Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128852918T>ACA369211228FLNC,FLNC-AS1c.6095T>A (p.Leu2032Gln)
c.5996T>A (p.Leu1999Gln)
n.215+367A>T
7g.128852918T>CCA369211229FLNC,FLNC-AS1c.6095T>C (p.Leu2032Pro)
c.5996T>C (p.Leu1999Pro)
n.215+367A>G
 ClinVar dbSNP gnomAD v4
7g.128852918T>GCA369211230FLNC,FLNC-AS1c.6095T>G (p.Leu2032Arg)
c.5996T>G (p.Leu1999Arg)
n.215+367A>C
7g.128852918T=CA1742575839FLNC,FLNC-AS1c.6095T= (p.Leu2032=)
c.5996T= (p.Leu1999=)
n.215+367A=
7g.128852919G>ACA457849500FLNC,FLNC-AS1c.6096G>A (p.Leu2032=)
c.5997G>A (p.Leu1999=)
n.215+366C>T
7g.128852919G>CCA457849501FLNC,FLNC-AS1c.6096G>C (p.Leu2032=)
c.5997G>C (p.Leu1999=)
n.215+366C>G
 dbSNP gnomAD v3 gnomAD v4
7g.128852919G=CA1742575843FLNC,FLNC-AS1c.6096G= (p.Leu2032=)
c.5997G= (p.Leu1999=)
n.215+366C=
7g.128852919G>TCA457849502FLNC,FLNC-AS1c.6096G>T (p.Leu2032=)
c.5997G>T (p.Leu1999=)
n.215+366C>A
7g.128852920G>ACA4475886FLNC,FLNC-AS1c.6097G>A (p.Val2033Met)
c.5998G>A (p.Val2000Met)
n.215+365C>T
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128852920G>CCA369211231FLNC,FLNC-AS1c.6097G>C (p.Val2033Leu)
c.5998G>C (p.Val2000Leu)
n.215+365C>G
7g.128852920G=CA1742575846FLNC,FLNC-AS1c.6097G= (p.Val2033=)
c.5998G= (p.Val2000=)
n.215+365C=
7g.128852920G>TCA369211232FLNC,FLNC-AS1c.6097G>T (p.Val2033Leu)
c.5998G>T (p.Val2000Leu)
n.215+365C>A
7g.128852921T>ACA369211233FLNC,FLNC-AS1c.6098T>A (p.Val2033Glu)
c.5999T>A (p.Val2000Glu)
n.215+364A>T
7g.128852921T>CCA4475887FLNC,FLNC-AS1c.6098T>C (p.Val2033Ala)
c.5999T>C (p.Val2000Ala)
n.215+364A>G
 dbSNP ExAC gnomAD v2
7g.128852921T>GCA369211234FLNC,FLNC-AS1c.6098T>G (p.Val2033Gly)
c.5999T>G (p.Val2000Gly)
n.215+364A>C
7g.128852921T=CA1742575869FLNC,FLNC-AS1c.6098T= (p.Val2033=)
c.5999T= (p.Val2000=)
n.215+364A=
7g.128852922G>ACA166190222FLNC,FLNC-AS1c.6099G>A (p.Val2033=)
c.6000G>A (p.Val2000=)
n.215+363C>T
 ClinVar dbSNP gnomAD v4
7g.128852922G>CCA457849503FLNC,FLNC-AS1c.6099G>C (p.Val2033=)
c.6000G>C (p.Val2000=)
n.215+363C>G
7g.128852922G=CA1742575871FLNC,FLNC-AS1c.6099G= (p.Val2033=)
c.6000G= (p.Val2000=)
n.215+363C=
7g.128852922G>TCA457849504FLNC,FLNC-AS1c.6099G>T (p.Val2033=)
c.6000G>T (p.Val2000=)
n.215+363C>A
7g.128852923G>ACA369211235FLNC,FLNC-AS1c.6100G>A (p.Gly2034Arg)
c.6001G>A (p.Gly2001Arg)
n.215+362C>T
7g.128852923G>CCA369211236FLNC,FLNC-AS1c.6100G>C (p.Gly2034Arg)
c.6001G>C (p.Gly2001Arg)
n.215+362C>G
 gnomAD v4
7g.128852923G>TCA369211237FLNC,FLNC-AS1c.6100G>T (p.Gly2034Trp)
c.6001G>T (p.Gly2001Trp)
n.215+362C>A
7g.128852924G>ACA369211238FLNC,FLNC-AS1c.6101G>A (p.Gly2034Glu)
c.6002G>A (p.Gly2001Glu)
n.215+361C>T
 dbSNP
7g.128852924G>CCA369211239FLNC,FLNC-AS1c.6101G>C (p.Gly2034Ala)
c.6002G>C (p.Gly2001Ala)
