Variant #0000714726 (NC_000007.13:g.298692G>A, NC_000007.13(NM_020223.3):c.1505+21G>A (FAM20C))
Chromosome |
7 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.298692G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
FAM20C_000060 |
Frequency |
1/4566 |
Freq. EA |
1/3182 |
Freq. AA |
0/1384 |
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 |
2014-02-18 20:42:23 +01:00 (CET) |

Variant on transcripts
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