Variant #0001081463 (NC_000017.10:g.?, NM_000213.3:c.? (ITGB4))

Chromosome 17
Allele Parent #1
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.?
DNA change (hg38) g.?
Published as exon 24-25 deletion (NM_001005731.2)
ISCN -
DB-ID ITGB4_000000
Variant remarks -
Reference PubMed: Liu 2026
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/7496 chromosomes
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Genomic location of variant could not be determined
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2026-08-03 14:41:16 +02:00 (CEST)
Date last edited N/A




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGB4 NM_000213.3 +?/. - c.? r.? p.?


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.