Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128851586G>ACA369208496FLNC,FLNC-AS1c.5800G>A (p.Asp1934Asn)
c.5701G>A (p.Asp1901Asn)
n.216-86C>T
7g.128851586G>CCA369208498FLNC,FLNC-AS1c.5800G>C (p.Asp1934His)
c.5701G>C (p.Asp1901His)
n.216-86C>G
7g.128851586G>TCA369208500FLNC,FLNC-AS1c.5800G>T (p.Asp1934Tyr)
c.5701G>T (p.Asp1901Tyr)
n.216-86C>A
7g.128851587A>CCA369208502FLNC,FLNC-AS1c.5801A>C (p.Asp1934Ala)
c.5702A>C (p.Asp1901Ala)
n.216-87T>G
7g.128851587A>GCA369208504FLNC,FLNC-AS1c.5801A>G (p.Asp1934Gly)
c.5702A>G (p.Asp1901Gly)
n.216-87T>C
 gnomAD v4
7g.128851587A>TCA369208505FLNC,FLNC-AS1c.5801A>T (p.Asp1934Val)
c.5702A>T (p.Asp1901Val)
n.216-87T>A
7g.128851588C>ACA369208507FLNC,FLNC-AS1c.5802C>A (p.Asp1934Glu)
c.5703C>A (p.Asp1901Glu)
n.216-88G>T
 dbSNP gnomAD v3 gnomAD v4
7g.128851588C=CA1742571617FLNC,FLNC-AS1c.5802C= (p.Asp1934=)
c.5703C= (p.Asp1901=)
n.216-88G=
7g.128851588C>GCA4475791FLNC,FLNC-AS1c.5802C>G (p.Asp1934Glu)
c.5703C>G (p.Asp1901Glu)
n.216-88G>C
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128851588C>TCA457849250FLNC,FLNC-AS1c.5802C>T (p.Asp1934=)
c.5703C>T (p.Asp1901=)
n.216-88G>A
 ClinVar
7g.128851589A=CA1742571641FLNC,FLNC-AS1c.5803A= (p.Lys1935=)
c.5704A= (p.Lys1902=)
n.216-89T=
7g.128851589A>CCA369208514FLNC,FLNC-AS1c.5803A>C (p.Lys1935Gln)
c.5704A>C (p.Lys1902Gln)
n.216-89T>G
7g.128851589A>GCA369208513FLNC,FLNC-AS1c.5803A>G (p.Lys1935Glu)
c.5704A>G (p.Lys1902Glu)
n.216-89T>C
 ClinVar dbSNP gnomAD v4
7g.128851589A>TCA369208511FLNC,FLNC-AS1c.5803A>T (p.Lys1935Ter)
c.5704A>T (p.Lys1902Ter)
n.216-89T>A
7g.128851590A>CCA369208517FLNC,FLNC-AS1c.5804A>C (p.Lys1935Thr)
c.5705A>C (p.Lys1902Thr)
n.216-90T>G
7g.128851590A>GCA369208520FLNC,FLNC-AS1c.5804A>G (p.Lys1935Arg)
c.5705A>G (p.Lys1902Arg)
n.216-90T>C
7g.128851590A>TCA369208519FLNC,FLNC-AS1c.5804A>T (p.Lys1935Met)
c.5705A>T (p.Lys1902Met)
n.216-90T>A
7g.128851591G>ACA4475792FLNC,FLNC-AS1c.5805G>A (p.Lys1935=)
c.5706G>A (p.Lys1902=)
n.216-91C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128851591G>CCA369208524FLNC,FLNC-AS1c.5805G>C (p.Lys1935Asn)
c.5706G>C (p.Lys1902Asn)
n.216-91C>G
7g.128851591G=CA1742571649FLNC,FLNC-AS1c.5805G= (p.Lys1935=)
c.5706G= (p.Lys1902=)
n.216-91C=
7g.128851591G>TCA369208522FLNC,FLNC-AS1c.5805G>T (p.Lys1935Asn)
c.5706G>T (p.Lys1902Asn)
n.216-91C>A
7g.128851592C>ACA369208526FLNC,FLNC-AS1c.5806C>A (p.His1936Asn)
c.5707C>A (p.His1903Asn)
n.216-92G>T
7g.128851592C>GCA369208529FLNC,FLNC-AS1c.5806C>G (p.His1936Asp)
c.5707C>G (p.His1903Asp)
n.216-92G>C
7g.128851592C>TCA369208527FLNC,FLNC-AS1c.5806C>T (p.His1936Tyr)
c.5707C>T (p.His1903Tyr)
n.216-92G>A
7g.128851593A=CA1742571660FLNC,FLNC-AS1c.5807A= (p.His1936=)
c.5708A= (p.His1903=)
n.216-93T=
7g.128851593A>CCA369208531FLNC,FLNC-AS1c.5807A>C (p.His1936Pro)
