Assay Details
Target Gene Details
Entrez Gene ID: | 54407 |
Gene Name: | solute carrier family 38 member 2 |
Gene Aliases: |
ATA2, PRO1068, SAT2, SNAT2 |
Location: |
Chr.12:46358188-46372862 on Build GRCh38 |
Assay Gene Location: | Within Exon 16 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC38A2 | NM_001307936.1 | 15 | 3270 | NP_001294865.1 |
NM_018976.4 | 16 | 3386 | NP_061849.2 | |
AB037803.2 | 15 | 2946 | BAA92620.2 | |
AF116620.2 | 1 | 936 | AAF71044.1 | |
AF259799.1 | 15 | 2966 | AAK38510.1 | |
AF298897.1 | 16 | 3297 | AAG24618.1 | |
AJ344099.1 | 16 | 3298 | CAC51434.1 | |
AK001700.1 | 15 | 3179 | BAA91846.1 | |
AK172784.1 | 9 | 2393 | BAD18765.1 | |
BC040342.1 | 16 | 3288 | AAH40342.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832398 | Chr.12:46217909 - 46431747 on Build GRCh38 | Gain | SLC38A1 LOC102723757 LOC100288798 SLC38A2 |
More Information
Additional Information:
For this assay, SNP(s) [rs76658095] 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 |