Variant #0000200380 (NC_000002.11:g.41612C>T, NM_001077710.2:c.962G>A (FAM110C))
Chromosome |
2 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41612C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
FAM110C_000001 |
Frequency |
2/11882 |
Freq. EA |
1/8178 |
Freq. AA |
1/3704 |
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 16:22:05 +02:00 (CEST) |
Date last edited |
2014-05-04 16:40:32 +02:00 (CEST) |

Variant on transcripts
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