Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.47733852T>ACA400059359TBX21c.398T>A (p.Val133Glu)
n.428T>A
17g.47733852T>CCA400059362TBX21c.398T>C (p.Val133Ala)
n.428T>C
17g.47733852T>GCA400059366TBX21c.398T>G (p.Val133Gly)
n.428T>G
dbSNP gnomAD v4
17g.47733852T=CA2262805826TBX21c.398T= (p.Val133=)
n.428T=
17g.47733853G>ACA500652442TBX21c.399G>A (p.Val133=)
n.429G>A
17g.47733853G>CCA500652444TBX21c.399G>C (p.Val133=)
n.429G>C
17g.47733853G>TCA500652445TBX21c.399G>T (p.Val133=)
n.429G>T
gnomAD v4
17g.47733854T>ACA400059375TBX21c.400T>A (p.Ser134Thr)
n.430T>A
17g.47733854T>CCA400059368TBX21c.400T>C (p.Ser134Pro)
n.430T>C
17g.47733854T>GCA400059373TBX21c.400T>G (p.Ser134Ala)
n.430T>G
17g.47733855C>ACA400059378TBX21c.401C>A (p.Ser134Ter)
n.431C>A
17g.47733855C>GCA400059380TBX21c.401C>G (p.Ser134Trp)
n.431C>G
17g.47733855C>TCA400059382TBX21c.401C>T (p.Ser134Leu)
n.431C>T
gnomAD v4
17g.47733856G>ACA500652446TBX21c.402G>A (p.Ser134=)
n.432G>A
gnomAD v4
17g.47733856G>CCA500652447TBX21c.402G>C (p.Ser134=)
n.432G>C
17g.47733856G>TCA500652448TBX21c.402G>T (p.Ser134=)
n.432G>T
gnomAD v4
17g.47733857G>ACA400059383TBX21c.403G>A (p.Gly135Arg)
n.433G>A
gnomAD v4
17g.47733857G>CCA400059385TBX21c.403G>C (p.Gly135Arg)
n.433G>C
gnomAD v4
17g.47733857G>TCA400059386TBX21c.403G>T (p.Gly135Trp)
n.433G>T
17g.47733858G>ACA400059392TBX21c.404G>A (p.Gly135Glu)
n.434G>A
17g.47733858G>CCA400059395TBX21c.404G>C (p.Gly135Ala)
n.434G>C
17g.47733858G>TCA400059397TBX21c.404G>T (p.Gly135Val)
n.434G>T
17g.47733859G>ACA500652454TBX21c.405G>A (p.Gly135=)
n.435G>A
17g.47733859G>CCA500652452TBX21c.405G>C (p.Gly135=)
n.435G>C
17g.47733859G>TCA500652453TBX21c.405G>T (p.Gly135=)
n.435G>T
17g.47733860A=CA2262805827TBX21c.406A= (p.Lys136=)
n.436A=
17g.47733860A>CCA400059401TBX21c.406A>C (p.Lys136Gln)
n.436A>C
17g.47733860A>GCA8626261TBX21c.406A>G (p.Lys136Glu)
n.436A>G
dbSNP ExAC gnomAD v2
17g.47733860A>TCA400059409TBX21c.406A>T (p.Lys136Ter)
n.436A>T
17g.47733861A>CCA400059413TBX21c.407A>C (p.Lys136Thr)
n.437A>C
gnomAD v4
17g.47733861A>GCA400059416TBX21c.407A>G (p.Lys136Arg)
n.437A>G
17g.47733861A>TCA400059415TBX21c.407A>T (p.Lys136Ile)
n.437A>T
17g.47733862A=CA2262805828TBX21c.408A= (p.Lys136=)
n.438A=
17g.47733862A>CCA400059420TBX21c.408A>C (p.Lys136Asn)
n.438A>C
17g.47733862A>GCA8626262TBX21c.408A>G (p.Lys136=)
n.438A>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47733862A>TCA400059429TBX21c.408A>T (p.Lys136Asn)
n.438A>T
17g.47733863C>ACA400059431TBX21c.409C>A (p.Leu137Met)
n.439C>A
17g.47733863C>GCA400059434TBX21c.409C>G (p.Leu137Val)
n.439C>G
17g.47733863C>TCA500652456TBX21c.409C>T (p.Leu137=)
