Chr Mutation (hg38) CAid Gene Transcript Linkouts
Xg.154367548_154367643delCA2824282109FLNAc.720+3_722del
c.639+3_641del
c.678+3_680del
Xg.154367628C=CA2466658951FLNAc.720+13G= (n.720+13G=)
c.639+13G= (n.639+13G=)
c.678+13G= (n.678+13G=)
Xg.154367628C>TCA10561375FLNAc.720+13G>A (n.720+13G>A)
c.639+13G>A (n.639+13G>A)
c.678+13G>A (n.678+13G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367629G>ACA10561376FLNAc.720+12C>T (n.720+12C>T)
c.639+12C>T (n.639+12C>T)
c.678+12C>T (n.678+12C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367629G=CA2466658952FLNAc.720+12C= (n.720+12C=)
c.639+12C= (n.639+12C=)
c.678+12C= (n.678+12C=)
Xg.154367631dupCA2695082969FLNAc.720+12dup (n.720+12dup)
c.639+12dup (n.639+12dup)
c.678+12dup (n.678+12dup)
 gnomAD v4
Xg.154367630G>ACA2466658954FLNAc.720+11C>T (n.720+11C>T)
c.639+11C>T (n.639+11C>T)
c.678+11C>T (n.678+11C>T)
 dbSNP gnomAD v4
Xg.154367630G=CA2466658953FLNAc.720+11C= (n.720+11C=)
c.639+11C= (n.639+11C=)
c.678+11C= (n.678+11C=)
Xg.154367631G>ACA337284220FLNAc.720+10C>T (n.720+10C>T)
c.639+10C>T (n.639+10C>T)
c.678+10C>T (n.678+10C>T)
 dbSNP gnomAD v3 gnomAD v4
Xg.154367631G=CA2466658955FLNAc.720+10C= (n.720+10C=)
c.639+10C= (n.639+10C=)
c.678+10C= (n.678+10C=)
Xg.154367632C>ACA10561378FLNAc.720+9G>T (n.720+9G>T)
c.639+9G>T (n.639+9G>T)
c.678+9G>T (n.678+9G>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC
Xg.154367632C=CA2466658956FLNAc.720+9G= (n.720+9G=)
c.639+9G= (n.639+9G=)
c.678+9G= (n.678+9G=)
Xg.154367632C>TCA10561377FLNAc.720+9G>A (n.720+9G>A)
c.639+9G>A (n.639+9G>A)
c.678+9G>A (n.678+9G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367633G>ACA10561379FLNAc.720+8C>T (n.720+8C>T)
c.639+8C>T (n.639+8C>T)
c.678+8C>T (n.678+8C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367633G=CA2466658957FLNAc.720+8C= (n.720+8C=)
c.639+8C= (n.639+8C=)
c.678+8C= (n.678+8C=)
Xg.154367635G>ACA2837554379FLNAc.720+6C>T (n.720+6C>T)
c.639+6C>T (n.639+6C>T)
c.678+6C>T (n.678+6C>T)
Xg.154367635G>CCA2466658959FLNAc.720+6C>G (n.720+6C>G)
c.639+6C>G (n.639+6C>G)
c.678+6C>G (n.678+6C>G)
 dbSNP
Xg.154367635G=CA2466658958FLNAc.720+6C= (n.720+6C=)
c.639+6C= (n.639+6C=)
c.678+6C= (n.678+6C=)
Xg.154367636T>ACA2466658961FLNAc.720+5A>T (n.720+5A>T)
c.639+5A>T (n.639+5A>T)
c.678+5A>T (n.678+5A>T)
 ClinVar dbSNP gnomAD v4
Xg.154367636T>GCA2695082972FLNAc.720+5A>C (n.720+5A>C)
c.639+5A>C (n.639+5A>C)
c.678+5A>C (n.678+5A>C)
 gnomAD v4
Xg.154367636T=CA2466658960FLNAc.720+5A= (n.720+5A=)
c.639+5A= (n.639+5A=)
c.678+5A= (n.678+5A=)
Xg.154367637delCA2695082973FLNAc.720+4del (n.720+4del)
c.639+4del (n.639+4del)
c.678+4del (n.678+4del)
 gnomAD v4
Xg.154367637G>ACA645290409FLNAc.720+4C>T (n.720+4C>T)
c.639+4C>T (n.639+4C>T)
c.678+4C>T (n.678+4C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v4
Xg.154367637G=CA2466658962FLNAc.720+4C= (n.720+4C=)
c.639+4C= (n.639+4C=)
c.678+4C= (n.678+4C=)
Xg.154367639A=CA2466658963FLNAc.720+2T= (n.720+2T=)
c.639+2T= (n.639+2T=)
c.678+2T= (n.678+2T=)
Xg.154367639A>CCA415248722FLNAc.720+2T>G (n.720+2T>G)
c.639+2T>G (n.639+2T>G)
c.678+2T>G (n.678+2T>G)
