Variant #0000000512 (NC_000001.10:g.876486C>T, NC_000001.10(NM_152486.2):c.707-38C>T (SAMD11))
Chromosome |
1 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.876486C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
SAMD11_000085 |
Frequency |
1/12796 |
Freq. EA |
1/8478 |
Freq. AA |
0/4318 |
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 16:20:35 +02:00 (CEST) |
Date last edited |
2014-04-27 20:45:39 +02:00 (CEST) |

Variant on transcripts
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