Genomic Map
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Target Gene Details
Entrez Gene ID: | 282618 |
Gene Name: | interferon lambda 1 |
Gene Aliases: |
IL-29, IL29 |
Location: |
Chr.19:39296325-39298672 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| IFNL1 | NM_172140.1 | 1 | 195 | NP_742152.1 |
| AY129150.1 | 1 | 195 | AAN28265.1 | |
| AY184372.1 | 1 | 98 | AAN86125.1 | |
| AY336716.1 | 1 | 101 | AAR24511.1 | |
| BC074985.2 | 1 | 118 | AAH74985.1 | |
| BC117482.1 | 1 | 143 | ||
| BC126183.1 | 1 | 143 | ||
| HQ214053.1 | 1 | 98 | ||
| JF268782.1 | 1 | 98 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv833830 | Chr.19:39218898 - 39347206 on Build GRCh38 | Loss |
 IFNL4
IFNL2
LRFN1
GMFG
IFNL3
IFNL1
SAMD4B
|
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Additional Information:
For this assay, SNP(s) [rs114823100] 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
|
Panther Classification:
Gene Ontology Categories:
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