Variant #0000000555 (NC_000020.10:g.43052879G>A, NM_175914.4:c.1048G>A (HNF4A))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Effect unknown
DNA change (genomic) (Relative to hg19 / GRCh37) g.43052879G>A
Reference -
DB-ID HNF4A_000005
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 14:06:47 +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.1048G>A r.(?) p.(Glu350Lys)