Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128851536C>ACA369208295FLNC,FLNC-AS1c.5750C>A (p.Ser1917Tyr)
c.5651C>A (p.Ser1884Tyr)
n.216-36G>T
7g.128851536C>GCA369208296FLNC,FLNC-AS1c.5750C>G (p.Ser1917Cys)
c.5651C>G (p.Ser1884Cys)
n.216-36G>C
 ClinVar
7g.128851536C>TCA369208299FLNC,FLNC-AS1c.5750C>T (p.Ser1917Phe)
c.5651C>T (p.Ser1884Phe)
n.216-36G>A
7g.128851537C>ACA457849196FLNC,FLNC-AS1c.5751C>A (p.Ser1917=)
c.5652C>A (p.Ser1884=)
n.216-37G>T
7g.128851537C>GCA457849195FLNC,FLNC-AS1c.5751C>G (p.Ser1917=)
c.5652C>G (p.Ser1884=)
n.216-37G>C
7g.128851537C>TCA457849194FLNC,FLNC-AS1c.5751C>T (p.Ser1917=)
c.5652C>T (p.Ser1884=)
n.216-37G>A
7g.128851538T>ACA369208305FLNC,FLNC-AS1c.5752T>A (p.Tyr1918Asn)
c.5653T>A (p.Tyr1885Asn)
n.216-38A>T
7g.128851538T>CCA369208303FLNC,FLNC-AS1c.5752T>C (p.Tyr1918His)
c.5653T>C (p.Tyr1885His)
n.216-38A>G
 gnomAD v4
7g.128851538T>GCA369208301FLNC,FLNC-AS1c.5752T>G (p.Tyr1918Asp)
c.5653T>G (p.Tyr1885Asp)
n.216-38A>C
7g.128851539A=CA1742571307FLNC,FLNC-AS1c.5753A= (p.Tyr1918=)
c.5654A= (p.Tyr1885=)
n.216-39T=
7g.128851539A>CCA369208307FLNC,FLNC-AS1c.5753A>C (p.Tyr1918Ser)
c.5654A>C (p.Tyr1885Ser)
n.216-39T>G
 gnomAD v4
7g.128851539A>GCA369208311FLNC,FLNC-AS1c.5753A>G (p.Tyr1918Cys)
c.5654A>G (p.Tyr1885Cys)
n.216-39T>C
 ClinVar dbSNP
7g.128851539A>TCA369208309FLNC,FLNC-AS1c.5753A>T (p.Tyr1918Phe)
c.5654A>T (p.Tyr1885Phe)
n.216-39T>A
7g.128851540delCA1682913318FLNC,FLNC-AS1c.5754del (p.Leu1919CysfsTer?)
c.5655del (p.Leu1886CysfsTer?)
n.216-40del
7g.128851540T>ACA369208313FLNC,FLNC-AS1c.5754T>A (p.Tyr1918Ter)
c.5655T>A (p.Tyr1885Ter)
n.216-40A>T
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.128851540T>CCA4475771FLNC,FLNC-AS1c.5754T>C (p.Tyr1918=)
c.5655T>C (p.Tyr1885=)
n.216-40A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.128851540T>GCA369208316FLNC,FLNC-AS1c.5754T>G (p.Tyr1918Ter)
c.5655T>G (p.Tyr1885Ter)
n.216-40A>C
7g.128851540T=CA1742571320FLNC,FLNC-AS1c.5754T= (p.Tyr1918=)
c.5655T= (p.Tyr1885=)
n.216-40A=
7g.128851541C>ACA369208318FLNC,FLNC-AS1c.5755C>A (p.Leu1919Met)
c.5656C>A (p.Leu1886Met)
n.216-41G>T
 dbSNP gnomAD v3 gnomAD v4
7g.128851541C=CA1742571330FLNC,FLNC-AS1c.5755C= (p.Leu1919=)
c.5656C= (p.Leu1886=)
n.216-41G=
7g.128851541C>GCA369208320FLNC,FLNC-AS1c.5755C>G (p.Leu1919Val)
c.5656C>G (p.Leu1886Val)
n.216-41G>C
7g.128851541C>TCA457849200FLNC,FLNC-AS1c.5755C>T (p.Leu1919=)
c.5656C>T (p.Leu1886=)
n.216-41G>A
 dbSNP gnomAD v2
7g.128851542T>ACA369208322FLNC,FLNC-AS1c.5756T>A (p.Leu1919Gln)
c.5657T>A (p.Leu1886Gln)
n.216-42A>T
7g.128851542T>CCA369208324FLNC,FLNC-AS1c.5756T>C (p.Leu1919Pro)
c.5657T>C (p.Leu1886Pro)
n.216-42A>G
7g.128851542T>GCA369208326FLNC,FLNC-AS1c.5756T>G (p.Leu1919Arg)
c.5657T>G (p.Leu1886Arg)
n.216-42A>C
