{{Rsnum
|rsid=80358249
|Chromosome=19
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=TNNT1
|position=55137176
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=TNNT1
}}{{omim
|id=191041
|rsnum=80358249
|variant=0001
}}{{ClinVar
|rsid=80358249
|Reversed=1
|FwdREF=G
|FwdALT=T
|REF=C
|ALT=A
|RSPOS=55648544
|CHROM=19
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=TNNT1:7138
|GENE_NAME=TNNT1
|GENE_ID=7138
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000019.9:g.55648544C>A
|CLNSRC=GeneReviews; Leiden Muscular Dystrophy pages (TNNT1); OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1288; TNNT1_00001; 191041.0001
|CLNSIG=5
|CLNCUI=C1854380
|CLNDBN=Nemaline myopathy 5; not provided
|Disease=Nemaline myopathy 5; not provided
|CLNACC=RCV000020554.2; RCV000024549.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1288:C1854380:605355:607
}}{{PMID Auto
|PMID=10952871
|Title=A novel nemaline myopathy in the Amish caused by a mutation in troponin T1.
|OA=1
}}

{{PMID Auto
|PMID=12732643
|Title=Truncation by Glu180 nonsense mutation results in complete loss of slow skeletal muscle troponin T in a lethal nemaline myopathy.
}}

{{PMID Auto
|PMID=15665378
|Title=Cellular fate of truncated slow skeletal muscle troponin T produced by Glu180 nonsense mutation in amish nemaline myopathy.
}}