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) |
Probably affects function |
| 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 |
Florian Bayersdorfer |
| Database submission license |
No license selected |
| Created by |
N/A |
| Date created |
2019-05-21 13:29:46 +00:00 (UTC) |
| Date last edited |
2025-10-09 14:20:51 +00:00 (UTC) |

Variant on transcripts
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