Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.49255735C>ACA412951094FOXP3c.610G>T (p.Val204Leu)
c.715G>T (p.Val239Leu)
c.784G>T (p.Val262Leu)
c.565G>T (p.Val189Leu)
c.934G>T (p.Val312Leu)
c.733G>T (p.Val245Leu)
c.970G>T (p.Val324Leu)
c.661G>T (p.Val221Leu)
Xg.49255735C>GCA412951095FOXP3c.610G>C (p.Val204Leu)
c.715G>C (p.Val239Leu)
c.784G>C (p.Val262Leu)
c.565G>C (p.Val189Leu)
c.934G>C (p.Val312Leu)
c.733G>C (p.Val245Leu)
c.970G>C (p.Val324Leu)
c.661G>C (p.Val221Leu)
Xg.49255735C>TCA412951096FOXP3c.610G>A (p.Val204Ile)
c.715G>A (p.Val239Ile)
c.784G>A (p.Val262Ile)
c.565G>A (p.Val189Ile)
c.934G>A (p.Val312Ile)
c.733G>A (p.Val245Ile)
c.970G>A (p.Val324Ile)
c.661G>A (p.Val221Ile)
Xg.49255736C>ACA412951097FOXP3c.609G>T (p.Met203Ile)
c.714G>T (p.Met238Ile)
c.783G>T (p.Met261Ile)
c.564G>T (p.Met188Ile)
c.933G>T (p.Met311Ile)
c.732G>T (p.Met244Ile)
c.969G>T (p.Met323Ile)
c.660G>T (p.Met220Ile)
Xg.49255736C>GCA412951098FOXP3c.609G>C (p.Met203Ile)
c.714G>C (p.Met238Ile)
c.783G>C (p.Met261Ile)
c.564G>C (p.Met188Ile)
c.933G>C (p.Met311Ile)
c.732G>C (p.Met244Ile)
c.969G>C (p.Met323Ile)
c.660G>C (p.Met220Ile)
Xg.49255736C>TCA412951099FOXP3c.609G>A (p.Met203Ile)
c.714G>A (p.Met238Ile)
c.783G>A (p.Met261Ile)
c.564G>A (p.Met188Ile)
c.933G>A (p.Met311Ile)
c.732G>A (p.Met244Ile)
c.969G>A (p.Met323Ile)
c.660G>A (p.Met220Ile)
Xg.49255737A=CA2428552714FOXP3c.608T= (p.Met203=)
c.713T= (p.Met238=)
c.782T= (p.Met261=)
c.563T= (p.Met188=)
c.932T= (p.Met311=)
c.731T= (p.Met244=)
c.968T= (p.Met323=)
c.659T= (p.Met220=)
Xg.49255737A>CCA10411754FOXP3c.608T>G (p.Met203Arg)
c.713T>G (p.Met238Arg)
c.782T>G (p.Met261Arg)
c.563T>G (p.Met188Arg)
c.932T>G (p.Met311Arg)
c.731T>G (p.Met244Arg)
c.968T>G (p.Met323Arg)
c.659T>G (p.Met220Arg)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
Xg.49255737A>GCA412951101FOXP3c.608T>C (p.Met203Thr)
c.713T>C (p.Met238Thr)
c.782T>C (p.Met261Thr)
c.563T>C (p.Met188Thr)
c.932T>C (p.Met311Thr)
c.731T>C (p.Met244Thr)
c.968T>C (p.Met323Thr)
c.659T>C (p.Met220Thr)
Xg.49255737A>TCA412951100FOXP3c.608T>A (p.Met203Lys)
c.713T>A (p.Met238Lys)
c.782T>A (p.Met261Lys)
c.563T>A (p.Met188Lys)
c.932T>A (p.Met311Lys)
c.731T>A (p.Met244Lys)
c.968T>A (p.Met323Lys)
c.659T>A (p.Met220Lys)
Xg.49255738T>ACA412951102FOXP3c.607A>T (p.Met203Leu)
c.712A>T (p.Met238Leu)
c.781A>T (p.Met261Leu)
c.562A>T (p.Met188Leu)
c.931A>T (p.Met311Leu)
c.730A>T (p.Met244Leu)
c.967A>T (p.Met323Leu)
c.658A>T (p.Met220Leu)
Xg.49255738T>CCA412951103FOXP3c.607A>G (p.Met203Val)
c.712A>G (p.Met238Val)
c.781A>G (p.Met261Val)
c.562A>G (p.Met188Val)
c.931A>G (p.Met311Val)
c.730A>G (p.Met244Val)
c.967A>G (p.Met323Val)
c.658A>G (p.Met220Val)
Xg.49255738T>GCA412951104FOXP3c.607A>C (p.Met203Leu)
c.712A>C (p.Met238Leu)
c.781A>C (p.Met261Leu)
c.562A>C (p.Met188Leu)
c.931A>C (p.Met311Leu)
c.730A>C (p.Met244Leu)
c.967A>C (p.Met323Leu)
c.658A>C (p.Met220Leu)
Xg.49255745_49255746delCA2693705157FOXP3c.606_607del (p.Glu202AspfsTer?)