n.439C>T
17g.47733864T>ACA400059442TBX21c.410T>A (p.Leu137Gln)
n.440T>A
17g.47733864T>CCA400059443TBX21c.410T>C (p.Leu137Pro)
n.440T>C
17g.47733864T>GCA400059459TBX21c.410T>G (p.Leu137Arg)
n.440T>G
17g.47733865G>ACA500652458TBX21c.411G>A (p.Leu137=)
n.441G>A
dbSNP gnomAD v2 gnomAD v4
17g.47733865G>CCA500652459TBX21c.411G>C (p.Leu137=)
n.441G>C
17g.47733865G=CA2262805829TBX21c.411G= (p.Leu137=)
n.441G=
17g.47733865G>TCA500652457TBX21c.411G>T (p.Leu137=)
n.441G>T
17g.47733866A>CCA500652460TBX21c.412A>C (p.Arg138=)
n.442A>C
17g.47733866A>GCA400059463TBX21c.412A>G (p.Arg138Gly)
n.442A>G
17g.47733866A>TCA400059469TBX21c.412A>T (p.Arg138Trp)
n.442A>T
17g.47733867G>ACA400059471TBX21c.413G>A (p.Arg138Lys)
n.443G>A
17g.47733867G>CCA400059473TBX21c.413G>C (p.Arg138Thr)
n.443G>C
17g.47733867G>TCA400059475TBX21c.413G>T (p.Arg138Met)
n.443G>T
COSMIC
17g.47733868G>ACA500652462TBX21c.414G>A (p.Arg138=)
n.444G>A
gnomAD v4
17g.47733868G>CCA400059479TBX21c.414G>C (p.Arg138Ser)
n.444G>C
17g.47733868G>TCA400059480TBX21c.414G>T (p.Arg138Ser)
n.444G>T
gnomAD v4 COSMIC
17g.47733869G>ACA400059482TBX21c.415G>A (p.Val139Ile)
n.445G>A
17g.47733869G>CCA400059485TBX21c.415G>C (p.Val139Leu)
n.445G>C
17g.47733869G>TCA400059484TBX21c.415G>T (p.Val139Phe)
n.445G>T
17g.47733870T>ACA400059486TBX21c.416T>A (p.Val139Asp)
n.446T>A
17g.47733870T>CCA400059489TBX21c.416T>C (p.Val139Ala)
n.446T>C
17g.47733870T>GCA400059492TBX21c.416T>G (p.Val139Gly)
n.446T>G
17g.47733871C>ACA500652466TBX21c.417C>A (p.Val139=)
n.447C>A
gnomAD v4
17g.47733871C=CA2262805830TBX21c.417C= (p.Val139=)
n.447C=
17g.47733871C>GCA500652465TBX21c.417C>G (p.Val139=)
n.447C>G
17g.47733871C>TCA8626263TBX21c.417C>T (p.Val139=)
n.447C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47733872G>ACA400059496TBX21c.418G>A (p.Ala140Thr)
n.448G>A
17g.47733872G>CCA400059499TBX21c.418G>C (p.Ala140Pro)
n.448G>C
17g.47733872G>TCA400059501TBX21c.418G>T (p.Ala140Ser)
n.448G>T
17g.47733873C>ACA400059503TBX21c.419C>A (p.Ala140Glu)
n.449C>A
17g.47733873C>GCA400059506TBX21c.419C>G (p.Ala140Gly)
n.449C>G
17g.47733873C>TCA400059508TBX21c.419C>T (p.Ala140Val)
n.449C>T
17g.47733874G>ACA8626265TBX21c.420G>A (p.Ala140=)
n.450G>A
dbSNP ExAC gnomAD v2 gnomAD v4
17g.47733874G>CCA8626264TBX21c.420G>C (p.Ala140=)
n.450G>C
dbSNP ExAC gnomAD v2 gnomAD v4
17g.47733874G=CA2262805831TBX21c.420G= (p.Ala140=)
n.450G=
17g.47733874G>TCA500652467TBX21c.420G>T (p.Ala140=)
n.450G>T
17g.47733875C>ACA400059512TBX21c.421C>A (p.Leu141Ile)
n.451C>A
17g.47733875C>GCA400059519TBX21c.421C>G (p.Leu141Val)
n.451C>G
17g.47733875C>TCA400059516TBX21c.421C>T (p.Leu141Phe)
