Variant #0000791396 (NC_000016.9:g.2121926C>G, NM_000548.3:c.2088C>G (TSC2))
| Chromosome |
16 |
| 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.2121926C>G |
| DNA change (hg38) |
g.2071925C>G |
| Published as |
- |
| ISCN |
- |
| DB-ID |
TSC2_004332 See all 3 reported entries |
| Variant remarks |
- |
| 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 |
2021-07-22 13:30:05 +02:00 (CEST) |
| Date last edited |
2021-09-29 01:33:35 +02:00 (CEST) |

Variant on transcripts
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