T | |
17 | g.47733902T>A | CA400059790 | TBX21 | c.448T>A (p.Phe150Ile) n.478T>A | |
17 | g.47733902T>C | CA400059788 | TBX21 | c.448T>C (p.Phe150Leu) n.478T>C | |
17 | g.47733902T>G | CA400059785 | TBX21 | c.448T>G (p.Phe150Val) n.478T>G | COSMIC |
17 | g.47733903T>A | CA400059792 | TBX21 | c.449T>A (p.Phe150Tyr) n.479T>A | |
17 | g.47733903T>C | CA400059794 | TBX21 | c.449T>C (p.Phe150Ser) n.479T>C | |
17 | g.47733903T>G | CA400059796 | TBX21 | c.449T>G (p.Phe150Cys) n.479T>G | |
17 | g.47733904T>A | CA400059802 | TBX21 | c.450T>A (p.Phe150Leu) n.480T>A | |
17 | g.47733904T>C | CA500652497 | TBX21 | c.450T>C (p.Phe150=) n.480T>C | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47733904T>G | CA400059805 | TBX21 | c.450T>G (p.Phe150Leu) n.480T>G | |
17 | g.47733904T= | CA2262805837 | TBX21 | c.450T= (p.Phe150=) n.480T= | |
17 | g.47733905A>C | CA400059811 | TBX21 | c.451A>C (p.Asn151His) n.481A>C | |
17 | g.47733905A>G | CA400059812 | TBX21 | c.451A>G (p.Asn151Asp) n.481A>G | |
17 | g.47733905A>T | CA400059813 | TBX21 | c.451A>T (p.Asn151Tyr) n.481A>T | |
17 | g.47733906A>C | CA400059815 | TBX21 | c.452A>C (p.Asn151Thr) n.482A>C | |
17 | g.47733906A>G | CA400059818 | TBX21 | c.452A>G (p.Asn151Ser) n.482A>G | |
17 | g.47733906A>T | CA400059822 | TBX21 | c.452A>T (p.Asn151Ile) n.482A>T | |
17 | g.47733907T>A | CA400059824 | TBX21 | c.453T>A (p.Asn151Lys) n.483T>A | |
17 | g.47733907T>C | CA500652498 | TBX21 | c.453T>C (p.Asn151=) n.483T>C | gnomAD v4 |
17 | g.47733907T>G | CA400059825 | TBX21 | c.453T>G (p.Asn151Lys) n.483T>G | |
17 | g.47733908C>A | CA400059827 | TBX21 | c.454C>A (p.Gln152Lys) n.484C>A | dbSNP |
17 | g.47733908C= | CA2262805838 | TBX21 | c.454C= (p.Gln152=) n.484C= | |
17 | g.47733908C>G | CA400059830 | TBX21 | c.454C>G (p.Gln152Glu) n.484C>G | |
17 | g.47733908C>T | CA400059829 | TBX21 | c.454C>T (p.Gln152Ter) n.484C>T | |
17 | g.47733909A>C | CA400059833 | TBX21 | c.455A>C (p.Gln152Pro) n.485A>C | |
17 | g.47733909A>G | CA400059834 | TBX21 | c.455A>G (p.Gln152Arg) n.485A>G | |
17 | g.47733909A>T | CA400059835 | TBX21 | c.455A>T (p.Gln152Leu) n.485A>T | |
17 | g.47733910G>A | CA500652502 | TBX21 | c.456G>A (p.Gln152=) n.486G>A | |
17 | g.47733910G>C | CA400059836 | TBX21 | c.456G>C (p.Gln152His) n.486G>C | |
17 | g.47733910G>T | CA400059837 | TBX21 | c.456G>T (p.Gln152His) n.486G>T | |
17 | g.47733911C>A | CA400059838 | TBX21 | c.457C>A (p.His153Asn) n.487C>A | |
17 | g.47733911C>G | CA400059839 | TBX21 | c.457C>G (p.His153Asp) n.487C>G | |
