Variant #0000011242 (NC_000009.12:g.132896605C>T, TSC1(NM_000368.4):c.3125G>A)
| Individual ID |
00004204 |
| Chromosome |
9 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| DNA change (genomic) (Relative to hg38 / GRCh38) |
g.132896605C>T |
| Reference |
- |
| DB-ID |
TSC1_000011 |
| dbSNP ID |
- |
| Variant remarks |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Guillermo Alberto-Instituto Fleming |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Instituto Nacional del Cancer |

Variant on transcripts
Screenings
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