Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128851488A>CCA369208064FLNC,FLNC-AS1c.5702A>C (p.Lys1901Thr)
c.5603A>C (p.Lys1868Thr)
n.228T>G
 COSMIC
7g.128851488A>GCA369208067FLNC,FLNC-AS1c.5702A>G (p.Lys1901Arg)
c.5603A>G (p.Lys1868Arg)
n.228T>C
7g.128851488A>TCA369208066FLNC,FLNC-AS1c.5702A>T (p.Lys1901Met)
c.5603A>T (p.Lys1868Met)
n.228T>A
7g.128851488_128851489delinsAGCA1742571110FLNC,FLNC-AS1c.5702_5703delinsAG (p.Lys1901=)
c.5603_5604delinsAG (p.Lys1868=)
n.227_228delinsCT
7g.128851489G>ACA457849140FLNC,FLNC-AS1c.5703G>A (p.Lys1901=)
c.5604G>A (p.Lys1868=)
n.227C>T
 ClinVar dbSNP gnomAD v4
7g.128851489G>CCA369208069FLNC,FLNC-AS1c.5703G>C (p.Lys1901Asn)
c.5604G>C (p.Lys1868Asn)
n.227C>G
7g.128851489G=CA1742571117FLNC,FLNC-AS1c.5703G= (p.Lys1901=)
c.5604G= (p.Lys1868=)
n.227C=
7g.128851489G>TCA369208070FLNC,FLNC-AS1c.5703G>T (p.Lys1901Asn)
c.5604G>T (p.Lys1868Asn)
n.227C>A
7g.128851490delCA645372844FLNC,FLNC-AS1c.5704del (p.Ala1902GlnfsTer?)
c.5605del (p.Ala1869GlnfsTer?)
n.227del
 ClinVar dbSNP
7g.128851490G>ACA369208072FLNC,FLNC-AS1c.5704G>A (p.Ala1902Thr)
c.5605G>A (p.Ala1869Thr)
n.226C>T
7g.128851490G>CCA369208075FLNC,FLNC-AS1c.5704G>C (p.Ala1902Pro)
c.5605G>C (p.Ala1869Pro)
n.226C>G
7g.128851490G>TCA369208074FLNC,FLNC-AS1c.5704G>T (p.Ala1902Ser)
c.5605G>T (p.Ala1869Ser)
n.226C>A
7g.128851491C>ACA369208078FLNC,FLNC-AS1c.5705C>A (p.Ala1902Glu)
c.5606C>A (p.Ala1869Glu)
n.225G>T
 ClinVar
7g.128851491C>GCA369208080FLNC,FLNC-AS1c.5705C>G (p.Ala1902Gly)
c.5606C>G (p.Ala1869Gly)
n.225G>C
7g.128851491C>TCA369208081FLNC,FLNC-AS1c.5705C>T (p.Ala1902Val)
c.5606C>T (p.Ala1869Val)
n.225G>A
7g.128851492A>CCA457849149FLNC,FLNC-AS1c.5706A>C (p.Ala1902=)
c.5607A>C (p.Ala1869=)
n.224T>G
7g.128851492A>GCA457849151FLNC,FLNC-AS1c.5706A>G (p.Ala1902=)
c.5607A>G (p.Ala1869=)
n.224T>C
7g.128851492A>TCA457849153FLNC,FLNC-AS1c.5706A>T (p.Ala1902=)
c.5607A>T (p.Ala1869=)
n.224T>A
7g.128851493G>ACA369208084FLNC,FLNC-AS1c.5707G>A (p.Glu1903Lys)
c.5608G>A (p.Glu1870Lys)
n.223C>T
 gnomAD v4
7g.128851493G>CCA369208086FLNC,FLNC-AS1c.5707G>C (p.Glu1903Gln)
c.5608G>C (p.Glu1870Gln)
n.223C>G
7g.128851493G>TCA369208087FLNC,FLNC-AS1c.5707G>T (p.Glu1903Ter)
c.5608G>T (p.Glu1870Ter)
n.223C>A
7g.128851494A>CCA369208089FLNC,FLNC-AS1c.5708A>C (p.Glu1903Ala)
c.5609A>C (p.Glu1870Ala)
n.222T>G
7g.128851494A>GCA369208091FLNC,FLNC-AS1c.5708A>G (p.Glu1903Gly)
c.5609A>G (p.Glu1870Gly)
n.222T>C
7g.128851494A>TCA369208092FLNC,FLNC-AS1c.5708A>T (p.Glu1903Val)
c.5609A>T (p.Glu1870Val)
n.222T>A
7g.128851495G>ACA457849154FLNC,FLNC-AS1c.5709G>A (p.Glu1903=)
c.5610G>A (p.Glu1870=)
n.221C>T
 ClinVar dbSNP gnomAD v4
