Variant #0000000557 (NC_000020.10:g.43047122T>A, NM_175914.4:c.640T>A (HNF4A))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
DNA change (genomic) (Relative to hg19 / GRCh37) g.43047122T>A
Reference -
DB-ID HNF4A_000007
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 14:08:07 +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 +?/+? 6 c.640T>A r.(?) p.(Ser214Thr)