Variant #0000000079 (NC_000020.10:g.43052788G>A, NM_175914.4:c.957G>A (HNF4A))
Chromosome |
20 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Probably affects function |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.43052788G>A |
Reference |
- |
DB-ID |
HNF4A_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 |
2019-05-21 14:13:33 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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