{{Rsnum
|rsid=80358248
|Chromosome=1
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TPM3
|position=154191925
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TPM3
}}{{omim
|id=191030
|rsnum=80358248
|variant=0004
}}{{ClinVar
|rsid=80358248
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=154191925
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000605000002110100
|GENEINFO=TPM3:7170
|GENE_NAME=TPM3
|GENE_ID=7170
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.154191925G>A
|CLNSRC=ClinVar; GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_152263.3:c.94C>T; NR_103460.1:n.143C>T; NBK1288; 191030.0004
|CLNSIG=5
|CLNCUI=C1836448; C1836448
|CLNDBN=Nemaline myopathy 1
|Disease=Nemaline myopathy 1
|CLNACC=RCV000013262.24
|Tags=RV;PM;PMC;S3D;SLO;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1259:NBK1288:C1836448:609284:ORPHA171881:ORPHA607
}}{{PMID Auto
|PMID=10619715
|Title=Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathy.
}}