Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.128335455C>ACA360757891FBN2n.631G>T
n.712G>T
c.3847G>T (p.Asp1283Tyr)
c.397G>T (p.Asp133Tyr)
c.3748G>T (p.Asp1250Tyr)
c.3844G>T (p.Asp1282Tyr)
c.3694G>T (p.Asp1232Tyr)
5g.128335455C>GCA360757893FBN2n.631G>C
n.712G>C
c.3847G>C (p.Asp1283His)
c.397G>C (p.Asp133His)
c.3748G>C (p.Asp1250His)
c.3844G>C (p.Asp1282His)
c.3694G>C (p.Asp1232His)
5g.128335455C>TCA360757892FBN2n.631G>A
n.712G>A
c.3847G>A (p.Asp1283Asn)
c.397G>A (p.Asp133Asn)
c.3748G>A (p.Asp1250Asn)
c.3844G>A (p.Asp1282Asn)
c.3694G>A (p.Asp1232Asn)
5g.128335456T>ACA446310113FBN2n.630A>T
n.711A>T
c.3846A>T (p.Ala1282=)
c.396A>T (p.Ala132=)
c.3747A>T (p.Ala1249=)
c.3843A>T (p.Ala1281=)
c.3693A>T (p.Ala1231=)
5g.128335456T>CCA446310114FBN2n.630A>G
n.711A>G
c.3846A>G (p.Ala1282=)
c.396A>G (p.Ala132=)
c.3747A>G (p.Ala1249=)
c.3843A>G (p.Ala1281=)
c.3693A>G (p.Ala1231=)
5g.128335456T>GCA446310115FBN2n.630A>C
n.711A>C
c.3846A>C (p.Ala1282=)
c.396A>C (p.Ala132=)
c.3747A>C (p.Ala1249=)
c.3843A>C (p.Ala1281=)
c.3693A>C (p.Ala1231=)
5g.128335457G>ACA360757894FBN2n.629C>T
n.710C>T
c.3845C>T (p.Ala1282Val)
c.395C>T (p.Ala132Val)
c.3746C>T (p.Ala1249Val)
c.3842C>T (p.Ala1281Val)
c.3692C>T (p.Ala1231Val)
5g.128335457G>CCA360757895FBN2n.629C>G
n.710C>G
c.3845C>G (p.Ala1282Gly)
c.395C>G (p.Ala132Gly)
c.3746C>G (p.Ala1249Gly)
c.3842C>G (p.Ala1281Gly)
c.3692C>G (p.Ala1231Gly)
5g.128335457G>TCA360757896FBN2n.629C>A
n.710C>A
c.3845C>A (p.Ala1282Glu)
c.395C>A (p.Ala132Glu)
c.3746C>A (p.Ala1249Glu)
c.3842C>A (p.Ala1281Glu)
c.3692C>A (p.Ala1231Glu)
5g.128335458C>ACA360757897FBN2n.628G>T
n.709G>T
c.3844G>T (p.Ala1282Ser)
c.394G>T (p.Ala132Ser)
c.3745G>T (p.Ala1249Ser)
c.3841G>T (p.Ala1281Ser)
c.3691G>T (p.Ala1231Ser)
5g.128335458C>GCA360757898FBN2n.628G>C
n.709G>C
c.3844G>C (p.Ala1282Pro)
c.394G>C (p.Ala132Pro)
c.3745G>C (p.Ala1249Pro)
c.3841G>C (p.Ala1281Pro)
c.3691G>C (p.Ala1231Pro)
5g.128335458C>TCA360757899FBN2n.628G>A
n.709G>A
c.3844G>A (p.Ala1282Thr)
c.394G>A (p.Ala132Thr)
c.3745G>A (p.Ala1249Thr)
c.3841G>A (p.Ala1281Thr)
c.3691G>A (p.Ala1231Thr)
5g.128335459A>CCA360757900FBN2n.627T>G
n.708T>G
c.3843T>G (p.Cys1281Trp)
