Disease-causing mutations in the human cardiac alpha-Actin gene

hypertrophic cardiomyopathy mutations
MutationDiseaseposition in ACTC_genomic.fasUCSC hg17 positionexon/intron
Glu101LysHCM2411328728912
Pro166AlaHCM3281328720213
Tyr168CysHCM3288328720143
Ala232ValHCM3606328716964
Ala297SerHCM4594328707085
Met307LeuHCM4624328706785
Ala333ProHCM5260328700426

dilated cardiomyopathy mutations
MutationDiseaseposition in ACTC_genomic.fasUCSC hg17 positionexon/intron
Arg314HisDCM4646328706565
Glu363GlyDCM5351328699516


Last modified: April 24, 2006