Xg.154367639A>GCA278875FLNAc.720+2T>C (n.720+2T>C)
c.639+2T>C (n.639+2T>C)
c.678+2T>C (n.678+2T>C)
 ClinVar dbSNP
Xg.154367639A>TCA415248723FLNAc.720+2T>A (n.720+2T>A)
c.639+2T>A (n.639+2T>A)
c.678+2T>A (n.678+2T>A)
Xg.154367640C>ACA415248724FLNAc.720+1G>T (n.720+1G>T)
c.639+1G>T (n.639+1G>T)
c.678+1G>T (n.678+1G>T)
Xg.154367640C>GCA415248725FLNAc.720+1G>C (n.720+1G>C)
c.639+1G>C (n.639+1G>C)
c.678+1G>C (n.678+1G>C)
Xg.154367640C>TCA415248726FLNAc.720+1G>A (n.720+1G>A)
c.639+1G>A (n.639+1G>A)
c.678+1G>A (n.678+1G>A)
Xg.154367641C>ACA415248727FLNAc.720G>T (p.Gln240His)
c.639G>T (p.Gln213His)
c.678G>T (p.Gln226His)
Xg.154367641C>GCA415248728FLNAc.720G>C (p.Gln240His)
c.639G>C (p.Gln213His)
c.678G>C (p.Gln226His)
Xg.154367641C>TCA519709729FLNAc.720G>A (p.Gln240=)
c.639G>A (p.Gln213=)
c.678G>A (p.Gln226=)
Xg.154367642T>ACA415248729FLNAc.719A>T (p.Gln240Leu)
c.638A>T (p.Gln213Leu)
c.677A>T (p.Gln226Leu)
Xg.154367642T>CCA415248730FLNAc.719A>G (p.Gln240Arg)
c.638A>G (p.Gln213Arg)
c.677A>G (p.Gln226Arg)
Xg.154367642T>GCA415248731FLNAc.719A>C (p.Gln240Pro)
c.638A>C (p.Gln213Pro)
c.677A>C (p.Gln226Pro)
Xg.154367643G>ACA415248732FLNAc.718C>T (p.Gln240Ter)
c.637C>T (p.Gln213Ter)
c.676C>T (p.Gln226Ter)
Xg.154367643G>CCA415248734FLNAc.718C>G (p.Gln240Glu)
c.637C>G (p.Gln213Glu)
c.676C>G (p.Gln226Glu)
Xg.154367643G>TCA415248733FLNAc.718C>A (p.Gln240Lys)
c.637C>A (p.Gln213Lys)
c.676C>A (p.Gln226Lys)
Xg.154367644G>ACA519709747FLNAc.717C>T (p.Pro239=)
c.636C>T (p.Pro212=)
c.675C>T (p.Pro225=)
 ClinVar dbSNP gnomAD v4
Xg.154367644G>CCA337284231FLNAc.717C>G (p.Pro239=)
c.636C>G (p.Pro212=)
c.675C>G (p.Pro225=)
 dbSNP
Xg.154367644G=CA2466658964FLNAc.717C= (p.Pro239=)
c.636C= (p.Pro212=)
c.675C= (p.Pro225=)
Xg.154367644G>TCA519709748FLNAc.717C>A (p.Pro239=)
c.636C>A (p.Pro212=)
c.675C>A (p.Pro225=)
Xg.154367645G>ACA415248735FLNAc.716C>T (p.Pro239Leu)
c.635C>T (p.Pro212Leu)
c.674C>T (p.Pro225Leu)
Xg.154367645G>CCA415248736FLNAc.716C>G (p.Pro239Arg)
c.635C>G (p.Pro212Arg)
c.674C>G (p.Pro225Arg)
Xg.154367645G>TCA415248737FLNAc.716C>A (p.Pro239His)
c.635C>A (p.Pro212His)
c.674C>A (p.Pro225His)
 gnomAD v4
Xg.154367646G>ACA415248738FLNAc.715C>T (p.Pro239Ser)
c.634C>T (p.Pro212Ser)
c.673C>T (p.Pro225Ser)
Xg.154367646G>CCA415248739FLNAc.715C>G (p.Pro239Ala)
c.634C>G (p.Pro212Ala)
c.673C>G (p.Pro225Ala)
Xg.154367646G>TCA415248740FLNAc.715C>A (p.Pro239Thr)
c.634C>A (p.Pro212Thr)
c.673C>A (p.Pro225Thr)
Xg.154367647G>ACA519709767FLNAc.714C>T (p.Ile238=)
c.633C>T (p.Ile211=)
c.672C>T (p.Ile224=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367647G>CCA415248741FLNAc.714C>G (p.Ile238Met)
c.633C>G (p.Ile211Met)
c.672C>G (p.Ile224Met)
 ClinVar dbSNP
Xg.154367647G=CA2466658965FLNAc.714C= (p.Ile238=)
c.633C= (p.Ile211=)
c.672C= (p.Ile224=)
Xg.154367647G>TCA519709769FLNAc.714C>A (p.Ile238=)
c.633C>A (p.Ile211=)
c.672C>A (p.Ile224=)
Xg.154367648A>CCA415248742FLNAc.713T>G (p.Ile238Ser)
c.632T>G (p.Ile211Ser)
c.671T>G (p.Ile224Ser)
Xg.154367648A>GCA415248743FLNAc.713T>C (p.Ile238Thr)
c.632T>C (p.Ile211Thr)
c.671T>C (p.Ile224Thr)
