{{Rsnum
|rsid=121964853
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=TPM3
|position=154176194
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM3
}}{{omim
|id=191030
|rsnum=121964853
|variant=0007
}}{{ClinVar
|rsid=121964853
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=154176194
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368480a05000002110100
|GENEINFO=TPM3:7170
|GENE_NAME=TPM3
|GENE_ID=7170
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.154176194G>T
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001043353.1:c.187C>A; NM_001278188.1:c.69-2993C>A; NM_001278191.1:c.-84C>A; NR_103461.1:n.317C>A; NBK1259; 191030.0007
|CLNSIG=5
|CLNCUI=C0546264
|CLNDBN=Congenital myopathy with fiber type disproportion
|Disease=Congenital myopathy with fiber type disproportion
|CLNACC=RCV000013267.22
|Tags=RV;PM;PMC;S3D;SLO;NSM;REF;U5;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1259:C0546264:255310:ORPHA2020:240084007
}}{{PMID|18300303}} Mutations in TPM3 are a common cause of congenital fiber type disproportion.