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 1 |
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 | CRAT37 |
nsv833094 | Chr.15:91288643 - 91497082 on Build GRCh38 | Gain | CRAT37 SV2B |
esv2760055 | Chr.15:91288620 - 91497082 on Build GRCh38 | Gain | CRAT37 SV2B |
More Information
Additional Information:
For this assay, SNP(s) [rs80076207] 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: |
Intragenic Intronic Non-exonic DGV Variation |