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: | Overlaps Intron 4 - Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BPIFA3 | NM_001042439.2 | NP_001035904.1 | ||
NM_178466.4 | NP_848561.2 | |||
AI073399.1 | ||||
AI638623.1 | ||||
AW082233.1 | ||||
BC066354.1 | AAH66354.1 |
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 | BPIFB2 LOC105372714 LOC101929698 COMMD7 LOC149950 BPIFB4 MAPRE1 BPIFA4P BPIFA2 BPIFB6 NOL4L C20orf203 SUN5 BPIFB1 BPIFB3 BPIFA1 BPIFA3 EFCAB8 DNMT3B |
esv2751912 | Chr.20:33179619 - 33248657 on Build GRCh38 | Loss | BPIFA1 BPIFA3 BPIFA4P BPIFA2 |
nsv1060241 | Chr.20:33172902 - 33244962 on Build GRCh38 | Loss | BPIFA1 BPIFA3 BPIFA4P BPIFA2 |
nsv458964 | Chr.20:33152998 - 33229798 on Build GRCh38 | Loss | LOC105372714 BPIFA3 BPIFA4P BPIFA2 |
More Information
Additional Information:
For this assay, SNP(s) [rs74640466] 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: |
Intragenic Non-exonic DGV Variation |