Variant #0000670373 (NC_000015.9:g.(?_22770421)_(23282799_?)del)
| Individual ID |
00305552 |
| Chromosome |
15 |
| 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.(?_22770421)_(23282799_?)del |
| DNA change (hg38) |
- |
| Published as |
chr15:22770421-23282799 |
| ISCN |
15q11.2del |
| DB-ID |
chr15_005419 |
| Variant remarks |
- |
| Reference |
PubMed: Vissers 2020 |
| 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 |
2020-06-28 11:11:46 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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