Variant #0001043378 (NC_000011.9:g.193689G>A, NC_000011.9(NM_145651.2):c.56-23G>A (SCGB1C1))
Chromosome |
11 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.193689G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
SCGB1C1_000013 |
Frequency |
1/12740 |
Freq. EA |
0/8468 |
Freq. AA |
1/4272 |
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 |
2014-03-14 05:53:29 +01:00 (CET) |

Variant on transcripts
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