Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154367704G>ACA519709647FLNAc.657C>T (p.Ser219=)
c.576C>T (p.Ser192=)
c.615C>T (p.Ser205=)
Xg.154367704G>CCA415248872FLNAc.657C>G (p.Ser219Arg)
c.576C>G (p.Ser192Arg)
c.615C>G (p.Ser205Arg)
Xg.154367704G>TCA415248873FLNAc.657C>A (p.Ser219Arg)
c.576C>A (p.Ser192Arg)
c.615C>A (p.Ser205Arg)
Xg.154367705delCA2573159434FLNAc.656del (p.Ser219ThrfsTer23)
c.575del (p.Ser192ThrfsTer23)
c.614del (p.Ser205ThrfsTer23)
 ClinVar dbSNP
Xg.154367705C>ACA415248874FLNAc.656G>T (p.Ser219Ile)
c.575G>T (p.Ser192Ile)
c.614G>T (p.Ser205Ile)
Xg.154367705C=CA2466658981FLNAc.656G= (p.Ser219=)
c.575G= (p.Ser192=)
c.614G= (p.Ser205=)
Xg.154367705C>GCA415248875FLNAc.656G>C (p.Ser219Thr)
c.575G>C (p.Ser192Thr)
c.614G>C (p.Ser205Thr)
 dbSNP
Xg.154367705C>TCA415248876FLNAc.656G>A (p.Ser219Asn)
c.575G>A (p.Ser192Asn)
c.614G>A (p.Ser205Asn)
 gnomAD v4
Xg.154367706T>ACA415248877FLNAc.655A>T (p.Ser219Cys)
c.574A>T (p.Ser192Cys)
c.613A>T (p.Ser205Cys)
Xg.154367706T>CCA415248878FLNAc.655A>G (p.Ser219Gly)
c.574A>G (p.Ser192Gly)
c.613A>G (p.Ser205Gly)
Xg.154367706T>GCA415248879FLNAc.655A>C (p.Ser219Arg)
c.574A>C (p.Ser192Arg)
c.613A>C (p.Ser205Arg)
Xg.154367707G>ACA519709653FLNAc.654C>T (p.Ala218=)
c.573C>T (p.Ala191=)
c.612C>T (p.Ala204=)
Xg.154367707G>CCA519709654FLNAc.654C>G (p.Ala218=)
c.573C>G (p.Ala191=)
c.612C>G (p.Ala204=)
 dbSNP gnomAD v2 gnomAD v4
Xg.154367707G=CA2466658982FLNAc.654C= (p.Ala218=)
c.573C= (p.Ala191=)
c.612C= (p.Ala204=)
Xg.154367707G>TCA519709655FLNAc.654C>A (p.Ala218=)
c.573C>A (p.Ala191=)
c.612C>A (p.Ala204=)
Xg.154367708G>ACA415248880FLNAc.653C>T (p.Ala218Val)
c.572C>T (p.Ala191Val)
c.611C>T (p.Ala204Val)
Xg.154367708G>CCA415248881FLNAc.653C>G (p.Ala218Gly)
c.572C>G (p.Ala191Gly)
c.611C>G (p.Ala204Gly)
Xg.154367708G>TCA415248882FLNAc.653C>A (p.Ala218Asp)
c.572C>A (p.Ala191Asp)
c.611C>A (p.Ala204Asp)
Xg.154367709C>ACA415248883FLNAc.652G>T (p.Ala218Ser)
c.571G>T (p.Ala191Ser)
c.610G>T (p.Ala204Ser)
 dbSNP gnomAD v2
Xg.154367709C=CA2466658983FLNAc.652G= (p.Ala218=)
c.571G= (p.Ala191=)
c.610G= (p.Ala204=)
Xg.154367709C>GCA415248884FLNAc.652G>C (p.Ala218Pro)
c.571G>C (p.Ala191Pro)
c.610G>C (p.Ala204Pro)
 gnomAD v4
Xg.154367709C>TCA10561381FLNAc.652G>A (p.Ala218Thr)
c.571G>A (p.Ala191Thr)
c.610G>A (p.Ala204Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367710G>ACA10561382FLNAc.651C>T (p.Asp217=)
c.570C>T (p.Asp190=)
c.609C>T (p.Asp203=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367710G>CCA415248885FLNAc.651C>G (p.Asp217Glu)
c.570C>G (p.Asp190Glu)
c.609C>G (p.Asp203Glu)
Xg.154367710G=CA2466658984FLNAc.651C= (p.Asp217=)
c.570C= (p.Asp190=)
c.609C= (p.Asp203=)
Xg.154367710G>TCA415248886FLNAc.651C>A (p.Asp217Glu)
c.570C>A (p.Asp190Glu)
c.609C>A (p.Asp203Glu)
Xg.154367711T>ACA415248887FLNAc.650A>T (p.Asp217Val)
c.569A>T (p.Asp190Val)
c.608A>T (p.Asp203Val)
Xg.154367711T>CCA415248888FLNAc.650A>G (p.Asp217Gly)
