Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128852818C=CA1742575447FLNC,FLNC-AS1c.6005-10C= (n.6005-10C=)
c.5906-10C= (n.5906-10C=)
n.215+467G=
7g.128852818C>TCA578150602FLNC,FLNC-AS1c.6005-10C>T (n.6005-10C>T)
c.5906-10C>T (n.5906-10C>T)
n.215+467G>A
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.128852819T>CCA202655FLNC,FLNC-AS1c.6005-9T>C (n.6005-9T>C)
c.5906-9T>C (n.5906-9T>C)
n.215+466A>G
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128852819T=CA1742575450FLNC,FLNC-AS1c.6005-9T= (n.6005-9T=)
c.5906-9T= (n.5906-9T=)
n.215+466A=
7g.128852821T>CCA915945514FLNC,FLNC-AS1c.6005-7T>C (n.6005-7T>C)
c.5906-7T>C (n.5906-7T>C)
n.215+464A>G
 ClinVar dbSNP gnomAD v4
7g.128852821T=CA1742575460FLNC,FLNC-AS1c.6005-7T= (n.6005-7T=)
c.5906-7T= (n.5906-7T=)
n.215+464A=
7g.128852822C=CA1742575468FLNC,FLNC-AS1c.6005-6C= (n.6005-6C=)
c.5906-6C= (n.5906-6C=)
n.215+463G=
7g.128852822C>TCA166190100FLNC,FLNC-AS1c.6005-6C>T (n.6005-6C>T)
c.5906-6C>T (n.5906-6C>T)
n.215+463G>A
 dbSNP
7g.128852823C>TCA2579014565FLNC,FLNC-AS1c.6005-5C>T (n.6005-5C>T)
c.5906-5C>T (n.5906-5C>T)
n.215+462G>A
 ClinVar gnomAD v4
7g.128852825C=CA1742575471FLNC,FLNC-AS1c.6005-3C= (n.6005-3C=)
c.5906-3C= (n.5906-3C=)
n.215+460G=
7g.128852825C>TCA166190102FLNC,FLNC-AS1c.6005-3C>T (n.6005-3C>T)
c.5906-3C>T (n.5906-3C>T)
n.215+460G>A
 dbSNP
7g.128852826A=CA1742575473FLNC,FLNC-AS1c.6005-2A= (n.6005-2A=)
c.5906-2A= (n.5906-2A=)
n.215+459T=
7g.128852826A>CCA369210854FLNC,FLNC-AS1c.6005-2A>C (n.6005-2A>C)
c.5906-2A>C (n.5906-2A>C)
n.215+459T>G
7g.128852826A>GCA369210856FLNC,FLNC-AS1c.6005-2A>G (n.6005-2A>G)
c.5906-2A>G (n.5906-2A>G)
n.215+459T>C
7g.128852826A>TCA166190104FLNC,FLNC-AS1c.6005-2A>T (n.6005-2A>T)
c.5906-2A>T (n.5906-2A>T)
n.215+459T>A
 dbSNP
7g.128852827G>ACA369210861FLNC,FLNC-AS1c.6005-1G>A (n.6005-1G>A)
c.5906-1G>A (n.5906-1G>A)
n.215+458C>T
7g.128852827G>CCA369210858FLNC,FLNC-AS1c.6005-1G>C (n.6005-1G>C)
c.5906-1G>C (n.5906-1G>C)
n.215+458C>G
7g.128852827G>TCA369210860FLNC,FLNC-AS1c.6005-1G>T (n.6005-1G>T)
c.5906-1G>T (n.5906-1G>T)
n.215+458C>A
7g.128852828G>ACA369210864FLNC,FLNC-AS1c.6005G>A (p.Gly2002Glu)
c.5906G>A (p.Gly1969Glu)
n.215+457C>T
7g.128852828G>CCA369210866FLNC,FLNC-AS1c.6005G>C (p.Gly2002Ala)
c.5906G>C (p.Gly1969Ala)
n.215+457C>G
 gnomAD v4
7g.128852828G=CA1742575482FLNC,FLNC-AS1c.6005G= (p.Gly2002=)
c.5906G= (p.Gly1969=)
n.215+457C=
7g.128852828G>TCA4475869FLNC,FLNC-AS1c.6005G>T (p.Gly2002Val)
c.5906G>T (p.Gly1969Val)
n.215+457C>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128852829G>ACA166190122FLNC,FLNC-AS1c.6006G>A (p.Gly2002=)
c.5907G>A (p.Gly1969=)
n.215+456C>T
 dbSNP gnomAD v3 gnomAD v4
7g.128852829G>CCA457849430FLNC,FLNC-AS1c.6006G>C (p.Gly2002=)
c.5907G>C (p.Gly1969=)
n.215+456C>G
 ClinVar dbSNP gnomAD v2 gnomAD v4
