Product Details

Assay Reference Genome
Location

Chr.15:38262357 on build GRCh38
Cytoband
15q14
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs72709667] 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.

Target Gene Details

Entrez Gene ID
161742
Gene Symbol
SPRED1
Gene Name
sprouty related EVH1 domain containing 1
Gene Aliases
NFLS, PPP1R147, hSpred1, spred-1
Location
Chr.15:38252087-38357249 on build GRCh38
Assay Gene Location
Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
SPRED1 NM_152594.2 NP_689807.1
XM_005254202.3 XP_005254259.1
AK091222.1 BAC03614.1
AY299089.1 AAP59414.1
BC018015.1
BC137480.1
BC137481.1
DA405650.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv3892674 Chr15:37311235 - 38400599 on Build GRCh38 Gain LOC101928227 SPRED1 TMCO5A
nsv832974 Chr15:38206405 - 38398384 on Build GRCh38 Loss SPRED1
nsv832973 Chr15:38151604 - 38352681 on Build GRCh38 Gain SPRED1

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