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
|