Assay Details
Target Gene Details
Entrez Gene ID: | 10017 |
Gene Name: | BCL2 like 10 |
Gene Aliases: |
BCL-B, Boo, Diva, bcl2-L-10 |
Location: |
Chr.15:52109263-52112775 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BCL2L10 | NM_001306168.1 | NP_001293097.1 | ||
NM_020396.3 | NP_065129.1 | |||
AF285092.1 | AAG00503.1 | |||
AF326964.1 | AAK48715.1 | |||
BC093826.1 | AAH93826.1 | |||
BC093828.1 | AAH93828.1 | |||
BC104442.1 | AAI04443.1 | |||
BC104443.1 | AAI04444.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv952627 | Chr.15:52110004 - 52113203 on Build GRCh38 | Deletion | BCL2L10 |
nsv471244 | Chr.15:52013266 - 52219268 on Build GRCh38 | Gain | LOC100129973 GNB5 MYO5C BCL2L10 MAPK6 |
nsv833005 | Chr.15:52097672 - 52249133 on Build GRCh38 | Gain | LOC100129973 GNB5 MYO5C BCL2L10 |
More Information
Additional Information:
For this assay, SNP(s) [rs77272195] 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 |