n.215+361C>G
7g.128852924G=CA1742575875FLNC,FLNC-AS1c.6101G= (p.Gly2034=)
c.6002G= (p.Gly2001=)
n.215+361C=
7g.128852924G>TCA369211240FLNC,FLNC-AS1c.6101G>T (p.Gly2034Val)
c.6002G>T (p.Gly2001Val)
n.215+361C>A
7g.128852925G>ACA457849505FLNC,FLNC-AS1c.6102G>A (p.Gly2034=)
c.6003G>A (p.Gly2001=)
n.215+360C>T
 gnomAD v4
7g.128852925G>CCA457849506FLNC,FLNC-AS1c.6102G>C (p.Gly2034=)
c.6003G>C (p.Gly2001=)
n.215+360C>G
7g.128852925G>TCA457849507FLNC,FLNC-AS1c.6102G>T (p.Gly2034=)
c.6003G>T (p.Gly2001=)
n.215+360C>A
 gnomAD v4
7g.128852926C>ACA369211241FLNC,FLNC-AS1c.6103C>A (p.Pro2035Thr)
c.6004C>A (p.Pro2002Thr)
n.215+359G>T
7g.128852926C=CA1742575920FLNC,FLNC-AS1c.6103C= (p.Pro2035=)
c.6004C= (p.Pro2002=)
n.215+359G=
7g.128852926C>GCA369211242FLNC,FLNC-AS1c.6103C>G (p.Pro2035Ala)
c.6004C>G (p.Pro2002Ala)
n.215+359G>C
7g.128852926C>TCA4475888FLNC,FLNC-AS1c.6103C>T (p.Pro2035Ser)
c.6004C>T (p.Pro2002Ser)
n.215+359G>A
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
7g.128852927C>ACA369211245FLNC,FLNC-AS1c.6104C>A (p.Pro2035Gln)
c.6005C>A (p.Pro2002Gln)
n.215+358G>T
7g.128852927C=CA1742575931FLNC,FLNC-AS1c.6104C= (p.Pro2035=)
c.6005C= (p.Pro2002=)
n.215+358G=
7g.128852927C>GCA369211246FLNC,FLNC-AS1c.6104C>G (p.Pro2035Arg)
c.6005C>G (p.Pro2002Arg)
n.215+358G>C
7g.128852927C>TCA369211243FLNC,FLNC-AS1c.6104C>T (p.Pro2035Leu)
c.6005C>T (p.Pro2002Leu)
n.215+358G>A
 ClinVar dbSNP
7g.128852928A>CCA457849508FLNC,FLNC-AS1c.6105A>C (p.Pro2035=)
c.6006A>C (p.Pro2002=)
n.215+357T>G
7g.128852928A>GCA457849509FLNC,FLNC-AS1c.6105A>G (p.Pro2035=)
c.6006A>G (p.Pro2002=)
n.215+357T>C
 ClinVar dbSNP gnomAD v4
7g.128852928A>TCA457849510FLNC,FLNC-AS1c.6105A>T (p.Pro2035=)
c.6006A>T (p.Pro2002=)
n.215+357T>A
7g.128852929T>ACA369211247FLNC,FLNC-AS1c.6106T>A (p.Ser2036Thr)
c.6007T>A (p.Ser2003Thr)
n.215+356A>T
7g.128852929T>CCA369211249FLNC,FLNC-AS1c.6106T>C (p.Ser2036Pro)
c.6007T>C (p.Ser2003Pro)
n.215+356A>G
7g.128852929T>GCA369211248FLNC,FLNC-AS1c.6106T>G (p.Ser2036Ala)
c.6007T>G (p.Ser2003Ala)
n.215+356A>C
 ClinVar
7g.128852930C>ACA369211250FLNC,FLNC-AS1c.6107C>A (p.Ser2036Tyr)
c.6008C>A (p.Ser2003Tyr)
n.215+355G>T
7g.128852930C>GCA369211251FLNC,FLNC-AS1c.6107C>G (p.Ser2036Cys)
c.6008C>G (p.Ser2003Cys)
n.215+355G>C
7g.128852930C>TCA369211252FLNC,FLNC-AS1c.6107C>T (p.Ser2036Phe)
c.6008C>T (p.Ser2003Phe)
n.215+355G>A
7g.128852931T>ACA457849511FLNC,FLNC-AS1c.6108T>A (p.Ser2036=)
c.6009T>A (p.Ser2003=)
n.215+354A>T
7g.128852931T>CCA457849513FLNC,FLNC-AS1c.6108T>C (p.Ser2036=)
c.6009T>C (p.Ser2003=)
n.215+354A>G
 ClinVar dbSNP gnomAD v3 gnomAD v4
7g.128852931T>GCA457849512FLNC,FLNC-AS1c.6108T>G (p.Ser2036=)
c.6009T>G (p.Ser2003=)
n.215+354A>C
 gnomAD v4

Number of alleles fetched