17 | g.47733911C>T | CA400059841 | TBX21 | c.457C>T (p.His153Tyr) n.487C>T | gnomAD v4 |
17 | g.47733912A>C | CA400059842 | TBX21 | c.458A>C (p.His153Pro) n.488A>C | |
17 | g.47733912A>G | CA400059843 | TBX21 | c.458A>G (p.His153Arg) n.488A>G | |
17 | g.47733912A>T | CA400059845 | TBX21 | c.458A>T (p.His153Leu) n.488A>T | |
17 | g.47733913C>A | CA400059850 | TBX21 | c.459C>A (p.His153Gln) n.489C>A | |
17 | g.47733913C>G | CA400059847 | TBX21 | c.459C>G (p.His153Gln) n.489C>G | |
17 | g.47733913C>T | CA500652503 | TBX21 | c.459C>T (p.His153=) n.489C>T | |
17 | g.47733914C>A | CA400059854 | TBX21 | c.460C>A (p.Gln154Lys) n.490C>A | |
17 | g.47733914C>G | CA400059858 | TBX21 | c.460C>G (p.Gln154Glu) n.490C>G | gnomAD v4 |
17 | g.47733914C>T | CA400059856 | TBX21 | c.460C>T (p.Gln154Ter) n.490C>T | |
17 | g.47733918_47733921del | CA2638460879 | TBX21 | c.464_467del (p.Thr155ArgfsTer2) n.494_497del | gnomAD v4 |
17 | g.47733915A= | CA2262805839 | TBX21 | c.461A= (p.Gln154=) n.491A= | |
17 | g.47733915A>C | CA400059859 | TBX21 | c.461A>C (p.Gln154Pro) n.491A>C | |
17 | g.47733915A>G | CA400059860 | TBX21 | c.461A>G (p.Gln154Arg) n.491A>G | dbSNP |
17 | g.47733915A>T | CA400059861 | TBX21 | c.461A>T (p.Gln154Leu) n.491A>T | dbSNP gnomAD v2 gnomAD v4 COSMIC |
17 | g.47733916G>A | CA500652508 | TBX21 | c.462G>A (p.Gln154=) n.492G>A | |
17 | g.47733916G>C | CA400059862 | TBX21 | c.462G>C (p.Gln154His) n.492G>C | dbSNP |
17 | g.47733916G= | CA2262805840 | TBX21 | c.462G= (p.Gln154=) n.492G= | |
17 | g.47733916G>T | CA400059863 | TBX21 | c.462G>T (p.Gln154His) n.492G>T | |
17 | g.47733917A>C | CA400059864 | TBX21 | c.463A>C (p.Thr155Pro) n.493A>C | |
17 | g.47733917A>G | CA400059866 | TBX21 | c.463A>G (p.Thr155Ala) n.493A>G | |
17 | g.47733917A>T | CA400059871 | TBX21 | c.463A>T (p.Thr155Ser) n.493A>T | |
17 | g.47733918C>A | CA400059874 | TBX21 | c.464C>A (p.Thr155Lys) n.494C>A | |
17 | g.47733918C>G | CA400059877 | TBX21 | c.464C>G (p.Thr155Arg) n.494C>G | |
17 | g.47733918C>T | CA400059879 | TBX21 | c.464C>T (p.Thr155Ile) n.494C>T | |
17 | g.47733919A= | CA2262805841 | TBX21 | c.465A= (p.Thr155=) n.495A= | |
17 | g.47733919A>C | CA500652512 | TBX21 | c.465A>C (p.Thr155=) n.495A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47733919A>G | CA291302322 | TBX21 | c.465A>G (p.Thr155=) n.495A>G | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47733919A>T | CA500652513 | TBX21 | c.465A>T (p.Thr155=) n.495A>T | |
17 | g.47733920G>A | CA400059886 | TBX21 | c.466G>A (p.Glu156Lys) n.496G>A | |
