Assay Details
Target Gene Details
Entrez Gene ID: | 56301 |
Gene Name: | solute carrier family 7 member 10 |
Gene Aliases: |
ASC1, HASC-1, asc-1 |
Location: |
Chr.19:33208664-33225850 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC7A10 | NM_019849.2 | NP_062823.1 | ||
| XM_006723284.2 | XP_006723347.1 | |||
| XM_011527119.1 | XP_011525421.1 | |||
| XM_011527120.1 | XP_011525422.1 | |||
| AB037670.1 | BAB03213.1 | |||
| AJ277731.1 | CAC81900.1 | |||
| AK307527.1 | ||||
| AK316594.1 | ||||
| BC035627.1 | AAH35627.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833808 | Chr.19:33130887 - 33350702 on Build GRCh38 | Loss |
|
| nsv953277 | Chr.19:33192995 - 33270394 on Build GRCh38 | Deletion |
|
More Information
Additional Information:
For this assay, SNP(s) [rs112167751] 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: |
|

Genomic Map