Variant #0000927011 (NC_000020.10:g.43034889dup, NC_000020.10(NM_175914.4):c.224+17dup (HNF4A))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43034889dup
DNA change (hg38) -
Published as HNF4A(NM_000457.4):c.290+17dup (p.(=)), HNF4A(NM_001287182.2):c.215+17dupT
ISCN -
DB-ID HNF4A_000036 See all 8 reported entries
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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +02:00 (CEST)
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_000457.4 -?/. - c.290+17dup r.(=) p.(=)
HNF4A NM_175914.4 -?/. - c.224+17dup r.(=) p.(=)


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