c.569A>G (p.Asp190Gly)
c.608A>G (p.Asp203Gly)
Xg.154367711T>GCA415248889FLNAc.650A>C (p.Asp217Ala)
c.569A>C (p.Asp190Ala)
c.608A>C (p.Asp203Ala)
Xg.154367712C>ACA415248890FLNAc.649G>T (p.Asp217Tyr)
c.568G>T (p.Asp190Tyr)
c.607G>T (p.Asp203Tyr)
Xg.154367712C=CA2466658985FLNAc.649G= (p.Asp217=)
c.568G= (p.Asp190=)
c.607G= (p.Asp203=)
Xg.154367712C>GCA415248891FLNAc.649G>C (p.Asp217His)
c.568G>C (p.Asp190His)
c.607G>C (p.Asp203His)
Xg.154367712C>TCA415248892FLNAc.649G>A (p.Asp217Asn)
c.568G>A (p.Asp190Asn)
c.607G>A (p.Asp203Asn)
 dbSNP gnomAD v2 gnomAD v4
Xg.154367714delCA2579738362FLNAc.649del (p.Asp217ThrfsTer25)
c.568del (p.Asp190ThrfsTer25)
c.607del (p.Asp203ThrfsTer25)
Xg.154367713C>ACA415248894FLNAc.648G>T (p.Trp216Cys)
c.567G>T (p.Trp189Cys)
c.606G>T (p.Trp202Cys)
Xg.154367713C>GCA415248895FLNAc.648G>C (p.Trp216Cys)
c.567G>C (p.Trp189Cys)
c.606G>C (p.Trp202Cys)
Xg.154367713C>TCA415248893FLNAc.648G>A (p.Trp216Ter)
c.567G>A (p.Trp189Ter)
c.606G>A (p.Trp202Ter)
Xg.154367714C>ACA415248896FLNAc.647G>T (p.Trp216Leu)
c.566G>T (p.Trp189Leu)
c.605G>T (p.Trp202Leu)
Xg.154367714C>GCA415248897FLNAc.647G>C (p.Trp216Ser)
c.566G>C (p.Trp189Ser)
c.605G>C (p.Trp202Ser)
Xg.154367714C>TCA415248898FLNAc.647G>A (p.Trp216Ter)
c.566G>A (p.Trp189Ter)
c.605G>A (p.Trp202Ter)
Xg.154367715A>CCA415248899FLNAc.646T>G (p.Trp216Gly)
c.565T>G (p.Trp189Gly)
c.604T>G (p.Trp202Gly)
Xg.154367715A>GCA415248900FLNAc.646T>C (p.Trp216Arg)
c.565T>C (p.Trp189Arg)
c.604T>C (p.Trp202Arg)
Xg.154367715A>TCA415248901FLNAc.646T>A (p.Trp216Arg)
c.565T>A (p.Trp189Arg)
c.604T>A (p.Trp202Arg)
Xg.154367716A=CA2466658986FLNAc.645T= (p.Ser215=)
c.564T= (p.Ser188=)
c.603T= (p.Ser201=)
Xg.154367716A>CCA519709685FLNAc.645T>G (p.Ser215=)
c.564T>G (p.Ser188=)
c.603T>G (p.Ser201=)
Xg.154367716A>GCA519709686FLNAc.645T>C (p.Ser215=)
c.564T>C (p.Ser188=)
c.603T>C (p.Ser201=)
 dbSNP
Xg.154367716A>TCA519709687FLNAc.645T>A (p.Ser215=)
c.564T>A (p.Ser188=)
c.603T>A (p.Ser201=)
 dbSNP
Xg.154367717G>ACA415248902FLNAc.644C>T (p.Ser215Phe)
c.563C>T (p.Ser188Phe)
c.602C>T (p.Ser201Phe)
Xg.154367717G>CCA415248903FLNAc.644C>G (p.Ser215Cys)
c.563C>G (p.Ser188Cys)
c.602C>G (p.Ser201Cys)
Xg.154367717G=CA2466658987FLNAc.644C= (p.Ser215=)
c.563C= (p.Ser188=)
c.602C= (p.Ser201=)
Xg.154367717G>TCA415248904FLNAc.644C>A (p.Ser215Tyr)
c.563C>A (p.Ser188Tyr)
c.602C>A (p.Ser201Tyr)
 dbSNP
Xg.154367718A>CCA415248905FLNAc.643T>G (p.Ser215Ala)
c.562T>G (p.Ser188Ala)
c.601T>G (p.Ser201Ala)
Xg.154367718A>GCA415248906FLNAc.643T>C (p.Ser215Pro)
c.562T>C (p.Ser188Pro)
c.601T>C (p.Ser201Pro)
Xg.154367718A>TCA415248907FLNAc.643T>A (p.Ser215Thr)
c.562T>A (p.Ser188Thr)
c.601T>A (p.Ser201Thr)
Xg.154367719G>ACA519709698FLNAc.642C>T (p.Asp214=)
c.561C>T (p.Asp187=)
c.600C>T (p.Asp200=)
Xg.154367719G>CCA415248908FLNAc.642C>G (p.Asp214Glu)
c.561C>G (p.Asp187Glu)
c.600C>G (p.Asp200Glu)
Xg.154367719G>TCA415248909FLNAc.642C>A (p.Asp214Glu)
