Assay Details
Target Gene Details
Entrez Gene ID: | 100996348 |
Gene Name: | CA3 antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.8:85441806-85464915 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CA3-AS1 | NR_121630.1 | |||
NR_121631.1 | ||||
DA940436.1 | ||||
DB177224.1 | ||||
DB196812.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831377 | Chr.8:85350878 - 85531912 on Build GRCh38 | Gain | CA2 CA1 CA3-AS1 CA3 |
nsv1028148 | Chr.8:85398341 - 85640901 on Build GRCh38 | Gain | CA2 CA3-AS1 CA3 |
esv2761206 | Chr.8:85398353 - 85556639 on Build GRCh38 | Gain | CA2 CA3-AS1 CA3 |
nsv483126 | Chr.8:83687766 - 85887771 on Build GRCh38 | Gain+Loss | LRRCC1 LOC100288562 LOC101929627 CA3-AS1 RALYL REXO1L1P LOC101929601 C8orf59 CA13 CA2 CA1 LOC107986879 LOC102723322 REXO1L2P CA3 E2F5 |
More Information
Additional Information:
For this assay, SNP(s) [rs77250341] 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 |