Variant #0000592007 (NC_000009.11:g.(135810483_135819929)_(135820020_?)del, NC_000009.11(NM_000368.4):c.(?_-234)_(-144+1_-143-1)del (TSC1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (dominant) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(135810483_135819929)_(135820020_?)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_000512 See all 11 reported entries |
| Variant remarks |
TSC1 exon 1 and at least 23kb upstream deleted; deletion removes the promoter region reported between nts. -157bp and -744bp |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| 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 |
2019-08-07 16:14:03 +02:00 (CEST) |
| Date last edited |
2020-08-15 20:04:04 +02:00 (CEST) |

Variant on transcripts
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