c.561C>A (p.Asp187Glu)
c.600C>A (p.Asp200Glu)
Xg.154367720T>ACA415248910FLNAc.641A>T (p.Asp214Val)
c.560A>T (p.Asp187Val)
c.599A>T (p.Asp200Val)
Xg.154367720T>CCA415248911FLNAc.641A>G (p.Asp214Gly)
c.560A>G (p.Asp187Gly)
c.599A>G (p.Asp200Gly)
 ClinVar dbSNP
Xg.154367720T>GCA415248912FLNAc.641A>C (p.Asp214Ala)
c.560A>C (p.Asp187Ala)
c.599A>C (p.Asp200Ala)
Xg.154367721C>ACA415248913FLNAc.640G>T (p.Asp214Tyr)
c.559G>T (p.Asp187Tyr)
c.598G>T (p.Asp200Tyr)
Xg.154367721C>GCA415248914FLNAc.640G>C (p.Asp214His)
c.559G>C (p.Asp187His)
c.598G>C (p.Asp200His)
Xg.154367721C>TCA415248915FLNAc.640G>A (p.Asp214Asn)
c.559G>A (p.Asp187Asn)
c.598G>A (p.Asp200Asn)
Xg.154367722C>ACA415248916FLNAc.639G>T (p.Trp213Cys)
c.558G>T (p.Trp186Cys)
c.597G>T (p.Trp199Cys)
Xg.154367722C>GCA415248917FLNAc.639G>C (p.Trp213Cys)
c.558G>C (p.Trp186Cys)
c.597G>C (p.Trp199Cys)
Xg.154367722C>TCA415248918FLNAc.639G>A (p.Trp213Ter)
c.558G>A (p.Trp186Ter)
c.597G>A (p.Trp199Ter)
Xg.154367723C>ACA415248919FLNAc.638G>T (p.Trp213Leu)
c.557G>T (p.Trp186Leu)
c.596G>T (p.Trp199Leu)
Xg.154367723C>GCA415248920FLNAc.638G>C (p.Trp213Ser)
c.557G>C (p.Trp186Ser)
c.596G>C (p.Trp199Ser)
Xg.154367723C>TCA415248921FLNAc.638G>A (p.Trp213Ter)
c.557G>A (p.Trp186Ter)
c.596G>A (p.Trp199Ter)
Xg.154367724A>CCA415248923FLNAc.637T>G (p.Trp213Gly)
c.556T>G (p.Trp186Gly)
c.595T>G (p.Trp199Gly)
Xg.154367724A>GCA415248924FLNAc.637T>C (p.Trp213Arg)
c.556T>C (p.Trp186Arg)
c.595T>C (p.Trp199Arg)
Xg.154367724A>TCA415248922FLNAc.637T>A (p.Trp213Arg)
c.556T>A (p.Trp186Arg)
c.595T>A (p.Trp199Arg)
Xg.154367725G>ACA519709710FLNAc.636C>T (p.Asp212=)
c.555C>T (p.Asp185=)
c.594C>T (p.Asp198=)
 gnomAD v4
Xg.154367725G>CCA415248925FLNAc.636C>G (p.Asp212Glu)
c.555C>G (p.Asp185Glu)
c.594C>G (p.Asp198Glu)
Xg.154367725G>TCA415248926FLNAc.636C>A (p.Asp212Glu)
c.555C>A (p.Asp185Glu)
c.594C>A (p.Asp198Glu)
 gnomAD v4
Xg.154367726T>ACA415248927FLNAc.635A>T (p.Asp212Val)
c.554A>T (p.Asp185Val)
c.593A>T (p.Asp198Val)
Xg.154367726T>CCA415248928FLNAc.635A>G (p.Asp212Gly)
c.554A>G (p.Asp185Gly)
c.593A>G (p.Asp198Gly)
Xg.154367726T>GCA415248929FLNAc.635A>C (p.Asp212Ala)
c.554A>C (p.Asp185Ala)
c.593A>C (p.Asp198Ala)
Xg.154367727C>ACA415248930FLNAc.634G>T (p.Asp212Tyr)
c.553G>T (p.Asp185Tyr)
c.592G>T (p.Asp198Tyr)
Xg.154367727C>GCA415248931FLNAc.634G>C (p.Asp212His)
c.553G>C (p.Asp185His)
c.592G>C (p.Asp198His)
 gnomAD v4
Xg.154367727C>TCA415248932FLNAc.634G>A (p.Asp212Asn)
c.553G>A (p.Asp185Asn)
c.592G>A (p.Asp198Asn)
Xg.154367728A>CCA519709727FLNAc.633T>G (p.Pro211=)
c.552T>G (p.Pro184=)
c.591T>G (p.Pro197=)
Xg.154367728A>GCA519709723FLNAc.633T>C (p.Pro211=)
c.552T>C (p.Pro184=)
c.591T>C (p.Pro197=)
Xg.154367728A>TCA519709725FLNAc.633T>A (p.Pro211=)
c.552T>A (p.Pro184=)
c.591T>A (p.Pro197=)
Xg.154367729G>ACA415248933FLNAc.632C>T (p.Pro211Leu)
c.551C>T (p.Pro184Leu)
c.590C>T (p.Pro197Leu)
Xg.154367729G>CCA16043290FLNAc.632C>G (p.Pro211Arg)
