Variant #0000879124 (NC_000021.8:g.46330183T>C, NC_000021.8(NM_000211.3):c.147+16A>G (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.46330183T>C |
| DNA change (hg38) |
g.44910268T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ITGB2_000220 |
| 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) |
0.05669 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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