Assay Details
Target Gene Details
Entrez Gene ID: | 100506733 |
Gene Name: | FAM170B antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.10:49121839-49151547 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM170B-AS1 | NR_038973.1 | |||
AK093055.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1042677 | Chr.10:47993784 - 49928329 on Build GRCh38 | Loss | PGBD3 FRMPD2 SLC18A3 MAPK8 CHAT VSTM4 AGAP12P FAM25C FAM170B ERCC6 MIR4294 DRGX C10orf53 ARHGAP22 LRRC18 C10orf128 WDFY4 C10orf71-AS1 FAM170B-AS1 OGDHL C10orf71 PARG |
More Information
Additional Information:
For this assay, SNP(s) [rs77499685] 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 |