Variant #0000484324 (NC_000001.10:g.59251097T>G, NM_002228.3:c.-2355A>C (JUN))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.59251097T>G
DNA change (hg38) g.58785425T>G
Published as -1318T>G
ISCN -
DB-ID JUN_000003 See all 3 reported entries
Variant remarks expression cloning in Caco2 and SW480 cells shows increased promoter activity
Reference PubMed: Chen 2011
ClinVar ID -
dbSNP ID rs2760501
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2019-06-06 14:31:44 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
JUN NM_002228.3 +/. _1 c.-2355A>C r.(=) p.(=)


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