Assay Details
Target Gene Details
Entrez Gene ID: | 120114 |
Gene Name: | FAT atypical cadherin 3 |
Gene Aliases: |
CDHF15, CDHR10, hFat3 |
Location: |
Chr.11:92224636-92896473 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
FAT3 | XM_017017178.1 | XP_016872667.1 | ||
XM_017017179.1 | XP_016872668.1 | |||
XM_017017180.1 | XP_016872669.1 | |||
XM_017017181.1 | XP_016872670.1 | |||
XM_017017182.1 | XP_016872671.1 | |||
XM_017017183.1 | XP_016872672.1 | |||
XM_017017184.1 | XP_016872673.1 | |||
XM_017017186.1 | XP_016872675.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv555902 | Chr.11:92195159 - 92251289 on Build GRCh38 | Loss | FAT3 |
nsv832229 | Chr.11:92151270 - 92341658 on Build GRCh38 | Gain | FAT3 |
esv3580015 | Chr.11:91820356 - 92847634 on Build GRCh38 | Gain | FAT3 |
nsv832230 | Chr.11:92219476 - 92379180 on Build GRCh38 | Gain | FAT3 |
More Information
Additional Information:
For this assay, SNP(s) [rs77172924] 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 |