Assay Details
Target Gene Details
Entrez Gene ID: | 4689 |
Gene Name: | neutrophil cytosolic factor 4 |
Gene Aliases: |
CGD3, NCF, P40PHOX, SH3PXD4 |
Location: |
Chr.22:36860988-36878017 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NCF4 | NM_000631.4 | 1 | 83 | NP_000622.2 |
NM_013416.3 | 1 | 83 | NP_038202.2 | |
AK223324.1 | BAD97044.1 | |||
AK290924.1 | ||||
BC002798.1 | 1 | 83 | AAH02798.1 | |
BX355636.2 | ||||
CR456528.1 | CAG30414.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3647697 | Chr.22:36860183 - 36866802 on Build GRCh38 | Gain | NCF4 |
nsv3619 | Chr.22:36856525 - 36877665 on Build GRCh38 | Insertion | NCF4 |
esv2758837 | Chr.22:36779110 - 36964864 on Build GRCh38 | Gain+Loss | CSF2RB PVALB NCF4 |
More Information
Additional Information:
For this assay, SNP(s) [rs148141762] 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 Exonic DGV Variation |