n.451C>T
17g.47733876T>ACA400059523TBX21c.422T>A (p.Leu141His)
n.452T>A
17g.47733876T>CCA400059526TBX21c.422T>C (p.Leu141Pro)
n.452T>C
17g.47733876T>GCA400059529TBX21c.422T>G (p.Leu141Arg)
n.452T>G
17g.47733877C>ACA500652468TBX21c.423C>A (p.Leu141=)
n.453C>A
17g.47733877C>GCA500652469TBX21c.423C>G (p.Leu141=)
n.453C>G
17g.47733877C>TCA500652470TBX21c.423C>T (p.Leu141=)
n.453C>T
gnomAD v4
17g.47733878A>CCA400059540TBX21c.424A>C (p.Asn142His)
n.454A>C
17g.47733878A>GCA400059541TBX21c.424A>G (p.Asn142Asp)
n.454A>G
17g.47733878A>TCA400059546TBX21c.424A>T (p.Asn142Tyr)
n.454A>T
17g.47733879A=CA2262805832TBX21c.425A= (p.Asn142=)
n.455A=
17g.47733879A>CCA400059551TBX21c.425A>C (p.Asn142Thr)
n.455A>C
17g.47733879A>GCA291302310TBX21c.425A>G (p.Asn142Ser)
n.455A>G
dbSNP gnomAD v4
17g.47733879A>TCA400059558TBX21c.425A>T (p.Asn142Ile)
n.455A>T
17g.47733880C>ACA400059562TBX21c.426C>A (p.Asn142Lys)
n.456C>A
17g.47733880C>GCA400059564TBX21c.426C>G (p.Asn142Lys)
n.456C>G
17g.47733880C>TCA500652474TBX21c.426C>T (p.Asn142=)
n.456C>T
17g.47733881A>CCA400059569TBX21c.427A>C (p.Asn143His)
n.457A>C
17g.47733881A>GCA400059567TBX21c.427A>G (p.Asn143Asp)
n.457A>G
17g.47733881A>TCA400059565TBX21c.427A>T (p.Asn143Tyr)
n.457A>T
17g.47733882A=CA2262805833TBX21c.428A= (p.Asn143=)
n.458A=
17g.47733882A>CCA291302312TBX21c.428A>C (p.Asn143Thr)
n.458A>C
dbSNP
17g.47733882A>GCA400059573TBX21c.428A>G (p.Asn143Ser)
n.458A>G
17g.47733882A>TCA400059574TBX21c.428A>T (p.Asn143Ile)
n.458A>T
17g.47733883C>ACA400059577TBX21c.429C>A (p.Asn143Lys)
n.459C>A
17g.47733883C>GCA400059583TBX21c.429C>G (p.Asn143Lys)
n.459C>G
17g.47733883C>TCA500652475TBX21c.429C>T (p.Asn143=)
n.459C>T
gnomAD v4
17g.47733884C>ACA400059586TBX21c.430C>A (p.His144Asn)
n.460C>A
17g.47733884C=CA2262805834TBX21c.430C= (p.His144=)
n.460C=
17g.47733884C>GCA400059588TBX21c.430C>G (p.His144Asp)
n.460C>G
17g.47733884C>TCA8626266TBX21c.430C>T (p.His144Tyr)
n.460C>T
dbSNP ExAC gnomAD v2 gnomAD v4
17g.47733885A>CCA400059604TBX21c.431A>C (p.His144Pro)
n.461A>C
17g.47733885A>GCA400059608TBX21c.431A>G (p.His144Arg)
n.461A>G
17g.47733885A>TCA400059613TBX21c.431A>T (p.His144Leu)
n.461A>T
17g.47733886C>ACA400059616TBX21c.432C>A (p.His144Gln)
n.462C>A
ClinVar
17g.47733886C=CA2262805835TBX21c.432C= (p.His144=)
n.462C=
17g.47733886C>GCA400059627TBX21c.432C>G (p.His144Gln)
n.462C>G
17g.47733886C>TCA500652479TBX21c.432C>T (p.His144=)
n.462C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.47733887C>ACA400059633TBX21c.433C>A (p.Leu145Met)
n.463C>A
17g.47733887C=CA2262805836TBX21c.433C= (p.Leu145=)
n.463C=
