Assay Details
Target Gene Details
Entrez Gene ID: | 284904 |
Gene Name: | SEC14 like lipid binding 4 |
Gene Aliases: |
TAP3 |
Location: |
Chr.22:30488150-30505711 on Build GRCh38 |
Assay Gene Location: | Within Exon 7 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SEC14L4 | NM_001161368.1 | 5 | 400 | NP_001154840.1 |
NM_174977.3 | 5 | 400 | NP_777637.1 | |
XM_006724235.2 | 5 | 416 | XP_006724298.1 | |
XM_011530164.2 | 5 | 580 | XP_011528466.1 | |
XM_017028787.1 | 4 | 529 | XP_016884276.1 | |
XM_017028788.1 | 4 | 530 | XP_016884277.1 | |
XM_017028789.1 | 4 | 202 | XP_016884278.1 | |
XM_017028790.1 | 4 | 537 | XP_016884279.1 | |
XM_017028791.1 | 4 | 229 | XP_016884280.1 | |
AK092002.1 | 6 | 449 | ||
AK093418.1 | 5 | 417 | ||
AK093448.1 | 5 | 384 | ||
AY158085.1 | 5 | 300 | AAO21869.1 | |
BC136358.1 | 5 | 372 | ||
BC136359.1 | 5 | 372 | ||
BC139912.1 | 5 | 339 | ||
CR456346.1 | 3 | 159 | CAG30232.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv829171 | Chr.22:30202041 - 30647591 on Build GRCh38 | Loss | OSM TCN2 HORMAD2 SDC4P GATSL3 MGC20647 SEC14L6 CCDC157 KIAA1656 PES1 TBC1D10A LIF MTFP1 RNF215 GAL3ST1 SEC14L2 SLC35E4 SF3A1 SEC14L4 SEC14L3 |
More Information
Additional Information:
For this assay, SNP(s) [rs80195131] 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 |