Gene entry
TPRN
taperin
- Chromosome
- 9
- Cytoband
- 9q34.3
- Variants (rsID)
- 4
TPRN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 9 (region 9q34.3). Its official name is “taperin”. The reference table lists 4 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs139459217Benignsingle nucleotide variant
- rs147404722Benignsingle nucleotide variant
- rs139520402Conflicting interpretationssingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 79
- rs727503520Likely benignsingle nucleotide variantAutosomal recessive nonsyndromic hearing loss 79
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.