Variant #0000660353 (NC_000006.11:g.44281032C>T, NM_020745.2:c.29G>A (AARS2))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.44281032C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AARS2_000232
Frequency 1/10206
Freq. EA 0/6908
Freq. AA 1/3298
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 13:09:06 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AARS2 NM_020745.2 ?/? c.29G>A r.(?) p.(Arg10Gln)