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

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
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
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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)