Variant #0000439322 (NC_000002.11:g.220290442A>C, NM_001927.3:c.1346A>C (DES))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.220290442A>C
DNA change (hg38) g.219425720A>C
Published as -
ISCN -
DB-ID DES_000044 See all 4 reported entries
Variant remarks cloned in pIRES GFP-DES, expressed in SW-13 and C2C12 cells; normal IF
Reference PubMed: Bar 2007
ClinVar ID -
dbSNP ID -
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 2008-06-20 20:39:37 +02:00 (CEST)
Date last edited 2020-07-14 21:54:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DES NM_001927.3 ?/. 8 c.1346A>C r.(?) p.Lys449Thr


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