Product Details

Assay Reference Genome Location: Chr.5:148987673 on build GRCh38
Cytoband: 5q32
Species: Homo sapiens
Variation Type: Copy Number

Additional Information

For this assay, SNP(s) [rs75086059] 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: 79628
Gene Symbol: SH3TC2
Gene Name: SH3 domain and tetratricopeptide repeats 2
Gene Aliases: CMT4C, MNMN
Location: Chr.5:148982150-149063174 on build GRCh38
Assay Gene Location: Within Exon 17

Gene Symbol	Transcript Accession	Exon Location	Assay Location	Protein ID
SH3TC2	NM_024577.3	17	21057	NP_078853.2

Target Copy Number Variation Details

DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv830517	Chr5:148953659 - 149171578 on Build GRCh38	Gain	LOC255187 MIR584 ABLIM3 SH3TC2

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