c.711_712del (p.Glu237AspfsTer?)
c.780_781del (p.Glu260AspfsTer?)
c.561_562del (p.Glu187AspfsTer?)
c.930_931del (p.Glu310AspfsTer?)
c.729_730del (p.Glu243AspfsTer?)
c.966_967del (p.Glu322AspfsTer?)
c.657_658del (p.Glu219AspfsTer?)
gnomAD v4
Xg.49255739C>ACA412951105FOXP3c.606G>T (p.Glu202Asp)
c.711G>T (p.Glu237Asp)
c.780G>T (p.Glu260Asp)
c.561G>T (p.Glu187Asp)
c.930G>T (p.Glu310Asp)
c.729G>T (p.Glu243Asp)
c.966G>T (p.Glu322Asp)
c.657G>T (p.Glu219Asp)
gnomAD v4
Xg.49255739C=CA2428552715FOXP3c.606G= (p.Glu202=)
c.711G= (p.Glu237=)
c.780G= (p.Glu260=)
c.561G= (p.Glu187=)
c.930G= (p.Glu310=)
c.729G= (p.Glu243=)
c.966G= (p.Glu322=)
c.657G= (p.Glu219=)
Xg.49255739C>GCA412951106FOXP3c.606G>C (p.Glu202Asp)
c.711G>C (p.Glu237Asp)
c.780G>C (p.Glu260Asp)
c.561G>C (p.Glu187Asp)
c.930G>C (p.Glu310Asp)
c.729G>C (p.Glu243Asp)
c.966G>C (p.Glu322Asp)
c.657G>C (p.Glu219Asp)
Xg.49255739C>TCA516397359FOXP3c.606G>A (p.Glu202=)
c.711G>A (p.Glu237=)
c.780G>A (p.Glu260=)
c.561G>A (p.Glu187=)
c.930G>A (p.Glu310=)
c.729G>A (p.Glu243=)
c.966G>A (p.Glu322=)
c.657G>A (p.Glu219=)
ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.49255740T>ACA412951107FOXP3c.605A>T (p.Glu202Val)
c.710A>T (p.Glu237Val)
c.779A>T (p.Glu260Val)
c.560A>T (p.Glu187Val)
c.929A>T (p.Glu310Val)
c.728A>T (p.Glu243Val)
c.965A>T (p.Glu322Val)
c.656A>T (p.Glu219Val)
Xg.49255740T>CCA412951109FOXP3c.605A>G (p.Glu202Gly)
c.710A>G (p.Glu237Gly)
c.779A>G (p.Glu260Gly)
c.560A>G (p.Glu187Gly)
c.929A>G (p.Glu310Gly)
c.728A>G (p.Glu243Gly)
c.965A>G (p.Glu322Gly)
c.656A>G (p.Glu219Gly)
Xg.49255740T>GCA412951108FOXP3c.605A>C (p.Glu202Ala)
c.710A>C (p.Glu237Ala)
c.779A>C (p.Glu260Ala)
c.560A>C (p.Glu187Ala)
c.929A>C (p.Glu310Ala)
c.728A>C (p.Glu243Ala)
c.965A>C (p.Glu322Ala)
c.656A>C (p.Glu219Ala)
Xg.49255741C>ACA412951110FOXP3c.604G>T (p.Glu202Ter)
c.709G>T (p.Glu237Ter)
c.778G>T (p.Glu260Ter)
c.559G>T (p.Glu187Ter)
c.928G>T (p.Glu310Ter)
c.727G>T (p.Glu243Ter)
c.964G>T (p.Glu322Ter)
c.655G>T (p.Glu219Ter)
