Variant #0000004713 (NC_000016.9:g.2103392A>T, TSC2(NM_000548.3):c.275A>T)
| Individual ID |
00004713 |
| Chromosome |
16 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2103392A>T |
| Reference |
Dunlop EA1, Dodd KM, Land SC, Davies PA, Martins N, Stuart H, McKee S, Kingswood C, Saggar A, Corderio I, Medeira AM, Kingston H, Sampson JR, Davies (2011) |
| DB-ID |
TSC2_000186 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0.001 View details |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
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