Assay Details
Target Gene Details
Entrez Gene ID: | 51439 |
Gene Name: | family with sequence similarity 8 member A1 |
Gene Aliases: |
AHCP |
Location: |
Chr.6:17600287-17611719 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM8A1 | NM_016255.2 | 5 | 4328 | NP_057339.1 |
| AF097027.1 | 5 | 4260 | AAF07850.1 | |
| AK074301.1 | 1 | 2639 | ||
| AL050128.1 | 1 | 1539 | ||
| BQ015864.1 | 1 | 435 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv5922n100 | Chr.6:17490857 - 17921391 on Build GRCh38 | Gain |
|
| nsv516012 | Chr.6:17459945 - 17876993 on Build GRCh38 | Gain+Loss |
|
| nsv601046 | Chr.6:17492862 - 17893291 on Build GRCh38 | Gain |
|
| dgv1715e212 | Chr.6:17457368 - 17679729 on Build GRCh38 | Gain |
|
| nsv830596 | Chr.6:17597791 - 17767811 on Build GRCh38 | Gain |
|
| nsv1027813 | Chr.6:17457369 - 17630059 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73722989] 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: |
|

Genomic Map