Variant #0000915371 (NC_000020.10:g.42984454G>A, NM_175914.4:c.10G>A (HNF4A))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.42984454G>A
DNA change (hg38) -
Published as HNF4A(NM_001030003.2):c.10G>A (p.(Val4Met))
ISCN -
DB-ID HNF4A_000332
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HNF4A NM_000457.4 ?/. - c.-45559G>A r.(?) p.(=)
HNF4A NM_175914.4 ?/. - c.10G>A r.(?) p.(Val4Met)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.