Variant #0001061378 (NC_000017.10:g.45360909C>T, NM_000212.2:c.355C>T (ITGB3))
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
NA |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45360909C>T |
| DNA change (hg38) |
g.47283543C>T |
| Published as |
- |
| ISCN |
- |
| DB-ID |
ITGB3_000089 See all 3 reported entries |
| Variant remarks |
in vitro expression analysis shows pronounced reduction in αIIb and β3 surface expression, loss of PAC-1 binding; authors suggest classification of variant as "pathogenic" |
| 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) |
3.0E-5 View details |
| 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 09:45:01 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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