Variant #0000693908 (NC_000017.10:g.(?_954760)_(1235739_?)dup)
| Individual ID |
00311169 |
| Chromosome |
17 |
| Allele |
Unknown |
| 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.(?_954760)_(1235739_?)dup |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
17p13.3 (954,760-1,235,739)x3 |
| DB-ID |
chr17_008082 |
| Variant remarks |
- |
| Reference |
PubMed: Cristofoli 2020 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline/De novo (untested) |
| 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 |
2020-09-20 10:25:05 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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