{{Rsnum
|rsid=199474718
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TPM3
|position=154170442
|Gene_s=TPM3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=C
|CHROM=1
|CLNACC=RCV000034945.1
|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.154170442T>C
|CLNSIG=5
|CLNSRC=ClinVar; GeneReviews
|CLNSRCID=NM_001043353.1:c.622A>G; NR_103461.1:n.748A>G; NBK1259
|Disease=Congenital myopathy with fiber type disproportion
|FwdALT=G
|FwdREF=A
|GENEINFO=TPM3:7170
|GENE_ID=7170
|GENE_NAME=TPM3
|REF=T
|RSPOS=154170442
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050368000a05000002110100
|WGT=1
|dbSNPBuildID=136
|rsid=199474718
|CLNORIGIN=0
}}{{PMID Auto
|PMID=18300303
|Title=Mutations in TPM3 are a common cause of congenital fiber type disproportion.
}}