Assay Details
Target Gene Details
Entrez Gene ID: | 101926928 |
Gene Name: | cervical cancer-associated transcript 37 |
Gene Aliases: |
- |
Location: |
Chr.15:91463339-91494850 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CRAT37 | NR_110106.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833095 | Chr.15:91463563 - 91607946 on Build GRCh38 | Loss |
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nsv833094 | Chr.15:91288643 - 91497082 on Build GRCh38 | Gain |
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esv2760055 | Chr.15:91288620 - 91497082 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs149136134] 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.
Set Membership: |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)