Gene entry
TPM3
tropomyosin 3
- Chromosome
- 1
- Cytoband
- 1q21.3
- Variants (rsID)
- 10
TPM3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1q21.3). Its official name is “tropomyosin 3”. The reference table lists 10 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs62000429Benignsingle nucleotide variantNemaline myopathy 1|Congenital myopathy with fiber type disproportion|Nemaline myopathy 1|Congenital myopathy with fiber type disproportion
- rs41265215Likely benignsingle nucleotide variant
- rs121964854Pathogenicsingle nucleotide variantCongenital myopathy with fiber type disproportion|Nemaline myopathy 1|Nemaline myopathy 1|Congenital myopathy with fiber type disproportion
- rs142817656Uncertain significancesingle nucleotide variantNemaline myopathy 1|Congenital myopathy with fiber type disproportion
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.