Genomic Map
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Target Gene Details
Entrez Gene ID: | 317716 |
Gene Name: | BPI fold containing family A member 4, pseudogene |
Gene Aliases: |
BASE |
Location: |
Chr.20:33193605-33210462 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BPIFA4P | NR_026760.1 | |||
| AY180924.1 | AAO17728.1 | |||
| BC128240.1 | ||||
| BC128241.1 |
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 |
 LOC101929698
COMMD7
SUN5
LOC105372714
BPIFB2
BPIFA2
BPIFB6
BPIFA1
LOC149950
BPIFA3
C20orf203
MAPRE1
BPIFB1
DNMT3B
NOL4L
EFCAB8
BPIFB4
BPIFB3
BPIFA4P
|
| esv2751912 | Chr.20:33179619 - 33248657 on Build GRCh38 | Loss |
BPIFA3
BPIFA2
BPIFA1
BPIFA4P
|
| nsv1060241 | Chr.20:33172902 - 33244962 on Build GRCh38 | Loss |
BPIFA3
BPIFA2
BPIFA1
BPIFA4P
|
| nsv458964 | Chr.20:33152998 - 33229798 on Build GRCh38 | Loss |
BPIFA3
LOC105372714
BPIFA2
BPIFA4P
|
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Additional Information:
For this assay, SNP(s) [rs73904633] 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
Intronic
Non-exonic
DGV Variation
|
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