Variant #0000459015 (NC_000024.9:g.(24070914_24639666)_(24876071_25505070)del)
| Individual ID |
00225595 |
| Chromosome |
Y |
| Allele |
Paternal (inferred) |
| 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.(24070914_24639666)_(24876071_25505070)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
chrY_000133 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Csilla Gabriella Krausz |
| Database submission license |
No license selected |
| Created by |
Csilla Gabriella Krausz |
| Date created |
2019-02-18 17:02:45 +01:00 (CET) |
| Date last edited |
2019-02-18 22:08:55 +01:00 (CET) |

Variant on transcripts
Screenings
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