Variant #0000921829 (NC_000016.9:g.67200495_67200499del, NM_001374675.1:c.596_600del (HSF4))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.67200495_67200499del
DNA change (hg38) g.67166592_67166596del
Published as 595_599delGGGCC
ISCN -
DB-ID HSF4_000015 See all 3 reported entries
Variant remarks cDNA expression cloning shows normal protein stability, normal subcellular localization and significantly reduced transactivation potential
Reference PubMed: Merath 2013
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2023-03-21 18:55:55 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF4 NM_001374675.1 +/. - c.596_600del - p.Gly199GlufsTer15


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