Variant #0000874476 (NC_000005.9:g.(?_83112653)_(85261932_?)del)
| Individual ID |
00415130 |
| Chromosome |
5 |
| 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.(?_83112653)_(85261932_?)del |
| DNA change (hg38) |
- |
| Published as |
(83112653–85261932)x1 |
| ISCN |
- |
| DB-ID |
chr5_006411 |
| Variant remarks |
5q14.3 deletion |
| Reference |
PubMed: Vitobello 2022, Journal: Vitobello 2022 |
| 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 |
2022-08-08 16:10:42 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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