c.5708A>C (p.His1903Pro)
n.216-93T>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.128851593A>GCA369208535FLNC,FLNC-AS1c.5807A>G (p.His1936Arg)
c.5708A>G (p.His1903Arg)
n.216-93T>C
7g.128851593A>TCA369208533FLNC,FLNC-AS1c.5807A>T (p.His1936Leu)
c.5708A>T (p.His1903Leu)
n.216-93T>A
7g.128851594C>ACA369208538FLNC,FLNC-AS1c.5808C>A (p.His1936Gln)
c.5709C>A (p.His1903Gln)
n.216-94G>T
7g.128851594C>GCA369208539FLNC,FLNC-AS1c.5808C>G (p.His1936Gln)
c.5709C>G (p.His1903Gln)
n.216-94G>C
7g.128851594C>TCA457849265FLNC,FLNC-AS1c.5808C>T (p.His1936=)
c.5709C>T (p.His1903=)
n.216-94G>A
 ClinVar dbSNP
7g.128851595A>CCA369208542FLNC,FLNC-AS1c.5809A>C (p.Ile1937Leu)
c.5710A>C (p.Ile1904Leu)
n.216-95T>G
7g.128851595A>GCA369208544FLNC,FLNC-AS1c.5809A>G (p.Ile1937Val)
c.5710A>G (p.Ile1904Val)
n.216-95T>C
 gnomAD v4
7g.128851595A>TCA369208546FLNC,FLNC-AS1c.5809A>T (p.Ile1937Phe)
c.5710A>T (p.Ile1904Phe)
n.216-95T>A
7g.128851596T>ACA369208548FLNC,FLNC-AS1c.5810T>A (p.Ile1937Asn)
c.5711T>A (p.Ile1904Asn)
n.216-96A>T
 ClinVar dbSNP
7g.128851596T>CCA369208550FLNC,FLNC-AS1c.5810T>C (p.Ile1937Thr)
c.5711T>C (p.Ile1904Thr)
n.216-96A>G
7g.128851596T>GCA369208552FLNC,FLNC-AS1c.5810T>G (p.Ile1937Ser)
c.5711T>G (p.Ile1904Ser)
n.216-96A>C
7g.128851596T=CA1742571666FLNC,FLNC-AS1c.5810T= (p.Ile1937=)
c.5711T= (p.Ile1904=)
n.216-96A=
7g.128851597C>ACA457849272FLNC,FLNC-AS1c.5811C>A (p.Ile1937=)
c.5712C>A (p.Ile1904=)
n.216-97G>T
7g.128851597C>GCA369208554FLNC,FLNC-AS1c.5811C>G (p.Ile1937Met)
c.5712C>G (p.Ile1904Met)
n.216-97G>C
7g.128851597C>TCA457849273FLNC,FLNC-AS1c.5811C>T (p.Ile1937=)
c.5712C>T (p.Ile1904=)
n.216-97G>A
7g.128851598C>ACA369208557FLNC,FLNC-AS1c.5812C>A (p.Pro1938Thr)
c.5713C>A (p.Pro1905Thr)
n.216-98G>T
7g.128851598C>GCA369208559FLNC,FLNC-AS1c.5812C>G (p.Pro1938Ala)
c.5713C>G (p.Pro1905Ala)
n.216-98G>C
7g.128851598C>TCA369208561FLNC,FLNC-AS1c.5812C>T (p.Pro1938Ser)
c.5713C>T (p.Pro1905Ser)
n.216-98G>A
 COSMIC
7g.128851599C>ACA369208567FLNC,FLNC-AS1c.5813C>A (p.Pro1938Gln)
c.5714C>A (p.Pro1905Gln)
n.216-99G>T
7g.128851599C=CA1742571682FLNC,FLNC-AS1c.5813C= (p.Pro1938=)
c.5714C= (p.Pro1905=)
n.216-99G=
7g.128851599C>GCA4475793FLNC,FLNC-AS1c.5813C>G (p.Pro1938Arg)
c.5714C>G (p.Pro1905Arg)
n.216-99G>C
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.128851599C>TCA369208563FLNC,FLNC-AS1c.5813C>T (p.Pro1938Leu)
c.5714C>T (p.Pro1905Leu)
n.216-99G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
7g.128851600G>ACA4475794FLNC,FLNC-AS1c.5814G>A (p.Pro1938=)
c.5715G>A (p.Pro1905=)
n.216-100C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128851600G>CCA457849281FLNC,FLNC-AS1c.5814G>C (p.Pro1938=)
c.5715G>C (p.Pro1905=)
n.216-100C>G
 ClinVar dbSNP

Number of alleles fetched