17 | g.47733920G>C | CA400059881 | TBX21 | c.466G>C (p.Glu156Gln) n.496G>C | |
17 | g.47733920G>T | CA400059884 | TBX21 | c.466G>T (p.Glu156Ter) n.496G>T | |
17 | g.47733920_47733925delinsAGTTTA | CA2573054468 | TBX21 | c.466_471delinsAGTTTA (p.Glu156_Met157delinsSerLeu) n.496_501delinsAGTTTA | ClinVar dbSNP |
17 | g.47733921A>C | CA400059888 | TBX21 | c.467A>C (p.Glu156Ala) n.497A>C | |
17 | g.47733921A>G | CA400059889 | TBX21 | c.467A>G (p.Glu156Gly) n.497A>G | |
17 | g.47733921A>T | CA400059892 | TBX21 | c.467A>T (p.Glu156Val) n.497A>T | |
17 | g.47733922G>A | CA500652514 | TBX21 | c.468G>A (p.Glu156=) n.498G>A | |
17 | g.47733922G>C | CA400059899 | TBX21 | c.468G>C (p.Glu156Asp) n.498G>C | |
17 | g.47733922G>T | CA400059900 | TBX21 | c.468G>T (p.Glu156Asp) n.498G>T | |
17 | g.47733923A>C | CA400059903 | TBX21 | c.469A>C (p.Met157Leu) n.499A>C | |
17 | g.47733923A>G | CA400059916 | TBX21 | c.469A>G (p.Met157Val) n.499A>G | |
17 | g.47733923A>T | CA400059919 | TBX21 | c.469A>T (p.Met157Leu) n.499A>T | |
17 | g.47733924T>A | CA400059921 | TBX21 | c.470T>A (p.Met157Lys) n.500T>A | |
17 | g.47733924T>C | CA400059922 | TBX21 | c.470T>C (p.Met157Thr) n.500T>C | |
17 | g.47733924T>G | CA400059925 | TBX21 | c.470T>G (p.Met157Arg) n.500T>G | |
17 | g.47733925G>A | CA400059933 | TBX21 | c.471G>A (p.Met157Ile) n.501G>A | |
17 | g.47733925G>C | CA400059937 | TBX21 | c.471G>C (p.Met157Ile) n.501G>C | |
17 | g.47733925G>T | CA400059928 | TBX21 | c.471G>T (p.Met157Ile) n.501G>T | |
17 | g.47733926A>C | CA400059942 | TBX21 | c.472A>C (p.Ile158Leu) n.502A>C | |
17 | g.47733926A>G | CA400059944 | TBX21 | c.472A>G (p.Ile158Val) n.502A>G | |
17 | g.47733926A>T | CA400059947 | TBX21 | c.472A>T (p.Ile158Phe) n.502A>T | |
17 | g.47733927T>A | CA400059950 | TBX21 | c.473T>A (p.Ile158Asn) n.503T>A | |
17 | g.47733927T>C | CA400059952 | TBX21 | c.473T>C (p.Ile158Thr) n.503T>C | |
17 | g.47733927T>G | CA400059957 | TBX21 | c.473T>G (p.Ile158Ser) n.503T>G | |
17 | g.47733928C>A | CA500652519 | TBX21 | c.474C>A (p.Ile158=) n.504C>A | |
17 | g.47733928C= | CA2262805842 | TBX21 | c.474C= (p.Ile158=) n.504C= | |
17 | g.47733928C>G | CA400059960 | TBX21 | c.474C>G (p.Ile158Met) n.504C>G | |
17 | g.47733928C>T | CA291302323 | TBX21 | c.474C>T (p.Ile158=) n.504C>T | dbSNP gnomAD v2 gnomAD v4 |
17 | g.47733929A>C | CA400059961 | TBX21 | c.475A>C (p.Ile159Leu) n.505A>C | |
17 | g.47733929A>G | CA400059962 | TBX21 | c.475A>G (p.Ile159Val) n.505A>G | |
17 | g.47733929A>T | CA400059963 | TBX21 | c.475A>T (p.Ile159Phe) n.505A>T | |
