Variant #0001128268 (NC_000011.9:g.76751760T>C, NM_138706.3:c.*7T>C (B3GNT6))

Chromosome 11
DNA change (genomic) (Relative to hg19 / GRCh37) g.76751760T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID B3GNT6_000030
Frequency 1/12428
Freq. EA 1/8380
Freq. AA 0/4048
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 23:54:08 +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.*7T>C r.(=) p.(=)