Variant #0001055622 (NC_000016.9:g.67201124C>T, NM_001374675.1:c.728C>T (HSF4))

Chromosome 16
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.67201124C>T
DNA change (hg38) -
Published as HSF4(NM_001374675.1):c.728C>T (p.(Ser243Leu))
ISCN -
DB-ID FBXL8_000019
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) 2.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KIAA0895L NM_001040715.1 ?/. - c.*9590G>A r.(=) p.(=)
HSF4 NM_001374675.1 ?/. - c.728C>T r.(?) p.(Ser243Leu)
FBXL8 NM_018378.2 ?/. - c.*3401C>T r.(=) p.(=)


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