Assay Details
Target Gene Details
Entrez Gene ID: | 128861 |
Gene Name: | BPI fold containing family A member 3 |
Gene Aliases: |
C20orf71, SPLUNC3 |
Location: |
Chr.20:33217310-33227806 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BPIFA3 | NM_001042439.2 | NP_001035904.1 | ||
NM_178466.4 | NP_848561.2 | |||
BC066354.1 | AAH66354.1 | |||
BF966133.1 | ||||
DB446335.1 | ||||
HY050111.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1056411 | Chr.20:32469234 - 33355029 on Build GRCh38 | Loss |
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esv2751912 | Chr.20:33179619 - 33248657 on Build GRCh38 | Loss |
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nsv1060241 | Chr.20:33172902 - 33244962 on Build GRCh38 | Loss |
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nsv458964 | Chr.20:33152998 - 33229798 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) [rs146326443] 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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Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)