Variant #0000061595 (NC_000009.11:g.(3735202_3781683)_(4161396_4258380)dup)
| Individual ID |
00034435 |
| Chromosome |
9 |
| 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.(3735202_3781683)_(4161396_4258380)dup |
| DNA change (hg38) |
- |
| Published as |
g.(3735202_3781683)_(4161396_4258380)dup |
| ISCN |
- |
| DB-ID |
chr9_000457 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
no |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Marta Sanchez Castro |
| Database submission license |
No license selected |
| Created by |
Marta Sanchez Castro |
| Date created |
2015-03-19 01:33:53 +01:00 (CET) |
| Date last edited |
2015-05-05 14:19:05 +02:00 (CEST) |

Variant on transcripts
Screenings
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