Variant #0001508329 (NC_000016.9:g.70303580G>A, NM_001605.2:c.903C>T (AARS))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.70303580G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AARS_000172
Frequency 6378/12996
Freq. EA 4307/8600
Freq. AA 2071/4396
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 16:42:42 +02:00 (CEST)
Date last edited 2018-08-23 10:00:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AARS NM_001605.2 ?/? c.903C>T r.(=) p.(=)