Assay Details
Target Gene Details
Entrez Gene ID: | 113146 |
Gene Name: | AHNAK nucleoprotein 2 |
Gene Aliases: |
C14orf78 |
Location: |
Chr.14:104937253-104978357 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
AHNAK2 | NM_138420.2 | NP_612429.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1438 | Chr.14:104946391 - 104991244 on Build GRCh38 | Deletion | AHNAK2 C14orf79 |
nsv566141 | Chr.14:104938047 - 105089059 on Build GRCh38 | Gain | CDCA4 AHNAK2 C14orf79 GPR132 |
esv3635634 | Chr.14:104965985 - 105147574 on Build GRCh38 | Gain | CDCA4 JAG2 AHNAK2 C14orf79 GPR132 LOC102723354 |
nsv952276 | Chr.14:104922864 - 105021963 on Build GRCh38 | Deletion | PLD4 CDCA4 AHNAK2 C14orf79 |
nsv1049253 | Chr.14:104918622 - 105005518 on Build GRCh38 | Gain | PLD4 AHNAK2 C14orf79 |
nsv1054574 | Chr.14:103210111 - 105365114 on Build GRCh38 | Loss | C14orf2 PLD4 LOC105370708 MIR203A MARK3 RD3L LOC388022 LOC105370687 C14orf180 EIF5 KLC1 CKB INF2 JAG2 SNORA28 CEP170B AHNAK2 PACS2 LOC105370691 BAG5 XRCC3 LOC105378183 APOPT1 MIR203B BTBD6 BRF1 CDCA4 ADSSL1 TMEM179 KIF26A ASPG TDRD9 TRMT61A MIR4710 C14orf79 GPR132 LOC107984648 PPP1R13B ZBTB42 NUDT14 SIVA1 LINC00638 ZFYVE21 AKT1 LINC00637 LOC101929634 LOC102723354 MIR6765 |
nsv1052190 | Chr.14:104957424 - 105256316 on Build GRCh38 | Gain | BTBD6 BRF1 CDCA4 JAG2 AHNAK2 C14orf79 GPR132 LOC102723354 NUDT14 MIR6765 |
nsv566150 | Chr.14:104969312 - 105223755 on Build GRCh38 | Loss | BRF1 CDCA4 JAG2 AHNAK2 C14orf79 GPR132 LOC102723354 NUDT14 MIR6765 |
More Information
Additional Information:
For this assay, SNP(s) [rs73357588] 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 |