Assay Details
Target Gene Details
Entrez Gene ID: | 961 |
Gene Name: | CD47 molecule |
Gene Aliases: |
IAP, MER6, OA3 |
Location: |
Chr.3:108043094-108094200 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CD47 | NM_001777.3 | 11 | 4176 | NP_001768.1 |
NM_198793.2 | 9 | 4118 | NP_942088.1 | |
XM_005247908.1 | 10 | 4113 | XP_005247965.1 | |
XM_005247909.1 | 8 | 4056 | XP_005247966.1 | |
AK096670.1 | 1 | 1587 | ||
AL832675.1 | 2 | 5833 | ||
BC037306.1 | 10 | 4030 | AAH37306.1 | |
BX640889.1 | 1 | 2745 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1011158 | Chr.3:107746970 - 108629120 on Build GRCh38 | Gain | LINC00636 KIAA1524 DZIP3 MYH15 CD47 BBX IFT57 HHLA2 LINC00635 LINC01215 |
More Information
Additional Information:
For this assay, SNP(s) [rs115142863] 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 |