Variant #0000610386 (NC_000005.9:g.176637776C>G, NM_172349.2:c.1569C>G (NSD1))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.176637776C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NSD1_000079
Frequency 2/13006
Freq. EA 0/8600
Freq. AA 2/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:26:58 +02:00 (CEST)
Date last edited 2013-05-04 08:24:50 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NSD1 NM_172349.2 ?/? c.1569C>G r.(?) p.(Cys523Trp)