Product Details
- Assay Reference Genome
Location
Chr.7:96157091 on build GRCh38
- Cytoband
- 7q21.3
- Species
- Homo sapiens
- Variation Type
- Copy Number
Additional Information
For this assay, SNP(s) [rs114109456] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Target Gene Details
- Entrez Gene ID
- 10165
- Gene Symbol
- SLC25A13
- Gene Name
- solute carrier family 25 member 13
- Gene Aliases
- ARALAR2, CITRIN, CTLN2
- Location
- Chr.7:96120220-96322147 on build GRCh38
- Assay Gene Location
- Within Intron 16
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