Variant #0000620089 (NC_000016.9:g.(?_2098587)_(2121936_2122241)del, NC_000016.9(NM_000548.3):c.(?_-29-1)_(2097+1_2098-1)del (TSC2))
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_2098587)_(2121936_2122241)del |
| DNA change (hg38) |
g.(?_2048586)_(2071935_2072240)del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_001253 See all 2 reported entries |
| Variant remarks |
TSC2 exons 2-19 deleted |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Rosemary Ekong |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Rosemary Ekong |
| Date created |
2019-11-15 19:28:56 +01:00 (CET) |
| Date last edited |
2021-08-18 14:44:30 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|