Variant #0000001407 (NC_000004.11:g.74606024A>T, NM_000584.3:c.-352A>T (IL8))

Individual ID 00000161
Chromosome 4
Allele Both (homozygous)
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74606024A>T
DNA change (hg38) g.73740307A>T
Published as -
ISCN -
DB-ID IL8_000001 See all 4 reported entries
Variant remarks -
Reference PubMed: Hollegaard 2013
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 45/197 cases
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Mads V Hollegaard
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2012-07-11 16:42:46 +02:00 (CEST)
Date last edited 2019-10-27 12:56:34 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
IL8 NM_000584.3 -?/. - c.-352A>T r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000000150 DNA arraySNP - - IL8 2 Mads V Hollegaard


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