Assay Details
Target Gene Details
Entrez Gene ID: | 2272 |
Gene Name: | fragile histidine triad |
Gene Aliases: |
AP3Aase, FRA3B |
Location: |
Chr.3:59747278-61251474 on Build GRCh38 |
Assay Gene Location: | Within Exon 16 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FHIT | NM_001166243.2 | NP_001159715.1 | ||
NM_001320899.1 | 9 | 2105 | NP_001307828.1 | |
NM_001320900.1 | 10 | 2199 | NP_001307829.1 | |
NM_001320901.1 | 7 | 2029 | NP_001307830.1 | |
NM_002012.3 | NP_002003.1 | |||
NR_135491.1 | 7 | 2114 | ||
XM_017005880.1 | 10 | 2153 | XP_016861369.1 | |
XM_017005881.1 | 9 | 2115 | XP_016861370.1 | |
XM_017005882.1 | 10 | 2138 | XP_016861371.1 | |
XM_017005883.1 | XP_016861372.1 | |||
XM_017005884.1 | XP_016861373.1 | |||
XM_017005885.1 | 6 | 2060 | XP_016861374.1 | |
XM_017005886.1 | 6 | 2820 | XP_016861375.1 | |
AK127931.1 | 7 | 1827 | ||
BC032336.1 | AAH32336.1 | |||
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 | Chr.3:58504269 - 60219035 on Build GRCh38 | Gain | C3orf67-AS1 ACOX2 FHIT FAM3D FAM107A LOC339902 C3orf67 FAM3D-AS1 |
nsv1014601 | Chr.3:59680883 - 59902440 on Build GRCh38 | Loss | FHIT |
More Information
Additional Information:
For this assay, SNP(s) [rs76124633,rs77913208] 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 Exonic DGV Variation |