Variant #0000000080 (NC_000020.10:g.42984446T>C, NM_175914.4:c.2T>C (HNF4A))
Chromosome |
20 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42984446T>C |
Reference |
- |
DB-ID |
HNF4A_000002 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0 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 14:22:43 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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