Variant #0000439315 (NC_000002.11:g.220284876C>T, NM_001927.3:c.638C>T (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.220284876C>T
DNA change (hg38) g.219420154C>T
Published as -
ISCN -
DB-ID DES_000020 See all 20 reported entries
Variant remarks cloned in pcDNA3, expressed in SW13 and C2C12 cells; DES normal
Reference PubMed: Goudeau 2006
ClinVar ID -
dbSNP ID rs41272699
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00932 View details
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 ?/. 2 c.638C>T r.(?) p.Ala213Val


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