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 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
AHNAK2 | NM_138420.2 | NP_612429.2 | ||
XM_005267299.1 | XP_005267356.1 | |||
AK094143.1 |
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 | C14orf79 AHNAK2 |
nsv566141 | Chr.14:104938047 - 105089059 on Build GRCh38 | Gain | C14orf79 AHNAK2 CDCA4 GPR132 |
esv3635634 | Chr.14:104965985 - 105147574 on Build GRCh38 | Gain | C14orf79 AHNAK2 LOC102723354 CDCA4 GPR132 JAG2 |
nsv952276 | Chr.14:104922864 - 105021963 on Build GRCh38 | Deletion | C14orf79 AHNAK2 CDCA4 PLD4 |
nsv1049253 | Chr.14:104918622 - 105005518 on Build GRCh38 | Gain | C14orf79 AHNAK2 PLD4 |
nsv1054574 | Chr.14:103210111 - 105365114 on Build GRCh38 | Loss | RD3L BAG5 MIR4710 MIR6765 APOPT1 MIR203B SNORA28 PPP1R13B EIF5 C14orf2 SIVA1 PACS2 LOC101929634 JAG2 AKT1 ASPG XRCC3 LOC105378183 AHNAK2 LOC102723354 KLC1 TDRD9 C14orf180 LINC00637 MARK3 C14orf79 CEP170B CKB BTBD6 LOC105370687 TMEM179 ZFYVE21 LINC00638 GPR132 LOC388022 NUDT14 KIF26A TRMT61A ZBTB42 ADSSL1 MIR203A BRF1 LOC105370691 CDCA4 INF2 LOC105370708 PLD4 LOC107984648 |
nsv1052190 | Chr.14:104957424 - 105256316 on Build GRCh38 | Gain | MIR6765 C14orf79 BTBD6 BRF1 AHNAK2 LOC102723354 CDCA4 GPR132 JAG2 NUDT14 |
nsv566150 | Chr.14:104969312 - 105223755 on Build GRCh38 | Loss | MIR6765 C14orf79 BRF1 AHNAK2 LOC102723354 CDCA4 GPR132 JAG2 NUDT14 |
More Information
Additional Information:
For this assay, SNP(s) [rs151130395] 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 |