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 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-09-27 13:36:02 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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