Variant #0000021691 (NC_000024.9:g.(15009431_15017731)_(15030038_15104000)del)
| Individual ID |
00003244 |
| Chromosome |
Y |
| Allele |
Paternal (inferred) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(15009431_15017731)_(15030038_15104000)del |
| DNA change (hg38) |
- |
| Published as |
AZFa deletion |
| ISCN |
- |
| DB-ID |
chrY_000090 See all 5 reported entries |
| Variant remarks |
AZFa deletion (sY87+, GY6_DBY3'del, 475TEL+); undeleted father or brother |
| Reference |
PubMed: Foresta 2000 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
1/41 cases |
| 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 |
2013-11-03 11:44:46 +01:00 (CET) |
| Date last edited |
2013-11-03 13:25:56 +01:00 (CET) |

Variant on transcripts
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