Assay Details
Target Gene Details
Entrez Gene ID: | 100526694 |
Gene Name: | MSANTD3-TMEFF1 readthrough |
Gene Aliases: |
C9orf3-TMEFF1, C9orf30-TMEFF1 |
Location: |
Chr.9:100441906-100577636 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
MSANTD3-TMEFF1 | NM_001198812.1 | NP_001185741.1 | ||
AL831919.1 | CAD38580.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3306071 | Chr.9:100461107 - 100461108 on Build GRCh38 | Mobile Element Insertion |
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esv3408660 | Chr.9:100461119 - 100461137 on Build GRCh38 | Insertion |
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nsv825012 | Chr.9:100389923 - 100493999 on Build GRCh38 | Gain |
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nsv614955 | Chr.9:100419314 - 100498945 on Build GRCh38 | Loss |
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esv3437174 | Chr.9:100461106 - 100461123 on Build GRCh38 | Insertion |
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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) [rs200530134] 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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