Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.128344385C>ACA360761630FBN2c.3343G>T (p.Asp1115Tyr)
c.3244G>T (p.Asp1082Tyr)
c.3340G>T (p.Asp1114Tyr)
c.3190G>T (p.Asp1064Tyr)
5g.128344385C=CA1581273725FBN2c.3343G= (p.Asp1115=)
c.3244G= (p.Asp1082=)
c.3340G= (p.Asp1114=)
c.3190G= (p.Asp1064=)
5g.128344385C>GCA281516FBN2c.3343G>C (p.Asp1115His)
c.3244G>C (p.Asp1082His)
c.3340G>C (p.Asp1114His)
c.3190G>C (p.Asp1064His)
ClinVar dbSNP
5g.128344385C>TCA360761631FBN2c.3343G>A (p.Asp1115Asn)
c.3244G>A (p.Asp1082Asn)
c.3340G>A (p.Asp1114Asn)
c.3190G>A (p.Asp1064Asn)
5g.128344386C>ACA446311188FBN2c.3342G>T (p.Thr1114=)
c.3243G>T (p.Thr1081=)
c.3339G>T (p.Thr1113=)
c.3189G>T (p.Thr1063=)
5g.128344386C=CA1581273726FBN2c.3342G= (p.Thr1114=)
c.3243G= (p.Thr1081=)
c.3339G= (p.Thr1113=)
c.3189G= (p.Thr1063=)
5g.128344386C>GCA446311187FBN2c.3342G>C (p.Thr1114=)
c.3243G>C (p.Thr1081=)
c.3339G>C (p.Thr1113=)
c.3189G>C (p.Thr1063=)
5g.128344386C>TCA3395268FBN2c.3342G>A (p.Thr1114=)
c.3243G>A (p.Thr1081=)
c.3339G>A (p.Thr1113=)
c.3189G>A (p.Thr1063=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.128344387G>ACA325281FBN2c.3341C>T (p.Thr1114Met)
c.3242C>T (p.Thr1081Met)
c.3338C>T (p.Thr1113Met)
c.3188C>T (p.Thr1063Met)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.128344387G>CCA360761635FBN2c.3341C>G (p.Thr1114Arg)
c.3242C>G (p.Thr1081Arg)
c.3338C>G (p.Thr1113Arg)
c.3188C>G (p.Thr1063Arg)
5g.128344387G=CA1581273727FBN2c.3341C= (p.Thr1114=)
c.3242C= (p.Thr1081=)
c.3338C= (p.Thr1113=)
c.3188C= (p.Thr1063=)
5g.128344387G>TCA360761638FBN2c.3341C>A (p.Thr1114Lys)
c.3242C>A (p.Thr1081Lys)
c.3338C>A (p.Thr1113Lys)
c.3188C>A (p.Thr1063Lys)
5g.128344388T>ACA360761639FBN2c.3340A>T (p.Thr1114Ser)
c.3241A>T (p.Thr1081Ser)
c.3337A>T (p.Thr1113Ser)
c.3187A>T (p.Thr1063Ser)
5g.128344388T>CCA360761640FBN2c.3340A>G (p.Thr1114Ala)
c.3241A>G (p.Thr1081Ala)
c.3337A>G (p.Thr1113Ala)
c.3187A>G (p.Thr1063Ala)
5g.128344388T>GCA360761642FBN2c.3340A>C (p.Thr1114Pro)
c.3241A>C (p.Thr1081Pro)
c.3337A>C (p.Thr1113Pro)
c.3187A>C (p.Thr1063Pro)
5g.128344389G>ACA446311189FBN2c.3339C>T (p.Cys1113=)
c.3240C>T (p.Cys1080=)
c.3336C>T (p.Cys1112=)
c.3186C>T (p.Cys1062=)
dbSNP gnomAD v3 gnomAD v4
5g.128344389G>CCA360761645FBN2c.3339C>G (p.Cys1113Trp)