c.551C>G (p.Pro184Arg)
c.590C>G (p.Pro197Arg)
 ClinVar dbSNP
Xg.154367729G=CA2466658988FLNAc.632C= (p.Pro211=)
c.551C= (p.Pro184=)
c.590C= (p.Pro197=)
Xg.154367729G>TCA415248934FLNAc.632C>A (p.Pro211His)
c.551C>A (p.Pro184His)
c.590C>A (p.Pro197His)
Xg.154367730G>ACA415248935FLNAc.631C>T (p.Pro211Ser)
c.550C>T (p.Pro184Ser)
c.589C>T (p.Pro197Ser)
Xg.154367730G>CCA415248936FLNAc.631C>G (p.Pro211Ala)
c.550C>G (p.Pro184Ala)
c.589C>G (p.Pro197Ala)
Xg.154367730G>TCA415248937FLNAc.631C>A (p.Pro211Thr)
c.550C>A (p.Pro184Thr)
c.589C>A (p.Pro197Thr)
Xg.154367731A>CCA415248938FLNAc.630T>G (p.Cys210Trp)
c.549T>G (p.Cys183Trp)
c.588T>G (p.Cys196Trp)
Xg.154367731A>GCA519709740FLNAc.630T>C (p.Cys210=)
c.549T>C (p.Cys183=)
c.588T>C (p.Cys196=)
Xg.154367731A>TCA415248939FLNAc.630T>A (p.Cys210Ter)
c.549T>A (p.Cys183Ter)
c.588T>A (p.Cys196Ter)
Xg.154367734_154367735delCA2695236982FLNAc.629_630del (p.Cys210SerfsTer2)
c.548_549del (p.Cys183SerfsTer2)
c.587_588del (p.Cys196SerfsTer2)
Xg.154367732C>ACA256064FLNAc.629G>T (p.Cys210Phe)
c.548G>T (p.Cys183Phe)
c.587G>T (p.Cys196Phe)
 ClinVar dbSNP
Xg.154367732C=CA2466658989FLNAc.629G= (p.Cys210=)
c.548G= (p.Cys183=)
c.587G= (p.Cys196=)
Xg.154367732C>GCA415248940FLNAc.629G>C (p.Cys210Ser)
c.548G>C (p.Cys183Ser)
c.587G>C (p.Cys196Ser)
Xg.154367732C>TCA415248941FLNAc.629G>A (p.Cys210Tyr)
c.548G>A (p.Cys183Tyr)
c.587G>A (p.Cys196Tyr)
Xg.154367733A>CCA415248942FLNAc.628T>G (p.Cys210Gly)
c.547T>G (p.Cys183Gly)
c.586T>G (p.Cys196Gly)
Xg.154367733A>GCA415248943FLNAc.628T>C (p.Cys210Arg)
c.547T>C (p.Cys183Arg)
c.586T>C (p.Cys196Arg)
Xg.154367733A>TCA415248944FLNAc.628T>A (p.Cys210Ser)
c.547T>A (p.Cys183Ser)
c.586T>A (p.Cys196Ser)
Xg.154367734C>ACA519709749FLNAc.627G>T (p.Leu209=)
c.546G>T (p.Leu182=)
c.585G>T (p.Leu195=)
Xg.154367734C=CA2466658990FLNAc.627G= (p.Leu209=)
c.546G= (p.Leu182=)
c.585G= (p.Leu195=)
Xg.154367734C>GCA519709750FLNAc.627G>C (p.Leu209=)
c.546G>C (p.Leu182=)
c.585G>C (p.Leu195=)
Xg.154367734C>TCA10561383FLNAc.627G>A (p.Leu209=)
c.546G>A (p.Leu182=)
c.585G>A (p.Leu195=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367735A>CCA415248945FLNAc.626T>G (p.Leu209Arg)
c.545T>G (p.Leu182Arg)
c.584T>G (p.Leu195Arg)
Xg.154367735A>GCA415248946FLNAc.626T>C (p.Leu209Pro)
c.545T>C (p.Leu182Pro)
c.584T>C (p.Leu195Pro)
Xg.154367735A>TCA415248947FLNAc.626T>A (p.Leu209Gln)
c.545T>A (p.Leu182Gln)
c.584T>A (p.Leu195Gln)
Xg.154367736G>ACA519709758FLNAc.625C>T (p.Leu209=)
c.544C>T (p.Leu182=)
c.583C>T (p.Leu195=)
Xg.154367736G>CCA415248948FLNAc.625C>G (p.Leu209Val)
c.544C>G (p.Leu182Val)
c.583C>G (p.Leu195Val)
Xg.154367736G>TCA415248949FLNAc.625C>A (p.Leu209Met)
c.544C>A (p.Leu182Met)
c.583C>A (p.Leu195Met)
Xg.154367737G>ACA519709765FLNAc.624C>T (p.Gly208=)
c.543C>T (p.Gly181=)
c.582C>T (p.Gly194=)
Xg.154367737G>CCA519709766FLNAc.624C>G (p.Gly208=)
c.543C>G (p.Gly181=)
c.582C>G (p.Gly194=)
