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 InternationalCreative Commons License
Created by Sabine Heber
Date created 2019-05-21 14:13:33 +00:00 (UTC)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF4A NM_175914.4 ?/+? 8 c.957G>A r.(=) p.(=)