Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128840123_128840136delCA2695208476FLNCc.1512_1525del (p.Gly505GlnfsTer?)
7g.128840126_128840131dupCA4474363FLNCc.1515_1520dup (p.Gly507_Glu508insSerGly)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.128840126_128840133delinsCAGCGGGGCA1742545938FLNCc.1515_1522delinsCAGCGGGG (p.Gly505=)
7g.128840130_128840136delCA658657716FLNCc.1519_1525del (p.Gly507SerfsTer15)
ClinVar dbSNP
7g.128840128G>ACA369225796FLNCc.1517G>A (p.Ser506Asn)
ClinVar dbSNP gnomAD v4
7g.128840128G>CCA369225798FLNCc.1517G>C (p.Ser506Thr)
7g.128840128G=CA1742545939FLNCc.1517G= (p.Ser506=)
7g.128840128G>TCA369225799FLNCc.1517G>T (p.Ser506Ile)
gnomAD v4
7g.128840129C>ACA369225803FLNCc.1518C>A (p.Ser506Arg)
7g.128840129C=CA1742545940FLNCc.1518C= (p.Ser506=)
7g.128840129C>GCA369225801FLNCc.1518C>G (p.Ser506Arg)
7g.128840129C>TCA4474367FLNCc.1518C>T (p.Ser506=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128840130G>ACA4474368FLNCc.1519G>A (p.Gly507Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128840130G>CCA369225804FLNCc.1519G>C (p.Gly507Arg)
7g.128840130G=CA1742545941FLNCc.1519G= (p.Gly507=)
7g.128840130G>TCA369225805FLNCc.1519G>T (p.Gly507Trp)
7g.128840131G>ACA369225806FLNCc.1520G>A (p.Gly507Glu)
dbSNP gnomAD v3 gnomAD v4
7g.128840131G>CCA369225808FLNCc.1520G>C (p.Gly507Ala)
7g.128840131G=CA1742545942FLNCc.1520G= (p.Gly507=)
7g.128840131G>TCA369225810FLNCc.1520G>T (p.Gly507Val)
7g.128840132G>ACA457582796FLNCc.1521G>A (p.Gly507=)
dbSNP
7g.128840132G>CCA457582798FLNCc.1521G>C (p.Gly507=)
7g.128840132G>TCA457582800FLNCc.1521G>T (p.Gly507=)
7g.128840133G>ACA369225813FLNCc.1522G>A (p.Glu508Lys)
7g.128840133G>CCA369225815FLNCc.1522G>C (p.Glu508Gln)
COSMIC
7g.128840133G>TCA369225817FLNCc.1522G>T (p.Glu508Ter)
7g.128840134A>CCA369225819FLNCc.1523A>C (p.Glu508Ala)
ClinVar
7g.128840134A>GCA369225821FLNCc.1523A>G (p.Glu508Gly)
7g.128840134A>TCA369225823FLNCc.1523A>T (p.Glu508Val)
7g.128840135G>ACA457582818FLNCc.1524G>A (p.Glu508=)
7g.128840135G>CCA369225824FLNCc.1524G>C (p.Glu508Asp)
7g.128840135G>TCA369225825FLNCc.1524G>T (p.Glu508Asp)
7g.128840136C>ACA369225831FLNCc.1525C>A (p.Leu509Ile)
7g.128840136C>GCA369225827FLNCc.1525C>G (p.Leu509Val)
ClinVar
7g.128840136C>TCA369225829FLNCc.1525C>T (p.Leu509Phe)
gnomAD v4
7g.128840137T>ACA369225833FLNCc.1526T>A (p.Leu509His)
7g.128840137T>CCA4474369FLNCc.1526T>C (p.Leu509Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.128840137T>GCA369225835FLNCc.1526T>G (p.Leu509Arg)
dbSNP gnomAD v3 gnomAD v4
7g.128840137T=CA1742545943FLNCc.1526T= (p.Leu509=)
7g.128840138C>ACA457582828FLNCc.1527C>A (p.Leu509=)
7g.128840138C=CA1742545944FLNCc.1527C= (p.Leu509=)
7g.128840138C>GCA457582831FLNCc.1527C>G (p.Leu509=)
COSMIC
7g.128840138C>TCA4474370FLNCc.1527C>T (p.Leu509=)
dbSNP ExAC gnomAD v2 gnomAD v4
7g.128840139A=CA1742545945FLNCc.1528A= (p.Lys510=)
7g.128840139A>CCA16618350FLNCc.1528A>C (p.Lys510Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.128840139A>GCA369225839FLNCc.1528A>G (p.Lys510Glu)
gnomAD v4
7g.128840139A>TCA369225840FLNCc.1528A>T (p.Lys510Ter)
7g.128840140A=CA1742545946FLNCc.1529A= (p.Lys510=)
7g.128840140A>CCA369225842FLNCc.1529A>C (p.Lys510Thr)
7g.128840140A>GCA369225843FLNCc.1529A>G (p.Lys510Arg)
dbSNP

Number of alleles fetched