Variant #0000714690 (NC_000007.13:g.208992_208993insG, NC_000007.13(NM_020223.3):c.863+16_863+17insG (FAM20C))
Chromosome |
7 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.208992_208993insG |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
FAM20C_000024 |
Frequency |
2/11876 |
Freq. EA |
2/7980 |
Freq. AA |
0/3896 |
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 16:28:58 +02:00 (CEST) |
Date last edited |
2014-06-15 21:42:04 +02:00 (CEST) |

Variant on transcripts
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