Assay Details
Target Gene Details
Entrez Gene ID: | 115019 |
Gene Name: | solute carrier family 26 member 9 |
Gene Aliases: |
- |
Location: |
Chr.1:205913048-205943472 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC26A9 | NM_052934.3 | 21 | 4427 | NP_443166.1 |
NM_134325.2 | 22 | 4250 | NP_599152.2 | |
XM_011509121.2 | 20 | 4290 | XP_011507423.1 | |
XM_011509122.2 | 18 | 3979 | XP_011507424.1 | |
AF314958.1 | 21 | 4138 | AAL26867.1 | |
AF331525.1 | 21 | 4427 | AAK95667.1 | |
AK091876.1 | 2 | 2073 | BAC03763.1 | |
AK127491.1 | 13 | 3697 | ||
BC151208.1 | 21 | 4386 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832392 | Chr.1:205882365 - 205944905 on Build GRCh38 | Gain | LOC284581 SLC26A9 LOC103021296 |
nsv549045 | Chr.1:205909560 - 205915146 on Build GRCh38 | Loss | SLC26A9 |
More Information
Additional Information:
For this assay, SNP(s) [rs78944112] 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 Exonic DGV Variation |