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: | Within Intron 11 |
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 CARD8-AS1 |
nsv9739 | Chr.19:47901840 - 50143063 on Build GRCh38 | Gain+Loss | PLEKHA4 SNORD34 CGB2 SIGLEC11 TSKS CGB5 TBC1D17 RASIP1 C19orf73 FUT1 SNAR-A2 AKT1S1 BCL2L12 SCAF1 NOSIP HRC PLA2G4C-AS1 DHDH SNAR-C5 GRWD1 RUVBL2 PPP1R15A LHB FLJ26850 PTOV1-AS2 FUZ SNRNP70 GRIN2D SNAR-D SNORD32A SNAR-A3 CGB3 MIR4750 ADM5 TMEM143 IRF3 MIR6799 SPHK2 KCNJ14 SNAR-A6 ALDH16A1 AP2A1 RPS11 SLC17A7 SNAR-A12 PRR12 CABP5 CD37 RCN3 CGB7 PRMT1 SNAR-A10 KDELR1 SNAR-G2 SNAR-B1 SYNGR4 LMTK3 PIH1D1 HSD17B14 SNAR-G1 SLC6A16 SNORD35A TULP2 SULT2B1 EMP3 SPACA4 NUP62 SNAR-A5 LOC101059948 MIR150 SNAR-C3 GFY CYTH2 PLA2G4C IZUMO1 SNAR-C4 IL4I1 PTOV1-AS1 MIR5088 NTN5 CGB8 MIR4751 MAMSTR SNAR-A8 MED25 SNAR-B2 SNORD33 MIR6800 NUCB1-AS1 PNKP PPFIA3 ELSPBP1 SNAR-C2 BCAT2 FLT3LG CARD8-AS1 C19orf68 FCGRT MIR4324 VRK3 ATF5 RRAS FTL LOC101928295 SIGLEC16 LOC105447645 BSPH1 BAX SNAR-A4 SNAR-A9 CCDC114 CCDC155 NUCB1 CA11 SNAR-A1 LIG1 CGB1 DBP PTOV1 LOC100287477 SNAR-A11 LIN7B MIR4749 RPL18 FGF21 FAM83E NTF4 ZNF114 ZNF473 LOC105372430 MIR6798 TRPM4 PTH2 RPL13A CARD8 SNAR-A13 SNORD35B GYS1 DKKL1 PRRG2 KCNA7 SNAR-C1 SNAR-A7 SEC1P TEAD2 CPT1C FUT2 SNAR-A14 |
dgv3614n100 | Chr.19:48224334 - 48283199 on Build GRCh38 | Gain | CARD8 ZNF114 CARD8-AS1 |
nsv469623 | Chr.19:48209728 - 48360236 on Build GRCh38 | Loss | CARD8 ZNF114 TMEM143 CCDC114 CARD8-AS1 EMP3 |
esv34181 | Chr.19:48009377 - 48416682 on Build GRCh38 | Loss | C19orf68 CABP5 GRIN2D CARD8 LIG1 TMEM143 KDELR1 SYNGR4 ELSPBP1 ZNF114 PLA2G4C PLA2G4C-AS1 CCDC114 CARD8-AS1 EMP3 |
nsv579902 | Chr.19:48208219 - 48239130 on Build GRCh38 | Loss | CARD8 |
More Information
Additional Information:
For this assay, SNP(s) [rs75912729] 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 |