Variant: rs121912673 

    present in Gene: ACTC1;LOC101928174
    present in Chromosome: 15
    Position on Chromosome: 34791163
    Alleles of this Variant: C/T

rs121912673 in ACTC1;LOC101928174 gene and Atrial Septal Defect 5 PMID 24736382 2014 Altered interactions between cardiac myosin binding protein-C and α-cardiac actin variants associated with cardiomyopathies.

PMID 22590617 2012 Subdomain location of mutations in cardiac actin correlate with type of functional change.

PMID 19799913 2010 Human actin mutations associated with hypertrophic and dilated cardiomyopathies demonstrate distinct thin filament regulatory properties in vitro.

PMID 9563954 1998 Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.

PMID 23283745 2013 Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy.

rs121912673 in ACTC1;LOC101928174 gene and CARDIOMYOPATHY, DILATED, 1R PMID 9563954 1998 Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.

PMID 22590617 2012 Subdomain location of mutations in cardiac actin correlate with type of functional change.

PMID 24736382 2014 Altered interactions between cardiac myosin binding protein-C and α-cardiac actin variants associated with cardiomyopathies.

PMID 23283745 2013 Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy.

PMID 19799913 2010 Human actin mutations associated with hypertrophic and dilated cardiomyopathies demonstrate distinct thin filament regulatory properties in vitro.

rs121912673 in ACTC1;LOC101928174 gene and Cardiomyopathy, Familial Hypertrophic, 11 PMID 9563954 1998 Actin mutations in dilated cardiomyopathy, a heritable form of heart failure.

PMID 23283745 2013 Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy.

PMID 24736382 2014 Altered interactions between cardiac myosin binding protein-C and α-cardiac actin variants associated with cardiomyopathies.

PMID 19799913 2010 Human actin mutations associated with hypertrophic and dilated cardiomyopathies demonstrate distinct thin filament regulatory properties in vitro.

PMID 22590617 2012 Subdomain location of mutations in cardiac actin correlate with type of functional change.