Variant #0000971558 (NC_000013.10:g.(?_66878526)_(66911784_?)del)
| Individual ID |
00410919 |
| Chromosome |
13 |
| Allele |
Paternal (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.(?_66878526)_(66911784_?)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
hg19 13q21.32(66878526-66911784)x1 |
| DB-ID |
chr13_002445 |
| Variant remarks |
- |
| Reference |
PubMed: Del Rocio Perez Baca 2024 |
| 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 |
2024-03-07 11:35:50 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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