Variant #0000000074 (NC_000012.11:g.121426645G>A, NM_000545.5:c.336G>A (HNF1A))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.121426645G>A |
Reference |
- |
DB-ID |
HNF1A_000002 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.00048 View details |
Owner |
Sabine Heber |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Sabine Heber |
Date created |
2019-05-21 13:15:39 +00:00 (UTC) |
Date last edited |
2019-05-21 13:51:55 +00:00 (UTC) |
Variant on transcripts
|
|