Variant #0001042012 (NC_000017.10:g.56565441_56565446dup, NM_001080439.1:c.197_202dup (HSF5))

Chromosome 17
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.56565441_56565446dup
DNA change (hg38) -
Published as HSF5(NM_001080439.3):c.197_202dup (p.(Gly66_Ala67dup))
ISCN -
DB-ID HSF5_000004
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HSF5 NM_001080439.1 -?/. - c.197_202dup r.(?) p.(Gly66_Ala67dup)
MTMR4 NM_004687.4 -?/. - c.*3585_*3590dup r.(=) p.(=)


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