Assay Details
Target Gene Details
Entrez Gene ID: | 51741 |
Gene Name: | WW domain containing oxidoreductase |
Gene Aliases: |
D16S432E, EIEE28, FOR, FRA16D, HHCMA56, PRO0128, SCAR12, SDR41C1, WOX1 |
Location: |
Chr.16:78099413-79212667 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
WWOX | NM_001291997.1 | NP_001278926.1 | ||
NM_016373.3 | NP_057457.1 | |||
NM_130791.3 | NP_570607.1 | |||
NR_120436.1 | ||||
XM_011523101.2 | XP_011521403.1 | |||
XM_011523103.2 | XP_011521405.1 | |||
XM_011523104.2 | XP_011521406.1 | |||
XM_011523105.2 | XP_011521407.1 | |||
XM_017023278.1 | XP_016878767.1 | |||
AF187015.1 | AAF31694.1 | |||
AF211943.1 | AAF27049.1 | |||
AF227526.1 | AAF82053.1 | |||
AF227527.1 | AAF82054.1 | |||
AF227528.1 | AAF82055.1 | |||
AF395123.1 | AAK81727.1 | |||
AF395124.1 | AAK81728.1 | |||
AK027626.1 | ||||
AK290438.1 | ||||
AK291300.1 | ||||
AK298322.1 | ||||
AW874692.1 | ||||
AY256821.1 | AAP94227.1 | |||
BC003184.1 | AAH03184.1 | |||
BU157392.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv539e214 | Chr.16:78117264 - 78142432 on Build GRCh38 | Loss | WWOX |
dgv3031n100 | Chr.16:77892138 - 78561070 on Build GRCh38 | Gain | WWOX CLEC3A VAT1L |
nsv1056016 | Chr.16:77990656 - 78129245 on Build GRCh38 | Loss | WWOX CLEC3A |
nsv833293 | Chr.16:77932757 - 78134791 on Build GRCh38 | Gain | WWOX CLEC3A VAT1L |
esv2760418 | Chr.16:77894064 - 78560274 on Build GRCh38 | Gain+Loss | WWOX CLEC3A VAT1L |
esv3892902 | Chr.16:78049580 - 78674801 on Build GRCh38 | Gain | WWOX |
nsv520408 | Chr.16:78117849 - 78137411 on Build GRCh38 | Loss | WWOX |
nsv573133 | Chr.16:78078366 - 78181055 on Build GRCh38 | Gain | WWOX |
More Information
Additional Information:
For this assay, SNP(s) [rs76796549] 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 |