Variant #0000461228 (NC_000024.9:g.(23978074_24354700)_(25316178_25505734)del)
| Individual ID |
00226112 |
| Chromosome |
Y |
| Allele |
Unknown |
| 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.(23978074_24354700)_(25316178_25505734)del |
| DNA change (hg38) |
- |
| Published as |
b1/b3 deletion |
| ISCN |
- |
| DB-ID |
chrY_000135 |
| Variant remarks |
sY142+, sY1196_sY1189del, sY254+ |
| Reference |
Moreno-Mendoza, submitted |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
? |
| Frequency |
1/497 |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Elena Casamonti |
| Database submission license |
No license selected |
| Created by |
Elena Casamonti |
| Date created |
2019-02-26 20:11:41 +01:00 (CET) |
| Date last edited |
2019-02-27 15:33:59 +01:00 (CET) |

Variant on transcripts
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