7g.128851495G>CCA369208094FLNC,FLNC-AS1c.5709G>C (p.Glu1903Asp)
c.5610G>C (p.Glu1870Asp)
n.221C>G
7g.128851495G=CA1742571130FLNC,FLNC-AS1c.5709G= (p.Glu1903=)
c.5610G= (p.Glu1870=)
n.221C=
7g.128851495G>TCA369208097FLNC,FLNC-AS1c.5709G>T (p.Glu1903Asp)
c.5610G>T (p.Glu1870Asp)
n.221C>A
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.128851496A>CCA369208103FLNC,FLNC-AS1c.5710A>C (p.Ile1904Leu)
c.5611A>C (p.Ile1871Leu)
n.220T>G
7g.128851496A>GCA369208099FLNC,FLNC-AS1c.5710A>G (p.Ile1904Val)
c.5611A>G (p.Ile1871Val)
n.220T>C
 COSMIC
7g.128851496A>TCA369208101FLNC,FLNC-AS1c.5710A>T (p.Ile1904Phe)
c.5611A>T (p.Ile1871Phe)
n.220T>A
7g.128851497T>ACA4475763FLNC,FLNC-AS1c.5711T>A (p.Ile1904Asn)
c.5612T>A (p.Ile1871Asn)
n.219A>T
 dbSNP ExAC gnomAD v2 gnomAD v4
7g.128851497T>CCA369208106FLNC,FLNC-AS1c.5711T>C (p.Ile1904Thr)
c.5612T>C (p.Ile1871Thr)
n.219A>G
7g.128851497T>GCA369208108FLNC,FLNC-AS1c.5711T>G (p.Ile1904Ser)
c.5612T>G (p.Ile1871Ser)
n.219A>C
7g.128851497T=CA1742571183FLNC,FLNC-AS1c.5711T= (p.Ile1904=)
c.5612T= (p.Ile1871=)
n.219A=
7g.128851498C>ACA457849158FLNC,FLNC-AS1c.5712C>A (p.Ile1904=)
c.5613C>A (p.Ile1871=)
n.218G>T
7g.128851498C>GCA369208110FLNC,FLNC-AS1c.5712C>G (p.Ile1904Met)
c.5613C>G (p.Ile1871Met)
n.218G>C
7g.128851498C>TCA457849159FLNC,FLNC-AS1c.5712C>T (p.Ile1904=)
c.5613C>T (p.Ile1871=)
n.218G>A
7g.128851499A=CA1742571190FLNC,FLNC-AS1c.5713A= (p.Thr1905=)
c.5614A= (p.Thr1872=)
n.217T=
7g.128851499A>CCA369208113FLNC,FLNC-AS1c.5713A>C (p.Thr1905Pro)
c.5614A>C (p.Thr1872Pro)
n.217T>G
7g.128851499A>GCA369208114FLNC,FLNC-AS1c.5713A>G (p.Thr1905Ala)
c.5614A>G (p.Thr1872Ala)
n.217T>C
 ClinVar dbSNP
7g.128851499A>TCA369208117FLNC,FLNC-AS1c.5713A>T (p.Thr1905Ser)
c.5614A>T (p.Thr1872Ser)
n.217T>A
7g.128851500C>ACA369208119FLNC,FLNC-AS1c.5714C>A (p.Thr1905Asn)
c.5615C>A (p.Thr1872Asn)
n.216G>T
 gnomAD v4
7g.128851500C=CA1742571192FLNC,FLNC-AS1c.5714C= (p.Thr1905=)
c.5615C= (p.Thr1872=)
n.216G=
7g.128851500C>GCA369208121FLNC,FLNC-AS1c.5714C>G (p.Thr1905Ser)
c.5615C>G (p.Thr1872Ser)
n.216G>C
7g.128851500C>TCA369208123FLNC,FLNC-AS1c.5714C>T (p.Thr1905Ile)
c.5615C>T (p.Thr1872Ile)
n.216G>A
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.128851501C>ACA457849161FLNC,FLNC-AS1c.5715C>A (p.Thr1905=)
c.5616C>A (p.Thr1872=)
n.216-1G>T
7g.128851501C>GCA457849163FLNC,FLNC-AS1c.5715C>G (p.Thr1905=)
c.5616C>G (p.Thr1872=)
n.216-1G>C
7g.128851501C>TCA457849162FLNC,FLNC-AS1c.5715C>T (p.Thr1905=)
c.5616C>T (p.Thr1872=)
n.216-1G>A
 gnomAD v4
7g.128851502T>ACA369208128FLNC,FLNC-AS1c.5716T>A (p.Cys1906Ser)
c.5617T>A (p.Cys1873Ser)
n.216-2A>T

Number of alleles fetched