Assay Details
Target Gene Details
Entrez Gene ID: | 23359 |
Gene Name: | family with sequence similarity 189 member A1 |
Gene Aliases: |
TMEM228 |
Location: |
Chr.15:29120252-29570723 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAM189A1 | NM_015307.1 | NP_056122.1 | ||
XM_011521407.2 | XP_011519709.1 | |||
AB011146.1 | BAA25500.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1040778 | Chr.15:28689598 - 30515727 on Build GRCh38 | Loss |
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nsv515798 | Chr.15:29068198 - 29146274 on Build GRCh38 | Gain+Loss |
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nsv471232 | Chr.15:29087561 - 29139979 on Build GRCh38 | Loss |
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nsv527255 | Chr.15:28754022 - 30074044 on Build GRCh38 | Gain |
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esv2751526 | Chr.15:28724519 - 30687025 on Build GRCh38 | Loss |
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nsv1039798 | Chr.15:28724126 - 30158154 on Build GRCh38 | Gain |
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nsv568675 | Chr.15:29035149 - 29916451 on Build GRCh38 | Gain |
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nsv524362 | Chr.15:29089598 - 29155854 on Build GRCh38 | Loss |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs113139734] 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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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)