Xg.49255741C>GCA412951111FOXP3c.604G>C (p.Glu202Gln)
c.709G>C (p.Glu237Gln)
c.778G>C (p.Glu260Gln)
c.559G>C (p.Glu187Gln)
c.928G>C (p.Glu310Gln)
c.727G>C (p.Glu243Gln)
c.964G>C (p.Glu322Gln)
c.655G>C (p.Glu219Gln)
Xg.49255741C>TCA412951112FOXP3c.604G>A (p.Glu202Lys)
c.709G>A (p.Glu237Lys)
c.778G>A (p.Glu260Lys)
c.559G>A (p.Glu187Lys)
c.928G>A (p.Glu310Lys)
c.727G>A (p.Glu243Lys)
c.964G>A (p.Glu322Lys)
c.655G>A (p.Glu219Lys)
Xg.49255742T>ACA412951113FOXP3c.603A>T (p.Arg201Ser)
c.708A>T (p.Arg236Ser)
c.777A>T (p.Arg259Ser)
c.558A>T (p.Arg186Ser)
c.927A>T (p.Arg309Ser)
c.726A>T (p.Arg242Ser)
c.963A>T (p.Arg321Ser)
c.654A>T (p.Arg218Ser)
Xg.49255742T>CCA516397367FOXP3c.603A>G (p.Arg201=)
c.708A>G (p.Arg236=)
c.777A>G (p.Arg259=)
c.558A>G (p.Arg186=)
c.927A>G (p.Arg309=)
c.726A>G (p.Arg242=)
c.963A>G (p.Arg321=)
c.654A>G (p.Arg218=)
Xg.49255742T>GCA412951114FOXP3c.603A>C (p.Arg201Ser)
c.708A>C (p.Arg236Ser)
c.777A>C (p.Arg259Ser)
c.558A>C (p.Arg186Ser)
c.927A>C (p.Arg309Ser)
c.726A>C (p.Arg242Ser)
c.963A>C (p.Arg321Ser)
c.654A>C (p.Arg218Ser)
Xg.49255743C>ACA412951115FOXP3c.602G>T (p.Arg201Ile)
c.707G>T (p.Arg236Ile)
c.776G>T (p.Arg259Ile)
c.557G>T (p.Arg186Ile)
c.926G>T (p.Arg309Ile)
c.725G>T (p.Arg242Ile)
c.962G>T (p.Arg321Ile)
c.653G>T (p.Arg218Ile)
Xg.49255743C=CA2428552716FOXP3c.602G= (p.Arg201=)
c.707G= (p.Arg236=)
c.776G= (p.Arg259=)
c.557G= (p.Arg186=)
c.926G= (p.Arg309=)
c.725G= (p.Arg242=)
c.962G= (p.Arg321=)
c.653G= (p.Arg218=)
Xg.49255743C>GCA412951116FOXP3c.602G>C (p.Arg201Thr)
c.707G>C (p.Arg236Thr)
c.776G>C (p.Arg259Thr)
c.557G>C (p.Arg186Thr)
c.926G>C (p.Arg309Thr)
c.725G>C (p.Arg242Thr)
c.962G>C (p.Arg321Thr)
c.653G>C (p.Arg218Thr)
Xg.49255743C>TCA412951117FOXP3c.602G>A (p.Arg201Lys)
c.707G>A (p.Arg236Lys)
c.776G>A (p.Arg259Lys)
c.557G>A (p.Arg186Lys)
c.926G>A (p.Arg309Lys)
c.725G>A (p.Arg242Lys)
c.962G>A (p.Arg321Lys)
c.653G>A (p.Arg218Lys)
dbSNP
Xg.49255744T>ACA412951118FOXP3c.601A>T (p.Arg201Ter)
c.706A>T (p.Arg236Ter)
