Variant #0000001602 (NC_000005.10:g.132664098G>A, NM_002188.2:c.*3816G>A (IL13))

Individual ID 00000347
Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.132664098G>A
Published as 4257G>A
Reference Ammu Kutty Radhakrishnan et al. (2013)
DB-ID IL13_000001 See all 2 reported entries
dbSNP ID -
Frequency 39/87
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nuur Athirah Binti Mohd Daud
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nuur Athirah Binti Mohd Daud
Date created 2021-01-12 15:29:21 +08:00 (CST)
Date last edited 2021-01-14 12:55:34 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

GVS function     

Clinical classification     
IL13 NM_002188.2 +/. - c.*3816G>A - r.(=) p.(=) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000361 DNA PCR IL13 2 Nuur Athirah Binti Mohd Daud