17g.47733887C>GCA400059630TBX21c.433C>G (p.Leu145Val)
n.463C>G
17g.47733887C>TCA291302319TBX21c.433C>T (p.Leu145=)
n.463C>T
dbSNP gnomAD v3 gnomAD v4
17g.47733888T>ACA400059653TBX21c.434T>A (p.Leu145Gln)
n.464T>A
17g.47733888T>CCA400059661TBX21c.434T>C (p.Leu145Pro)
n.464T>C
17g.47733888T>GCA400059655TBX21c.434T>G (p.Leu145Arg)
n.464T>G
17g.47733889G>ACA500652483TBX21c.435G>A (p.Leu145=)
n.465G>A
17g.47733889G>CCA500652484TBX21c.435G>C (p.Leu145=)
n.465G>C
17g.47733889G>TCA500652485TBX21c.435G>T (p.Leu145=)
n.465G>T
17g.47733890T>ACA400059672TBX21c.436T>A (p.Leu146Met)
n.466T>A
17g.47733890T>CCA500652486TBX21c.436T>C (p.Leu146=)
n.466T>C
gnomAD v4
17g.47733890T>GCA400059680TBX21c.436T>G (p.Leu146Val)
n.466T>G
17g.47733891T>ACA400059682TBX21c.437T>A (p.Leu146Ter)
n.467T>A
17g.47733891T>CCA400059687TBX21c.437T>C (p.Leu146Ser)
n.467T>C
17g.47733891T>GCA400059683TBX21c.437T>G (p.Leu146Trp)
n.467T>G
17g.47733892G>ACA500652487TBX21c.438G>A (p.Leu146=)
n.468G>A
gnomAD v4
17g.47733892G>CCA400059691TBX21c.438G>C (p.Leu146Phe)
n.468G>C
17g.47733892G>TCA400059697TBX21c.438G>T (p.Leu146Phe)
n.468G>T
17g.47733893T>ACA400059702TBX21c.439T>A (p.Trp147Arg)
n.469T>A
17g.47733893T>CCA400059703TBX21c.439T>C (p.Trp147Arg)
n.469T>C
17g.47733893T>GCA400059704TBX21c.439T>G (p.Trp147Gly)
n.469T>G
17g.47733894G>ACA400059709TBX21c.440G>A (p.Trp147Ter)
n.470G>A
gnomAD v4
17g.47733894G>CCA400059716TBX21c.440G>C (p.Trp147Ser)
n.470G>C
17g.47733894G>TCA400059719TBX21c.440G>T (p.Trp147Leu)
n.470G>T
17g.47733895G>ACA400059721TBX21c.441G>A (p.Trp147Ter)
n.471G>A
17g.47733895G>CCA400059722TBX21c.441G>C (p.Trp147Cys)
n.471G>C
17g.47733895G>TCA400059728TBX21c.441G>T (p.Trp147Cys)
n.471G>T
17g.47733896T>ACA400059740TBX21c.442T>A (p.Ser148Thr)
n.472T>A
17g.47733896T>CCA400059737TBX21c.442T>C (p.Ser148Pro)
n.472T>C
17g.47733896T>GCA400059731TBX21c.442T>G (p.Ser148Ala)
n.472T>G
17g.47733897C>ACA400059746TBX21c.443C>A (p.Ser148Tyr)
n.473C>A
17g.47733897C>GCA400059751TBX21c.443C>G (p.Ser148Cys)
n.473C>G
17g.47733897C>TCA400059753TBX21c.443C>T (p.Ser148Phe)
n.473C>T
17g.47733898C>ACA500652490TBX21c.444C>A (p.Ser148=)
n.474C>A
17g.47733898C>GCA500652491TBX21c.444C>G (p.Ser148=)
n.474C>G
17g.47733898C>TCA500652493TBX21c.444C>T (p.Ser148=)
n.474C>T
17g.47733899A>CCA400059759TBX21c.445A>C (p.Lys149Gln)
n.475A>C
17g.47733899A>GCA400059764TBX21c.445A>G (p.Lys149Glu)
n.475A>G
17g.47733899A>TCA400059765TBX21c.445A>T (p.Lys149Ter)
n.475A>T
17g.47733900A>CCA400059768TBX21c.446A>C (p.Lys149Thr)
n.476A>C
17g.47733900A>GCA400059771TBX21c.446A>G (p.Lys149Arg)
n.476A>G
gnomAD v4
17g.47733900A>TCA400059778TBX21c.446A>T (p.Lys149Met)