Xg.154367737G>TCA519709770FLNAc.624C>A (p.Gly208=)
c.543C>A (p.Gly181=)
c.582C>A (p.Gly194=)
Xg.154367738C>ACA415248950FLNAc.623G>T (p.Gly208Val)
c.542G>T (p.Gly181Val)
c.581G>T (p.Gly194Val)
Xg.154367738C>GCA415248952FLNAc.623G>C (p.Gly208Ala)
c.542G>C (p.Gly181Ala)
c.581G>C (p.Gly194Ala)
Xg.154367738C>TCA415248951FLNAc.623G>A (p.Gly208Asp)
c.542G>A (p.Gly181Asp)
c.581G>A (p.Gly194Asp)
Xg.154367740_154367842delCA519709779FLNAc.622+2_623del
c.541+2_542del
c.580+2_581del
Xg.154367739C>ACA415248953FLNAc.623-1G>T (n.623-1G>T)
c.542-1G>T (n.542-1G>T)
c.581-1G>T (n.581-1G>T)
Xg.154367739C>GCA415248954FLNAc.623-1G>C (n.623-1G>C)
c.542-1G>C (n.542-1G>C)
c.581-1G>C (n.581-1G>C)
Xg.154367739C>TCA415248955FLNAc.623-1G>A (n.623-1G>A)
c.542-1G>A (n.542-1G>A)
c.581-1G>A (n.581-1G>A)
Xg.154367740T>ACA415248956FLNAc.623-2A>T (n.623-2A>T)
c.542-2A>T (n.542-2A>T)
c.581-2A>T (n.581-2A>T)
Xg.154367740T>CCA337284275FLNAc.623-2A>G (n.623-2A>G)
c.542-2A>G (n.542-2A>G)
c.581-2A>G (n.581-2A>G)
 ClinVar dbSNP
Xg.154367740T>GCA415248957FLNAc.623-2A>C (n.623-2A>C)
c.542-2A>C (n.542-2A>C)
c.581-2A>C (n.581-2A>C)
Xg.154367740T=CA2466658991FLNAc.623-2A= (n.623-2A=)
c.542-2A= (n.542-2A=)
c.581-2A= (n.581-2A=)
Xg.154367741G>CCA221727FLNAc.623-3C>G (n.623-3C>G)
c.542-3C>G (n.542-3C>G)
c.581-3C>G (n.581-3C>G)
 ClinVar dbSNP
Xg.154367741G=CA2466658992FLNAc.623-3C= (n.623-3C=)
c.542-3C= (n.542-3C=)
c.581-3C= (n.581-3C=)
Xg.154367743G>ACA337284290FLNAc.623-5C>T (n.623-5C>T)
c.542-5C>T (n.542-5C>T)
c.581-5C>T (n.581-5C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367743G=CA2466658993FLNAc.623-5C= (n.623-5C=)
c.542-5C= (n.542-5C=)
c.581-5C= (n.581-5C=)
Xg.154367745C=CA2466658994FLNAc.623-7G= (n.623-7G=)
c.542-7G= (n.542-7G=)
c.581-7G= (n.581-7G=)
Xg.154367745C>GCA2573159435FLNAc.623-7G>C (n.623-7G>C)
c.542-7G>C (n.542-7G>C)
c.581-7G>C (n.581-7G>C)
 ClinVar dbSNP gnomAD v4
Xg.154367745C>TCA245194FLNAc.623-7G>A (n.623-7G>A)
c.542-7G>A (n.542-7G>A)
c.581-7G>A (n.581-7G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154367746G>ACA645290446FLNAc.623-8C>T (n.623-8C>T)
c.542-8C>T (n.542-8C>T)
c.581-8C>T (n.581-8C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367746G>CCA337284299FLNAc.623-8C>G (n.623-8C>G)
c.542-8C>G (n.542-8C>G)
c.581-8C>G (n.581-8C>G)
 dbSNP
Xg.154367746G=CA2466658995FLNAc.623-8C= (n.623-8C=)
c.542-8C= (n.542-8C=)
c.581-8C= (n.581-8C=)
Xg.154367746G>TCA1139667849FLNAc.623-8C>A (n.623-8C>A)
c.542-8C>A (n.542-8C>A)
c.581-8C>A (n.581-8C>A)
 ClinVar dbSNP
Xg.154367747C>GCA2695082980FLNAc.623-9G>C (n.623-9G>C)
c.542-9G>C (n.542-9G>C)
c.581-9G>C (n.581-9G>C)
 gnomAD v4
Xg.154367748A=CA2466658997FLNAc.623-10T= (n.623-10T=)
c.542-10T= (n.542-10T=)
c.581-10T= (n.581-10T=)
Xg.154367748A>TCA2466658996FLNAc.623-10T>A (n.623-10T>A)
c.542-10T>A (n.542-10T>A)
c.581-10T>A (n.581-10T>A)
 ClinVar dbSNP
Xg.154367749A>CCA2824282192FLNAc.623-11T>G (n.623-11T>G)
