Variant #0000525815 (NC_000005.9:g.52385852_52385853insT, NM_002203.3:c.3425_3426insT (ITGA2))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.52385852_52385853insT |
DNA change (hg38) |
g.53090022_53090023insT |
Published as |
ITGA2(NM_002203.3):c.3425_3426insT (p.I1143Nfs*22) |
ISCN |
- |
DB-ID |
ITGA2_000015 |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2020-06-17 10:13:28 +02:00 (CEST) |

Variant on transcripts
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