Variant #0001043366 (NC_000011.9:g.193096T>C, NM_145651.2:c.-4T>C (SCGB1C1))
Chromosome |
11 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.193096T>C |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
SCGB1C1_000001 |
Frequency |
6093/12800 |
Freq. EA |
4199/8524 |
Freq. AA |
1894/4276 |
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 16:37:25 +02:00 (CEST) |
Date last edited |
2014-05-02 14:30:22 +02:00 (CEST) |

Variant on transcripts
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