Variant #0000699602 (NC_000009.11:g.(135782758_135785957)_(135786080_135786388)del, NC_000009.11(NM_000368.4):c.(1141+1_1142-1)_(1263+1_1264-1)del (TSC1))
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(135782758_135785957)_(135786080_135786388)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC1_001379 See all 2 reported entries |
| Variant remarks |
exon 12 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 |
2020-11-02 10:52:17 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|