7g.128852829G=CA1742575488FLNC,FLNC-AS1c.6006G= (p.Gly2002=)
c.5907G= (p.Gly1969=)
n.215+456C=
7g.128852829G>TCA457849431FLNC,FLNC-AS1c.6006G>T (p.Gly2002=)
c.5907G>T (p.Gly1969=)
n.215+456C>A
7g.128852830A>CCA369210869FLNC,FLNC-AS1c.6007A>C (p.Ile2003Leu)
c.5908A>C (p.Ile1970Leu)
n.215+455T>G
7g.128852830A>GCA369210871FLNC,FLNC-AS1c.6007A>G (p.Ile2003Val)
c.5908A>G (p.Ile1970Val)
n.215+455T>C
7g.128852830A>TCA369210873FLNC,FLNC-AS1c.6007A>T (p.Ile2003Phe)
c.5908A>T (p.Ile1970Phe)
n.215+455T>A
7g.128852831T>ACA369210875FLNC,FLNC-AS1c.6008T>A (p.Ile2003Asn)
c.5909T>A (p.Ile1970Asn)
n.215+454A>T
 ClinVar
7g.128852831T>CCA369210877FLNC,FLNC-AS1c.6008T>C (p.Ile2003Thr)
c.5909T>C (p.Ile1970Thr)
n.215+454A>G
 dbSNP
7g.128852831T>GCA369210879FLNC,FLNC-AS1c.6008T>G (p.Ile2003Ser)
c.5909T>G (p.Ile1970Ser)
n.215+454A>C
7g.128852831T=CA1742575494FLNC,FLNC-AS1c.6008T= (p.Ile2003=)
c.5909T= (p.Ile1970=)
n.215+454A=
7g.128852832delCA2580611033FLNC,FLNC-AS1c.6009del (p.Ser2004ProfsTer12)
c.5910del (p.Ser1971ProfsTer12)
n.215+453del
 ClinVar
7g.128852832C>ACA457849433FLNC,FLNC-AS1c.6009C>A (p.Ile2003=)
c.5910C>A (p.Ile1970=)
n.215+453G>T
 ClinVar dbSNP gnomAD v4
7g.128852832C>GCA369210881FLNC,FLNC-AS1c.6009C>G (p.Ile2003Met)
c.5910C>G (p.Ile1970Met)
n.215+453G>C
7g.128852832C>TCA457849434FLNC,FLNC-AS1c.6009C>T (p.Ile2003=)
c.5910C>T (p.Ile1970=)
n.215+453G>A
 ClinVar gnomAD v4
7g.128852834_128852836delCA2695203152FLNC,FLNC-AS1c.6011_6013del (p.Ser2004del)
c.5912_5914del (p.Ser1971del)
n.215+451_215+453del
7g.128852833T>ACA369210883FLNC,FLNC-AS1c.6010T>A (p.Ser2004Thr)
c.5911T>A (p.Ser1971Thr)
n.215+452A>T
7g.128852833T>CCA369210885FLNC,FLNC-AS1c.6010T>C (p.Ser2004Pro)
c.5911T>C (p.Ser1971Pro)
n.215+452A>G
7g.128852833T>GCA369210887FLNC,FLNC-AS1c.6010T>G (p.Ser2004Ala)
c.5911T>G (p.Ser1971Ala)
n.215+452A>C
7g.128852834C>ACA369210890FLNC,FLNC-AS1c.6011C>A (p.Ser2004Tyr)
c.5912C>A (p.Ser1971Tyr)
n.215+451G>T
7g.128852834C>GCA369210893FLNC,FLNC-AS1c.6011C>G (p.Ser2004Cys)
c.5912C>G (p.Ser1971Cys)
n.215+451G>C
7g.128852834C>TCA369210891FLNC,FLNC-AS1c.6011C>T (p.Ser2004Phe)
c.5912C>T (p.Ser1971Phe)
n.215+451G>A
 ClinVar
7g.128852835C>ACA457849436FLNC,FLNC-AS1c.6012C>A (p.Ser2004=)
c.5913C>A (p.Ser1971=)
n.215+450G>T
 gnomAD v4
7g.128852835C>GCA457849437FLNC,FLNC-AS1c.6012C>G (p.Ser2004=)
c.5913C>G (p.Ser1971=)
n.215+450G>C
 ClinVar
7g.128852835C>TCA457849438FLNC,FLNC-AS1c.6012C>T (p.Ser2004=)
c.5913C>T (p.Ser1971=)
n.215+450G>A
7g.128852836T>ACA369210896FLNC,FLNC-AS1c.6013T>A (p.Phe2005Ile)
c.5914T>A (p.Phe1972Ile)
n.215+449A>T
7g.128852836T>CCA369210898FLNC,FLNC-AS1c.6013T>C (p.Phe2005Leu)
c.5914T>C (p.Phe1972Leu)
n.215+449A>G
7g.128852836T>GCA369210900FLNC,FLNC-AS1c.6013T>G (p.Phe2005Val)
c.5914T>G (p.Phe1972Val)
n.215+449A>C

Number of alleles fetched