Variant #0000169460 (NC_000023.10:g.(pter_cen_qter)sup)
| Individual ID |
00103955 |
| 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.(pter_cen_qter)sup |
| DNA change (hg38) |
- |
| Published as |
47,XXY |
| ISCN |
47,XXY |
| DB-ID |
chrX_002751 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Le Gall |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-05-05 20:05:45 +02:00 (CEST) |
| Date last edited |
2020-05-10 14:24:38 +02:00 (CEST) |
Variant on transcripts
Screenings
|