Variant #0000598221 (NC_000016.9:g.2122986_2122989del, NC_000016.9(NM_000548.3):c.2355+2_2355+5del (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.2122986_2122989del |
| DNA change (hg38) |
g.2072985_2072988del |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_000254 See all 17 reported entries |
| Variant remarks |
4bp deletion of TAGG |
| 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 |
2019-10-12 14:26:04 +02:00 (CEST) |
| Date last edited |
2021-08-18 14:44:30 +02:00 (CEST) |

Variant on transcripts
|