Variant #0000000554 (NC_000020.10:g.43052699C>T, NM_175914.4:c.868C>T (HNF4A))

Chromosome 20
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.43052699C>T
Reference -
DB-ID HNF4A_000004
Frequency -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Florian Bayersdorfer
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Florian Bayersdorfer
Date created 2024-05-07 14:06:13 +00:00 (UTC)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF4A NM_175914.4 +/+ 8 c.868C>T r.(?) p.(Arg290Cys)