Assay Details
Target Gene Details
Entrez Gene ID: | 9420 |
Gene Name: | cytochrome P450 family 7 subfamily B member 1 |
Gene Aliases: |
CBAS3, CP7B, SPG5A |
Location: |
Chr.8:64590851-64798791 on Build GRCh38 |
Assay Gene Location: | Within Intron 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CYP7B1 | NM_001324112.1 | NP_001311041.1 | ||
NM_004820.4 | NP_004811.1 | |||
XM_017014002.1 | XP_016869491.1 | |||
AF029403.1 | AAC95426.1 | |||
AF127090.1 | AAD20021.1 | |||
BC029155.1 | ||||
BC136574.1 | ||||
BM729103.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv611449 | Chr.8:64598475 - 64630844 on Build GRCh38 | Loss | CYP7B1 |
More Information
Additional Information:
For this assay, SNP(s) [rs148775285] 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 |