Product Details

Assay Reference Genome
Location

Chr.3:59752396 on build GRCh38
Cytoband
3p14.2
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs78168437] 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
2272
Gene Symbol
FHIT
Gene Name
fragile histidine triad
Gene Aliases
AP3Aase, FRA3B
Location
Chr.3:59747278-61251474 on build GRCh38
Assay Gene Location
Within Intron 15
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
FHIT NM_001166243.2 NP_001159715.1
NM_001320899.1 NP_001307828.1
NM_001320900.1 NP_001307829.1
NM_001320901.1 NP_001307830.1
NM_002012.3 NP_002003.1
NR_135491.1
XM_017005880.1 XP_016861369.1
XM_017005881.1 XP_016861370.1
XM_017005882.1 XP_016861371.1
XM_017005883.1 XP_016861372.1
XM_017005884.1 XP_016861373.1
XM_017005885.1 XP_016861374.1
XM_017005886.1 XP_016861375.1
AK127931.1
AK289824.1
BC032336.1 AAH32336.1
DB131595.1
DQ120721.1 AAZ23623.1
KJ534835.1
U46922.1 AAA99013.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
dgv4749n100 Chr3:58504269 - 60219035 on Build GRCh38 Gain ACOX2 FAM3D-AS1 FAM3D FAM107A FHIT LOC339902 C3orf67-AS1 C3orf67
nsv1014601 Chr3:59680883 - 59902440 on Build GRCh38 Loss FHIT

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