c.3240C>G (p.Cys1080Trp)
c.3336C>G (p.Cys1112Trp)
c.3186C>G (p.Cys1062Trp)
5g.128344389G=CA1581273728FBN2c.3339C= (p.Cys1113=)
c.3240C= (p.Cys1080=)
c.3336C= (p.Cys1112=)
c.3186C= (p.Cys1062=)
5g.128344389G>TCA360761646FBN2c.3339C>A (p.Cys1113Ter)
c.3240C>A (p.Cys1080Ter)
c.3336C>A (p.Cys1112Ter)
c.3186C>A (p.Cys1062Ter)
5g.128344389dupCA2675118134FBN2c.3339dup (p.Thr1114HisfsTer11)
c.3240dup (p.Thr1081HisfsTer11)
c.3336dup (p.Thr1113HisfsTer11)
c.3186dup (p.Thr1063HisfsTer11)
gnomAD v4
5g.128344390C>ACA360761648FBN2c.3338G>T (p.Cys1113Phe)
c.3239G>T (p.Cys1080Phe)
c.3335G>T (p.Cys1112Phe)
c.3185G>T (p.Cys1062Phe)
dbSNP gnomAD v2 gnomAD v4
5g.128344390C=CA1581273729FBN2c.3338G= (p.Cys1113=)
c.3239G= (p.Cys1080=)
c.3335G= (p.Cys1112=)
c.3185G= (p.Cys1062=)
5g.128344390C>GCA360761649FBN2c.3338G>C (p.Cys1113Ser)
c.3239G>C (p.Cys1080Ser)
c.3335G>C (p.Cys1112Ser)
c.3185G>C (p.Cys1062Ser)
5g.128344390C>TCA360761651FBN2c.3338G>A (p.Cys1113Tyr)
c.3239G>A (p.Cys1080Tyr)
c.3335G>A (p.Cys1112Tyr)
c.3185G>A (p.Cys1062Tyr)
5g.128344391A=CA1581273730FBN2c.3337T= (p.Cys1113=)
c.3238T= (p.Cys1080=)
c.3334T= (p.Cys1112=)
c.3184T= (p.Cys1062=)
5g.128344391A>CCA360761653FBN2c.3337T>G (p.Cys1113Gly)
c.3238T>G (p.Cys1080Gly)
c.3334T>G (p.Cys1112Gly)
c.3184T>G (p.Cys1062Gly)
5g.128344391A>GCA360761654FBN2c.3337T>C (p.Cys1113Arg)
c.3238T>C (p.Cys1080Arg)
c.3334T>C (p.Cys1112Arg)
c.3184T>C (p.Cys1062Arg)
gnomAD v4
5g.128344391A>TCA127018175FBN2c.3337T>A (p.Cys1113Ser)
c.3238T>A (p.Cys1080Ser)
c.3334T>A (p.Cys1112Ser)
c.3184T>A (p.Cys1062Ser)
dbSNP gnomAD v4
5g.128344392G>ACA446311190FBN2c.3336C>T (p.Asn1112=)
c.3237C>T (p.Asn1079=)
c.3333C>T (p.Asn1111=)
c.3183C>T (p.Asn1061=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.128344392G>CCA360761659FBN2c.3336C>G (p.Asn1112Lys)
c.3237C>G (p.Asn1079Lys)
c.3333C>G (p.Asn1111Lys)
c.3183C>G (p.Asn1061Lys)
5g.128344392G=CA1581273731FBN2c.3336C= (p.Asn1112=)
c.3237C= (p.Asn1079=)
c.3333C= (p.Asn1111=)
c.3183C= (p.Asn1061=)
5g.128344392G>TCA360761658FBN2c.3336C>A (p.Asn1112Lys)
c.3237C>A (p.Asn1079Lys)
c.3333C>A (p.Asn1111Lys)
c.3183C>A (p.Asn1061Lys)
5g.128344393T>ACA360761661FBN2c.3335A>T (p.Asn1112Ile)
c.3236A>T (p.Asn1079Ile)
c.3332A>T (p.Asn1111Ile)
c.3182A>T (p.Asn1061Ile)