c.542-11T>G (n.542-11T>G)
c.581-11T>G (n.581-11T>G)
Xg.154367749_154367758delinsAGGGAGGCTGCA2466658998FLNAc.623-20_623-11delinsCAGCCTCCCT (n.623-20_623-11delinsCAGCCTCCCT)
c.542-20_542-11delinsCAGCCTCCCT (n.542-20_542-11delinsCAGCCTCCCT)
c.581-20_581-11delinsCAGCCTCCCT (n.581-20_581-11delinsCAGCCTCCCT)
Xg.154367750G>ACA2573159436FLNAc.623-12C>T (n.623-12C>T)
c.542-12C>T (n.542-12C>T)
c.581-12C>T (n.581-12C>T)
 ClinVar dbSNP
Xg.154367750G>CCA2695082981FLNAc.623-12C>G (n.623-12C>G)
c.542-12C>G (n.542-12C>G)
c.581-12C>G (n.581-12C>G)
 gnomAD v4
Xg.154367750_154367758delCA274745FLNAc.623-20_623-12del (n.623-20_623-12del)
c.542-20_542-12del (n.542-20_542-12del)
c.581-20_581-12del (n.581-20_581-12del)
 ClinVar dbSNP
Xg.154367754G>ACA2695082982FLNAc.623-16C>T (n.623-16C>T)
c.542-16C>T (n.542-16C>T)
c.581-16C>T (n.581-16C>T)
 gnomAD v4
Xg.154367756_154367758delinsCTGCA2466658999FLNAc.623-20_623-18delinsCAG (n.623-20_623-18delinsCAG)
c.542-20_542-18delinsCAG (n.542-20_542-18delinsCAG)
c.581-20_581-18delinsCAG (n.581-20_581-18delinsCAG)
Xg.154367759_154367760delCA2466659000FLNAc.623-20_623-19del (n.623-20_623-19del)
c.542-20_542-19del (n.542-20_542-19del)
c.581-20_581-19del (n.581-20_581-19del)
 dbSNP
Xg.154367760G>ACA2466659002FLNAc.623-22C>T (n.623-22C>T)
c.542-22C>T (n.542-22C>T)
c.581-22C>T (n.581-22C>T)
 dbSNP
Xg.154367760G=CA2466659001FLNAc.623-22C= (n.623-22C=)
c.542-22C= (n.542-22C=)
c.581-22C= (n.581-22C=)
Xg.154367762G>ACA2695082983FLNAc.623-24C>T (n.623-24C>T)
c.542-24C>T (n.542-24C>T)
c.581-24C>T (n.581-24C>T)
 gnomAD v4
Xg.154367763T>ACA10561384FLNAc.623-25A>T (n.623-25A>T)
c.542-25A>T (n.542-25A>T)
c.581-25A>T (n.581-25A>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154367763T=CA2466659003FLNAc.623-25A= (n.623-25A=)
c.542-25A= (n.542-25A=)
c.581-25A= (n.581-25A=)
Xg.154367766G>CCA1138571931FLNAc.623-28C>G (n.623-28C>G)
c.542-28C>G (n.542-28C>G)
c.581-28C>G (n.581-28C>G)
 dbSNP gnomAD v3 gnomAD v4
Xg.154367766G=CA2466659004FLNAc.623-28C= (n.623-28C=)
c.542-28C= (n.542-28C=)
c.581-28C= (n.581-28C=)
Xg.154367770delCA2579738363FLNAc.623-28del (n.623-28del)
c.542-28del (n.542-28del)
c.581-28del (n.581-28del)
 gnomAD v4
Xg.154367767G>ACA2695082984FLNAc.623-29C>T (n.623-29C>T)
c.542-29C>T (n.542-29C>T)
c.581-29C>T (n.581-29C>T)
 gnomAD v4
Xg.154367768G>CCA2695082985FLNAc.623-30C>G (n.623-30C>G)
c.542-30C>G (n.542-30C>G)
c.581-30C>G (n.581-30C>G)
 gnomAD v4
Xg.154367769G>ACA873345202FLNAc.623-31C>T (n.623-31C>T)
c.542-31C>T (n.542-31C>T)
c.581-31C>T (n.581-31C>T)
 dbSNP gnomAD v3 gnomAD v4
Xg.154367769G=CA2466659005FLNAc.623-31C= (n.623-31C=)
c.542-31C= (n.542-31C=)
c.581-31C= (n.581-31C=)
Xg.154367770G=CA2466659007FLNAc.623-32C= (n.623-32C=)
c.542-32C= (n.542-32C=)
c.581-32C= (n.581-32C=)
Xg.154367770G>TCA645290447FLNAc.623-32C>A (n.623-32C>A)
c.542-32C>A (n.542-32C>A)
c.581-32C>A (n.581-32C>A)
 dbSNP gnomAD v2 gnomAD v4
