Variant #0000597996 (NC_000009.11:g.(?_135766735)_?del(147000), NM_000368.4:c.(?_-234)_?del(147000) (TSC1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(?_135766735)_?del(147000) |
| DNA change (hg38) |
g.(?_132891348)_?del(147000) |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_001345 See all 2 reported entries |
| Variant remarks |
147kb deletion involving part of TSC1, GF11B and GTF3C5 (both genes at 5’ of TSC1); deletedTSC1 exons not mentioned and extent of deletion into TSC1 undetermined |
| 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 |
2019-10-11 19:09:07 +02:00 (CEST) |
| Date last edited |
2022-08-17 17:24:06 +02:00 (CEST) |

Variant on transcripts
|