Assay Details
Target Gene Details
Entrez Gene ID: | 22900 |
Gene Name: | caspase recruitment domain family member 8 |
Gene Aliases: |
CARDINAL, DACAR, DAKAR, NDPP, NDPP1, TUCAN |
Location: |
Chr.19:48203148-48256269 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 8 - Exon 9 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv3613n100 | Chr.19:48220413 - 48256972 on Build GRCh38 | Gain | CARD8-AS1 CARD8 |
nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss | SULT2B1 SNAR-A9 SYNGR4 SIGLEC16 NUCB1-AS1 LOC105372430 MIR4324 SNORD34 SCAF1 CD37 SEC1P SPHK2 SNAR-D PTOV1-AS2 SPACA4 SNAR-A7 SNORD35A C19orf73 ADM5 CGB5 SNAR-A1 DBP CCDC114 FCGRT CGB1 MIR4751 RCN3 PPFIA3 LOC101059948 RPS11 PRMT1 FAM83E CA11 CGB8 LOC105447645 SNAR-C2 SNAR-B2 NTF4 LOC101928295 C19orf68 SNAR-A10 NOSIP GFY AKT1S1 VRK3 PIH1D1 SNAR-G1 PLEKHA4 EMP3 LIG1 LIN7B ALDH16A1 NTN5 FLJ26850 SNAR-C4 SLC17A7 SNAR-A11 NUCB1 SNAR-C1 SNORD32A KCNJ14 MIR5088 KDELR1 CGB2 MED25 SNAR-G2 TULP2 RUVBL2 GRIN2D HSD17B14 MIR150 CPT1C RASIP1 AP2A1 CGB7 DKKL1 IZUMO1 SNAR-B1 BAX SNORD35B TEAD2 SNAR-C5 ELSPBP1 DHDH CGB3 PTOV1 ATF5 BCL2L12 TSKS PNKP CABP5 FLT3LG PRRG2 HRC ZNF114 SNAR-A2 MIR4750 PTOV1-AS1 FUZ SNAR-A4 RPL18 SNAR-A5 MIR6799 ZNF473 GYS1 NUP62 MIR6798 SNAR-A6 PTH2 CYTH2 GRWD1 SNAR-A8 BCAT2 MAMSTR SNORD33 FUT1 SIGLEC11 TBC1D17 CARD8-AS1 FTL BSPH1 SLC6A16 CARD8 FUT2 PRR12 PPP1R15A RPL13A PLA2G4C LMTK3 IRF3 SNAR-A3 KCNA7 TMEM143 SNAR-C3 FGF21 MIR6800 TRPM4 LHB SNRNP70 MIR4749 LOC100287477 PLA2G4C-AS1 SNAR-A12 IL4I1 SNAR-A13 SNAR-A14 CCDC155 RRAS |
dgv3614n100 | Chr.19:48224334 - 48283199 on Build GRCh38 | Gain | CARD8-AS1 CARD8 ZNF114 |
nsv469623 | Chr.19:48209728 - 48360236 on Build GRCh38 | Loss | EMP3 CARD8-AS1 TMEM143 CARD8 CCDC114 ZNF114 |
esv34181 | Chr.19:48009377 - 48416682 on Build GRCh38 | Loss | SYNGR4 EMP3 TMEM143 LIG1 GRIN2D CABP5 ZNF114 PLA2G4C-AS1 CARD8-AS1 C19orf68 CARD8 KDELR1 CCDC114 PLA2G4C ELSPBP1 |
nsv579902 | Chr.19:48208219 - 48239130 on Build GRCh38 | Loss | CARD8 |
More Information
Additional Information:
For this assay, SNP(s) [rs140826611] 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 Non-exonic DGV Variation |