Xg.154367648A>TCA415248744FLNAc.713T>A (p.Ile238Asn)
c.632T>A (p.Ile211Asn)
c.671T>A (p.Ile224Asn)
Xg.154367649T>ACA415248745FLNAc.712A>T (p.Ile238Phe)
c.631A>T (p.Ile211Phe)
c.670A>T (p.Ile224Phe)
Xg.154367649T>CCA415248747FLNAc.712A>G (p.Ile238Val)
c.631A>G (p.Ile211Val)
c.670A>G (p.Ile224Val)
Xg.154367649T>GCA415248746FLNAc.712A>C (p.Ile238Leu)
c.631A>C (p.Ile211Leu)
c.670A>C (p.Ile224Leu)
Xg.154367650G>ACA519709778FLNAc.711C>T (p.Gly237=)
c.630C>T (p.Gly210=)
c.669C>T (p.Gly223=)
Xg.154367650G>CCA519709780FLNAc.711C>G (p.Gly237=)
c.630C>G (p.Gly210=)
c.669C>G (p.Gly223=)
Xg.154367650G>TCA519709781FLNAc.711C>A (p.Gly237=)
c.630C>A (p.Gly210=)
c.669C>A (p.Gly223=)
Xg.154367651C>ACA415248748FLNAc.710G>T (p.Gly237Val)
c.629G>T (p.Gly210Val)
c.668G>T (p.Gly223Val)
Xg.154367651C=CA2466658966FLNAc.710G= (p.Gly237=)
c.629G= (p.Gly210=)
c.668G= (p.Gly223=)
Xg.154367651C>GCA415248750FLNAc.710G>C (p.Gly237Ala)
c.629G>C (p.Gly210Ala)
c.668G>C (p.Gly223Ala)
Xg.154367651C>TCA415248749FLNAc.710G>A (p.Gly237Asp)
c.629G>A (p.Gly210Asp)
c.668G>A (p.Gly223Asp)
 dbSNP
Xg.154367652C>ACA415248751FLNAc.709G>T (p.Gly237Cys)
c.628G>T (p.Gly210Cys)
c.667G>T (p.Gly223Cys)
Xg.154367652C>GCA415248753FLNAc.709G>C (p.Gly237Arg)
c.628G>C (p.Gly210Arg)
c.667G>C (p.Gly223Arg)
Xg.154367652C>TCA415248752FLNAc.709G>A (p.Gly237Ser)
c.628G>A (p.Gly210Ser)
c.667G>A (p.Gly223Ser)
Xg.154367653C>ACA519709788FLNAc.708G>T (p.Leu236=)
c.627G>T (p.Leu209=)
c.666G>T (p.Leu222=)
Xg.154367653C>GCA519709790FLNAc.708G>C (p.Leu236=)
c.627G>C (p.Leu209=)
c.666G>C (p.Leu222=)
 ClinVar
Xg.154367653C>TCA519709789FLNAc.708G>A (p.Leu236=)
c.627G>A (p.Leu209=)
c.666G>A (p.Leu222=)
 ClinVar dbSNP gnomAD v4
Xg.154367654A>CCA415248754FLNAc.707T>G (p.Leu236Arg)
c.626T>G (p.Leu209Arg)
c.665T>G (p.Leu222Arg)
Xg.154367654A>GCA415248756FLNAc.707T>C (p.Leu236Pro)
c.626T>C (p.Leu209Pro)
c.665T>C (p.Leu222Pro)
Xg.154367654A>TCA415248755FLNAc.707T>A (p.Leu236Gln)
c.626T>A (p.Leu209Gln)
c.665T>A (p.Leu222Gln)
Xg.154367655G>ACA519709794FLNAc.706C>T (p.Leu236=)
c.625C>T (p.Leu209=)
c.664C>T (p.Leu222=)
 dbSNP
Xg.154367655G>CCA415248757FLNAc.706C>G (p.Leu236Val)
c.625C>G (p.Leu209Val)
c.664C>G (p.Leu222Val)
Xg.154367655G=CA2466658967FLNAc.706C= (p.Leu236=)
c.625C= (p.Leu209=)
c.664C= (p.Leu222=)
Xg.154367655G>TCA415248758FLNAc.706C>A (p.Leu236Met)
c.625C>A (p.Leu209Met)
c.664C>A (p.Leu222Met)
Xg.154367656C>ACA415248759FLNAc.705G>T (p.Trp235Cys)
c.624G>T (p.Trp208Cys)
c.663G>T (p.Trp221Cys)
Xg.154367656C=CA2466658968FLNAc.705G= (p.Trp235=)
c.624G= (p.Trp208=)
c.663G= (p.Trp221=)
Xg.154367656C>GCA415248761FLNAc.705G>C (p.Trp235Cys)
c.624G>C (p.Trp208Cys)
c.663G>C (p.Trp221Cys)
Xg.154367656C>TCA415248760FLNAc.705G>A (p.Trp235Ter)
c.624G>A (p.Trp208Ter)
c.663G>A (p.Trp221Ter)
 ClinVar dbSNP
Xg.154367657C>ACA415248762FLNAc.704G>T (p.Trp235Leu)
c.623G>T (p.Trp208Leu)
c.662G>T (p.Trp221Leu)
Xg.154367657C>GCA415248764FLNAc.704G>C (p.Trp235Ser)
c.623G>C (p.Trp208Ser)
c.662G>C (p.Trp221Ser)
Xg.154367657C>TCA415248763FLNAc.704G>A (p.Trp235Ter)
c.623G>A (p.Trp208Ter)
c.662G>A (p.Trp221Ter)
Xg.154367658A>CCA415248765FLNAc.703T>G (p.Trp235Gly)
