Variant #0001261966 (NC_000012.11:g.125591844C>T, NC_000012.11(NM_023928.3):c.915+30C>T (AACS))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.125591844C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AACS_000068
Frequency 3696/13006
Freq. EA 2460/8600
Freq. AA 1236/4406
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 2018-08-23 03:33:40 +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.915+30C>T r.(=) p.(=)