c.393T>G (p.Cys131Trp)
c.3744T>G (p.Cys1248Trp)
c.3840T>G (p.Cys1280Trp)
c.3690T>G (p.Cys1230Trp)
5g.128335459A>GCA446310117FBN2n.627T>C
n.708T>C
c.3843T>C (p.Cys1281=)
c.393T>C (p.Cys131=)
c.3744T>C (p.Cys1248=)
c.3840T>C (p.Cys1280=)
c.3690T>C (p.Cys1230=)
5g.128335459A>TCA360757901FBN2n.627T>A
n.708T>A
c.3843T>A (p.Cys1281Ter)
c.393T>A (p.Cys131Ter)
c.3744T>A (p.Cys1248Ter)
c.3840T>A (p.Cys1280Ter)
c.3690T>A (p.Cys1230Ter)
5g.128335460C>ACA360757902FBN2n.626G>T
n.707G>T
c.3842G>T (p.Cys1281Phe)
c.392G>T (p.Cys131Phe)
c.3743G>T (p.Cys1248Phe)
c.3839G>T (p.Cys1280Phe)
c.3689G>T (p.Cys1230Phe)
5g.128335460C>GCA360757903FBN2n.626G>C
n.707G>C
c.3842G>C (p.Cys1281Ser)
c.392G>C (p.Cys131Ser)
c.3743G>C (p.Cys1248Ser)
c.3839G>C (p.Cys1280Ser)
c.3689G>C (p.Cys1230Ser)
5g.128335460C>TCA360757904FBN2n.626G>A
n.707G>A
c.3842G>A (p.Cys1281Tyr)
c.392G>A (p.Cys131Tyr)
c.3743G>A (p.Cys1248Tyr)
c.3839G>A (p.Cys1280Tyr)
c.3689G>A (p.Cys1230Tyr)
5g.128335461A>CCA360757905FBN2n.625T>G
n.706T>G
c.3841T>G (p.Cys1281Gly)
c.391T>G (p.Cys131Gly)
c.3742T>G (p.Cys1248Gly)
c.3838T>G (p.Cys1280Gly)
c.3688T>G (p.Cys1230Gly)
5g.128335461A>GCA360757907FBN2n.625T>C
n.706T>C
c.3841T>C (p.Cys1281Arg)
c.391T>C (p.Cys131Arg)
c.3742T>C (p.Cys1248Arg)
c.3838T>C (p.Cys1280Arg)
c.3688T>C (p.Cys1230Arg)
5g.128335461A>TCA360757906FBN2n.625T>A
n.706T>A
c.3841T>A (p.Cys1281Ser)
c.391T>A (p.Cys131Ser)
c.3742T>A (p.Cys1248Ser)
c.3838T>A (p.Cys1280Ser)
c.3688T>A (p.Cys1230Ser)
5g.128335462C>ACA446310118FBN2n.624G>T
n.705G>T
c.3840G>T (p.Ser1280=)
c.390G>T (p.Ser130=)
c.3741G>T (p.Ser1247=)
c.3837G>T (p.Ser1279=)
c.3687G>T (p.Ser1229=)
5g.128335462C=CA1581269595FBN2n.624G=
n.705G=
c.3840G= (p.Ser1280=)
c.390G= (p.Ser130=)
c.3741G= (p.Ser1247=)
c.3837G= (p.Ser1279=)
c.3687G= (p.Ser1229=)
5g.128335462C>GCA446310119FBN2n.624G>C
n.705G>C
c.3840G>C (p.Ser1280=)
c.390G>C (p.Ser130=)
c.3741G>C (p.Ser1247=)
c.3837G>C (p.Ser1279=)
c.3687G>C (p.Ser1229=)
5g.128335462C>TCA3395131FBN2n.624G>A
n.705G>A
c.3840G>A (p.Ser1280=)
c.390G>A (p.Ser130=)
c.3741G>A (p.Ser1247=)
c.3837G>A (p.Ser1279=)
c.3687G>A (p.Ser1229=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.128335463G>ACA324510FBN2n.623C>T
