{{Rsnum
|rsid=199474719
|Chromosome=1
|Orientation=minus
|geno1=(-;-)
|geno2=(-;A)
|geno3=(A;A)
|Gene=TPM3
|position=154167940
|Gene_s=TPM3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=199474719
|Reversed=1
|FwdREF=A
|FwdALT=
|REF=AT
|ALT=A
|RSPOS=154167939
|CHROM=1
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050168081205000002110200
|WGT=1
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.154167940delT
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_001043351.1:c.664+2460delA; NM_152263.3:c.855delA; 191030.0006
|CLNSIG=5
|CLNCUI=C1836448
|CLNDBN=Nemaline myopathy 1
|Disease=Nemaline myopathy 1
|CLNACC=RCV000013266.23
|Tags=RV;PM;PMC;SLO;NSF;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1259:NBK1288:C1836448:609284:ORPHA171881:ORPHA607
|GENEINFO=TPM3:7170
|GENE_ID=7170
|GENE_NAME=TPM3
}}{{PMID Auto
|PMID=18382475
|Title=Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish origin.
}}