Variant #0000879121 (NC_000021.8:g.46330670C>T, NM_000211.3:c.28G>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.46330670C>T |
DNA change (hg38) |
g.44910755C>T |
Published as |
- |
ISCN |
- |
DB-ID |
ITGB2_000237 |
Variant remarks |
- |
Reference |
PubMed: Roos 2023, Journal: Roos 2023 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00446 View details |
Owner |
Dirk Roos |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2022-09-27 13:39:00 +02:00 (CEST) |
Date last edited |
2025-01-23 20:49:25 +01:00 (CET) |

Variant on transcripts
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