Xg.154367770_154367771delinsGCCA2466659006FLNAc.623-33_623-32delinsGC (n.623-33_623-32delinsGC)
c.542-33_542-32delinsGC (n.542-33_542-32delinsGC)
c.581-33_581-32delinsGC (n.581-33_581-32delinsGC)
Xg.154367772delCA645290448FLNAc.623-33del (n.623-33del)
c.542-33del (n.542-33del)
c.581-33del (n.581-33del)
 dbSNP gnomAD v2 gnomAD v4
Xg.154367772C=CA2466659008FLNAc.623-34G= (n.623-34G=)
c.542-34G= (n.542-34G=)
c.581-34G= (n.581-34G=)
Xg.154367772C>TCA10561385FLNAc.623-34G>A (n.623-34G>A)
c.542-34G>A (n.542-34G>A)
c.581-34G>A (n.581-34G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367773G>ACA10561386FLNAc.623-35C>T (n.623-35C>T)
c.542-35C>T (n.542-35C>T)
c.581-35C>T (n.581-35C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154367773G>CCA645290449FLNAc.623-35C>G (n.623-35C>G)
c.542-35C>G (n.542-35C>G)
c.581-35C>G (n.581-35C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367773G=CA2466659009FLNAc.623-35C= (n.623-35C=)
c.542-35C= (n.542-35C=)
c.581-35C= (n.581-35C=)
Xg.154367774C=CA2466659010FLNAc.623-36G= (n.623-36G=)
c.542-36G= (n.542-36G=)
c.581-36G= (n.581-36G=)
Xg.154367774C>TCA2466659011FLNAc.623-36G>A (n.623-36G>A)
c.542-36G>A (n.542-36G>A)
c.581-36G>A (n.581-36G>A)
 dbSNP gnomAD v3 gnomAD v4
Xg.154367775A=CA2466659012FLNAc.623-37T= (n.623-37T=)
c.542-37T= (n.542-37T=)
c.581-37T= (n.581-37T=)
Xg.154367775A>CCA2695082986FLNAc.623-37T>G (n.623-37T>G)
c.542-37T>G (n.542-37T>G)
c.581-37T>G (n.581-37T>G)
 gnomAD v4
Xg.154367775A>GCA873345209FLNAc.623-37T>C (n.623-37T>C)
c.542-37T>C (n.542-37T>C)
c.581-37T>C (n.581-37T>C)
 dbSNP gnomAD v4
Xg.154367779C>ACA645290450FLNAc.623-41G>T (n.623-41G>T)
c.542-41G>T (n.542-41G>T)
c.581-41G>T (n.581-41G>T)
 dbSNP gnomAD v2 gnomAD v4
Xg.154367779C=CA2466659013FLNAc.623-41G= (n.623-41G=)
c.542-41G= (n.542-41G=)
c.581-41G= (n.581-41G=)
Xg.154367779C>GCA645290451FLNAc.623-41G>C (n.623-41G>C)
c.542-41G>C (n.542-41G>C)
c.581-41G>C (n.581-41G>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367779C>TCA10561387FLNAc.623-41G>A (n.623-41G>A)
c.542-41G>A (n.542-41G>A)
c.581-41G>A (n.581-41G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154367780C>TCA2695082987FLNAc.623-42G>A (n.623-42G>A)
c.542-42G>A (n.542-42G>A)
c.581-42G>A (n.581-42G>A)
 gnomAD v4
Xg.154367781C>TCA2558130291FLNAc.623-43G>A (n.623-43G>A)
c.542-43G>A (n.542-43G>A)
c.581-43G>A (n.581-43G>A)
 gnomAD v4
Xg.154367783C>GCA2503638722FLNAc.623-45G>C (n.623-45G>C)
c.542-45G>C (n.542-45G>C)
c.581-45G>C (n.581-45G>C)
 gnomAD v4
Xg.154367784T>GCA2579738364FLNAc.623-46A>C (n.623-46A>C)
c.542-46A>C (n.542-46A>C)
c.581-46A>C (n.581-46A>C)
Xg.154367787A=CA2466659014FLNAc.623-49T= (n.623-49T=)
c.542-49T= (n.542-49T=)
c.581-49T= (n.581-49T=)
Xg.154367787A>GCA10561388FLNAc.623-49T>C (n.623-49T>C)
c.542-49T>C (n.542-49T>C)
c.581-49T>C (n.581-49T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367788G>ACA873345212FLNAc.623-50C>T (n.623-50C>T)
