Variant #0001081463 (NC_000017.10:g.?, NM_000213.3:c.? (ITGB4))
| Chromosome |
17 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
| DNA change (hg38) |
g.? |
| Published as |
exon 24-25 deletion (NM_001005731.2) |
| ISCN |
- |
| DB-ID |
ITGB4_000000 |
| Variant remarks |
- |
| Reference |
PubMed: Liu 2026 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
1/7496 chromosomes |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2026-08-03 14:41:16 +02:00 (CEST) |
| Date last edited |
N/A |
Variant on transcripts
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