Variant #0000781986 (NC_000007.13:g.121757026T>C, NC_000007.13(NM_005763.3):c.688-15A>G (AASS))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.121757026T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AASS_000132
Frequency 1438/13004
Freq. EA 599/8598
Freq. AA 839/4406
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 16:28:58 +02:00 (CEST)
Date last edited 2018-08-23 04:34:13 +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.688-15A>G r.(=) p.(=)