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 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PALM3 | NM_001145028.1 | NP_001138500.1 | ||
XM_005259891.4 | XP_005259948.1 | |||
XM_011527965.2 | XP_011526267.1 | |||
CR747190.1 |
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 | C19orf67 PALM3 MIR1199 IL27RA PRKACA RFX1 ASF1B MISP3 SAMD1 RLN3 |
nsv578642 | Chr.19:14028192 - 14187630 on Build GRCh38 | Gain | C19orf67 PALM3 MIR1199 IL27RA PRKACA ASF1B ADGRL1 MISP3 SAMD1 RLN3 LOC100507373 |
More Information
Additional Information:
For this assay, SNP(s) [rs78497170] 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 |