c.622T>G (p.Trp208Gly)
c.661T>G (p.Trp221Gly)
Xg.154367658A>GCA415248766FLNAc.703T>C (p.Trp235Arg)
c.622T>C (p.Trp208Arg)
c.661T>C (p.Trp221Arg)
Xg.154367658A>TCA415248767FLNAc.703T>A (p.Trp235Arg)
c.622T>A (p.Trp208Arg)
c.661T>A (p.Trp221Arg)
Xg.154367659G>ACA519709806FLNAc.702C>T (p.Asp234=)
c.621C>T (p.Asp207=)
c.660C>T (p.Asp220=)
Xg.154367659G>CCA415248768FLNAc.702C>G (p.Asp234Glu)
c.621C>G (p.Asp207Glu)
c.660C>G (p.Asp220Glu)
Xg.154367659G>TCA415248769FLNAc.702C>A (p.Asp234Glu)
c.621C>A (p.Asp207Glu)
c.660C>A (p.Asp220Glu)
Xg.154367660T>ACA415248770FLNAc.701A>T (p.Asp234Val)
c.620A>T (p.Asp207Val)
c.659A>T (p.Asp220Val)
Xg.154367660T>CCA415248771FLNAc.701A>G (p.Asp234Gly)
c.620A>G (p.Asp207Gly)
c.659A>G (p.Asp220Gly)
Xg.154367660T>GCA415248772FLNAc.701A>C (p.Asp234Ala)
c.620A>C (p.Asp207Ala)
c.659A>C (p.Asp220Ala)
Xg.154367661C>ACA415248775FLNAc.700G>T (p.Asp234Tyr)
c.619G>T (p.Asp207Tyr)
c.658G>T (p.Asp220Tyr)
Xg.154367661C>GCA415248774FLNAc.700G>C (p.Asp234His)
c.619G>C (p.Asp207His)
c.658G>C (p.Asp220His)
Xg.154367661C>TCA415248773FLNAc.700G>A (p.Asp234Asn)
c.619G>A (p.Asp207Asn)
c.658G>A (p.Asp220Asn)
Xg.154367662A=CA2466658969FLNAc.699T= (p.Asp233=)
c.618T= (p.Asp206=)
c.657T= (p.Asp219=)
Xg.154367662A>CCA415248776FLNAc.699T>G (p.Asp233Glu)
c.618T>G (p.Asp206Glu)
c.657T>G (p.Asp219Glu)
Xg.154367662A>GCA519709818FLNAc.699T>C (p.Asp233=)
c.618T>C (p.Asp206=)
c.657T>C (p.Asp219=)
 dbSNP
Xg.154367662A>TCA415248777FLNAc.699T>A (p.Asp233Glu)
c.618T>A (p.Asp206Glu)
c.657T>A (p.Asp219Glu)
Xg.154367663delCA2695236981FLNAc.698del (p.Asp233ValfsTer9)
c.617del (p.Asp206ValfsTer9)
c.656del (p.Asp219ValfsTer9)
Xg.154367663T>ACA415248778FLNAc.698A>T (p.Asp233Val)
c.617A>T (p.Asp206Val)
c.656A>T (p.Asp219Val)
Xg.154367663T>CCA415248779FLNAc.698A>G (p.Asp233Gly)
c.617A>G (p.Asp206Gly)
c.656A>G (p.Asp219Gly)
Xg.154367663T>GCA415248780FLNAc.698A>C (p.Asp233Ala)
c.617A>C (p.Asp206Ala)
c.656A>C (p.Asp219Ala)
Xg.154367664C>ACA415248781FLNAc.697G>T (p.Asp233Tyr)
c.616G>T (p.Asp206Tyr)
c.655G>T (p.Asp219Tyr)
Xg.154367664C>GCA415248782FLNAc.697G>C (p.Asp233His)
c.616G>C (p.Asp206His)
c.655G>C (p.Asp219His)
Xg.154367664C>TCA415248783FLNAc.697G>A (p.Asp233Asn)
c.616G>A (p.Asp206Asn)
c.655G>A (p.Asp219Asn)
 gnomAD v4
Xg.154367665C>ACA519709826FLNAc.696G>T (p.Ala232=)
c.615G>T (p.Ala205=)
c.654G>T (p.Ala218=)
Xg.154367665C=CA2466658970FLNAc.696G= (p.Ala232=)
c.615G= (p.Ala205=)
c.654G= (p.Ala218=)
Xg.154367665C>GCA519709827FLNAc.696G>C (p.Ala232=)
c.615G>C (p.Ala205=)
c.654G>C (p.Ala218=)
Xg.154367665C>TCA337284233FLNAc.696G>A (p.Ala232=)
c.615G>A (p.Ala205=)
c.654G>A (p.Ala218=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367666G>ACA415248785FLNAc.695C>T (p.Ala232Val)
c.614C>T (p.Ala205Val)
c.653C>T (p.Ala218Val)
 ClinVar dbSNP
Xg.154367666G>CCA415248786FLNAc.695C>G (p.Ala232Gly)
c.614C>G (p.Ala205Gly)
c.653C>G (p.Ala218Gly)
 ClinVar
Xg.154367666G=CA2466658971FLNAc.695C= (p.Ala232=)
c.614C= (p.Ala205=)
c.653C= (p.Ala218=)
Xg.154367666G>TCA415248784FLNAc.695C>A (p.Ala232Glu)
c.614C>A (p.Ala205Glu)
