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 InternationalCreative Commons License
Created by Sabine Heber
Date created 2019-05-21 14:22:43 +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 ./? 1D c.2T>C r.? p.(Met1Thr)