Assay Details
Target Gene Details
Entrez Gene ID: | 116832 |
Gene Name: | ribosomal protein L39 like |
Gene Aliases: |
RPL39L1 |
Location: |
Chr.3:187120953-187139475 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RPL39L | NM_052969.1 | NP_443201.1 | ||
AB063610.1 | BAC19837.1 | |||
BC012328.1 | AAH12328.1 | |||
L05096.1 | AAC15859.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv4157 | Chr.3:187094850 - 187129650 on Build GRCh38 | Insertion | RPL39L |
nsv1004008 | Chr.3:186879814 - 187204053 on Build GRCh38 | Gain | RPL39L ST6GAL1 LOC101929106 RTP1 |
nsv1014596 | Chr.3:187106902 - 187410668 on Build GRCh38 | Gain | MASP1 RPL39L LOC101929106 RTP4 LOC101929130 RTP1 |
nsv965243 | Chr.3:187118443 - 187122168 on Build GRCh38 | Duplication | RPL39L |
More Information
Additional Information:
For this assay, SNP(s) [rs113814489] 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 |