Variant #0001061373 (NC_000017.10:g.42462676C>G, NM_000419.3:c.602G>C (ITGA2B))

Chromosome 17
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.42462676C>G
DNA change (hg38) g.44385308C>G
Published as -
ISCN -
DB-ID ITGA2B_000140
Variant remarks in vitro expression analysis shows abolished αIIb and β3 surface expression and no
PAC-1 binding following activation; authors suggest classification of variant as "pathogenic"
Reference PubMed: Kosaka 2025
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 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 2025-12-15 09:18:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
ITGA2B NM_000419.3 +/. - c.602G>C - p.Gly201Ala -


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