{{Rsnum
|rsid=199474711
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TPM3
|position=154192008
|Gene_s=TPM3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000034941.1
|CLNALLE=1
|CLNDBN=Congenital myopathy with fiber type disproportion
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1259:C0546264:255310:ORPHA2020:240084007
|CLNHGVS=NC_000001.11:g.154192008G>A
|CLNORIGIN=0
|CLNSIG=5
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_152263.3:c.11C>T; NR_103460.1:n.60C>T; NBK1259
|Disease=Congenital myopathy with fiber type disproportion
|FwdALT=T
|FwdREF=C
|GENEINFO=TPM3:7170
|GENE_ID=7170
|GENE_NAME=TPM3
|REF=G
|RSPOS=154192008
|Reversed=1
|SAO=1
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000a05000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=199474711
}}{{PMID Auto
|PMID=19953533
|Title=Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.
|OA=1
}}