n.704C>T
c.3839C>T (p.Ser1280Leu)
c.389C>T (p.Ser130Leu)
c.3740C>T (p.Ser1247Leu)
c.3836C>T (p.Ser1279Leu)
c.3686C>T (p.Ser1229Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
5g.128335463G>CCA360757908FBN2n.623C>G
n.704C>G
c.3839C>G (p.Ser1280Trp)
c.389C>G (p.Ser130Trp)
c.3740C>G (p.Ser1247Trp)
c.3836C>G (p.Ser1279Trp)
c.3686C>G (p.Ser1229Trp)
5g.128335463G=CA1581269596FBN2n.623C=
n.704C=
c.3839C= (p.Ser1280=)
c.389C= (p.Ser130=)
c.3740C= (p.Ser1247=)
c.3836C= (p.Ser1279=)
c.3686C= (p.Ser1229=)
5g.128335463G>TCA360757909FBN2n.623C>A
n.704C>A
c.3839C>A (p.Ser1280Ter)
c.389C>A (p.Ser130Ter)
c.3740C>A (p.Ser1247Ter)
c.3836C>A (p.Ser1279Ter)
c.3686C>A (p.Ser1229Ter)
5g.128335464A>CCA360757910FBN2n.622T>G
n.703T>G
c.3838T>G (p.Ser1280Ala)
c.388T>G (p.Ser130Ala)
c.3739T>G (p.Ser1247Ala)
c.3835T>G (p.Ser1279Ala)
c.3685T>G (p.Ser1229Ala)
5g.128335464A>GCA360757911FBN2n.622T>C
n.703T>C
c.3838T>C (p.Ser1280Pro)
c.388T>C (p.Ser130Pro)
c.3739T>C (p.Ser1247Pro)
c.3835T>C (p.Ser1279Pro)
c.3685T>C (p.Ser1229Pro)
5g.128335464A>TCA360757912FBN2n.622T>A
n.703T>A
c.3838T>A (p.Ser1280Thr)
c.388T>A (p.Ser130Thr)
c.3739T>A (p.Ser1247Thr)
c.3835T>A (p.Ser1279Thr)
c.3685T>A (p.Ser1229Thr)
5g.128335465T>ACA360757913FBN2n.621A>T
n.702A>T
c.3837A>T (p.Arg1279Ser)
c.387A>T (p.Arg129Ser)
c.3738A>T (p.Arg1246Ser)
c.3834A>T (p.Arg1278Ser)
c.3684A>T (p.Arg1228Ser)
5g.128335465T>CCA446310120FBN2n.621A>G
n.702A>G
c.3837A>G (p.Arg1279=)
c.387A>G (p.Arg129=)
c.3738A>G (p.Arg1246=)
c.3834A>G (p.Arg1278=)
c.3684A>G (p.Arg1228=)
5g.128335465T>GCA360757914FBN2n.621A>C
n.702A>C
c.3837A>C (p.Arg1279Ser)
c.387A>C (p.Arg129Ser)
c.3738A>C (p.Arg1246Ser)
c.3834A>C (p.Arg1278Ser)
c.3684A>C (p.Arg1228Ser)
5g.128335466C>ACA360757915FBN2n.620G>T
n.701G>T
c.3836G>T (p.Arg1279Ile)
c.386G>T (p.Arg129Ile)
c.3737G>T (p.Arg1246Ile)
c.3833G>T (p.Arg1278Ile)
c.3683G>T (p.Arg1228Ile)
5g.128335466C>GCA360757916FBN2n.620G>C
n.701G>C
c.3836G>C (p.Arg1279Thr)
c.386G>C (p.Arg129Thr)
c.3737G>C (p.Arg1246Thr)
c.3833G>C (p.Arg1278Thr)
c.3683G>C (p.Arg1228Thr)
5g.128335466C>TCA360757917FBN2n.620G>A
n.701G>A
c.3836G>A (p.Arg1279Lys)
c.386G>A (p.Arg129Lys)
c.3737G>A (p.Arg1246Lys)
