Variant #0000000447 (NC_000001.10:g.865738A>G, NC_000001.10(NM_152486.2):c.254+22A>G (SAMD11))
Chromosome |
1 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.865738A>G |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
SAMD11_000020 |
Frequency |
34/12974 |
Freq. EA |
31/8588 |
Freq. AA |
3/4386 |
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 |
2021-08-02 16:07:23 +02:00 (CEST) |

Variant on transcripts
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