Variant #0001595518 (NC_000017.10:g.41105712C>T, NC_000017.10(NM_001261434.1):c.1008+29G>A (AARSD1))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.41105712C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AARSD1_000026
Frequency 51/13006
Freq. EA 6/8600
Freq. AA 45/4406
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 16:44:12 +02:00 (CEST)
Date last edited 2018-08-23 12:19:55 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AARSD1 NM_001261434.1 ?/? c.1008+29G>A r.(=) p.(=)