Variant #0001080685 (NC_000011.9:g.44639921C>T, NC_000011.9(NM_001024844.1):c.567+6C>T (CD82))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.44639921C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CD82_000072
Frequency 6350/12956
Freq. EA 4714/8570
Freq. AA 1636/4386
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 22:20:38 +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.567+6C>T r.(=) p.(=)