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 6 |
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 | ||||
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 |
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nsv1160586 | Chr.19:12597480 - 12823909 on Build GRCh38 | Duplication |
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dgv138n111 | Chr.19:12627853 - 12810372 on Build GRCh38 | Deletion |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs75188411] 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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Panther Classification:
Gene Ontology Categories:
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