Variant #0000971564 (NC_000024.9:g.pter_qtersup)
| Individual ID |
00448099 |
| Chromosome |
Y |
| Allele |
Paternal (inferred) |
| 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.pter_qtersup |
| DNA change (hg38) |
g.pter_qtersup |
| Published as |
- |
| ISCN |
47,XYY |
| DB-ID |
chrY_000180 |
| Variant remarks |
- |
| Reference |
PubMed: Del Rocio Perez Baca 2024 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline/De novo (untested) |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2024-03-07 11:54:26 +01:00 (CET) |
| Date last edited |
N/A |
Variant on transcripts
Screenings
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