Variant #0000714678 (NC_000007.13:g.195679C>T, NM_020223.3:c.731C>T (FAM20C))
Chromosome |
7 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.195679C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
FAM20C_000012 |
Frequency |
19/12598 |
Freq. EA |
0/8410 |
Freq. AA |
19/4188 |
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 20:59:34 +02:00 (CEST) |

Variant on transcripts
|
|