Variant #0000880228 (NC_000009.11:g.146178C>T, NC_000009.11(NM_018491.3):c.708-20G>A (CBWD1))
Chromosome |
9 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.146178C>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
CBWD1_000022 |
Frequency |
22/5842 |
Freq. EA |
2/4014 |
Freq. AA |
20/1828 |
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 16:29:58 +02:00 (CEST) |
Date last edited |
2020-08-30 01:32:46 +02:00 (CEST) |

Variant on transcripts
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