n.476A>T
17g.47733901G>ACA500652495TBX21c.447G>A (p.Lys149=)
n.477G>A
17g.47733901G>CCA400059780TBX21c.447G>C (p.Lys149Asn)
n.477G>C
17g.47733901G>TCA400059781TBX21c.447G>T (p.Lys149Asn)
n.477G>T
17g.47733902T>ACA400059790TBX21c.448T>A (p.Phe150Ile)
n.478T>A
17g.47733902T>CCA400059788TBX21c.448T>C (p.Phe150Leu)
n.478T>C
17g.47733902T>GCA400059785TBX21c.448T>G (p.Phe150Val)
n.478T>G
COSMIC
17g.47733903T>ACA400059792TBX21c.449T>A (p.Phe150Tyr)
n.479T>A
17g.47733903T>CCA400059794TBX21c.449T>C (p.Phe150Ser)
n.479T>C
17g.47733903T>GCA400059796TBX21c.449T>G (p.Phe150Cys)
n.479T>G
17g.47733904T>ACA400059802TBX21c.450T>A (p.Phe150Leu)
n.480T>A
17g.47733904T>CCA500652497TBX21c.450T>C (p.Phe150=)
n.480T>C
dbSNP gnomAD v3 gnomAD v4
17g.47733904T>GCA400059805TBX21c.450T>G (p.Phe150Leu)
n.480T>G
17g.47733904T=CA2262805837TBX21c.450T= (p.Phe150=)
n.480T=
17g.47733905A>CCA400059811TBX21c.451A>C (p.Asn151His)
n.481A>C
17g.47733905A>GCA400059812TBX21c.451A>G (p.Asn151Asp)
n.481A>G
17g.47733905A>TCA400059813TBX21c.451A>T (p.Asn151Tyr)
n.481A>T
17g.47733906A>CCA400059815TBX21c.452A>C (p.Asn151Thr)
n.482A>C
17g.47733906A>GCA400059818TBX21c.452A>G (p.Asn151Ser)
n.482A>G
17g.47733906A>TCA400059822TBX21c.452A>T (p.Asn151Ile)
n.482A>T
17g.47733907T>ACA400059824TBX21c.453T>A (p.Asn151Lys)
n.483T>A
17g.47733907T>CCA500652498TBX21c.453T>C (p.Asn151=)
n.483T>C
gnomAD v4
17g.47733907T>GCA400059825TBX21c.453T>G (p.Asn151Lys)
n.483T>G
17g.47733908C>ACA400059827TBX21c.454C>A (p.Gln152Lys)
n.484C>A
dbSNP
17g.47733908C=CA2262805838TBX21c.454C= (p.Gln152=)
n.484C=
17g.47733908C>GCA400059830TBX21c.454C>G (p.Gln152Glu)
n.484C>G
17g.47733908C>TCA400059829TBX21c.454C>T (p.Gln152Ter)
n.484C>T
17g.47733909A>CCA400059833TBX21c.455A>C (p.Gln152Pro)
n.485A>C
17g.47733909A>GCA400059834TBX21c.455A>G (p.Gln152Arg)
n.485A>G
17g.47733909A>TCA400059835TBX21c.455A>T (p.Gln152Leu)
n.485A>T
17g.47733910G>ACA500652502TBX21c.456G>A (p.Gln152=)
n.486G>A
17g.47733910G>CCA400059836TBX21c.456G>C (p.Gln152His)
n.486G>C
17g.47733910G>TCA400059837TBX21c.456G>T (p.Gln152His)
n.486G>T
17g.47733911C>ACA400059838TBX21c.457C>A (p.His153Asn)
n.487C>A
17g.47733911C>GCA400059839TBX21c.457C>G (p.His153Asp)
n.487C>G
17g.47733911C>TCA400059841TBX21c.457C>T (p.His153Tyr)
n.487C>T
gnomAD v4
17g.47733912A>CCA400059842TBX21c.458A>C (p.His153Pro)
n.488A>C
17g.47733912A>GCA400059843TBX21c.458A>G (p.His153Arg)
n.488A>G
17g.47733912A>TCA400059845TBX21c.458A>T (p.His153Leu)
n.488A>T
17g.47733913C>ACA400059850TBX21c.459C>A (p.His153Gln)
n.489C>A
17g.47733913C>GCA400059847TBX21c.459C>G (p.His153Gln)
n.489C>G
17g.47733913C>TCA500652503TBX21c.459C>T (p.His153=)
