Assay Details
Target Gene Details
Entrez Gene ID: | 10535 |
Gene Name: | ribonuclease H2 subunit A |
Gene Aliases: |
AGS4, JUNB, RNASEHI, RNHIA, RNHL |
Location: |
Chr.19:12802054-12813648 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RNASEH2A | NM_006397.2 | NP_006388.2 | ||
| XM_006722619.2 | XP_006722682.1 | |||
| AK315327.1 | ||||
| AY363912.1 | AAQ64005.1 | |||
| BC011748.2 | AAH11748.1 | |||
| BG825340.1 | ||||
| BM664190.1 | ||||
| CB240995.1 | ||||
| CR456841.1 | CAG33122.1 | |||
| Z97029.1 | CAB09725.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv953977 | Chr.19:12666887 - 13095486 on Build GRCh38 | Deletion |
|
| nsv1160586 | Chr.19:12597480 - 12823909 on Build GRCh38 | Duplication |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73503455] 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: |
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Genomic Map