Gene entry
TAP1
transporter 1, ATP binding cassette subfamily B member
- Chromosome
- 6
- Cytoband
- 6p21.32
- Variants (rsID)
- 23
TAP1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 6 (region 6p21.32). Its official name is “transporter 1, ATP binding cassette subfamily B member”. The reference table lists 23 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs1057149Benignsingle nucleotide variantMHC class I deficiency
- rs1135216Benignsingle nucleotide variantPEPTIDE TRANSPORTER PSF1 POLYMORPHISM|MHC class I deficiency
- rs2127679Benignsingle nucleotide variantMHC class I deficiency
- rs2228110Benignsingle nucleotide variantMHC class I deficiency
- rs41551515Benignsingle nucleotide variantMHC class I deficiency
- rs41561219Benignsingle nucleotide variantMHC class I deficiency
- rs121917702Likely benignsingle nucleotide variantTAP1 deficiency, somatic|MHC class I deficiency
- rs2228108Likely benignsingle nucleotide variantMHC class I deficiency
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.