{{Rsnum
|rsid=104894505
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPM1
|position=63044072
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM1
}}{{omim
|id=191010
|rsnum=104894505
|variant=0004
}}{{ClinVar
|rsid=104894505
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=63336271
|CHROM=15
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=TPM1:7168
|GENE_NAME=TPM1
|GENE_ID=7168
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000015.9:g.63336271G>A
|CLNSRC=Leiden Muscular Dystrophy pages (TPM1); OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=TPM1_00002; 191010.0004
|CLNSIG=5
|CLNCUI=C2678476
|CLNDBN=Dilated cardiomyopathy 1Y
|Disease=Dilated cardiomyopathy 1Y
|CLNACC=RCV000013274.21
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1309:C2678476:611878:154:54260
}}{{PMID|11273725}} Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy.