Variant #0001508363 (NC_000016.9:g.70316485T>C, NC_000016.9(NM_001605.2):c.144+38A>G (AARS))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.70316485T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AARS_000206
Frequency 4/12996
Freq. EA 3/8600
Freq. AA 1/4396
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 2018-08-22 23:46:01 +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.144+38A>G r.(=) p.(=)