Assay Details
Target Gene Details
Entrez Gene ID: | 375061 |
Gene Name: | family with sequence similarity 89 member A |
Gene Aliases: |
C1orf153 |
Location: |
Chr.1:231018958-231040249 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM89A | NM_198552.2 | NP_940954.1 | ||
BC009447.1 | AAH09447.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3589093 | Chr.1:230482037 - 231277190 on Build GRCh38 | Gain |
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nsv1011066 | Chr.1:230940432 - 231242850 on Build GRCh38 | Gain |
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nsv1000488 | Chr.1:230799658 - 231269735 on Build GRCh38 | Gain |
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More Information
Additional Information:
For this assay, SNP(s) [rs116699533] 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: |
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Panther Classification:
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