Assay Details
Target Gene Details
Entrez Gene ID: | 6510 |
Gene Name: | solute carrier family 1 member 5 |
Gene Aliases: |
AAAT, ASCT2, ATBO, M7V1, M7VS1, R16, RDRC |
Location: |
Chr.19:46759685-46788622 on Build GRCh38 |
Assay Gene Location: | Within Intron 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC1A5 | XM_005259167.4 | XP_005259224.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3644536 | Chr.19:46768258 - 46772221 on Build GRCh38 | Loss |
|
| nsv833850 | Chr.19:46703285 - 46867053 on Build GRCh38 | Loss |
|
| dgv3608n100 | Chr.19:46757741 - 46865807 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs72477169] 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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Genomic Map