Variant #0000575955 (NC_000023.10:g.41201999_41202000del, NM_001356.3:c.453_454del (DDX3X))
| Chromosome |
X |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41201999_41202000del |
| DNA change (hg38) |
g.41342746_41342747del |
| Published as |
DDX3X(NM_001356.4):c.453_454delTT (p.S152Wfs*7) |
| ISCN |
- |
| DB-ID |
DDX3X_000078 |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2020-07-19 19:06:50 +02:00 (CEST) |

Variant on transcripts
|