c.653C>A (p.Ala218Glu)
Xg.154367667C>ACA415248787FLNAc.694G>T (p.Ala232Ser)
c.613G>T (p.Ala205Ser)
c.652G>T (p.Ala218Ser)
Xg.154367667C>GCA415248788FLNAc.694G>C (p.Ala232Pro)
c.613G>C (p.Ala205Pro)
c.652G>C (p.Ala218Pro)
Xg.154367667C>TCA415248789FLNAc.694G>A (p.Ala232Thr)
c.613G>A (p.Ala205Thr)
c.652G>A (p.Ala218Thr)
Xg.154367668C>ACA415248790FLNAc.693G>T (p.Gln231His)
c.612G>T (p.Gln204His)
c.651G>T (p.Gln217His)
Xg.154367668C>GCA415248791FLNAc.693G>C (p.Gln231His)
c.612G>C (p.Gln204His)
c.651G>C (p.Gln217His)
Xg.154367668C>TCA519709843FLNAc.693G>A (p.Gln231=)
c.612G>A (p.Gln204=)
c.651G>A (p.Gln217=)
 ClinVar dbSNP
Xg.154367669T>ACA415248792FLNAc.692A>T (p.Gln231Leu)
c.611A>T (p.Gln204Leu)
c.650A>T (p.Gln217Leu)
Xg.154367669T>CCA415248793FLNAc.692A>G (p.Gln231Arg)
c.611A>G (p.Gln204Arg)
c.650A>G (p.Gln217Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
Xg.154367669T>GCA415248794FLNAc.692A>C (p.Gln231Pro)
c.611A>C (p.Gln204Pro)
c.650A>C (p.Gln217Pro)
Xg.154367669T=CA2466658972FLNAc.692A= (p.Gln231=)
c.611A= (p.Gln204=)
c.650A= (p.Gln217=)
Xg.154367670G>ACA415248795FLNAc.691C>T (p.Gln231Ter)
c.610C>T (p.Gln204Ter)
c.649C>T (p.Gln217Ter)
 ClinVar
Xg.154367670G>CCA415248796FLNAc.691C>G (p.Gln231Glu)
c.610C>G (p.Gln204Glu)
c.649C>G (p.Gln217Glu)
Xg.154367670G>TCA415248797FLNAc.691C>A (p.Gln231Lys)
c.610C>A (p.Gln204Lys)
c.649C>A (p.Gln217Lys)
Xg.154367671C>ACA415248799FLNAc.690G>T (p.Gln230His)
c.609G>T (p.Gln203His)
c.648G>T (p.Gln216His)
Xg.154367671C=CA2466658973FLNAc.690G= (p.Gln230=)
c.609G= (p.Gln203=)
c.648G= (p.Gln216=)
Xg.154367671C>GCA415248798FLNAc.690G>C (p.Gln230His)
c.609G>C (p.Gln203His)
c.648G>C (p.Gln216His)
Xg.154367671C>TCA519709851FLNAc.690G>A (p.Gln230=)
c.609G>A (p.Gln203=)
c.648G>A (p.Gln216=)
 ClinVar dbSNP gnomAD v4
Xg.154367672T>ACA415248800FLNAc.689A>T (p.Gln230Leu)
c.608A>T (p.Gln203Leu)
c.647A>T (p.Gln216Leu)
Xg.154367672T>CCA415248801FLNAc.689A>G (p.Gln230Arg)
c.608A>G (p.Gln203Arg)
c.647A>G (p.Gln216Arg)
Xg.154367672T>GCA415248802FLNAc.689A>C (p.Gln230Pro)
c.608A>C (p.Gln203Pro)
c.647A>C (p.Gln216Pro)
Xg.154367673G>ACA415248803FLNAc.688C>T (p.Gln230Ter)
c.607C>T (p.Gln203Ter)
c.646C>T (p.Gln216Ter)
Xg.154367673G>CCA415248804FLNAc.688C>G (p.Gln230Glu)
c.607C>G (p.Gln203Glu)
c.646C>G (p.Gln216Glu)
Xg.154367673G>TCA415248805FLNAc.688C>A (p.Gln230Lys)
c.607C>A (p.Gln203Lys)
c.646C>A (p.Gln216Lys)
Xg.154367674C>ACA10604670FLNAc.687G>T (p.Met229Ile)
c.606G>T (p.Met202Ile)
c.645G>T (p.Met215Ile)
 ClinVar dbSNP
Xg.154367674C=CA2466658974FLNAc.687G= (p.Met229=)
c.606G= (p.Met202=)
c.645G= (p.Met215=)
Xg.154367674C>GCA415248806FLNAc.687G>C (p.Met229Ile)
c.606G>C (p.Met202Ile)
c.645G>C (p.Met215Ile)
Xg.154367674C>TCA415248807FLNAc.687G>A (p.Met229Ile)
c.606G>A (p.Met202Ile)
c.645G>A (p.Met215Ile)
 ClinVar dbSNP
Xg.154367675A>CCA415248808FLNAc.686T>G (p.Met229Arg)
c.605T>G (p.Met202Arg)
c.644T>G (p.Met215Arg)
Xg.154367675A>GCA415248809FLNAc.686T>C (p.Met229Thr)
c.605T>C (p.Met202Thr)
c.644T>C (p.Met215Thr)
Xg.154367675A>TCA415248810FLNAc.686T>A (p.Met229Lys)
c.605T>A (p.Met202Lys)
c.644T>A (p.Met215Lys)
