Variant #0001176749 (NC_000012.11:g.9258953_9258954insA, NC_000012.11(NM_000014.4):c.995-13_995-12insT (A2M))
| Chromosome |
12 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.9258953_9258954insA |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
A2M_000168 |
| Frequency |
1/11328 |
| Freq. EA |
0/7798 |
| Freq. AA |
1/3530 |
| 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 16:39:18 +02:00 (CEST) |
| Date last edited |
2018-08-23 09:14:52 +02:00 (CEST) |

Variant on transcripts
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