Assay Details
Target Gene Details
Entrez Gene ID: | 8795 |
Gene Name: | TNF receptor superfamily member 10b |
Gene Aliases: |
CD262, DR5, KILLER, KILLER/DR5, TRAIL-R2, TRAILR2, TRICK2, TRICK2A, TRICK2B, TRICKB, ZTNFR9 |
Location: |
Chr.8:23020133-23069187 on Build GRCh38 |
Assay Gene Location: | Within Intron 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TNFRSF10B | NM_003842.4 | NP_003833.4 | ||
NM_147187.2 | NP_671716.2 | |||
NR_027140.1 | ||||
XM_017013944.1 | XP_016869433.1 | |||
AB451272.1 | ||||
AB451399.1 | ||||
AF012535.1 | AAB67103.1 | |||
AF012628.1 | AAB67109.1 | |||
AF016266.1 | AAB81180.1 | |||
AF016268.1 | AAC01565.1 | |||
AF016849.1 | AAC51778.1 | |||
AF018657.1 | AAB70577.1 | |||
AF018658.1 | AAB70578.1 | |||
AF020501.1 | AAB71412.1 | |||
AF022386.1 | AAB71949.1 | |||
AF153687.1 | AAF75587.1 | |||
AF192548.1 | AAF07175.1 | |||
AK291216.1 | ||||
AK296128.1 | ||||
AK298602.1 | ||||
AY358277.1 | AAQ88644.1 | |||
BC001281.1 | AAH01281.1 | |||
BX537617.1 | CAD97801.1 | |||
BX538104.1 | CAD98017.1 | |||
BX538179.1 | CAD98053.1 | |||
CR541898.1 | CAG46696.1 | |||
CX870630.1 | ||||
FJ200482.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1027718 | Chr.8:22805950 - 23258334 on Build GRCh38 | Gain | CHMP7 LOC101929237 TNFRSF10C LOC389641 LOC254896 PEBP4 LOC286059 RHOBTB2 TNFRSF10D LOC107984124 TNFRSF10B TNFRSF10A |
nsv524231 | Chr.8:23003729 - 23028617 on Build GRCh38 | Loss | RHOBTB2 TNFRSF10B |
nsv1025672 | Chr.8:22868571 - 23130480 on Build GRCh38 | Gain | LOC101929237 TNFRSF10C LOC254896 PEBP4 LOC286059 RHOBTB2 LOC107984124 TNFRSF10B |
esv2759604 | Chr.8:20675533 - 23254096 on Build GRCh38 | Loss | NUDT18 BIN3 CHMP7 LOC100507071 LOC254896 GFRA2 PDLIM2 C8orf58 RHOBTB2 BMP1 TNFRSF10B LOC101929172 PHYHIP LOC102467222 XPO7 TNFRSF10C PEBP4 EGR3 SORBS3 FAM160B2 SLC39A14 FGF17 LOC107986876 LOC107984124 POLR3D REEP4 SFTPC CCAR2 BIN3-IT1 LOC286059 NPM2 LOC286114 DMTN TNFRSF10A DOK2 LGI3 LOC101929237 PPP3CC LOC389641 PIWIL2 MIR320A HR TNFRSF10D |
nsv1017570 | Chr.8:22969562 - 23544783 on Build GRCh38 | Gain | CHMP7 LOC254896 LOC286059 RHOBTB2 TNFRSF10B ENTPD4 R3HCC1 TNFRSF10A TNFRSF10C LOC389641 LOC100507156 SLC25A37 TNFRSF10D LOC107984124 LOXL2 |
More Information
Additional Information:
For this assay, SNP(s) [rs199547541] 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 |