Variant #0000009626 (NC_000016.10:g.2079165G>T, NM_000548.3:c.3100G>A (TSC2))
Individual ID |
00002313 |
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.2079165G>T |
Reference |
- |
DB-ID |
TSC2_000003 |
dbSNP ID |
rs146745242 |
Variant remarks |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Claudia Martin-Hospital de Córdoba |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Instituto Nacional del Cancer |
Date created |
2023-12-06 14:52:16 -02:00 (-02) |
Date last edited |
N/A |
Variant on transcripts
Screenings
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