Variant #0001128260 (NC_000011.9:g.76751188C>G, NM_138706.3:c.593C>G (B3GNT6))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.76751188C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID B3GNT6_000022
Frequency 1/12952
Freq. EA 1/8560
Freq. AA 0/4392
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 23:54:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
B3GNT6 NM_138706.3 ?/? c.593C>G r.(?) p.(Thr198Arg)