Variant #0001169977 (NC_000012.11:g.6346887G>C, NC_000012.11(NM_001769.3):c.622-42G>C (CD9))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.6346887G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CD9_000074
Frequency 389/13006
Freq. EA 5/8600
Freq. AA 384/4406
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 01:27:02 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CD9 NM_001769.3 ?/? c.622-42G>C r.(=) p.(=)