Variant #0000000076 (NC_000017.10:g.36093699A>G, NM_000458.2:c.660T>C (HNF1B))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.36093699A>G |
Reference |
- |
DB-ID |
HNF1B_000001 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
5.0E-5 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 13:29:46 +00:00 (UTC) |
Date last edited |
2019-05-21 13:46:56 +00:00 (UTC) |
Variant on transcripts
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