Gene entry
TRIOBP
TRIO and F-actin binding protein
- Chromosome
- 22
- Cytoband
- 22q13.1
- Variants (rsID)
- 25
TRIOBP is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 22 (region 22q13.1). Its official name is “TRIO and F-actin binding protein”. The reference table lists 25 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs138139146Benignsingle nucleotide variant
- rs183455182Benignsingle nucleotide variant
- rs183941928Benignsingle nucleotide variant
- rs200359708Benignsingle nucleotide variant
- rs34066624Benignsingle nucleotide variantDeafness|Autosomal recessive nonsyndromic hearing loss 28
- rs61737841Benignsingle nucleotide variant
- rs9610841Benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 28
- rs368119524Conflicting interpretationssingle nucleotide variant
- rs147273930Likely benignsingle nucleotide variant
- rs147691840Uncertain significancesingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 28
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.