Variant #0000782098 (NC_000016.9:g.(?_2097990)_?del(75000), NM_000548.3:c.(?_-106)_?del(75000) (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.(?_2097990)_?del(75000) |
| DNA change (hg38) |
g.(?_2047989)_?del(75000) |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_001298 See all 2 reported entries |
| Variant remarks |
deletion of ~75kb; part of TSC2 but not PKD1 deleted; adjacent SLC9A3R2 (OCTS2) and NTHL1 (OCTS3) genes also deleted; proximal deletion breakpoint within TSC2 but distal end uncertain |
| 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 |
2021-05-04 16:22:13 +02:00 (CEST) |
| Date last edited |
2022-06-29 23:30:16 +02:00 (CEST) |

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