c.775A>T (p.Arg259Ter)
c.556A>T (p.Arg186Ter)
c.925A>T (p.Arg309Ter)
c.724A>T (p.Arg242Ter)
c.961A>T (p.Arg321Ter)
c.652A>T (p.Arg218Ter)
Xg.49255744T>CCA412951119FOXP3c.601A>G (p.Arg201Gly)
c.706A>G (p.Arg236Gly)
c.775A>G (p.Arg259Gly)
c.556A>G (p.Arg186Gly)
c.925A>G (p.Arg309Gly)
c.724A>G (p.Arg242Gly)
c.961A>G (p.Arg321Gly)
c.652A>G (p.Arg218Gly)
Xg.49255744T>GCA516397373FOXP3c.601A>C (p.Arg201=)
c.706A>C (p.Arg236=)
c.775A>C (p.Arg259=)
c.556A>C (p.Arg186=)
c.925A>C (p.Arg309=)
c.724A>C (p.Arg242=)
c.961A>C (p.Arg321=)
c.652A>C (p.Arg218=)
Xg.49255745C>ACA412951120FOXP3c.600G>T (p.Gln200His)
c.705G>T (p.Gln235His)
c.774G>T (p.Gln258His)
c.555G>T (p.Gln185His)
c.924G>T (p.Gln308His)
c.723G>T (p.Gln241His)
c.960G>T (p.Gln320His)
c.651G>T (p.Gln217His)
Xg.49255745C>GCA412951121FOXP3c.600G>C (p.Gln200His)
c.705G>C (p.Gln235His)
c.774G>C (p.Gln258His)
c.555G>C (p.Gln185His)
c.924G>C (p.Gln308His)
c.723G>C (p.Gln241His)
c.960G>C (p.Gln320His)
c.651G>C (p.Gln217His)
Xg.49255745C>TCA516397378FOXP3c.600G>A (p.Gln200=)
c.705G>A (p.Gln235=)
c.774G>A (p.Gln258=)
c.555G>A (p.Gln185=)
c.924G>A (p.Gln308=)
c.723G>A (p.Gln241=)
c.960G>A (p.Gln320=)
c.651G>A (p.Gln217=)
Xg.49255746T>ACA412951122FOXP3c.599A>T (p.Gln200Leu)
c.704A>T (p.Gln235Leu)
c.773A>T (p.Gln258Leu)
c.554A>T (p.Gln185Leu)
c.923A>T (p.Gln308Leu)
c.722A>T (p.Gln241Leu)
c.959A>T (p.Gln320Leu)
c.650A>T (p.Gln217Leu)
Xg.49255746T>CCA412951124FOXP3c.599A>G (p.Gln200Arg)
c.704A>G (p.Gln235Arg)
c.773A>G (p.Gln258Arg)
c.554A>G (p.Gln185Arg)
c.923A>G (p.Gln308Arg)
c.722A>G (p.Gln241Arg)
c.959A>G (p.Gln320Arg)
c.650A>G (p.Gln217Arg)
Xg.49255746T>GCA412951123FOXP3c.599A>C (p.Gln200Pro)
c.704A>C (p.Gln235Pro)
c.773A>C (p.Gln258Pro)
c.554A>C (p.Gln185Pro)
c.923A>C (p.Gln308Pro)
c.722A>C (p.Gln241Pro)
c.959A>C (p.Gln320Pro)
c.650A>C (p.Gln217Pro)
Xg.49255747G>ACA412951125FOXP3c.598C>T (p.Gln200Ter)
c.703C>T (p.Gln235Ter)
c.772C>T (p.Gln258Ter)
c.553C>T (p.Gln185Ter)
c.922C>T (p.Gln308Ter)
c.721C>T (p.Gln241Ter)
