Assay Details
Target Gene Details
Entrez Gene ID: | 100287944 |
Gene Name: | uncharacterized LOC100287944 |
Gene Aliases: |
- |
Location: |
Chr.12:106496410-106774831 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
LOC100287944 | NR_040246.1 | |||
DA250223.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832511 | Chr.12:106551876 - 106714050 on Build GRCh38 | Gain | RFX4 LOC100287944 LOC100505978 |
nsv832510 | Chr.12:106393952 - 106557362 on Build GRCh38 | Loss | LOC100287944 POLR3B |
nsv560090 | Chr.12:106541358 - 106830191 on Build GRCh38 | Gain | RFX4 LOC100287944 RIC8B LOC100505978 |
More Information
Additional Information:
For this assay, SNP(s) [rs75240325,rs75308344] 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 |