7g.128851543G>ACA457849201FLNC,FLNC-AS1c.5757G>A (p.Leu1919=)
c.5658G>A (p.Leu1886=)
n.216-43C>T
7g.128851543G>CCA457849203FLNC,FLNC-AS1c.5757G>C (p.Leu1919=)
c.5658G>C (p.Leu1886=)
n.216-43C>G
7g.128851543G>TCA457849202FLNC,FLNC-AS1c.5757G>T (p.Leu1919=)
c.5658G>T (p.Leu1886=)
n.216-43C>A
7g.128851544C>ACA4475773FLNC,FLNC-AS1c.5758C>A (p.Pro1920Thr)
c.5659C>A (p.Pro1887Thr)
n.216-44G>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128851544C=CA1742571340FLNC,FLNC-AS1c.5758C= (p.Pro1920=)
c.5659C= (p.Pro1887=)
n.216-44G=
7g.128851544C>GCA369208330FLNC,FLNC-AS1c.5758C>G (p.Pro1920Ala)
c.5659C>G (p.Pro1887Ala)
n.216-44G>C
7g.128851544C>TCA4475772FLNC,FLNC-AS1c.5758C>T (p.Pro1920Ser)
c.5659C>T (p.Pro1887Ser)
n.216-44G>A
 dbSNP ExAC gnomAD v2
7g.128851545C>ACA369208332FLNC,FLNC-AS1c.5759C>A (p.Pro1920Gln)
c.5660C>A (p.Pro1887Gln)
n.216-45G>T
7g.128851545C=CA1742571347FLNC,FLNC-AS1c.5759C= (p.Pro1920=)
c.5660C= (p.Pro1887=)
n.216-45G=
7g.128851545C>GCA369208334FLNC,FLNC-AS1c.5759C>G (p.Pro1920Arg)
c.5660C>G (p.Pro1887Arg)
n.216-45G>C
7g.128851545C>TCA4475774FLNC,FLNC-AS1c.5759C>T (p.Pro1920Leu)
c.5660C>T (p.Pro1887Leu)
n.216-45G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128851546G>ACA4475775FLNC,FLNC-AS1c.5760G>A (p.Pro1920=)
c.5661G>A (p.Pro1887=)
n.216-46C>T
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128851546G>CCA457849205FLNC,FLNC-AS1c.5760G>C (p.Pro1920=)
c.5661G>C (p.Pro1887=)
n.216-46C>G
7g.128851546G=CA1742571357FLNC,FLNC-AS1c.5760G= (p.Pro1920=)
c.5661G= (p.Pro1887=)
n.216-46C=
7g.128851546G>TCA457849207FLNC,FLNC-AS1c.5760G>T (p.Pro1920=)
c.5661G>T (p.Pro1887=)
n.216-46C>A
7g.128851547A>CCA369208338FLNC,FLNC-AS1c.5761A>C (p.Thr1921Pro)
c.5662A>C (p.Thr1888Pro)
n.216-47T>G
7g.128851547A>GCA369208342FLNC,FLNC-AS1c.5761A>G (p.Thr1921Ala)
c.5662A>G (p.Thr1888Ala)
n.216-47T>C
7g.128851547A>TCA369208340FLNC,FLNC-AS1c.5761A>T (p.Thr1921Ser)
c.5662A>T (p.Thr1888Ser)
n.216-47T>A
7g.128851548C>ACA369208344FLNC,FLNC-AS1c.5762C>A (p.Thr1921Asn)
c.5663C>A (p.Thr1888Asn)
n.216-48G>T
7g.128851548C>GCA369208346FLNC,FLNC-AS1c.5762C>G (p.Thr1921Ser)
c.5663C>G (p.Thr1888Ser)
n.216-48G>C
7g.128851548C>TCA369208348FLNC,FLNC-AS1c.5762C>T (p.Thr1921Ile)
c.5663C>T (p.Thr1888Ile)
n.216-48G>A
 gnomAD v4 COSMIC
7g.128851549delCA2580076615FLNC,FLNC-AS1c.5763del (p.Ala1922ArgfsTer?)
c.5664del (p.Ala1889ArgfsTer?)
n.216-49del
 ClinVar
7g.128851549T>ACA457849210FLNC,FLNC-AS1c.5763T>A (p.Thr1921=)
c.5664T>A (p.Thr1888=)
n.216-49A>T
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.128851549T>CCA152871FLNC,FLNC-AS1c.5763T>C (p.Thr1921=)
c.5664T>C (p.Thr1888=)
n.216-49A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128851549T>GCA457849212FLNC,FLNC-AS1c.5763T>G (p.Thr1921=)
c.5664T>G (p.Thr1888=)
n.216-49A>C

Number of alleles fetched