Assay Details
Target Gene Details
Entrez Gene ID: | 342979 |
Gene Name: | paralemmin 3 |
Gene Aliases: |
- |
Location: |
Chr.19:14053367-14062137 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PALM3 | XM_005259891.4 | XP_005259948.1 | ||
XM_011527965.2 | XP_011526267.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv833761 | Chr.19:13998659 - 14136778 on Build GRCh38 | Loss | RLN3 IL27RA MIR1199 PRKACA PALM3 C19orf67 MISP3 SAMD1 ASF1B RFX1 |
nsv828452 | Chr.19:14059742 - 14148154 on Build GRCh38 | Loss | MIR1199 PRKACA LOC100507373 PALM3 C19orf67 MISP3 SAMD1 ASF1B ADGRL1 |
nsv578642 | Chr.19:14028192 - 14187630 on Build GRCh38 | Gain | RLN3 IL27RA MIR1199 PRKACA LOC100507373 PALM3 C19orf67 MISP3 SAMD1 ASF1B ADGRL1 |
More Information
Additional Information:
For this assay, SNP(s) [rs75426611] 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 |