Gene entry
CPT1C
carnitine palmitoyltransferase 1C
- Chromosome
- 19
- Cytoband
- 19q13.33
- Variants (rsID)
- 11
CPT1C is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19q13.33). Its official name is “carnitine palmitoyltransferase 1C”. The reference table lists 11 variants (rsID) for this gene.
Clinically classified variants
2 reference-table entries with clinical significance.
- rs61747405Benignsingle nucleotide variantHereditary spastic paraplegia 73
- rs200190780Uncertain significancesingle nucleotide variantHereditary spastic paraplegia 73
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.