Variant #0001012108 (NC_000023.10:g.(148800000_148830445)_(149029121_149050000)del)
| Individual ID |
00455956 |
| Chromosome |
X |
| Allele |
Maternal (confirmed) |
| 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.(148800000_148830445)_(149029121_149050000)del |
| DNA change (hg38) |
- |
| Published as |
hg19 148830445–149029121del |
| ISCN |
- |
| DB-ID |
chrX_019430 |
| Variant remarks |
198.7 kb deletion |
| Reference |
PubMed: Zanetti 2014 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| 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 |
2024-10-21 18:59:27 +02:00 (CEST) |
| Date last edited |
2024-10-21 19:03:43 +02:00 (CEST) |

Variant on transcripts
Screenings
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