Variant #0000117393 (NC_000023.10:g.(?_24942199)_(31315935_?)dup)
| Individual ID |
00073549 |
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_24942199)_(31315935_?)dup |
| DNA change (hg38) |
- |
| Published as |
chrX:24,942,199-31,315,935dup |
| ISCN |
- |
| DB-ID |
chrX_002746 |
| Variant remarks |
FISH confirms duplication on X-chromosome |
| Reference |
PubMed: Paderova 2016, Journal: Paderova 2016 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| 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 |
2016-06-10 23:01:39 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
Screenings
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