Variant #0000660296 (NC_000006.11:g.44274797T>C, NC_000006.11(NM_020745.2):c.1041-29A>G (AARS2))
Chromosome |
6 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44274797T>C |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
AARS2_000169 |
Frequency |
11541/13006 |
Freq. EA |
8309/8600 |
Freq. AA |
3232/4406 |
Average frequency (gnomAD v.2.1.1) |
- |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Ivo F.A.C. Fokkema |
Date created |
2013-05-03 16:27:59 +02:00 (CEST) |
Date last edited |
2018-08-23 03:54:04 +02:00 (CEST) |

Variant on transcripts
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