Variant #0000855682 (NC_000008.10:g.104153137_104153138insG, NM_001024372.1:c.12_13insG (BAALC))

Chromosome 8
DNA change (genomic) (Relative to hg19 / GRCh37) g.104153137_104153138insG
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID BAALC_000002
Frequency 124/9154
Freq. EA 80/6220
Freq. AA 44/2934
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 16:29:29 +02:00 (CEST)
Date last edited 2013-05-04 15:21:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
BAALC NM_001024372.1 ?/? c.12_13insG r.(?) p.(Ser6Glufs*66)