c.3833G>A (p.Arg1278Lys)
c.3683G>A (p.Arg1228Lys)
5g.128335467T>ACA360757918FBN2n.619A>T
n.700A>T
c.3835A>T (p.Arg1279Ter)
c.385A>T (p.Arg129Ter)
c.3736A>T (p.Arg1246Ter)
c.3832A>T (p.Arg1278Ter)
c.3682A>T (p.Arg1228Ter)
5g.128335467T>CCA360757919FBN2n.619A>G
n.700A>G
c.3835A>G (p.Arg1279Gly)
c.385A>G (p.Arg129Gly)
c.3736A>G (p.Arg1246Gly)
c.3832A>G (p.Arg1278Gly)
c.3682A>G (p.Arg1228Gly)
ClinVar dbSNP
5g.128335467T>GCA446310121FBN2n.619A>C
n.700A>C
c.3835A>C (p.Arg1279=)
c.385A>C (p.Arg129=)
c.3736A>C (p.Arg1246=)
c.3832A>C (p.Arg1278=)
c.3682A>C (p.Arg1228=)
5g.128335467T=CA1581269597FBN2n.619A=
n.700A=
c.3835A= (p.Arg1279=)
c.385A= (p.Arg129=)
c.3736A= (p.Arg1246=)
c.3832A= (p.Arg1278=)
c.3682A= (p.Arg1228=)
5g.128335468C>ACA446310124FBN2n.618G>T
n.699G>T
c.3834G>T (p.Gly1278=)
c.384G>T (p.Gly128=)
c.3735G>T (p.Gly1245=)
c.3831G>T (p.Gly1277=)
c.3681G>T (p.Gly1227=)
5g.128335468C>GCA446310122FBN2n.618G>C
n.699G>C
c.3834G>C (p.Gly1278=)
c.384G>C (p.Gly128=)
c.3735G>C (p.Gly1245=)
c.3831G>C (p.Gly1277=)
c.3681G>C (p.Gly1227=)
5g.128335468C>TCA446310123FBN2n.618G>A
n.699G>A
c.3834G>A (p.Gly1278=)
c.384G>A (p.Gly128=)
c.3735G>A (p.Gly1245=)
c.3831G>A (p.Gly1277=)
c.3681G>A (p.Gly1227=)
gnomAD v4 COSMIC COSMIC
5g.128335469C>ACA360757920FBN2n.617G>T
n.698G>T
c.3833G>T (p.Gly1278Val)
c.383G>T (p.Gly128Val)
c.3734G>T (p.Gly1245Val)
c.3830G>T (p.Gly1277Val)
c.3680G>T (p.Gly1227Val)
5g.128335469C=CA1581269598FBN2n.617G=
n.698G=
c.3833G= (p.Gly1278=)
c.383G= (p.Gly128=)
c.3734G= (p.Gly1245=)
c.3830G= (p.Gly1277=)
c.3680G= (p.Gly1227=)
5g.128335469C>GCA360757921FBN2n.617G>C
n.698G>C
c.3833G>C (p.Gly1278Ala)
c.383G>C (p.Gly128Ala)
c.3734G>C (p.Gly1245Ala)
c.3830G>C (p.Gly1277Ala)
c.3680G>C (p.Gly1227Ala)
5g.128335469C>TCA3395132FBN2n.617G>A
n.698G>A
c.3833G>A (p.Gly1278Glu)
c.383G>A (p.Gly128Glu)
c.3734G>A (p.Gly1245Glu)
c.3830G>A (p.Gly1277Glu)
c.3680G>A (p.Gly1227Glu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
5g.128335470C>ACA360757922FBN2n.616G>T
n.697G>T
c.3832G>T (p.Gly1278Trp)
c.382G>T (p.Gly128Trp)
c.3733G>T (p.Gly1245Trp)
c.3829G>T (p.Gly1277Trp)
c.3679G>T (p.Gly1227Trp)
gnomAD v4

Number of alleles fetched