17 | g.47733930T>A | CA400059964 | TBX21 | c.476T>A (p.Ile159Asn) n.506T>A | |
17 | g.47733930T>C | CA400059966 | TBX21 | c.476T>C (p.Ile159Thr) n.506T>C | |
17 | g.47733930T>G | CA400059969 | TBX21 | c.476T>G (p.Ile159Ser) n.506T>G | |
17 | g.47733931C>A | CA8626267 | TBX21 | c.477C>A (p.Ile159=) n.507C>A | dbSNP ExAC gnomAD v4 |
17 | g.47733931C= | CA2262805843 | TBX21 | c.477C= (p.Ile159=) n.507C= | |
17 | g.47733931C>G | CA400059972 | TBX21 | c.477C>G (p.Ile159Met) n.507C>G | |
17 | g.47733931C>T | CA500652520 | TBX21 | c.477C>T (p.Ile159=) n.507C>T | |
17 | g.47733932A>C | CA400059982 | TBX21 | c.478A>C (p.Thr160Pro) n.508A>C | |
17 | g.47733932A>G | CA400059984 | TBX21 | c.478A>G (p.Thr160Ala) n.508A>G | |
17 | g.47733932A>T | CA400059987 | TBX21 | c.478A>T (p.Thr160Ser) n.508A>T | |
17 | g.47733933C>A | CA400059989 | TBX21 | c.479C>A (p.Thr160Asn) n.509C>A | |
17 | g.47733933C>G | CA400059998 | TBX21 | c.479C>G (p.Thr160Ser) n.509C>G | |
17 | g.47733933C>T | CA400060000 | TBX21 | c.479C>T (p.Thr160Ile) n.509C>T | |
17 | g.47733934C>A | CA500652521 | TBX21 | c.480C>A (p.Thr160=) n.510C>A | gnomAD v4 |
17 | g.47733934C= | CA2262805844 | TBX21 | c.480C= (p.Thr160=) n.510C= | |
17 | g.47733934C>G | CA500652522 | TBX21 | c.480C>G (p.Thr160=) n.510C>G | dbSNP |
17 | g.47733934C>T | CA500652523 | TBX21 | c.480C>T (p.Thr160=) n.510C>T | |
17 | g.47733935A>C | CA400060003 | TBX21 | c.481A>C (p.Lys161Gln) n.511A>C | |
17 | g.47733935A>G | CA400060004 | TBX21 | c.481A>G (p.Lys161Glu) n.511A>G | |
17 | g.47733935A>T | CA400060008 | TBX21 | c.481A>T (p.Lys161Ter) n.511A>T | |
17 | g.47733936A>C | CA400060026 | TBX21 | c.482A>C (p.Lys161Thr) n.512A>C | |
17 | g.47733936A>G | CA400060029 | TBX21 | c.482A>G (p.Lys161Arg) n.512A>G | |
17 | g.47733936A>T | CA400060036 | TBX21 | c.482A>T (p.Lys161Met) n.512A>T | gnomAD v4 |
17 | g.47733937G>A | CA500652524 | TBX21 | c.483G>A (p.Lys161=) n.513G>A | dbSNP gnomAD v4 |
17 | g.47733937G>C | CA400060039 | TBX21 | c.483G>C (p.Lys161Asn) n.513G>C | |
17 | g.47733937G= | CA2262805845 | TBX21 | c.483G= (p.Lys161=) n.513G= | |
17 | g.47733937G>T | CA400060050 | TBX21 | c.483G>T (p.Lys161Asn) n.513G>T | gnomAD v4 |
17 | g.47733938C>A | CA400060058 | TBX21 | c.484C>A (p.Gln162Lys) n.514C>A | |
17 | g.47733938C>G | CA400060059 | TBX21 | c.484C>G (p.Gln162Glu) n.514C>G | gnomAD v4 |
17 | g.47733938C>T | CA400060055 | TBX21 | c.484C>T (p.Gln162Ter) n.514C>T | |
17 | g.47733939A= | CA2262805846 | TBX21 | c.485A= (p.Gln162=) n.515A= | |
