Variant #0001436435 (NC_000016.9:g.105908T>G, NC_000016.9(NM_024571.3):c.266+26T>G (SNRNP25))
| Chromosome |
16 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.105908T>G |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
SNRNP25_000027 |
| Frequency |
1/13004 |
| Freq. EA |
0/8600 |
| Freq. AA |
1/4404 |
| 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 |
2014-05-04 13:21:08 +02:00 (CEST) |

Variant on transcripts
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