Variant #0000000036 (NC_000012.11:g.121435388_121435391dupAGCC, NM_000545.5:c.1421_1424dupAGCC (HNF1A))
Chromosome |
12 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.121435388_121435391dupAGCC |
Reference |
- |
DB-ID |
HNF1A_000001 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Sabine Heber |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Sabine Heber |
Date created |
2018-04-05 11:22:57 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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