Variant #0001261990 (NC_000012.11:g.125603363G>A, NC_000012.11(NM_023928.3):c.1121+52G>A (AACS))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.125603363G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AACS_000085
Frequency 13/7272
Freq. EA 0/4618
Freq. AA 13/2654
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 2018-08-23 07:19:27 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AACS NM_023928.3 ?/? c.1121+52G>A r.(=) p.(=)