Variant #0000879111 (NC_000021.8:g.46326929C>T, NM_000211.3:c.229G>A (ITGB2))

Chromosome 21
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46326929C>T
DNA change (hg38) g.44907014C>T
Published as -
ISCN -
DB-ID ITGB2_000214
Variant remarks -
Reference PubMed: Van De Vijver 2012, Journal: Van De Vijver
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00073 View details
Owner Dirk Roos
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-09-27 13:36:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGB2 NM_000211.3 -/. 4 c.229G>A r.(?) p.(Asp77Asn)


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