Variant #0001208178 (NC_000012.11:g.53715141C>T, NM_001173466.1:c.109G>A (AAAS))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.53715141C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAAS_000117
Frequency 1/13002
Freq. EA 1/8598
Freq. AA 0/4404
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 01:11:06 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAAS NM_001173466.1 ?/? c.109G>A r.(?) p.(Asp37Asn)