Variant #0001436448 (NC_000016.9:g.106629G>A, NC_000016.9(NM_024571.3):c.341+16G>A (SNRNP25))
Chromosome |
16 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.106629G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
SNRNP25_000040 |
Frequency |
2/13006 |
Freq. EA |
2/8600 |
Freq. AA |
0/4406 |
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 16:42:42 +02:00 (CEST) |
Date last edited |
2014-11-21 01:30:16 +01:00 (CET) |

Variant on transcripts
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