Assay Details
Target Gene Details
Entrez Gene ID: | 8492 |
Gene Name: | protease, serine 12 |
Gene Aliases: |
BSSP-3, BSSP3, MRT1 |
Location: |
Chr.4:118280038-118353042 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PRSS12 | NM_003619.3 | 13 | 3357 | NP_003610.2 |
| AJ001531.1 | CAA04816.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2759279 | Chr.4:117557693 - 118753587 on Build GRCh38 | Gain |
|
| esv34038 | Chr.4:118113969 - 118534236 on Build GRCh38 | Loss |
|
| nsv1002771 | Chr.4:118204206 - 118650082 on Build GRCh38 | Gain |
|
| dgv5372n100 | Chr.4:118028335 - 118350088 on Build GRCh38 | Loss |
|
| esv3894015 | Chr.4:118188365 - 118489227 on Build GRCh38 | Gain |
|
| nsv519017 | Chr.4:117907652 - 118850326 on Build GRCh38 | Loss |
|
| esv34354 | Chr.4:117643184 - 118666956 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs72919299] 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