n.489C>T
17g.47733914C>ACA400059854TBX21c.460C>A (p.Gln154Lys)
n.490C>A
17g.47733914C>GCA400059858TBX21c.460C>G (p.Gln154Glu)
n.490C>G
gnomAD v4
17g.47733914C>TCA400059856TBX21c.460C>T (p.Gln154Ter)
n.490C>T
17g.47733918_47733921delCA2638460879TBX21c.464_467del (p.Thr155ArgfsTer2)
n.494_497del
gnomAD v4
17g.47733915A=CA2262805839TBX21c.461A= (p.Gln154=)
n.491A=
17g.47733915A>CCA400059859TBX21c.461A>C (p.Gln154Pro)
n.491A>C
17g.47733915A>GCA400059860TBX21c.461A>G (p.Gln154Arg)
n.491A>G
dbSNP
17g.47733915A>TCA400059861TBX21c.461A>T (p.Gln154Leu)
n.491A>T
dbSNP gnomAD v2 gnomAD v4 COSMIC
17g.47733916G>ACA500652508TBX21c.462G>A (p.Gln154=)
n.492G>A
17g.47733916G>CCA400059862TBX21c.462G>C (p.Gln154His)
n.492G>C
dbSNP
17g.47733916G=CA2262805840TBX21c.462G= (p.Gln154=)
n.492G=
17g.47733916G>TCA400059863TBX21c.462G>T (p.Gln154His)
n.492G>T
17g.47733917A>CCA400059864TBX21c.463A>C (p.Thr155Pro)
n.493A>C
17g.47733917A>GCA400059866TBX21c.463A>G (p.Thr155Ala)
n.493A>G
17g.47733917A>TCA400059871TBX21c.463A>T (p.Thr155Ser)
n.493A>T
17g.47733918C>ACA400059874TBX21c.464C>A (p.Thr155Lys)
n.494C>A
17g.47733918C>GCA400059877TBX21c.464C>G (p.Thr155Arg)
n.494C>G
17g.47733918C>TCA400059879TBX21c.464C>T (p.Thr155Ile)
n.494C>T
17g.47733919A=CA2262805841TBX21c.465A= (p.Thr155=)
n.495A=
17g.47733919A>CCA500652512TBX21c.465A>C (p.Thr155=)
n.495A>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.47733919A>GCA291302322TBX21c.465A>G (p.Thr155=)
n.495A>G
dbSNP gnomAD v3 gnomAD v4
17g.47733919A>TCA500652513TBX21c.465A>T (p.Thr155=)
n.495A>T
17g.47733920G>ACA400059886TBX21c.466G>A (p.Glu156Lys)
n.496G>A
17g.47733920G>CCA400059881TBX21c.466G>C (p.Glu156Gln)
n.496G>C
17g.47733920G>TCA400059884TBX21c.466G>T (p.Glu156Ter)
n.496G>T
17g.47733920_47733925delinsAGTTTACA2573054468TBX21c.466_471delinsAGTTTA (p.Glu156_Met157delinsSerLeu)
n.496_501delinsAGTTTA
ClinVar dbSNP
17g.47733921A>CCA400059888TBX21c.467A>C (p.Glu156Ala)
n.497A>C
17g.47733921A>GCA400059889TBX21c.467A>G (p.Glu156Gly)
n.497A>G
17g.47733921A>TCA400059892TBX21c.467A>T (p.Glu156Val)
n.497A>T
17g.47733922G>ACA500652514TBX21c.468G>A (p.Glu156=)
n.498G>A
17g.47733922G>CCA400059899TBX21c.468G>C (p.Glu156Asp)
n.498G>C
17g.47733922G>TCA400059900TBX21c.468G>T (p.Glu156Asp)
n.498G>T
17g.47733923A>CCA400059903TBX21c.469A>C (p.Met157Leu)
n.499A>C
17g.47733923A>GCA400059916TBX21c.469A>G (p.Met157Val)
n.499A>G
17g.47733923A>TCA400059919TBX21c.469A>T (p.Met157Leu)
n.499A>T
17g.47733924T>ACA400059921TBX21c.470T>A (p.Met157Lys)
n.500T>A
17g.47733924T>CCA400059922TBX21c.470T>C (p.Met157Thr)
n.500T>C
