Assay Details
Target Gene Details
Entrez Gene ID: | 54979 |
Gene Name: | HRAS like suppressor 2 |
Gene Aliases: |
PLA1/2-2 |
Location: |
Chr.11:63552759-63565072 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
HRASLS2 | NM_017878.1 | NP_060348.1 | ||
XM_011545120.2 | XP_011543422.1 | |||
AB453251.1 | ||||
AK000563.1 | BAA91256.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv3626646 | Chr.11:63549774 - 63585192 on Build GRCh38 | Gain | PLA2G16 HRASLS2 |
nsv352 | Chr.11:63555836 - 63589650 on Build GRCh38 | Insertion | PLA2G16 HRASLS2 |
nsv509417 | Chr.11:63485643 - 63569743 on Build GRCh38 | Insertion | RARRES3 HRASLS5 LGALS12 HRASLS2 |
More Information
Additional Information:
For this assay, SNP(s) [rs115908514] 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 |