Variant #0000781939 (NC_000007.13:g.121738928_121738929dup, NC_000007.13(NM_005763.3):c.1407-9_1407-8dup (AASS))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.121738928_121738929dup
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AASS_000086
Frequency 1478/8720
Freq. EA 950/6040
Freq. AA 528/2680
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 16:28:58 +02:00 (CEST)
Date last edited 2018-08-23 13:10:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AASS NM_005763.3 ?/? c.1407-9_1407-8dup r.(=) p.(=)