5g.128344393T>CCA360761663FBN2c.3335A>G (p.Asn1112Ser)
c.3236A>G (p.Asn1079Ser)
c.3332A>G (p.Asn1111Ser)
c.3182A>G (p.Asn1061Ser)
ClinVar
5g.128344393T>GCA360761664FBN2c.3335A>C (p.Asn1112Thr)
c.3236A>C (p.Asn1079Thr)
c.3332A>C (p.Asn1111Thr)
c.3182A>C (p.Asn1061Thr)
dbSNP gnomAD v2 gnomAD v4
5g.128344393T=CA1581273732FBN2c.3335A= (p.Asn1112=)
c.3236A= (p.Asn1079=)
c.3332A= (p.Asn1111=)
c.3182A= (p.Asn1061=)
5g.128344394T>ACA360761666FBN2c.3334A>T (p.Asn1112Tyr)
c.3235A>T (p.Asn1079Tyr)
c.3331A>T (p.Asn1111Tyr)
c.3181A>T (p.Asn1061Tyr)
5g.128344394T>CCA360761667FBN2c.3334A>G (p.Asn1112Asp)
c.3235A>G (p.Asn1079Asp)
c.3331A>G (p.Asn1111Asp)
c.3181A>G (p.Asn1061Asp)
5g.128344394T>GCA360761668FBN2c.3334A>C (p.Asn1112His)
c.3235A>C (p.Asn1079His)
c.3331A>C (p.Asn1111His)
c.3181A>C (p.Asn1061His)
5g.128344395T>ACA360761669FBN2c.3333A>T (p.Arg1111Ser)
c.3234A>T (p.Arg1078Ser)
c.3330A>T (p.Arg1110Ser)
c.3180A>T (p.Arg1060Ser)
5g.128344395T>CCA446311191FBN2c.3333A>G (p.Arg1111=)
c.3234A>G (p.Arg1078=)
c.3330A>G (p.Arg1110=)
c.3180A>G (p.Arg1060=)
5g.128344395T>GCA360761670FBN2c.3333A>C (p.Arg1111Ser)
c.3234A>C (p.Arg1078Ser)
c.3330A>C (p.Arg1110Ser)
c.3180A>C (p.Arg1060Ser)
5g.128344396C>ACA360761673FBN2c.3332G>T (p.Arg1111Ile)
c.3233G>T (p.Arg1078Ile)
c.3329G>T (p.Arg1110Ile)
c.3179G>T (p.Arg1060Ile)
gnomAD v4
5g.128344396C>GCA360761675FBN2c.3332G>C (p.Arg1111Thr)
c.3233G>C (p.Arg1078Thr)
c.3329G>C (p.Arg1110Thr)
c.3179G>C (p.Arg1060Thr)
5g.128344396C>TCA360761677FBN2c.3332G>A (p.Arg1111Lys)
c.3233G>A (p.Arg1078Lys)
c.3329G>A (p.Arg1110Lys)
c.3179G>A (p.Arg1060Lys)
5g.128344397T>ACA360761681FBN2c.3331A>T (p.Arg1111Ter)
c.3232A>T (p.Arg1078Ter)
c.3328A>T (p.Arg1110Ter)
c.3178A>T (p.Arg1060Ter)
5g.128344397T>CCA360761683FBN2c.3331A>G (p.Arg1111Gly)
c.3232A>G (p.Arg1078Gly)
c.3328A>G (p.Arg1110Gly)
c.3178A>G (p.Arg1060Gly)
ClinVar dbSNP
5g.128344397T>GCA446311192FBN2c.3331A>C (p.Arg1111=)
c.3232A>C (p.Arg1078=)
c.3328A>C (p.Arg1110=)
c.3178A>C (p.Arg1060=)
5g.128344397T=CA1581273733FBN2c.3331A= (p.Arg1111=)
c.3232A= (p.Arg1078=)
c.3328A= (p.Arg1110=)
c.3178A= (p.Arg1060=)
5g.128344398T>ACA360761686FBN2c.3330A>T (p.Glu1110Asp)
c.3231A>T (p.Glu1077Asp)
c.3327A>T (p.Glu1109Asp)
c.3177A>T (p.Glu1059Asp)
COSMIC COSMIC

Number of alleles fetched