Assay Details
Target Gene Details
Entrez Gene ID: | 9531 |
Gene Name: | BCL2 associated athanogene 3 |
Gene Aliases: |
BAG-3, BIS, CAIR-1, MFM6 |
Location: |
Chr.10:119651347-119677819 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BAG3 | NM_004281.3 | NP_004272.2 | ||
XM_005270287.1 | XP_005270344.1 | |||
AF071218.2 | AAF69592.2 | |||
AF095193.2 | AAD16122.2 | |||
AF127139.1 | AAF26839.1 | |||
AK222800.1 | BAD96520.1 | |||
AK291333.1 | ||||
AK313026.1 | ||||
AL137582.1 | CAB70824.1 | |||
BC006418.1 | AAH06418.1 | |||
BC014656.1 | AAH14656.1 | |||
BC107786.1 | AAI07787.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv825585 | Chr.10:119648080 - 119761531 on Build GRCh38 | Gain | INPP5F BAG3 |
nsv1045668 | Chr.10:119611032 - 119859464 on Build GRCh38 | Gain | INPP5F BAG3 MCMBP |
More Information
Additional Information:
For this assay, SNP(s) [rs77116325] 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 |