Variant #0001061129 (NC_000017.10:g.45368454G>A, NM_000212.2:c.1260G>A (ITGB3))

Chromosome 17
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.45368454G>A
DNA change (hg38) g.47291088G>A
Published as [1143A>C;1260G>A]
ISCN -
DB-ID ITGB3_000060 See all 5 reported entries
Variant remarks analysis shows no effect on splicing only when combined with 1143C in cis
Reference PubMed: Jin 1996
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 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 2025-12-12 09:06:13 +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     
ITGB3 NM_000212.2 -/. 9 c.1260G>A r.1260G>A p.Thr420= -


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