Assay Details
Target Gene Details
Entrez Gene ID: | 64421 |
Gene Name: | DNA cross-link repair 1C |
Gene Aliases: |
A-SCID, DCLREC1C, RS-SCID, SCIDA, SNM1C |
Location: |
Chr.10:14897853-14954432 on Build GRCh38 |
Assay Gene Location: | Within Intron 12 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv469720 | Chr.10:14865281 - 15037379 on Build GRCh38 | Gain | HSPA14 SUV39H2 MEIG1 DCLRE1C LOC105376432 LOC105376430 |
dgv68n27 | Chr.10:14913179 - 15018884 on Build GRCh38 | Gain | MEIG1 DCLRE1C LOC105376432 LOC105376430 |
dgv961n54 | Chr.10:14910793 - 15028616 on Build GRCh38 | Gain | MEIG1 DCLRE1C LOC105376432 LOC105376430 |
esv2760142 | Chr.10:14930788 - 15024489 on Build GRCh38 | Gain | MEIG1 DCLRE1C LOC105376432 LOC105376430 |
nsv831793 | Chr.10:14870604 - 15058763 on Build GRCh38 | Loss | HSPA14 SUV39H2 MEIG1 DCLRE1C OLAH LOC105376432 LOC105376430 |
More Information
Additional Information:
For this assay, SNP(s) [rs115449302] 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 |