Genomic Map
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Target Gene Details
Entrez Gene ID: | 580 |
Gene Name: | BRCA1 associated RING domain 1 |
Gene Aliases: |
- |
Location: |
Chr.2:214725645-214809711 on Build GRCh38 |
Assay Gene Location: | Within Intron 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BARD1 | NM_000465.3 | NP_000456.2 | ||
| NM_001282543.1 | NP_001269472.1 | |||
| NM_001282545.1 | NP_001269474.1 | |||
| NM_001282548.1 | NP_001269477.1 | |||
| NM_001282549.1 | NP_001269478.1 | |||
| NR_104212.1 | ||||
| NR_104215.1 | ||||
| NR_104216.1 | ||||
| XM_017004613.1 | XP_016860102.1 | |||
| AK223409.1 | BAD97129.1 | |||
| AK301843.1 | ||||
| AK314260.1 | ||||
| AX794378.1 | CAE48237.1 | |||
| BC126426.1 | ||||
| BC126428.1 | ||||
| BU677525.1 | ||||
| BX098964.1 | ||||
| JF790280.1 | ||||
| JF790281.1 | ||||
| JF790282.1 | ||||
| JF790283.1 | ||||
| JF790284.1 | ||||
| JF790285.1 | ||||
| JF790286.1 | ||||
| U76638.1 | AAB38316.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv584436 | Chr.2:214680236 - 214768739 on Build GRCh38 | Gain |
 BARD1
|
| esv3893552 | Chr.2:214697853 - 214755197 on Build GRCh38 | Gain |
BARD1
|
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Additional Information:
For this assay, SNP(s) [rs78513346] 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
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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