Variant #0001045048 (NC_000017.10:g.45385008G>A, NC_000017.10(NM_000212.2):c.2301+5G>A (ITGB3))

Chromosome 17
Allele Unknown
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.45385008G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ITGB3_000045
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2547623844
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-05-24 12:42:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGB3 NM_000212.2 +?/. - c.2301+5G>A r.(?) p.(?)


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