Xg.154367676T>ACA415248812FLNAc.685A>T (p.Met229Leu)
c.604A>T (p.Met202Leu)
c.643A>T (p.Met215Leu)
Xg.154367676T>CCA415248813FLNAc.685A>G (p.Met229Val)
c.604A>G (p.Met202Val)
c.643A>G (p.Met215Val)
Xg.154367676T>GCA415248811FLNAc.685A>C (p.Met229Leu)
c.604A>C (p.Met202Leu)
c.643A>C (p.Met215Leu)
Xg.154367677G>ACA519709863FLNAc.684C>T (p.Ala228=)
c.603C>T (p.Ala201=)
c.642C>T (p.Ala214=)
Xg.154367677G>CCA519709868FLNAc.684C>G (p.Ala228=)
c.603C>G (p.Ala201=)
c.642C>G (p.Ala214=)
Xg.154367677G>TCA519709870FLNAc.684C>A (p.Ala228=)
c.603C>A (p.Ala201=)
c.642C>A (p.Ala214=)
Xg.154367678G>ACA415248816FLNAc.683C>T (p.Ala228Val)
c.602C>T (p.Ala201Val)
c.641C>T (p.Ala214Val)
Xg.154367678G>CCA415248814FLNAc.683C>G (p.Ala228Gly)
c.602C>G (p.Ala201Gly)
c.641C>G (p.Ala214Gly)
Xg.154367678G>TCA415248815FLNAc.683C>A (p.Ala228Asp)
c.602C>A (p.Ala201Asp)
c.641C>A (p.Ala214Asp)
Xg.154367679C>ACA415248817FLNAc.682G>T (p.Ala228Ser)
c.601G>T (p.Ala201Ser)
c.640G>T (p.Ala214Ser)
 ClinVar dbSNP
Xg.154367679C>GCA415248818FLNAc.682G>C (p.Ala228Pro)
c.601G>C (p.Ala201Pro)
c.640G>C (p.Ala214Pro)
Xg.154367679C>TCA415248819FLNAc.682G>A (p.Ala228Thr)
c.601G>A (p.Ala201Thr)
c.640G>A (p.Ala214Thr)
Xg.154367680C>ACA415248820FLNAc.681G>T (p.Glu227Asp)
c.600G>T (p.Glu200Asp)
c.639G>T (p.Glu213Asp)
Xg.154367680C>GCA415248821FLNAc.681G>C (p.Glu227Asp)
c.600G>C (p.Glu200Asp)
c.639G>C (p.Glu213Asp)
Xg.154367680C>TCA519709875FLNAc.681G>A (p.Glu227=)
c.600G>A (p.Glu200=)
c.639G>A (p.Glu213=)
Xg.154367681T>ACA415248822FLNAc.680A>T (p.Glu227Val)
c.599A>T (p.Glu200Val)
c.638A>T (p.Glu213Val)
Xg.154367681T>CCA415248823FLNAc.680A>G (p.Glu227Gly)
c.599A>G (p.Glu200Gly)
c.638A>G (p.Glu213Gly)
Xg.154367681T>GCA415248824FLNAc.680A>C (p.Glu227Ala)
c.599A>C (p.Glu200Ala)
c.638A>C (p.Glu213Ala)
Xg.154367682C>ACA415248827FLNAc.679G>T (p.Glu227Ter)
c.598G>T (p.Glu200Ter)
c.637G>T (p.Glu213Ter)
Xg.154367682C>GCA415248826FLNAc.679G>C (p.Glu227Gln)
c.598G>C (p.Glu200Gln)
c.637G>C (p.Glu213Gln)
Xg.154367682C>TCA415248825FLNAc.679G>A (p.Glu227Lys)
c.598G>A (p.Glu200Lys)
c.637G>A (p.Glu213Lys)
Xg.154367683T>ACA519709881FLNAc.678A>T (p.Arg226=)
c.597A>T (p.Arg199=)
c.636A>T (p.Arg212=)
Xg.154367683T>CCA519709883FLNAc.678A>G (p.Arg226=)
c.597A>G (p.Arg199=)
c.636A>G (p.Arg212=)
Xg.154367683T>GCA519709884FLNAc.678A>C (p.Arg226=)
c.597A>C (p.Arg199=)
c.636A>C (p.Arg212=)
Xg.154367684C>ACA415248828FLNAc.677G>T (p.Arg226Leu)
c.596G>T (p.Arg199Leu)
c.635G>T (p.Arg212Leu)
Xg.154367684C=CA2466658975FLNAc.677G= (p.Arg226=)
c.596G= (p.Arg199=)
c.635G= (p.Arg212=)
Xg.154367684C>GCA415248829FLNAc.677G>C (p.Arg226Pro)
c.596G>C (p.Arg199Pro)
c.635G>C (p.Arg212Pro)
Xg.154367684C>TCA415248830FLNAc.677G>A (p.Arg226Gln)
c.596G>A (p.Arg199Gln)
c.635G>A (p.Arg212Gln)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
Xg.154367685G>ACA415248831FLNAc.676C>T (p.Arg226Ter)
c.595C>T (p.Arg199Ter)
c.634C>T (p.Arg212Ter)
 ClinVar dbSNP
Xg.154367685G>CCA415248832FLNAc.676C>G (p.Arg226Gly)
c.595C>G (p.Arg199Gly)
c.634C>G (p.Arg212Gly)
 ClinVar dbSNP
Xg.154367685G=CA2466658976FLNAc.676C= (p.Arg226=)