c.958C>T (p.Gln320Ter)
c.649C>T (p.Gln217Ter)
Xg.49255747G>CCA412951126FOXP3c.598C>G (p.Gln200Glu)
c.703C>G (p.Gln235Glu)
c.772C>G (p.Gln258Glu)
c.553C>G (p.Gln185Glu)
c.922C>G (p.Gln308Glu)
c.721C>G (p.Gln241Glu)
c.958C>G (p.Gln320Glu)
c.649C>G (p.Gln217Glu)
Xg.49255747G>TCA412951127FOXP3c.598C>A (p.Gln200Lys)
c.703C>A (p.Gln235Lys)
c.772C>A (p.Gln258Lys)
c.553C>A (p.Gln185Lys)
c.922C>A (p.Gln308Lys)
c.721C>A (p.Gln241Lys)
c.958C>A (p.Gln320Lys)
c.649C>A (p.Gln217Lys)
gnomAD v4
Xg.49255748G>ACA516397386FOXP3c.597C>T (p.Leu199=)
c.702C>T (p.Leu234=)
c.771C>T (p.Leu257=)
c.552C>T (p.Leu184=)
c.921C>T (p.Leu307=)
c.720C>T (p.Leu240=)
c.957C>T (p.Leu319=)
c.648C>T (p.Leu216=)
ClinVar dbSNP gnomAD v4
Xg.49255748G>CCA516397389FOXP3c.597C>G (p.Leu199=)
c.702C>G (p.Leu234=)
c.771C>G (p.Leu257=)
c.552C>G (p.Leu184=)
c.921C>G (p.Leu307=)
c.720C>G (p.Leu240=)
c.957C>G (p.Leu319=)
c.648C>G (p.Leu216=)
dbSNP
Xg.49255748G=CA2428552717FOXP3c.597C= (p.Leu199=)
c.702C= (p.Leu234=)
c.771C= (p.Leu257=)
c.552C= (p.Leu184=)
c.921C= (p.Leu307=)
c.720C= (p.Leu240=)
c.957C= (p.Leu319=)
c.648C= (p.Leu216=)
Xg.49255748G>TCA516397390FOXP3c.597C>A (p.Leu199=)
c.702C>A (p.Leu234=)
c.771C>A (p.Leu257=)
c.552C>A (p.Leu184=)
c.921C>A (p.Leu307=)
c.720C>A (p.Leu240=)
c.957C>A (p.Leu319=)
c.648C>A (p.Leu216=)
Xg.49255749A>CCA412951128FOXP3c.596T>G (p.Leu199Arg)
c.701T>G (p.Leu234Arg)
c.770T>G (p.Leu257Arg)
c.551T>G (p.Leu184Arg)
c.920T>G (p.Leu307Arg)
c.719T>G (p.Leu240Arg)
c.956T>G (p.Leu319Arg)
c.647T>G (p.Leu216Arg)
Xg.49255749A>GCA412951129FOXP3c.596T>C (p.Leu199Pro)
c.701T>C (p.Leu234Pro)
c.770T>C (p.Leu257Pro)
c.551T>C (p.Leu184Pro)
c.920T>C (p.Leu307Pro)
c.719T>C (p.Leu240Pro)
c.956T>C (p.Leu319Pro)
c.647T>C (p.Leu216Pro)
Xg.49255749A>TCA412951130FOXP3c.596T>A (p.Leu199His)
c.701T>A (p.Leu234His)
c.770T>A (p.Leu257His)
c.551T>A (p.Leu184His)
c.920T>A (p.Leu307His)
c.719T>A (p.Leu240His)
c.956T>A (p.Leu319His)
c.647T>A (p.Leu216His)

Number of alleles fetched