Gene entry
TCAP
titin-cap
- Chromosome
- 17
- Cytoband
- 17q12
- Variants (rsID)
- 9
TCAP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17q12). Its official name is “titin-cap”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
9 reference-table entries with clinical significance.
- rs45458802Benignsingle nucleotide variantHypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy|Cardiovascular phenotype|Cardiomyopathy|Hypertrophic cardiomyopathy|Long QT syndrome
- rs45578741Benignsingle nucleotide variantPrimary familial hypertrophic cardiomyopathy|Cardiovascular phenotype|Cardiomyopathy|Hypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy|Autosomal recessive limb-girdle muscular dystrophy type 2G|Hypertrophic cardiomyopathy 25|Hypertrophic cardiomyopathy
- rs143233087Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Cardiomyopathy|Hypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy|Hypertrophic cardiomyopathy 1
- rs146502276Conflicting interpretationssingle nucleotide variantCardiovascular phenotype|Hypertrophic cardiomyopathy 25|Autosomal recessive limb-girdle muscular dystrophy type 2G|Hypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy
- rs149585781Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 25|Autosomal recessive limb-girdle muscular dystrophy type 2G|Hypertrophic cardiomyopathy 25|Hypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy
- rs397516861Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy|Cardiomyopathy
- rs45614332Conflicting interpretationssingle nucleotide variantHypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy
- rs104894655Pathogenicsingle nucleotide variantAutosomal recessive limb-girdle muscular dystrophy type 2G|Hypertrophic cardiomyopathy 25|Primary dilated cardiomyopathy|Hypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy
- rs45509691Uncertain significancesingle nucleotide variantCardiomyopathy|Hypertrophic cardiomyopathy 25|Primary familial hypertrophic cardiomyopathy|Cardiovascular phenotype|Hypertrophic cardiomyopathy 25|Autosomal recessive limb-girdle muscular dystrophy type 2G
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.