Genomic Map
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Target Gene Details
Entrez Gene ID: | 388650 |
Gene Name: | family with sequence similarity 69 member A |
Gene Aliases: |
- |
Location: |
Chr.1:92832729-92961522 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| FAM69A | NM_001006605.4 | NP_001006606.2 | ||
| NM_001252269.1 | NP_001239198.1 | |||
| NM_001252270.1 | NP_001239199.1 | |||
| NM_001252271.1 | NP_001239200.1 | |||
| NM_001252273.1 | NP_001239202.1 | |||
| AK303700.1 | ||||
| AL536469.3 | ||||
| AL702320.1 | ||||
| BC070342.1 | AAH70342.1 | |||
| BF979329.1 | ||||
| DA141589.1 | ||||
| DA155419.1 | ||||
| DA348631.1 | ||||
| DA736826.1 | ||||
| DB199113.1 | ||||
| DB475309.1 | ||||
| DB498496.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv508393 | Chr.1:92824956 - 92879367 on Build GRCh38 | Deletion |
 RPL5
SNORD21
FAM69A
SNORA66
|
| esv2714684 | Chr.1:91095800 - 93049130 on Build GRCh38 | Deletion |
HFM1
RPL5
RPAP2
KIAA1107
SNORD21
SETSIP
FAM69A
C1orf146
GFI1
EPHX4
SNORA66
EVI5
CDC7
GLMN
BRDT
BTBD8
HSP90B3P
TGFBR3
|
| nsv1008602 | Chr.1:92711254 - 93175251 on Build GRCh38 | Gain |
MTF2
RPL5
TMED5
SNORD21
FAM69A
SNORA66
EVI5
|
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Additional Information:
For this assay, SNP(s) [rs79666458] 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
|
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