Variant #0000660334 (NC_000006.11:g.44279309C>T, NC_000006.11(NM_020745.2):c.436-37G>A (AARS2))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.44279309C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AARS2_000213
Frequency 3790/13006
Freq. EA 2071/8600
Freq. AA 1719/4406
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 16:27:59 +02:00 (CEST)
Date last edited 2018-08-23 00:51:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AARS2 NM_020745.2 ?/? c.436-37G>A r.(=) p.(=)