Variant #0000000078 (NC_000012.11:g.121416568A>G, NM_000545.5:c.-4A>G (HNF1A))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.121416568A>G |
Reference |
- |
DB-ID |
HNF1A_000004 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.00083 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 14:06:27 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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