17g.47733924T>GCA400059925TBX21c.470T>G (p.Met157Arg)
n.500T>G
17g.47733925G>ACA400059933TBX21c.471G>A (p.Met157Ile)
n.501G>A
17g.47733925G>CCA400059937TBX21c.471G>C (p.Met157Ile)
n.501G>C
17g.47733925G>TCA400059928TBX21c.471G>T (p.Met157Ile)
n.501G>T
17g.47733926A>CCA400059942TBX21c.472A>C (p.Ile158Leu)
n.502A>C
17g.47733926A>GCA400059944TBX21c.472A>G (p.Ile158Val)
n.502A>G
17g.47733926A>TCA400059947TBX21c.472A>T (p.Ile158Phe)
n.502A>T
17g.47733927T>ACA400059950TBX21c.473T>A (p.Ile158Asn)
n.503T>A
17g.47733927T>CCA400059952TBX21c.473T>C (p.Ile158Thr)
n.503T>C
17g.47733927T>GCA400059957TBX21c.473T>G (p.Ile158Ser)
n.503T>G
17g.47733928C>ACA500652519TBX21c.474C>A (p.Ile158=)
n.504C>A
17g.47733928C=CA2262805842TBX21c.474C= (p.Ile158=)
n.504C=
17g.47733928C>GCA400059960TBX21c.474C>G (p.Ile158Met)
n.504C>G
17g.47733928C>TCA291302323TBX21c.474C>T (p.Ile158=)
n.504C>T
dbSNP gnomAD v2 gnomAD v4
17g.47733929A>CCA400059961TBX21c.475A>C (p.Ile159Leu)
n.505A>C
17g.47733929A>GCA400059962TBX21c.475A>G (p.Ile159Val)
n.505A>G
17g.47733929A>TCA400059963TBX21c.475A>T (p.Ile159Phe)
n.505A>T
17g.47733930T>ACA400059964TBX21c.476T>A (p.Ile159Asn)
n.506T>A
17g.47733930T>CCA400059966TBX21c.476T>C (p.Ile159Thr)
n.506T>C
17g.47733930T>GCA400059969TBX21c.476T>G (p.Ile159Ser)
n.506T>G
17g.47733931C>ACA8626267TBX21c.477C>A (p.Ile159=)
n.507C>A
dbSNP ExAC gnomAD v4
17g.47733931C=CA2262805843TBX21c.477C= (p.Ile159=)
n.507C=
17g.47733931C>GCA400059972TBX21c.477C>G (p.Ile159Met)
n.507C>G
17g.47733931C>TCA500652520TBX21c.477C>T (p.Ile159=)
n.507C>T
17g.47733932A>CCA400059982TBX21c.478A>C (p.Thr160Pro)
n.508A>C
17g.47733932A>GCA400059984TBX21c.478A>G (p.Thr160Ala)
n.508A>G
17g.47733932A>TCA400059987TBX21c.478A>T (p.Thr160Ser)
n.508A>T
17g.47733933C>ACA400059989TBX21c.479C>A (p.Thr160Asn)
n.509C>A
17g.47733933C>GCA400059998TBX21c.479C>G (p.Thr160Ser)
n.509C>G
17g.47733933C>TCA400060000TBX21c.479C>T (p.Thr160Ile)
n.509C>T
17g.47733934C>ACA500652521TBX21c.480C>A (p.Thr160=)
n.510C>A
gnomAD v4
17g.47733934C=CA2262805844TBX21c.480C= (p.Thr160=)
n.510C=
17g.47733934C>GCA500652522TBX21c.480C>G (p.Thr160=)
n.510C>G
dbSNP
17g.47733934C>TCA500652523TBX21c.480C>T (p.Thr160=)
n.510C>T
17g.47733935A>CCA400060003TBX21c.481A>C (p.Lys161Gln)
n.511A>C
17g.47733935A>GCA400060004TBX21c.481A>G (p.Lys161Glu)
n.511A>G
17g.47733935A>TCA400060008TBX21c.481A>T (p.Lys161Ter)
n.511A>T
17g.47733936A>CCA400060026TBX21c.482A>C (p.Lys161Thr)
n.512A>C
17g.47733936A>GCA400060029TBX21c.482A>G (p.Lys161Arg)
n.512A>G
17g.47733936A>TCA400060036TBX21c.482A>T (p.Lys161Met)
n.512A>T
gnomAD v4
17g.47733937G>ACA500652524TBX21c.483G>A (p.Lys161=)