c.595C= (p.Arg199=)
c.634C= (p.Arg212=)
Xg.154367685G>TCA519709890FLNAc.676C>A (p.Arg226=)
c.595C>A (p.Arg199=)
c.634C>A (p.Arg212=)
Xg.154367686C>ACA519709891FLNAc.675G>T (p.Ala225=)
c.594G>T (p.Ala198=)
c.633G>T (p.Ala211=)
 dbSNP gnomAD v2 gnomAD v4
Xg.154367686C=CA2466658977FLNAc.675G= (p.Ala225=)
c.594G= (p.Ala198=)
c.633G= (p.Ala211=)
Xg.154367686C>GCA519709892FLNAc.675G>C (p.Ala225=)
c.594G>C (p.Ala198=)
c.633G>C (p.Ala211=)
Xg.154367686C>TCA10561380FLNAc.675G>A (p.Ala225=)
c.594G>A (p.Ala198=)
c.633G>A (p.Ala211=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367687G>ACA415248833FLNAc.674C>T (p.Ala225Val)
c.593C>T (p.Ala198Val)
c.632C>T (p.Ala211Val)
 gnomAD v4 COSMIC COSMIC
Xg.154367687G>CCA415248834FLNAc.674C>G (p.Ala225Gly)
c.593C>G (p.Ala198Gly)
c.632C>G (p.Ala211Gly)
Xg.154367687G>TCA415248835FLNAc.674C>A (p.Ala225Glu)
c.593C>A (p.Ala198Glu)
c.632C>A (p.Ala211Glu)
Xg.154367688C>ACA415248836FLNAc.673G>T (p.Ala225Ser)
c.592G>T (p.Ala198Ser)
c.631G>T (p.Ala211Ser)
Xg.154367688C>GCA415248837FLNAc.673G>C (p.Ala225Pro)
c.592G>C (p.Ala198Pro)
c.631G>C (p.Ala211Pro)
Xg.154367688C>TCA415248838FLNAc.673G>A (p.Ala225Thr)
c.592G>A (p.Ala198Thr)
c.631G>A (p.Ala211Thr)
Xg.154367689A>CCA415248840FLNAc.672T>G (p.Asn224Lys)
c.591T>G (p.Asn197Lys)
c.630T>G (p.Asn210Lys)
Xg.154367689A>GCA519709904FLNAc.672T>C (p.Asn224=)
c.591T>C (p.Asn197=)
c.630T>C (p.Asn210=)
Xg.154367689A>TCA415248839FLNAc.672T>A (p.Asn224Lys)
c.591T>A (p.Asn197Lys)
c.630T>A (p.Asn210Lys)
Xg.154367690T>ACA415248841FLNAc.671A>T (p.Asn224Ile)
c.590A>T (p.Asn197Ile)
c.629A>T (p.Asn210Ile)
Xg.154367690T>CCA415248842FLNAc.671A>G (p.Asn224Ser)
c.590A>G (p.Asn197Ser)
c.629A>G (p.Asn210Ser)
 ClinVar
Xg.154367690T>GCA415248843FLNAc.671A>C (p.Asn224Thr)
c.590A>C (p.Asn197Thr)
c.629A>C (p.Asn210Thr)
Xg.154367691T>ACA415248844FLNAc.670A>T (p.Asn224Tyr)
c.589A>T (p.Asn197Tyr)
c.628A>T (p.Asn210Tyr)
Xg.154367691T>CCA415248845FLNAc.670A>G (p.Asn224Asp)
c.589A>G (p.Asn197Asp)
c.628A>G (p.Asn210Asp)
Xg.154367691T>GCA415248846FLNAc.670A>C (p.Asn224His)
c.589A>C (p.Asn197His)
c.628A>C (p.Asn210His)
Xg.154367692G>ACA519709913FLNAc.669C>T (p.Thr223=)
c.588C>T (p.Thr196=)
c.627C>T (p.Thr209=)
Xg.154367692G>CCA519709914FLNAc.669C>G (p.Thr223=)
c.588C>G (p.Thr196=)
c.627C>G (p.Thr209=)
Xg.154367692G>TCA519709916FLNAc.669C>A (p.Thr223=)
c.588C>A (p.Thr196=)
c.627C>A (p.Thr209=)
Xg.154367693G>ACA415248847FLNAc.668C>T (p.Thr223Ile)
c.587C>T (p.Thr196Ile)
c.626C>T (p.Thr209Ile)
 gnomAD v4
Xg.154367693G>CCA415248848FLNAc.668C>G (p.Thr223Ser)
c.587C>G (p.Thr196Ser)
c.626C>G (p.Thr209Ser)
Xg.154367693G>TCA415248849FLNAc.668C>A (p.Thr223Asn)
c.587C>A (p.Thr196Asn)
c.626C>A (p.Thr209Asn)
Xg.154367694T>ACA415248850FLNAc.667A>T (p.Thr223Ser)
c.586A>T (p.Thr196Ser)
c.625A>T (p.Thr209Ser)
Xg.154367694T>CCA415248851FLNAc.667A>G (p.Thr223Ala)
c.586A>G (p.Thr196Ala)
c.625A>G (p.Thr209Ala)
Xg.154367694T>GCA415248852FLNAc.667A>C (p.Thr223Pro)
c.586A>C (p.Thr196Pro)
c.625A>C (p.Thr209Pro)
Xg.154367695A=CA2466658978FLNAc.666T= (p.Val222=)
c.585T= (p.Val195=)
c.624T= (p.Val208=)
