Variant #0000000289 (NC_000002.11:g.220286137A>G, NM_001927.3:c.1099A>G (DES))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.220286137A>G
Reference -
DB-ID DES_000001
Frequency -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2023-06-29 13:04:17 +00:00 (UTC)
Date last edited 2024-10-28 10:19:02 +00:00 (UTC)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DES NM_001927.3 ?/? - c.1099A>G r.(?) p.(Ile367Val)