Variant #0001080696 (NC_000011.9:g.44640151T>C, NC_000011.9(NM_001024844.1):c.568-39T>C (CD82))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.44640151T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CD82_000083
Frequency 1/13004
Freq. EA 0/8598
Freq. AA 1/4406
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 16:37:25 +02:00 (CEST)
Date last edited 2013-05-04 22:20:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CD82 NM_001024844.1 ?/? c.568-39T>C r.(=) p.(=)