c.542-50C>T (n.542-50C>T)
c.581-50C>T (n.581-50C>T)
 dbSNP gnomAD v3 gnomAD v4
Xg.154367788G=CA2466659015FLNAc.623-50C= (n.623-50C=)
c.542-50C= (n.542-50C=)
c.581-50C= (n.581-50C=)
Xg.154367789G>ACA2579738365FLNAc.623-51C>T (n.623-51C>T)
c.542-51C>T (n.542-51C>T)
c.581-51C>T (n.581-51C>T)
 gnomAD v4
Xg.154367789G>TCA2503392806FLNAc.623-51C>A (n.623-51C>A)
c.542-51C>A (n.542-51C>A)
c.581-51C>A (n.581-51C>A)
Xg.154367790G>ACA2824282208FLNAc.623-52C>T (n.623-52C>T)
c.542-52C>T (n.542-52C>T)
c.581-52C>T (n.581-52C>T)
Xg.154367791C>TCA2579738366FLNAc.622+51G>A (n.622+51G>A)
c.541+51G>A (n.541+51G>A)
c.580+51G>A (n.580+51G>A)
Xg.154367792C>ACA2695082988FLNAc.622+50G>T (n.622+50G>T)
c.541+50G>T (n.541+50G>T)
c.580+50G>T (n.580+50G>T)
 gnomAD v4
Xg.154367795C=CA2466659016FLNAc.622+47G= (n.622+47G=)
c.541+47G= (n.541+47G=)
c.580+47G= (n.580+47G=)
Xg.154367796C>TCA2529390332FLNAc.622+46G>A (n.622+46G>A)
c.541+46G>A (n.541+46G>A)
c.580+46G>A (n.580+46G>A)
Xg.154367796_154367797insTCCA10561389FLNAc.622+46_622+47insAG (n.622+46_622+47insAG)
c.541+46_541+47insAG (n.541+46_541+47insAG)
c.580+46_580+47insAG (n.580+46_580+47insAG)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367797A=CA2466659017FLNAc.622+45T= (n.622+45T=)
c.541+45T= (n.541+45T=)
c.580+45T= (n.580+45T=)
Xg.154367797A>GCA915938875FLNAc.622+45T>C (n.622+45T>C)
c.541+45T>C (n.541+45T>C)
c.580+45T>C (n.580+45T>C)
 dbSNP gnomAD v2
Xg.154367798T>ACA10561390FLNAc.622+44A>T (n.622+44A>T)
c.541+44A>T (n.541+44A>T)
c.580+44A>T (n.580+44A>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367798T>GCA2824282211FLNAc.622+44A>C (n.622+44A>C)
c.541+44A>C (n.541+44A>C)
c.580+44A>C (n.580+44A>C)
Xg.154367798T=CA2466659018FLNAc.622+44A= (n.622+44A=)
c.541+44A= (n.541+44A=)
c.580+44A= (n.580+44A=)
Xg.154367799G=CA2466659019FLNAc.622+43C= (n.622+43C=)
c.541+43C= (n.541+43C=)
c.580+43C= (n.580+43C=)
Xg.154367799G>TCA10561391FLNAc.622+43C>A (n.622+43C>A)
c.541+43C>A (n.541+43C>A)
c.580+43C>A (n.580+43C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154367800G>ACA10561392FLNAc.622+42C>T (n.622+42C>T)
c.541+42C>T (n.541+42C>T)
c.580+42C>T (n.580+42C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
Xg.154367800G=CA2466659020FLNAc.622+42C= (n.622+42C=)
c.541+42C= (n.541+42C=)
c.580+42C= (n.580+42C=)
Xg.154367801G>ACA2695082989FLNAc.622+41C>T (n.622+41C>T)
c.541+41C>T (n.541+41C>T)
c.580+41C>T (n.580+41C>T)
 dbSNP gnomAD v4
Xg.154367802T>ACA645290452FLNAc.622+40A>T (n.622+40A>T)
c.541+40A>T (n.541+40A>T)
c.580+40A>T (n.580+40A>T)
 dbSNP gnomAD v2 gnomAD v4
Xg.154367802T=CA2466659021FLNAc.622+40A= (n.622+40A=)
c.541+40A= (n.541+40A=)
c.580+40A= (n.580+40A=)
Xg.154367803G>TCA2695082990FLNAc.622+39C>A (n.622+39C>A)
c.541+39C>A (n.541+39C>A)
c.580+39C>A (n.580+39C>A)
 gnomAD v4
Xg.154367804A>GCA2533405665FLNAc.622+38T>C (n.622+38T>C)
c.541+38T>C (n.541+38T>C)
c.580+38T>C (n.580+38T>C)

Number of alleles fetched