Variant #0001491247 (NC_000016.9:g.50826462G>T, NC_000016.9(NM_001042355.1):c.2233-46G>T (CYLD))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.50826462G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CYLD_000088
Frequency 1248/11714
Freq. EA 585/8092
Freq. AA 663/3622
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 16:42:42 +02:00 (CEST)
Date last edited 2013-05-05 13:44:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CYLD NM_001042355.1 ?/? c.2233-46G>T r.(=) p.(=)