Variant #0000509792 (NC_000004.11:g.123813337T>C, NC_000004.11(NM_002006.4):c.682-29T>C (FGF2))
| Chromosome |
4 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.123813337T>C |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
FGF2_000033 |
| Frequency |
1/12992 |
| Freq. EA |
0/8596 |
| Freq. AA |
1/4396 |
| 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 16:25:12 +02:00 (CEST) |
| Date last edited |
2013-05-04 05:37:25 +02:00 (CEST) |

Variant on transcripts
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