Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.128840046G>ACA4474348FLNCc.1435G>A (p.Ala479Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128840046G>CCA369225481FLNCc.1435G>C (p.Ala479Pro)
dbSNP gnomAD v2 COSMIC
7g.128840046G=CA1742545897FLNCc.1435G= (p.Ala479=)
7g.128840046G>TCA369225483FLNCc.1435G>T (p.Ala479Ser)
7g.128840047C>ACA369225487FLNCc.1436C>A (p.Ala479Asp)
7g.128840047C=CA1742545898FLNCc.1436C= (p.Ala479=)
7g.128840047C>GCA369225489FLNCc.1436C>G (p.Ala479Gly)
7g.128840047C>TCA369225490FLNCc.1436C>T (p.Ala479Val)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
7g.128840048C>ACA457582519FLNCc.1437C>A (p.Ala479=)
7g.128840048C=CA1742545899FLNCc.1437C= (p.Ala479=)
7g.128840048C>GCA457582518FLNCc.1437C>G (p.Ala479=)
7g.128840048C>TCA4474349FLNCc.1437C>T (p.Ala479=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
7g.128840049T>ACA369225494FLNCc.1438T>A (p.Ser480Thr)
7g.128840049T>CCA369225496FLNCc.1438T>C (p.Ser480Pro)
ClinVar
7g.128840049T>GCA369225497FLNCc.1438T>G (p.Ser480Ala)
7g.128840050C>ACA369225498FLNCc.1439C>A (p.Ser480Tyr)
7g.128840050C>GCA369225499FLNCc.1439C>G (p.Ser480Cys)
7g.128840050C>TCA369225501FLNCc.1439C>T (p.Ser480Phe)
7g.128840051T>ACA457582521FLNCc.1440T>A (p.Ser480=)
7g.128840051T>CCA457582523FLNCc.1440T>C (p.Ser480=)
7g.128840051T>GCA457582522FLNCc.1440T>G (p.Ser480=)
7g.128840052G>ACA369225503FLNCc.1441G>A (p.Gly481Arg)
gnomAD v4
7g.128840052G>CCA369225505FLNCc.1441G>C (p.Gly481Arg)
7g.128840052G>TCA369225507FLNCc.1441G>T (p.Gly481Trp)
7g.128840053G>ACA369225513FLNCc.1442G>A (p.Gly481Glu)
7g.128840053G>CCA369225511FLNCc.1442G>C (p.Gly481Ala)
gnomAD v4
7g.128840053G>TCA369225509FLNCc.1442G>T (p.Gly481Val)
7g.128840054G>ACA457582526FLNCc.1443G>A (p.Gly481=)
7g.128840054G>CCA457582527FLNCc.1443G>C (p.Gly481=)
7g.128840054G>TCA457582528FLNCc.1443G>T (p.Gly481=)
7g.128840055C>ACA457582529FLNCc.1444C>A (p.Arg482=)
7g.128840055C=CA1742545900FLNCc.1444C= (p.Arg482=)
7g.128840055C>GCA369225514FLNCc.1444C>G (p.Arg482Gly)
7g.128840055C>TCA369225516FLNCc.1444C>T (p.Arg482Ter)
ClinVar dbSNP gnomAD v2 gnomAD v4
7g.128840056G>ACA4474350FLNCc.1445G>A (p.Arg482Gln)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
7g.128840056G>CCA369225518FLNCc.1445G>C (p.Arg482Pro)
7g.128840056G=CA1742545901FLNCc.1445G= (p.Arg482=)
7g.128840056G>TCA369225521FLNCc.1445G>T (p.Arg482Leu)
7g.128840057A>CCA457582533FLNCc.1446A>C (p.Arg482=)
7g.128840057A>GCA457582534FLNCc.1446A>G (p.Arg482=)
7g.128840057A>TCA457582535FLNCc.1446A>T (p.Arg482=)
7g.128840058G>ACA369225523FLNCc.1447G>A (p.Gly483Ser)
7g.128840058G>CCA369225525FLNCc.1447G>C (p.Gly483Arg)
7g.128840058G>TCA369225527FLNCc.1447G>T (p.Gly483Cys)
7g.128840059G>ACA369225530FLNCc.1448G>A (p.Gly483Asp)
ClinVar dbSNP gnomAD v4
7g.128840059G>CCA369225531FLNCc.1448G>C (p.Gly483Ala)
gnomAD v4
7g.128840059G=CA1742545902FLNCc.1448G= (p.Gly483=)
7g.128840059G>TCA369225533FLNCc.1448G>T (p.Gly483Val)
7g.128840060C>ACA457582537FLNCc.1449C>A (p.Gly483=)
7g.128840060C>GCA457582538FLNCc.1449C>G (p.Gly483=)
ClinVar

Number of alleles fetched