17 | g.47733939A>C | CA400060064 | TBX21 | c.485A>C (p.Gln162Pro) n.515A>C | |
17 | g.47733939A>G | CA400060063 | TBX21 | c.485A>G (p.Gln162Arg) n.515A>G | dbSNP gnomAD v2 gnomAD v4 |
17 | g.47733939A>T | CA400060065 | TBX21 | c.485A>T (p.Gln162Leu) n.515A>T | |
17 | g.47733940G>A | CA291302324 | TBX21 | c.486G>A (p.Gln162=) n.516G>A | dbSNP |
17 | g.47733940G>C | CA291302325 | TBX21 | c.486G>C (p.Gln162His) n.516G>C | dbSNP |
17 | g.47733940G= | CA2262805847 | TBX21 | c.486G= (p.Gln162=) n.516G= | |
17 | g.47733940G>T | CA400060066 | TBX21 | c.486G>T (p.Gln162His) n.516G>T | |
17 | g.47733941G>A | CA400060069 | TBX21 | c.487G>A (p.Gly163Arg) n.517G>A | COSMIC |
17 | g.47733941G>C | CA400060070 | TBX21 | c.487G>C (p.Gly163Arg) n.517G>C | |
17 | g.47733941G>T | CA400060085 | TBX21 | c.487G>T (p.Gly163Ter) n.517G>T | gnomAD v4 |
17 | g.47733942G>A | CA400060094 | TBX21 | c.488G>A (p.Gly163Glu) n.518G>A | |
17 | g.47733942G>C | CA400060092 | TBX21 | c.488G>C (p.Gly163Ala) n.518G>C | |
17 | g.47733942G>T | CA400060090 | TBX21 | c.488G>T (p.Gly163Val) n.518G>T | |
17 | g.47733943A= | CA2262805848 | TBX21 | c.489A= (p.Gly163=) n.519A= | |
17 | g.47733943A>C | CA500652526 | TBX21 | c.489A>C (p.Gly163=) n.519A>C | |
17 | g.47733943A>G | CA8626268 | TBX21 | c.489A>G (p.Gly163=) n.519A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47733943A>T | CA500652525 | TBX21 | c.489A>T (p.Gly163=) n.519A>T | |
17 | g.47733944C>A | CA500652527 | TBX21 | c.490C>A (p.Arg164=) n.520C>A | |
17 | g.47733944C>G | CA400060103 | TBX21 | c.490C>G (p.Arg164Gly) n.520C>G | |
17 | g.47733944C>T | CA400060104 | TBX21 | c.490C>T (p.Arg164Trp) n.520C>T | |
17 | g.47733945G>A | CA400060105 | TBX21 | c.491G>A (p.Arg164Gln) n.521G>A | |
17 | g.47733945G>C | CA400060106 | TBX21 | c.491G>C (p.Arg164Pro) n.521G>C | |
17 | g.47733945G>T | CA400060108 | TBX21 | c.491G>T (p.Arg164Leu) n.521G>T | gnomAD v4 |
17 | g.47733946G>A | CA400060111 | TBX21 | c.491+1G>A (n.491+1G>A) n.521+1G>A | |
17 | g.47733946G>C | CA400060118 | TBX21 | c.491+1G>C (n.491+1G>C) n.521+1G>C | |
17 | g.47733946G>T | CA400060114 | TBX21 | c.491+1G>T (n.491+1G>T) n.521+1G>T | |
17 | g.47733947T>A | CA400060121 | TBX21 | c.491+2T>A (n.491+2T>A) n.521+2T>A | |
17 | g.47733947T>C | CA400060127 | TBX21 | c.491+2T>C (n.491+2T>C) n.521+2T>C | |
17 | g.47733947T>G | CA400060130 | TBX21 | c.491+2T>G (n.491+2T>G) n.521+2T>G | |
17 | g.47733948G>T | CA2638460929 | TBX21 | c.491+3G>T (n.491+3G>T) n.521+3G>T | gnomAD v4 |