Gene entry
TTC19
tetratricopeptide repeat domain 19
- Chromosome
- 17
- Cytoband
- 17p12
- Variants (rsID)
- 16
TTC19 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 17 (region 17p12). Its official name is “tetratricopeptide repeat domain 19”. The reference table lists 16 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs73981411Benignsingle nucleotide variant
- rs200004394Conflicting interpretationssingle nucleotide variantMitochondrial complex III deficiency nuclear type 1
- rs753100200Conflicting interpretationssingle nucleotide variantMitochondrial complex III deficiency nuclear type 1
- rs77955179Conflicting interpretationssingle nucleotide variantMitochondrial complex III deficiency nuclear type 2
- rs78882347Conflicting interpretationssingle nucleotide variantMitochondrial complex III deficiency nuclear type 2
- rs79724115Conflicting interpretationssingle nucleotide variantMitochondrial complex III deficiency nuclear type 1
- rs117087989Uncertain significancesingle nucleotide variantMitochondrial complex III deficiency nuclear type 2
- rs192522753Uncertain significancesingle nucleotide variant
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.