n.513G>A
dbSNP gnomAD v4
17g.47733937G>CCA400060039TBX21c.483G>C (p.Lys161Asn)
n.513G>C
17g.47733937G=CA2262805845TBX21c.483G= (p.Lys161=)
n.513G=
17g.47733937G>TCA400060050TBX21c.483G>T (p.Lys161Asn)
n.513G>T
gnomAD v4
17g.47733938C>ACA400060058TBX21c.484C>A (p.Gln162Lys)
n.514C>A
17g.47733938C>GCA400060059TBX21c.484C>G (p.Gln162Glu)
n.514C>G
gnomAD v4
17g.47733938C>TCA400060055TBX21c.484C>T (p.Gln162Ter)
n.514C>T
17g.47733939A=CA2262805846TBX21c.485A= (p.Gln162=)
n.515A=
17g.47733939A>CCA400060064TBX21c.485A>C (p.Gln162Pro)
n.515A>C
17g.47733939A>GCA400060063TBX21c.485A>G (p.Gln162Arg)
n.515A>G
dbSNP gnomAD v2 gnomAD v4
17g.47733939A>TCA400060065TBX21c.485A>T (p.Gln162Leu)
n.515A>T
17g.47733940G>ACA291302324TBX21c.486G>A (p.Gln162=)
n.516G>A
dbSNP
17g.47733940G>CCA291302325TBX21c.486G>C (p.Gln162His)
n.516G>C
dbSNP
17g.47733940G=CA2262805847TBX21c.486G= (p.Gln162=)
n.516G=
17g.47733940G>TCA400060066TBX21c.486G>T (p.Gln162His)
n.516G>T
17g.47733941G>ACA400060069TBX21c.487G>A (p.Gly163Arg)
n.517G>A
COSMIC
17g.47733941G>CCA400060070TBX21c.487G>C (p.Gly163Arg)
n.517G>C
17g.47733941G>TCA400060085TBX21c.487G>T (p.Gly163Ter)
n.517G>T
gnomAD v4
17g.47733942G>ACA400060094TBX21c.488G>A (p.Gly163Glu)
n.518G>A
17g.47733942G>CCA400060092TBX21c.488G>C (p.Gly163Ala)
n.518G>C
17g.47733942G>TCA400060090TBX21c.488G>T (p.Gly163Val)
n.518G>T
17g.47733943A=CA2262805848TBX21c.489A= (p.Gly163=)
n.519A=
17g.47733943A>CCA500652526TBX21c.489A>C (p.Gly163=)
n.519A>C
17g.47733943A>GCA8626268TBX21c.489A>G (p.Gly163=)
n.519A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.47733943A>TCA500652525TBX21c.489A>T (p.Gly163=)
n.519A>T
17g.47733944C>ACA500652527TBX21c.490C>A (p.Arg164=)
n.520C>A
17g.47733944C>GCA400060103TBX21c.490C>G (p.Arg164Gly)
n.520C>G
17g.47733944C>TCA400060104TBX21c.490C>T (p.Arg164Trp)
n.520C>T
17g.47733945G>ACA400060105TBX21c.491G>A (p.Arg164Gln)
n.521G>A
17g.47733945G>CCA400060106TBX21c.491G>C (p.Arg164Pro)
n.521G>C
17g.47733945G>TCA400060108TBX21c.491G>T (p.Arg164Leu)
n.521G>T
gnomAD v4
17g.47733946G>ACA400060111TBX21c.491+1G>A (n.491+1G>A)
n.521+1G>A
17g.47733946G>CCA400060118TBX21c.491+1G>C (n.491+1G>C)
n.521+1G>C
17g.47733946G>TCA400060114TBX21c.491+1G>T (n.491+1G>T)
n.521+1G>T
17g.47733947T>ACA400060121TBX21c.491+2T>A (n.491+2T>A)
n.521+2T>A
17g.47733947T>CCA400060127TBX21c.491+2T>C (n.491+2T>C)
n.521+2T>C
17g.47733947T>GCA400060130TBX21c.491+2T>G (n.491+2T>G)
n.521+2T>G
17g.47733948G>TCA2638460929TBX21c.491+3G>T (n.491+3G>T)
n.521+3G>T
gnomAD v4
17g.47733952G>TCA2638460930TBX21c.491+7G>T (n.491+7G>T)
n.521+7G>T
gnomAD v4

Number of alleles fetched