Variant #0001061374 (NC_000017.10:g.42462679G>A, NM_000419.3:c.599C>T (ITGA2B))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42462679G>A |
| DNA change (hg38) |
g.44385311G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ITGA2B_000141 |
| Variant remarks |
in vitro expression analysis shows normal αIIb and β3 surface expression and normal PAC-1 binding following activation |
| Reference |
PubMed: Kosaka 2025 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
In vitro (cloned) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2025-12-15 09:20:49 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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