Variant #0000921831 (NC_000016.9:g.67203255A>G, NM_001374675.1:c.1255_1324del (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.67203255A>G
DNA change (hg38) g.67169352A>G
Published as 1327+4A>G
ISCN -
DB-ID HSF4_000017 See all 3 reported entries
Variant remarks variant linked to c.1324+4A>G; 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) 1.0E-5 View details
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 2023-03-21 18:56:48 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF4 NM_001374675.1 +/. - c.1255_1324del - p.Met419GlufsTer29


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