Xg.154367695A>CCA519709617FLNAc.666T>G (p.Val222=)
c.585T>G (p.Val195=)
c.624T>G (p.Val208=)
Xg.154367695A>GCA519709619FLNAc.666T>C (p.Val222=)
c.585T>C (p.Val195=)
c.624T>C (p.Val208=)
Xg.154367695A>TCA519709620FLNAc.666T>A (p.Val222=)
c.585T>A (p.Val195=)
c.624T>A (p.Val208=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367696A>CCA415248855FLNAc.665T>G (p.Val222Gly)
c.584T>G (p.Val195Gly)
c.623T>G (p.Val208Gly)
Xg.154367696A>GCA415248853FLNAc.665T>C (p.Val222Ala)
c.584T>C (p.Val195Ala)
c.623T>C (p.Val208Ala)
Xg.154367696A>TCA415248854FLNAc.665T>A (p.Val222Asp)
c.584T>A (p.Val195Asp)
c.623T>A (p.Val208Asp)
Xg.154367697C>ACA415248856FLNAc.664G>T (p.Val222Phe)
c.583G>T (p.Val195Phe)
c.622G>T (p.Val208Phe)
Xg.154367697C=CA2466658979FLNAc.664G= (p.Val222=)
c.583G= (p.Val195=)
c.622G= (p.Val208=)
Xg.154367697C>GCA415248857FLNAc.664G>C (p.Val222Leu)
c.583G>C (p.Val195Leu)
c.622G>C (p.Val208Leu)
Xg.154367697C>TCA337284253FLNAc.664G>A (p.Val222Ile)
c.583G>A (p.Val195Ile)
c.622G>A (p.Val208Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
Xg.154367698G>ACA288871FLNAc.663C>T (p.Pro221=)
c.582C>T (p.Pro194=)
c.621C>T (p.Pro207=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
Xg.154367698G>CCA519709625FLNAc.663C>G (p.Pro221=)
c.582C>G (p.Pro194=)
c.621C>G (p.Pro207=)
Xg.154367698G=CA2466658980FLNAc.663C= (p.Pro221=)
c.582C= (p.Pro194=)
c.621C= (p.Pro207=)
Xg.154367698G>TCA519709626FLNAc.663C>A (p.Pro221=)
c.582C>A (p.Pro194=)
c.621C>A (p.Pro207=)
 ClinVar gnomAD v4
Xg.154367699G>ACA415248858FLNAc.662C>T (p.Pro221Leu)
c.581C>T (p.Pro194Leu)
c.620C>T (p.Pro207Leu)
Xg.154367699G>CCA415248859FLNAc.662C>G (p.Pro221Arg)
c.581C>G (p.Pro194Arg)
c.620C>G (p.Pro207Arg)
Xg.154367699G>TCA415248860FLNAc.662C>A (p.Pro221His)
c.581C>A (p.Pro194His)
c.620C>A (p.Pro207His)
Xg.154367700G>ACA415248861FLNAc.661C>T (p.Pro221Ser)
c.580C>T (p.Pro194Ser)
c.619C>T (p.Pro207Ser)
Xg.154367700G>CCA415248862FLNAc.661C>G (p.Pro221Ala)
c.580C>G (p.Pro194Ala)
c.619C>G (p.Pro207Ala)
Xg.154367700G>TCA415248863FLNAc.661C>A (p.Pro221Thr)
c.580C>A (p.Pro194Thr)
c.619C>A (p.Pro207Thr)
Xg.154367701C>ACA415248864FLNAc.660G>T (p.Lys220Asn)
c.579G>T (p.Lys193Asn)
c.618G>T (p.Lys206Asn)
Xg.154367701C>GCA415248865FLNAc.660G>C (p.Lys220Asn)
c.579G>C (p.Lys193Asn)
c.618G>C (p.Lys206Asn)
Xg.154367701C>TCA519709635FLNAc.660G>A (p.Lys220=)
c.579G>A (p.Lys193=)
c.618G>A (p.Lys206=)
 gnomAD v4
Xg.154367702T>ACA415248867FLNAc.659A>T (p.Lys220Met)
c.578A>T (p.Lys193Met)
c.617A>T (p.Lys206Met)
Xg.154367702T>CCA415248868FLNAc.659A>G (p.Lys220Arg)
c.578A>G (p.Lys193Arg)
c.617A>G (p.Lys206Arg)
 ClinVar
Xg.154367702T>GCA415248866FLNAc.659A>C (p.Lys220Thr)
c.578A>C (p.Lys193Thr)
c.617A>C (p.Lys206Thr)
Xg.154367703T>ACA415248870FLNAc.658A>T (p.Lys220Ter)
c.577A>T (p.Lys193Ter)
c.616A>T (p.Lys206Ter)
Xg.154367703T>CCA415248869FLNAc.658A>G (p.Lys220Glu)
c.577A>G (p.Lys193Glu)
c.616A>G (p.Lys206Glu)
Xg.154367703T>GCA415248871FLNAc.658A>C (p.Lys220Gln)
c.577A>C (p.Lys193Gln)
c.616A>C (p.Lys206Gln)
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=)

Number of alleles fetched