Variant #0000570840 (NC_000021.8:g.46326996C>T, NM_000211.3:c.162G>A (ITGB2))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.46326996C>T
DNA change (hg38) g.44907081C>T
Published as ITGB2(NM_000211.3):c.162G>A (p.P54=), ITGB2(NM_001127491.3):c.162G>A (p.P54=)
ISCN -
DB-ID ITGB2_000013 See all 4 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00169 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ITGB2 NM_000211.3 -?/. - c.162G>A r.(?) p.(Pro54=)


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