Assay Details
Target Gene Details
Entrez Gene ID: | 84324 |
Gene Name: | SAP domain containing ribonucleoprotein |
Gene Aliases: |
CIP29, HCC1, HSPC316, THO1 |
Location: |
Chr.12:55752463-55817756 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SARNP | NM_033082.3 | 11 | 781 | NP_149073.1 |
NR_026722.1 | ||||
NR_026723.1 | ||||
AF161434.1 | 11 | 751 | AAF28994.1 | |
AK290508.1 | ||||
BC007099.1 | 11 | 747 | AAH07099.1 | |
BC093051.1 | AAH93051.1 | |||
BI520421.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832423 | Chr.12:55687038 - 55859914 on Build GRCh38 | Gain | ORMDL2 GDF11 RDH5 TMEM198B CD63 BLOC1S1-RDH5 ITGA7 SARNP BLOC1S1 MMP19 DNAJC14 |
nsv559004 | Chr.12:55704254 - 55777109 on Build GRCh38 | Loss | GDF11 RDH5 CD63 BLOC1S1-RDH5 ITGA7 SARNP BLOC1S1 |
More Information
Additional Information:
For this assay, SNP(s) [rs76956510] 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 |